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Middle-level production supervisor & technology transfer specialist

Peschiera Borromeo
Contratto a tempo indeterminato
Adecco Italia
Pubblicato il 31 luglio
Descrizione

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.

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