We are currently looking for a Documentation Control Specialist to join a leading Pharmaceutical company based in Ireland.
As the Documentation Control Specialist you will help support an important project by ensuring the creation, storage, issuance, and retrieval of all documentation in a manner which meets cGMP requirements.
This is a contract opportunity until the end of December 2024.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Documentation Control Specialist will be varied however the key duties and responsibilities are as follows:
1. Responsible for defining, managing and maintaining a documentation control system for QC projects & BAU cGMP documents.
2. Responsible for supporting and reporting right first-time documentation findings to support continuous improvement initiatives.
3. As the Documentation Control Specialist you will participate in internal audits, support all external audits and any key quality Initiatives.
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4. You will also help maintain QC project key metrics ensuring site visibility, strong internal customer satisfaction and trending to support continuous improvement activities.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Documentation Control Specialist we are looking to identify the following on your profile and past history:
1. Good knowledge of cGMP in a regulated.
2. Excellent accuracy and attention to detail.
3. Ability to work independently and to your own initiative.
Key Words: QC / Documentation / Control Specialist / Documentation Control Specialist / Luna / GMP /
You must have the right to work in Ulster.
- Agency: Hyper Recruitment Solutions
- Reference: J5637455
Website: Hyper Recruitment Solutions
- Posted: 13th January 2023
- Expires: 10th February 2023
