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Process Expert

Linthwaite Facility




ONE STADA – communication and teamwork, it’s our path into the future together.

AGILITY – do you have the flexibility and decisiveness to drive change?

ENTREPRENEURSHIP – will you thrive in one of the fastest growing pharmaceutical businesses in Europe?

INTEGRITY – we are driven by trust, respect, and honesty, are you?


About the Company:

Like all success stories, our company history started with a great idea. In 1895, a group of pharmacists had a common objective: The standardized production of medicinal products to ensure an effective and reasonable provision of healthcare for the many. This was the beginning of STADA’s impressive development.


We are now a leading manufacturer of high-quality pharmaceuticals. With a long-standing heritage rooted in pharmacies, we continue to be a reliable and trustworthy partner. We help people regain and protect a dignified and able life.


As STADA, we fundamentally care for people’s health as a trusted partner.


If you are ready for new challenges where you can make a difference to people’s health, you have come to the right place. We are looking for people with a great attitude and passion, who care about making a difference in the world.


About the Role:

In this role within MS&T, you'll be responsible for providing front line expert support for all process-specific issues to production, continuously improving in quality and efficiency, performed in compliance to GMPs, SOPs and applicable guidelines. In this highly varied and fast paced role you will help to support the delivery of our strategic vision of Caring for People as a Trusted Partner.

Key Responsibilities

  • Support the execution of process validations, re-validations, Annual Batch Monitoring and short-term improvement projects, liaising with all the relevant parties to ensure accurate execution.
  • Execute process improvements, raw material assessments and scale-up.
  • Support Project Engineering in process related projects.
  • Support the selection and installation of new equipment and validation activities
  • Lead product and process related investigations and deviations
  • Be a resource to other departments as Subject Matter Expert for the product and process knowledge.


About You:

At STADA we talk about diversity as Uniqueness. Everyone is unique and we recognise our differences as a strength. Our values Entrepreneurship, Integrity, Agility and One STADA ensure our uniqueness thrives, enabling us to care for people’s health as a trusted partner. Empower your Uniqueness, bring your whole self to STADA.


If you’re keen to add value and see results, thrive under pressure and have the can-do spirit that’s spearheading our success, bring those unique qualities, with the following skills and qualifications:


  • A minimum of 5 years of combined experience in Pharmaceutical (i.e., Validation / QA) or allied industries with exposure to cGMP and GDP.
  • In-depth knowledge of GMPs and current validation sciences.
  • Proven process understanding (Pharma, GMP, Regulatory aspects)
  • Analytical thinking / problem solving skills


What’s in it for you?

Rewarding our employees is important to us, which is why we offer a range of fantastic benefits, such as:


  • Competitive base salary
  • Annual company performance-based bonus.
  • 25 days annual leave (plus bank holidays) with the opportunity to buy an additional 5 days leave.
  • Generous Company Pension Scheme
  • Life Assurance
  • Employee Assistance Programme

Apply now »