Associate Manager - Quality Assurance
AI summary
Shalina Healthcare is hiring an Associate Manager – Quality Assurance to support the Quality Management System and ensure manufacturing processes, documentation, and products meet GMP, WHO, and NAFDAC standards. The role involves overseeing validation activities, batch release, deviations, CAPA, audits, and cross-functional compliance within the pharmaceutical facility. Candidates need a relevant science degree and 10–15 years of pharma manufacturing experience, including 2–3 years in a QA supervisory role.
- Pharmaceutical QA leadership role with batch release and QMS ownership
- Requires 10–15 years pharma manufacturing experience, including 2–3 years in QA supervision
- Must know GMP, GDP, NAFDAC, WHO, and ISO regulatory requirements
- Involves audits, validation, deviations, CAPA, and cross-functional compliance
- Bachelor’s degree in pharmacy, microbiology, biochemistry, chemistry, or related field required
AI job guide
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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?
- Required10+ years of relevant experienceThe job post includes a minimum experience signal.
- RequiredEducation or certification mentioned in the postThe captured text mentions education, a diploma, certificate, or licence.
- PreferredPractical evidence in cleaning, factory, internshipThe 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
- Role specificAcademic or professional certificates
- VerifyID or passport only after verifying the employer
Application tips for this job
- Place your strongest Associate Manager - Quality Assurance 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 cleaning, factory, internship, 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.
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Interview preparation
- What experience makes you a strong fit for this Associate Manager - Quality Assurance role in cleaning, factory?
- 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 role ensures that all manufacturing processes, documentation, and quality systems meet established standards and that products are consistently produced and controlled to quality specifications. The QA Associate Manager is responsible for supporting the implementation and maintenance of the Quality Management System (QMS) in compliance with regulatory requirements: such as GMP, WHO, and NAFDAC standards. Key Responsibilities: Oversee validation and qualification activities (process validation, cleaning validation, equipment qualification). Support the QA Manager in overseeing all Quality Assurance activities within the manufacturing facility. Ensure compliance with cGMP, WHO guidelines, and NAFDAC regulations. Support regulatory inspections and ensure timely closure of audit findings. Collaborate with Production, QC, Engineering, and Warehouse to ensure quality compliance. Monitor environmental conditions and ensure compliance with required standards. Review and approve Standard Operating Procedures (SOPs), batch manufacturing records (BMR), and batch packaging records (BPR). Monitor and ensure proper documentation practices (GDP) across departments. Maintain and improve the Quality Management System (QMS). Review and approve product release documentation and support batch disposition. Manage deviations, CAPA (Corrective and Preventive Actions), change controls, and investigations. Coordinate and participate in internal and external audits (regulatory, customer, and certification audits). Ensure proper training and compliance of staff on quality systems and SOPs. Qualifications & Experience: Experience: in handling audits and regulatory inspections. Strong knowledge of GMP, GDP, and regulatory requirements: (NAFDAC, WHO, ISO). 10–15 years experience: in pharmaceutical manufacturing, with at least 2–3 years in a supervisory / lead role in QA. Bachelor’s Degree in pharmacy, Microbiology, Biochemistry, Chemistry, or related field. How to Apply Interested and qualified candidates should: Click here to apply online View all Jobs in Nigeria Ogun State