1

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

Sr. QC Manager

Waltham, MA · On-site

$150 - $170/hr

Analyze quality, yield, reliability, complaint, nonconformance, and production output data to ... Experience linking QC trends, nonconformances, complaint investigations, and manufacturing ...

Showing results 21-40

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.

Supervisor, Qc Analytical

PCI Pharma Services

Bedford, NH • On-site

Full-time

Posted 25 days ago


PCI Pharma Services rating

6.3

Company rating: 6.3 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

492nd of 545 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.

The QC Analytical Supervisor will have responsibility for supporting all activities in the Quality Control Laboratory including completing the majority of the peer review in the department and approving the majority of procedures used in the analytical department. The work includes the testing of in-process samples, finished product samples and raw materials. The QC Analytical Supervisor will communicate with clients regarding Out of Specification and other Quality System Events. The person in this position has knowledge of commonly-used analytic concepts, practices, and procedures within the field of his/her responsibilities. Also, must be familiar with cGMPs as they relate to analytical test methodologies and practices.

Essential Duties and Responsibilities: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The essential duties and responsibilities include the following but other duties may be assigned.

  • Prioritize and distribute work to the analysts working in the QC Analytical laboratory

  • Conduct OOS and customer complaint investigations

  • Complete peer review of work executed within the analytical laboratory

  • Train new Employees

  • Routine Analytical testing of samples supporting incoming raw materials, in-process production and finished product testing

  • Performs analytical testing using HPLC, Karl Fischer, Particle Size Analyzer, UV Vis, Densitometer, Osmometer and other instrumentation as required

  • Perform instrument calibrations and preventative maintenance as needed

  • Documents laboratory work using laboratory worksheets/notebooks. Documentation must be detailed and meet CGMP requirements

  • Write, review and revise SOPs as required

  • Other duties as assigned or required

Special Demands: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. The employee must be physically capable to perform the duties listed below with or without reasonable accommodations which may be made to enable individuals with disabilities to perform the essential functions.

  • Routine work requires walking, standing, bending, reaching, climbing stairs, lifting or carrying objects that typically weigh less than 50 lbs.

  • Capacity to work on several tasks simultaneously.

  • Able to organize and prioritize work activities.

  • Must be able to walk and drive between locations

  • Physically able to wear laboratory protective gowning and equipment, including but not limited to gowning, goggles, face shields, respirators, and protective gloves

  • Comfortable with working/handling of hazardous materials

Work Environment: The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  • Works closely with Quality Assurance and Quality Control staff in performing varied work procedures and activities.

  • Interacts with Operations staff, Research and Development staff and clients on a regular basis.

  • Supervises the employees in the QC Analytical departmen

  • TRAVEL - <10%

Qualifications: The requirements listed below are representative of the knowledge, skill, and/or ability required for the stated position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

  • 5+ years relevant Analytical Chemistry experience, preferably in Quality Control, in a pharmaceutical manufacturing company

  • Experience working in a cGMP laboratory required

  • Experience working in a CMO (contact manufacturing/development organization) preferred

  • Prior leadership experience is preferred

  • Bachelor of Science in a scientific area of study

  • Master of Science in a scientific area of study and 3+ years Analytical Chemistry experience, preferably in Quality Control, in a pharmaceutical manufacturing company

  • Ability to prioritize tasks for staff

  • Ability to make informed decisions

  • Detail oriented

  • Strong oral and written communication skills

  • Excellent organization skills

  • Office Suite experience (Excel, Word, Access, and PowerPoint)Bachelor of Science in a scientific area of study

  • Excellent interpersonal skills and the ability to communicate well both orally and in in writing

  • Ability to multi-task in a dynamic environment with changing priorities

  • Resilient, can quickly move forward despite challenges

  • A drive to achieve results for self, and the team, and is cable of working with limited supervision

  • Positive attitude and strong team, cross team collaboration

  • Honesty, integrity, respect and courtesy with leadership and peers

  • Strong commitment to conducting PCI PHARMA SERVICES business according to the highest legal and ethical standards, and to continually pursue excellence in the manufacturing and delivery of PCI PHARMA SERVICES products and services

#LI-RS1

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.


What PCI Pharma Services employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom