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Qc Associate Jobs in Boston, MA (NOW HIRING)

Atrium

Quality Control Senior Associate

Boston, MA · On-site

$30 - $33/hr

The Quality Control Senior Associate will perform in-process, release, and stability testing while supporting laboratory operations and maintaining compliance with cGMP standards. The ideal Quality ...

ZwitterCo

Quality Control Technician

Woburn, MA · On-site

$20.50 - $26.25/hr

Technical training, certificate, or associate degree preferred * 3-5 years of experience in quality control, inspection, or manufacturing role required * Solid understanding of quality inspection ...

ZwitterCo

Quality Control Technician

Woburn, MA

$20.50 - $26.25/hr

Technical training, certificate, or associate degree preferred * 3-5 years of experience in quality control, inspection, or manufacturing role required * Solid understanding of quality inspection ...

ZwitterCo

Quality Control Technician

Woburn, MA

$20.50 - $26.25/hr

High school diploma or equivalent required Technical training, certificate, or associate degree preferred 3-5 years of experience in quality control, inspection, or manufacturing role required Solid ...

Adecco

Quality Control Inspector

Peabody, MA

$27 - $32/hr

Adecco is hiring for QC Inspectors in Peabody, MA on 1st and 2nd shift! These are temp to perm ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

Adecco

QC Inspector

Tyngsboro, MA

$21/hr

Adecco is hiring for a QC Inspector in Tyngsboro, MA! This is a temp to perm opportunity on 1st ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

Adecco

Quality Control Inspector

Peabody, MA

$27 - $32/hr

Adecco is hiring for QC Inspectors in Peabody, MA on 1st and 2nd shift! These are temp to perm ... In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other ...

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How much do qc associate jobs pay per hour?

As of May 28, 2026, the average hourly pay for qc associate in Boston, MA is $27.66, according to ZipRecruiter salary data. Most workers in this role earn between $20.10 and $33.70 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a QC Associate, and why are they important?

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 are some common challenges faced by QC Associates 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.

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.
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Qc Associate jobs near you
Infographic showing various Qc Associate job openings in Boston, MA as of May 2026, with employment types broken down into 92% Full Time, 3% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $57,538 per year, or $27.7 per hour.

Quality Control Associate

Meet Life Sciences

Watertown, MA • On-site

Other

Posted 7 days ago

Job description

Job Summary

Seeking a detail-oriented Associate II, Analytical Development/Quality Control professional to support analytical testing, method development, and quality control activities within a regulated pharmaceutical or biotech environment. This role is responsible for executing analytical assays, maintaining data integrity, supporting investigations, and collaborating cross-functionally to ensure product quality and compliance with cGMP standards.


Responsibilities

  • Perform routine and non-routine analytical testing of raw materials, in-process samples, and finished products.
  • Support Environmental Monitoring activities and laboratory operations.
  • Execute analytical assays using techniques such as HPLC/UPLC, GC, UV-Vis, and microscopy.
  • Record, review, and maintain accurate laboratory data and documentation in compliance with GMP and GDP requirements.
  • Assist with investigations related to out-of-specification (OOS) results and deviations.
  • Support analytical method development, optimization, qualification, and transfer activities.
  • Prepare technical documents including protocols, reports, and data summaries.
  • Perform data review, trending, and quality assessments.
  • Collaborate with Manufacturing, Quality Assurance, and Project Management teams to support project and client needs.
  • Communicate testing results, observations, and issues clearly to stakeholders.


Qualifications

  • Bachelor’s or Master’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific field.
  • 0–3+ years of experience in pharmaceutical, biotech, or CDMO environments.
  • Hands-on experience with analytical techniques, including HPLC/UPLC preferred.
  • Understanding of cGMP, GDP, and laboratory compliance standards.
  • Strong documentation, organizational, and data integrity skills.
  • Ability to manage multiple priorities in a fast-paced, client-driven environment.

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