Cannabis jobs at Red Mesa Science and Refining, LLC

Red Mesa Science & Refining is a large-scale raw materials manufacturer and supplier of CBD and CBG isolate and distillate as well as several other minor cannabinoids. As a B2B producer our customers are wholesale end product formulating businesses that specialize in contract manufacturing, white labeling and private labeling activities. We are searching for a talented and experienced Quality Assurance Manager who supports the delivery of products to consistently meet internal and customer expectations.

As a science-based business that operates in a ISO9001:2015 and cGMP environment, prior experience in this professional setting is a must. The Quality Assurance Manager maintains quality standards at RMSR in accordance with local, state, federal regulations and standards, with consideration for applicable international markets. This individual is responsible for the maintenance and administration of the Quality Management System.

This position is located in St. George, Utah. This is beautiful red rock country surrounded by world-famous national and state parks, reservoirs, trails and mountains. In 2022, St. George hosted the IRONMAN World Championships along with several other world-class athletic and ATV/Jeep events. The cost of living is a welcome relief to many who come from other western states to make this their home. This is a great place to raise a family, grow a career, and reap the benefits of retirement. “We have an emerging tech sector, a state of the art healthcare industry, a college and a university, a medical school, a bustling construction sector, and an entrepreneurial spirit that sees new businesses being developed daily.” (St. George Area Chamber of Commerce)

Responsibilities

· Own the process for maintaining controlled documented information.

· Own the effective management of the change control process.

· Approve documents originating from your area or appoint a delegate to do so on your behalf.

· Approval authority on relevant QMS documented information.

· Approve new suppliers to be included on the Approved Supplier List.

· Monitor/support monitoring of qualified approved suppliers for their capacity to continue serving the needs of RMSR, and maintain records associated with them.

· Approve purchase requests originating from your area.

· Assess whether customer complaints require Nonconformance or CAPA investigation.

· Assess and identify the need for recall as defined by procedure.

· Monitor and maintain records for relevant equipment assets and their maintenance cycles.

· Own, monitor, review, and improve the Audit Program.

· Act as a liaison and lead point of contact for external audits at RMSR.

· Design sampling protocols in accordance with the Sampling Protocol Owner.

· Own and facilitate nonconformance, occurrence, or CAPA investigations.

· Assign QMS-relevant training; develop and maintain the training program and the method for assessing competency for employees in your area of responsibility.

· Utilize critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm and implement creative solutions.

· Work with relevant departments to formulate strategies to increase productivity.

· Identify, lead, and develop talent to maximize individual, team, and organizational effectiveness to meet company goals.

· Analyze data to find areas for growth and improvement.

· Review processes to ensure they are operationally relevant with current practices or trends.

· Reports to Director of Quality.

· Direct Reports – Quality Engineers, Quality Assurance Associates, Document Control Specialist

Key Qualifications

· Bachelor’s degree preferably in Engineering, Biological/Physical sciences, or equivalent scientific focus of study from an accredited university or college

· 5+ years’ experience in a highly regulated industry: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis. Highly desirable: FDA, PCQI trained, ISO9001:2015

· Prior experience in regulatory agency inspections and correspondence.

· Prior experience in third-party certification audits.

· Ability to follow written procedures and support others for adherence to written procedures.

· Ability to create or update written procedures with onsite personnel.

· Strong written and verbal communication skills, including writing executive summaries and communicating with senior level operations, quality management team, and regulatory agencies.

· Must be able to use computers and generate reports.

· Ability to analyze data and create and review processes, excellent attention to detail.

· Willingness to assist other departments to develop solutions and metrics that improve company quality standards.

· Work closely with all departments to implement best practices and drive continuous improvement.

· Must be able to sit or stand for extended periods of time.

· Must be able to adapt quickly to changes in policy, procedure, and technique.

· Must be at least 18 years of age and must pass UT and Federal background checks.

Salary commensurate with experience and track record.

You must be up to date on COVID vaccinations in order to be considered for this position. Preference will be given to applicants who take the Indeed Skills assessments.

Job Type: Full-time

Pay: $85,000.00 - $110,000.00 per year

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Health savings account
• Paid time off
• Vision insurance

Schedule:

• Monday to Friday
• Weekend availability

Experience:

• ISO 9001: 1 year (Required)

Work Location: One location

Apply for this job with Red Mesa Science and Refining, LLC

Apply now →

By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company. Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply. Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.

Red Mesa Science & Refining is a large-scale raw materials manufacturer and supplier of CBD and CBG isolate and distillate as well as several other minor cannabinoids. As a B2B producer our customers are wholesale end product formulating businesses that specialize in contract manufacturing, white labeling and private labeling activities. We are searching for a talented and experienced Quality Assurance Manager who supports the delivery of products to consistently meet internal and customer expectations.

As a science-based business that operates in a ISO9001:2015 and cGMP environment, prior experience in this professional setting is a must. The Quality Assurance Manager maintains quality standards at RMSR in accordance with local, state, federal regulations and standards, with consideration for applicable international markets. This individual is responsible for the maintenance and administration of the Quality Management System.

This position is located in St. George, Utah. This is beautiful red rock country surrounded by world-famous national and state parks, reservoirs, trails and mountains. In 2022, St. George hosted the IRONMAN World Championships along with several other world-class athletic and ATV/Jeep events. The cost of living is a welcome relief to many who come from other western states to make this their home. This is a great place to raise a family, grow a career, and reap the benefits of retirement. “We have an emerging tech sector, a state of the art healthcare industry, a college and a university, a medical school, a bustling construction sector, and an entrepreneurial spirit that sees new businesses being developed daily.” (St. George Area Chamber of Commerce)

Responsibilities

· Own the process for maintaining controlled documented information.

