Calibration Specialist

LSC, Life Science Consultants

Limerick

On-site

EUR 55,000 - 75,000

Full time

18 hours ago
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Job summary

Life Science Consultants in Limerick is seeking a Calibration Specialist to own the site calibration program, ensuring instrumentation is maintained to regulatory standards and supporting startup activities with technical expertise. This role involves working on next-gen manufacturing technologies, data collection platforms, and audits with health authorities to drive quality and reliability on site.

You will develop SOPs, lead continuous improvement in calibration practices, and collaborate

Qualifications

  • Experience owning calibration programs in pharma or regulated environments.
  • Familiar with IEC/ISO/ISA standards and EU directives (ATEX where applicable).
  • Strong troubleshooting and root-cause analysis capabilities.
  • Experience with calibration upgrades, obsolescence management and reliability projects.
  • Proficient in data analysis, CMMS, and predictive maintenance.

Responsibilities

  • Own and manage the site calibration program to regulatory standards.
  • Provide expert support on electrical and instrumentation issues during startup and operations.
  • Collaborate with authorities during audits and regulatory engagements.
  • Roll out new calibration strategies in line with best practices.
  • Support maintenance with technical guidance, training and troubleshooting.
  • Lead continuous improvement of calibration and maintenance processes.
  • Develop and maintain SOPs, data sheets and job plans.
  • Carry out internal GMP audits to verify compliance.
  • Analyze condition monitoring data for proactive maintenance.

Skills

Calibration programs
Electrical & instrumentation
Troubleshooting
CMMS
Data analysis
GMP/HSE
Communication

Education

Level 8 Degree in Electrical & Instrumentation Eng

Job description

LSC have a great contract opportunity for a Calibration Specialist to join a Limerick based Biotech Drug Substance Manufacturing Facility.

This is an exciting opportunity to work with next-gen manufacturing technologies, advanced data collection and analysis platforms that will result in safety and quality improvements, increased productivity, and variability reduction.

If you have at least 5 years of relevant experience in a cGMP environment and ready for your next challenge, this could be the perfect project for you!

Calibration Specialist

Are you a knowledgeable Calibration Specialist ready to lead instrumentation and calibration excellence in a dynamic pharmaceutical environment? Join a pioneering team in Limerick for Phase 2 of an innovative project, where your expertise will be pivotal in maintaining the highest standards of equipment reliability and compliance. This is an exciting opportunity to apply your skills in a role that blends technical mastery with regulatory engagement, ensuring quality and operational excellence on site.

What You'll Do:
  • Own and manage the site calibration program, ensuring all instrumentation equipment is maintained to regulatory standards.
  • Provide expert support and guidance on electrical and instrumentation issues during startup and ongoing operations.
  • Collaborate with health and regulatory authorities, representing site calibration practices during audits.
  • Initiate and roll out new calibration strategies in line with industry best practices.
  • Support maintenance teams with technical support, training, and troubleshooting.
  • Lead continuous improvement initiatives to enhance calibration and maintenance processes.
  • Develop and maintain SOPs, job plans, and data sheets, ensuring accuracy and compliance.
  • Carry out internal audits to verify GMP compliance and drive quality standards.
  • Analyze condition monitoring data to identify proactive maintenance opportunities.
Key Skills & Responsibilities:
  • Proven experience owning and managing calibration programs, ideally within pharma or a highly regulated industry.
  • Strong knowledge of electrical and instrumentation standards, including IEC, ISO, ISA, and relevant EU directives (e.g., ATEX).
  • Demonstrated ability to troubleshoot complex equipment failures and perform root cause analysis.
  • Hands-on experience with calibration, equipment upgrades, obsolescence management, and reliability improvement projects.
  • Proficiency with CMMS systems, data analysis, and predictive maintenance techniques.
  • Excellent communication skills for liaising with internal teams, suppliers, and external regulatory bodies.
  • Ability to work independently, demonstrating strong organizational and problem-solving capabilities.
  • Knowledge of GMP, HSE standards, and internal quality systems.
Preferred Education & Experience:
  • Level 8 Degree in Electrical & Instrumentation Engineering or a related field.
  • At least 5 years' experience in maintenance or engineering roles, preferably within the pharmaceutical or biotech sectors.
  • Familiarity with global and local standards and directives relevant to pharmaceutical manufacturing.
  • Experience supporting calibration standards development and uncertainty measurement programs.

For our contracting positions in Ireland's pharmaceutical industry, applicants must possess a Stamp 1G or a Stamp 4 visa. We apologize for any inconvenience, as visa sponsorship is not available at this time. Thank you for your attention.

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