About the Role
Our client, a dynamic and growing pharmaceutical manufacturing company based in Upington, Northern Cape , is seeking an experienced Senior Pharmaceutical Manufacturing Operations Specialist. This role is integral to overseeing and optimizing day-to-day manufacturing activities, ensuring the efficient and compliant production of high-quality pharmaceutical products. You will be involved in process monitoring, troubleshooting, continuous improvement initiatives, and ensuring adherence to stringent GMP standards. This position offers a hybrid work arrangement, combining essential on-site operational management with remote planning and reporting. The ideal candidate will possess a strong understanding of pharmaceutical manufacturing processes and a proven ability to lead teams and drive operational excellence. This is a significant opportunity to contribute to the success of a key player in the pharmaceutical industry.
Key Responsibilities
- Oversee and manage daily pharmaceutical manufacturing operations, including production scheduling, resource allocation, and workflow management.
- Ensure all manufacturing activities are conducted in strict accordance with Good Manufacturing Practices (GMP) and company Standard Operating Procedures (SOPs).
- Monitor production performance, identify deviations, and implement corrective actions to minimize downtime and ensure product quality.
- Lead and mentor manufacturing teams, providing guidance, training, and performance feedback.
- Participate in process validation activities and support technology transfer initiatives.
- Identify and implement continuous improvement opportunities to enhance efficiency, reduce costs, and improve quality.
- Collaborate with Quality Assurance, Quality Control, Engineering, and Supply Chain departments to ensure seamless operations.
- Maintain detailed production records and documentation, ensuring accuracy and completeness.
- Ensure a safe working environment by promoting and enforcing safety regulations.
- Stay updated with industry trends and best practices in pharmaceutical manufacturing.
Requirements
- Bachelor's degree in Pharmacy, Chemical Engineering, Industrial Engineering, or a related field.
- Minimum of 5 years of experience in pharmaceutical manufacturing operations.
- Thorough understanding of GMP regulations and pharmaceutical manufacturing processes (e.g., sterile manufacturing, solid dosage forms).
- Proven experience in process monitoring, troubleshooting, and continuous improvement.
- Strong leadership and team management skills.
- Excellent problem-solving, analytical, and organizational abilities.
- Effective communication and interpersonal skills, with the ability to collaborate across departments.
- Proficiency in manufacturing execution systems (MES) and enterprise resource planning (ERP) software is a plus.
- Ability to adapt to a hybrid work environment, balancing on-site and remote responsibilities.
- Commitment to quality, safety, and regulatory compliance.
Benefits
- Our client provides a competitive salary package, including performance bonuses and overtime pay opportunities.
- The hybrid work model offers flexibility and work‑life balance.
- Comprehensive medical aid and a retirement fund are included.
- Paid annual leave and sick leave are generous.
- Opportunities for professional development, including leadership training and specialized courses, are provided.
- Employees work in a supportive and safety‑conscious environment.
- Life insurance and disability benefits are also part of the package.