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Quality Specialist
4 weeks ago
PE Global is currently recruiting a Quality Specialist (Quality Systems) for an 11-month contract with a leading multi-national client based in Cork.
This is initially an 11-month contract position, offering a lucrative hourly rate.
The role is a shift, full-time onsite role providing quality oversight to operational areas. This role is integrated into the production area.
This position within the QA department will provide quality oversight, support, and knowledge to activities relating to Quality Systems across the site and in meeting the company priorities of: Compliance, Supply, Strategy, and Profit Plan.
The team working style is one of collaboration, coaching, and facilitation to ensure the success of the site. The Quality Specialist is accountable for the Quality Systems within the site.
This role requires the delivery of a robust Quality Management System to support a flexible, collaborative, multi-skilled teamwork environment.
The Quality Specialist will have proven capability in the development of Quality Systems as an active member across cross-functional teams to deliver process improvement. The Quality Specialist will model the company leadership behaviors and understand the MPS principles to drive a culture of continuous improvement building a High-Performance Organisation.
The Quality Specialist will participate and comply with the company Quality Management System (QMS) requirements, including ownership as required.
Duties of the role/Responsibilities:
- Provides expertise in Quality Systems and/or Operational Quality, including Quality Notifications/Investigations/Change Management; environment monitoring programs; sterility assurance/low bioburden manufacturing; etc.
- Uses knowledge to improve Quality Systems and/or Operational Quality; solve complex problems, provide continuous improvement and execute tasks.
- Acts as a resource to colleagues with less experience in Quality Systems and/or Operational Quality.
- Understands and applies regulatory/compliance requirements to their role together with remaining current on upcoming regulatory and compliance changes.
- Required to be proficient in Quality approval and oversight for Commissioning and Qualification activities (IQ/OQ/PQ).
- Interprets customer needs, assesses requirements, and identifies solutions to non-standard requests.
- Makes decisions within guidelines and policies which impact Product Quality, Projects, and Quality Systems.
- Provides compliance contribution to project teams and leads small projects.
- Coaches and guides colleagues within the site.
- Supports Corporate Quality to ensure actions related to Quality Systems at the site are executed.
- Participates in inspections of the site by Divisional/Regulatory Bodies/third parties together with follow-up actions where applicable.
- Participates in GMP Walkthroughs.
- Deviation Management & Change Control approval.
- Ensures supply of high-quality product through the implementation and oversight of the Quality Management System for the site.
- Champions the highest Quality and Compliance standards for the site.
- Ensures the highest safety standards.
- Additional activities as requested by QA Lead.
Education/Experience:
- Degree or 3rd level qualification (Science, Quality).
- Demonstrated knowledge in more than one pharmaceutical and/or chemical manufacturing operation.
- 5 years' experience in the pharmaceutical industry or a similar operating environment which includes experience in a Quality function.
- Quality Assurance SME knowledge, from both operational and educational experience, is required.
- Knowledge and experience in interpreting current regulatory requirements and providing independent support to the site.
- Demonstrated ability to work independently and fully realize improvement initiatives with a moderate level of guidance.
- Demonstrated ability to work and succeed within teams as well as leading small project teams.
- Demonstrated ability to drive the completion of tasks.
- Proven track record of providing independent Quality support to the site.
- Advanced PC skills such as Excel, Word, PowerPoint.
- Stakeholder management of multiple decision-makers, auditors, cross-functional teams by demonstrating the ability to maintain and strengthen trust relationships with people on all levels.
- Proven decision-making capability with full accountability and responsibility.
- Energetic with a proactive & positive attitude.
- Demonstrated coaching skills.
- Demonstrated ability to solve problems.
Interested candidates should submit an updated CV.
Please click the link below to apply, call Chloe on 086 0200448 or alternatively send an up-to-date CV to chloe.slingsby@peglobal.net.
***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland.***
Seniority level- Associate
- Contract
- Quality Assurance and Science
- Industries: Pharmaceutical Manufacturing
