About this role
Production Pharmacist (Entry-Level) at Proten
Location: Lagos
Job Summary
- The Production Pharmacist will support pharmaceutical manufacturing operations, ensuring that production activities comply with Good Manufacturing Practice (GMP), quality standards, and regulatory requirements.
- The role involves assisting with batch manufacturing, packaging, documentation, quality procedures, and continuous process improvement.
Responsibilities
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Assist in supervising production activities, including batch manufacturing, filling, labelling, and packaging.
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Support the implementation of quality control procedures to ensure products meet established standards.
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Ensure compliance with GMP, relevant regulatory requirements, and company procedures.
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Assist in reviewing batch records, certificates of analysis, and other production documentation.
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Report and support investigations into production deviations, discrepancies, and product complaints.
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Maintain accurate records of production, quality checks, and regulatory activities.
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Participate in production process improvements and initiatives to enhance efficiency and product quality.
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Support internal audits, regulatory inspections, and customer audits where required.
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Collaborate with Quality Assurance, Research and Development, Regulatory Affairs, and other relevant departments.
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Participate in training on production procedures, quality standards, and workplace safety.
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Requirements & Qualification
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Bachelor of Pharmacy (B.Pharm) degree.
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Minimum of 0–1 year of relevant experience in pharmaceutical or industrial manufacturing.
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Basic understanding of pharmaceutical production processes and Good Manufacturing Practice (GMP).
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Knowledge of production documentation and quality assurance procedures is an advantage.
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Strong communication and interpersonal skills.
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Good time management, organisational, and problem-solving abilities.
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Willingness to learn, attention to detail, and ability to work effectively in a team.
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Check how your CV matches this job
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Note: Only qualified candidates would be contacted.
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Deadline: 11 November 2026
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