About this opportunity
Zenith LifeScience lists this Quality Control Scientist opportunity in westborough, Massachusetts. Review the employer’s description below for duties, qualifications and application requirements.
Job description
The Scientist II QC Microbiology serves as senior technical subject matter expert responsible for overseeing microbiological testing programs supporting GMP operations. This role provides technical leadership across QC Microbiology and Manufacturing by ensuring effective microbiological testing, mentoring laboratory staff, supporting quality systems and delivering aseptic technique training to maintain compliance with GMP and contamination control requirements.
Job Responsibilities:
Serve as subject matter expert for microbiological testing programs including environmental monitoring, sterility, endotoxin, mycoplasma, microbial identification, and contamination control.
Support QC Microbiology Senior Manager in oversight of laboratory operations, technical initiatives, and microbiological program execution.
Develop and deliver aseptic technique and contamination control training for manufacturing and QC personnel to maintain compliance with GMP and cleanroom practices.
Track and support quality system activities including deviations, investigations, CAPAs, Change Control and trending associated with QC microbiology operations.
Review and approve microbiological data, protocols, quarterly reports , SOPs and other technical documentation.
Lead data trending and interpretation of environmental monitoring and microbiological data to identify risks and support contamination control strategy.
Provide technical leadership and mentorship to microbiologists and junior scientist within QC microbiology laboratory.
Author and review SOPs, protocols, validation reports, investigation reports and technical documents in accordance with GMP requirements.
Lead or support method qualification, validation, and technology implementation for microbiological assays.
Collaborate cross-functionally with Manufacturing, QA , Facilities and other teams to support manufacturing operations and process improvements.
Support regulatory inspections, audits and responses by providing technical justification and documentation.
Required Qualifications
BS degree in Biology/Microbiology with 10+ years or M.S. with 6+ years of relevant experience in a GMP QC microbiology laboratory.
Demonstrated advanced expertise in microbiological testing including environmental monitoring, bioburden, endotoxin, sterility, mycoplasma and microbial identification.
Experience supporting aseptic manufacturing environments and cleanroom operations.
Demonstrated experience mentoring laboratory staff and providing technical training.
Strong knowledge of cGMP regulations and microbiological control strategies.
Excellent technical writing and communication skills.
Strong interpersonal skills, highly collaborative within a multi-disciplinary team and contributes to a supportive and positive work environment.
This role is scheduled to work during day shift (8 am to 5 pm) Monday to Friday.
Flexibility to work weekend hours may be required to support GMP Operations.
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Worksite address
westborough, MA, 01581, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.