Production Pharmacist at Shalina Healthcare

Job Summary

• To ensure the efficient, compliant, and safe manufacturing of pharmaceutical products by supervising production activities, monitoring adherence to cGMP and regulatory requirements, and supporting continuous process improvement

Key Responsibilities

• Supervise and coordinate day-to-day production operations in accordance with approved SOPs, cGMP, and regulatory standards.
• Ensure proper documentation of batch manufacturing records, logbooks, and related documents in compliance with GDP.
• Monitor in-process operations to ensure quality, safety, and efficiency of production.
• Conduct line clearance, equipment checks, and ensure proper cleaning and sanitization before and after production.
• Collaborate with QA, QC, Engineering, and Supply Chain to ensure smooth production flow.
• Train, guide, and monitor operators/technicians on production processes, hygiene, and safety practices.
• Identify deviations, report non-conformances, and support implementation of corrective and preventive actions (CAPA).
• Assist in validation and qualification of equipment, processes, and cleaning procedures.
• Maintain strict compliance with EHS (Environment, Health & Safety) policies and ensure safe workplace practices.
• Participate in audits (internal, external, regulatory) and ensure readiness of production area at all times.
• Contribute to continuous improvement initiatives aimed at enhancing productivity, minimizing wastage, and optimizing resources.

Key Performance Indicators (KPIs)

• Compliance with cGMP and SOPs (zero critical deviations).
• Batch rejection and rework rates.
• Production yield and efficiency.
• Timely completion of production schedules.
• Audit readiness and compliance status.
• Staff training and competency development.

Qualifications & Experience

• Bachelor of Pharmacy (B.Pharm) or Doctor of Pharmacy (Pharm.D).
• Current registration with Pharmacists Council of [Country].
• 2–5 years of experience in pharmaceutical production, preferably in [dosage forms: tablets, capsules, injectables, creams, etc.].
• Strong knowledge of cGMP, GDP, and regulatory requirements (NAFDAC, WHO, FDA, etc.).
• Proficiency in documentation and compliance with pharmaceutical manufacturing guidelines.

Skills & Competencies:

• Strong attention to detail and commitment to quality.
• Good leadership, supervisory, and team management skills.
• Excellent problem-solving and decision-making ability.
• Strong communication and interpersonal skills.
• Ability to work under pressure and meet production timelines.
• Computer literacy (MS Office, ERP systems preferred).