What are the responsibilities and job description for the Calibration Specialist position at ClinLab Solutions Group?
Calibration Specialist-St Louis, MO
Position Summary
The Calibration Specialist is responsible for performing, documenting, and maintaining instrument calibrations to ensure compliance with regulatory standards and operational excellence in a pharmaceutical manufacturing environment. This role supports product quality, equipment reliability, and regulatory readiness through precise calibration practices and adherence to cGMP requirements.
Key Responsibilities
- Calibration ExecutionPerform routine and complex calibrations on temperature, pressure, flow, and analytical instruments (including pH and conductivity).
- Ensure all equipment operates within specified tolerances to maintain process accuracy and reliability.
- Regulatory Compliance (cGMP)Maintain strict adherence to Current Good Manufacturing Practices (cGMP) and site-specific Standard Operating Procedures (SOPs).
- Ensure all calibration activities meet internal and external regulatory requirements.
- Documentation & Data IntegrityAccurately complete calibration records in compliance with ALCOA data integrity standards.
- Maintain clear, complete, and audit-ready documentation for all calibration activities.
- NIST TraceabilityEnsure all calibration standards and master test equipment are properly certified and traceable to NIST.
- Monitor and maintain calibration status of all reference standards.
- Out-of-Tolerance (OOT) InvestigationsSupport investigations related to out-of-tolerance conditions.
- Assess potential impact of instrumentation issues on product quality and manufacturing processes.
- Calibration Management Systems (CCMS)Utilize systems such as Blue Mountain or Maximo to manage calibration schedules, records, and asset histories.
- Ensure timely completion of scheduled calibrations and system updates.
- Troubleshooting & MaintenanceDiagnose, repair, and resolve instrumentation issues to minimize downtime.
- Support high-speed and sterile manufacturing operations with rapid response to equipment failures.
- Audit & Inspection SupportProvide technical expertise during internal audits and regulatory inspections (e.g., FDA).
- Present documentation and explain calibration processes as required.
- Safety & Cleanroom ComplianceFollow all safety procedures, including Lockout/Tagout (LOTO).
- Comply with aseptic gowning and cleanroom protocols.
- Vendor & Contractor OversightCoordinate and oversee third-party calibration vendors.
- Ensure contractor work meets company quality, safety, and compliance standards.
Qualifications
- Education & ExperienceAssociate’s or Bachelor’s degree in Engineering, Life Sciences, or related technical field (or equivalent experience).
- Experience in calibration within pharmaceutical, biotech, or regulated manufacturing environments preferred.
- Technical SkillsKnowledge of calibration principles for process and analytical instrumentation.
- Familiarity with cGMP regulations and FDA compliance requirements.
- Experience with calibration management software (e.g., Blue Mountain, Maximo).