Quality Control Microbiology Analyst

$35.00/hr - $38.00/hr

Title: Quality Control Microbiology Analyst II

Location: Norton, MA

Duration: 6 Months+

Overview: The Quality Control Microbiology Analyst II plays a role in supporting the department's efforts to maintain the highest standards of quality and compliance from development through to commercialization. In addition to executing routine and non-routine testing in support of development through commercial programs, the Analyst II may participate in data trending, investigations, and laboratory operations. By ensuring these critical activities are executed within project milestones and timelines, the Analyst II contributes to routine laboratory operations, thereby enhancing the overall efficiency and effectiveness of the QC functions.

This position is onsite and will be primarily located in Norton, MA, with occasional responsibilities at a secondary location in Cambridge, MA.

• Perform routine and non-routine microbiological assays (bioburden, TOC, endotoxin, conductivity), with increasing complexity, to support critical utility samples, in-process samples, and product release, following established SOPs
• Maintain up-to-date training records, adhere to the testing schedule, and ensure the timely completion of all assignments to support the seamless operation of QC activities and uphold the department's commitment to meeting project timelines and quality metrics
• Assist in the maintenance of laboratory equipment and inventory to ensure smooth laboratory operations
• Ensure data is submitted timely; may qualify as a data reviewer to ensure timely and efficient data availability.
• Perform role‑specific operational assignments (e.g., critical utility sampling, environmental monitoring, product testing, etc.).
• Contribute to the revision and updating of controlled documents, including SOPs, work instructions, and test methods, to ensure continuous improvement and compliance with ALNY requirements
• Adhere to internal standards, policies, and SOPs, as well as regulatory and industry standards (e.g., GMP, GLP, ICH guidelines) to maintain the highest levels of quality and compliance.
• Collaborate with QC and cross‑functional teams to ensure seamless quality control operations and to support the collective company goals
• Participate in inspection readiness activities as well as supporting onsite audits and inspections, as needed.
• Support continuous improvement initiatives aimed at enhancing QC processes and procedures, increasing laboratory efficiency and effectiveness.
• Collaborate with other organizational functions including Manufacturing, Materials Management, and Quality Assurance to ensure alignment with overall business goals.
• Support various quality events as needed (i.e., investigations, deviations, CAPAs, change controls)

• B.S. in biology, biochemistry, chemistry, or related scientific field;
  Associate’s degree, Biotech Certificate, or equivalent considered
• Pharmaceutical/Biotech industry experience with 2 years in a regulated laboratory setting, Quality Control, or equivalent
• Demonstrated prior experience/understanding of microbiology testing and EM/CU sampling
• Experience with quality events preferred (i.e., investigations, deviations, CAPAs, change controls)
• Data analysis experience preferred
• Ability to work under direction, with attention to detail, in an environment where priorities shift
• Good communication and teamwork abilities, capable of working effectively in a collaborative environment
• Knowledge of LIMS, Excel, Word, and PowerPoint is helpful

Mid‑Senior level

Contract

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Pharmaceutical Manufacturing and Biotechnology Research