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Quality and Compliance Analyst
Eingestellt von Optimus Search Limited
Gesuchte Skills: Engineering
Projektbeschreibung
Quality and Compliance Analyst
A fantastic new opportunity has arisen for an experienced Quality and Compliance Analyst to join a global pharmaceutical/manufacturing organization in Belgium. The successful candidate will start ASAP as the position is urgent.
Tasks and responsibilities:
- Implementation and maintenance of Standard Operating Procedures, work instructions and templates
- Maintenance and review of qualification documents and coordination of corrective actions
- Qualification planning and cooperation with project teams to ensure qualification activities are performed
- Identify and implement process and/or application improvements
Required profile:
- At least 3 years experience in the pharmaceutical industry
- 3 years experience in technical writing CSV, SDLC, GxP
- Strong tracking, coordination and project planning skills
- Master and/or Bachelor Degree in Mathematics, Engineering, Computer Science, Chemistry or Bioinformatics OR equivalent through experience
- English and Dutch spoken and written
The successful candidate will enjoy working as part of an experienced and passionate team. They will have the chance to make an impact within a well-known organisation whilst enjoying a competitive salary and benefits package.
For more information, please forward your CV for immediate consideration. We also offer a generous referral bonus of £400 for any referral that results in employment so if you know of anyone suitable please put them in touch.
A fantastic new opportunity has arisen for an experienced Quality and Compliance Analyst to join a global pharmaceutical/manufacturing organization in Belgium. The successful candidate will start ASAP as the position is urgent.
Tasks and responsibilities:
- Implementation and maintenance of Standard Operating Procedures, work instructions and templates
- Maintenance and review of qualification documents and coordination of corrective actions
- Qualification planning and cooperation with project teams to ensure qualification activities are performed
- Identify and implement process and/or application improvements
Required profile:
- At least 3 years experience in the pharmaceutical industry
- 3 years experience in technical writing CSV, SDLC, GxP
- Strong tracking, coordination and project planning skills
- Master and/or Bachelor Degree in Mathematics, Engineering, Computer Science, Chemistry or Bioinformatics OR equivalent through experience
- English and Dutch spoken and written
The successful candidate will enjoy working as part of an experienced and passionate team. They will have the chance to make an impact within a well-known organisation whilst enjoying a competitive salary and benefits package.
For more information, please forward your CV for immediate consideration. We also offer a generous referral bonus of £400 for any referral that results in employment so if you know of anyone suitable please put them in touch.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Ingenieurwesen/Technik