- QA Specialist - 6 month fixed term contract - Athlone, Ireland-121138
Due to continued growth, PPD is recruiting for a QA Specialist to work on a 6 month basis at our Athlone Global Clinical Supplies Depot. Working within the Quality Management Services group, the role will be to provide expertise to the QA department in a variety of specialized quality management areas; including all aspects of GMP manufacturing, quality systems audits, manufacturing investigations, route cause analysis for critical and non-critical quality events, complaints and recalls. ...
- QA CSV Specialist
Excellent opportunity to join the Global QA IT team of a Biotechnology company based in Switzerland.
- RA\QA Specialist
Employment type: Permanent, full-time
Clinical Professionals are currently working with one of the globe’s leading Medical Devices distribution firms, based in Germany, who are looking for individuals to undertake a role as a Regulatory/Quality Specialist.
- Quality Assurance Specialist
You will be working in the setting of the oldest City in Ireland. This is an excellent opportunity for an experienced Quality assurance Specialist to join a very progressive and dynamic role within a busy GMP environment. This quality assurance role will report directly into the QA ManagerI have an immediate opening for a Quality Assurance Specialist position in a leading medical device company based in Co.Waterford. ...
- Quality Management Specialist – Clinical Technologies – London, UK
Quality Management Specialist – Meet are partnering with a leading Clinical Technologies who pride themselves on offering the best service to their clients. They are recruiting for a Quality Management Specialist to take full ownership of the Quality Management system within this leading Global organization.
- QA Specialist - 6 month Fixed Term Contract. Job
Position Specialist, QASupervisor Associate Director, Quality Compliance – Celgene EuropePrerequisites BS (or equivalent) in a technical of scientific discipline.Demonstrated pharmaceutical (or other related industry) quality experience. ...
- QA Specialist GMP
I am currently working with an expanding client who want bring on a new Quality Officer to join a fast pace and diverse role and team. This is an excellent sociable working environment within a company who offer excellent training and progression prospects. It will also allow successful applicants the opportunity to work from early stage through to manufacture.
- Qualities Systems Specialist
Qualities Systems Specialist: South of England
Rate: 300 per day
Our Client is a large well established pharmaceutical company based in Kent. Looking for a Qualities Systems Specialist with experience within GMP and FDA Guild lines.
- Quality Specialist –Lifecycle Validation– Noord Brabant
As a Quality Specialist you are responsible to ensure new products are introduced in a compliant and efficient manner, by keeping focus on regulatory, quality and supply needs. Additionally, you will support product lifecycle activities in QA support for variation management.
- QA Specialist
Primary Tasks and Responsibilities Supports the management of GMP compliance systems through the following activities: • Assesses compliance systems on ongoing basis to identify opportunities for process improvement. • Carries out tasks related to the administration of project and site nonconformance management systems: • Reviews and/or approves nonconformance investigations and their associated documentation. • Manages entry of nonconformance records into the appropriate electronic system. ...