QC Manager - Pharma
Pharmaceutical Company - API's - QC Manager - Principi Attivi - Azienda Farmaceutica
La tua nuova azienda
Il tuo nuovo ruolo
Di cosa hai bisogno per aver successo
Location: Malta
Cosa devi fare ora
If you are interested in this opportunity, click on "Apply Now" to submit an updated copy of your CV. If this opportunity does not align with your expectations, but you are looking for a new job, visit our website to discover new opportunities. Candidates of both sexes, after viewing the mandatory privacy notice on the website www.hays.it, are requested to send their CV in Word format, indicating the reference (Ref. 947202) and their consent to the processing of personal data pursuant to D.LGS. 196/03. Min. Auth. No. 13/I/0007145/03.04 of April 1, 2008.
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Our Client, is a leading pharmaceutical company, organization located in the Mediterranean. It focuses on the development and production of high-quality pharmaceutical products, utilizing advanced technologies and modern facilities. Committed to innovation and regulatory compliance, it collaborates with global partners and continuously invests in infrastructure and sustainability.
Il tuo nuovo ruolo
In view of expanding our workforce, we are seeking a QC Manager. For this role, the following responsibilities are expected:
Coordination: Supervising subordinate functions to meet long- and short-term deadlines while collaborating with other departments and/or company direction.
Budget: Defining and adhering to the annual Quality Control (QC) budget.
QC Strategies: Acting as a reference person for strategy definition for QC laboratories.
Programming and Analysis: Responsible for planning and executing analyses of raw materials, intermediates, and active pharmaceutical ingredients.
Documentation and Regulations: Managing GMP documentation, SOPs, analytical methods, and validation documents.
Non-Conformities: Supervising investigations into deviations and non-conformities and implementing CAPA measures.
Batch Approval: Final approval or rejection of batches/intermediates.
Audits: Participating in internal/external audits as auditor and auditee.
Training and Personnel: Supervising personnel training, task distribution, and organization of work shifts.
Instruments and Reagents: Managing instrument calibration and procurement of reagents and consumables.
Method Transfer: Overseeing transfer and validation of analytical methods.
Extraordinary Activities: Coordinating extraordinary activities with other company functions or suppliers.
Electronic Data: Managing GMP electronic data storage and backup.
Certificates: Issuing certificates of analysis (CoA) and handling sample management.
Substitution: Acting as Stability Manager replacement when absent, reporting to the Head of Quality Unit and Direction.
Di cosa hai bisogno per aver successo
For this role, the following qualifications are required:
A Scientific Degree (e.g., Pharmaceutical Chemistry and Technology, Pharmacy, Biology, etc.);
At least 5 years of solid experience in a pharmaceutical production environment (preferably APIs);
Fluent knowledge of the English language is mandatory.
Location: Malta
Cosa devi fare ora
If you are interested in this opportunity, click on "Apply Now" to submit an updated copy of your CV. If this opportunity does not align with your expectations, but you are looking for a new job, visit our website to discover new opportunities. Candidates of both sexes, after viewing the mandatory privacy notice on the website www.hays.it, are requested to send their CV in Word format, indicating the reference (Ref. 947202) and their consent to the processing of personal data pursuant to D.LGS. 196/03. Min. Auth. No. 13/I/0007145/03.04 of April 1, 2008.
#LI-DNI
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Riepilogo
- Tipologia di lavoro
- Tempo indeterminato
- Settore
- Industria e Produzione
- Sede di lavoro
- ITALIA
- Divisione
- Life Sciences
- Rif:
- 947202
Consulente di riferimento
Il Consulente Martina D'andrea, è il nostro esperto che gestisce questa opportunità di lavoro, con sede a Milano
Hays, Corso Italia, 13 - Milano
Telefono: 02 888 93 300
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