Fresh Jobs at Morison Industries Plc

Job Summary

• Morison Industries Plc is seeking a qualified and detail-oriented Documentation & In-Process Officer to join its pharmaceutical manufacturing team. The successful candidate will be responsible for maintaining accurate production documentation, monitoring in-process quality checks, and ensuring compliance with Good Manufacturing Practices (GMP), Standard Operating Procedures (SOPs), and regulatory requirements. The ideal candidate should possess excellent documentation skills, a strong quality mindset, and the ability to work effectively in a regulated manufacturing environment.

Key Responsibilities

• Prepare, issue, reconcile, and archive Batch Manufacturing Records (BMRs), Batch Packaging Records (BPRs), and other controlled production documents.
• Review production documentation for completeness, accuracy, and compliance before submission to Quality Assurance.
• Perform and document in-process quality checks during manufacturing and packaging operations in accordance with approved procedures.
• Monitor critical process parameters and ensure compliance with established specifications.
• Verify line clearance activities before commencement of manufacturing and packaging operations.
• Record, investigate, and report in-process deviations, non-conformances, and abnormalities to the appropriate departments.
• Ensure all production records are completed in real time and maintained in compliance with data integrity requirements (ALCOA+ principles).
• Coordinate with Production, Quality Assurance (QA), and Quality Control (QC) to resolve documentation discrepancies.
• Assist in GMP documentation training for production personnel.
• Participate in internal audits, regulatory inspections, process validation, and continuous improvement initiatives.
• Ensure controlled documents are properly managed, distributed, and archived according to document control procedures.

Skills and Qualifications

Applicants must possess:

• Bachelor's Degree in Pharmacy, Biochemistry, Microbiology, Industrial Chemistry, Chemistry, or a related science discipline.
• Post-NYSC experience in pharmaceutical manufacturing, quality assurance, documentation, or in-process quality control.
• Good knowledge of Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and pharmaceutical regulatory requirements.
• Excellent attention to detail and documentation skills.
• Strong analytical, organizational, and problem-solving abilities.
• Good communication and interpersonal skills.
• Proficiency in Microsoft Office applications and electronic documentation systems.
• Ability to work independently and under pressure while maintaining accuracy.

Working Conditions

• Full-time, on-site position based in Lagos.
• Pharmaceutical manufacturing environment requiring strict adherence to GMP, GDP, and workplace safety procedures.
• May require occasional overtime depending on production schedules.

Performance Indicators

Success in this role will be measured by:

• Accuracy and completeness of production documentation.
• Compliance with GMP, GDP, and regulatory requirements.
• Timely completion and review of batch records.
• Reduction in documentation errors and deviations.
• Effectiveness of in-process monitoring and compliance.
• Successful internal and regulatory audit outcomes.

Education

• Bachelor's Degree in Pharmacy, Biochemistry, Microbiology, Industrial Chemistry, Chemistry, or a related science discipline (Required).

Professional Certification

• Relevant professional registration (where applicable) is an added advantage. For Pharmacy graduates, a valid PCN practising licence is desirable; for other science graduates, membership of a relevant professional body is an added advantage.

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Job Summary

• Morison Industries Plc is seeking a qualified and experienced Production Chemist to join its pharmaceutical manufacturing team. The successful candidate will be responsible for supporting and coordinating manufacturing operations, ensuring production processes comply with Good Manufacturing Practices (GMP), Standard Operating Procedures (SOPs), and applicable regulatory requirements. The ideal candidate should possess sound technical knowledge, strong problem-solving skills, and a commitment to producing high-quality pharmaceutical products.

Key Responsibilities

• Supervise and monitor daily manufacturing activities in accordance with approved production schedules.
• Ensure compliance with Good Manufacturing Practices (GMP), Standard Operating Procedures (SOPs), and company quality policies.
• Prepare, review, and maintain production records, equipment logs, and manufacturing documentation.
• Monitor critical production parameters to ensure consistent product quality and process efficiency.
• Coordinate with Quality Assurance (QA) and Quality Control (QC) teams to ensure timely sampling, testing, and product release.
• Ensure proper cleaning, operation, and maintenance of production equipment and manufacturing areas.
• Investigate production deviations, assist with root cause analysis, and implement Corrective and Preventive Actions (CAPA).
• Monitor raw material usage, minimize process waste, and improve production efficiency.
• Train and guide production personnel on GMP, safety procedures, and manufacturing best practices.
• Participate in process validation, internal audits, regulatory inspections, and continuous improvement initiatives.
• Ensure adherence to environmental health and safety (EHS) policies within the production area.

Skills and Qualifications

Applicants must possess:

• Bachelor's Degree in Chemistry, Industrial Chemistry, Applied Chemistry, or a related discipline.
• Post-NYSC experience in pharmaceutical manufacturing or a regulated manufacturing environment.
• Sound knowledge of GMP, pharmaceutical production processes, and regulatory requirements.
• Strong analytical, problem-solving, and organizational skills.
• Good leadership, communication, and interpersonal skills.
• Proficiency in Microsoft Office applications and production documentation.
• Ability to work effectively under pressure and meet production deadlines.

Working Conditions

• Full-time, on-site position based in Lagos.
• Manufacturing environment requiring strict adherence to GMP and workplace safety procedures.
• May require occasional overtime or shift work depending on production schedules.

Performance Indicators

Success in this role will be measured by:

• Achievement of production targets.
• Compliance with GMP and company quality standards.
• Reduction in production deviations and process losses.
• Efficient utilization of raw materials.
• Consistent product quality and manufacturing efficiency.

Education

• Bachelor's Degree in Chemistry, Industrial Chemistry, Applied Chemistry, or a related field (Required).

Professional Certification

• Membership of the Chemical Society of Nigeria (CSN) or other relevant professional body is an added advantage.