обновлено 4 дня назад
Secondary Packaging pMDI Supervisor (Biologics Manufacturing)
39 000€
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Secondary Packaging pMDI Supervisor (Biologics Manufacturing): Building and starting up a secondary packaging production department for a greenfield biologics manufacturing site with an accent on GMP-compliant process design, equipment qualification, and operational standards. Focus on supervising daily manufacturing, leading operators, managing deviations and investigations, and driving quality, safety, and continuous improvement.
Location: Nerviano, Milan, Italy
Salary: Minimum €39,000 per year, with the final offer based on skills, experience, qualifications, and internal equity.
Company
is an international research-focused biopharmaceutical group operating in more than 30 countries, with over 8,000 employees and manufacturing sites in Italy, France, and Brazil.
What you will do
- Support process and facility design, layout reviews, equipment URS definition, procurement, commissioning, and qualification for secondary packaging manufacturing lines.
- Participate in FAT/SAT activities and help establish operational workflows for a greenfield biologics manufacturing project.
- Develop SOPs, batch records, training programs, and operational standards in collaboration with MS&T, Engineering, QA, and Validation.
- Supervise day-to-day secondary packaging manufacturing operations and ensure compliance with EHS, quality, GMP, and ALCOA+ requirements.
- Lead and coach operators while monitoring production performance, deviations, investigations, and inspection readiness.
- Drive timely resolution, continuous improvement, and a strong quality and safety culture.
Requirements
- Degree in Biotechnology, Pharmacy, Biology, Chemical Engineering, or a related scientific discipline.
- 3–5 years of experience in secondary packaging manufacturing.
- Knowledge of GMP, GDP, and regulatory requirements for pharmaceutical packaging.
- Familiarity with process validation and equipment qualification.
- Strong documentation and deviation management capabilities.
Nice to have
- Previous experience supervising or leading production teams.
- Strong leadership, communication, and problem-solving skills.
- Experience managing OEE, productivity, quality, and schedule-adherence KPIs.
Culture & Benefits
- Purpose-driven environment focused on sustainable innovation, reliability, transparency, and ethical behaviour.
- Comprehensive pension, private medical insurance, wellbeing, and flexible benefits programs.
- Work-life balance initiatives, training, development resources, and performance bonuses.
- Relocation support and tax assistance services for foreign colleagues.
- Equal-opportunity workplace with a strong focus on diversity and inclusion.
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