Cannabis jobs at Open Book Extracts
We know of 7 jobs at Open Book Extracts as of May 2024, including roles such as R&D Technician, Product Development, Assistant Manager, Finished Goods Production, Lab Technician - Day Three Labs, and Manufacturing Manager/Director.
More than 30+ days
THE COMPANY
Headquartered in Roxboro, N.C., Open Book Extracts is a cGMP-certified manufacturer of premium plant-based cannabinoid products, aiming to be the industry's true north by delivering premium products, exceptional service, and industry-leading transparency. With control of the entire supply chain, a state-of-the-art extraction campus near North Carolina's Research Triangle, proprietary refinement and conversion methods backed by a growing IP portfolio, and a team of PhD chemists and seasoned business leaders, OBX is positioned to be the trusted partner for global brands seeking to enter the marketplace. OBX Asia, with its headquarters in Hong Kong, provides strategic guidance and on-the-ground support for our Asia customers.
THE POSITION
We are seeking an entry level R&D Technician who will be responsible for assisting the development of new products from concept to commercialization that support company growth. Position will also assist enhancement and improvement upon current products. Serves as a technical aid that supports product development and improvements, quality improvements, and customer requests. Assist the R&D team with the activities and operations required to complete the functions of the research and development department. Study and comprehend all policies, procedures and operational guidelines set by the management team. Is responsible for generation of representative pilot samples and production batches for internal and external customer evaluations through the use of appropriate scale-down process models. Other duties include assisting process optimization and product enhancement activities.
RESPONSIBILITIES
- Assists new product process from development to commercialization, within defined company, industry, and regulatory parameters*
- Executes lab scale and small batch experimentation to support all levels of formulation, analytics, and processing for multiple cannabis-based research.
- Assists in new research and development procedures and techniques under the supervision of the Senior Formulation Scientists
- Executes individual project goals and follows outlined priorities for research and development endeavors.
- Records and aids maintenance of technical documents, databases, and reports.
- Follows SOPs, formulation spreadsheets, inventories, traceability logs, tracking logs, etc.
- Aids in the maintenance of inventories for research and developments raw materials, chemicals, and equipment.
- Follows complex instructions and formulations in the preparation of cannabis extract, concentrates, and infused products.
- Follows guidelines for acceptance and testing of chemical raw-materials in finished blends
- Operates within company's Quality Management System
- Participates in team driven activities to facilitate on- going production improvements or new product development projects.
- Familiarity with scientific principles and research and development laboratory experience. Can follow written direction and maintain a laboratory notebook.
- Practices highly sterile laboratory cleaning procedures throughout the facility with focus and personal contributions towards a clean and organized assigned work area at the end of the assigned shift.
- Capability of troubleshooting, fixing, and services a wide range of equipment and software with little to no assistance.
- Promotes a positive can-do attitude
- Communicates effectively and consistently in writing and verbally with all levels of staff
- Collaborates in cross functional teams to meet research and development schedules.
- Understands and meets daily goals, expectations, and deadlines.
- Consistently enforces all company policies & procedures.
- Conducts stability studies on formulations
- Writes necessary documents for manufacturing feasibility
- Prepares product registration documentation and product chemistry packages to meet regulatory requirements.
- Responsible for batch production from pilot scale to process validation.
- Performs additional special projects as assigned.
EXPERIENCE
- Bachelor's degree preferred or equivalent experience in research and development, chemical or pharmaceutical manufacturing
- Experience with HPLC testing and other stability testing methods.
- Proven problem-solving skills and track record of successful technical accomplishments
- Ability to establish and maintain effective working relationships with all employees.
- Ability to take direction and initiative.
- Skills in intermediate math.
- Excellent verbal and written communication skills with coworkers and management.
- Enthusiasm for research and formulating/improving product formulations.
- Ability to be detail oriented, multi-task and produce results.
- Superior organizational skills.
