Equipment Specialist

Job Description

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).  SPL has an exciting opportunity to join the team as an Equipment Specialist.

Under general supervision, our Equipment Specialist is responsible for the operation, inspection, maintenance, troubleshooting, and repair of manufacturing, utility, and production support equipment. The incumbent assists in ensuring equipment reliability, minimizes downtime, and supports safe and compliant operations within a regulated manufacturing environment. The Equipment Specialist performs routine maintenance activities, responds to equipment issues, and works with senior maintenance personnel on more complex repairs and projects.

Responsibilities:

• Perform routine inspections, startup activities, and operational checks on manufacturing and utility equipment.
• Monitor equipment performance and identify issues requiring corrective action.
• Troubleshoot and perform repairs on production support and utility equipment within established skill level.
• Conduct preventive maintenance activities according to established schedules and procedures.
• Assist with equipment calibration, adjustment, and testing to ensure proper operation.
• Support maintenance and operation of plant utility systems, including boilers, HVAC systems, water systems, and related equipment.
• Assist with troubleshooting and maintenance of process equipment, including freeze dryers and other manufacturing equipment.
• Perform basic electrical, mechanical, piping, and instrumentation maintenance tasks.
• Document maintenance activities, repairs, inspections, and equipment performance data accurately.
• Follow Standard Operating Procedures (SOPs), Good Manufacturing Practices (GMP), and safety requirements.
• Collaborate with Manufacturing, Engineering, Validation, and Maintenance personnel to resolve equipment-related issues.
• Escalate complex equipment malfunctions to senior technicians or supervisors as needed.
• Participate in continuous improvement initiatives to enhance equipment reliability and operational efficiency.
• Maintain a clean, organized, and safe work environment.

Job Requirements and Qualifications

Required:

This position is open to candidates with a range of relevant experience levels. Candidates meeting the minimum qualifications are encouraged to apply. Final job level and compensation will be determined based on the selected candidate’s education, experience, skills, and overall qualifications.

• High school diploma or GED.
• Minimum of 3 years of maintenance or equipment support experience in manufacturing, pharmaceutical, food processing, chemical, or related industrial environment.
• Basic knowledge of mechanical, electrical, instrumentation, or HVAC systems.
• Experience performing preventive maintenance, calibration and equipment troubleshooting.
• Ability to read and interpret equipment manuals, work instructions, schematics, and technical drawings.
• Working knowledge of boilers, PW/WFI systems, solvent recovery systems, plant peptone concentration system, and other plant utilities.
• Basic understanding of industrial control systems and instrumentation.
• Strong problem-solving and organizational skills.
• Ability to work independently and as part of a team.
• Must be available to work 2nd shift (Monday - Friday, 3pm - 11:30pm).

Preferred:

• Technical training in Industrial Maintenance, Mechanical Systems, HVAC, Electrical Technology, Instrumentation, or related field.
• Experience supporting utility systems, process equipment, or production support equipment.
• Familiarity with computerized maintenance management systems (CMMS).
• Minimum of 5+ years of maintenance or equipment support experience in manufacturing, pharmaceutical, food processing, chemical, or related industrial environment.
• Knowledge of GMP and industrial safety practices.

WHY JOIN SPL?

Our employees are our success!  We recruit motivated people, recognize their contributions, and support their development to reach their full potential.  

Perks include: competitive compensation; 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; 401k; advancement opportunities; team-oriented environment; community involvement; company events and more!

SPL is an equal opportunity employer. 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. 

 

Company 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. 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.

Company 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. 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.