Pharmaceutical Production Supervisor

Placements24; London Borough of Newham; On-site; GBP 22,000 - 32,000; Full time

Benefits offered by this job

Medical aid

Retirement fund contributions

Career advancement

Job summary

Placements24 is seeking a Pharmaceutical Production Supervisor for our East London, Eastern Cape facility. You will lead a team of production operators, oversee daily GMP-compliant manufacturing, and ensure safety and quality on the floor.

The ideal candidate has a Diploma or Bachelors in Pharmacy or related field, at least 5 years in pharmaceutical manufacturing with 2+ in supervision, strong leadership, and experience with MES/ERP systems.

Qualifications

• Minimum 5 years in pharmaceutical manufacturing with at least 2 years in a supervisory role.
• Strong GMP, SOPs, and regulatory knowledge with leadership experience.
• Excellent troubleshooting, communication, and problem-solving skills.

Responsibilities

• Supervise day-to-day pharmaceutical production activities ensuring targets are met.
• Lead, train, and motivate a team of production operators for safe, efficient output.
• Maintain compliance with GMP, SOPs, and regulatory guidelines.
• Monitor equipment, identify deviations, and implement corrective actions.
• Document batch records, logs, and CAPA investigations in a timely manner.
• Collaborate with QA, Engineering and Maintenance to support continuous improvement.
• Manage material flow and inventory within the production area.

Skills

Pharma manufacturing

Leadership

GMP knowledge

MES/ERP familiarity

Education

Diploma or Bachelor's in Pharmacy

Tools

MES software

ERP software

Job description

About the Role

Our client, a prominent pharmaceutical manufacturer dedicated to producing high-quality medicines, is seeking an experienced and detail-oriented Pharmaceutical Production Supervisor for their facility in **East London, Eastern Cape**. This role is crucial for overseeing daily production operations, ensuring efficiency, safety, and adherence to strict Good Manufacturing Practices (GMP). You will lead a team of production operators, guiding them in executing manufacturing processes, troubleshooting issues, and maintaining a productive workflow. The ideal candidate will have a strong background in pharmaceutical manufacturing, excellent leadership skills, and a commitment to upholding the highest standards of quality and compliance. This is a hands‑on role requiring active engagement with the production floor and a proactive approach to problem‑solving.

Key Responsibilities

• Supervise and manage day-to-day pharmaceutical production activities, ensuring targets are met efficiently and effectively.
• Lead, train, and motivate a team of production operators to achieve optimal performance and safety.
• Ensure all manufacturing processes are conducted in strict compliance with GMP, SOPs (Standard Operating Procedures), and regulatory guidelines.
• Monitor production equipment and processes, identifying and resolving any operational issues or deviations promptly.
• Oversee the accurate documentation of all production activities, batch records, and equipment logs.
• Conduct regular safety inspections and enforce safety protocols to maintain a secure working environment.
• Participate in quality investigations, root cause analysis, and the implementation of corrective and preventive actions (CAPA).
• Collaborate with Quality Assurance, Engineering, and Maintenance departments to ensure smooth operations and continuous improvement.
• Manage material flow and inventory within the production area, ensuring adequate supplies are available.
• Promote a culture of continuous improvement and operational excellence on the production floor.

Requirements

• Diploma or Bachelor's degree in Pharmacy, Chemical Engineering, Biotechnology, or a related field.
• Minimum of 5 years of experience in pharmaceutical manufacturing, with at least 2 years in a supervisory or team lead role.
• In-depth knowledge of GMP, pharmaceutical production processes, and regulatory requirements.
• Proven ability to lead and develop a team.
• Strong understanding of process validation and quality control principles.
• Excellent troubleshooting and problem‑solving skills.
• Proficiency in using manufacturing execution systems (MES) and enterprise resource planning (ERP) software is an advantage.
• Strong communication and interpersonal skills.
• Ability to work shifts and flexible hours as required by production schedules.
• Commitment to maintaining a safe and compliant work environment in **East London, Eastern Cape**.

Benefits

• Our client offers a competitive salary, performance-based bonuses, comprehensive medical aid, retirement fund contributions, and ample opportunities for career advancement within the pharmaceutical industry.
• We provide a supportive work environment focused on employee development and well‑being.
• This role is based at our state‑of‑the‑art facility in **East London, Eastern Cape**.