QC Analyst- Chemistry

Scientific Protein Laboratories, LLC; Waunakee (WI); On-site; USD 60,000 - 80,000; Full time

Job summary

Join a leading biopharmaceutical company as a QC Analyst in Waunakee, WI. This role involves performing laboratory analyses, following strict guidelines, and ensuring quality standards are met. Candidates should have a high school diploma and preferably a degree in chemistry, with knowledge of FDA regulations being a plus. Enjoy competitive compensation and a supportive work environment.

Benefits

Competitive compensation

Medical, Dental, and Vision on Day 1

401k with advancement opportunities

Generous vacation and paid holidays

Qualifications

• QC Analyst position requires strong analytical and detail-oriented skills.
• Bachelor’s degree preferred, with 2+ years of experience for the role.
• Knowledge of cGMP/FDA guidelines is beneficial.

Responsibilities

• Perform laboratory analyses on APIs following strict procedures.
• Record and communicate results accurately, ensuring SOP compliance.
• Participate in calibration and maintenance of laboratory equipment.

Skills

Attention to detail

Analytical skills

Teamwork

Education

High School Diploma or G.E.D.

Bachelor’s degree in biochemistry or Chemistry

Job description

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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 a QC Analyst.

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 a QC Analyst.

This position is responsible for performing simple and complex routine laboratory analyses on APIs following strict written procedures derived from the United States Pharmacopoeia and/or other documents, to meet strict compendial and custom specifications. This work is performed under the cGMP/FDA guidelines. Participates in analytical and systems-improvement projects.

Responsibilities Include

• Follow Standard Operating Procedures (SOPs) to obtain accurate results.
• Perform the scheduled laboratory testing of raw material, in-process, finished product APIs and special products.
• Properly record all data results on appropriate documents and in electronic files, including immediate communication of problems to management.
• With assistance from management, author and/or execute laboratory experiments, analytical method and instrument validation efforts as necessary.
• Perform routine calibration and preventive maintenance of laboratory equipment.
• Review/Revise SOPs to ensure compliance with compendial documents.
• Review and interpret the work of other analysts.
  
  

Job Requirements And Qualifications

Position will be filled up to the Sr QC Analyst level and determined at discretion of the hiring manager.

Associate QC Analyst

Experience: none required, 2+ years preferred

Education: High School Diploma or G.E.D. required, bachelor’s degree or above in biochemistry or Chemistry or related discipline preferred

QC Analyst

Experience: 2+ years required, 5+ years preferred

Education: High School Diploma or G.E.D. required, bachelor’s degree or above in biochemistry or Chemistry or related discipline preferred

Sr QC Analyst

Experience: 5+ years required, 10+ years preferred

Education: High School Diploma or G.E.D. required, bachelor’s degree or above in biochemistry or Chemistry or related discipline preferred

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.

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Other

Job function

• Job function

  Quality Assurance

• Industries

  Pharmaceutical Manufacturing

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