Cleaning Validation Engineer

WeQuelHelsingborgJob.bopublished 10/26/2026
Must-have:HealthTech

About the company

Cleaning Validation Engineer – Helsingborg At WeQuel, we connect skilled specialists with exciting assignments across Life Science and industry. We are now looking for an energetic Cleaning Validation Engineer for an assignment with a global consumer healthcare company at its manufacturing site in Helsingborg. The site produces over-the-counter medicines for the global market. You will join the Technical Operations team.

Your tasks

The assignment You will be responsible for cleaning validation and re-validation of the process and packaging equipment used for the site’s marketed products. You will assess and set acceptance criteria for cleaning validation. You will also help improve cleaning validation processes and systems so the cleaning processes stay in a validated state.

  • Prepare cleaning validation protocols and reports on time, in line with the Validation Master Plan (VMP) and project timelines.
  • Execute cleaning validation, including:
  • preparing the documentation needed for the validation runs
  • training and coordinating the production staff involved
  • performing sampling and analysis of samples.
  • Calculate cleaning limits and set acceptance criteria.
  • Collaborate with all departments to make validation and re-validation successful.
  • Update and improve cleaning instructions and validation processes as needed.
  • Follow the relevant SOPs and complete the training required for the role.

Requirements

  • Bachelor’s degree in Chemistry, Chemical Engineering, Pharmaceutics or equivalent.
  • Proven hands-on experience of cleaning validation, including sampling techniques.
  • Fluent Swedish and English, spoken and written.

Meriting

  • Experience of calculating cleaning limits.
  • Experience of analytical methods.
  • Experience of leading a project team towards a defined goal.
  • Strong technical writing and documentation skills to GMP standards.
  • Excellent knowledge of GMP requirements.

You are energetic, driven and have a strong work ethic. You know cleaning validation thoroughly and enjoy working close to production. You thrive in a Technical Operations team, collaborate easily with colleagues across functions, and can plan and drive activities on your own.

How to apply

Send your application today. We review applications continuously and the position may be filled before the application deadline.

Other

Assignment details

  • Location: Helsingborg
  • Scope: full time (100%)
  • Remote: on site (0% remote)
  • Start: 1/12-26

Det här har jag medvetet utelämnat ur annonsen: kundens namn, produkt- och varumärkesnamn samt pris. Startdatum, slutdatum och omfattning fanns inte i underlaget. Jag har därför skrivit “as agreed”, 100 % och onsite som standardvärden. Justera dem om kunden har angett något annat.