QA Associate - EMEA

Job title : QA Associate - EMEA
Location : Brussels, Belgium
Job type : Contract/Freelance
Salary : Negotiable
Contact name : Jayne Stiff
Contact email : jayne.stiff@secpharma.com

A global CRO is looking for an experienced QA Associate to join them in their friendly, fast paced, professional team.

Client: Global CRO
Duration: 6 Months
Location: Remote - Able to travel to the Brussels area as necessary
Rate: Negotiable based on experience

The QA Associate will need to be experienced with SOPs, GLP/GMP and be able to perform audits

As a QA Associate Specialist, you will:
*Monitor the quality of laboratory data and reports.
*Review chromatographic data and related notebooks as specified by Standard Operating Procedures (SOPs).
*Evaluate data to ensure compliance with analytical methods, client criteria, Good Laboratory Practices (GLP) or Good Manufacturing Practices (GMP).

Essential duties and responsibilities (include but not limited to):
*Perform internal and vendor audits
*Participate in client and regulatory
*Institute and administer systems for tracking of manufacturing / laboratory investigations.
*Be involved in training activity
*Contribute to policy-making decisions as an expert in your field
*Building peer level relationships between onsite QA services and the QA management of designated customers.

Skills/experience required:
*Bachelor's degree or equivalent and relevant formal academic / vocational qualification
*Minimum of 2 years previous experience that provides the knowledge, skills, and abilities to perform the job
*Thorough knowledge of SOPs and Federal Regulations to include GLP and GMP
*Thorough knowledge of chromatography and divisional SOPs
*Strong technical knowledge including an understanding of laboratory procedures, methodology and standards
*Business proficiency in English and Dutch
*Strong verbal and written communication skills
*Strong attention to detail
*Ability to train staff Ability to independently review laboratory reports and analytical methods
*Ability to deal with multiple and changing priorities Ability to provide clear and concise feedback and/or documentation of results
*Ability to work in a collaborative team environment
*Must live in Belgium or Netherlands
*Occasional drives to site locations with occasional travel both domestic and international.

If you are interested in applying for this role, send your CV to Jayne.Stiff@secpharma.com or give me a call on +44(0)207 255 6630 to discuss this further.