SUMMARY:
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POSITION INFO:
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.