· Own the effective management of the change control process.

· Approve documents originating from your area or appoint a delegate to do so on your behalf.

· Approval authority on relevant QMS documented information.

· Approve new suppliers to be included on the Approved Supplier List.

· Monitor/support monitoring of qualified approved suppliers for their capacity to continue serving the needs of RMSR, and maintain records associated with them.

· Approve purchase requests originating from your area.

· Assess whether customer complaints require Nonconformance or CAPA investigation.

· Assess and identify the need for recall as defined by procedure.

· Monitor and maintain records for relevant equipment assets and their maintenance cycles.

· Own, monitor, review, and improve the Audit Program.

· Act as a liaison and lead point of contact for external audits at RMSR.

· Design sampling protocols in accordance with the Sampling Protocol Owner.

· Own and facilitate nonconformance, occurrence, or CAPA investigations.

· Assign QMS-relevant training; develop and maintain the training program and the method for assessing competency for employees in your area of responsibility.

· Utilize critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm and implement creative solutions.

· Work with relevant departments to formulate strategies to increase productivity.

· Identify, lead, and develop talent to maximize individual, team, and organizational effectiveness to meet company goals.

· Analyze data to find areas for growth and improvement.

· Review processes to ensure they are operationally relevant with current practices or trends.

· Reports to Director of Quality.

· Direct Reports – Quality Engineers, Quality Assurance Associates, Document Control Specialist

Key Qualifications

· Bachelor’s degree preferably in Engineering, Biological/Physical sciences, or equivalent scientific focus of study from an accredited university or college

· 5+ years’ experience in a highly regulated industry: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis. Highly desirable: FDA, PCQI trained, ISO9001:2015

· Prior experience in regulatory agency inspections and correspondence.

· Prior experience in third-party certification audits.

· Ability to follow written procedures and support others for adherence to written procedures.

· Ability to create or update written procedures with onsite personnel.

· Strong written and verbal communication skills, including writing executive summaries and communicating with senior level operations, quality management team, and regulatory agencies.

· Must be able to use computers and generate reports.

· Ability to analyze data and create and review processes, excellent attention to detail.

· Willingness to assist other departments to develop solutions and metrics that improve company quality standards.

· Work closely with all departments to implement best practices and drive continuous improvement.

· Must be able to sit or stand for extended periods of time.

· Must be able to adapt quickly to changes in policy, procedure, and technique.

· Must be at least 18 years of age and must pass UT and Federal background checks.

Salary commensurate with experience and track record.

You must be up to date on COVID vaccinations in order to be considered for this position. Preference will be given to applicants who take the Indeed Skills assessments.

Job Type: Full-time

Pay: $85,000.00 - $110,000.00 per year

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Health savings account
• Paid time off
• Vision insurance

Schedule:

• Monday to Friday
• Weekend availability

Experience:

• ISO 9001: 1 year (Required)

Work Location: One location

Apply for this job with Red Mesa Science and Refining, LLC

Apply now →

By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company. Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply. Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.

Red Mesa Science & Refining is a large-scale raw materials manufacturer and supplier of CBD and CBG isolate and distillate as well as several other minor cannabinoids. As a B2B producer our customers are wholesale end product formulating businesses that specialize in contract manufacturing, white labeling and private labeling activities. We are searching for a talented and experienced Quality Assurance Manager who supports the delivery of products to consistently meet internal and customer expectations.

As a science-based business that operates in a ISO9001:2015 and cGMP environment, prior experience in this professional setting is a must. The Quality Assurance Manager maintains quality standards at RMSR in accordance with local, state, federal regulations and standards, with consideration for applicable international markets. This individual is responsible for the maintenance and administration of the Quality Management System.

This position is located in St. George, Utah. This is beautiful red rock country surrounded by world-famous national and state parks, reservoirs, trails and mountains. In 2022, St. George hosted the IRONMAN World Championships along with several other world-class athletic and ATV/Jeep events. The cost of living is a welcome relief to many who come from other western states to make this their home. This is a great place to raise a family, grow a career, and reap the benefits of retirement. “We have an emerging tech sector, a state of the art healthcare industry, a college and a university, a medical school, a bustling construction sector, and an entrepreneurial spirit that sees new businesses being developed daily.” (St. George Area Chamber of Commerce)

Responsibilities

· Own the process for maintaining controlled documented information.

· Own the effective management of the change control process.

· Approve documents originating from your area or appoint a delegate to do so on your behalf.

· Approval authority on relevant QMS documented information.

· Approve new suppliers to be included on the Approved Supplier List.

· Monitor/support monitoring of qualified approved suppliers for their capacity to continue serving the needs of RMSR, and maintain records associated with them.

· Approve purchase requests originating from your area.

· Assess whether customer complaints require Nonconformance or CAPA investigation.

· Assess and identify the need for recall as defined by procedure.

· Monitor and maintain records for relevant equipment assets and their maintenance cycles.

· Own, monitor, review, and improve the Audit Program.

· Act as a liaison and lead point of contact for external audits at RMSR.

· Design sampling protocols in accordance with the Sampling Protocol Owner.

· Own and facilitate nonconformance, occurrence, or CAPA investigations.

· Assign QMS-relevant training; develop and maintain the training program and the method for assessing competency for employees in your area of responsibility.

· Utilize critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm and implement creative solutions.

· Work with relevant departments to formulate strategies to increase productivity.