- Strong understanding of cGMP guidelines and FDA regulations related to the pharmaceutical industry *
- Proficient using MS Office applications.*
- Experience with FDA and other regulatory agency requirements
OTHER DETAILS
- This is a full-time position based out of Roxboro, NC or Raleigh/Durham, NC.
- Compensation commensurate with experience.
- Background and reference checks required.
- Periodically required to be available to virtually meet with international clients during non-traditional business hours.
PHYSICAL DEMANDS AND WORKING ENVIRONMENT:
- Must be able to lift, carry and balance up to 50 pounds
- While performing the duties of this job, the employee is regularly required to perform grasping, talking, hearing, seeing and repetitive motions.
- Ability to walk and stand for long periods of time (4-6 hours) with frequent kneeling and bending.
- Working in limited climate-controlled facilities and may experience extreme heat or cold
- Work with heavy fumes, plants, airborne particles and chemicals
- Must be comfortable working with and around heavy machinery
- May experience moderately high noise levels
EQUAL EMPLOYMENT OPPORTUNITY STATEMENT
Open Book Extracts is proud to be an equal opportunity employer. We embrace diversity and are committed to building a team that represents a variety of backgrounds, perspectives, and skills. The more inclusive we are, the better our work will be.
Apply for this job with Open Book Extracts
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.
Open Book Extracts
Assistant Manager, Finished Goods Production
The Company
Headquartered in Roxboro, N.C., Open Book Extracts is a cGMP-certified manufacturer of premium plant-based cannabinoid products, aiming to be the industry's true north by delivering premium products, exceptional service, and industry-leading transparency. With control of the entire supply chain, a state-of-the-art extraction campus near North Carolina's Research Triangle, proprietary refinement and conversion methods backed by a growing IP portfolio, and a team of PhD chemists and seasoned business leaders, OBX is positioned to be the trusted partner for global brands seeking to enter or expand their presence in the marketplace.
Job Summary
The Assistant Manager will oversee the day-to-day finished goods production operations for a wide range of manufactured ingestible products in a cGMP facility. You will report to the Production Manager and oversee the production staff as well as any other function that may be assigned to ensure on-time production of products for third party clients. We expect you to possess strong people management, team building, problem solving, scheduling, and process improvement skills with relevant experience in consumer products and/or manufacturing. Proven experience managing teams, deploying company performance policies, exercising sound judgment in escalating staff complaints, and implementing HR directives is required. Ability to direct personnel towards maximum performance will set you apart as a leader. The goal is to ensure an efficient and productive manufacturing process that meets customer requirements, and be a leader who personifies the company culture.
Responsibilities
- Design and implement operational systems to ensure on-time manufacturing, accurate quoting, and forecasting.
- Support the Manager's hiring and staff management objectives required to meet company objectives.
- Oversee staff management of both full time employees and part-time labor at the direction of the Manager.
- Serve as a leader and a pace setter in a fast paced environment in order to ensure production timelines are met.
- Enforce company attendance, performance management, time clock utilization, and any additional HR policy objectives at the company.
- Participate in cross departmental collaboration liaising with QA/QC, product development, facility + equipment, supply chain, fulfillment, and sales departments.
- Work closely with the Equipment and Facilities team to support the commissioning, repair, and preventative maintenance of equipment on an ongoing basis.
- Manage daily production schedules and organize workflow daily to meet specifications and deadlines.
- Develop and Implement team goals with the Manager including KPI's on a daily, monthly, and quarterly basis.
- Monitor production to resolve issues as they arise and communicate schedule impacts to the Manager and cross departmentally as directed.
- Supervise and evaluate performance of production personnel.
- Deploy and implement a rigorous culture of quality control and collaborate with the Quality Assurance team to ensure compliance with the numerous certifications at the facility including, but not limited to cGMP (111 and 117), PCQI, Organic, Halal, Kosher, NASC.
- Support quality assurance department during customer and regulatory audits as requested.
- Serve as a leader in the implementation and enforcement of company health and safety directives including adherence to OSHA protocols.
Skills & Abilities
- Excellent organizational and planning skills.
