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- Write/prepare analytical methods and specifications of analysis docs, chromatographic proformas and analytical records
- Support in documentation related to method validation, process validation, cleaning validation, and stability studies
- Issue of COAs for QC Management approval
- Assist the QC Manager in drafting/revising SOPs relevant to QC operations
- Ensure that all pharmacopeial standards are in compliance with current pharmacopoeias and are reflected in internal documents
- Participate in the management, coordination and timely execution/closure of change controls, deviations and CAPAs
- Creation of specifications and master of tests in the MRP system
- Co-ordination and management of client sample requests
- In possession of a higher qualification in Chemistry or Pharmaceutical Science
- A minimum of two years experience in a pharmaceutical QC environment
- Extremely organised and possess excellent communication skills
- Able to work independently as well as in a team environment
- Self-motivated and have excellent attention to detail
- Results-oriented and will display an attitude that reflects our Company values
Quality Control Documentation Officer - Birżebbuġa, Malta - Quad Consultancy
Description
Industry: Pharma
Location: Malta
Basis: Full time
Remuneration: Salary + Benefits
Main Duties:
What skills do you need?
Eligibility to work in the EU is a must
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