· Identify, lead, and develop talent to maximize individual, team, and organizational effectiveness to meet company goals.

· Analyze data to find areas for growth and improvement.

· Review processes to ensure they are operationally relevant with current practices or trends.

· Reports to Director of Quality.

· Direct Reports – Quality Engineers, Quality Assurance Associates, Document Control Specialist

Key Qualifications

· Bachelor’s degree preferably in Engineering, Biological/Physical sciences, or equivalent scientific focus of study from an accredited university or college

· 5+ years’ experience in a highly regulated industry: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis. Highly desirable: FDA, PCQI trained, ISO9001:2015

· Prior experience in regulatory agency inspections and correspondence.

· Prior experience in third-party certification audits.

· Ability to follow written procedures and support others for adherence to written procedures.

· Ability to create or update written procedures with onsite personnel.

· Strong written and verbal communication skills, including writing executive summaries and communicating with senior level operations, quality management team, and regulatory agencies.

· Must be able to use computers and generate reports.

· Ability to analyze data and create and review processes, excellent attention to detail.

· Willingness to assist other departments to develop solutions and metrics that improve company quality standards.

· Work closely with all departments to implement best practices and drive continuous improvement.

· Must be able to sit or stand for extended periods of time.

· Must be able to adapt quickly to changes in policy, procedure, and technique.

· Must be at least 18 years of age and must pass UT and Federal background checks.

Salary commensurate with experience and track record.

You must be up to date on COVID vaccinations in order to be considered for this position. Preference will be given to applicants who take the Indeed Skills assessments.

Job Type: Full-time

Pay: $85,000.00 - $110,000.00 per year

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Health savings account
• Paid time off
• Vision insurance

Schedule:

• Monday to Friday
• Weekend availability

Experience:

• ISO 9001: 1 year (Required)

Work Location: One location

Apply for this job with Red Mesa Science and Refining, LLC

Apply now →

By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company. Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply. Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.

Red Mesa Science & Refining is a large-scale raw materials manufacturer and supplier of CBD and CBG isolate and distillate as well as several other minor cannabinoids. As a B2B producer our customers are wholesale end product formulating businesses that specialize in contract manufacturing, white labeling and private labeling activities. We are searching for a talented and experienced Quality Assurance Manager who supports the delivery of products to consistently meet internal and customer expectations.

As a science-based business that operates in a ISO9001:2015 and cGMP environment, prior experience in this professional setting is a must. The Quality Assurance Manager maintains quality standards at RMSR in accordance with local, state, federal regulations and standards, with consideration for applicable international markets. This individual is responsible for the maintenance and administration of the Quality Management System.

This position is located in St. George, Utah. This is beautiful red rock country surrounded by world-famous national and state parks, reservoirs, trails and mountains. In 2022, St. George hosted the IRONMAN World Championships along with several other world-class athletic and ATV/Jeep events. The cost of living is a welcome relief to many who come from other western states to make this their home. This is a great place to raise a family, grow a career, and reap the benefits of retirement. “We have an emerging tech sector, a state of the art healthcare industry, a college and a university, a medical school, a bustling construction sector, and an entrepreneurial spirit that sees new businesses being developed daily.” (St. George Area Chamber of Commerce)

Responsibilities

· Own the process for maintaining controlled documented information.

· Own the effective management of the change control process.

· Approve documents originating from your area or appoint a delegate to do so on your behalf.

· Approval authority on relevant QMS documented information.

· Approve new suppliers to be included on the Approved Supplier List.

· Monitor/support monitoring of qualified approved suppliers for their capacity to continue serving the needs of RMSR, and maintain records associated with them.

· Approve purchase requests originating from your area.

· Assess whether customer complaints require Nonconformance or CAPA investigation.

· Assess and identify the need for recall as defined by procedure.

· Monitor and maintain records for relevant equipment assets and their maintenance cycles.

· Own, monitor, review, and improve the Audit Program.

· Act as a liaison and lead point of contact for external audits at RMSR.

· Design sampling protocols in accordance with the Sampling Protocol Owner.

· Own and facilitate nonconformance, occurrence, or CAPA investigations.

· Assign QMS-relevant training; develop and maintain the training program and the method for assessing competency for employees in your area of responsibility.

· Utilize critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm and implement creative solutions.

· Work with relevant departments to formulate strategies to increase productivity.

· Identify, lead, and develop talent to maximize individual, team, and organizational effectiveness to meet company goals.

· Analyze data to find areas for growth and improvement.

· Review processes to ensure they are operationally relevant with current practices or trends.

· Reports to Director of Quality.

· Direct Reports – Quality Engineers, Quality Assurance Associates, Document Control Specialist

Key Qualifications

· Bachelor’s degree preferably in Engineering, Biological/Physical sciences, or equivalent scientific focus of study from an accredited university or college

· 5+ years’ experience in a highly regulated industry: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis. Highly desirable: FDA, PCQI trained, ISO9001:2015

· Prior experience in regulatory agency inspections and correspondence.

· Prior experience in third-party certification audits.

· Ability to follow written procedures and support others for adherence to written procedures.

· Ability to create or update written procedures with onsite personnel.

· Strong written and verbal communication skills, including writing executive summaries and communicating with senior level operations, quality management team, and regulatory agencies.

· Must be able to use computers and generate reports.

· Ability to analyze data and create and review processes, excellent attention to detail.

· Willingness to assist other departments to develop solutions and metrics that improve company quality standards.

· Work closely with all departments to implement best practices and drive continuous improvement.

