JTL Services, Inc.
Overview
JTL Services, Inc. has been retained to find top candidates for this growing business.
Responsibilities
Responsible for the receipt, preparation, analysis, and timely reporting of results from the production samples, incoming raw materials, or investigatory samples.
Execute analytical and microbiological testing to support GMP production of commercial and pre-commercial RNA-based products, following approved methods and batch records.
Conduct the analysis and routine maintenance of the complex instrumentation and wet chemical determinations conducted in the laboratory.
Responsible for always maintaining a safe work environment for all employees.
Support the analytical needs of production research, product and process support, development of sample methods, preparation of standards, and, when needed, support the development of in-house test methods of analysis to solve product and process challenges.
Participate in daily Quality Control operations to support production and ensure compliance with the Quality Management System.
Adhere to ensuring that timely and accurate sample processing, data analysis, and reporting are consistent.
Perform in-process and final product testing, including HPLC, wet chemistry, gel electrophoresis, and enzymology.
Monitor and maintain method QC statistics, perform QC release of intermediates and final products, and troubleshoot analytical methods as needed.
Contribute to continuous improvement initiatives to enhance quality systems and operational excellence.
Maintain and calibrate laboratory equipment, manage reagent preparation, and oversee inventory and supply chain for quality operations.
Utilize LIMS and QMS platforms for data entry, document control, training, and nonconformance management.
Practice the proper use of personal protective equipment and the proper handling and disposal of commonly used hazardous chemicals in the laboratory.
Education and Qualifications
Bachelor’s degree in a technical field (e.g., Chemistry, Biochemistry, Microbiology, Biotechnology) or equivalent experience.
2+ years of relevant work experience in a biochemical, biotechnology, or food processing environment, including laboratory-based roles.
Experience working in ISO 9001:2015 and/or ISO 17025 certified environments.
Proficiency in laboratory techniques such as HPLC, wet chemistry, gel electrophoresis, and enzymology.
Strong understanding of Quality Control processes, including troubleshooting methods and process control tracking.
Experience with LIMS and QMS software (Document Control, Training, CAPA, Nonconformance Management).
High attention to detail, strong organizational and time management skills, and effective problem-solving abilities.
Proficiency in Microsoft Office tools (Excel, PowerPoint, Word, Outlook, Teams).
Strong communication and leadership skills, with the ability to supervise and mentor team.
Required Skills
Proficiency in laboratory techniques such as HPLC, wet chemistry, gel electrophoresis, and enzymology.
Strong understanding of Quality Control processes, including troubleshooting methods and process control tracking.
Experience with LIMS and QMS software (Document Control, Training, CAPA, Nonconformance Management).
High attention to detail, strong organizational and time management skills, and effective problem-solving abilities.
Proficiency in Microsoft Office tools (Excel, PowerPoint, Word, Outlook, Teams).
Working Conditions
Work is performed in a GMP controlled environment with strict adherence to contamination control and PPE protocols.
This job operates in a professional lab environment. This role routinely uses lab equipment such as computers, HPLC, and analyzers. Tolerance of odors and incidental chemical exposure is required in the laboratory environment.
Requires standing, walking, and hands-on laboratory work for extended periods.
May involve occasional extended hours or weekend work to support production schedules or investigations.
Responsible for maintaining audit readiness through accurate documentation, procedural compliance, and team oversight.
While performing the duties of this job, the employee is regularly required to talk or hear. The employee is frequently required to stand; walk; use hands to finger, handle or feel; and reach with hands and arms.
The employee is occasionally required to sit, climb, balance, stoop, kneel, crouch or crawl. The employee may frequently lift and move up to 15 pounds and occasionally lift and move objects up to 50 pounds.
Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus.
Required to wear all appropriate PPE which may include a lab coat, gloves, dust mask, goggles, safety glasses or a face mask when environment conditions deem necessary.
For more information, send your updated resume to the hiring contact at JTL Services, Inc.
