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Added 5 days ago
Head of Project Engineering
Scientific Protein Laboratories
Waunakee, WI
Added 5 days ago
Sr Manager Automation & Electrical Maintenance Engineering
Scientific Protein Laboratories
Waunakee, WI
Added 5 days ago
CDL A Shipping & Warehouse Specialist (Tanker Endorsement Required)
Scientific Protein Laboratories
Sioux City, IA
Added 11 days ago
Supervisor Quality Control
Scientific Protein Laboratories
Waunakee, WI
Added 15 days ago
Process Operator - 1st Shift (Multiple Openings & Schedule Options Available)
Scientific Protein Laboratories
Waunakee, WI
Added 16 days ago
Reliability Engineer
Scientific Protein Laboratories
Waunakee, WI
Added 16 days ago
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Scientific Protein Laboratories
Waunakee, WI
Added 16 days ago
Supervisor, Manufacturing - Pancreatin
Scientific Protein Laboratories
Waunakee, WI
Added 16 days ago
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Scientific Protein Laboratories
Waunakee, WI
Added 16 days ago
Automation Engineer
Scientific Protein Laboratories
Waunakee, WI
Added 16 days ago
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Scientific Protein Laboratories
Waunakee, WI
Added 16 days ago
Process Development Engineer
Scientific Protein Laboratories
Waunakee, WI
Added 16 days ago
Manufacturing Technician- 3rd Shift
Scientific Protein Laboratories
Waunakee, WI
Added 16 days ago
Process Operator- 3rd Shift - (Multiple Openings & Schedule Options Available)
Scientific Protein Laboratories
Waunakee, WI
Added 16 days ago
Manufacturing Technician - 1st shift, Weekends
Scientific Protein Laboratories
Waunakee, WI
Added 16 days ago
Controls Engineer
Scientific Protein Laboratories
Waunakee, WI
Added 16 days ago
On-Site QA Specialist
Scientific Protein Laboratories
Waunakee, WI
Added 16 days ago
Maintenance Supervisor
Scientific Protein Laboratories
Waunakee, WI
Added 16 days ago
Head of Planning S&OP
Scientific Protein Laboratories
Waunakee, WI
Added 16 days ago
Planning Specialist
Scientific Protein Laboratories
Waunakee, WI
Added 16 days ago
Manager Regulatory Affairs
Scientific Protein Laboratories
Waunakee, WI
Added 16 days ago
Quality Systems eQMS Technical Manager
Scientific Protein Laboratories
Waunakee, WI
Added 16 days ago
Equipment Specialist
Scientific Protein Laboratories
Waunakee, WI
Added 16 days ago
Quality Systems QA Manager
Scientific Protein Laboratories
Waunakee, WI
Added 16 days ago
CSV & DI Compliance Manager
Scientific Protein Laboratories
Waunakee, WI

Closed listing

Scientific Protein Laboratories

On-Site QA Supervisor

Waunakee, WI, United States

This opening has closed.

The original listing is kept below for reference.

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Job details

Posting language: English
Posted: Jul 29, 2026

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Original job description

Archived listing. The details below describe a past opening.

JOB SUMMARY

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 On-Site QA Supervisor. This is a 1st shift position.

This position is responsible for supervision of the sites on-site Quality Assurance responsibilities including but not limited to on-site inspection, batch record review and raw material inspection/release. Develops and maintains cGMP-compliant Quality Management Systems. Responsible for management of SPL's quality compliance throughout SPL which includes operational activities such as: release of intermediate product, release assessment of finished product; review of batch records; review of investigations, deviations, change controls and CAPAs; pest control; raw material inspections/release. The supervisor is responsible for personnel activities such as: reviews, workload management and coordination of training.

Responsibilities include:

Oversee the functions of the on-site QA staff to include but are not limited to on-site inspection of manufacturing/testing areas, sampling and release of raw materials, pest control, review of manufacturing and packaging batch records and
Organize the establishment/maintenance of relevant procedures/documents.
Assists all departments in the identification and evaluation of facility events. Assures proper documentation is initiated to capture the event.
Determine disposition of packaging materials, in-process materials and products on the basis of approved specifications.
Participates in the preparation of Annual Product Review documentation for all SPL Marketed Products.
Provide appropriate data and QA support for SPL regulatory functions.
Coordinates/reviews deviations, investigations, change controls and CAPAs
Participates in audits and addresses audit findings where necessary.
Performs intermediate product release and finished product release assessments.
Product shipping release.
Responsible for continuous improvement of SPL cGMP Quality Systems to support on-site QA in compliance with FDA, ICH, USDA, ISPE and other pertinent pharma industry requirements.
Compiles and communicates metrics associated with on-site QA to management as required.

Job Requirements and Qualifications:

Education: Associate’s degree required, Bachelor’s degree or above preferred
Experience: 5+ years’ required, 10+ years preferred
Schedule: 1st shift

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.

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Skills

Quality assurance
Inspection
Quality assurance procedures
Regulatory compliance
Packaging
Documentation
Process improvement
Quality control systems
Pharmaceutical industry

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