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Senior TS/MS Specialist (m/f/d) · Pharma

Anzeige auf Englisch

ArbeitsortCuxhaven
Gehalt65.000–85.000 € brutto/Jahr
HomeofficeKeine Angabe

Location: Cuxhaven

Responsibilities

  • Lateral Leadership: Lead and inspire diverse cross‑functional teams (Production, Quality Assurance, Engineering) to achieve project milestones through influence and collaboration.
  • Process Scale‑up: Drive the seamless transfer and scale‑up of vaccine manufacturing processes from pilot to industrial level, ensuring deep alignment with GMP and pharmaceutical regulatory frameworks.
  • Data‑Driven Decision Making: Leverage complex data analysis to optimize equipment utilisation and strategic staffing requirements.
  • Operational Excellence: Champion a continuous improvement mindset by implementing operational standards, managing critical deviations and leading Root Cause Investigations (RCI) and CAPA processes.
  • Risk & Compliance: Maintain the validated state of manufacturing processes and lead technical risk assessments (e.g., FMEA) to ensure robust business continuity and high‑quality outcomes.
  • Strategic Sourcing: Execute the technical implementation of secondary suppliers, ensuring full compliance with internal and external quality and regulatory requirements.
  • Strategic Partnership: Act as a key technical consultant for cross‑functional departments to develop and maintain scalable, cost‑effective, and safe production processes.
  • Audit Excellence: Represent the technical site functions during regulatory inspections and lead expert discussions with auditors.
  • Technical Diplomacy: Synthesize complex technical challenges into clear, strategic updates for site leadership and global stakeholders.

Profile

  • Education: University degree (Master’s or equivalent) in Biology, Chemistry, Veterinary Medicine, Biotechnology, or a related life science discipline.
  • Experience: At least 5 years of professional experience in a pharmaceutical environment, specifically within pharmaceutical production.
  • Compliance & Technical Knowledge: Familiarity with Global Quality Standards (FDA, EU‑GMP) and a solid understanding of aseptic processes.
  • Languages: Excellent written and spoken communication skills in both German and English, with effective communication skills in multicultural settings.
  • Analytical & IT Skills: Strong analytical capabilities and proficiency in MS Office (Excel, Word); experience with statistical software (e.g., JMP) is highly desirable.

Desired Skills

  • Strategic Thinking: Ability to develop and implement long‑term strategies aligned with business goals.
  • Conflict Resolution: Effectively resolving conflicts and fostering a positive team environment.
  • Change Management: Leading and managing change effectively within the team and across departments.
  • Continuous Improvement Mindset: Proactive approach to identifying and implementing process improvements.
  • Cross‑Functional Collaboration: Effectively collaborating with other departments, such as Production units, R&D, Quality Assurance, and Supply Chain.
  • Adaptability and Flexibility: Responding effectively to changing priorities and demands.
  • Problem‑Solving and Decision‑Making: Demonstrated ability to analyse complex situations and make sound decisions.

Benefits

  • Competitive Compensation: An attractive salary package and participation in the company's success through our bonus scheme.
  • Autonomy & Growth: Room for personal initiative and independent action within a modern, growing global pharmaceutical company.
  • Career Development: Access to our internal global career network with exciting development and training opportunities.
  • Dynamic Environment: Work in a diverse and interesting environment where your contribution directly impacts animal health worldwide.

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