Meet...

Aneta Jell

Presenter

Aneta Jell is a seasoned Quality Assurance professional with over 20 years of experience across manufacturing, contract operations, and quality leadership in the pharmaceutical industry. Currently serving as Quality and training manager at PaulPalmer limited she oversees global contract manufacturing quality, ensuring GxP compliance, regulatory alignment, and supply chain integrity. Her expertise spans GMP, ISO 9001, ISO 17025, and QMS administration, with proven strength in audits, CAPA, deviations, and technical agreements. A qualified QMS lead auditor with bilingual proficiency in English and Slovak, Aneta is recognised for driving continuous improvement, fostering compliance culture, and leading high-performing quality and HSE teams.

Aneta Jell’s courses

  • 18 Nov • 1 day course

Root Cause Analysis and Critical Thinking

Live online

  • 01 Dec • 2 day course

Process Validation with Qualification

Live online

  • 04 Dec • 1 day course

CAPA (Corrective and Preventative Action)

Live online

  • 08 Dec • 1 day course

Data Integrity and Document Management

Live online

  • 08 Dec • 2 day course

Effective Technology Transfer

Live online

  • 10 Dec • 2 day course

Mastering Computer System Validation

Live online

  • 24 Jun • 1 day course

ICH Q9(R1) Quality Risk Management (QRM)

Live online

Reviews for Aneta’s courses

I wanted to gain the knowledge from other SOP writers, especially from another country. I found that the US and the UK have very similar ways to create SOPs and Process Maps. I found the whole experience informative and well put together. I would reccomend it to others.

26 Mar 2026

Writing Inspection-Ready SOPs: Best Practice for Compliance and Control

Laura was very professional, knowledgeable, and had a relaxed manner that made a somewhat dry subject easy to follow and engage with. The documentation was useful, and having never had formal SOPs writing training before now.

26 Mar 2026

Writing Inspection-Ready SOPs: Best Practice for Compliance and Control

Laura was very good, easy to understand and answered any questions

18 Dec 2025

Data Integrity and Document Management

I really liked this webinar and I would suggest it to other colleagues

4 Dec 2025

Writing Inspection-Ready SOPs: Best Practice for Compliance and Control

Overall, I enjoyed the course and got a lot of worthwhile knowledge and ideas for improving the SOP system I work with currently. Laura was very knowledgeable and led the course well. She was accommodating for delegates of varying levels of experience. I enjoyed the mind mapping and flow chart exercises.

4 Dec 2025

Writing Inspection-Ready SOPs: Best Practice for Compliance and Control

Very good. Also the form of how it was conducted with the exercises

24 Nov 2025

Root Cause Analysis and Critical Thinking

Overall, the webinar was good. The content was informative, the presentation was clear.

24 Nov 2025

Mastering Computer System Validation

I was hoping to gain knowledge and be exposed to different interpretations of the guidelines. I accomplished this. It was a great opportunity to see the guidelines from a pharmaceutical perspective. I enjoyed seeing the tolerances the most, in terms of aspects that do not have specific guidelines but would be considered best practice. I have a positive opinion of the webinar, content and presentation. I also enjoyed the way it was clearly broken down into distinct parts, being able to see the exercises in advance [to help] pay particular attention on those parts, and apply what I have just been taught. The speakers were of high quality, and knowledgeable within the field delivering a highly engaging session.

10 Nov 2025

Stability Testing of Pharmaceuticals and Biopharmaceuticals

Very good. I was expected to improve my knowledge and get some tips and I did it.

17 Jul 2025

Writing Inspection-Ready SOPs: Best Practice for Compliance and Control

I particularly liked working groups. Very good!

17 Jul 2025

Writing Inspection-Ready SOPs: Best Practice for Compliance and Control