NextPharma
NextPharma is a leading European pharmaceutical CDMO focused on attractive technology niches.
Since its foundation in 1989, the Livingston site has evolved into a global player in the development and application of both traditional and novel drug encapsulation technologies that are supported by modern and commercial scale manufacturing facilities.
Our Vision:
Our vision is to be the leading and most trusted, reliable and innovative Europe-based CDMO by upholding the highest industry standards and exceeding customer expectations, while driving strong, sustainable growth for the company.
Job Summary:
We are seeking a detail-oriented and experienced Production Shift Team Leader to manage pharmaceutical manufacturing operations during back 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.
· Back Shift hours Monday-Friday, including public holidays (Excluding Christmas & New Year) and occasional weekends as needed.
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.
Remuneration Package:
Basic Salary: £DOE
Private Medical Insurance
Health Cash Plan
Contributory pension scheme
Life Insurance
Income Protection
Employee Assistance Program
Please note: Only candidates with permanent Right to Work in the UK will be considered.
NextPharma is an equal opportunities employer and positively encourages applications from suitably qualified and eligible candidates regardless of sex, race, disability, age, sexual orientation, marriage or civil partnership, pregnancy or maternity, religion or belief.
Job Types: Full-time, Permanent
Benefits:
- Company pension
- Cycle to work scheme
- Free parking
- Health & wellbeing programme
- Life insurance
- On-site parking
- Private medical insurance
- Referral programme
Schedule:
- 8 hour shift
- Monday to Friday
Ability to commute/relocate:
- Livingston EH53 0TH: reliably commute or plan to relocate before starting work (required)
Experience:
- Pharmaceutical: 3 years (required)
Work authorisation:
- United Kingdom (required)
Work Location: In person
