Associate Manager - Quality Control
AI summary
Shalina Healthcare is hiring an Associate Manager - Quality Control at its pharmaceutical manufacturing facility in Odeda, Ogun. The role oversees QC laboratory operations, ensures compliance with GMP, NAFDAC, WHO and other regulatory standards, and leads investigations on deviations and out-of-specification results. This is a permanent, full-time position.
- Permanent full-time role in pharmaceutical quality control
- Oversees chemical, microbiological and instrumental lab analysis
- Ensures compliance with GMP, GLP, WHO and NAFDAC standards
- Leads OOS, OOT and deviation investigations
- Manages and mentors QC staff and laboratory operations
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?
- UnclearRelated work experienceThe text mentions experience, but the exact level should be confirmed at source.
- RequiredEducation or certification mentioned in the postThe captured text mentions education, a diploma, certificate, or licence.
- PreferredPractical evidence in internship, Quality Control, Quality AssuranceThe 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
- Role specificAcademic or professional certificates
- VerifyID or passport only after verifying the employer
Application tips for this job
- Place your strongest Associate Manager - Quality Control 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.
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- 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 Control role in internship, Quality Control?
- 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?
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Original source description
Associate Manager - Quality Control at Shalina Healthcare
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Sep 28, 2026, 2:01 PM
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View all Medical & Healthcare jobs
Shalina Healthcare is one of the largest pharmaceutical companies in sub-Saharan Africa. For the last 35 years, we have made it our mission to provide quality medicines to those who need it the most. We manufacture and distribute branded prescription and over-the-counter pharmaceutical and consumer products across various therapeutic groups, including anti-malarial, antibiotics, anti-inflammatory, and nutrition. We have a track record few can match and our brands are among the most trusted in Africa.
We are recruiting to fill the position below:
Job Title: Associate Manager - Quality Control
Location: : Odeda, Ogun
Job Type: Permanent / Full time
About the job
The role ensures compliance with Good Manufacturing Practices (GMP), regulatory guidelines, and company quality policies.
The Quality Control Associate QC Manager is responsible for overseeing all quality control activities within the pharmaceutical manufacturing facility.
This includes ensuring that raw materials, in-process products, and finished goods meet established quality standards and regulatory requirements.
Key Responsibilities
- Develop, review, and update Standard Operating Procedures (SOPs), specifications, and test methods.
- Support internal and external audits, including regulatory inspections.
- Manage and supervise all Quality Control laboratory operations, including chemical, microbiological, and instrumental analysis.
- Review and approve laboratory results, certificates of analysis (CoA), and test reports.
- Manage and mentor QC staff, including training and performance evaluation.
- Ensure proper documentation practices and data integrity in line with regulatory expectations.
- Ensure compliance with regulatory requirements such as GMP, GLP, WHO, NAFDAC, and other applicable standards.
- Ensure testing of raw materials, packaging materials, in-process samples, and finished products in accordance with approved specifications and methods.
- Collaborate with Production, Quality Assurance, and other departments to ensure product quality and compliance.
- Lead investigations on Out-of-Specification (OOS), Out-of-Trend (OOT), and deviations, and ensure proper documentation and closure.
- Coordinate stability studies and ensure proper documentation and reporting.
- Oversee calibration, qualification, and maintenance of laboratory equipment.
- Monitor laboratory inventory and ensure availability of reagents, chemicals, and consumables.
- Qualifications & Requirements
- Experience with analytical instruments such as HPLC, GC, UV Spectrophotometer, etc.
- 10–15 years of experience in pharmaceutical manufacturing, with at least 3–5 years in a managerial role.
- Strong knowledge of GMP, GLP, and regulatory requirements (e.g., NAFDAC, WHO).
- Strong leadership, organizational, and problem-solving skills.
- High attention to detail and commitment to quality.
- Bachelor’s Degree in pharmacy, Chemistry, Biochemistry, Microbiology, or a related field (master’s degree is an advantage).
- Excellent communication and report-writing skills.
- Key Competencies:
- Regulatory Compliance
- Analytical and Critical Thinking
- Leadership and Team Management
- Time Management.
- Attention to Detail
- Decision-Making Ability
- How to Apply
- Interested and qualified candidates should:
- Click here to apply online
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- Ogun State