QC Chemistry Associate II

Randstad USA; Norwood (MA); On-site; USD 66,124; Full time

Job summary

A staffing and workforce solutions company is looking for a QC Chemistry Associate II in Norwood, MA for a 6-month contract position, potentially extendable. The role involves conducting analytical testing, ensuring compliance with FDA standards, and operating lab instrumentation like HPLC and UPLC. Candidates should have a BA/BS in Chemistry with at least two years of experience in a quality control laboratory. Join a team that emphasizes learning and innovation in the biotechnology sector.

Qualifications

• 2+ years of experience in a pharmaceutical quality control lab.
• Strong understanding of FDA, ICH regulations, and internal SOPs.
• Passion for rapid learning and technical growth.

Responsibilities

• Conduct in-process, release, and stability testing.
• Operate laboratory instrumentation and document results.
• Assist with deviation investigations and implement CAPAs.
• Utilize advanced digital tools to enhance patient health.

Skills

Analytical Testing

Instrumentation operation

Data Integrity

Lab Investigations

Innovation in lab techniques

Education

BA/BS in Chemistry or relevant scientific discipline

Tools

HPLC

UPLC

UV plate readers

Karl Fischer (KF) analyzers

Osmolality analyzers

Job description

Quality Control Chemistry Associate II (Contingent) - Norwood, MA

Contract 6 months with possible extension

Randstad is currently seeking a highly technical QC Chemistry Associate II to support a world-class Quality Control organization in Norwood.

This is a critical role ensuring the integrity of life-changing therapeutics through robust, compliant analytical testing in a fast-paced, digital-first environment.

The Opportunity:

• Pay Rate: Up to $48.00 per hour.
• Schedule: Monday – Friday, 2nd Shift (Onsite).
• Duration: 6-month contract with a possibility for extension.
• Location: Norwood, MA.

Key Responsibilities:

• Analytical Testing: Conduct in-process, release, and stability testing for drug substances and final products.
• Instrumentation: Operate HPLC, UPLC, UV plate readers, Karl Fischer (KF), and osmolality analyzers.
• Data Integrity: Accurately document results using LIMS following GDP and cGMP requirements.
• Lab Investigations: Assist with deviation investigations (OOS, OOT, OOE) and implement CAPAs.
• Innovation: Utilize advanced digital tools and automation systems to maximize impact on patient health.

Qualifications:

• Education: BA/BS in Chemistry (preferred) or a relevant scientific discipline.
• Experience: Minimum of 2 years in a pharmaceutical company quality control laboratory.
• Mindset: A passion for rapid learning and technical growth in a complex lab setting.
• Compliance: Strong understanding of FDA, ICH regulations, and internal SOPs.

Apply today to join a team that "obsesses over learning" and pushes the boundaries of what is possible in biotechnology.