· Must be able to sit or stand for extended periods of time.

· Must be able to adapt quickly to changes in policy, procedure, and technique.

· Must be at least 18 years of age and must pass UT and Federal background checks.

Salary commensurate with experience and track record.

You must be up to date on COVID vaccinations in order to be considered for this position. Preference will be given to applicants who take the Indeed Skills assessments.

Job Type: Full-time

Pay: $85,000.00 - $110,000.00 per year

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Health savings account
• Paid time off
• Vision insurance

Schedule:

• Monday to Friday
• Weekend availability

Experience:

• ISO 9001: 1 year (Required)

Work Location: One location

Apply for this job with Red Mesa Science and Refining, LLC

Apply now →

By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company. Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply. Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.

Red Mesa Science & Refining is a large-scale raw materials manufacturer and supplier of CBD and CBG isolate and distillate as well as several other minor cannabinoids. As a B2B producer our customers are wholesale end product formulating businesses that specialize in contract manufacturing, white labeling and private labeling activities. We are searching for a talented and experienced Quality Assurance Manager who supports the delivery of products to consistently meet internal and customer expectations.

As a science-based business that operates in a ISO9001:2015 and cGMP environment, prior experience in this professional setting is a must. The Quality Assurance Manager maintains quality standards at RMSR in accordance with local, state, federal regulations and standards, with consideration for applicable international markets. This individual is responsible for the maintenance and administration of the Quality Management System.

This position is located in St. George, Utah. This is beautiful red rock country surrounded by world-famous national and state parks, reservoirs, trails and mountains. In 2022, St. George hosted the IRONMAN World Championships along with several other world-class athletic and ATV/Jeep events. The cost of living is a welcome relief to many who come from other western states to make this their home. This is a great place to raise a family, grow a career, and reap the benefits of retirement. “We have an emerging tech sector, a state of the art healthcare industry, a college and a university, a medical school, a bustling construction sector, and an entrepreneurial spirit that sees new businesses being developed daily.” (St. George Area Chamber of Commerce)

Responsibilities

· Own the process for maintaining controlled documented information.

· Own the effective management of the change control process.

· Approve documents originating from your area or appoint a delegate to do so on your behalf.

· Approval authority on relevant QMS documented information.

· Approve new suppliers to be included on the Approved Supplier List.

· Monitor/support monitoring of qualified approved suppliers for their capacity to continue serving the needs of RMSR, and maintain records associated with them.

· Approve purchase requests originating from your area.

· Assess whether customer complaints require Nonconformance or CAPA investigation.

· Assess and identify the need for recall as defined by procedure.

· Monitor and maintain records for relevant equipment assets and their maintenance cycles.

· Own, monitor, review, and improve the Audit Program.

· Act as a liaison and lead point of contact for external audits at RMSR.

· Design sampling protocols in accordance with the Sampling Protocol Owner.

· Own and facilitate nonconformance, occurrence, or CAPA investigations.

· Assign QMS-relevant training; develop and maintain the training program and the method for assessing competency for employees in your area of responsibility.

· Utilize critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm and implement creative solutions.

· Work with relevant departments to formulate strategies to increase productivity.

· Identify, lead, and develop talent to maximize individual, team, and organizational effectiveness to meet company goals.

· Analyze data to find areas for growth and improvement.

· Review processes to ensure they are operationally relevant with current practices or trends.

· Reports to Director of Quality.

· Direct Reports – Quality Engineers, Quality Assurance Associates, Document Control Specialist

Key Qualifications

· Bachelor’s degree preferably in Engineering, Biological/Physical sciences, or equivalent scientific focus of study from an accredited university or college

· 5+ years’ experience in a highly regulated industry: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis. Highly desirable: FDA, PCQI trained, ISO9001:2015

· Prior experience in regulatory agency inspections and correspondence.

· Prior experience in third-party certification audits.

· Ability to follow written procedures and support others for adherence to written procedures.

· Ability to create or update written procedures with onsite personnel.

· Strong written and verbal communication skills, including writing executive summaries and communicating with senior level operations, quality management team, and regulatory agencies.

· Must be able to use computers and generate reports.

· Ability to analyze data and create and review processes, excellent attention to detail.

· Willingness to assist other departments to develop solutions and metrics that improve company quality standards.

· Work closely with all departments to implement best practices and drive continuous improvement.

· Must be able to sit or stand for extended periods of time.

· Must be able to adapt quickly to changes in policy, procedure, and technique.

· Must be at least 18 years of age and must pass UT and Federal background checks.

Salary commensurate with experience and track record.

You must be up to date on COVID vaccinations in order to be considered for this position. Preference will be given to applicants who take the Indeed Skills assessments.

Job Type: Full-time

Pay: $85,000.00 - $110,000.00 per year

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Health savings account
• Paid time off
• Vision insurance

Schedule:

• Monday to Friday
• Weekend availability

Experience:

• ISO 9001: 1 year (Required)

Work Location: One location

Apply for this job with Red Mesa Science and Refining, LLC

Apply now →

By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company. Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply. Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.

Red Mesa Science & Refining is a large-scale raw materials manufacturer and supplier of CBD and CBG isolate and distillate as well as several other minor cannabinoids. As a B2B producer our customers are wholesale end product formulating businesses that specialize in contract manufacturing, white labeling and private labeling activities. We are searching for a talented and experienced Quality Assurance Manager who supports the delivery of products to consistently meet internal and customer expectations.

