- Our client has developed a stand-out culture of innovation, inclusion and development, and consistently features as a great place to work.
- You enjoy working on exciting projects and want to work with a global manufacturing site in the midlands.
- Provides guidance to global GMP/GDP business partners to support compliant and timely execution of quality management systems (QMS) records such as deviations, investigations, CAPAs, change controls and laboratory investigations.
- Integrates knowledge and experience as skilled specialist with knowledge of corporate and industry standards with respect to area.
- Creates and delivers QMS training and coaching (process and technical).
- Creates, owns, and manages deviations, change controls, and CAPA in TrackWise.
- Creates, updates, reviews, approves and implements QMS procedural documentation and work instructions with accuracy and clarity.
- Completes assigned projects, supporting delivery on time and in full. Provides regular updates on progress.
- Leads and participates in internal forums, for example Change Control Review Board, CAPA Review Board and Communities of Practice.
- Compiles and analyses QMS data to assess compliance, identify trends and generate new insights. Provides recommendations for continuous improvement supported by data and analysis.
- Participates in inspection readiness activities and internal/external audits and inspections.
- Bachelor's degree (or equivalent) in a technical or life sciences discipline (ex. Chemistry, Biology, Biotechnology)
- 6 years' + experience in Pharmaceutical, Device or Commercial Quality Assurance within the biopharmaceutical or pharmaceutical industry.
- Prior experience creating and delivering training required.
- Direct experience with development and approval of deviations, CAPAs, Change Controls and laboratory investigations.
- Prior experience in a Global QA role preferred.
- Able to plan, prioritize and manage workload and manage shifting priorities to ensure commitments are met.
- Demonstrated critical thinking and problem-solving skills.
- Knowledge of global GMP and GDP requirements for quality systems, medical devices, and combination products.
- Excellent written and verbal communication skills.
- Experience using TrackWise required.
- Experience using Veeva Vault eQMS desired.
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Assoc Research Scientist
1 week ago
Thermo Fisher Scientific Athlone, Ireland Full timeAssoc Research Scientist – Biopharma · At PPD, part of Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and ...
Senior Specialist QA Scientific - Westmeath, Ireland - TEAM HORIZON
Description
Team Horizon is seeking a Senior Specialist QA Scientific for our client based in Dublin. The Senior Specialist, Quality Systems, to join the Central Quality Systems and Compliance team.This role serves as a pharmaceutical quality subject matter expert and supports global colleagues across Operations, Commercial, Device, IT and Quality partners. The successful candidate for this role must be able to work onsite in line with company requirements.
Why you should apply:
What you will be doing:
What you need to apply:
