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Employers

Senior Quality Operations Manager/QP, Sligo

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Location:

Sligo, Ireland 

Job Category:

Biotech/Pharma, Science
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EU work permit required:

Yes
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Job Reference:

1778

Job Views:

111

Posted:

11.09.2020

Expiry Date:

26.10.2020
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Job Description:

We are seeking applications for an experienced Senior Quality Operations Manager for our Clients exciting biologics expansion project. The successful candidate will be a strong No. 2 to the Site Quality Head.

This role is a key role in developing Quality Heads (Directors) within our Clients manufacturing network. This position requires a strong leader who will be the Quality Director delegate as needed and partner closely with the Senior Leadership team.  With an international manufacturing presence and a strong pipeline of products there will be continuous opportunities to be involved in Global Projects and to grow your career.

Why you should apply:

  • As this expansion is a start-up project, in this role you will have the opportunity to build your very own team from scratch and then lead and coach this diverse, technical team of expert Quality professionals. You will be responsible for leading the complete product lifecycle - from the technical transfer of investigational new products and the monitoring of overall performance of these products through to implementation of post-approval changes.

What you will be doing:

  • Recruit & lead the QP & QA Operations group, including batch release, product performance, Data Analytics, new products introduction (NPI), and interface with HPRA and FDA.
  • In this role, you will act as the primary delegate to the Quality Director and regularly interact with the Senior Management Team.
  • NPI is key to the growth of our business. As the Senior Quality Operations Manager, you will support the effective transfer of NPIs to site and into commercial manufacturing; coordinating with external global teams including, but not limited to S&T, Regulatory and CMC QA.
  • You will empower your team to ensure any deviations or planned changes in production or quality control have been addressed according to all relevant regulatory requirements and company policies and procedures. As manager, you will mentor and coach your QPs, building their technical expertise.
  • Ensure product manufacture is in accordance with Good Manufacturing Practice and meets requirements of our patients, Regulatory Authorities (FDA, HPRA etc.) and of the company
  • Partner with internal and external Regulatory groups, FDA, HPRA etc. while liaising with operations, technical operations, science & technology teams in relation to product filing support.
  • Have responsibility for the oversight of product performance process, product quality Review, complaints and product track and trend
  • Ensure compliance with all processes and procedures while maintaining the Quality Risk Management (QRM) program on site
  • Have knowledge and experience up to date on market and product (technical and scientific) progress and changes in regulations and quality management related to our range of products.

What you need to apply:

  • Third level qualification in a relevant science discipline with minimum 5 years’ experience in the pharmaceutical industry
  • MSc in Industrial Pharmaceutical Science or similar course recognized by Regulatory Authority to permit Qualified Person (QP) status as per Article 49 of Directive 2001/83/EC desirable.
  • Minimum 5 years industrial experience gained in an FDA and EMA approved pharmaceutical environment.
  • Minimum 3 years’ experience in an aseptic sterile fill finish manufacturing environment an advantage
  • People Management experience is required
Company Info
Team Horizon
1 Cedar Crescent, Cedar Park, Westport, Co. Mayo
Westport, Ireland
Phone: +353 98 50600
Web Site: http://www.teamhorizon.ie
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