#J-18808-Ljbffr
Responsibilities
Responsible for the receipt, preparation, analysis, and timely reporting of results from the production samples, incoming raw materials, or investigatory samples.
Execute analytical and microbiological testing to support GMP production of commercial and pre-commercial RNA-based products, following approved methods and batch records.
Conduct the analysis and routine maintenance of the complex instrumentation and wet chemical determinations conducted in the laboratory.
Responsible for always maintaining a safe work environment for all employees.
Support the analytical needs of production research, product and process support, development of sample methods, preparation of standards, and, when needed, support the development of in-house test methods of analysis to solve product and process challenges.
Participate in daily Quality Control operations to support production and ensure compliance with the Quality Management System.
Adhere to ensuring that timely and accurate sample processing, data analysis, and reporting are consistent.
Perform in-process and final product testing, including HPLC, wet chemistry, gel electrophoresis, and enzymology.
Monitor and maintain method QC statistics, perform QC release of intermediates and final products, and troubleshoot analytical methods as needed.
Contribute to continuous improvement initiatives to enhance quality systems and operational excellence.
Maintain and calibrate laboratory equipment, manage reagent preparation, and oversee inventory and supply chain for quality operations.
Utilize LIMS and QMS platforms for data entry, document control, training, and nonconformance management.
Practice the proper use of personal protective equipment and the proper handling and disposal of commonly used hazardous chemicals in the laboratory.
Education and Qualifications
Bachelor’s degree in a technical field (e.g., Chemistry, Biochemistry, Microbiology, Biotechnology) or equivalent experience.
2+ years of relevant work experience in a biochemical, biotechnology, or food processing environment, including laboratory-based roles.
Experience working in ISO 9001:2015 and/or ISO 17025 certified environments.
Proficiency in laboratory techniques such as HPLC, wet chemistry, gel electrophoresis, and enzymology.
Strong understanding of Quality Control processes, including troubleshooting methods and process control tracking.
Experience with LIMS and QMS software (Document Control, Training, CAPA, Nonconformance Management).
High attention to detail, strong organizational and time management skills, and effective problem-solving abilities.
Proficiency in Microsoft Office tools (Excel, PowerPoint, Word, Outlook, Teams).
Strong communication and leadership skills, with the ability to supervise and mentor team.
Required Skills
Proficiency in laboratory techniques such as HPLC, wet chemistry, gel electrophoresis, and enzymology.
Strong understanding of Quality Control processes, including troubleshooting methods and process control tracking.
Experience with LIMS and QMS software (Document Control, Training, CAPA, Nonconformance Management).
High attention to detail, strong organizational and time management skills, and effective problem-solving abilities.
Proficiency in Microsoft Office tools (Excel, PowerPoint, Word, Outlook, Teams).
Working Conditions
Work is performed in a GMP controlled environment with strict adherence to contamination control and PPE protocols.
This job operates in a professional lab environment. This role routinely uses lab equipment such as computers, HPLC, and analyzers. Tolerance of odors and incidental chemical exposure is required in the laboratory environment.
Requires standing, walking, and hands-on laboratory work for extended periods.
May involve occasional extended hours or weekend work to support production schedules or investigations.
Responsible for maintaining audit readiness through accurate documentation, procedural compliance, and team oversight.
While performing the duties of this job, the employee is regularly required to talk or hear. The employee is frequently required to stand; walk; use hands to finger, handle or feel; and reach with hands and arms.
The employee is occasionally required to sit, climb, balance, stoop, kneel, crouch or crawl. The employee may frequently lift and move up to 15 pounds and occasionally lift and move objects up to 50 pounds.
Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus.
Required to wear all appropriate PPE which may include a lab coat, gloves, dust mask, goggles, safety glasses or a face mask when environment conditions deem necessary.
For more information, send your updated resume to the hiring contact at JTL Services, Inc.
#J-18808-Ljbffr