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Senior Validation Specialist
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Senior Validation Specialist

Type of work
Full-time
Experience
Senior
Employment Type
Permanent, B2B
Operating mode
Remote
Transition Technologies MS

Transition Technologies MS

We are a rapidly growing IT company with global reach. We deal with IT outsourcing and implementation projects in flexible cooperation models, providing access to competence and experts in technologies from mainstream to cloud. TTMS' greatest strength is its skilled professionals, so people are at the heart of our organisational culture.

Tech stack

    English

    C1

    CSV

    master

    GAMP

    master

Job description

Online interview
Friendly offer

Your responsibilities:


  • Development and implementation of validation strategies for MES systems at several international locations
  • Ensuring compliance with regulatory requirements, especially GxP, as well as internal quality guidelines
  • Creation, review and approval of validation documentation such as risk analyses, test plans and reports
  • Support in the implementation and qualification of new technologies taking compliance requirements into account
  • Collaboration with interdisciplinary teams to establish efficient and sustainable validation processes



We are looking for you, if you have:


  • Experience in validating IT systems, ideally in the area of ​​manufacturing
  • In-depth knowledge of regulatory requirements (e.g. GxP, FDA, ISO 13485)
  • Experience in creating and implementing validation documentation and processes
  • Experience in an international environment and in working with global teams
  • Strong communication skills and ability to communicate complex regulatory requirements in an understandable manner
  • 3+ years experience in IT & Software Validation (CSV, GAMP), preferably in pharma environment
  • Experience in authoring or reviewing validation related deliverables, records and other evidences
  • Experience in software development lifecycle processes (SDLC), models, standards in pharmaceutical industry (or other regulated)
  • 3+ years experience in IT & Software Validation (CSV, GAMP), preferably in pharma environment
  • Experience in leading validation for projects and systems maintenance
  • Experience in authoring validation plans, reports and deliverable registries
  • Experience in authoring or reviewing validation related deliverables, records and other evidences
  • Experience in software development lifecycle processes (SDLC), models, standards in pharmaceutical industry (or other regulated)
  • Experience in Lean and/or Agile approaches
  • Experience in maintenance and support of applications under global inspection agencies, CFR 21 FDA Part 11, Annex 11
  • English language mandatory (C1)


We offer:


  • Interesting and challenging projects
  • Flexible working hours
  • Friendly, non-corporate atmosphere
  • Stable working conditions (CoE or B2B)
  • Possibility for self-development and promotion in the company
  • Rich benefits package


We reserve the right to contact the selected candidates.



Undisclosed Salary

Permanent, B2B