Piramal Pharma Solutions
Guus Jellema has a diverse work experience in the pharmaceutical and medical industries. Guus started their career as a Design Assurance Engineer at Phillips-Medisize in July 2016. Guus then worked as a Qualified Person/QPPV and RP at Linde Gas Benelux from January 2017. In June 2017, they joined Zimmerbiomet as a sr.QA specialist. In February 2018, they took on the role of Lead Auditor and Technical Expert in Medical Devices and Pharma at SGS Antwerp Belgium. Guus also worked as a GTX Eindhoven Medical QA at GTX medical starting from September 2018. Guus shifted to Allergan as a QA Manager QP/RP starting from October 2018 until December 2019. Guus then became a Senior Regulatory Affairs at GSK from February 2019 until July 2019. Guus briefly worked as a Senior Manager and QP Head of the Release Department at TEVA from August 2019 to October 2019. Finally, they worked as a Principal EU QP at Piramal Pharma Solutions from January 2022 till present.
Guus Jellema pursued their PhD in Organic Chemistry and Medical Biochemistry at Leiden University from 1978 to 1984.
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Piramal Pharma Solutions
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Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug product. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovator and generic companies worldwide.