QA Validation Engineer
3 weeks ago
Social network you want to login/join with:
Team Horizon is seeking a QA Validation Engineer for a 12 Month contract on behalf of our client, a leading medical device manufacturer in the Connaught region.
Why you should apply:
- Opportunity to cooordinate the development and maintenance of the site validation program and ensure external regulatory, quality, and compliance requirements are met
- Work with a diverse & talented team on exciting projects
What you will be doing:
- Coordination / direction and active participation in the validation and quality assurance of site equipment, utilities, processes and software in compliance with company policies, FDA, European cGMP and GAMP standards.
- Generation/maintenance/execution of the Site Validation Master Plan.
- Generation/maintenance/execution of Project Validation Plans and schedules.
- Generation of validation protocols and final reports to cGMP standards.
- Generation of validation investigations and implementation of corrective actions.
- Creation/Review/Approval of various quality documents and test data.
- Management of validation, exception event, and change control processes.
- Maintenance and tracking of validation equipment, if applicable.
- Completing all required training before executing a task.
- Documenting all activities in line with cGMP requirements.
- Updating of validation procedures, job instructions and batch documentation to reflect current best practices.
- Performing cross training within the team and training of new team members.
- Participation in continuous improvement programs to implement improvements in manufacturing, quality, safety and training systems.
- Coordinating activities to maximize the effectiveness of all of the team members.
- Maintaining the overall cGMP compliance of the production areas.
- Communicating with peers and management regarding activities in the area, including elevation of events or concerns.
What you need to apply:
- Qualification and/or degree in engineering or scientific discipline
- 3 years plus validation/Quality experience in medical device plastics processing, moulding or assembly operations.
- 3 years plus of knowledge of cGMP and regulatory requirements relating to the medical device industry.
-
Qa Validation Engineer
3 weeks ago
Sligo, Sligo, Ireland Gertek Project Management Full timeJob Title: Equipment Validation Engineer Summary: Responsible for the planning, execution, and documentation of equipment qualification and validation activities within a GMP-regulated pharmaceutical manufacturing environment.Ensures that all equipment meets regulatory requirements and company quality standards.Responsibilities: Develop and execute...
-
QA Validation Engineer Only 24h Left
2 weeks ago
Sligo, Sligo, Ireland Gertek Project Management Full timeJob Title: Equipment Validation Engineer Summary: Responsible for the planning, execution, and documentation of equipment qualification and validation activities within a GMP-regulated pharmaceutical manufacturing environment. Ensures that all equipment meets regulatory requirements and company quality standards. Responsibilities: Develop and execute...
-
QA Validation Engineer 3 Days Left
2 weeks ago
Sligo, Sligo, Ireland Gertek Project Management Full timeJob Title: Equipment Validation EngineerSummary:Responsible for the planning, execution, and documentation of equipment qualification and validation activities within a GMP-regulated pharmaceutical manufacturing environment. Ensures that all equipment meets regulatory requirements and company quality standards.Responsibilities:Develop and execute validation...
-
Validation Engineer Position
2 weeks ago
Sligo, Sligo, Ireland beBee Careers Full timeJob RequirementsWe are looking for a highly skilled QA Validation Engineer with experience in validation/Quality in medical device plastics processing, moulding or assembly operations.Qualifications:Qualification and/or degree in engineering or scientific discipline3 years plus validation/Quality experience in medical device plastics processing, moulding or...
-
QA Professional
1 week ago
Sligo, Sligo, Ireland beBee Careers Full timeAs a QA Specialist, you will play a crucial role in ensuring product manufacturing complies with GMP and Regulatory standards.The responsibilities of this individual contributor role include validating facility, equipment, and utilities, as well as reviewing and approving validation documentation. This requires a self-starter with expertise in QA and...
-
Qa Specialist
2 weeks ago
Sligo, Sligo, Ireland Phibro Animal Health Corporation Full timePosition Details Job Purpose: The QA Specialist will be responsible for delivery of Quality Assurance activities to ensure product is manufactured in accordance with GMP and Regulatory requirements.The role will also include the review and approval of validation documentation and activities related to the qualification of the facility, equipment, and...
-
QA Compliance Specialist
6 days ago
Sligo, Sligo, Ireland beBee Careers Full timeAs a QA Specialist, you will play a crucial role in ensuring product manufacturing complies with GMP and Regulatory standards.Responsibilities:Provide technical expertise and guidance on QA and compliance topics, including validation strategy, new product introduction, and manufacturing issue resolution.Manage assigned QMS areas, including Deviation, Change...
-
Quality Assurance Validation Engineer
2 days ago
Sligo, Sligo, Ireland Sigmar Recruitment Full timeAbout Your New Company You will be joining a global biopharmaceutical company that focus on developing, and commercializing products contributing to oncology and eye role is a 12-month contract in Sligo.As a QA Validation engineer you will coordinate the development and maintenance of the site validation program and ensure quality requirements are met.About...
-
Validation Specialist
2 weeks ago
Sligo, Sligo, Ireland beBee Careers Full timeThe role of QA Validation Engineer is critical in ensuring that equipment, utilities, processes, and software meet clients' policies, FDA, European cGMP, and GAMP standards.Responsibilities:Developing and executing project validation plans and schedules.Crafting validation protocols and final reports that adhere to cGMP standards.SUPPORTING QUALITY ASSURANCE...
-
QA Specialist
7 days ago
Sligo, Sligo, Ireland Phibro Animal Health Full timeAbout Phibro Animal Health CorporationPhibro Animal Health Corporation is a publicly traded, global organization with a rich history in animal health and nutrition as a manufacturer and marketer of medicated feed additives, vaccines, nutritional specialty products, and mineral nutrition. We strive to be a trusted partner with livestock producers, farmers,...