CQV Lead – Client Side at DPS Group
Dublin, County Dublin, Ireland -
Full Time


Start Date

Immediate

Expiry Date

19 Aug, 25

Salary

0.0

Posted On

19 May, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Project Management Skills, Interpersonal Skills, Regulatory Requirements, Ema, Gmp

Industry

Pharmaceuticals

Description

Arcadis DPS are seeking a CQV Lead on contract basis for a client side position with a leading pharmaceutical company in Dublin
Job Description:
We are seeking a Contract CQV (Commissioning, Qualification, and Validation) Lead to oversee and manage CQV activities for our client-side operations in Dublin. The successful candidate will be responsible for ensuring that all systems and processes meet regulatory compliance and quality standards.

Key Responsibilities:

  • Lead and manage CQV activities for manufacturing and utility systems.
  • Develop and implement CQV strategies and plans.
  • Coordinate with cross-functional teams to ensure project timelines are met.
  • Review and approve CQV documentation, including protocols and reports.
  • Ensure compliance with industry regulations and standards.
  • Provide technical expertise and guidance to the project team.
  • Identify and resolve issues related to CQV processes.
  • Conduct risk assessments and implement mitigation strategies.

Required Skills and Qualifications:

  • Bachelor’s degree in Engineering, Science, or related field.
  • Extensive experience in CQV activities within the pharmaceutical or biotech industry.
  • In-depth knowledge of regulatory requirements and industry standards (e.g., FDA, EMA, GMP).
  • Strong leadership and project management skills.
  • Excellent communication and interpersonal skills.
  • Ability to work collaboratively with cross-functional teams.
  • Detail-oriented with strong problem-solving capabilities.

Interested candidates should submit their resume and cover letter detailing relevant experience and qualifications

Responsibilities
  • Lead and manage CQV activities for manufacturing and utility systems.
  • Develop and implement CQV strategies and plans.
  • Coordinate with cross-functional teams to ensure project timelines are met.
  • Review and approve CQV documentation, including protocols and reports.
  • Ensure compliance with industry regulations and standards.
  • Provide technical expertise and guidance to the project team.
  • Identify and resolve issues related to CQV processes.
  • Conduct risk assessments and implement mitigation strategies
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