Emzor Pharmaceutical Industries Limited is a wholly private indigenous pharmaceutical manufacturing group founded in 1984 by Dr. Stella C. Okoli, OON. The company is into the manufacture of high quality pharmaceutical products and medical consumables. Today, Emzor has become a household name in Nigeria and a leader in the pharmaceutical market that is known ...
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We are seeking an experienced and meticulous Microbiology Officer to lead microbiological quality control operations at our Oral Solid Dosage (OSD) facility in Sagamu.
This role is responsible for overseeing microbiological testing activities and environmental monitoring programs to ensure full compliance with cGMP, internal quality systems, and regulatory expectations.
Responsibilities
Coordinate and oversee daily microbiological testing, including raw materials, in-process samples, finished products, and water systems (PW/WFI).
Supervise environmental and personnel monitoring in cleanrooms and other controlled environments.
Review and approve microbiological test reports and ensure data integrity in all records.
Lead qualification, validation, and trend analysis of microbiological methods and EM systems.
Ensure adherence to WHO, NAFDAC, cGMP, and other regulatory guidelines.
Investigate microbiological deviations, OOS results, and oversee implementation of CAPAs.
Provide technical guidance and mentoring to microbiology supervisors and analysts.
Monitor and manage inventory of microbiology lab supplies and consumables.
Prepare technical reports for audits, inspections, and internal reviews.
Collaborate with QA, Production, and Engineering to support compliance and continuous improvement.
Qualification & Experience
B.Sc./M.Sc. in Microbiology, Industrial Microbiology, or a related field.
4 – 6 years experience in pharmaceutical microbiology, preferably in OSD manufacturing.
Proven leadership or coordination experience in microbiological quality control.
Strong knowledge of microbial limit testing, water testing, cleanroom standards, and aseptic techniques.
Familiarity with pharmacopeial and regulatory standards (USP, BP, WHO, NAFDAC).
Key Competencies:
Strong technical expertise in pharmaceutical microbiology and aseptic practices.
Proven ability to lead teams and coordinate cross-functional quality activities.
Sound judgment in investigations, CAPA implementation, and regulatory compliance.
Excellent documentation skills with a focus on data integrity and audit readiness.
Proficient in LIMS, lab software, and Microsoft Office tools.
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