Cannabis jobs at RDP Development

We are a Cannabis Testing Lab based in Las Vegas. Our goal is to protect patients and consumers by certifying that the product they are consuming have undergone the same level of stringent testing as other drug and food products.

Quality Manager

Responsibilities within the ISO 17025:2017 Quality Management System
The Quality Manager has defined responsibility and authority for ensuring that the quality management system related to quality in the laboratory is implemented and followed at all times. The Quality Manager has direct access to the highest level of management where decisions are made on laboratory policy or resources.

The Quality Manager maintains the master list identifying
the current revision status and distribution of documents in the QMS to prevent the use of obsolete documents.

Required Qualifications, Training & Skills

Must be self-motivated, energetic and possess the ability to work in a diverse GLP laboratory environment under a QMS. Candidate must have deep understanding of analytical techniques with hands-on experience in method development leading to the creation of SOPs, LIMS interface and basic chemistry techniques e.g. HPLC, GC-MS, LC-MS.

This position requires the candidates to have adequate statistical analysis skills, good concept of quantification, accuracy/variation, and organizational skills. Candidates must have the ability to work independently with minimal supervision; have strong trouble-shooting, computer and record keeping skills and problem-solving skills.

Specifically

• Serves as the focal point for the QMS

• Oversees and provides secondary approval for all certificates of analyses published by lab
• Approves all controlled laboratory documentation
• Oversees quality control data.
• Evaluates data objectively and performs assessments without managerial influence.
• Maintains ISO 17025 accreditation and compliance with State and local regulatory requirements, including quality checks and compliance of safety standards such as, but not limited to, OSHA, Fire Marshall and Police
• Oversees the Quality Assurance and Control Program
• Manages and maintains all laboratory controlled documentation
• Performs internal audits, including both technical and quality systems and direct any necessary corrective action notifying management of deficiencies or opportunities for improvement
• Develops and maintains laboratory policy and procedural manuals, quality procedures, SOPs, equipment requirements, and evaluating and implementing new procedures as necessary.

• Performs, schedules, and records internal laboratory inspections as necessary
• Oversees the LIMS and general records management.
• Provides oversight of human resources and any adherences required as an equal opportunity facility
• Serves as the laboratory safety officer with oversight on all safety systems in adherence with ISO 17025, OSHA, NAC 453A, and any other laboratory safety organizations

• Maintains chemical/equipment traceability records and generating control charts.

• Maintains training records for all lab staff.

• Generates training plans for all laboratory staff.
• Creates and maintains internal training processes for all laboratory staff including (but not limited to) any necessary retrainings, safety training, good laboratory practices, quality assurance programs, and continuing education

• Schedules proficiency testing for all analytes
• Monitors CAPAs, non-conformances, OOS, failed tests, repeat tests employee incidents, and client complaints for areas of improvement

• May oversee and sign-off on any laboratory documentation as needed
• May step in and perform any tasks assigned in the lab as needed

Desired Skills

Demonstrated expertise in sample chain of custody protocols, large dataset analysis, should be aware of emerging analytical techniques, experience using LIMS, familiar with cGMP and GLP requirements, as well as working under a Quality Management System are favored.

Required Education, Expertise & Experience

A Bachelor’s Degree (BS) or greater in chemistry, biochemistry, microbiology or equivalent with 5 years of relevant experience is REQUIRED.

Excellent written and oral communication skills, previously demonstrated successful managerial or supervisory experience and previously demonstrated successful ability to contribute in a team Quality Management System environment are essential.

Job Type: Full-time

Pay: $50,000.00 - $75,000.00 per year

Benefits:

• Health insurance
• Paid time off

Schedule:

• Monday to Friday

Experience:

• ISO 9001: 3 years (Preferred)
• Quality assurance: 4 years (Preferred)
• Quality control: 4 years (Preferred)
• lab: 4 years (Preferred)

Work Location: One location

Apply for this job with RDP Development

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.

We are a independent cannabis testing lab looking for motivated Sample Pick Up Tech to join our team!

The Sample Pick Up Tech is responsible for transporting and accurately documenting laboratory samples.

Duties

• Scheduling and coordinating sample pickups
• Cleaning and preparing sampling tools and instruments
• Communicating pickup times with clients
• Driving to and from client facilities
• Documenting routes and mileage
• Collecting and accurately documenting sample details

Requirements

• Reliable and insured vehicle with a locking trunk and alarm system
• Experience in the cannabis industry - preferred
• Laboratory and or cannabis industry experience is preferable

Skills

• Customer service orientated
• Microsoft Word and Excel,
• Metrc

Job Type: Full-time

Pay: $13.00 - $16.00 per hour

Schedule:

• Monday to Friday

Experience:

• Customer service: 2 years (Preferred)

Work Location: One location

Apply for this job with RDP Development

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.

