Middle-Level Production Supervisor & Technology Transfer Specialist
Descrizione dell'offerta
Adecco Life Science is looking for a Middle-Level Production Supervisor & Technology Transfer Specialist on behalf of a pharmaceutical company operating in the development and manufacturing of semi-solid and liquid dosage forms.
Responsibilities:
- Oversee daily production activities and ensure optimal allocation of resources.
- Supervise and motivate production teams, ensuring adherence to safety regulations, GMP standards, and internal procedures.
- Collaborate with cross-functional departments such as Quality, R&D, Procurement, and Engineering to achieve organizational goals.
- Drive continuous improvement initiatives focused on performance, quality, safety, and operational efficiency.
- Participate in technical feasibility evaluations, new product introductions, and technology transfer activities.
- Draft, review, and maintain GMP documentation, including SOPs, batch records, and deviation reports.
- Support the optimization of manufacturing processes and manage production and packaging activities for new product launches or process improvements.
Required Qualifications:
- A degree in scientific disciplines such as Pharmaceutical Chemistry, Pharmacy, or related fields.
- 3–5 years of experience in production roles, preferably with team supervision responsibilities.
- Proven expertise in technology transfer processes for semi-solid and liquid products, including compounding, filling, and packaging operations.
- Previous experience in continuous improvement projects with a lean approach.
- A strong analytical mindset and ability to identify and implement process optimizations.
Additional Preferred Skills:
- Background in R&D with demonstrated leadership capabilities and familiarity with process improvement methodologies.
- Prior experience in a CDMO environment is considered an asset.
- Excellent interpersonal and communication skills to foster collaboration with internal and external stakeholders.
- Proficiency in English, both written and spoken.
Additional Information:
- Contract Type: Permanent, regulated under CCNL Chimico Farmaceutico.
- Work Environment: A dynamic, innovative, and international company that promotes collaboration and professional growth.
- Compensation: Competitive remuneration aligned with experience and industry standards.
Working Hours: Full-time availability required.
Workplace: Metropolitan City of Milan.