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Quality Control Analyst Jobs in Lawrence, MA (NOW HIRING)

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 ...

Manager, Quality Control

Bedford, MA · On-site

$122 - $152/hr

Manager, Quality Control Regular Full-Time Bedford, MA, Bedford, MA, US 3 days ago Requisition ID ... Provide technical oversight of analytical instrumentation, including UV-Vis spectrophotometers ...

Manager, Quality Control

Bedford, MA · On-site

$120 - $170/hr

What You'll Do The Manager, Quality Control leads daily operations of the analytical testing laboratory, ensuring raw materials, in-process samples, and finished products meet established quality and ...

New

Quality Control Technician ???? Lowell, MA ???? $20-$24/hour, depending on experience ... analytical tests . * Conduct in-process and finished-product inspections to verify quality and ...

Quality Control Technician Lowell, MA $20-$24/hour, depending on experience Full-Time | Monday ... analytical tests . * Conduct in-process and finished-product inspections to verify quality and ...

Quality Control Technician Lowell, MA $20-$24/hour, depending on experience Full-Time | Monday ... analytical tests . * Conduct in-process and finished-product inspections to verify quality and ...

Quality Control Manager

Lowell, MA · On-site

$130 - $165/hr

Analytical problem‑solving skills and decision‑making abilities * Communication skills with the ... Professional quality control or construction management certifications (ISO 9001, ASQ CQE, etc.

Showing results 41-60

Quality Control Analyst information

See Lawrence, MA salary details

$17

$29

$43

How much do quality control analyst jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for quality control 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.

What is a quality control analyst?

A quality control (QC) analyst or quality assurance analyst tests computer programs to ensure that software applications function properly before being deployed in production or going to market. As a quality control analyst, your job is to identify and fix bugs in software applications and computer systems and make recommendations to management about how to improve a software application’s functionality, user experience (UX), and user interface (UI). Your QC process typically involves a significant amount of collaboration with other analysts and software developers.

What are the key skills and qualifications needed to thrive as a quality control analyst?

To thrive as a Quality Control Analyst, you need a solid understanding of quality assurance principles, data analysis, and laboratory or manufacturing processes, often supported by a degree in a related scientific or technical field. Familiarity with tools such as LIMS (Laboratory Information Management Systems), statistical software, and regulatory standards (like GMP or ISO) is typically required. Attention to detail, problem-solving abilities, and strong communication skills help analysts identify issues and collaborate effectively with team members. These skills ensure products or processes consistently meet quality standards, safeguarding consumer safety and organizational reputation.

What are some common challenges faced by quality control analysts, and how can they be effectively managed?

Quality Control Analysts often encounter challenges such as tight production deadlines, variability in sample quality, and adapting to frequent changes in testing protocols or regulatory standards. Managing these challenges involves strong organizational skills, proactive communication with production and laboratory teams, and staying current with industry regulations. Developing efficient documentation practices and using digital tools for data management can also help maintain accuracy and streamline workflow, ultimately supporting consistent product quality.

What is the difference between Quality Control Analyst vs Quality Assurance Specialist?

AspectQuality Control AnalystQuality Assurance Specialist
CertificationsOften requires certifications like ASQ CQE or ISO auditorSimilar certifications, with focus on process audits
Work EnvironmentLaboratory, manufacturing, or production settingsOffice-based, process review, and compliance environments
Primary FocusTesting products, identifying defects, ensuring quality standardsDeveloping and maintaining quality systems, preventing defects
Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, software, healthcare industries

While both roles aim to ensure product quality, the Quality Control Analyst primarily tests and inspects products to identify defects, whereas the Quality Assurance Specialist focuses on creating and improving processes to prevent defects. Both roles often require similar certifications and work in related environments, but their core responsibilities differ in focus and approach.

How much does a quality control analyst earn?

The average salary for a quality control analyst typically ranges from $45,000 to $70,000 per year, depending on experience, industry, and location. Entry-level positions may start lower, while experienced analysts with certifications can earn higher salaries. Many roles also include benefits such as health insurance and paid time off.