As a science-based business that operates in a ISO9001:2015 and cGMP environment, prior experience in this professional setting is a must. The Quality Assurance Manager maintains quality standards at RMSR in accordance with local, state, federal regulations and standards, with consideration for applicable international markets. This individual is responsible for the maintenance and administration of the Quality Management System.

This position is located in St. George, Utah. This is beautiful red rock country surrounded by world-famous national and state parks, reservoirs, trails and mountains. In 2022, St. George hosted the IRONMAN World Championships along with several other world-class athletic and ATV/Jeep events. The cost of living is a welcome relief to many who come from other western states to make this their home. This is a great place to raise a family, grow a career, and reap the benefits of retirement. “We have an emerging tech sector, a state of the art healthcare industry, a college and a university, a medical school, a bustling construction sector, and an entrepreneurial spirit that sees new businesses being developed daily.” (St. George Area Chamber of Commerce)

Responsibilities

· Own the process for maintaining controlled documented information.

· Own the effective management of the change control process.

· Approve documents originating from your area or appoint a delegate to do so on your behalf.

· Approval authority on relevant QMS documented information.

· Approve new suppliers to be included on the Approved Supplier List.

· Monitor/support monitoring of qualified approved suppliers for their capacity to continue serving the needs of RMSR, and maintain records associated with them.

· Approve purchase requests originating from your area.

· Assess whether customer complaints require Nonconformance or CAPA investigation.

· Assess and identify the need for recall as defined by procedure.

· Monitor and maintain records for relevant equipment assets and their maintenance cycles.

· Own, monitor, review, and improve the Audit Program.

· Act as a liaison and lead point of contact for external audits at RMSR.

· Design sampling protocols in accordance with the Sampling Protocol Owner.

· Own and facilitate nonconformance, occurrence, or CAPA investigations.

· Assign QMS-relevant training; develop and maintain the training program and the method for assessing competency for employees in your area of responsibility.

· Utilize critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm and implement creative solutions.

· Work with relevant departments to formulate strategies to increase productivity.

· Identify, lead, and develop talent to maximize individual, team, and organizational effectiveness to meet company goals.

· Analyze data to find areas for growth and improvement.

· Review processes to ensure they are operationally relevant with current practices or trends.

· Reports to Director of Quality.

· Direct Reports – Quality Engineers, Quality Assurance Associates, Document Control Specialist

Key Qualifications

· Bachelor’s degree preferably in Engineering, Biological/Physical sciences, or equivalent scientific focus of study from an accredited university or college

· 5+ years’ experience in a highly regulated industry: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis. Highly desirable: FDA, PCQI trained, ISO9001:2015

· Prior experience in regulatory agency inspections and correspondence.

· Prior experience in third-party certification audits.

· Ability to follow written procedures and support others for adherence to written procedures.

· Ability to create or update written procedures with onsite personnel.

· Strong written and verbal communication skills, including writing executive summaries and communicating with senior level operations, quality management team, and regulatory agencies.

· Must be able to use computers and generate reports.

· Ability to analyze data and create and review processes, excellent attention to detail.

· Willingness to assist other departments to develop solutions and metrics that improve company quality standards.

· Work closely with all departments to implement best practices and drive continuous improvement.

· Must be able to sit or stand for extended periods of time.

· Must be able to adapt quickly to changes in policy, procedure, and technique.

· Must be at least 18 years of age and must pass UT and Federal background checks.

Salary commensurate with experience and track record.

You must be up to date on COVID vaccinations in order to be considered for this position. Preference will be given to applicants who take the Indeed Skills assessments.

Job Type: Full-time

Pay: $85,000.00 - $110,000.00 per year

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Health savings account
• Paid time off
• Vision insurance

Schedule:

• Monday to Friday
• Weekend availability

Experience:

• ISO 9001: 1 year (Required)

Work Location: One location

Apply for this job with Red Mesa Science and Refining, LLC

Apply now →

By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company. Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply. Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.

Red Mesa Science & Refining is a large-scale raw materials manufacturer and supplier of CBD and CBG isolate and distillate as well as several other minor cannabinoids. As a B2B producer our customers are wholesale end product formulating businesses that specialize in contract manufacturing, white labeling and private labeling activities. We are searching for a talented and experienced Quality Assurance Manager who supports the delivery of products to consistently meet internal and customer expectations.

As a science-based business that operates in a ISO9001:2015 and cGMP environment, prior experience in this professional setting is a must. The Quality Assurance Manager maintains quality standards at RMSR in accordance with local, state, federal regulations and standards, with consideration for applicable international markets. This individual is responsible for the maintenance and administration of the Quality Management System.

You must be up to date on COVID vaccinations in order to be considered for this position. Preference will be given to applicants who take the Indeed Skills assessments.

Responsibilities

· Own the process for maintaining controlled documented information.

· Own the effective management of the change control process.

· Approve documents originating from your area or appoint a delegate to do so on your behalf.

· Approval authority on relevant QMS documented information.

· Approve new suppliers to be included on the Approved Supplier List.

· Monitor/support monitoring of qualified approved suppliers for their capacity to continue serving the needs of RMSR, and maintain records associated with them.

· Approve purchase requests originating from your area.

· Assess whether customer complaints require Nonconformance or CAPA investigation.

· Assess and identify the need for recall as defined by procedure.

· Monitor and maintain records for relevant equipment assets and their maintenance cycles.

· Own, monitor, review, and improve the Audit Program.

· Act as a liaison and lead point of contact for external audits at RMSR.

· Design sampling protocols in accordance with the Sampling Protocol Owner.

· Own and facilitate nonconformance, occurrence, or CAPA investigations.