Rapidly growing cannabis testing laboratory located in Nevada is looking to hire a full time general manager to oversee the laboratory operations and employees. Laboratory General Manager will develop safe and effective cannabis-based products by supervising production and implementing standard operating procedures (SOPs). The successful candidate will be able to oversee testing formulated products, generate quality assurance/quality control (QA/QC) reports, oversee general laboratory day to day operations, and assist with marketing, networking, and bringing in new clients to use our testing services.

Qualifications:

• Bachelor’s degree required (preferred degree in business management, chemistry, engineering, or biology/microbiology)
• Prior sales and management experience of at least 3 year required
• Must be highly organized, have a team player mentality, and be able to multi task
• Must be able to intelligently communicate to lab employees as well as upper management on a daily basis
• Prior laboratory experience a plus but not required
• Experience with analytical testing (HPLC) and microbiology including working in aseptic conditions is a plus

Responsibilities:

• Adhere to protocols and laboratory SOPs
• Oversee and help assist with sales
• Problem-solving skills and troubleshooting of products and equipment
• Manage laboratory operations and ensure safety of employees

Job Type: Full-time

Pay: $90,000.00 - $115,000.00 per year

Benefits:

• Health insurance

Schedule:

• Monday to Friday

Experience:

• management: 5 years (Preferred)
• Laboratory: 4 years (Preferred)
• SOP: 4 years (Preferred)

Work Location: One location

Apply for this job with RDP Development

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.

We are a Cannabis Testing Lab based in Las Vegas. Our goal is to protect patients and consumers by certifying that the product they are consuming have undergone the same level of stringent testing as other drug and food products.

Quality Manager

Responsibilities within the ISO 17025:2017 Quality Management System
The Quality Manager has defined responsibility and authority for ensuring that the quality management system related to quality in the laboratory is implemented and followed at all times. The Quality Manager has direct access to the highest level of management where decisions are made on laboratory policy or resources.

The Quality Manager maintains the master list identifying
the current revision status and distribution of documents in the QMS to prevent the use of obsolete documents.

Required Qualifications, Training & Skills

Must be self-motivated, energetic and possess the ability to work in a diverse GLP laboratory environment under a QMS. Candidate must have deep understanding of analytical techniques with hands-on experience in method development leading to the creation of SOPs, LIMS interface and basic chemistry techniques e.g. HPLC, GC-MS, LC-MS.

This position requires the candidates to have adequate statistical analysis skills, good concept of quantification, accuracy/variation, and organizational skills. Candidates must have the ability to work independently with minimal supervision; have strong trouble-shooting, computer and record keeping skills and problem-solving skills.

Specifically

• Serves as the focal point for the QMS

• Oversees and provides secondary approval for all certificates of analyses published by lab
• Approves all controlled laboratory documentation
• Oversees quality control data.
• Evaluates data objectively and performs assessments without managerial influence.
• Maintains ISO 17025 accreditation and compliance with State and local regulatory requirements, including quality checks and compliance of safety standards such as, but not limited to, OSHA, Fire Marshall and Police
• Oversees the Quality Assurance and Control Program
• Manages and maintains all laboratory controlled documentation
• Performs internal audits, including both technical and quality systems and direct any necessary corrective action notifying management of deficiencies or opportunities for improvement
• Develops and maintains laboratory policy and procedural manuals, quality procedures, SOPs, equipment requirements, and evaluating and implementing new procedures as necessary.

• Performs, schedules, and records internal laboratory inspections as necessary
• Oversees the LIMS and general records management.
• Provides oversight of human resources and any adherences required as an equal opportunity facility
• Serves as the laboratory safety officer with oversight on all safety systems in adherence with ISO 17025, OSHA, NAC 453A, and any other laboratory safety organizations

• Maintains chemical/equipment traceability records and generating control charts.

• Maintains training records for all lab staff.

• Generates training plans for all laboratory staff.
• Creates and maintains internal training processes for all laboratory staff including (but not limited to) any necessary retrainings, safety training, good laboratory practices, quality assurance programs, and continuing education

• Schedules proficiency testing for all analytes
• Monitors CAPAs, non-conformances, OOS, failed tests, repeat tests employee incidents, and client complaints for areas of improvement

• May oversee and sign-off on any laboratory documentation as needed
• May step in and perform any tasks assigned in the lab as needed

Desired Skills

Demonstrated expertise in sample chain of custody protocols, large dataset analysis, should be aware of emerging analytical techniques, experience using LIMS, familiar with cGMP and GLP requirements, as well as working under a Quality Management System are favored.

