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Jen Postlethwaite Bpharm Mrpharms

Senior Regulatory Affairs Specialist at Kindeva Drug Delivery

Jen Postlethwaite BPharm MRPharmS has extensive experience in regulatory affairs and pharmaceutical operations, currently serving as a Senior Regulatory Affairs Specialist at Kindeva Drug Delivery since August 2020, where responsibilities include supporting the development and commercialization of inhalation and transdermal products. Prior to this role, Jen worked as a Regulatory Affairs Contractor at 3M Health Care Ltd from June 2017 to July 2020, providing regulatory compliance guidance and strategic planning. Jen also held leadership positions, such as Director of Manufacturing Operations at Quotient Clinical Ltd and Head of BCM Specials & Analytical Services at BCM LTD, where significant improvements in productivity and compliance were achieved. Educational background includes a Bachelor of Pharmacy degree from the University of Nottingham.

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Kindeva Drug Delivery

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Kindeva Drug Delivery is a global contract development and manufacturing organization (CDMO) in the pharmaceutical industry.


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501-1,000

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