- Strong verbal and written communication skills.
- Excellent interpersonal skills and the proven ability to work well with all levels of management and staff.
- Progressive experience in successful leadership and management of teams in a cGMP and OSHA compliant environment.
- Deep knowledge of production management.
- Proficient with scheduling and inventory reporting systems.
- Understanding of quality standards and health & safety regulations.
- Experience in reporting on key production metrics.
- Proficient in MS Office, Google Suite, and ERP software.
- Attention to detail, and a natural problem solver.
- Strong decision-making skills and a results-driven approach.
Education & Experience
- Minimum 5 years relevant experience in a production management leadership position.
- Bachelor's degree required, graduate degree in a relevant field a plus. Cannabis, hemp, consumer products, food production, or white/private label experience is a plus.
Additional Details
- This is a full-time position based out of Roxboro, NC.
- Flexibility to work days/evenings/weekends depending on production schedules required.
Physical Demands and Working Environment
- May be required to stand and/or walk for extended periods of time
- Must be able to lift, carry and balance up to 50 pounds
- While performing the duties of this job, the employee is regularly required to perform grasping, talking, hearing, seeing and repetitive motions.
- Ability to walk and stand for long periods of time (4-6 hours) with frequent kneeling and bending.
- Working in limited climate-controlled facilities and experience extreme heat or cold
- Work with heavy fumes, plants, airborne particles and chemicals
- Must be comfortable working with and around heavy machinery
- May experience moderately high noise levels
Equal Employment Opportunity (EEO) Statement
Open Book Extracts is proud to be an equal opportunity employer. We embrace diversity and are committed to building a team that represents a variety of backgrounds, perspectives, and skills. The more inclusive we are, the better our work will be.
This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.
Apply for this job with Open Book Extracts
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.
THE COMPANY
Headquartered in Roxboro, N.C., Open Book Extracts is a cGMP-certified manufacturer of premium plant-based cannabinoid products, aiming to be the industry's true north by delivering premium products, exceptional service, and industry-leading transparency. With control of the entire supply chain, a state-of-the-art extraction campus near North Carolina's Research Triangle, proprietary refinement and conversion methods backed by a growing IP portfolio, and a team of PhD chemists and seasoned business leaders, OBX is positioned to be the trusted partner for global brands seeking to enter the marketplace. OBX Asia, with its headquarters in Hong Kong, provides strategic guidance and on-the-ground support for our Asia customers.
THE POSITION
We are seeking an entry level R&D Technician who will be responsible for assisting the development of new products from concept to commercialization that support company growth. Position will also assist enhancement and improvement upon current products. Serves as a technical aid that supports product development and improvements, quality improvements, and customer requests. Assist the R&D team with the activities and operations required to complete the functions of the research and development department. Study and comprehend all policies, procedures and operational guidelines set by the management team. Is responsible for generation of representative pilot samples and production batches for internal and external customer evaluations through the use of appropriate scale-down process models. Other duties include assisting process optimization and product enhancement activities.
RESPONSIBILITIES
- Assists new product process from development to commercialization, within defined company, industry, and regulatory parameters*
- Executes lab scale and small batch experimentation to support all levels of formulation, analytics, and processing for multiple cannabis-based research.
- Assists in new research and development procedures and techniques under the supervision of the Senior Formulation Scientists
- Executes individual project goals and follows outlined priorities for research and development endeavors.
- Records and aids maintenance of technical documents, databases, and reports.
- Follows SOPs, formulation spreadsheets, inventories, traceability logs, tracking logs, etc.
- Aids in the maintenance of inventories for research and developments raw materials, chemicals, and equipment.
- Follows complex instructions and formulations in the preparation of cannabis extract, concentrates, and infused products.
- Follows guidelines for acceptance and testing of chemical raw-materials in finished blends
- Operates within company's Quality Management System
- Participates in team driven activities to facilitate on- going production improvements or new product development projects.
- Familiarity with scientific principles and research and development laboratory experience. Can follow written direction and maintain a laboratory notebook.
