Production Supervisor
AI summary
Shalina Healthcare is hiring a Production Supervisor to oversee day-to-day pharmaceutical production activities in Nigeria. The role involves supervising manufacturing processes, ensuring GMP and SOP compliance, coordinating with QA/QC and Engineering teams, and achieving production targets. Candidates should have a B.Sc./B.Pharm/HND in a relevant science or engineering field and 5–10 years of pharmaceutical manufacturing experience.
- Pharmaceutical production supervision role with GMP and SOP compliance focus
- Requires 5–10 years of relevant manufacturing experience
- Supervisory or team-lead experience preferred
- Apply online via the Apply Online Now button on the job page
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?
- Required5+ 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 factory, internship, armazemThe 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 Production Supervisor 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 factory, internship, armazem, ideally with measurable outcomes or clear responsibilities.
- Follow the instructions from My NGO Jobs 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
- My NGO Jobs 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 Production Supervisor role in factory, internship?
- 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
Job Purpose To supervise and coordinate day-to-day pharmaceutical production activities, ensuring that products are manufactured safely, efficiently, and in compliance with GMP, SOPs, quality standards, and regulatory requirements. The Production Supervisor will lead production personnel, monitor manufacturing processes, and ensure that production targets are achieved without compromising product quality or safety. Key Responsibilities: Production Operations: Supervise daily production activities in assigned manufacturing areas. Ensure production targets are achieved according to approved production plans and schedules. Monitor manufacturing processes including dispensing, granulation, blending, compression, encapsulation, coating, and packaging, as applicable. Ensure proper utilization of production equipment, materials, and manpower. Monitor production output, process efficiency, downtime, and rejection rates. Coordinate with Warehouse, Quality Assurance, Quality Control, and Engineering teams to resolve production issues. Ensure proper line clearance and equipment readiness before commencement of production activities. GMP & Compliance: Ensure all production activities are performed in accordance with Good Manufacturing Practices (GMP) and approved SOPs. Ensure production personnel follow approved Batch Manufacturing Records (BMRs), Batch Packaging Records (BPRs), and other controlled documents. Ensure proper documentation and recording of production activities in real time. Report deviations, incidents, non-conformances, and abnormal process conditions promptly. Support investigations, CAPA implementation, change controls, and other quality-related activities. Maintain high standards of hygiene, housekeep Qualifications B.Sc./B.Pharm/HND in Pharmacy, Pharmaceutical Technology, Biochemistry, Chemistry, Microbiology, Chemical Engineering, or a related discipline. Relevant professional certification or membership will be an added advantage. Good knowledge of GMP, GLP, SOPs, Good Documentation Practices (GDP), and pharmaceutical manufacturing processes. Experience: 5–10 years of relevant experience: in pharmaceutical manufacturing. Previous experience: in a supervisory or team-lead position is preferred. Experience: in tablet, capsule, liquid, or other pharmaceutical production operations is an advantage. Practical knowledge of pharmaceutical production equipment and manufacturing processes. Method of Application Interested and qualified candidates should apply below USING APPLY ONLINE NOW BUTTON Premium NGO Service Increase your chances of getting this job! Let our experts professionally update your CV and Cover Letter to meet international NGO standards. Get Started Now From ₦700 only