Are you looking to broaden your experience in a diverse setting that will give you exposure to a range of quality activities?
Partnering with an evolving business that has been investing heavily within their quality team over the past 6 months, I am now supporting the hire of a Quality Specialist to add further experience to the team.
With a global presence, you will have the opportunity to work on a range of projects supplying critical medicine across the world.
Given the nature of this being a contract site, versatility is key and that is reflected in the role responsibilities – batch review, auditing and supplier management to name just a few.
You don’t need to have worked in each of these areas before but what you do need is to be able to bring a solid early background in QA activities in a GMP setting, as well as a positive and flexible attitude to the site, with a continuous learning approach.
· Experienced in a Quality Assurance capacity within a GMP setting
· Pharmaceutical experience preferred but alternative GMP environments could be considered
· Educated to degree level from a relevant technical background
· Experience across some of batch review, investigations, auditing, supplier management and system controls.
· Good understanding of the range of quality responsibilities on a testing, manufacturing and packaging facility
· Flexible approach who can learn and adapt quickly
Please apply below or contact Mark Bux-Ryan for more information.
Quality, QA, assurance, GMP, manufacturing, distribution, packaging, CDMO, pharmaceutical, batch, release, systems, compliance, regulatory, specialist, investigations, CAPA, deviation, change, control, operations
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