- Practices highly sterile laboratory cleaning procedures throughout the facility with focus and personal contributions towards a clean and organized assigned work area at the end of the assigned shift.
- Capability of troubleshooting, fixing, and services a wide range of equipment and software with little to no assistance.
- Promotes a positive can-do attitude
- Communicates effectively and consistently in writing and verbally with all levels of staff
- Collaborates in cross functional teams to meet research and development schedules.
- Understands and meets daily goals, expectations, and deadlines.
- Consistently enforces all company policies & procedures.
- Conducts stability studies on formulations
- Writes necessary documents for manufacturing feasibility
- Prepares product registration documentation and product chemistry packages to meet regulatory requirements.
- Responsible for batch production from pilot scale to process validation.
- Performs additional special projects as assigned.
EXPERIENCE
- Bachelor's degree preferred or equivalent experience in research and development, chemical or pharmaceutical manufacturing
- Experience with HPLC testing and other stability testing methods.
- Proven problem-solving skills and track record of successful technical accomplishments
- Ability to establish and maintain effective working relationships with all employees.
- Ability to take direction and initiative.
- Skills in intermediate math.
- Excellent verbal and written communication skills with coworkers and management.
- Enthusiasm for research and formulating/improving product formulations.
- Ability to be detail oriented, multi-task and produce results.
- Superior organizational skills.
- Strong understanding of cGMP guidelines and FDA regulations related to the pharmaceutical industry *
- Proficient using MS Office applications.*
- Experience with FDA and other regulatory agency requirements
OTHER DETAILS
- This is a full-time position based out of Roxboro, NC or Raleigh/Durham, NC.
- Compensation commensurate with experience.
- Background and reference checks required.
- Periodically required to be available to virtually meet with international clients during non-traditional business hours.
PHYSICAL DEMANDS AND WORKING ENVIRONMENT:
- Must be able to lift, carry and balance up to 50 pounds
- While performing the duties of this job, the employee is regularly required to perform grasping, talking, hearing, seeing and repetitive motions.
- Ability to walk and stand for long periods of time (4-6 hours) with frequent kneeling and bending.
- Working in limited climate-controlled facilities and may experience extreme heat or cold
- Work with heavy fumes, plants, airborne particles and chemicals
- Must be comfortable working with and around heavy machinery
- May experience moderately high noise levels
EQUAL EMPLOYMENT OPPORTUNITY STATEMENT
Open Book Extracts is proud to be an equal opportunity employer. We embrace diversity and are committed to building a team that represents a variety of backgrounds, perspectives, and skills. The more inclusive we are, the better our work will be.
Apply for this job with Open Book Extracts
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.
Day Three Labs (DTL) is a cannabinoid CPG ingredient manufacturer specializing in the development and commercialization of novel cannabis product solutions. With headquarters in Denver, Colorado, and research operations in Israel. DTL can tap into over 50 years of scientific research and plant studies to reimagine existing cannabis offerings by delivering Israeli innovation and ingenuity to the global cannabis industry. Our portfolio includes proprietary pharmaceutical-grade infusion technologies with the objective of handing control of the cannabis experience to the everyday consumer.
DTL's production partner on the hemp-derived cannabinoid side of the cannabis industry is Open Book Extracts (OBX), located north of Durham, North Carolina. DTL is looking for a Lab Technician who will be responsible for directly supporting operations and manufacturing efforts in OBX's production facility. The lab technician will perform general lab and production operations, duties crucial to the overall manufacturing process. This role includes, but is not limited to, operating and maintaining lab equipment, adhering to approved SOPs, ensuring high quality production, and maintaining a clean and safe laboratory working environment. This role will report directly to the Chief Manufacturing Officer (CMO) and will include frequent communication with senior-level employees and external clients.
Job Duties & Responsibilities:
Operate, clean and maintain lab instruments and equipment such as - a Tangential Flow Filtration Skid (TFF), Spray Dryer, and Microplate Reader.- Closely follow approved manufacturing Standard Operating Procedures (SOPs).
