Microbiologist / Pharma Manufacturing

Microbiologist This organization is a well-established and reputable medium-sized company in the CPG sector. Known for its focus on innovation and high-quality standards, the company is dedicated to delivering exceptional products to its customers while fostering a supportive and professional work environment.

Job Description Perform and oversee microbiological testing of raw materials, in-process materials, finished products, and packaging components per applicable regulatory and internal specifications. Author, review, and revise Standard Operating Procedures (SOPs), validation protocols, test methods, and controlled documents. Serve as the microbiology subject matter expert during audits, inspections, and product quality investigations. Oversee environmental monitoring programs (air, surface, water, personnel) and trend/report results. Develop, execute, and document validation protocols for cleaning, equipment, and process changes. Collaborate cross-functionally with Quality, Manufacturing, and Sanitation teams on microbiological risk and process impact. Conduct validation activities including environmental monitoring assessments, cleaning verification, and risk evaluations. Support contamination control strategies and microbiological risk assessments across departments. Train and mentor junior staff on laboratory methods, aseptic technique, and compliance requirements. Maintain and troubleshoot laboratory equipment while ensuring ongoing GMP and GLP compliance. Stay current on industry trends, emerging pathogens, and regulatory updates. Review outsourced microbiological results and investigate discrepancies. Ensure adherence to laboratory safety practices and response procedures. ATP testing, swabbing). Develop and implement microbiological testing methods, including rapid methods where applicable. Analyze complex data, identify trends, and present findings to management. Lead investigations into out-of-specification (OOS) or atypical results, including root cause analysis and CAPA. Support customer complaint investigations related to microbiological quality. Provide input on specifications, regulatory compliance, and client-facing discussions. Deliver microbiology and GMP training to laboratory and production personnel. Maintain accurate documentation in alignment with data integrity and traceability requirements. Support facility cleaning and sanitization programs. Participate in internal audits, supplier audits, and regulatory inspections. MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants. Michael Page will consider for employment qualified applicants with criminal histories in a manner consistent with the Los Angeles Fair Chance Initiative for Hiring Ordinance.

The Successful Applicant A successful Microbiologist should have: Minimum 3+ years of experience in a GMP-regulated microbiology laboratory (dietary supplements, pharmaceuticals, or food manufacturing preferred). Experience working with applicable regulatory frameworks (e.g., Demonstrated experience with method validation, investigations, and technical report writing. Familiarity with laboratory documentation practices and data integrity principles. Experience using LIMS or similar digital laboratory systems. Hands-on experience with microbiological testing (e.g., APC, yeast and mold, coliforms, pathogens). Experience supporting audits or inspections (FDA, NSF, UL, or similar).

Comprehensive 401(k) retirement plan. Opportunities for professional growth and development in the FMCG industry. If you're passionate about microbiology and want to make an impact in the CPG industry, we encourage you to apply!