Assistant Manager, Quality Assurance
AI summary
Emzor Pharmaceutical Industries Limited is hiring an Assistant Manager, Quality Assurance for its API manufacturing facility in Sagamu, Ogun State. The role involves coordinating QA activities, QMS documentation, validation, batch release, audit compliance, and handling deviations, CAPAs, and product recalls. The position is full-time and targets candidates with 5–8 years of QA experience in pharmaceutical API or regulated chemical manufacturing.
- Full-time role at a leading Nigerian pharmaceutical company
- Based at the API manufacturing facility in Sagamu, Ogun State
- Requires 5–8 years QA experience in pharma API or regulated chemical manufacturing
- Involves QMS coordination, validation, batch release, and audit compliance
- Offers medical insurance, pension, and performance-based bonus
AI job guide
Use this guide to check salary signals, requirements, documents, application steps and safety before you apply.
AI salary guide
Source salary availableThe source lists Competitive salary and performance-based bonus. Confirm the final pay, benefits, contract terms and allowances directly with the employer before accepting an offer.
Can you qualify for this role?
- Required5+ years of relevant experienceThe job post includes a minimum experience signal.
- PreferredPractical evidence in cleaning, Quality Assurance, Quality ManagementThe tags and summary point to skills connected with this role.
- RequiredAvailability to work in Not specifiedThe vacancy is associated with this location.
- UnclearComfort with the Full Time contract termsConfirm hours, duration, probation and benefits at the original source.
Documents to prepare
- Likely requiredUpdated CV
- Role specificCover letter or short employer message
- OptionalProfessional references
- VerifyID or passport only after verifying the employer
Application tips for this job
- Place your strongest Assistant Manager, Quality Assurance evidence in the first half of your CV.
- In your cover letter or employer message, connect your experience to Emzor Pharmaceutical Industries Limited and the role in Not specified.
- Add concrete examples related to cleaning, Quality Assurance, Quality Management, ideally with measurable outcomes or clear responsibilities.
- Follow the instructions from Jobzilla Nigeria; avoid sending documents to unofficial contacts or copied links.
- Confirm the deadline, interview location and employer contact before sharing personal documents.
Source and safety check
- Jobzilla Nigeria
- Original source link available
- Application method is clear
- Deadline not specified
- No major risk signal was detected in the captured text.
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Interview preparation
- What experience makes you a strong fit for this Assistant Manager, Quality Assurance role in cleaning, Quality Assurance?
- How have you handled responsibilities similar to those in this job post?
- Are you available to work in Not specified under the listed contract or schedule?
- Prepare examples with clear responsibilities, tools used and measurable outcomes.
- Review the source and research Emzor Pharmaceutical Industries Limited before the interview.
Ask what the first priorities will be in the role and how success will be measured.
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Original source description
Job Title: Assistant Manager, Quality Assurance
Assistant Manager, Quality Assurance at Emzor Pharmaceutical Industries Limited
⏲
Sep 21, 2026, 12:18 PM
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View all Pharmaceutical jobs
Emzor Pharmaceutical Industries is a leading pharmaceutical company in Nigeria, with over 40 years of excellence in producing high-quality, affordable, and innovative healthcare products. In line with our mission to promote Unlimited Wellness, we are recruiting for various positions at our world-class Active Pharmaceutical Ingredients (API) manufacturing facility in Sagamu, Ogun State.
We are recruiting to fill the position below:
Location: Sagamu, Ogun
Employment Type: Full-time
Role Summary
To support and coordinate Quality Assurance activities including QMS coordination, quality documentation, qualification, validation, batch-related quality review and audit compliance activities.
Key Responsibilities
- Co-ordinate dispatch related activity. To handle the return goods / Recall. To prepare & review APQR. To review TR & COA before batch release
- Co-ordinate audit compliance report of various customer, QMR related activity and vendor audit.
- Perform the qualification of equipment, instrument and validation for process & cleaning as per ICH Q7 guideline.
- Coordinate and fill customer questionnaire. To coordinate for customer queries. To Co-ordinate for Quality Agreement / Technical Agreement. To prepare & review the site quality risk assessment. To coordinate for external communication.
- Prepare & review the quality documents (SMF/VMP/QM etc.) & it’s up-dation. To prepare & review the Technical Agreement / Quality Agreement. To prepare & review QMS trends.
- Co-ordinate, handle and review of change control, deviation, market complaint, OOS, OOT, returned goods, CAPA, QRM, product recall and other QMS related activities. To prepare & review SOPs and other quality related documents as per the requirement. To review the specification / method of analysis / test report.
- Qualifications &
Experience
5-8 years of Quality Assurance
in the pharmaceutical API or regulated chemical manufacturing industry.
B.Pharm./B.Sc./HND in Biochemistry, Microbiology or a related discipline.
What We Offer
Comprehensive medical insurance, pension, and other employee benefits.
A supportive and dynamic work environment with clear career growth opportunities.
Competitive salary and performance-based bonuses.
How to Apply
Interested and qualified candidates should:
Click here to apply online
Application
Deadline:
30th October, 2026.
View all Jobs in Nigeria
Ogun State and 1 other location
Ogun State
,
Sagamu