- Ensure the CMO is informed of progress, priorities, deadlines, and regulatory challenges.
- Follow all SOPs regarding Quality Control/Quality Assurance.
- Maintain a clean and safe work environment.
- Independently perform special projects that require a combined knowledge of technical operations.
- Complete accurate and detailed production batch sheets and maintain an up-to-date laboratory notebook.
- Be available for job-related tasks during regular business working hours and occasionally during off-hours (evenings and weekends).
- Participates in team driven activities to facilitate on- going production improvements and GMP standards.
- Other duties as required.
Qualifications & Skills:
- 3+ years of experience working in a laboratory and/or manufacturing environment.
- Experience in a life science (biotech, pharma, diagnostics, chemistry, or biology) or cannabis company is preferred.
- Ability to thrive in a fast-paced environment and operate independently with a high sense of urgency.
- Ability to anticipate needs, consistently strive for excellence and exercise good judgment. Resourcefulness and responsiveness are essential.
- Ability to observe strict confidentiality in all aspects of services provided.
- Strong interpersonal skills with the ability to interface effectively with a wide variety of internal and external clients.
- Highly developed written communication skills, including report writing, presentations, email correspondence and verbal communication skills.
- Excellent calendar management skills and demonstrated history of complex scheduling with consistent follow through.
- Ability to quickly learn how to operate, maintain, and troubleshoot laboratory equipment.
- Strong understanding of cGMP guidelines and FDA regulations related to the pharmaceutical industry
- Proficient in MS Office Suite, HubSpot or other CRM systems.
- High School diploma required. College degree is preferred.
DTL offers a competitive benefits package that contributes to employees' overall total compensation package.
Posting Instructions
Please send your application to [email protected].
Applications without a cover letter will not be considered.
DTL is an equal opportunity employer and will not discriminate against an applicant or employee based on race, color, religion, creed, national origin or ancestry, sex, sexual orientation, gender identity, age, physical or mental disability, veteran or military status, genetic information, union membership, or any other legally recognized protected basis under federal, state, or local law. The information collected by this application is solely to determine suitability for employment, verify identity, and maintain employment statistics on applicants.
Applicants with disabilities may be entitled to reasonable accommodation under the Americans with Disabilities Act and certain state or local laws. A reasonable accommodation is a change in the way things are normally done which will ensure an equal employment opportunity without imposing undue hardship on DTL. Please let us know by emailing [email protected] if you need assistance completing this application or to otherwise participate in the application process.
Apply for this job with Open Book Extracts
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.
The Company
Open Book Extracts is the complete source for all your hemp-derived cannabinoids, including wholesale raw ingredients, finished goods, and custom solutions - the singular destination for excellence in cultivation, extraction, processing, manufacturing, R&D, traceability, and fulfillment.
Job Summary
We are looking for an experienced Manufacturing Manager/Director (experience dependant) to oversee the manufacturing of finished goods for a wide range of ingestible products in a cGMP facility. You will be responsible for running and scaling this business line, and implementing systems to ensure on-time production for third party clients. We expect you to possess strong project management, team building, and process improvement skills with relevant experience in consumer products and/or food manufacturing. Ability to direct personnel towards maximum performance will set you apart as a leader. Decision-making, problem-solving, and cross departmental communication will take up a great part of your day. The goal is to ensure an efficient and productive manufacturing process that meets customer requirements. This position reports to the Chief Operating Officer or Chief Strategy Officer.
Responsibilities
- Design and implement operational systems to ensure on-time manufacturing, accurate quoting, and forecasting.
- Direct hiring and staff management with executive collaboration and approval, including making organizational chart recommendations required to meet objectives.
- Oversee staff management of both full time employees and part-time labor as needed to meet objectives.
- Lead cross departmental collaboration liaising with QA/QC, product development, facility + equipment, supply chain, fulfillment, and sales departments.
- Provide input to the Equipment and Facilities team regarding new equipment selection, commissioning, and repair on an ongoing basis.
