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Posted 2 months ago

Validation & Compliance EngineerUSPF PROJECT FARMA

Validation & Compliance Engineer

MSD (Switzerland) - Customer SiteHybridFull-time

AI Summary

Validates and maintains test and data analysis equipment and systems for phase 1 and phase 2 manufacturing at a customer site, ensuring compliance with cGMP, Annex 1, and regulatory requirements.

About this role

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!

Skills

Annex 1CalibrationCAPACGMPChange ManagementDeviation TrackingEU Regulatory RequirementsFDAGDocPGLPGMPPharmacopeiaQualificationSwissmedicValidation

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