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Qc Associate Jobs in Boston, MA (NOW HIRING)

Adecco

QC Inspector

Chelmsford, MA

$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 ...

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 ...

TScan Therapeutics

Director, Quality Control

Waltham, MA

$210K - $220K/yr

Reporting to the Associate Vice President of QC and AD, the ideal candidate should have relevant experience in compendial, cellular, molecular, and environmental monitoring in a cGMP facility, and ...

TScan Therapeutics

Director, Quality Control

Waltham, MA · On-site

$210K - $220K/yr

Reporting to the Associate Vice President of QC and AD, the ideal candidate should have relevant experience in compendial, cellular, molecular, and environmental monitoring in a cGMP facility, and ...

TScan Therapeutics

Director, Quality Control

Waltham, MA · On-site

$210K - $220K/yr

Reporting to the Associate Vice President of QC and AD, the ideal candidate should have relevant experience in compendial, cellular, molecular, and environmental monitoring in a cGMP facility, and ...

Sloan

Be Seen First

Quality Control Inspector

Andover, MA · On-site

$54K - $60K/yr

The Quality Control Inspector will be responsible for testing and inspecting components and ... Associate Degree. * Hazardous Waste & USDOT Hazardous Materials. * Power Industrial Truck ...

Amrize

Quality Control Technician II

Saugus, MA

$19 - $24.50/hr

Quality Control Technician II | Req ID: 16555 | HR Contact: Roscoe Chambers | Location: Saugus ... Associate's degree Required Work Experience: 3-5 year Required Training/Certifications: State ...

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Qc Associate information

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How much do qc associate jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for qc associate in Boston, MA is $27.70, according to ZipRecruiter salary data. Most workers in this role earn between $20.14 and $33.75 per hour, depending on experience, location, and employer.

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 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 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.

What are the most commonly searched types of Qc jobs in Boston, MA?

The most popular types of Qc jobs in Boston, MA are:

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For Qc Associate jobs in Boston, MA, the most frequently searched job titles are:

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Qc Associate jobs near you
Infographic showing various Qc Associate job openings in Boston, MA as of August 2026, with employment types broken down into 1% As Needed, 71% Full Time, 25% Part Time, 1% Temporary, and 2% Contract. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $57,609 per year, or $27.7 per hour.

Associate Director, Quality Control (56861)

Praxis Precision Medicines, Inc

Boston, MA • On-site, Remote

$150K - $169K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 14 days ago

Job description

Associate Director, Quality Control
Reports to: Senior Director, Quality Operations, CMC
Location: This position may be performed remotely with travel to the Boston area as needed.
Position Summary
Praxis is seeking a highly experienced, motivated, and innovative quality leader with strong experience in late-stage development and commercialization to join our Quality team as Associate Director, Quality Control to support QC product release and stability activities. Reporting to Senior Director, Quality Operations CMC, this position will be responsible for managing and executing Quality Control activities in support of product testing, release, and stability, and toxicology studies test material inventory support. Ensure GMP activities are conducted in accordance with applicable SOPs, compendia, approved methods, and in accordance with company's and regulatory agencies' policies and procedures.
Primary Responsibilities
  • Quality control oversight of contract lab activities e.g. routine testing, testing results review and approval, generation of Certificate of Analysis, review/approval of technical documents such as method validation and qualification protocols/reports, and regulatory filing documents per project needs as required
  • Manage and lead clinical and commercial quality control compliance for stability, reference standard, and specification programs
  • Support the establishment of QC systems such as product specifications, product expiry, reference standard program, QC documentation including SOP's, material specifications and other quality documents, etc.
  • Support CMC Analytical Development in a QC aspect by review and approval of applicable documents in support of activities such as method development, transfer, characterization, comparability investigations, analytical test method qualification plans/protocols and reports
  • Perform data review of trending for in-process testing, release, and stability and identify data trends, to ensure compliance with regulatory filings and ICH or other global health authority guidance documents, as applicable
  • Support technology transfer and process performance qualification with product characterization/process validation activities
  • QC support in the generation, quality, and compliance review of bioanalytical data from preclinical and clinical projects for proprietary compounds and in some cases support for sample analysis projects
  • Support tox material inventory monitoring process, to ensure no impediments to completing studies
  • Additional responsibilities and ad hoc projects as required

Qualifications and Key Success Factors
  • Bachelors degree strongly preferred, with minimum of 6 years of experience in cGMP Quality Control environment
  • In-depth technical and regulatory understanding of GMP biologics manufacturing and testing including applicable international regulations/standards (GMP and ICH guidelines) in all phases of product development and commercialization
  • Experience managing third party assay laboratories, collaborations, and relevant bioanalytical vendors preferred
  • Extensive knowledge of GMP regulations, ICH guidelines, and stability testing requirements.
  • Proven track record of managing stability programs and COA processes for clinical and commercial products
  • Experience working in QC lab environment with hands-on experience in running, qualifying, and validating analytical methods
  • Ability to work effectively in a fast-paced, dynamic environment
  • Experience managing Contract Test Labs activities
  • Experience with regulatory inspections and interactions with health authorities
  • Excellent communication skills and ability to build key networks and business relationships across all levels of the business

Compensation & Benefits
At Praxis, we're proud to offer an exceptional benefits package that includes:
  • 99% premium cost covered for medical (Blue Cross Blue Shield), dental, and vision plans
  • Bonus program structured to pay on a quarterly basis
  • 401k plan with 100% match up to 6% of employee's contribution (Traditional & Roth)
  • Wellness benefit of $200/month towards incredibly flexible options including travel, fitness equipment & memberships, student loan repayment, sports fees and much more
  • Unlimited PTO, (2) weeklong shutdowns each year, and a generous extended family leave benefit
  • Eligibility for equity awards and Employee Stock Purchase Plan (15% discount)

To round out this world-class total rewards package, we provide base salary compensation in the range of $150,000 to $169,000 annualized. Final salary range may be modified commensurate with job level, education, and experience.
Company Overview
Praxis Precision Medicines is a clinical-stage biopharmaceutical company translating genetic insights into the development of therapies for central nervous system disorders characterized by neuronal imbalance. At Praxis we share a common vision of reshaping the human condition into a more freeing and fulfilled existence by developing high impact medicines for patients and families affected by and living with complex brain disorders. Our core Values of Trust, Ownership, Curiosity and Results are foundational to every aspect of our business and are exemplified by each and every one of our team members.
Diversity, Equity & Inclusion
Guided by our core values, at Praxis Precision Medicines, Inc. we continue to DARE FOR MORE ® to advance, promote, and champion diversity, equity, and inclusion by encouraging individuals to bring their authentic selves and perspectives to work each day. We are an equal opportunity employer and committed to providing opportunities to all qualified applicants without regard to race, religious creed, color, gender identity or expression, age, national origin, sexual orientation, disability, genetics, military service and veteran status, or any other characteristic protected by federal, state, or local laws.
Attention: Job Scam Alert
Praxis has recently become aware of fraudulent job recruitment postings from individuals claiming to represent Praxis. These postings seek financial information in connection with fraudulent opportunities for employment. If you suspect any fraudulent activity or misrepresentation in connection with a Praxis job opportunity, please report it to careers@praxismedicines.com.
Praxis does not accept unsolicited submissions from recruitment agencies for open positions. We ask all recruitment agencies to refrain from contacting any Praxis employee regarding any position. All unsolicited resumes submitted by recruitment agencies to any Praxis employee in any form or method will be deemed to be the property of Praxis, and Praxis explicitly reserves the right to hire those candidate(s) without any financial obligation to the recruitment agency.

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