Quality Control Analyst II — Onsite QC & Data Review

YOH Services LLC; Norton (MA); On-site; USD 41,000 - 59,000; Full time

Benefits offered by this job

Medical, Prescription, Dental & Vision

Health Savings Account (HSA)

Life & Disability Insurance

401K Retirement Savings Plan

Employee Assistance Program (EAP)

Direct Deposit & weekly epayroll

Referral Bonus Programs

Certification and training opportunit

Job summary

Yoh, a Day & Zimmermann company, is hiring an Analyst II – Quality Control Operations to support testing from development through commercialization at our Norton, MA site, with occasional duties in Cambridge, MA.

The role involves routine and non-routine analytical assays, data trending, investigations, and participation in method transfers and validation under GMP/GLP guidelines. Candidates should have 4–8 years in pharma/biotech QC and strong data analysis and teamwork skills.

Qualifications

• Bachelor's degree in chemistry, biology, biochemistry, or related field; associate degree or equivalent considered.
• 4–8 years of pharma/biotech regulated lab QC experience.
• Strong attention to detail and teamwork in a fast-changing environment.

Responsibilities

• Perform routine and non-routine analytical assays to support materials and product release.
• Maintain training records and testing schedules to support timelines.
• Assist with equipment and inventory maintenance and reagent preparation.
• Submit data accurately and support data review for regulatory submissions.
• Support audits, inspections, and continuous QC process improvements.

Skills

Data analysis

Attention to detail

Communication

Teamwork

Education

Bachelor's degree in chemistry/biology/biochemistry or related field

Tools

LIMS

Excel

Word

PowerPoint

Job description

Yoh, a Day & Zimmermann company, is hiring an Analyst II – Quality Control Operations to support testing from development through commercialization at our Norton, MA site, with occasional duties in Cambridge, MA.

The role involves routine and non-routine analytical assays, data trending, investigations, and participation in method transfers and validation under GMP/GLP guidelines. Candidates should have 4–8 years in pharma/biotech QC and strong data analysis and teamwork skills.