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Associate Engineer Validation Ops​/temporary contrac

Job in 2000, Neuchâtel, Neuchâtel, Switzerland
Listing for: AurigaVision AG
Seasonal/Temporary, Contract position
Listed on 2026-02-17
Job specializations:
  • Engineering
    Validation Engineer, Quality Engineering, Pharma Engineer
Salary/Wage Range or Industry Benchmark: 80000 - 100000 CHF Yearly CHF 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Position: Associate Engineer Validation Ops (Ref. Nr. 2729) - start June 1st / 8 months temporary contrac[...]

For our client, an innovative pharmaceutical company with its international headquarter based in Neuchâtel, we are searching for a:

Associate Engineer Validation Ops (. 2729) - start June 1st / 8 months temporary contract, junior profiles welcome

In this hands‑on role, you will support validation and qualification activities for GMP‑regulated equipment and systems across the site. You will collaborate closely with cross‑functional teams within Manufacturing, Technical Services, Quality, and Engineering, ensuring that periodic reviews, risk assessments, and technical documentation meet regulatory and internal standards. This role offers an excellent opportunity to gain experience within a dynamic and highly regulated environment.

  • Implement and optimize periodic review processes for GMP equipment and systems across the site.
  • Determine review criticality and frequency in accordance with qualification and periodic review procedures.
  • Develop templates and evaluate workload requirements for system and equipment periodic reviews.
  • Support qualification and validation activities, including execution, requalification, and documentation.
  • Maintain and update equipment risk assessments, integrating new equipment as needed.
  • Contribute to the creation and improvement of local procedures and validation documentation.
  • Collaborate with cross‑functional teams while ensuring adherence to internal procedures and regulatory expectations.

Your profile

  • Degree in Biology, Biochemistry, Quality Engineering
    , or a comparable scientific/technical field.
  • Strong analytical, structured, and solution‑oriented mindset with excellent organizational skills.
  • Good interpersonal and writing skills; able to work autonomously and propose improvements proactively.
  • Knowledge of GMP guidelines and risk‑analysis methodologies (an advantage).
  • Proficient in Microsoft tools and comfortable working with technical documentation.
  • Ability to work in a dynamic, fast‑paced environment with cross‑functional interfaces.
  • Ability to communicate in French preferred;
    English skills are a strong asset

Domagoj Odrljin is looking forward to receiving your application documents via our job portal (CV, diploma, reference letters; no motivational letter necessary).

Full discretion is guaranteed and we will gladly answer any additional questions.

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Position Requirements
10+ Years work experience
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