Description
For our client, a leading multinational company, we are searching for a QA Method Validation Analist to work in The Netherlands (West) for 3 months plus possible extensions.
Main tasks:
Review and approval of analytical method validation documentation (protocols and reports); these activities are done on documentation and studies prepared by a contract manufacturer/laboratory. If the consultant would have the appropriate background and expertise, we would consider deploying this person for some other QA tasks as well in the same project (eg, on process characterization, raw material qualification, etc).
Experience:
- 3-5 years in the industry
- Candidate should have some demonstrable affinity with analytical techniques used in biotech: PCR, ELISA, IEF, SDS-PAGE, OD, Western Blot, HPLC, etc.
Candidate should be able to work independently. He/she should have the proper experience to make fair judgements on issues that may be encountered, ie, the candidate must be able to separate the vital few issues from the useful many. He/she must have good problem solving skills to ensure that issues are dealt with in a manner that is always GMP compliant and scientifically sound.
As the candidate works with an outside party as well as with several internal parties, he/she should have good communication skills.
Candidate should have proficient skills in English, both oral and written.
If you are interested in this position, please respond within 24 hours with your CV in Word format so MBA can contact you. MBA do have a policy to fulfil job requests within 24 hours therefore a quick response is important.
Michael Bailey International is acting as an Employment Business in relation to this vacancy.