Job Description
Our client in the pharmaceutical industry is seeking an experienced Production Technician to manage and oversee operations within the production department on a 1-month contract. This role focuses on ensuring the cost-effective production of anti-venom products in compliance with Good Manufacturing Practice (GMP), Medical Control Council, and South African pharmaceutical requirements. The ideal candidate will be well-versed in quality management systems and play a crucial role in ensuring the production of safe, efficacious, and high-quality products.
Key Responsibilities:
– Manage daily production operations to maximize output while ensuring compliance with GMP and industry standards.
– Implement and maintain QA processes and Standard Operating Procedures (SOPs) in line with GMP requirements.
– Ensure all SOPs are current, providing coaching and training to staff on GMP compliance and production policies.
– Oversee equipment calibration, maintenance, and liaise with external contractors to maintain and validate equipment as per schedule.
– Manage departmental assets, including CAPEX planning and stock level monitoring for seamless operations.
– Compile and review management reports and ensure effective communication with other departments.
– Provide coaching, training, performance reviews, and continuous development opportunities for staff.
– Ensure safety compliance according to OHSA to maintain a safe working environment.
– Oversee and ensure accurate documentation of SOPs and production-related activities.
– Manage and monitor stock, workflows, and turnaround times.
– Lead the department in meeting SANAS accreditation requirements and ensure quality control results are audited and appropriate actions are taken.
Minimum Requirements & Competencies:
– Four-year Degree/Diploma in Pharmacy (B.Pharm).
– Registration with the South African Pharmacy Council as a Pharmacist.
– Minimum of 6 years experience in the pharmaceutical manufacturing industry.
– At least 1 year of experience in aseptic processing.
– 2 years of supervisory experience in the pharmaceutical industry.
– Strong knowledge of GMP, aseptic techniques, sterilization methods, and validation processes.
– Basic financial knowledge and experience managing assets and consumables.
– Knowledge of OHSA regulations.
– Strong computer, general management, communication, and interpersonal skills.
– Problem-solving and troubleshooting ability with high attention to detail.
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