Job description

The Quality Control Lab Supervisor is responsible to supervise and direct the day-to-day activities of the laboratory division.

This role will be on 2nd shift (3:00pm to 11:30pm)

Essential Duties and Responsibilities:

• Responsible for supervising the activities of the analytical staff in a cGMP QC laboratory environment
• Direct/Coordinate the quality lab activities to plan and establish work schedules, and assignments in support of production and organizational goals
• Support laboratory staff; access to training, manage performance and development of staff
• Reports on performance, and metrics for each analyst to QC Manager
• Ensures that all testing is performed in a timely manner and with accuracy to support the release of the product
• Initiates and Performs laboratory investigation when necessary based on the outcome of testing performed.
• Ensures raw material testing for approval and supply chain management is performed, documented, and communicated to the appropriate departments as needed
• Assists with new product development and timelines
• Ability to write/execute protocols, and write reports for method validations
• Perform the qualifications and validations of test methods, and instruments
• Performs impurity, supplier approval, and research testing
• Troubleshoots and maintains instrumentation
• Develop, maintain and communicate all applicable SOP’s (Standard Operating Procedures)
• Maintains proper record keeping, calibration, and repair of analytical instruments to ensure compliance with GLP and GMP
• Reviews and approves laboratory notebooks
• Maintains inventory and ordering of laboratory supplies
• Maintain all housekeeping, regulatory and GMP requirements
• Other duties may be assigned as deemed appropriate by management.

Qualifications:

• Bachelors of Science degree in Science or related field
• 2-5 years previous quality laboratory experience in a fast-paced regulated manufacturing environment preferred.
• Must possess excellent communication (oral and written), organizational, and interpersonal skills with the ability to multitask while working under restrictive timelines.
• Must be proficient with MS Office applications
• Prior experience working in a cGMP/GLP environment required
• Solid critical thinking skills and ability to create new, innovative ways to handle the quality function
• Must be able to read, write, speak, and understand English
• Ability to maintain absolute confidentiality at all times and in all situations
• Must be able to lift, bend, stoop, reach, climb ladder, sit or stand throughout shift
• Must be able to distinguish color and color change

Job Type: Full-time

Pay: From $65,000.00 per year

Benefits:

• 401(k)
• 401(k) matching
• Dental insurance
• Employee assistance program
• Health insurance
• Life insurance
• Paid time off
• Parental leave
• Professional development assistance
• Referral program
• Vision insurance

Schedule:

• 8 hour shift
• Monday to Friday

Work Location: One location

offroadmanagementgroup.com is the go-to platform for job seekers looking for the best job postings from around the web. With a focus on quality, the platform guarantees that all job postings are from reliable sources and are up-to-date. It also offers a variety of tools to help users find the perfect job for them, such as searching by location and filtering by industry. Furthermore, offroadmanagementgroup.com provides helpful resources like resume tips and career advice to give job seekers an edge in their search. With its commitment to quality and user-friendliness, offroadmanagementgroup.com is the ideal place to find your next job.