Description
To provide leadership and direction for process engineering matters connected with the development, industrialisation and routine manufacture of Pharmaceutical products.
Responsibilities
- To set standards for process engineering which ensure the safe and reliable manufacture of its drug products in accordance with cGMP and Sanofi quality standards and guidelines
- To provide guidance and expertise on process engineering issues relating to the design, specification and operation of process systems which may affect safety, product quality or regulatory compliance
- To ensure that requirements for process engineering work are properly specified and essential deliverables identified resulting in tangible benefits in drug product process efficiency and commercial effectiveness being delivered to the Company.
- To ensure that process engineering design and investigation work is carried out by appropriately qualified organisation/individuals and results are properly presented.
- To evaluate processes in development and operations, identify opportunities for continuous improvement and define any changes required.
Skills and Behaviours
- Broad understanding of Pharmaceutical Engineering, Industry standards and Process Control.
- Proven project management skills.
- Team worker operating effectively in multi-disciplinary technical teams with other engineers, technologists and production personnel.
- Excellent communication skills both written and verbal.
- Demonstrate LEAD competencies: Act for change, Cooperate Transversally, Strive for Results, Commit to Customers, Make Decisions, Think Strategically
Qualifications and Experience:
- Degree in Chemical Engineering with 5 years related experience.
- Member of a professional Engineering Body.