Skip to main content
Tallo logoTallo logo

Find Jobs

Find Jobs Near You – Available Work in Your Location

Skip to job details

Back to Results

Apply for this opportunity

To apply for this job, you'll continue to an external website or email application.

Randstad USA

Associate II, Quality Control Chemistry

Review key factors to help you decide if the role fits your goals.
Pay Growth
?
out of 5
Not enough data
Not enough info to score pay or growth
Job Security
?
out of 5
Not enough data
Calculating job security score...
Total Score
68
out of 100
Average of individual scores

Were these scores useful?

Job Description

associate ii, quality control chemistry.norwood, massachusettsposted september 18, 2026 job detailssummary$36 - $41 per hourcontractbachelor degreecategorylife, physical, and social science occupations reference 54596 job details job summary: Skip the routine data entry and step into a high-impact bench role where your analytical testing directly drives product release. Working 2nd shift, you will run advanced chromatography and spectroscopy systems, tackle real-time stat testing for manufacturing, and own cGMP quality workflows from raw data to CAPA resolution.
location:
Norwood, Massachusetts job type: Contract salary: $36 - 41 per hour work hours: 9 to 5 education: Bachelors responsibilities: Perform routine and high-priority stat cGMP analytical chemistry testing, including HPLC/UPLC, GC, UV-Vis, Particle Analysis, Dynamic Light Scattering (DLS), Karl Fischer (KF), and NaOH plate reader assays.

Execute data entry, sample result tracking, and Electronic Assay Forms within LIMS (LabVantage).Support active drug substance manufacturing operations through in-process, release, and stability testing.

Assist in troubleshooting analytical assay methods and laboratory equipment when testing anomalies arise.

Maintain laboratory readiness by preparing reagents, managing sample inventories, maintaining equipment, and stocking QC supplies.

Author, revise, and review SOPs, testing protocols, and technical reports.

Participate in quality systems management by authoring quality records, including investigations, deviations, change controls, and CAPAs.

Support the site stability program and assist junior team members with data review, onboarding training, and technical troubleshooting.

Complete and maintain cGMP documentation in strict alignment with Good Documentation Practices (GDP) and Data Integrity guidelines.
qualifications:
Required:
BA/BS in relevant scientific discipline2 years of Laboratory experience.

Demonstrated aptitude or ability to learn to gain a strong understanding of GxP regulations #LI-AH1 skills: Quality control, HPLC, SOP, CAPA, GMP (Good Manufacturing Practice)
Equal Opportunity Employer:
Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com. Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility). This posting is open for thirty (30) days. It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Benefits

  • 401(k) Plans
  • Dental Insurance
  • Disability Insurance
  • Life Insurance