What are the most commonly searched types of Quality Control Analyst jobs in Lawrence, MA?

The most popular types of Quality Control Analyst jobs in Lawrence, MA are:

What are popular job titles related to Quality Control Analyst jobs in Lawrence, MA?

For Quality Control Analyst jobs in Lawrence, MA, the most frequently searched job titles are:

What job categories do people searching Quality Control Analyst jobs in Lawrence, MA look for?

The top searched job categories for Quality Control Analyst jobs in Lawrence, MA are:

What cities near Lawrence, MA are hiring for Quality Control Analyst jobs?

Cities near Lawrence, MA with the most Quality Control Analyst job openings:

Infographic showing various Quality Control Analyst job openings in Lawrence, MA as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 16% Part Time, 3% Contract, and 1% Nights. Highlights an 86% Physical, 2% Hybrid, and 12% Remote job distribution, with an average salary of $60,918 per year, or $29.3 per hour.

Scientist, Quality Control (QC) Systems

Bristol-Myers Squibb Company

Devens, MA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 13 days ago


Bristol Myers Squibb rating

8.2

Company rating: 8.2 out of 10

Based on 51 frontline employees who took The Breakroom Quiz

33rd of 86 rated pharmaceutical


Job description

Working with Us
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.
Position Summary
The Scientist, QC Systems at the Cell Therapy Facility (CTF) is responsible for the development, configuration, and management of QC electronic systems and applications supporting QC operations. This role acts as a subject matter expert in providing electronic systems operational support and troubleshooting to QC end users and will interface with both internal and external functions to implement electronic system improvements to optimize business processes and improve efficiency.
Duties/Responsibilities
• Create, deploy, review and sustain electronic systems Master Data. Perform data verification, system integration (Smart-QC, LIMS, ERP, and MES) for electronic systems.
• Create and execute computer system validation documents (i.e., UAT, URS, OQ, PQ, etc.) as applicable and guide QC end users on the development of system enhancements with user requirements and business drivers.
• Provide electronic systems operational support and troubleshooting to end user.
• Own project, CAPA and deviation/ investigation related tasks and/ or continuous improvement efforts.
• Propose and implement improvements to electronic systems to optimize business process and improve efficiency. Collaborate with end users to develop business case.
• Anticipate mid- to long-term business needs and constraints. Support QC management in proposal and implementation of strategic initiatives.
• Anticipate and perform troubleshooting and problem solving independently.
• Train and mentor others on electronic systems use and operation.
• Translate business requirements into technical design requirements and communicate to partner organizations (e.g., IT) for system solution.
• Facilitate design, testing and subsequent deployment of solutions.
• Perform other tasks as assigned.
Reporting Relationship
The Scientist, Quality Control (QC) Systems will report to the Associate Director of QC Systems and Support.
Qualifications
Specific Knowledge, Skills, Abilities:
• Ability to accurately and completely understand, follow, interpret and apply Global Regulatory and cGMP requirements.
• Ability to work in a fast-paced team environment, meet deadlines, and prioritize work.
• Advanced technical, problem-solving skills and logical.
• Ability to communicate effectively with peers, department management and cross-functional peers.
• Demonstrated technical writing skills.
• Mentoring, coaching, influencing, negotiating and personnel interaction skills.
• Knowledge of analytical and microbiological test methods and environmental monitoring programs.
Education/Experience/ Licenses/Certifications:
• Bachelor's degree or equivalent required, preferably in science or related engineering field.
• 6+ years of relevant work experience in LIMS, ELN and laboratory software systems (e.g., Smart-QC), preferably in a regulated environment.
• An equivalent combination of education and experience may be considered.
• Demonstrated experience with validation and/or maintenance of laboratory electronic software systems.
Job Safety Requirements & Essential Physical Demands
  • Ability to perform lifting tasks up to 20 lbs (9 kg) at floor and waist height. Ability to lift up to 10 lbs (4.5 kg) overhead as well as push or maneuver carts to transport materials between locations.
  • Ability to perform frequent pipetting and related laboratory tasks within a biological safety cabinet, including extended periods of seated work.
  • Ability to independently don, doff, and wear required personal protective equipment such as but not limited to lab coat/frock, gloves, safety glasses/face shield for prolonged periods while performing laboratory work.
  • Ability to safely handle and use chemical disinfectants, flammable materials, and hazardous chemicals.
  • Work may involve handling of dry ice, liquid nitrogen, and cryogenically cooled materials.
  • Ability to use step stools while reaching and handling materials.
  • Ability to work in a Biosafety Level 2 (BSL-2) environment.
  • The laboratory employee is responsible for performing work safely in accordance with EHSS procedures. This includes identifying and controlling risks, proper use of personal protective equipment (PPE), safe handling of chemicals and biological agents, compliance with waste and emergency procedures, and active participation in training and safety programs.