- Organize workflow to meet specifications and deadlines.
- Identify and implement team goals including KPI's on a daily, monthly, and quarterly basis.
- Ensure accurate customer lead time quotes, cost estimates, and collaborate with the finance, product development, procurement, and sales departments for alignment.
- Prepare budgets as directed by the finance department.
- Monitor production to resolve issues as they arise and communicate schedule impacts cross departmentally to enable sales to manage customer communication.
- Supervise and evaluate performance of production personnel (quality inspectors, workers etc.)
- Determine the amount of necessary resources (workforce, raw materials, packaging materials) to be successful on an ongoing basis.
- Deploy and implement a rigorous culture of quality control and collaborate with the Quality team to ensure compliance with with the numerous certifications at the facility including, but not limited to cGMP (111 and 117), PCQI, Organic, Halal, Kosher, NASC.
- Support quality assurance department during customer and regulatory audits.
- Enforce health and safety precautions including adherence to OSHA protocols.
Skills and Abilities
- Experience managing and building teams in a cGMP and OSHA compliant environment.
- Deep knowledge of production management.
- Understanding of quality standards and health & safety regulations.
- Knowledge of performance evaluation and budgeting concepts.
- Experience in reporting on key production metrics.
- Proficient in MS Office and ERP software.
- Outstanding communication ability.
- Excellent organizational and leaderships skills.
- Attention to detail, and a natural problem solver.
- Strong decision-making skills and a results-driven approach.
- BSc/Ba in business administration or relevant field is preferred.
Education and Experience
- Minimum 5 years relevant experience in a production management leadership position. Bachelor's degree required, graduate degree in a relevant field a plus. Cannabis, hemp, consumer products, food production, or white/private label experience will distinguish you.
Additional Details:
- This is a full-time position based out of Roxboro, NC or Raleigh/Durham, NC.
- Flexibility to work days/evenings/weekends depending on production schedules required
Physical Demands and Working Environment:
- May be required to stand and/or walk for extended periods of time. Must be able to lift, carry and balance up to 50 pounds
- While performing the duties of this job, the employee is regularly required to perform grasping, talking, hearing, seeing and repetitive motions.
- Ability to walk and stand for long periods of time (4-6 hours) with frequent kneeling and bending.
- Working in limited climate-controlled facilities and experience extreme heat or cold
- Work with heavy fumes, plants, airborne particles and chemicals
- Must be comfortable working with and around heavy machinery
- May experience moderately high noise levels
Equal Employment Opportunity (EEO) Statement
Open Book Extracts is proud to be an equal opportunity employer. We embrace diversity and are committed to building a team that represents a variety of backgrounds, perspectives, and skills. The more inclusive we are, the better our work will be.
This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.
Apply for this job with Open Book Extracts
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.
The Company
Open Book Extracts is the complete source for all your hemp-derived cannabinoids, including wholesale raw ingredients, finished goods, and custom solutions - the singular destination for excellence in cultivation, extraction, processing, manufacturing, R&D, traceability, and fulfillment.
Job Summary
The Master Scheduler is responsible for planning, scheduling, coordinating, and monitoring products through the complete production cycle. Expertise in supply chain, production scheduling, inventory management, forecasting, and inventory management software is required. Strong initiative, attention to detail, communication skills, as well as strict adherence to local, state and federal regulations are critical to this role. This position reports to the Manufacturing Manager and also works closely with the Controller, Product Development, Sales, Fulfillment, and Executive teams.
Responsibilities
- Plan, schedule, coordinate, and monitor products through the complete production cycle.
- Maintain accurate inventories of raw materials and packaging materials needed for production.
- Communicate any obstacle impacting production efficiency on a daily and forward-looking basis.
- Create daily production schedules and ensure that all relevant staff members receive the production schedule.
- Record and communicate production progress daily.
- Check the quality of products to ensure that they meet client expectations and ensure that the quantity and specifications of products are correct.
