Cleaning Validation Engineer

Cleaning Validation Engineer – Pharmaceuticals / GMP / cleaning / validation / SOP / Swedish

Location: Helsingborg, Sweden

Company: Global Consumer Healthcare Company

Duration: 6 months, with extensions.

Overview

The Cleaning Validation Engineer is responsible for cleaning validation and re-validation of process equipment used for all marketed company products in Helsingborg. You will assess and determine the acceptance criteria for cleaning validation of the process and packaging equipment used on site. The role may also include work to improve the cleaning validation processes and systems in order to maintain the validated status of the cleaning processes at the Helsingborg plant.

Main responsibilities

• Prepare cleaning validation protocols and reports according to the Validation Master Plan (VMP) and project timelines.
• Execute the cleaning validation process, including:
• Create necessary documentation for validation runs.
• Train and coordinate with production staff involved in the validation activity.
• Conduct sampling and analysis of samples.
• Collaborate with all departments to ensure successful cleaning validation or re-validation.
• Follow designated Standard Operating Procedures (SOPs) and required training for the role.
• Enhance cleaning instructions or validation processes as needed through updates and improvements.

Must-have

• Bachelor’s degree with a major in e.g. Chemistry, Chemical engineering, pharmaceutics, or equivalent.
• Proficient in Swedish and English.
• Experience in the field of cleaning validation with proven knowledge of cleaning validation including sampling techniques.
• Experience in the execution of cleaning validation processes and calculating cleaning limits.
• Experience in analytical methods.
• Capability to lead a project team to achieve a defined goal.
• Strong interpersonal and collaborative skills to facilitate the planning and execution of activities.
• The ability to generate technical and user documentation to GMP standards and technical writing is also required.
• Excellent knowledge of GMP requirements.
• Full autonomy to work independently.

******To apply to this role you must be legally entitled to work in Sweden***

>>>>Apply directly here or send your CV to up@eu-recruit.com<<<<

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