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Qc Associate Jobs in Boston, MA (NOW HIRING)

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 ...

Quality Control Technician II

Saugus, MA · On-site

$19 - $24.50/hr

Provides QC support on various residential and commercial projects WHAT YOU'LL ACCOMPLISH ... Associate's degree Required Work Experience: 3-5 year Required Training/Certifications: State ...

Quality Control Technician II 1

Wrentham, MA

$20.50 - $26.25/hr

We're seeking a Quality Control Technician II who's ready to put your skills to work on projects ... Associate's degree Required Work Experience: 3-5 year Required Training/Certifications: State ...

Quality Control Technician II 1

Wrentham, MA · On-site

$20.50 - $26.25/hr

Provides QC support on various residential and commercial projects WHAT YOU'LL ACCOMPLISH ... Associate's degree Required Work Experience: 3-5 year Required Training/Certifications: State ...

QC Lab Tech I

Billerica, MA · On-site

$23.56 - $28.80/hr

Job Title: Quality Control Lab Tech Department: Quality Last Reviewed: September 2023 Levels ... An Associates of Science in Chemistry, Biology or advanced degrees are preferred. Physical ...

Showing results 41-60

Qc Associate information

See Boston, MA salary details

$12

$27

$41

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:

What are popular job titles related to Qc Associate jobs in Boston, MA?

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

What cities near Boston, MA are hiring for Qc Associate jobs?

Cities near Boston, MA with the most Qc Associate job openings:

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 Lab Automation

Initial Therapeutics, Inc.

Norwood, MA • On-site

$142.50 - $256.50/hr

Other

Medical, PTO

Posted 9 days ago


Job description

The Role

The Associate Director, Quality Control Lab Automation Strategy & Digital Integration is responsible for leading the strategy, implementation, and lifecycle management of laboratory automation and digital integration across Moderna’s Quality Control laboratories.

This role will define and execute the multi‑year roadmap for automation, robotics, integrated laboratory systems, and digital workflows, ensuring solutions are scalable, compliant, and aligned with business priorities and regulatory expectations. The Associate Director will work in a highly collaborative, cross‑functional environment, partnering closely with QC, Digital/IT, QA, Manufacturing, Analytical Development, AS&T, and Applied Technologies to drive the adoption of innovative automation technologies and connected laboratory solutions. This role will provide strategic direction and governance for automation programs, systems, policies, and standards while ensuring alignment with Moderna’s vision for a highly automated and data‑enabled laboratory ecosystem. The incumbent will be responsible for driving automation performance, operational efficiency, data integrity, and continuous improvement across the QC network. This includes supporting regulatory inspections, overseeing automation‑related investigations and quality systems, evaluating emerging technologies, and providing executive‑level communication of program progress, risks, and business value.

Success in this role requires strong expertise in GMP laboratory automation, digital systems integration, strategic leadership, and the ability to influence and align stakeholders across a complex matrix organization.

