QC Chemist I
Perrigo Company plc
August 11, 2026
Remote friendly (Covington, OH)
United States
Operations
Scope of the Role
- Collect samples including raw material, finished product, process equipment and environmental.
- Test purchased materials and/or Perrigo manufactured products per cGMP requirements and participate in laboratory investigations.
- Operate laboratory equipment.
- Participate in internal and external quality audits.
- Maintain personal laboratory work area and assist with general laboratory cleaning.
- Participate in training and development.
Experience Required
- Bachelor of Science degree in a scientific discipline (Chemistry or Food Science preferred, Biology) required; includes academic lab experience.
- 1–2 years’ experience working in a GMP/FDA regulated manufacturing environment preferred.
- Good written and verbal communication skills; excellent documentation and organizational skills.
- Demonstrated critical thinking skills, attention to detail, and ability to work independently and with others.
- Ability to take ownership of assigned tasks and responsibility for results.
- Ability to work overtime as required.
Benefits
- Competitive compensation, benefits tailored to supporting you and your family, and career development opportunities.
Application Instructions
- To apply, click the APPLY button at the bottom of the application; resumes/CVs must be submitted in English.
- Collect samples including raw material, finished product, process equipment and environmental.
- Test purchased materials and/or Perrigo manufactured products per cGMP requirements and participate in laboratory investigations.
- Operate laboratory equipment.
- Participate in internal and external quality audits.
- Maintain personal laboratory work area and assist with general laboratory cleaning.
- Participate in training and development.
Experience Required
- Bachelor of Science degree in a scientific discipline (Chemistry or Food Science preferred, Biology) required; includes academic lab experience.
- 1–2 years’ experience working in a GMP/FDA regulated manufacturing environment preferred.
- Good written and verbal communication skills; excellent documentation and organizational skills.
- Demonstrated critical thinking skills, attention to detail, and ability to work independently and with others.
- Ability to take ownership of assigned tasks and responsibility for results.
- Ability to work overtime as required.
Benefits
- Competitive compensation, benefits tailored to supporting you and your family, and career development opportunities.
Application Instructions
- To apply, click the APPLY button at the bottom of the application; resumes/CVs must be submitted in English.