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Qc Associate Jobs in Worcester, MA (NOW HIRING)

Quality Systems Associate Summary: Under the direct supervision of the Quality Systems Manager ... Completes weekly review of equipment QC and maintenance records. * Documents, investigates, and ...

Assistant Quality Manager

Putnam, CT · On-site

$55K - $75K/yr

Conduct QC testing and inspections to verify that products meet safety, customer, industry ... associate a general sense of the responsibilities and expectations of his/her position. As the ...

Showing results 41-60

Qc Associate information

See Worcester, MA salary details

$11

$25

$38

How much do qc associate jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for qc associate in Worcester, MA is $25.41, according to ZipRecruiter salary data. Most workers in this role earn between $18.46 and $30.96 per hour, depending on experience, location, and employer.

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 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 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 popular job titles related to Qc Associate jobs in Worcester, MA?

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

What job categories do people searching Qc Associate jobs in Worcester, MA look for?

The top searched job categories for Qc Associate jobs in Worcester, MA are:

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

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

Infographic showing various Qc Associate job openings in Worcester, MA as of August 2026, with employment types broken down into 1% As Needed, 75% Full Time, 22% Part Time, 1% Temporary, and 1% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $52,847 per year, or $25.4 per hour.

Technician I, QC Sample Management, Cell Therapy

Bristol Myers Squibb

Devens, MA

$27.35 - $33.14/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

New


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

At Bristol Myers Squibb, our employees often ask, "Who are you working for?"-a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it.


Position Summary

Responsible for handling of test samples throughout the sample lifecycle from receipt to disposal. Maintains inventory and support distribution of QC sample and materials to appropriate functional groups as scheduled or requested.

Shift/Days/Hours

This role works from 6AM to 6PM following a 12-hour rotating shift (36/48 hours over a 2-week period) which includes working every other weekend, holidays falling on scheduled workdays, and during adverse weather conditions in support of QC and the manufacturing facility. Flexibility to work irregular hours and short notice overtime may be required.

Duties/Responsibilities

  • Handle test samples and retains throughout the sample lifecycle: receipt, storage, distribution, transfer, and disposal. Facilitate cold chain transfers of samples.
  • Ensure samples and materials are appropriately labelled and maintain sample tracking, labelling and chain of custody records in accordance with written procedures.
  • Maintain inventory and support distribution of QC samples and materials to functional groups as scheduled or requested. Record performance metrics for the sample management group.
  • Follow lab procedures to maintain a safe and organized lab.
  • Perform other tasks as assigned.

Reporting Relationship

  • This position will report to QC management.

Qualifications

Specific Knowledge, Skills, Abilities:

  • Reliable and detail oriented with organizational skills.
  • Ability to understand and follow procedures.
  • Ability to work in a fast-paced team environment, meet deadlines, and adjust to changing priorities.
  • Ability to communicate effectively with peers and management regarding task completion, roadblocks, and needs.

Education/Experience/ Licenses/Certifications:

  • Associate's degree or higher. High school diploma/GED with 2+ years of relevant work experience will be considered.
    Netherlands: MLO level 3 is preferred. An equivalent combination of education and experience, preferably in a regulated environment, will be considered.
  • Knowledge of basic electronic systems (email, MS Office, etc.) required.

Job Safety Requirements& Essential Physical Demands

  • Abilitytoperform lifting tasks up to 20lbs(9 kg) at floor and waist height. Ability tolift upto 10lbs(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.
  • Workmayinvolvehandling ofdry 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 employeeis responsible forperforming work safelyin accordance withEHSS procedures. This includesidentifyingand 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.

We hire for skills and capabilities, not just credentials - if this role excites you, but doesn't perfectly match your resume, we encourage you to apply anyway.

Compensation Overview:

Devens - MA - US: $27.35 - $33.14per hour

The starting pay range(s) listed above is for full-time employees (FTE). You may also be eligible for additional discretionary incentive cash and stock opportunities. We determine starting pay thoughtfully - carefully considering the nature of the role, required skills, work location, schedule and the knowledge and experience you bring. Final compensation is guided by pay equity principles and applicable employment laws. Compensation programs are reviewed on an ongoing basis and may be adjusted over time to reflect evolving market factors, and individual, team or Company performance.


Benefits:


Subject to the terms and conditions of the applicable plans then in effect, you may be eligible to participate in our comprehensive benefit plans - including wellbeing support, retirement and financial protection benefits, and insurance offerings (medical, dental, vision, life and disability).


U.S.-based exempt employees are eligible for Flexible Time Off (FTO), which provides paid time off without a set accrual limit, subject to manager approval, along with 11 paid company holidays each year.


Non-exempt employees, RayzeBio employees, and employees located in Puerto Rico receive 160 hours of paid vacation annually for new hires (subject to manager approval), 11 paid company holidays, and 3 optional holidays.


Depending on eligibility, employees may also have access to additional time-off benefits, including paid sick leave, up to two paid volunteer days per year, summer hours flexibility, and leaves of absence for medical, personal, parental, caregiver, bereavement, or military needs. Eligible employees also enjoy an annual Global Shutdown between Christmas Day and New Year's Day.


U.S.-based job seekers can explore full benefit offerings at https://careers.bms.com/benefits


How We Work

Where you work matters - because collaboration, innovation and patient impact happen in many settings. Our roles are structured across four work models: site-essential, site-by-design, field-based and remote-by-design. The model assigned to this role is based on its core responsibilities. Learn more at https://careers.bms.com/ways-of-working.


Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplaceaccommodations/adjustmentsand ongoing support in their roles. Applicants can request a reasonable workplaceaccommodation/adjustmentprior to accepting a job offer. If you require reasonableaccommodations/adjustmentsin completing this application, or in any part of the recruitment process, direct your inquiries toadastaffingsupport@bms.com. Visitcareers.bms.com/eeo-accessibilityto access our complete Equal Employment Opportunity statement.


Candidate Rights

BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.


For roles based in Los Angeles County only: 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 athttps://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 this posting is missing required information required by local law or incorrect, contact BMS atTAEnablement@bms.comwith the Job Title and Requisition number. Do not send application-related inquiries to this email. To check your application status, please login to your Candidate Home Account.


R1605956 : Technician I, QC Sample Management, Cell Therapy

What Bristol Myers Squibb employees say

Pay

Benefits

Hours and flexibility

Workplace

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Bristol-Myers Squibb logo

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