Required Education, Expertise & Experience

A Bachelor’s Degree (BS) or greater in chemistry, biochemistry, microbiology or equivalent with 5 years of relevant experience is REQUIRED.

Excellent written and oral communication skills, previously demonstrated successful managerial or supervisory experience and previously demonstrated successful ability to contribute in a team Quality Management System environment are essential.

Job Type: Full-time

Pay: $50,000.00 - $75,000.00 per year

Benefits:

• Health insurance
• Paid time off

Schedule:

• Monday to Friday

Experience:

• ISO 9001: 3 years (Preferred)
• Quality assurance: 4 years (Preferred)
• Quality control: 4 years (Preferred)
• lab: 4 years (Preferred)

Work Location: One location

Apply for this job with RDP Development

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.

We are a Cannabis Testing Lab based in Las Vegas. Our goal is to protect patients and consumers by certifying that the product they are consuming have undergone the same level of stringent testing as other drug and food products.

Quality Manager

Responsibilities within the ISO 17025:2017 Quality Management System
The Quality Manager has defined responsibility and authority for ensuring that the quality management system related to quality in the laboratory is implemented and followed at all times. The Quality Manager has direct access to the highest level of management where decisions are made on laboratory policy or resources.

The Quality Manager maintains the master list identifying
the current revision status and distribution of documents in the QMS to prevent the use of obsolete documents.

Required Qualifications, Training & Skills

Must be self-motivated, energetic and possess the ability to work in a diverse GLP laboratory environment under a QMS. Candidate must have deep understanding of analytical techniques with hands-on experience in method development leading to the creation of SOPs, LIMS interface and basic chemistry techniques e.g. HPLC, GC-MS, LC-MS.

This position requires the candidates to have adequate statistical analysis skills, good concept of quantification, accuracy/variation, and organizational skills. Candidates must have the ability to work independently with minimal supervision; have strong trouble-shooting, computer and record keeping skills and problem-solving skills.

Specifically

• Serves as the focal point for the QMS
• Oversees and provides secondary approval for all certificates of analyses published by lab
• Approves all controlled laboratory documentation
• Oversees quality control data.
• Evaluates data objectively and performs assessments without managerial influence.
• Maintains ISO 17025 accreditation and compliance with State and local regulatory requirements, including quality checks and compliance of safety standards such as, but not limited to, OSHA, Fire Marshall and Police
• Oversees the Quality Assurance and Control Program
• Manages and maintains all laboratory controlled documentation
• Performs internal audits, including both technical and quality systems and direct any necessary corrective action notifying management of deficiencies or opportunities for improvement
• Develops and maintains laboratory policy and procedural manuals, quality procedures, SOPs, equipment requirements, and evaluating and implementing new procedures as necessary.
• Performs, schedules, and records internal laboratory inspections as necessary
• Oversees the LIMS and general records management.
• Provides oversight of human resources and any adherences required as an equal opportunity facility
• Serves as the laboratory safety officer with oversight on all safety systems in adherence with ISO 17025, OSHA, NAC 453A, and any other laboratory safety organizations
• Maintains chemical/equipment traceability records and generating control charts.
• Maintains training records for all lab staff.
• Generates training plans for all laboratory staff.
• Creates and maintains internal training processes for all laboratory staff including (but not limited to) any necessary retrainings, safety training, good laboratory practices, quality assurance programs, and continuing education
• Schedules proficiency testing for all analytes
• Monitors CAPAs, non-conformances, OOS, failed tests, repeat tests employee incidents, and client complaints for areas of improvement
• May oversee and sign-off on any laboratory documentation as needed
• May step in and perform any tasks assigned in the lab as needed

Desired Skills

Demonstrated expertise in sample chain of custody protocols, large dataset analysis, should be aware of emerging analytical techniques, experience using LIMS, familiar with cGMP and GLP requirements, as well as working under a Quality Management System are favored.

Required Education, Expertise & Experience

A Bachelor’s Degree (BS) or greater in chemistry, biochemistry, microbiology or equivalent with 5 years of relevant experience is REQUIRED.

Excellent written and oral communication skills, previously demonstrated successful managerial or supervisory experience and previously demonstrated successful ability to contribute in a team Quality Management System environment are essential.

