Compliance / Life Science Consultant

Epista Life Science Sweden is growing and they are looking to add Compliance/Life Science consultants to their team!

They a consultancy of more than 100 employees dedicated to continuously improving compliance and business in the Life Science industry. Epista has big ambitions for the future of Life Science, and want you to be a part of it and help them achieve those goals. If you’re interested in becoming the next addition to their team, get in touch, we want to hear from you.

General Consulting is one of their four strategic value propositions within Epista. General Consulting consists of a team of specialists working in a wide field of the Life Science industry. The team members have significant knowledge and experience from different GxP disciplines and areas from R&D to commercialisation to Supply Chain, QA/QC/QP, IT, and more. General Consulting is closely connected to the other Epista Business Units and supports these as appropriate, but in most cases, consultants in General Consulting conduct their assignments independently in the customer’s business environment. 

About the job;

Depending on your expertise and interests, you may work on:

  • QMS Development and Optimization (Pharma and Medical Devices)
  • QA / IT Validation
  • Audits
  • GMP Supply Chain Processes
  • Customer projects – identifying, planning, specification, and implementation.

The Epista team has extensive experience in various Life Science fields, in addition to technical expertise and project management. You’ll be part of a team that continuously works to increase the contribution of Life Science to society by turning compliance obstacles into business opportunities.

In addition, you have:

  • At least 5 years of experience in any of the following areas: Compliance, QMS, QA/QC, QP, computer system validation, auditing, or similar in a regulated industry
  • A driven, structured, result-oriented, and ambitious mindset
  • A desire to continuously improve your clients, your colleagues, your company, and yourself
  • Bonus: Experience in IT QA/QC in the pharmaceutical industry
  • Possibility for occasional travel as some of our customers are located at different locations.

On a typical day you might;

As an Epista consultant, you’ll be working at the intersection of compliance and business as a part of the highly skilled and dedicated team. You’ll be involved in a wide variety of projects and assignments and always in connection with various business areas. And the best part? You probably already have the skills and have done many of the tasks in your previous roles in the industry. But now, your time will be spent with the clients – international pharma and medical technology companies. Your daily activities might include:

  • Collaborating with colleagues both internally at Epista and at your clients
  • Developing, reviewing, and updating documentation
  • Understanding end users and applying their needs
  • Preparing and/or participating in workshops
  • Internal knowledge sharing
  • Business relationship building
  • Holding and facilitating training sessions.

Interested? Send your CV to

Computer System Validation Specialist


Compliance Consultant


Veeva Vault Implementation Specialist


Veeva Vault Managed Operations Specialist


Process Automation Consultant


IT Project Manager