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

Associate

Employment type

Full-time

Job function

Product Management

Industries

Pharmaceutical Manufacturing

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