Deputy FvP

CHF90 - CHF100 per hour
  1. Interim/Contract
Lucerne
  1. Quality Assurance
Posted: 08/06/2021
BBBH16693

This vacancy has now expired. Please see similar roles below...

Hobson Prior are seeking a Deputy FvP to join one of the world's leading research-based health organisations. Our client is looking for someone who can start by mid-July on a contract basis.

Please note that to be considered for this role you must have the right to work in this location.


Key Responsibilities:

  • Control of batch certificates and comparison with regulatory requirements.
  • Record and evaluate results of transport temperature monitoring.
  • Report temperature excursions and request disposition statements.
  • Artwork checks.
  • Process deviations.
  • Life-cycle management, administration and change control of standard operating procedures, work instructions, protocols, flow-charts, controlled job aids, and forms according to approved Master SOPs and valid templates.
  • Formal control of documents in review, support of SOP process owners and authors with structural and formatting rules during creation and review of SOPs.
  • Implementation of inputs during review of controlled documents.
  • Retrieve and ensure timely review of PQRs for authorized and marketed medicinal products, assure that time-lines for review are respected.
  • File the completed and reviewed PQRs, follow-up delayed PQRs.
  • Processing of Product Quality Complaints (receipt, classification, forwarding to manufacturer, tracking, feed-back to customers, metrics, periodical evaluations).
  • Timely information of Pharmacovigilance Country Lead in case of suspected AEs in connection with PQCs.
  • Support planning and monitoring of general GDP training of employees.
  • Prepare check-lists and protocols for annual self-inspection and mock recall.
  • Awareness and implementation of applicable regulations and dissemination to relevant colleagues.

Requirements:

  • Master's Degree in in pharmacy, medicine, biology or equivalent.
  • Minimum of 4-years' experience in Quality Assurance (GMP/GDP) within the pharmaceutical industry.
  • Documented experience with local Swiss, European and international GxP regulations.
  • Experience with quality management tools and/or workflow management tools.
  • English and German language - Proficiency at a business level. French knowledge is a plus.
  • Excellent analytical and problem-solving skills, based on science, data and understanding of regulatory requirements in a complex and evolving environment; ability to apply sound risk management.
  • Team work, communication and solution-oriented.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.

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