Product & Process Engineer: Validation & Innovation

Haleon plc.

Aprilia

On-site

EUR 41,000 - 56,000

Full time

3 days ago
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Job summary

Haleon plc. is seeking a Product and Process Engineer at the Aprilia site to drive development and validation of manufacturing processes and cleaning procedures. You will lead cross-functional teams, interact with Global R&D, and author validation reports while updating related SOPs.

The role emphasizes handling stability data, de-risking projects with suppliers and QA, and ensuring validation state control via CPV/PCS reviews. Fluency in English and a scientific background are required.

Qualifications

  • Scientific University degree in Chemistry, Pharmaceutical Chemistry, Chemical Engineering, Biology, Biotechnology, or related area.
  • 2–5 years of experience in a GxP pharmaceutical regulated environment.
  • Experience with process validation of pharmaceutical and dietary supplement products and cleaning validation in GMP production.

Responsibilities

  • Coordinate development and validation of manufacturing processes and equipment cleaning procedures.
  • Author protocols and reports, and update SOPs.
  • Analyze stability data for shelf-life and site programs.
  • Coordinate de-risking and business continuity projects with suppliers and QA.
  • Perform cleaning validation assessments for new products and materials.
  • Support CPV and data trending to ensure processes stay in a validated state.

Skills

GxP experience
Process validation
Cross-functional collaboration
English proficiency

Education

Scientific University degree in Chemistry, Pharmaceutical Chemistry, Chemical Engineering, Biology, Biotechnology, or related area

Job description

Haleon plc. is seeking a Product and Process Engineer at the Aprilia site to drive development and validation of manufacturing processes and cleaning procedures. You will lead cross-functional teams, interact with Global R&D, and author validation reports while updating related SOPs.

The role emphasizes handling stability data, de-risking projects with suppliers and QA, and ensuring validation state control via CPV/PCS reviews. Fluency in English and a scientific background are required.

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