Hobson Prior are looking for a QA Associate to join a leading pharmaceutical organisation in Slough, where you will support the other RQ Global Quality Lead auditors by assisting with all Good Laboratory Practice auditing activities.

Job Responsibilities:

• Review of Study Plans, Study/Phase Reports and Standard Operating Procedures (SOPs), for audit by team - utilising Veeva, TrackWise, Excel (database).
• Conducting process-based, system/facility-based audits (database).
• Writing of Audit Reports within TrackWise (database, Adobe Acrobat, MS Word).
• Drafting QA Statements from information within TrackWise (database, MS Word, Adobe Acrobat)
• Tracking CAPA and follow up within TrackWise; follow up with internal CAPA owners (database)
• Contributing to the review of process maps within RQ standard procedures, during the update of the SOPs (MS Word, Adobe Acrobat, MS Visio).
• Preparation / Review of GLP, GRP, GCP Lab Refresher training content (MS Powerpoint).
• Maintaining strict confidentiality and discretion concerning matters pertinent to the team.
• Perform any other duties as requested to help support the RQ team activities.

Key Skills:

• Excellent communication skills and the ability to build effective working relationships with business partners.
• Able to function as a team player, with a desire to seek alignment of understanding of tasks.
• Proficient in the use of Microsoft Office Suite (MS Teams, MS Word, MS Excel, MS Powerpoint, MS Whiteboard).
• Excellent planning and organizational skills.
• Flexible thinking / creative approach to problem solving.
• Action-oriented, and able to motivate self and others.
• Attention to detail and solution orientated.

Requirements:

• Digitally competent and confident in using databases and web-based software (eg TrackWise, Veeva Vault).
• Comfortable in conducting remote multi-site audits.
• Ability to work on multiple tasks with conflicting priorities and work under pressure (whilst utilising multiple systems, various business partners).
• Sufficient experience in GLP to be able to advise the business partners with respect to GLP regulations, and how to meet these requirements.
• Fluent in English both written and oral; French would be desirable.
• Working competency in the OECD GLP Regulations; GLP auditor experience (2-5 years).

Apply now:

If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.