Job type: 100%

Loading ...

Job content

To support the team in implementing a computerized systems validation strategy. (CSV), you are able to take the lead on all or part of the following business responsibilities:

Validation of PLCs, supervisors and MES (Manufacturing Execution System)

Functional analysis

Writing test protocols, change control and validation reports

Execution of IQ OQ PQ tests

GAMP, 21 CFR part 11, GMP compliance

Interface with suppliers and/or customers

You have a desire to professionalize yourself on any missing skills.

You are familiar with reference systems (GMP, 21 CFR Part11, GAMP) and with specific regulations in the field of computer validation.

You have already written test sheets and participated in qualification tests.

You have a degree from an engineering school, a 5-year degree or a Faculty of Pharmacy, with a focus on quality management, drug quality, and quality risk management.

You have a strong appetite for complex projects and problem solving. Your curiosity and your technical culture are recognized in the professional environment but also in the personal environment. You have an easy questioning and are constantly looking for ways to improve.

You undertake, carry out projects and commitments. You challenge your methods and ideas to surpass yourself and reach a high level of excellence. In this context, your drivers can be technical, financial or human, you will be valued on your performance and/or that of your team.

This position is open to people with disabilities, adaptations of the position can easily be put in place.

Remuneration will be based on years of experience and specific technical expertise.

Job Type: 100%

Salary: CHF80.00 - CHF140.00 per year

Schedule:

  • 8 Hour Shift
  • Day shift
  • Monday to Friday

Supplemental pay types:

  • Bonus pay
  • Overtime pay

Work Location: In person

Loading ...
Loading ...

Deadline: 13-05-2024

Click to apply for free candidate

Apply

Loading ...
Loading ...

SIMILAR JOBS

Loading ...
Loading ...