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