· Assign QMS-relevant training; develop and maintain the training program and the method for assessing competency for employees in your area of responsibility.

· Utilize critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm and implement creative solutions.

· Work with relevant departments to formulate strategies to increase productivity.

· Identify, lead, and develop talent to maximize individual, team, and organizational effectiveness to meet company goals.

· Analyze data to find areas for growth and improvement.

· Review processes to ensure they are operationally relevant with current practices or trends.

· Reports to Director of Quality.

· Direct Reports – Quality Engineers, Quality Assurance Associates, Document Control Specialist

Key Qualifications

· Bachelor’s degree preferably in Engineering, Biological/Physical sciences, or equivalent scientific focus of study from an accredited university or college

· 5+ years’ experience in a highly regulated industry: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis. Highly desirable: FDA, PCQI trained, ISO9001:2015

· Prior experience in regulatory agency inspections and correspondence.

· Prior experience in third-party certification audits.

· Ability to follow written procedures and support others for adherence to written procedures.

· Ability to create or update written procedures with onsite personnel.

· Strong written and verbal communication skills, including writing executive summaries and communicating with senior level operations, quality management team, and regulatory agencies.

· Must be able to use computers and generate reports.

· Ability to analyze data and create and review processes, excellent attention to detail.

· Willingness to assist other departments to develop solutions and metrics that improve company quality standards.

· Work closely with all departments to implement best practices and drive continuous improvement.

· Must be able to sit or stand for extended periods of time.

· Must be able to adapt quickly to changes in policy, procedure, and technique.

· Must be at least 18 years of age and must pass UT and Federal background checks.

Salary commensurate with experience and track record.

Job Type: Full-time

Pay: $85,000.00 - $110,000.00 per year

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Health savings account
• Paid time off
• Vision insurance

Schedule:

• Monday to Friday
• Weekend availability

Ability to commute/relocate:

• Saint George, UT 84790: Reliably commute or planning to relocate before starting work (Preferred)

Experience:

• ISO 9001: 1 year (Required)

Work Location: One location

Apply for this job with Red Mesa Science and Refining, LLC

Apply now →

By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company. Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply. Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.

Red Mesa Science & Refining is a large-scale raw materials manufacturer and supplier of CBD and CBG isolate and distillate as well as several other minor cannabinoids. As a B2B producer our customers are wholesale end product formulating businesses that specialize in contract manufacturing, white labeling and private labeling activities. We are searching for a talented and experienced Quality Assurance Manager who supports the delivery of products to consistently meet internal and customer expectations.

As a science-based business that operates in a ISO9001:2015 and cGMP environment, prior experience in this professional setting is a must. The Quality Assurance Manager maintains quality standards at RMSR in accordance with local, state, federal regulations and standards, with consideration for applicable international markets. This individual is responsible for the maintenance and administration of the Quality Management System.

You must be up to date on COVID vaccinations in order to be considered for this position. Preference will be given to applicants who take the Indeed Skills assessments.

Responsibilities

· Own the process for maintaining controlled documented information.

· Own the effective management of the change control process.

· Approve documents originating from your area or appoint a delegate to do so on your behalf.

· Approval authority on relevant QMS documented information.

· Approve new suppliers to be included on the Approved Supplier List.

· Monitor/support monitoring of qualified approved suppliers for their capacity to continue serving the needs of RMSR, and maintain records associated with them.

· Approve purchase requests originating from your area.

· Assess whether customer complaints require Nonconformance or CAPA investigation.

· Assess and identify the need for recall as defined by procedure.

· Monitor and maintain records for relevant equipment assets and their maintenance cycles.

· Own, monitor, review, and improve the Audit Program.

· Act as a liaison and lead point of contact for external audits at RMSR.

· Design sampling protocols in accordance with the Sampling Protocol Owner.

· Own and facilitate nonconformance, occurrence, or CAPA investigations.

· Assign QMS-relevant training; develop and maintain the training program and the method for assessing competency for employees in your area of responsibility.

· Utilize critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm and implement creative solutions.

· Work with relevant departments to formulate strategies to increase productivity.

· Identify, lead, and develop talent to maximize individual, team, and organizational effectiveness to meet company goals.

· Analyze data to find areas for growth and improvement.

· Review processes to ensure they are operationally relevant with current practices or trends.

· Reports to Director of Quality.

· Direct Reports – Quality Engineers, Quality Assurance Associates, Document Control Specialist

Key Qualifications

· Bachelor’s degree preferably in Engineering, Biological/Physical sciences, or equivalent scientific focus of study from an accredited university or college

· 5+ years’ experience in a highly regulated industry: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis. Highly desirable: FDA, PCQI trained, ISO9001:2015

· Prior experience in regulatory agency inspections and correspondence.

· Prior experience in third-party certification audits.

· Ability to follow written procedures and support others for adherence to written procedures.

· Ability to create or update written procedures with onsite personnel.

· Strong written and verbal communication skills, including writing executive summaries and communicating with senior level operations, quality management team, and regulatory agencies.

· Must be able to use computers and generate reports.

· Ability to analyze data and create and review processes, excellent attention to detail.

· Willingness to assist other departments to develop solutions and metrics that improve company quality standards.

· Work closely with all departments to implement best practices and drive continuous improvement.

· Must be able to sit or stand for extended periods of time.

· Must be able to adapt quickly to changes in policy, procedure, and technique.

· Must be at least 18 years of age and must pass UT and Federal background checks.

Salary commensurate with experience and track record.