- Determine optimized raw materials and packaging materials procurement and inventory based on Company orders and objectives with its clients.
- Collaborate with the executive, financial/accounting, manufacturing, and sales teams to ensure production alignment with company goals and objectives.
- Participate in meetings with clients for production scheduling input as needed.
- Implement inventory control procedures and integration with the company's inventory tracking software.
- Become an expert administrator of the company's inventory control software and train employees as necessary.
- Perform analytics and forecasting for manufacturing process and efficiency improvements.
- Convert rolling sales forecasts into detailed production scheduling.
- Collaborate with the fulfillment manager and perform daily quality control checks on shipment organization for finished goods and bulk wholesale orders.
- Monitor and reconcile all packaging sessions to ensure compliance between Company's inventory software, and physical inventory.
- Establish periodic and monthly inventory reconciliation procedures.
- Exercise significant authority over shipping label storage, creation, and accuracy.
Skills and Abilities
- Experience managing and building teams in a cGMP and OSHA compliant environment.
- Deep knowledge of production management.
- Prior experience in manufacturing, supply chain management or a related field a plus
- Excellent planning and time management skills.
- Excellent computer literacy skills and proficiency in MS Office and ERP software.
- Excellent interpersonal and communication skills.
- Understanding of quality standards and health & safety regulations.
- Knowledge of performance evaluation and budgeting concepts.
- Experience in reporting on key production metrics.
- Outstanding communication ability.
- Excellent organizational and leaderships skills.
- Attention to detail, and a natural problem solver.
- Strong decision-making skills and a results-driven approach.
- BSc/Ba in business administration or relevant field is preferred.
Education and Experience
- Bachelor's degree in related fields. Graduate degree desired.
- APICS certification(s) desired.
- 5+ years of management or related experience required.
- Cannabis, hemp, consumer products, food production, or white/private label experience desired.
- Strong software, analytics, and computer skills required.
- Thorough understanding of cGMP and/or ISO manufacturing operations desired.
- Comfortable working in a start-up environment.
- Proven project management, communication, leadership, and collaboration skills required.
Additional Details:
- This is a full-time position based out of Roxboro, NC or Raleigh/Durham, NC.
- Flexibility to work days/evenings/weekends depending on production schedules required
Physical Demands and Working Environment:
- May be required to stand and/or walk for extended periods of time. Must be able to lift, carry and balance up to 50 pounds
- While performing the duties of this job, the employee is regularly required to perform grasping, talking, hearing, seeing and repetitive motions.
- Ability to walk and stand for long periods of time (4-6 hours) with frequent kneeling and bending.
- Working in limited climate-controlled facilities and experience extreme heat or cold
- Work with heavy fumes, plants, airborne particles and chemicals
- Must be comfortable working with and around heavy machinery
- May experience moderately high noise levels
Equal Employment Opportunity (EEO) Statement
Open Book Extracts is proud to be an equal opportunity employer. We embrace diversity and are committed to building a team that represents a variety of backgrounds, perspectives, and skills. The more inclusive we are, the better our work will be.
This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.
Apply for this job with Open Book Extracts
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.
Open Book Extracts
Technologist, Product Development
THE COMPANY
Headquartered in Roxboro, N.C., Open Book Extracts is a cGMP-certified manufacturer of premium plant-based cannabinoid products, aiming to be the industry's true north by delivering premium products, exceptional service, and industry-leading transparency. With control of the entire supply chain, a state-of-the-art extraction campus near North Carolina's Research Triangle, proprietary refinement and conversion methods backed by a growing IP portfolio, and a team of PhD chemists and seasoned business leaders, OBX is positioned to be the trusted partner for global brands seeking to enter the marketplace. OBX Asia, with its headquarters in Hong Kong, provides strategic guidance and on-the-ground support for our Asia customers.
