Training consultant: Adam Slater

Adam is a Pharmaceutical/Biopharmaceutical  Quality Assurance (QA) professional, with over 35 years’ experience across GMP, GDP, ISO 9001, Pharmaceutical Quality Systems (PQS) and auditing. A Microbiology and Chemistry Graduate, Adam started his career in QC laboratories within the NHS, before moving into the private sector. He then moved into Quality Control (QC) and QA roles within different contract manufacturing companies, further enhancing his industry experience and expertise.

 

In 2004 Adam joined Wyeth (now Pfizer), leading a team responsible for contract manufacturing operations in Europe, Middle East and Africa. Adam also completed his EU Qualified Person training during this busy time.

 

Adam has an array of industry knowledge gained from a career spanning positions in QC, QA, regulatory, R&D, operations, technical support and validation. He is also very experienced when it comes to dosage forms, specialising in sterile manufacturing and US FDA PAI readiness and remediation.

In addition, Adam is an active, highly experienced international auditor and has worked extensively in India, China, Pakistan, Middle East, Japan and the US. 

 

Dedicated to promoting positive ‘Quality Culture’, Adam has used his senior leadership and board roles to help spread this message and established his own consultancy in July 2010.  

 

Passionate about passing on his personal experience onto others, Adam is involved in the education, coaching, mentoring and training of fellow professionals at any stage of their pharmaceutical career journey. 

 

 

Consultancy

 

Adam is nominated by the UK MHRA as a Compliance Monitor and enrolled on the MHRAs pilot compliance monitoring team. This is aimed at providing remediation support to organisations who have following inspection been required to provide closer oversight of their pharmaceutical quality system and progress to addressing identified concerns to the inspection body

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