Senior Pharmaceutical Production Supervisor

Placements24

United States

Hybrid

USD 71,000 - 107,000

Full time

26 hours ago
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Benefits offered by this job

Health insurance
Retirement annuity
Performance-based incentives
Hybrid work model

Job summary

Placements24 seeks a Senior Pharmaceutical Production Supervisor to oversee a team of operators and technicians in a hybrid work setting at a South African pharmaceutical production facility. You will ensure compliant manufacturing of oral solids and sterile injectables, lead continuous improvement initiatives, and maintain rigorous safety and quality standards.

The role requires a Bachelor's degree in Pharmacy or related field, 5+ years in pharma manufacturing with 2+ years in supervision, and

Qualifications

  • Bachelor's degree in Pharmacy, Chemical Engineering, Biotechnology, or related field.
  • Minimum of 5 years in pharmaceutical manufacturing, with at least 2 years in a supervisory role.
  • Strong knowledge of cGMP, pharmaceutical production processes, and regulatory compliance.
  • Proven experience in managing production teams and improving operational efficiency.
  • Excellent understanding of safety procedures and protocols in a manufacturing environment.
  • Strong leadership, communication, and interpersonal skills.
  • Ability to analyze production data and implement data-driven improvements.
  • Proficiency in MES/ERP systems is advantageous.

Responsibilities

  • Supervise daily production activities to meet targets for quantity, quality, and timelines.
  • Mentor a team of production operators and technicians with training and feedback.
  • Ensure strict adherence to cGMP, SOPs, and safety regulations across production processes.
  • Monitor equipment performance and coordinate with maintenance for repairs and preventive maintenance.
  • Oversee batch record review and reconciliation for accuracy and completeness.
  • Drive continuous improvement initiatives to optimize efficiency and reduce waste.
  • Participate in deviation investigations and CAPA implementations.
  • Collaborate with QA, QC, and Engineering to resolve production issues.
  • Maintain a safe and clean work environment and promote a strong safety culture.

Skills

Leadership
cGMP knowledge
Data analysis
MES/ERP proficiency

Education

Bachelor's degree in Pharmacy
Related scientific/technical degree

Tools

MES software
ERP systems

Job description

About the Role

Our client, a well-established pharmaceutical manufacturer, is seeking an experienced and dedicated Senior Pharmaceutical Production Supervisor to oversee their production operations in Klerksdorp, North West . This role is crucial for ensuring the efficient, safe, and compliant manufacturing of high-quality pharmaceutical products. You will lead a team of production operators and technicians, providing guidance, training, and supervision to meet production targets while adhering to strict regulatory standards. The position involves a hybrid work model, requiring on-site presence for core operational duties and offering flexibility for administrative tasks. The ideal candidate will possess strong leadership abilities, a comprehensive understanding of pharmaceutical manufacturing processes (e.g., oral solids, sterile injectables), and a commitment to maintaining a safe and productive work environment. You will play a key role in continuous improvement initiatives aimed at enhancing operational efficiency and product quality within the pharmaceutical production facility.

Key Responsibilities
  • Supervise daily production activities, ensuring targets are met in terms of quantity, quality, and timelines.
  • Manage and mentor a team of production operators and technicians, providing training, performance feedback, and support.
  • Ensure strict adherence to cGMP, SOPs, and safety regulations throughout all production processes.
  • Monitor production equipment performance and coordinate with maintenance teams for timely repairs and preventative maintenance.
  • Oversee batch record review and reconciliation, ensuring accuracy and completeness.
  • Implement and drive continuous improvement initiatives to optimize production efficiency and reduce waste.
  • Participate in deviation investigations and the implementation of corrective and preventive actions (CAPAs).
  • Collaborate with Quality Assurance, Quality Control, and Engineering departments to resolve production issues.
  • Maintain a safe and clean work environment, promoting a strong safety culture on the production floor.
Requirements
  • Bachelor's degree in Pharmacy, Chemical Engineering, Biotechnology, or a related scientific or technical field.
  • Minimum of 5 years of experience in pharmaceutical manufacturing, with at least 2 years in a supervisory or team lead role.
  • Strong knowledge of cGMP, pharmaceutical production processes, and regulatory compliance.
  • Proven experience in managing production teams and improving operational efficiency.
  • Excellent understanding of safety procedures and protocols in a manufacturing environment.
  • Strong leadership, communication, and interpersonal skills.
  • Ability to analyze production data and implement data-driven improvements.
  • Proficiency in using manufacturing execution systems (MES) and Enterprise Resource Planning (ERP) systems is advantageous.
  • Willingness to work a hybrid schedule, balancing on-site supervision with administrative responsibilities in Klerksdorp .
Benefits
  • Our client offers a competitive salary and a comprehensive benefits package including health insurance, a retirement annuity, and performance-based incentives.
  • Employees will have the opportunity to work in a modern pharmaceutical manufacturing facility in Klerksdorp and contribute to the production of vital medicines.
  • This hybrid role offers a degree of flexibility while ensuring hands-on operational involvement.
  • Professional development opportunities, including GMP training and leadership workshops, are provided to support career growth within the pharmaceutical industry.
  • The company culture emphasizes teamwork, safety, and continuous improvement.
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