Quality & Regulatory Administrator (Fixed Term - Clevedon, United Kingdom - DCC VITAL

DCC VITAL
DCC VITAL
Verified Company
Clevedon, United Kingdom

1 month ago

Tom O´Connor

Posted by:

Tom O´Connor

beBee Recruiter
Description

Req ID:6882
Company:

DCC Vital - Fannin UK
Salary:£22,000 - £24,000
Location:
Clevedon, GB, BS21 6TH
Contract Type:Fixed Term Contract
Date Posted:22 Feb 2024
Description:

Quality & Regulatory Administrator - Fixed-Term until end March 2025

Location:
Location: Clevedon, Kenn Road**
Reports to:Quality & Regulatory Manager**
Contract: Contract: Fixed-Term until the end of March 2025

Hours of Work:
Full-time (37.5 hours per week Monday to Friday)

About the Company:


DCC Vital:


  • DCC Vital is a division of DCC Healthcare, with revenues of + £500m, marketing and selling a broad range of own
- and third-party medical products in the Irish, British and DACH healthcare markets covering hospitals, pharmacy and community care, GPs, and other healthcare settings


DCC Vital Medical Devices:


  • Fannin (UK) Ltd manufactures and supplies of a range of tissue retrieval systems for laparoscopic surgery, in addition to providing sales, marketing and distribution services to third party manufacturers.
  • Fannin (UK) Ltd creates an atmosphere that encourages respect, growth and contributions of all associates and our success will be the achievement of longterm customer satisfaction.
  • In October 2022 DCC Vital announced the acquisition of
    Medi-Globe, a leading global player in developing, manufacturing, and distributing single use medical devices for endoscopy in gastroenterology and urology.

The Opportunity:


  • This role provides a good exposure to the workings of the Medical Devices industry especially on the demanding global Quality and Regulatory compliance framework which is critical for medical devices to be placed on the market.
    Duties & Responsibilities
  • To support the Quality & Regulatory management systems for Fannin (UK) Businesses covering manufacturing, distribution, and commercial activities.
  • To Support creation, revision, and control of quality system documents needed to ensure product quality and adherence to applicable regulations for Fannin (UK) businesses.
  • To Support with validation of equipment and processes in manufacturing.
  • To assist in planning and execution of the audit activities/Management Review's necessary for monitoring the Quality Management system and participate as a team member in all internal/external audits.
  • To track and support training activities to ensure on time training completion for all employees, this includes new employee training, skill training and change implementation training for new/revised procedures.
  • Manage and maintain good professional working relationships both internally and externally.
    Qualifications & Experience
  • A knowledge background of bio/life sciences.
  • Basic knowledge on Quality, Regulatory & ISO Systems would be beneficial.
  • Excellent computer literacy.
  • Proven verbal and written communication skills, and very good listening skills.
  • Ability to create a positive impact and convey confidence and credibility to others.
  • Establish and maintain good working and interpersonal relationships.
  • Ability to produce results, prioritise objectives & schedule work to best use time and resources
  • The role demands a wellorganized approach, underpinned by the ability to communicate effectively with people at all levels, both verbally and in writing.
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