Job Type: Full-time

Pay: $85,000.00 - $110,000.00 per year

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Health savings account
• Paid time off
• Vision insurance

Schedule:

• Monday to Friday
• Weekend availability

Ability to commute/relocate:

• Saint George, UT 84790: Reliably commute or planning to relocate before starting work (Preferred)

Education:

• Bachelor's (Preferred)

Experience:

• ISO 9001: 1 year (Required)
• working in highly regulated industry: 5 years (Preferred)

Work Location: One location

Apply for this job with Red Mesa Science and Refining, LLC

Apply now →

By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company. Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply. Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.

Red Mesa Science & Refining is a large-scale raw materials manufacturer and supplier of CBD and CBG isolate and distillate as well as several other minor cannabinoids. As a B2B producer our customers are wholesale end product formulating businesses that specialize in contract manufacturing, white labeling and private labeling activities. We are searching for a talented and experienced Quality Assurance Manager who supports the delivery of products to consistently meet internal and customer expectations.

As a science-based business that operates in a ISO9001:2015 and cGMP environment, prior experience in this professional setting is a must. The Quality Assurance Manager maintains quality standards at RMSR in accordance with local, state, federal regulations and standards, with consideration for applicable international markets. This individual is responsible for the maintenance and administration of the Quality Management System.

You must be up to date on COVID vaccinations in order to be considered for this position. Preference will be given to applicants who take the Indeed Skills assessments.

Responsibilities

· Own the process for maintaining controlled documented information.

· Own the effective management of the change control process.

· Approve documents originating from your area or appoint a delegate to do so on your behalf.

· Approval authority on relevant QMS documented information.

· Approve new suppliers to be included on the Approved Supplier List.

· Monitor/support monitoring of qualified approved suppliers for their capacity to continue serving the needs of RMSR, and maintain records associated with them.

· Approve purchase requests originating from your area.

· Assess whether customer complaints require Nonconformance or CAPA investigation.

· Assess and identify the need for recall as defined by procedure.

· Monitor and maintain records for relevant equipment assets and their maintenance cycles.

· Own, monitor, review, and improve the Audit Program.

· Act as a liaison and lead point of contact for external audits at RMSR.

· Design sampling protocols in accordance with the Sampling Protocol Owner.

· Own and facilitate nonconformance, occurrence, or CAPA investigations.

· Assign QMS-relevant training; develop and maintain the training program and the method for assessing competency for employees in your area of responsibility.

· Utilize critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm and implement creative solutions.

· Work with relevant departments to formulate strategies to increase productivity.

· Identify, lead, and develop talent to maximize individual, team, and organizational effectiveness to meet company goals.

· Analyze data to find areas for growth and improvement.

· Review processes to ensure they are operationally relevant with current practices or trends.

· Reports to Director of Quality.

· Direct Reports – Quality Engineers, Quality Assurance Associates, Document Control Specialist

Key Qualifications

· Bachelor’s degree preferably in Engineering, Biological/Physical sciences, or equivalent scientific focus of study from an accredited university or college

· 5+ years’ experience in a highly regulated industry: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis. Highly desirable: FDA, PCQI trained, ISO9001:2015

· Prior experience in regulatory agency inspections and correspondence.

· Prior experience in third-party certification audits.

· Ability to follow written procedures and support others for adherence to written procedures.

· Ability to create or update written procedures with onsite personnel.

· Strong written and verbal communication skills, including writing executive summaries and communicating with senior level operations, quality management team, and regulatory agencies.

· Must be able to use computers and generate reports.

· Ability to analyze data and create and review processes, excellent attention to detail.

· Willingness to assist other departments to develop solutions and metrics that improve company quality standards.

· Work closely with all departments to implement best practices and drive continuous improvement.

· Must be able to sit or stand for extended periods of time.

· Must be able to adapt quickly to changes in policy, procedure, and technique.

· Must be at least 18 years of age and must pass UT and Federal background checks.

Salary commensurate with experience and track record.

Job Type: Full-time

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Health savings account
• Paid time off
• Vision insurance

Schedule:

• Monday to Friday
• Weekend availability

Ability to commute/relocate:

• Saint George, UT 84790: Reliably commute or planning to relocate before starting work (Preferred)

Education:

• Bachelor's (Preferred)

Experience:

• ISO 9001: 1 year (Required)
• working in highly regulated industry: 5 years (Preferred)

Work Location: One location

Apply for this job with Red Mesa Science and Refining, LLC

Apply now →

By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company. Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply. Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.

ABOUT RED MESA SCIENCE AND REFINING

Red Mesa Science & Refining is a vertically integrated, industrial scale CBD extraction and processing facility located in St. George, UT. All processing activities are performed in house, including extraction, distillation, crystallization and chromatography. We manufacture a variety of products, including full and broad spectrum distillates and oils, cannabinoid crystalline isolates, and mixed cannabinoid oils. We utilize an in-house analytics lab that helps ensure quality throughout the manufacturing process.

Job Description

As a member of Top Management reporting to the CEO, the Director of Quality Assurance develops and maintains quality standards at RMSR in accordance with local, state, federal regulations and standards, with consideration for applicable international markets. This individual is responsible for managing QA/QC personnel in the maintenance and administration of the Quality Management System and the quality culture, and its adherence to applicable regulations and standards. Additional qualifications, responsibilities and authorities are described below.

Essential Work Experience and Qualifications

Bachelor’s degree in Engineering, Biological/Physical sciences, or equivalent scientific focus of study from an accredited university or college

5+ years experience in a highly regulated industry: healthcare, medical devices, pharmaceutical, consumer packaged goods (food), cannabis. Highly desirable: FDA, HACCP, ISO9001:2015

Prior experience in regulatory agency audits and correspondence.

