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Validation & Compliance Engineer

NewperkinelmerWorkdayMSD (Switzerland) - Customer Site
Posted 28 AugFound 28 OctSeen 22 hours ago

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The Posting

When joining PerkinElmer, you select an experienced and trusted leader in scientific solutions, with the support of a global service network and distribution centers, providing the right solution, at the right time, to meet critical customer needs. With over an 80+ year legacy of advancing science and a mission of innovating for a healthier world, our dedicated team collaborates closely with commercial, government, academic and healthcare customers to deliver our broad portfolio of analytical solutions, and OneSource services.

Job Title

Validation & Compliance Engineer

Location(s)

MSD (Switzerland) - Customer Site

Job Description

PerkinElmer's OneSource team is looking for a Validation & Compliance Engineer to support production environment on the Customer site (MSD) in Schachen.

More information about PerkinElmer and our business : PerkinElmer | Science with Purpose

More information about our OneSource services: OneSource Laboratory Solutions | PerkinElmer

Hybrid working model

Responsibilities:

  • Performs the review and validation of test and data analysis equipment and systems used for phase 1 and phase 2 manufacturing.
  • Maintains all documentation pertaining to maintenance and qualification/calibration, both original and electronic records into Customer systems.
  • May contribute to developing procedures and/or protocols.
  • Serves as information resource for validation technicians, contractors and vendors.
  • Contribute with Customer QA and Technical Unit in developing and implementing new specifications.
  • Contribute to change management and deviation tracking processes, including leading or contributing to CAPA.

Requirements

  • Bachelor’s degree in Life Sciences or Quality/Compliance discipline or equivalent experience preferred.
  • 3 to 5 years of relevant experience in a (Bio-)Pharma company in quality, validation or compliance roles
  • Knowledge of cGMP, Annex 1 and validation regulations and requirements.
  • Knowledge of GMP, GLP, GDocP, pharmacopeia and regulatory requirements preferred.
  • Developed Customer service mindset
  • Be passionate about detail and tech aspects
  • Strong written and verbal communication skills in English, German language knowledge will be beneficial.
  • Ability to work both independently and as a team member
  • Following customer SOPs and regulatory guidelines FDA, EU & SwissMedic

Join our Team!

We are strongly committed to the development of your career and giving you opportunities to learn and grow.

We make a difference for you while you make a difference in the world!

Facts

Source
Workday
External id
REQ-058081
Location
MSD, Switzerland
Remote
Not stated
Employment
Full time
Posted
28 Aug 2026
First seen
28 Oct 2026, 23:31
Last seen
1 Nov 2026, 00:29
Status
Not yet added
Posting id
02306a1d-86ab-51db-9de0-45ca0a78517f