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Qc Associate Jobs in Cambridge, MA (NOW HIRING)

Adecco

QC Inspector

Chelmsford, MA · On-site

$24.20/hr

Assists the QC Supervisor, QA Engineer and/or Quality Manager in the required areas as listed in ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

Adecco

QC Inspector

Chelmsford, MA · On-site

$24.20/hr

Assists the QC Supervisor, QA Engineer and/or Quality Manager in the required areas as listed in ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

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Qc Associate information

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$27

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How much do qc associate jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for qc associate in Cambridge, MA is $27.83, according to ZipRecruiter salary data. Most workers in this role earn between $20.24 and $33.89 per hour, depending on experience, location, and employer.

What is a QC associate?

A QC (Quality Control) Associate is a professional responsible for performing tests and inspections on products, materials, or processes to ensure they meet established quality standards. They work primarily in manufacturing, pharmaceutical, biotechnology, or food industries, helping to identify defects and maintain compliance with regulatory requirements. QC Associates document their findings, report issues, and may assist in implementing corrective actions to improve product quality. Their work is critical in ensuring that only safe and effective products reach customers.

What skills and qualifications are needed to be a QC associate?

To thrive as a QC Associate, you need a background in chemistry, biology, or a related scientific field, often supported by a relevant degree or laboratory experience. Familiarity with laboratory equipment, analytical instruments (like HPLC or GC), and quality management systems (such as GMP or ISO standards) is typically required. Attention to detail, strong organizational skills, and effective communication are crucial soft skills for ensuring accuracy and collaborating with team members. These competencies are essential for maintaining product quality, regulatory compliance, and operational efficiency in quality control environments.

What challenges do QC associates face when ensuring product quality, and how can they be addressed?

QC Associates often encounter challenges such as tight production deadlines, handling multiple testing protocols, and maintaining accuracy under pressure. Adapting to new technologies or updated regulatory standards can also present difficulties. To address these, strong organizational skills, continuous training, and effective communication with cross-functional teams are essential. Additionally, maintaining thorough documentation and proactively identifying potential issues can help ensure consistent product quality and compliance.

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Qc Associate jobs near you
Infographic showing various Qc Associate job openings in Cambridge, MA as of August 2026, with employment types broken down into 1% As Needed, 68% Full Time, 29% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $57,887 per year, or $27.8 per hour.

QC Associate, Raw Materials

JMD Technologies Inc.

Norwood, MA • On-site

$35 - $40/hr

Other

Posted 6 days ago

Job description

Title : QC Associate, Raw Materials I, II

Location: Norwood, MA (On-Site)

Employment Type: Contract

Status: Accepting Candidates


About the Role

The Quality Control Associate will support cGMP QC testing for raw materials, drug substances, and finished products at a manufacturing facility and affiliated contract organizations.

This role includes executing and troubleshooting analytical methods, supporting method transfers and qualification activities, and ensuring compliance with cGMP standards.


Key Responsibilities

QC Testing & Laboratory Support

  • Execute QC molecular biology and Bioassay methods, including mammalian cell-based potency, QPCR, sequencing, and protein analysis
  • Assist in troubleshooting equipment and assay issues
  • Perform reagent preparation, equipment maintenance, housekeeping, and logbook reviews
  • Establish and maintain a safe laboratory working environment


Documentation & Quality Systems

  • Write, revise, and maintain SOPs, protocols, and reports
  • Assist in execution of quality records, including investigations, change controls, and CAPAs
  • Ensure compliance with cGMP documentation and regulatory guidelines
  • Support training as assigned


Compliance & Continuous Improvement

  • Maintain mandatory training and assigned tasks
  • Provide support during audits
  • Collaborate on continuous improvement initiatives
  • Perform additional duties as assigned


Qualifications

BA/BS Degree

  • STEM degree with 3–5 years of experience in a cGMP laboratory setting


Hands-on experience with:

  • Mammalian cell culture
  • Cell-based and potency assays
  • ELISA
  • Molecular biology
  • Protein analysis


Preferred Qualifications

  • Method development/qualification experience with molecular biology, cell-based assays, or protein analysis methods
  • Experience with aseptic techniques and general laboratory instrumentation
  • Experience with pH meters, balances, and pipettes
  • Ability to prepare reagents and pipette small volumes
  • Experience working in a Biological Safety Cabinet
  • Laboratory equipment calibration and maintenance experience
  • Ability to work effectively in a fast-paced, cross-functional matrix environment
  • Familiarity with FDA, EU, ICH guidelines, and regulations


Compensation

  • Level I: $30–$35/hr (0–2 Years Experience)
  • Level II: $35–$40/hr (3–5 years' experience)
  • Norwood, MA – 100% On-Site
  • Monday–Friday, 8:00 AM–5:00 PM
  • 6+ Month Contract

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