About this opportunity
MMQCI lists this QC Technical Lead opportunity in saco, Maine. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Put Your Technical Expertise to Work in Quality Control!
MMQCI is seeking a Quality Control Technical Lead who enjoys overseeing and executing quality control release testing of MMQCI’s products using a variety of complex molecular test systems, performing statistical data analysis, troubleshooting instrumentation, data trends, and unexpected results.
The Technical Lead is a passionate problem-solver with a strong background in clinical molecular laboratory techniques. Responsibilities also include coordinating schedules, ensuring testing materials are available, and helping ensure QC lab deliverables are completed on time. The Technical Lead maintains a contamination-free lab by ensuring stringent adherence to established protocols, works cross-functionally with a variety of internal teams, and may occasionally interact with customers on technical questions and troubleshooting. This role reports to the Manager of Manufacturing Operations and is expected to work independently with minimal supervision.
What You Will Get to Do
Use technical expertise in molecular clinical diagnostic testing methods, instrumentation, and quality control principles and practices to mentor and train others
Performs and coordinates testing of MMQCI products for product releases, special testing, and investigations, while ensuring accurate test results and timelines are met
Author, review, and continuously improve QC standard operating procedures (SOPs)
Assists others with data analysis and review and performs QC-related issue/failure investigations, CAPA projects, and testing/evaluation for customer complaints
Helps coordinate transfer of new products/assays from R&D to QC. Collaborates with R&D and Discovery to establish/implement new test methods and release criteria
Stays current with equipment, technologies, and methodologies employed in sample preparation and testing of DNA and RNA products
Summarizes and communicates issues and data. Able to generate concise summary in written communications. Presents data to others as needed
Follows MMQCI’s quality systems in accordance with current Good Manufacturing Practice (cGMP)
Helps ensure proper product handling and cross-contamination practices are being followed in the QC area. May include training of cross functional personnel
Role model to help build a culture that understands and supports MMQCI’s quality plan, the need for accuracy, attention to detail, risk mitigation, contamination prevention, and continuous improvement
Carefully and consistently follows all MMQCI protocols to protect product integrity, including repetitive cleaning of benches, and donning of gloves, booties, lab coats, facemasks and hairnets and other Personal Protective Equipment (PPE) as appropriate
Required Skills & Experience
M.S. in Biology / Life Sciences with Molecular Biology focus and 3+ years applicable work experience or B.S. and 6+ years applicable work experience. Applicable work experience would be either molecular diagnostic clinical laboratory or performing testing in a medical device industrial setting. Medical Technologist MT (ASCP) certification is strongly preferred
Demonstrated mastery of a broad array of molecular biology assays across multiple testing platforms, featuring exceptional lab proficiency/pipetting accuracy
Proficient in lab techniques supporting molecular biology including accurate pipetting skills
Exceptional ability to identify questionable data trends or results and successfully lead root-cause investigations
Experience leading project teams, performing risk assessments, and successfully implementing new laboratory protocols
Proficiency in statistical techniques applicable to medical devices or patient sample monitoring (experience with JMP software is a plus)
Experience working with products requiring special handling and work area protocols to prevent contamination. Comfortable in a clean room laboratory environment where gowning and aseptic technique are required
Good communication skills, written and oral, strong computer skills, excellent mentorship and training skills
Experience in a CLIA, GMP or ISO certified industrial environment is required
Must be able to stand for several hours, lift approximately 30 lbs., reach overhead, and be able to climb ladder to reach and put away items on high shelves
Must have visual acuity to inspect testing materials, well plates, and analyze color coded results
Why You’ll Love Working Here
Opportunity to make a meaningful impact within a growing diagnostic company
Collaborative, mission-driven team environment
Competitive compensation and benefits
Benefits We Offer
Medical, dental, and vision insurance
401(k) retirement savings plan
Company profit sharing program
Paid time off: including vacation, holidays, and sick leave
Paid Parental Leave Program
The pay range for this position is $65,500 to $124,000 annually
Get to know the MMQCI team!
Maine Molecular Quality Controls, Inc. (MMQCI) designs, develops, manufactures, and sells unique quality control products used by hospital laboratories and manufacturers to monitor the accuracy of tests for genetic, oncologic, and infectious diseases. MMQCI has proprietary technologies to stabilize DNA and RNA for use as quality controls and continues to pursue the discovery of novel techniques useful for the development of new quality control products.
MMQCI is conveniently located in beautiful southern coastal Maine, minutes from the MaineTurnpike, Portland International Jetport, and less than 2 hours from Boston.Close by are fabulous Portland restaurants, sandy beaches, and a plentiful supply of Maine lobsters! Many terrific outdoor activities are easily accessible including hiking, biking, kayaking, fishing,skiingand snowshoeing.We’reina state-of-the-artfacility,locatedin Saco, right next to the Eastern Trail. Come join us!
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Worksite address
saco, ME, 04072, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.