Did you know that your Internet Explorer is out of date?
To get the best possible experience using our website we recommend that you upgrade to a newer version or download another web browser.A list of the most popular web browsers can be found below. Just click on the icons to get to the download page.
Google Chrome |
Internet Explorer |
Mozilla Firefox |
Opera |
Your browser will need to close to complete the installation and you will need to manually reload the site when finished
Apply for this job
Details
Qualified Person
Reference: | SCAXSG-348663 | Location: |
Limerick Limerick City |
Qualification: | Degree | Experience: | 5-7 Years |
Job Type: | Permanent | Salary: | Not Disclosed |
May be suitable for:
Qualified Person
Qualified Person
Our client, a global biotech,are seeking a highly motivated and detail-oriented Qualified Person to join the quality assurance team as the Lead QP onsite. The successful candidate will have previously been a named QP on a Irish licence previously.
Responsibilities
- Ensure manufactured biotech drug substance (DS) batches are certified in accordance with all required regulations and in compliance with IND/CTAs/ manufacturing authorisation/ marketing authorisation
- Ensure that biotech drug product batches are tested in compliance with manufacturing & marketing authorisations (BLA/MAAs/ROW CTDs)
- Is responsible for the final decision associated with batch certification
- Ensures that the principles and guidelines of GMP as stated in 2003/94EC, 2001/83EC, 536/2014 (repealing 2001/20/EC), associated EU GMP annexes, (e.g., Annex 13, Annex 16) and current product specification file (PSF) are met
- Provide Quality leadership, direction, training and governance for the specific area of responsibility
- Carry out day to day activities in compliance with site safety policy and procedure
- Promote and encourage safe practices and promptly report any safety concerns
- Continue to maintain knowledge and experience in line with technical and scientific progress for product(s) of responsibility in alignment with Annex 16 requirements.
- Communication and education of personnel in GMP requirements and regulations.
- Responsible for approving appropriate quality-related documents. An approval signature confirms that the company, GMP and relevant regulatory requirements have been met
- Review and approve change controls, deviations, failure investigations, suspect analytical results, product quality complaints, stability studies and reports associated with the manufactured batches
- Review and approve GMP documents associated with qualification and validation including but not limited to change controls, IQ/OQ/PQ & validation documents for facility, equipment, computer systems, GMP utilities, analytical methods, and processes, stability data and periodic review reports (PRR) and annual product reviews (APR) product quality evaluations
- Responsible for issuance of QP declarations where required
- Understand the conditions and requirements when a renewed authorisation is necessary and ensure they are complied with
- Evaluation and contribution of regulatory information to regulatory documents including review/approval of dossier sections as part of the product submission processes
- BSc, MSc, or PhD in Biology, Chemistry, Pharmacy, or related discipline
- Must be approved by member state as a licensed QP in order to be named on the company licence as a QP
- Minimum of 7 years of experience in quality assurance within a biotechnology or pharmaceutical manufacturing environment
- Must have been on an Irish license previously as QP
Group sites:
Medical Device Jobs |
Diagnostics Jobs |
Biopharmaceutical Jobs |
Quality Assurance Jobs |
Medical Affairs Jobs |
Biotechnology Jobs |
Supply Chain Jobs |
Clinical Research Jobs |
Contract Jobs |
Science Jobs |
Engineering Jobs |
Scientific Jobs |
Pharmaceutical Jobs |
Chemistry Jobs |
Connected Health Jobs |
Pharmaceutical | Tel:+353 1 685 4545 | Fax: +353 (0)1 443 05 24 | Email: [email protected] | Copyright © 2012 Life Science Recruitment Ltd
This site uses cookies. For more information on our cookie policy visit Privacy Policy | Terms of Use
Registered as a private limited company. No: 445328 |
Web Design / SEO by WebScience | Valid XHTML - CSS
Pharmaceutical | Tel:+353 1 685 4545 | Fax: +353 (0)1 443 05 24 | Email: [email protected] | Copyright © 2012 Life Science Recruitment Ltd
This site uses cookies. For more information on our cookie policy visit Privacy Policy | Terms of Use
Registered as a private limited company. No: 445328 |
Web Design / SEO by WebScience | Valid XHTML - CSS