Live opening · Posted 5 days ago

Calibration and Metrology Specialist - Torrance

PolyPeptide US · Torrance, CA, US
Teamtailor No
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At a glance

The key details from the original listing.

Posted 5 days ago
CompanyPolyPeptide US
LocationTorrance, CA, US
Work modeNo
SourceTeamtailor
Listed5 days ago

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About the role

Description supplied by the original job listing.

Calibration and Metrology Specialist
Location: Torrance, CA | Employment Type: Full-Time
Help Keep Critical GMP Equipment Accurate, Compliant, and Production-Ready
At PolyPeptide, we partner with pharmaceutical and biotech companies to support the development and manufacturing of peptide-based therapies. We are looking for a Calibration and Metrology Specialist to help ensure the instruments, equipment, and systems used in our GMP manufacturing, laboratory, and facility operations remain accurate, reliable, and compliant.
This role is a strong fit for someone who enjoys hands-on technical work, takes pride in precision and documentation, and understands the importance of calibration and metrology in a regulated pharmaceutical environment. In this position, your work will directly support product quality, equipment readiness, regulatory compliance, and on-time delivery to our customers.
About the Role
The Calibration and Metrology Specialist is responsible for performing calibration, routine maintenance, troubleshooting, documentation, and compliance activities for instruments and equipment used across manufacturing, laboratory, utility, and facility operations.
In this role, you will help maintain equipment in a validated and inspection-ready state, support investigations for out-of-tolerance or failed calibrations, coordinate with external vendors, and collaborate closely with Engineering, Quality Assurance, Manufacturing, and Laboratory teams.
This is an important technical role for someone who is detail-oriented, organized, and confident working in a GMP environment where accuracy, traceability, and compliance are essential.
What You Will Do
Perform calibrations and routine maintenance on laboratory, manufacturing, utility, and facility instruments and equipment.
Follow established calibration schedules, procedures, work instructions, and GMP documentation requirements.
Maintain accurate and up-to-date calibration records, certificates, and related documentation in accordance with cGMP, ISO, and company standards.
Troubleshoot and resolve equipment and instrument issues related to calibration, performance, and functionality.
Support investigations for out-of-tolerance or failed calibrations, including root cause analysis and CAPA implementation.
Coordinate with external vendors and contractors for third-party calibrations, repairs, and equipment qualifications.
Assist with the development, review, and improvement of calibration procedures, schedules, and work instructions.
Support compliance with 21 CFR Part 11, FDA, ICH, and other applicable regulatory requirements for instrumentation and metrology systems.
Provide calibration documentation and technical support during internal and external audits.
Participate in the implementation and continuous improvement of computerized calibration management systems, including CMMS.
Collaborate with Engineering, Quality Assurance, Manufacturing, Laboratory, and Facilities teams to support equipment readiness for production and testing operations.
Promote a strong culture of safety, quality, accuracy, and compliance.
What We Are Looking For
Education and Experience
Associate’s or Bachelor’s degree in Metrology, Engineering, Life Sciences, or a related technical field.
3+ years of calibration or metrology experience in a GMP-regulated pharmaceutical, biotech, CDMO, or similar regulated environment.
Experience supporting manufacturing, laboratory, utility, or facility equipment in a regulated setting preferred.
Technical Skills
Strong understanding of calibration standards, methods, tolerances, traceability, and regulatory compliance.
Hands-on experience with calibration tools and standards, such as weights, multimeters, RTDs, pressure gauges, pH meters, HPLCs, and related instrumentation.
Experience maintaining calibration records, certificates, and GMP documentation.
Ability to troubleshoot instrument performance, equipment functionality, and calibration-related issues.
Familiarity with computerized maintenance or calibration management systems, such as CMMS, preferred.
Understanding of cGMP, ISO, FDA, ICH, 21 CFR Part 11, and applicable quality system requirements.
Skills and Competencies
Strong attention to detail and commitment to documentation accuracy.
Accountability and strong compliance orientation.
Analytical thinking and problem-solving skills.
Ability to work independently while supporting cross-functional teams.
Strong communication and technical writing skills.
Ability to prioritize work and support equipment readiness in a fast-paced GMP environment.
Safety awareness and understanding of regulated laboratory and manufacturing practices.
Why Join PolyPeptide?
This is an opportunity to take on a hands-on technical role that has a direct impact on manufacturing readiness, laboratory reliability, regulatory compliance, and product quality.
As a Calibration and Metrology Specialist, you will help ensure critical equipment remains accurate, compliant, and ready to support GMP operations. Your work will support teams across Engineering, Quality, Manufacturing, Laboratories, and Facilities, making this a highly visible role within our operations.
This position is ideal for someone who values precision, enjoys solving technical problems, and wants to contribute to the reliable delivery of peptide-based therapies.
Join PolyPeptide and help ensure our critical instruments, equipment, and systems remain accurate, compliant, and ready to support high-quality GMP manufacturing and laboratory operations.
Salary: $90k-$100k
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity or expression, pregnancy, age, national origin, disability status, genetic information, protected veteran status, or any other characteristic protected by law.

Work arrangement
No

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