i-Pharm GxP
Overview
Senior Quality Control Microbiologist position in Norwood, MA. On-site role with 6-month initial contract. Job Title:
Senior Quality Control Microbiologist Location:
Norwood, MA – on site Rate:
Up to $25/h W2 Duration:
6-Month Contract Initially Shift Pattern:
Monday - Friday, First Shift We are seeking a
Senior Quality Control Microbiologist
with 3–5 years of relevant cGMP laboratory experience to join a high-profile biopharmaceutical manufacturing facility. This role will support cGMP QC activities for raw materials, drug substances, and finished products, ensuring compliance with regulatory standards and contributing to life-saving therapies. Responsibilities
Perform QC microbiology testing including bioburden, endotoxin, sterility, TOC, and enumeration. Maintain and troubleshoot laboratory equipment, and manage QC lab supplies. Draft, revise, and maintain SOPs, protocols, and reports. Participate in quality system activities such as deviations, CAPAs, change controls, and investigations. Support audits and continuous improvement initiatives. Maintain a safe and compliant laboratory environment. Qualifications
STEM degree with 3–5 years’ cGMP laboratory experience, preferably in microbiology. Proficient in aseptic techniques, microbiology methods, and laboratory instrumentation. Strong troubleshooting, documentation, and communication skills. Familiarity with Microsoft Office, LIMS, SAP, and eQMS. Ability to manage multiple projects in a fast-paced environment.
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Senior Quality Control Microbiologist position in Norwood, MA. On-site role with 6-month initial contract. Job Title:
Senior Quality Control Microbiologist Location:
Norwood, MA – on site Rate:
Up to $25/h W2 Duration:
6-Month Contract Initially Shift Pattern:
Monday - Friday, First Shift We are seeking a
Senior Quality Control Microbiologist
with 3–5 years of relevant cGMP laboratory experience to join a high-profile biopharmaceutical manufacturing facility. This role will support cGMP QC activities for raw materials, drug substances, and finished products, ensuring compliance with regulatory standards and contributing to life-saving therapies. Responsibilities
Perform QC microbiology testing including bioburden, endotoxin, sterility, TOC, and enumeration. Maintain and troubleshoot laboratory equipment, and manage QC lab supplies. Draft, revise, and maintain SOPs, protocols, and reports. Participate in quality system activities such as deviations, CAPAs, change controls, and investigations. Support audits and continuous improvement initiatives. Maintain a safe and compliant laboratory environment. Qualifications
STEM degree with 3–5 years’ cGMP laboratory experience, preferably in microbiology. Proficient in aseptic techniques, microbiology methods, and laboratory instrumentation. Strong troubleshooting, documentation, and communication skills. Familiarity with Microsoft Office, LIMS, SAP, and eQMS. Ability to manage multiple projects in a fast-paced environment.
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