Calibration Engineer

Job Description Join our team at Scientific Protein Laboratories (SPL), a world leader in biosourced pharmaceuticals, located just outside of Madison, Wisconsin in Waunakee! SPL is an innovative biopharmaceutical leader with unique products and services supporting the pharmaceutical industry globally. For over 40 years, SPL specializes in the development and cGMP compliant manufacturing of Active Pharmaceutical Ingredients (APIs). Our Metrology Calibration Specialist is responsible for the calibration, maintenance, troubleshooting, and documentation of test and measurement equipment used in a regulated pharmaceutical manufacturing environment. This role supports equipment reliability and compliance by performing calibration activities, maintaining accurate records, and assisting with quality and regulatory requirements. Perform calibration, maintenance, troubleshooting, and minor repairs on test, measurement, and diagnostic equipment (TMDE). Calibrate a variety of instruments including temperature, pressure, electrical, flow, mass, pH, dimensional, and analytical equipment. Support calibration activities for equipment such as recorders, controllers, transducers, moisture analyzers, gas sensors, autoclaves, bioreactors, and laboratory instrumentation. Maintain calibration standards and reference equipment in accordance with established procedures and traceability requirements. Accurately document calibration results and maintain calibration records within the Calibration Management Information System (CMMS/CMIS). Assist in coordinating internal and external calibration services to ensure equipment is calibrated on schedule. Participate in routine equipment inspections and help identify opportunities to improve calibration processes and equipment reliability. Collaborate with Quality, Manufacturing, Engineering, and Facilities teams to resolve routine equipment and measurement-related issues. Assist with the selection and qualification of measurement equipment for new or modified processes. Contribute to continuous improvement initiatives focused on reducing equipment downtime and improving workflow efficiency. Associate degree in Electronics, Engineering Technology, Instrumentation Technology, or a related technical field. Minimum of 5 years of calibration and instrumentation experience in a pharmaceutical, biotechnology, medical device, or other regulated manufacturing environment. Experience calibrating a broad range of instrumentations including temperature, pressure, electrical, flow, and analytical equipment. Bachelor’s degree in engineering or related technical discipline. ASQ Certified Calibration Technician (CCT) certification or willingness to obtain certification. excellent benefits package - including Medical, Dental and Vision on Day 1; Life and AD&D Insurance, and Short and Long-term Disability; Health and Flexible Saving Account options; Employee Assistance Program, generous vacation; paid Holidays; community involvement; All qualified applicants will receive consideration for employment without regard to age, color, creed, disability, gender identity, national origin, protected veteran status, race, religion, sex, sexual orientation, and any other status protected by applicable local, state or federal law. \nCompany Description SPL, a Hepalink Company, creates the Active Pharmaceutical Ingredients Heparin Sodium USP, Pancreatin USP, and Pancrelipase USP. We serve the pharmaceutical, veterinary, and food industries globally. Within the still-young biopharmaceutical industry, we are among a small group of companies with an established track record in efficient process development, analytical testing, quality assurance, and regulatory support required to provide our customers with cGMP compliant APIs at all phases of clinical development, straight through to commercial launch. SPL, a Hepalink Company, creates the Active Pharmaceutical Ingredients Heparin Sodium USP, Pancreatin USP, and Pancrelipase USP. We serve the pharmaceutical, veterinary, and food industries globally. We specialize in cGMP biopharmaceutical manufacturing. Within the still-young biopharmaceutical industry, we are among a small group of companies with an established track record in efficient process development, analytical testing, quality assurance, and regulatory support required to provide our customers with cGMP compliant APIs at all phases of clinical development, straight through to commercial launch.