Associate Manager – Quality Assurance (External Manufacturing)
AI summary
Shalina Healthcare is hiring an Associate Manager – Quality Assurance (External Manufacturing) in Nigeria. The role oversees compliance of externally manufactured pharmaceutical products with GMP, NAFDAC, and WHO standards, manages CMOs, conducts audits, reviews batch documentation, and supports regulatory submissions. Candidates need 8–10 years of QA experience in pharma, preferably with external manufacturing exposure.
- Pharmaceutical QA leadership role focused on external manufacturing and CMO oversight
- Requires 8–10 years of QA experience in the pharmaceutical industry
- Strong emphasis on GMP, NAFDAC, and WHO regulatory compliance
- Involves audits, batch release, deviations, CAPA, and change control management
- Application is via an online link provided on the posting
AI job guide
Use this guide to check salary signals, requirements, documents, application steps and safety before you apply.
AI salary guide
Not enough public dataNot enough public salary data is available for this exact role. Before applying, prepare to ask about gross pay, benefits, contract length, probation period, transport and any allowances.
Can you qualify for this role?
- Required8+ years of relevant experienceThe job post includes a minimum experience signal.
- PreferredPractical evidence in associate manager, mid-senior level, quality assuranceThe tags and summary point to skills connected with this role.
- RequiredAvailability to work in Not specifiedThe vacancy is associated with this location.
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 Associate Manager – Quality Assurance (External Manufacturing) evidence in the first half of your CV.
- In your cover letter or employer message, connect your experience to Shalina Healthcare and the role in Not specified.
- Add concrete examples related to associate manager, mid-senior level, quality assurance, 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.
- Prepare a polite question about pay, benefits and contract terms for later interview stages.
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.
Never pay for interviews, shortlisting, medical checks, uniforms, or job placement. Confirm every application at the original source before sharing personal documents. Report suspicious listing.
Interview preparation
- What experience makes you a strong fit for this Associate Manager – Quality Assurance (External Manufacturing) role in associate manager, mid-senior level?
- 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 Shalina Healthcare 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
The Associate Manager – Quality Assurance (External Manufacturing) is responsible for overseeing and ensuring compliance of all externally manufactured pharmaceutical products with regulatory requirements, company quality standards, and GMP guidelines. This role involves managing contract manufacturing organizations (CMOs), conducting audits, reviewing documentation, and ensuring product quality throughout the supply chain. Key Responsibilities: External Manufacturing Oversight: Ensure all contract manufacturers comply with GMP, regulatory, and company quality standards. Act as the primary QA contact for all external manufacturing partners. Vendor Qualification & Audits: Prepare audit reports and follow up on corrective and preventive actions (CAPAs). Perform qualification, requalification, and periodic audits of CMOs, suppliers, and service providers. Batch Documentation & Release: Review and approve batch manufacturing records, analytical reports, and related documents from CMOs. Support or authorize batch release in compliance with regulatory requirements. Quality Systems Management: Ensure implementation of quality systems at external sites (deviations, change controls, CAPA, OOS/OOT). Monitor and track quality metrics for external manufacturing operations. Regulatory Compliance: Ensure products meet NAFDAC, WHO, and other applicable regulatory requirements. Support regulatory submissions and inspections related to external manufacturing. Deviation & Investigation Handling: Review and approve deviations, investigations, and CAPAs from external partners. Ensure timely closure and effectiveness of corrective actions. Change Control Management: Evaluate and approve changes related to materials, processes, and equipment at CMOs. Assess impact on product quality and regulatory compliance. Qualifications Experience: 8–10 years of experience: in Quality Assurance within the pharmaceutical industry Experience: with external manufacturing or contract manufacturing organizations (CMOs) is highly preferred Skills & Competencies: Excellent documentation review and attention to detail Strong analytical and problem-solving skills Effective communication and stakeholder management Strong knowledge of GMP, GDP, and regulatory requirements: (NAFDAC, WHO,) Experience: in auditing and vendor management Ability to work independently and manage multiple priorities How to Apply Interested and qualified candidates should: Click here to apply online View all Jobs in Nigeria Ogun State