Senior Scientist MS&T (m/f/d) - Pharma

Elanco; Cuxhaven; Vor Ort; EUR 70.000 - 90.000; Vollzeit

Benefits dieser Stelle

Competitive compensation and bonus scheme

Career development opportunities

Dynamic work environment

Zusammenfassung

Elanco, located in Cuxhaven, is seeking a Senior TS/MS Specialist (m/f/d) to bridge R&D and commercial manufacturing. The role involves leading project management and ensuring compliance with regulatory standards.

The ideal candidate holds a Master’s degree in a life science and possesses at least 5 years of experience in pharmaceutical production. Strong analytical skills, bilingual proficiency in German and English, and expertise in quality standards are essential for this position.

Qualifikationen

• At least 5 years of experience in a pharmaceutical environment, specifically in production.
• Familiarity with Global Quality Standards (FDA, EU-GMP) and aseptic processes.
• Excellent communication skills in German and English.

Aufgaben

• Lead and inspire cross-functional teams to achieve project milestones.
• Drive the transfer of vaccine manufacturing processes.
• Maintain the validated state of manufacturing processes.

Kenntnisse

Cross-functional collaboration

Analytical skills

Change management

Ausbildung

University degree in Biology, Chemistry, or related

Tools

MS Office (Excel, Word)

Statistical software (e.g., JMP)

Jobbeschreibung

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

As a Senior Specialist in TS/MS – Technical Services / Manufacturing Science, you are part of the scientific heart of production, serving as the vital bridge between Research & Development (R&D) and commercial manufacturing. Our team ensures that manufacturing processes are robust, validated, and state‑of‑the‑art to guarantee a continuous supply of high-quality vaccines.

Your Responsibilities

TS/MS Project Management & Technical Leadership

• 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 utilization 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.

Collaboration and Communication

• 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.

YOUR PROFILE

Essential Qualifications

• 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 And Abilities

• Strategic Thinking: The 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: A 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 analyze complex situations and make sound decisions.

Your 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.

Elanco is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.