Your new company
Our client is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. The company focusses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people’s lives. A biotechnology pioneer since 1980, they have grown to be one of the world’s leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.
Your new role
Are you looking for a new role where you can provide QA guidance and support in production? We are looking for someone to perform batch record reviews of batches which are assembled, packaged and labelled onsite. In addition to this, an overview of your responsibilities will look like:
- Daily guidance of production staff in relation to compliance, SOPs and work instructions
- Act as a first point of contact for quality related questions during packaging and labelling
- Review and approve batch record data entries prior to production
- Carry out finished product checks during production runs
- Perform GMP compliance checks
- Initiate deviations, and review and approve deviation records
- Participate in QA production projects as needed
- Assist in various investigations
What you'll need to succeed
MBO or B.Sc. degree in Life Sciences with 3 years QA / quality related manufacturing in a pharmaceutical environment with experience in batch record review and investigations. Working knowledge and hands-on experience with GMP, GDP and or GCP. Experience in a manufacturing environment is highly desirable. Alongside these hard requirements, we are looking for:
- Knowledge of related industry regulations
- Ensures compliance with the regulatory environment
- Works under general direction
- Recognises and escalates problems
- Contribute to the team by ensuring the quality of tasks completed
- Establishing work relationships with other departments
- Excellent communication skills in English
What you'll get in return
Hays Detachering | This is a project that will start with a contract for 12 months through Hays. Extension to stay within the department is anticipated. In this position, you will get a competitive salary and your travel expenses are covered. This position is offered in shifts, therefore you must be available to work flexible hours, including weekends and nights. A shift allowance is offered for compensation.
What you need to do now
If you are interested in the role of Senior Associate QA GMP, click ‘Apply now’ to send an up-to-date CV, or give us a call! Is this job isn’t quite right for you, but are you still looking for a new position? Please contact us for a confidential discussion about your career.
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