Ability to follow written procedures and monitor others for adherence to written procedures.

Ability to create or update written procedures with site operations personnel.

Strong written and verbal communication skills, including writing executive summaries and communicating with senior level operations, quality management team, and regulatory agencies.

Must be able to use computers and generate reports.

Ability to analyze data and create and review processes, excellent attention to detail.

Willingness to assist other departments to develop solutions and metrics that improve company quality standards.

Work closely with department leadership to implement best practices, drive continuous improvement, and ensure policies are followed in daily processes.

Must be able to adapt quickly to changes in policy, procedure, and technique.

Must have a basic understanding of the Industrial Hemp Production and Medical Marijuana laws, rules and regulations set forth by the state.

Must be at least 21 years of age and must pass UT and Federal background checks.

Red Mesa Science and Refining, LLC’s Quality Management System (QMS) Responsibilities & Authority

Train and adhere to the documents and procedures applicable to your role.

Monitor Quality Management processes against delivery of their intended outputs.

Ensure federal, state, and local requirements are met for hygienic and safe operations.

Attend Management Review meetings, and report on the performance of the QMS and on opportunities for improvement for your department. Reporting includes but is not limited to changes in external or internal issues relevant to the QMS, internal/external audits, and monitoring and measurement metrics.

Ensure staff comply with company policies and Standard Operating Procedures, as well as take responsibility for staff completing training within a timely manner.

Demonstrate leadership and commitment to a culture of risk management defined by procedure. Serve as the Audit and Risk Committee lead if appointed to do so.

Monitor and review risks.

Identify and communicate new, emerging, and mitigated risks; support the Audit and Risk Committee by providing risk and mitigation information.

Review monthly customer feedback and complaint reports.

Ensure the timely review, distribution, implementation, and maintenance of all released documented information.

Contribute to the generation of supporting QMS relevant documentation where applicable.

Support or delegate in deviation response and Impact Assessment.

Train, motivate, coach, and correct employees to ensure that standards are met.

Perform internal audits as scheduled.

Support all change control in-process and completed documentation.

Support timeliness of recall activities as defined in procedure.

Promote customer focus throughout the organization.

Ensure staff training is completed in a timely manner.

Notify Facilities Personnel of any sightings or unusual level of pests.

Stop work in the event of an emergency, contain the emergency if able to do so safely, and notify the available Safety Officer(s) immediately.

Approve and support development of new products, processes, software, equipment, or facility areas.

Approve and support development of changes to products, processes, equipment, or facility areas.

Approval authority on all relevant QMS documented information.

Own the process for maintaining controlled documented information.

Own the effective management of the change control process.

Approve new and revisions to Standard Operating Procedures.

Approve documents originating from your area or appoint a delegate to do so on your behalf.

Approve or reject change control implementation and/or completion or appoint a delegate to do so on your behalf.

Monitor qualified approved suppliers for their capacity to continue serving the needs of RMSR, and maintain records associated with them.

Approve new suppliers to be included on the Approved Supplier List.

Approve purchase requests originating from your area.

Analyze and assess risks, determine appropriate mitigations, and accept residual risk (as appropriate).

Assess whether customer complaints require Nonconformance or CAPA investigation.

Assess and identify the need for recall as defined by procedure. Assign a Recall Coordinator with other members of Top Management.

Monitor and maintain records for relevant equipment assets and their maintenance cycles.

Own, monitor, review, and improve the Audit Program.

Act as a liaison and lead point of contact for external audits at RMSR.

Design sampling protocols in accordance with the Sampling Protocol Owner.

Own and facilitate all nonconformance, occurrence, or CAPA investigations.

Assign QMS-relevant training; develop and maintain the training program and the method for assessing competency for employees in your area of responsibility.

Approve staff promotions and new hires.

Make decisions regarding metrics discussed in Management Review meetings.

Make high-level decisions about policy and strategy.

Additional Responsibilities

Utilize critical thinking to troubleshoot issues, work collaboratively with a team to brainstorm solutions, and implement improvement solutions

Lead and drive effective efficiency improvement initiatives.

Identify, lead, and develop talent to maximize individual, team, and organizational effectiveness to meet company goals.

Job Type: Full-time

Pay: $90,000.00 - $100,000.00 per year

Benefits:

• Paid Time Off

Schedule:

• Holidays
• Monday to Friday
• On Call
• Weekends

Experience:

• Quality Management: 3 years (Required)

Education:

• Bachelor's (Required)

Location:

• Saint George, UT 84790 (Required)

Work authorization:

• United States (Required)

Work Location:

• One location

This Job Is Ideal for Someone Who Is:

• Detail-oriented -- would rather focus on the details of work than the bigger picture
• Achievement-oriented -- enjoys taking on challenges, even if they might fail
• Autonomous/Independent -- enjoys working with little direction

This Company Describes Its Culture as:

• Detail-oriented -- quality and precision-focused
• Innovative -- innovative and risk-taking
• Outcome-oriented -- results-focused with strong performance culture

Company's website:

• https://www.greenrockhempholdings.com/

Work Remotely:

• No

Apply for this job with Red Mesa Science and Refining, LLC

Apply now →

By clicking the "Apply now" button, you'll be leaving Fazow and going to an external job application page for this company. Please research all companies before applying. When applying for jobs, you should NOT have to pay to apply. Fazow accepts no liability or responsibility as a consequence of any reliance upon information on external sites or in jobs listed on fazow.com.