CQV Coordinator

vor 3 Wochen


Visp, Schweiz Randstad Vollzeit
Job Description

We are seeking a highly organized and detail-oriented CQV Coordinator to join our team. The ideal candidate will possess strong coordination skills, a proactive attitude, and attention to detail.

Key Responsibilities:
  • Act as the primary point of contact for all CQV-related requests, addressing inquiries promptly and coordinating follow-up support when necessary.
  • Assist in the CQV EHS team with reporting, metrics, and updating necessary documentation.
Organizational Coordination:
  • Regularly maintain and update the CQV organizational chart to ensure it reflects current team structures.
  • Oversee and update CQV Outlook groups, particularly for new starters, ensuring smooth support for OPS CQV activities and handling any required group changes.
Administrative Tasks:
  • Provide ad-hoc administrative support as needed, such as CQV container management, including updating metrics on whiteboards, supporting report updates, and handling the distribution of supplies.
  • Manage the stationery supplies for the CQV team and coordinate supply orders efficiently for all locations.
Requirements:
  • Prior experience in administrative support or a similar role (experience in pharma or CQV-related fields is a plus).
  • Strong organizational skills, with the ability to manage multiple tasks and prioritize effectively.
  • Proficient in Microsoft Outlook and other office software.
  • Excellent communication skills, both written and verbal, with a customer-service mindset.
  • Detail-oriented and able to maintain accuracy in documentation and reporting.
Preferred Skills:
  • Experience working in a pharmaceutical or biotech environment.
  • Knowledge of CQV processes or experience supporting CQV teams is a strong advantage.
  • Familiarity with EHS reporting and basic metrics management.
What We Offer:
  • An opportunity to work in a dynamic and supportive team environment.
  • Competitive salary and comprehensive benefits package.
  • The chance to contribute to cutting-edge projects in the pharmaceutical industry.

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