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Senior Associate QA
Biotechnology and BioPharma jobs, Holland, Europe
| Job ref: | J011433/CO |
|---|---|
| Position type | Permanent |
| Location | Holland |
| Industry | Biotechnology and BioPharma |
Vacancy details
Senior Associate QA required to join a biopharmaceutical company located in Holland on a permanent basis. The QA Associate will be responsible for ensuring new and revised artwork for commercial printed packaging components is compliant with approved text and GMP. They will also be required to work with RA and provide them with the appropriate samples and documents for registration purposes.
Role and Responsibilities
- Check content of artwork against approved text, Change record and other references.
- Review and approve new and revised artwork for commercial printed packaging components (manual and electronic proof reading).
- Act as first point of contact for RA for registration requests.
- Coordinate the timely supply of documents (all kinds of certificates), samples of products or printed components and reference standards for registration purposes.
- Participate in internal audits as needed.
- Participate in projects and improvement efforts.
- Responsible for preparation of monthly metrics.
- Own and maintain departmental performance board
Requirements
- Good knowledge of the Dutch language
- Three years experience within Quality Assurance or a Manufacturing discipline
- Understanding and application of principles, concepts, theories and standards of technical/scientific field
- Deepens technical knowledge through exposure and continuous learning
- Knowledge of related regulatory/industry considerations, compliance issues and/or scientific discovery
- Applies research, information gathering, analytical and interpretation skills to problems of diverse scope
- Ensures compliance within regulatory environment
- Develops solutions to technical problems of moderate complexity
- Screens, categorizes, evaluates, reconciles, reports and resolves data integrity issues
- Interprets generally defined practices and methods
- Autonomy
- Works under general direction
- Work is guided by objectives of the department or assignment
- Refers to technical standards, principles, theories and precedents as needed
- May set project timeframes and priorities based on project objectives and ongoing assignments
- Recognizes and escalates problems
If this is you please apply today.
Apply for this job:
Quanta's recruiter for this job is Caroline O'Sullivan
- +44 (0) 1442 869 202
- E-mail Caz
- Connect on LinkedIn
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