Aristo Group

Associate Scientist Cleaning Validation (m/w/d)

Mehr als 30 Tage alt

Angaben zum Job

Aristo Group
Firma Aristo Group Personalvermittler
Kategorie Forschung / Wissenschaft
Pensum 100%
Lohn (geschätzt) CHF 88'000 – 112'000 / Jahr
Einsatzort Boudry

Job-Inhalt

Industry: Pharma
Skills: QA,Cleaning Validation

Start of project: 01.09.2023

Duration of the project : 12 months

Project volume: 1920 Hour(s) 

Location: Boudry, Switzerland (on site)

Language: English and French

Tasks:

  • May be assigned Subject Matter Expert (SME) role for a defined validation/qualification area.
  • Ensure cleaning processes are qualified, validated and maintained in compliance with local policies, guidelines, and procedures during their lifecycle.
  • Author and when required review validation documents, including validation plans, protocols, reports, traceability matrix and summary reports.
  • Execute validations for cleaning across the site.
  • Co-ordinate activities interfacing with multiple sites, departments and external vendors.
  • Lead/participate to risk assessments and risk management teams.
  • Review change controls and maintenance interventions, evaluating the impact upon qualified systems & validated processes, and documents required actions.
  • Maintain procedures governing validation to ensure they are in compliance with corporate policies and regulatory requirements. Participate to the development and maintenance of the local site procedures.
  • Participate when required during internal and external audits for which they are a SME, by answering questions, reviewing qualifications and validations with auditors, and providing documentation.
  • Participates/lead projects and initiatives and contributes to continuous improvement exercises.
Qualifications & Experience
  • Degree in Engineering/Technical discipline or experience equivalent.
  • Experience (at least 5 years) in validation required, special focus on cleaning validation for small molecules
  • Familiarity with current international regulatory regulations, cGxP requirements and best practices, including 21 CFR part 11, 210 and 211, Annex 11n, EU-GMP guidelines and GAMP
  • Good communication skills in English and French with stakeholders and outside vendor groups
  • Automation knowledge advantageous
  • Team player: ability to interact effectively with team and customers
  • Proactively identifies problems and recommends solutions
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