THE POSITION
We are seeking an entry level Product Formulation Technologist who will be responsible for assisting the development of new products from concept to commercialization that support company growth. Position will also assist enhancement and improvement upon current products. Serves as a technical aid that supports product development and improvements, quality improvements, and customer requests. Assist the R&D team with the activities and operations required to complete the functions of the research and development department. Study and comprehend all policies, procedures and operational guidelines set by the management team. Is responsible for generation of representative pilot samples and production batches for internal and external customer evaluations through the use of appropriate scale-down process models. Other duties include assisting process optimization and product enhancement activities.
RESPONSIBILITIES
- Assists new product process from development to commercialization, within defined company, industry, and regulatory parameters*
- Executes lab scale and small batch experimentation to support all levels of formulation, analytics, and processing for multiple cannabis-based research.
- Assists in new research and development procedures and techniques under the supervision of the Senior Formulation Scientists
- Executes individual project goals and follows outlined priorities for research and development endeavors.
- Records and aids maintenance of technical documents, databases, and reports.
- Follows SOPs, formulation spreadsheets, inventories, traceability logs, tracking logs, etc.
- Aids in the maintenance of inventories for research and developments raw materials, chemicals, and equipment.
- Follows complex instructions and formulations in the preparation of cannabis extract, concentrates, and infused products.
- Follows guidelines for acceptance and testing of chemical raw-materials in finished blends
- Operates within company's Quality Management System
- Participates in team driven activities to facilitate on- going production improvements or new product development projects.
- Familiarity with scientific principles and research and development laboratory experience. Can follow written direction and maintain a laboratory notebook.
- Practices highly sterile laboratory cleaning procedures throughout the facility with focus and personal contributions towards a clean and organized assigned work area at the end of the assigned shift.
- Capability of troubleshooting, fixing, and services a wide range of equipment and software with little to no assistance.
- Promotes a positive can-do attitude
- Communicates effectively and consistently in writing and verbally with all levels of staff
- Collaborates in cross functional teams to meet research and development schedules.
- Understands and meets daily goals, expectations, and deadlines.
- Consistently enforces all company policies & procedures.
- Conducts stability studies on formulations
- Writes necessary documents for manufacturing feasibility
- Prepares product registration documentation and product chemistry packages to meet regulatory requirements.
- Responsible for batch production from pilot scale to process validation.
- Performs additional special projects as assigned.
EXPERIENCE
- Bachelor's degree preferred or equivalent experience in research and development, chemical or pharmaceutical manufacturing
- Experience with HPLC testing and other stability testing methods.
- Proven problem-solving skills and track record of successful technical accomplishments
- Ability to establish and maintain effective working relationships with all employees.
- Ability to take direction and initiative.
- Skills in intermediate math.
- Excellent verbal and written communication skills with coworkers and management.
- Enthusiasm for research and formulating/improving product formulations.
- Ability to be detail oriented, multi-task and produce results.
- Superior organizational skills.
- Strong understanding of cGMP guidelines and FDA regulations related to the pharmaceutical industry *
- Proficient using MS Office applications.*
- Experience with FDA and other regulatory agency requirements
OTHER DETAILS
- This is a full-time position based out of Roxboro, NC or Raleigh/Durham, NC.
- Compensation commensurate with experience.
- Background and reference checks required.
- Periodically required to be available to virtually meet with international clients during non-traditional business hours.
PHYSICAL DEMANDS AND WORKING ENVIRONMENT:
- Must be able to lift, carry and balance up to 50 pounds
- While performing the duties of this job, the employee is regularly required to perform grasping, talking, hearing, seeing and repetitive motions.
- Ability to walk and stand for long periods of time (4-6 hours) with frequent kneeling and bending.
- Working in limited climate-controlled facilities and may experience extreme heat or cold
- Work with heavy fumes, plants, airborne particles and chemicals
- Must be comfortable working with and around heavy machinery
- May experience moderately high noise levels
EQUAL EMPLOYMENT OPPORTUNITY STATEMENT
Open Book Extracts is proud to be an equal opportunity employer. We embrace diversity and are committed to building a team that represents a variety of backgrounds, perspectives, and skills. The more inclusive we are, the better our work will be.
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