Job Type: Full-time

Pay: $45,000.00 - $60,000.00 per year

Benefits:

• Health insurance
• Paid time off

Schedule:

• Monday to Friday

Ability to commute/relocate:

• Las Vegas, NV 89102: Reliably commute or planning to relocate before starting work (Preferred)

Experience:

• ISO 9001: 1 year (Preferred)

Work Location: One location

Apply for this job with RDP Development

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.

We are a Cannabis Testing Lab based in Las Vegas. Our goal is to protect patients and consumers by certifying that the product they are consuming have undergone the same level of stringent testing as other drug and food products.

Quality Manager

Responsibilities within the ISO 17025:2017 Quality Management System
The Quality Manager has defined responsibility and authority for ensuring that the quality management system related to quality in the laboratory is implemented and followed at all times. The Quality Manager has direct access to the highest level of management where decisions are made on laboratory policy or resources.

The Quality Manager maintains the master list identifying
the current revision status and distribution of documents in the QMS to prevent the use of obsolete documents.

Required Qualifications, Training & Skills

Must be self-motivated, energetic and possess the ability to work in a diverse GLP laboratory environment under a QMS. Candidate must have deep understanding of analytical techniques with hands-on experience in method development leading to the creation of SOPs, LIMS interface and basic chemistry techniques e.g. HPLC, GC-MS, LC-MS.

This position requires the candidates to have adequate statistical analysis skills, good concept of quantification, accuracy/variation, and organizational skills. Candidates must have the ability to work independently with minimal supervision; have strong trouble-shooting, computer and record keeping skills and problem-solving skills.

Specifically

• Serves as the focal point for the QMS
• Oversees and provides secondary approval for all certificates of analyses published by lab
• Approves all controlled laboratory documentation
• Oversees quality control data.
• Evaluates data objectively and performs assessments without managerial influence.
• Maintains ISO 17025 accreditation and compliance with State and local regulatory requirements, including quality checks and compliance of safety standards such as, but not limited to, OSHA, Fire Marshall and Police
• Oversees the Quality Assurance and Control Program
• Manages and maintains all laboratory controlled documentation
• Performs internal audits, including both technical and quality systems and direct any necessary corrective action notifying management of deficiencies or opportunities for improvement
• Develops and maintains laboratory policy and procedural manuals, quality procedures, SOPs, equipment requirements, and evaluating and implementing new procedures as necessary.
• Performs, schedules, and records internal laboratory inspections as necessary
• Oversees the LIMS and general records management.
• Provides oversight of human resources and any adherences required as an equal opportunity facility
• Serves as the laboratory safety officer with oversight on all safety systems in adherence with ISO 17025, OSHA, NAC 453A, and any other laboratory safety organizations
• Maintains chemical/equipment traceability records and generating control charts.
• Maintains training records for all lab staff.
• Generates training plans for all laboratory staff.
• Creates and maintains internal training processes for all laboratory staff including (but not limited to) any necessary retrainings, safety training, good laboratory practices, quality assurance programs, and continuing education
• Schedules proficiency testing for all analytes
• Monitors CAPAs, non-conformances, OOS, failed tests, repeat tests employee incidents, and client complaints for areas of improvement
• May oversee and sign-off on any laboratory documentation as needed
• May step in and perform any tasks assigned in the lab as needed

Desired Skills

Demonstrated expertise in sample chain of custody protocols, large dataset analysis, should be aware of emerging analytical techniques, experience using LIMS, familiar with cGMP and GLP requirements, as well as working under a Quality Management System are favored.

Required Education, Expertise & Experience

A Bachelor’s Degree (BS) or greater in chemistry, biochemistry, microbiology or equivalent with 5 years of relevant experience is REQUIRED.

Excellent written and oral communication skills, previously demonstrated successful managerial or supervisory experience and previously demonstrated successful ability to contribute in a team Quality Management System environment are essential.

Job Type: Full-time

Pay: $45,000.00 - $60,000.00 per year

Benefits:

• Health insurance
• Paid time off

Schedule:

• Monday to Friday

Ability to commute/relocate:

• Las Vegas, NV 89102: Reliably commute or planning to relocate before starting work (Preferred)

Experience:

• ISO 9001: 1 year (Preferred)

Work Location: One location

Apply for this job with RDP Development

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.

We are a independent cannabis testing lab looking for motivated Sample Pick Up Tech to join our team!

The Sample Pick Up Tech is responsible for transporting and accurately documenting laboratory samples.

