Middle-Level Production Supervisor & Technology Transfer Specialist

Middle-Level Production Supervisor & Technology Transfer Specialist

Middle-Level Production Supervisor & Technology Transfer Specialist

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Talent Acquisition & Recruiting Specialist Life Science @Adecco

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:

- 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: Northern Province of Milan, Italy

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Full-time

Job function

• Job function

  Product Management

• Industries

  Pharmaceutical Manufacturing

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