Mid-Senior Production Pharmacist - GMP & Quality Lead

Recordati S.p.A

Italia

In loco

EUR 70.000 - 90.000

Tempo pieno

9 giorni fa
Generatore di candidature

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Descrizione del lavoro

Recordati S.p.A. is seeking a Production Pharmacist to supervise pharmaceutical manufacturing and packaging operations on site at Ariana, TN. You will ensure GMP/BPF compliance, manage batch records, and support continuous improvement across production teams.

The role requires a Doctor of Pharmacy with active registration and experience in a pharmaceutical production environment. Familiarity with ISO 13485 is a plus for medical device contexts, and collaboration with Quality, QC, Maintenance and

Competenze

  • Doctor of Pharmacy degree.
  • Active pharmacist registration where required by local regulations.
  • Additional training in production, quality, GMP/BPF or industrial management preferred.
  • ISO 13485 knowledge is a plus when medical devices are in scope.

Mansioni

  • Supervise manufacturing and packaging activities according to production schedule.
  • Ensure compliance with GMP/BPF, internal procedures and ISO 13485 where applicable.
  • Oversee batch records, production records and documentation traceability.
  • Participate in deviations, non-conformities, CAPA, Change Control and risk analyses.
  • Support staff qualification and skill development of production teams.
  • Assist qualification, validation and control of processes.
  • Monitor team performance and drive continuous improvement.

Conoscenze

Pharma production experience
Team leadership
BPF/GMP knowledge
Regulatory compliance

Formazione

Doctor of Pharmacy
Pharmacist registration

Strumenti

Microsoft Office
ERP systems

Descrizione del lavoro

Recordati S.p.A. is seeking a Production Pharmacist to supervise pharmaceutical manufacturing and packaging operations on site at Ariana, TN. You will ensure GMP/BPF compliance, manage batch records, and support continuous improvement across production teams.

The role requires a Doctor of Pharmacy with active registration and experience in a pharmaceutical production environment. Familiarity with ISO 13485 is a plus for medical device contexts, and collaboration with Quality, QC, Maintenance and

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