Duties

• Scheduling and coordinating sample pickups
• Cleaning and preparing sampling tools and instruments
• Communicating pickup times with clients
• Driving to and from client facilities
• Documenting routes and mileage
• Collecting and accurately documenting sample details

Requirements

• Reliable and insured vehicle with a locking trunk and alarm system
• Experience in the cannabis industry - preferred
• Must be licensed, at least 21 years of age, and have a clean driving record
• Laboratory and or cannabis industry experience is preferable

Skills

• Customer service orientated
• Microsoft Word and Excel,
• Metrc

Job Type: Full-time

Pay: $12.00 - $15.00 per hour

Schedule:

• Monday to Friday

Application Question(s):

• Are you 21 years or older?
• Do you have LVMPD Marijuana Agent Card
• Do you have Nevada State Laboratory Agent Card
• Have you worked within the Cannabis space?
• Have you worked with Metrc?

Work Location: One location

Apply for this job with RDP Development

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.

We are a independent cannabis testing lab looking for motivated chemist with a strong knowledge of one or more of following: LC/MSMS, GC/MS , HPLC, GC and similar laboratory instrumentation.

Position will include working alongside chemists and director to ensure laboratory organization and efficiency in work flow.

Overview:

This position is to be a full time position. People with extensive analytical, academic, commercial, and/or laboratory consultation experience preferred.

• Conducting sample preparation and analysis of raw materials, finished products according to standard operating procedures and validated methods.
• Accurately record and keep QCs and sample information.
• Preparation and monitoring of standards, calibrators and QCs
• Operating analytical instruments such as HPLC, HPLC (MSMS), GC (MSD) and ICP (MS)
• Follow GLP and ISO quality standards
• Maintain daily housekeeping routines and perform routine instrument maintenance.
• Interface with LIMS software for recording and reporting analysis results.

Requirements

• Bachelor of Science in a natural or physical science (Chemistry, Biochemistry, Biology, Microbiology, etc.)
• Mass Spectrometry experience preferred.
• Knowledge of or the capability to learn and comply with Nevada Cannabis regulations.
• Able to work under pressure in a fast-paced laboratory setting.
• Method development and validation experience
• Knowledge of mass spectrometry (GC, LC/MS, and/or ICP), and/or live PCR
• Familiar with ISO 17025 certification
• Strong communication skill (written and oral)
• Team player

Position requires FBI background check

Job Type: Full-time

Salary: $45,000.00 to $55,000.00 /year

Experience:

• chemist: 3 years (Required)
• LC, GC , HPLC: 3 years (Required)

Education:

• Bachelor's (Required)

Location:

• Las Vegas, NV (Required)

Work authorization:

• United States (Required)

Application Question:

• Which specific instruments have you used?

Work Location:

• One location

Schedule:

• Monday to Friday

Apply for this job with RDP Development

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.

Job Description

We are a growing testing laboratory located in Las Vegas NV. We are currently looking to hire a full time assistant general manager to oversee the laboratory operations and employees. The laboratory assistant manager will ensure safe and effective cannabis-environment. The successful candidate will oversee general laboratory day to day operations and assist with bringing in new clients to use our testing facility and services.

Qualifications:

• Bachelor’s degree required (preferred degree in business management, chemistry, engineering, or biology/microbiology)
• Prior sales and management experience of at least 2 year required
• Must be highly organized, have a team player mentality, and be able to multi task
• Must be able to intelligently communicate to lab employees as well as senior management on a daily basis
• Prior laboratory experience a plus

Responsibilities:

• Oversee staff, manage day to day operations, and business development/sales
• Set-up, operate, maintain, and break down laboratory equipment as needed
• Maintain a clean and organized work environment
• Secure and organize all customer files and provide weekly updates
• Ensure development of tactical programs to pursue targeted goals and objectives
• Manage inventory and supplies
• Problem-solving skills and troubleshooting of products and equipment
• Manage laboratory operations and ensure safety of employees
• Ensure compliance with all state and local laws, regulations and ordinances
• Maintain a culture of high quality customer service and communication.

This a full time position with salary plus bonus and benefits.

Job Type: Full-time

Salary: $16.00 to $19.00 /hour

Pay may depend on skills and/or qualifications

Experience:

• Operations: 4 years (Required)
• Management: 3 years (Required)
• sales: 3 years (Required)

Location:

• Las Vegas, NV (Required)

Work authorization:

• United States (Required)

Work Location:

• One location

Schedule:

• Monday to Friday

Apply for this job with RDP Development

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.