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Quality Control Lab Analyst Jobs in Lawrence, MA

Dyne Tx

Director, Quality Control

Waltham, MA · On-site

$190 - $230/hr

The Director, Quality Control leads global Quality Control activities, including oversight of ... Leads analytical troubleshooting efforts in collaboration with contract laboratories * Ensures ...

TScan Therapeutics

Director, Quality Control

Waltham, MA · On-site

$210K - $220K/yr

Ensure GMP lab is maintained in a constant state of compliance and inspection readiness * Support QMS compliance through timely review of documents and ensuring QC support of Quality/CMC ...

Dyne Therapeutics

Director, Quality Control

Waltham, MA · On-site

$190K - $230K/yr

The Director, Quality Control leads global Quality Control activities, including oversight of ... Leads analytical troubleshooting efforts in collaboration with contract laboratories * Ensures ...

TScan Therapeutics

Director, Quality Control

Waltham, MA · On-site

$210K - $220K/yr

Ensure GMP lab is maintained in a constant state of compliance and inspection readiness * Support QMS compliance through timely review of documents and ensuring QC support of Quality/CMC ...

TScan Therapeutics

Director, Quality Control

Waltham, MA · On-site

$210 - $220/hr

Ensure GMP lab is maintained in a constant state of compliance and inspection readiness. * Support QMS compliance through timely review of documents and ensuring QC support of Quality/CMC ...

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All JobsQuality Control Lab Analyst JobsQuality Control Lab Analyst Jobs in Lawrence, MA

Quality Control Lab Analyst information

See Lawrence, MA salary details

$17

$29

$43

How much do quality control lab analyst jobs pay per hour?

As of Aug 10, 2026, the average hourly pay for quality control lab analyst in Lawrence, MA is $29.29, according to ZipRecruiter salary data. Most workers in this role earn between $24.23 and $32.55 per hour, depending on experience, location, and employer.

How much does a quality control lab analyst earn?

A quality control lab analyst typically earns between $40,000 and $70,000 annually, depending on experience, location, and industry. Entry-level positions may start lower, while experienced analysts with certifications can earn higher salaries, often with opportunities for overtime and benefits.

What does a quality control lab analyst do?

A quality control lab analyst tests and inspects products, raw materials, and processes to ensure they meet quality standards and regulatory requirements. They use laboratory equipment and techniques such as chromatography and spectroscopy, often following standard operating procedures and documenting results accurately.

What is the difference between Quality Control Lab Analyst vs Quality Control Technician?

AspectQuality Control Lab AnalystQuality Control Technician
CredentialsTypically requires a degree in science or related field; certifications like ASQ or laboratory-specific training are commonOften requires a high school diploma or associate degree; some certifications may be preferred
Work EnvironmentLaboratory setting, performing tests and analyses on samplesManufacturing or production environment, performing inspections and sample collection
Industry UsageUsed across pharmaceutical, biotech, food, and chemical industriesCommon in manufacturing, food production, and pharmaceuticals

The main difference is that a Quality Control Lab Analyst typically conducts detailed laboratory testing and analysis, often requiring more specialized education and certifications. In contrast, a Quality Control Technician focuses on sample collection, inspection, and basic testing in production environments. Both roles are essential for quality assurance but differ in scope and responsibilities.

What job categories do people searching Quality Control Lab Analyst jobs in Lawrence, MA look for? The top searched job categories for Quality Control Lab Analyst jobs in Lawrence, MA are:
What cities near Lawrence, MA are hiring for Quality Control Lab Analyst jobs? Cities near Lawrence, MA with the most Quality Control Lab Analyst job openings:
Quality Control Lab Analyst jobs near you

QC Specialist II, Analytical Investigations

PCI Pharma Services

Bedford, NH • On-site

Full-time

Re-posted 23 days ago

PCI Pharma Services rating

6.7

Company rating: 6.7 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

439th of 538 rated manufacturers

Job description

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.


We are PCI.


Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

What You'll Do

As a QC Specialist, you will:

  • Lead investigations into QC Analytical deviations, OOS/OOT/OOE results, and other quality issues.

  • Serve as a key point of contact during audits and inspections, ensuring timely and compliant responses.

  • Draft and revise change controls, technical reports, cGMP documents, and protocols.

  • Perform QC analytical testing, review data, and identify trends to proactively address risks.

  • Assist in managing analytical equipment to maintain compliance and efficiency.

  • Collaborate cross-functionally to close out quality events and audit findings on time.

  • Help shape and refine QC processes that support continuous improvement.

What You Bring

  • Education/Experience: Bachelor's degree in Analytical Chemistry, Chemistry, Pharmaceutical Sciences, or related field; 2-5 years of QC Analytical Chemistry experience (pharma experience preferred).

  • Technical Skills: Hands-on experience with UPLC, HPLC, GC, FTIR, UV/VIS, Karl Fisher, Particle Size Analyzer, Densitometer, and Osmometer.

  • Knowledge: Solid understanding of cGMP, ICH, USP, and global compendia guidelines, especially in analytical method validation and stability studies.

  • Strengths: Strong organizational and documentation skills, technical writing ability, and excellent communication skills (written and verbal).

  • Mindset: Ability to thrive in a fast-paced, dynamic environment, juggling multiple priorities while maintaining a sharp eye for detail.

  • Tech: Proficiency in MS Office; experience with lab-based data management systems a plus.

Why Join Us

  • Be part of a collaborative team where your expertise directly impacts patient safety and product quality.

  • Gain exposure to diverse analytical techniques and regulatory processes.

  • Opportunity to work in a GMP environment supporting both clinical and commercial product lifecycles.

  • Professional growth through hands-on problem solving, cross-functional collaboration, and continuous learning.

#LI-LL1

Join us and be part of building the bridge between life changing therapies and patients. Let's talk future

Equal Employment Opportunity (EEO) Statement:
PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

At PCI, Equity and Inclusion are at the core of our company's purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity - at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

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