Here’s What You’ll Do
  • Own the strategic direction, governance, and execution of the QC laboratory automation roadmap across Moderna's QC network.
  • Develop and maintain a multi‑year automation strategy aligned with QC business priorities, digital transformation objectives, and future laboratory operating models.
  • Lead governance and prioritization of the QC automation portfolio, ensuring initiatives are sequenced based on business value, compliance impact, technical readiness, resource capacity, and long‑term scalability.
  • Lead a portfolio of automation and digital enablement initiatives including liquid handling robotics, automated sample management, laboratory instrumentation integration, autonomous technologies, and digital laboratory workflows.
  • Partner with business owners of laboratory systems including Chromeleon, LES, LabVantage LIMS, LabX, MODA, and related platforms to ensure seamless integration of automation technologies within QC operations.
  • Establish automation standards, governance processes, and best practices to ensure scalable, compliant, and sustainable implementations across QC laboratories.
  • Provide strategic leadership and oversight for automation projects, including prioritization, resource planning, risk management, stakeholder alignment, and value realization.
  • Drive governance forums, executive communications, and strategic reviews including Steering Committee meetings, Quarterly Business Reviews, and senior leadership updates.
  • Ensure automation solutions comply with GMP requirements, ALCOA+ principles, data integrity expectations, Computer System Validation requirements, and applicable global regulations.
  • Own and oversee quality system records associated with automation initiatives, including change controls, deviations, CAPAs, investigations, and impact assessments.
  • Serve as the QC automation subject matter expert during regulatory inspections, audits, and health authority interactions.
  • Develop and monitor automation performance metrics, reliability measures, operational KPIs, and business value indicators to drive continuous improvement and investment decisions.
  • Partner with Manufacturing, Technical Development, Analytical Development, AS&T, and Quality organizations to support product lifecycle activities, investigations, and strategic business initiatives.
  • Evaluate emerging automation technologies, laboratory robotics, artificial intelligence applications, and digital capabilities to continuously advance Moderna's laboratory automation strategy.
  • Influence cross‑functional teams and senior leadership to drive alignment on automation priorities, technology investments, and long‑term laboratory transformation goals.
  • Foster a culture of innovation, collaboration, operational excellence, and continuous improvement across the QC organization.
Here’s What You’ll Need (Basic Qualifications)
  • Education: BS, MS, or PhD in Engineering, Computer Science, Automation, Life Sciences, or a related technical field.
  • Experience: BS degree with 10+ years, MS degree with 8+ years, or PhD with 5+ years of experience in automation design and implementation.
  • Specific Certifications or Training: None.
Here’s What You’ll Bring to the Table (Preferred Qualifications)
  • Significant experience in Quality Control, laboratory automation, analytical operations, digital lab systems, or GMP laboratory transformation.
  • Experience implementing robotics, integrated laboratory work‑cells, automated sample preparation, or digital method execution in a GMP environment.
  • Demonstrated experience implementing and managing laboratory automation technologies including liquid handling systems, robotics platforms, automated storage systems, and integrated laboratory workflows.
  • Experience developing and executing enterprise‑level automation strategies and roadmaps.
  • Proven success leading complex cross‑functional programs involving Quality, Digital, Manufacturing, Technical Development, and Regulatory stakeholders.
  • Strong business acumen with the ability to evaluate investment opportunities and communicate value realization to senior leadership.
  • Exceptional project and portfolio management skills with the ability to manage multiple strategic initiatives simultaneously.
  • Strong executive communication and presentation skills, including preparation of materials for senior leadership, Steering Committees, and executive governance forums.
  • Demonstrated ability to influence without authority and drive alignment across a highly matrixed organization.
  • Proven track record of identifying opportunities for innovation and delivering practical automation solutions that improve quality, compliance, efficiency, and business performance.
Pay & Benefits

The salary range for this role is $142,500.00 - $256,500.00. This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An individual’s position within the salary range will be based on several factors including, but not limited to, specific competencies, relevant education, qualifications, certifications, experience, skills, performance, and business or organizational needs. The successful candidate may be eligible for an annual discretionary bonus, other incentive compensation, or equity award, subject to company plan eligibility criteria and individual performance.

  • Best‑in‑class healthcare coverage, plus voluntary benefit programs to support your unique needs.
  • A holistic approach to well‑being, with access to fitness, mindfulness, and mental health support.
  • Family planning benefits, including fertility, adoption, and surrogacy support.
  • Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year‑end shutdown.
  • Savings and investment opportunities to help you plan for the future.
  • Location‑specific perks and extras.
Equal Opportunities

Moderna is committed to equal employment opportunity and non‑discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law. Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!

Moderna is an E‑Verify Employer in the United States. We consider qualified applicants regardless of criminal histories, consistent with legal requirements.

Accommodations

We’re focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best.

Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should contact the Accommodations team at leavesandaccommodations@modernatx.com.

Export Control Notice

This position may involve access to technology or data that is subject to U.S. export control laws, including the Export Administration Regulations (EAR). As such, employment is contingent upon the applicant’s ability to access export‑controlled information in accordance with U.S. law. Due to the nature of the work and regulatory requirements, only individuals who qualify as U.S. persons (citizens, permanent residents, asylees, or refugees) are eligible for this position. For this role Moderna is unable to sponsor non‑U.S. persons to apply for an export control license.

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