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Pale Blue Dot Recruitment | The Experts in MedTech Recruitment
An exciting opportunity has arisen for a Validation Engineer (Metrology) to support operations by executing the metrology schedule and helpdesk activities in a fast-paced, GMP-regulated environment. This role will be a key point of contact for all metrology-related activities, including calibration, qualification, preventative maintenance, and compliance with regulatory standards. The successful candidate will ensure that all internal client requirements are met or exceeded while maintaining the highest standards of quality and productivity.
Responsibilities Include But Are Not Limited to the Following:
* Perform calibration and qualification of equipment as per schedule, ensuring all documentation is accurate, timely, and compliant with GMP requirements.
* Manage the Metrology Helpdesk, generate reports, and track key performance metrics.
* Handle unscheduled calibration following repairs or equipment movement and maintain preventative maintenance records.
* Coordinate servicing and repairs, including liaising with vendors, arranging visits, and managing documentation post-repair.
* Maintain calibration, qualification, and preventative maintenance schedules.
* Review and approve external calibration certificates and generate internal certification records.
* Ensure all SOPs related to calibration and validation are up to date, periodically reviewed, and continuously improved.
* Support internal and external audits by providing documentation and assisting with compliance reviews.
* Monitor and address audit observations, change controls, CAPAs, and deviations.
* Adhere to all safety, housekeeping, and quality standards while maintaining a customer-centric approach to metrology operations.
Job Requirements
-Education & Qualifications:
* Bachelor's degree in Life Sciences, Engineering, or a related field.
* At least 3 years of experience in a laboratory or GMP-regulated environment, preferably with calibration experience.
-Experience & Skills:
* Familiarity with pharmaceutical equipment calibration and validation processes.
* Strong understanding of GMP regulations and quality systems.
* Experience in documenting analytical data, writing reports, and maintaining compliance.
* Ability to work independently or as part of a team in a fast-paced environment.
* Strong communication and organizational skills with a quality-first mindset.
* Experience using preventative maintenance systems and metrology tools.
-Personal Attributes:
* Detail-oriented with a strong commitment to compliance and continuous improvement.
* Proactive problem solver with a structured approach to troubleshooting and decision-making.
* Strong ability to collaborate with internal stakeholders and external vendors.
What's On Offer:
* Competitive salary package.
* Opportunities for career development and professional growth.
* A collaborative work environment with a focus on quality, innovation, and customer service.
* Exposure to a dynamic and regulated industry with global best practices.
Note: By applying for this position, you may also be considered by Pale Blue Dot Recruitment for other or future related vacancies.
-Pale Blue Dot Recruitment, The Resource for the MedTech Workforce-
Seniority level
* Seniority level
Mid-Senior level
Employment type
* Employment type
Full-time
Job function
* Job function
Engineering, Analyst, and Product Management
* Industries
Biotechnology Research and Medical Equipment Manufacturing
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