Shiftlead Bulk Production
Location:Livingston, GB, EH53 0TH
Job Function: Operations
Anticipated Start Date: 30 Jun 2025
Job Type: Full-Time
Are you looking for…
an exciting professional challenge?
We are one of the leading European contract manufacturers in the pharmaceutical, biotech and healthcare sectors, with some 2,500 employees in Germany, France, Finland, UK and Norway. For us, the next step is always the one that matters most. Our fast pace drives us forward, fills our working environment with life and spurs our growth. Our winning formula for shared success: room for passion. Because we know that passion is the best medicine when it comes to excellent service around the world. Welcome to NextPharma.
Job Summary:
We are seeking a detail-oriented and experienced Production Shift Team Leader to manage pharmaceutical manufacturing operations during assigned shifts. The ideal candidate will have a strong background in GMP-compliant environments and be responsible for leading production teams, ensuring adherence to quality and safety standards, and driving operational efficiency within a highly regulated setting.

Key Responsibilities:

• Lead, supervise, and support production operators and technicians to meet daily manufacturing targets while complying with Good Manufacturing Practice (GMP) guidelines.
• Ensure strict adherence to SOPs, batch manufacturing records (BMRs), and regulatory compliance across all shift activities.
• Monitor production processes, troubleshoot issues, and ensure timely completion of manufacturing orders.
• Conduct shift handovers, maintain accurate documentation, and report production metrics and deviations.
• Champion safety, quality, and hygiene standards; ensure the team adheres to site health and safety policies at all times.
• Collaborate with quality assurance, maintenance, and validation teams to address production issues and support investigations.
• Support the implementation of continuous improvement initiatives, including lean practices and 5S methodologies.
• Participate in internal and external audits, providing accurate documentation and responding to audit findings.
• Train and mentor team members on GMP, SOPs, and equipment operation to maintain a competent and compliant workforce.

Requirements:

• Previous experience (3+ years) in pharmaceutical manufacturing, preferably in a supervisory or team-lead capacity.
• In-depth knowledge of GMP, regulatory compliance, and pharmaceutical production processes preferred.
• Strong leadership, problem-solving, and decision-making skills.
• Excellent communication and organizational abilities.
• Comfortable working in cleanroom and controlled environments.
• Flexible to work rotating shifts, including public holidays and occasional weekends as needed.
• Potential for set shifts i.e. early or back shift

Preferred Qualifications:

• Diploma/certificate in scientific or a related field
• Experience with solid dosage forms preferred.
• Familiarity with ERP systems (e.g., SAP) and quality systems preferred.

It’s time for your next chapter:
We look forward to receiving your application.

• Lead, supervise, and support production operators and technicians to meet daily manufacturing targets while complying with Good Manufacturing Practice (GMP) guidelines.
• Ensure strict adherence to SOPs, batch manufacturing records (BMRs), and regulatory compliance across all shift activities.
• Monitor production processes, troubleshoot issues, and ensure timely completion of manufacturing orders.
• Conduct shift handovers, maintain accurate documentation, and report production metrics and deviations.
• Champion safety, quality, and hygiene standards; ensure the team adheres to site health and safety policies at all times.
• Collaborate with quality assurance, maintenance, and validation teams to address production issues and support investigations.
• Support the implementation of continuous improvement initiatives, including lean practices and 5S methodologies.
• Participate in internal and external audits, providing accurate documentation and responding to audit findings.
• Train and mentor team members on GMP, SOPs, and equipment operation to maintain a competent and compliant workforce