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Cleaning Validation Engineer

WeQuel AB
  • OrtHelsingborg
  • OmfattningHeltid
  • Sista ansökan30 dagar kvar
  • Publicerad26 okt.

Om tjänsten

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.

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.

Your responsibilities

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.

Who you are

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.

Assignment details

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

Apply

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

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.

Vill du att jag skapar uppdraget i Cinode (Sales Pipeline, inkorg) med den här annonsen som rollbeskrivning?

Krav- & nyckelordscheck

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