If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.
Compensation Overview:
Devens - MA - US: $107,100 - $129,780
The starting compensation range(s) for this role are listed above for a full-time employee (FTE) basis. Additional incentive cash and stock opportunities (based on eligibility) may be available. The starting pay rate takes into account characteristics of the job, such as required skills, where the job is performed, the employee's work schedule, job-related knowledge, and experience. Final, individual compensation will be decided based on demonstrated experience.
Eligibility for specific benefits listed on our careers site may vary based on the job and location. For more on benefits, please visit https://careers.bms.com/life-at-bms/.
Benefit offerings are subject to the terms and conditions of the applicable plans in effect at the time and may require enrollment. Our benefits include:
  • Health Coverage: Medical, pharmacy, dental, and vision care.
  • Wellbeing Support: Programs such as BMS Well-Being Account, BMS Living Life Better, and Employee Assistance Programs (EAP).
  • Financial Well-being and Protection: 401(k) plan, short- and long-term disability, life insurance, accident insurance, supplemental health insurance, business travel protection, personal liability protection, identity theft benefit, legal support, and survivor support.

Work-life benefits include:
Paid Time Off
  • US Exempt Employees: flexible time off (unlimited, with manager approval, 11 paid national holidays (not applicable to employees in Phoenix, AZ, Puerto Rico or Rayzebio employees)
  • Phoenix, AZ, Puerto Rico and Rayzebio Exempt, Non-Exempt, Hourly Employees: 160 hours annual paid vacation for new hires with manager approval, 11 national holidays, and 3 optional holidays

Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
All global employees full and part-time who are actively employed at and paid directly by BMS at the end of the calendar year are eligible to take advantage of the Global Shutdown.
*Eligibility Disclosure: The summer hours program is for United States (U.S.) office-based employees due to the unique nature of their work. Summer hours are generally not available for field sales and manufacturing operations and may also be limited for the capability centers. Employees in remote-by-design or lab-based roles may be eligible for summer hours, depending on the nature of their work, and should discuss eligibility with their manager. Employees covered under a collective bargaining agreement should consult that document to determine if they are eligible. Contractors, leased workers and other service providers are not eligible to participate in the program.
Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as "Transforming patients' lives through science™ ", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.
On-site Protocol
BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.
Supporting People with Disabilities
BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.
Candidate Rights
BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/
Data Protection
We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.
Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.
If you believe that the job posting is missing information required by local law or incorrect in any way, please contact BMS at TAEnablement@bms.com. Please provide the Job Title and Requisition number so we can review. Communications related to your application should not be sent to this email and you will not receive a response. Inquiries related to the status of your application should be directed to Chat with Ripley.
R1605428 : Scientist, Quality Control (QC) Systems

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About Bristol-Myers Squibb

Sourced by ZipRecruiter

Bristol-Myers Squibb is a world-renowned global Biopharmaceutical company headquartered in New York, NY, US. Established in 1887, the company has more than 130 years’ worth of history dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. The company operates in the healthcare industry and thrives on providing a range of pharmaceutical products and services for various medical fields, like oncology, cardiovascular diseases, and immunoscience. Notably, Bristol-Myers Squibb is known for its commitment to relentless research and innovative drug development, which has led to breakthroughs like Opdivo, one of the first immunotherapies.

Industry

Scientific research and development services and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

New York, NY, US