{"id":5564,"date":"2026-08-19T11:45:02","date_gmt":"2026-08-19T11:45:02","guid":{"rendered":"https:\/\/jobs.dataaxisnode.com\/nigeria\/uncategorized\/documentation-compliance-officer\/"},"modified":"2026-08-19T11:45:02","modified_gmt":"2026-08-19T11:45:02","slug":"documentation-compliance-officer","status":"publish","type":"post","link":"https:\/\/jobs.dataaxisnode.com\/nigeria\/jobs\/lagos\/documentation-compliance-officer\/","title":{"rendered":"Documentation \/ Compliance Officer"},"content":{"rendered":"<p><script type=\"application\/ld+json\">{\"@context\": \"https:\/\/schema.org\/\", \"@type\": \"JobPosting\", \"title\": \"Documentation \/ Compliance Officer\", \"description\": \"Key Responsibilities\\nRegulatory Compliance: Ensure company operations follow NAFDAC regulations and global Good Manufacturing Practice GMP standards.\\nDocument Control: Create, review, update, and archive Standard Operating Procedures SOPs, batch records, and quality manuals\\n.Audit Management: Lead internal quality audits and prepare the facility for external NAFDAC inspections or regulatory audits.\\nTraining Coordination: Train staff on compliance policies, document control systems, and current GMP guidelines.\\nDeviation & CAPA Tracking: Log quality deviations, manage investigations, and monitor Corrective and Preventive Actions CAPAs.\\nRequirements and Qualifications\\nA Bachelor's Degree in Pharmacy B.Pharm, Industrial Chemistry, Microbiology, Biochemistry, or a related science field.\\nMore than 5 years of experience in quality assurance, regulatory affairs, or document control within a regulated manufacturing environment.\\nSkills: Strong knowledge of NAFDAC\/WHO GMP guidelines, excellent attention to detail, strong technical writing skills, and good computer literacy.\", \"datePosted\": \"2026-08-18\", \"hiringOrganization\": {\"@type\": \"Organization\", \"name\": \"Chemo-Pharma Laboratories\"}, \"jobLocation\": {\"@type\": \"Place\", \"address\": {\"@type\": \"PostalAddress\", \"addressLocality\": \"Lagos\", \"addressCountry\": \"NG\"}}, \"directApply\": true, \"validThrough\": \"2026-09-01T23:59:59\", \"employmentType\": \"FULL_TIME\"}<\/script><\/p>\n<p><strong>Company:<\/strong> Chemo-Pharma Laboratories<\/p>\n<p><strong>Location:<\/strong> Lagos<\/p>\n<p><strong>Job Type:<\/strong> Full Time<\/p>\n<p><strong>Apply Before:<\/strong> 2026-09-01<\/p>\n<h3>Job Description<\/h3>\n<p>Key Responsibilities<br \/>Regulatory Compliance: Ensure company operations follow NAFDAC regulations and global Good Manufacturing Practice GMP standards.<br \/>Document Control: Create, review, update, and archive Standard Operating Procedures SOPs, batch records, and quality manuals<br \/>.Audit Management: Lead internal quality audits and prepare the facility for external NAFDAC inspections or regulatory audits.<br \/>Training Coordination: Train staff on compliance policies, document control systems, and current GMP guidelines.<br \/>Deviation &#038; CAPA Tracking: Log quality deviations, manage investigations, and monitor Corrective and Preventive Actions CAPAs.<br \/>Requirements and Qualifications<br \/>A Bachelor&#8217;s Degree in Pharmacy B.Pharm, Industrial Chemistry, Microbiology, Biochemistry, or a related science field.<br \/>More than 5 years of experience in quality assurance, regulatory affairs, or document control within a regulated manufacturing environment.<br \/>Skills: Strong knowledge of NAFDAC\/WHO GMP guidelines, excellent attention to detail, strong technical writing skills, and good computer literacy.<\/p>\n<h3>How to Apply<\/h3>\n<p>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.<br \/>Build your CV for free. Download in different templates.<\/p>\n<p><a href=\"mailto:hr@chemopharmalabs.com\" target=\"_blank\" rel=\"noopener\" style=\"display:inline-block;padding:10px 20px;background:#2271b1;color:#fff;text-decoration:none;border-radius:4px;\">Apply Now<\/a><\/p>\n<p><small>Source: MyJobMag<\/small><\/p>\n<p><!-- job-expiry: 2026-09-01 --><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Company: Chemo-Pharma Laboratories Location: Lagos Job Type: Full Time Apply Before: 2026-09-01 Job Description Key ResponsibilitiesRegulatory 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 [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[13,21],"tags":[1267,51,18,17],"class_list":["post-5564","post","type-post","status-publish","format-standard","hentry","category-jobs","category-lagos","tag-chemo-pharma-laboratories","tag-full-time","tag-job-listing","tag-myjobmag"],"_links":{"self":[{"href":"https:\/\/jobs.dataaxisnode.com\/nigeria\/wp-json\/wp\/v2\/posts\/5564","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/jobs.dataaxisnode.com\/nigeria\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/jobs.dataaxisnode.com\/nigeria\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/jobs.dataaxisnode.com\/nigeria\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/jobs.dataaxisnode.com\/nigeria\/wp-json\/wp\/v2\/comments?post=5564"}],"version-history":[{"count":0,"href":"https:\/\/jobs.dataaxisnode.com\/nigeria\/wp-json\/wp\/v2\/posts\/5564\/revisions"}],"wp:attachment":[{"href":"https:\/\/jobs.dataaxisnode.com\/nigeria\/wp-json\/wp\/v2\/media?parent=5564"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/jobs.dataaxisnode.com\/nigeria\/wp-json\/wp\/v2\/categories?post=5564"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/jobs.dataaxisnode.com\/nigeria\/wp-json\/wp\/v2\/tags?post=5564"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}