Documentation / Compliance Officer
AI summary
Chemo-Pharma Labs Limited is hiring a Documentation / Compliance Officer in Lagos to ensure NAFDAC and GMP compliance, manage document control, lead audits, and track deviations and CAPAs. Candidates need a B.Pharm or related science degree and over five years of experience in a regulated manufacturing environment. Applications should be sent by email with the job title as the subject.
- Full-time compliance role in a Lagos-based pharmaceutical manufacturer
- Requires B.Pharm, Industrial Chemistry, Microbiology, Biochemistry, or related field
- Over 5 years of QA, regulatory affairs, or document control experience needed
- Strong NAFDAC and WHO GMP knowledge required
- Apply by emailing hr@chemopharmalabs.com and copying info@chemopharmalabs.com
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 internship, Quality Assurance, Regulatory AffairsThe 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 Documentation / Compliance Officer evidence in the first half of your CV.
- In your cover letter or employer message, connect your experience to Chemo-Pharma Labs Limited and the role in Not specified.
- Add concrete examples related to internship, Quality Assurance, Regulatory Affairs, ideally with measurable outcomes or clear responsibilities.
- Follow the instructions from MyJobMag 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
- MyJobMag 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 Documentation / Compliance Officer role in internship, 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 Chemo-Pharma Labs 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
We are a leading manufacturing pharmaceutical company whose major priority centers on the healthy well being of everyone. Our mission is to build a healthier tomorrow for patients , provision of health facilities for the creation of a healthy nation. Documentation / Compliance Officer Job Type Full Time Qualification BA/BSc/HND Experience: 5 years Location Lagos Job Field Pharmaceutical Key Responsibilities: Regulatory Compliance: Ensure company operations follow NAFDAC regulations and global Good Manufacturing Practice (GMP) standards. Document Control: Create, review, update, and archive Standard Operating Procedures (SOPs), batch records, and quality manuals .Audit Management: Lead internal quality audits and prepare the facility for external NAFDAC inspections or regulatory audits. Training Coordination: Train staff on compliance policies, document control systems, and current GMP guidelines. Deviation & CAPA Tracking: Log quality deviations, manage investigations, and monitor Corrective and Preventive Actions (CAPAs). Requirements: and Qualifications A Bachelor's Degree in Pharmacy (B.Pharm), Industrial Chemistry, Microbiology, Biochemistry, or a related science field. More than 5 years of experience: in quality assurance, regulatory affairs, or document control within a regulated manufacturing environment. Skills: Strong knowledge of NAFDAC/WHO GMP guidelines, excellent attention to detail, strong technical writing skills, and good computer literacy. Check how your CV aligns with this job Method of Application Interested and qualified candidates should send their Resume to: hr@chemopharmalabs.com and copy info@chemopharmalabs.com using the Job Title as the subject of the mail. Build your CV for free. Download in different templates.