Production Operations Specialist
3 days ago
Job Title:
Operations SupervisorThe Operations Supervisor is responsible for overseeing and managing the production operations of a Pharmaceutical company. This includes ensuring timely production, maintaining compliance with current good manufacturing practices (cGMP), achieving quality and quantity targets, and managing resources efficiently across all production areas.
Key Responsibilities:
- Supervise and manage day-to-day production operations of all sections.
- Ensure manufacturing is carried out as per batch production records (BPRs), standard operating procedures (SOPs), and cGMP guidelines.
- Coordinate with Quality Assurance (QA), Quality Control (QC), Engineering, and Supply Chain departments to ensure smooth and compliant production processes.
- Monitor production output and ensure achievement of planned production targets with minimal downtime and optimal resource utilization.
- Lead root cause analysis and corrective/preventive actions in case of deviations, breakdowns, or non-conformities.
- Train, supervise, and evaluate performance of production staff and line supervisors.
- Maintain strict compliance with safety, health, and environmental protocols.
- Ensure cleanliness, calibration, validation, and maintenance of all production equipment and areas.
- Prepare and maintain production reports, yields, and variance records.
- Participate in regulatory and internal audits; ensure readiness and compliance at all times.
- Lead and implement continuous improvement initiatives to enhance productivity and reduce waste.
Required Skills & Qualifications:
- Bachelor's or Master's degree in Pharmacy (Pharm-D or B.Pharm).
- Minimum 12–15 years of hands-on experience in pharmaceutical production, with proven expertise in Tablet, Liquid, Cream & Ointment, Injectables and Cephalosporin manufacturing.
- In-depth knowledge of cGMP, drug regulations, and international quality standards.
- Strong leadership, communication, and team management skills.
- Experience with production planning, Enterprise Resource Planning (ERP) systems, and documentation.
- Ability to troubleshoot manufacturing issues and work under pressure in a fast-paced environment.
Preferred:
- Certification in GMP, Lean Manufacturing, or Six Sigma will be an advantage.
- Prior experience with regulatory audits will be beneficial.
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