Our Team

As we have grown our team our core values revolve around:

  • People – investing in and developing our employees
  • Professionalism – providing our Clients with clear technical solutions, efficiently.
  • Passion & Participation – creating an environment of knowledge transfer
  • Performance – delivering on commitments to clients
  • Process – Understanding and strict compliance with all regulatory frameworks

We are proud of our heritage which is one of technical excellence and strong core values.

Meet the management team

Jo Bunyan

Managing Director

Jo was co-founder of the group and has over 25 years experience in Regulatory affairs and Pharmacovigilance. She holds an MSc. In Pharmacovigilance and is a QPPV.

Steve Davenport

Technical Director

Steve has over 25 years experience in the Pharmaceutical industry working in a manufacturing environment and obtaining QP status in 2005.

Andy Smith

Technical Manager

Andy has worked for over 35 years in the Pharmaceutical Industry for both Blue Chip and privately owned companies producing OTC and Prescription Medicines. He has held roles within Manufacturing, Packaging and Quality Assurance.  As a TQP and IRCA Certified PQS auditor with experience of auditing in the UK, Europe and India, Andy has a depth of experience and knowledge of the industry.

Lisa Sproat

Technical Manager

Lisa has over 15 years’ experience working within the Pharmaceutical & healthcare sector and is in the final stages of QP qualification. She is a qualified lead auditor with a strong background working in GMP and auditing a range of API and finished product sites worldwide. Experienced in GDP and completed Cogent Gold Standard training, she also acts as a Responsible Person.

Jim Johnston

Quality Manager

Jim is a chemist and has worked in the pharmaceutical, Contract Manufacturing industry for 17 years in human, veterinary and special medicines. He has worked extensively in R&D, Quality Control, Qualification, Validation, Quality Assurance Management and has a strong Technical background in relation to regulatory requirements. Jim is an approved MHRA and HPRA Responsible Person and is currently in the final stages of QP qualification.

Batch release of human & veterinary medicines to market, Qualified Person (QP) services & pharmaceutical auditing from Elara Pharmaservices. MHRA & VMD approved.

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