QC Associate II
Westborough, MA · On-site
$48/hr
Job Title: QC Associate II Location: Westborough, MA Zip Code: 01581 Duration: 12 Months Pay Rate: $48/hr. Keyword's: #Westboroughjobs; #QCAssociatejobs; Start Date: Immediate We provide a ...
QC Associate II
Westborough, MA · On-site
$48/hr
Job Title: QC Associate II Location: Westborough, MA Zip Code: 01581 Duration: 12 Months Pay Rate: $48/hr. Keyword's: #Westboroughjobs; #QCAssociatejobs; Start Date: Immediate We provide a ...
QC Associate II
Westborough, MA · On-site
$48/hr
Job Title: QC Associate II Location: Westborough, MA Zip Code: 01581 Duration: 12 Months Pay Rate: $48/hr. Keyword's: #Westboroughjobs; #QCAssociatejobs; Start Date: Immediate We provide a ...
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QC Associate II
Westborough, MA · On-site
$48/hr
Job Title: QC Associate II Location: Westborough, MA Zip Code: 01581 Duration: 12 Months Pay Rate: $48/hr. Keyword's: #Westboroughjobs; #QCAssociatejobs; Start Date: Immediate We provide a ...
Cell Therapy QC Associate
Westborough, MA · On-site
Position Title : QC Associate II Work Location: 9 Technology Drive, Westborough, MA, 01581 Assignment Duration: 12 months Work Arrangement: Mon - Friday (onsite) Description : Purpose & Scope: AIRM ...
Cell Therapy QC Associate
Westborough, MA · On-site
Position Title : QC Associate II Work Location: 9 Technology Drive, Westborough, MA, 01581 Assignment Duration: 12 months Work Arrangement: Mon - Friday (onsite) Description : Purpose & Scope: AIRM ...
The QC Associate is responsible for supporting Quality Control microbiological in-process, release, and stability testing of clinical and commercial cell therapy drug product. Additionally, the QC ...
The QC Associate is responsible for supporting Quality Control microbiological in-process, release, and stability testing of clinical and commercial cell therapy drug product. Additionally, the QC ...
Associate, QC Microbiology, (A1), Cell Therapy
Devens, MA · On-site
$35.03 - $42.45/hr
The QC Associate is responsible for supporting Quality Control microbiological in-process, release, and stability testing of clinical and commercial cell therapy drug product. Additionally, the QC ...
Associate, QC Microbiology, (A1), Cell Therapy
Devens, MA · On-site
$35.03 - $42.45/hr
The QC Associate is responsible for supporting Quality Control microbiological in-process, release, and stability testing of clinical and commercial cell therapy drug product. Additionally, the QC ...
The Associate I, QC Microbiology is responsible for performing routine activities at our Waltham facility. This role will be responsible for ensuring daily functions and responsibilities of the QC ...
The Associate I, QC Microbiology is responsible for performing routine activities at our Waltham facility. This role will be responsible for ensuring daily functions and responsibilities of the QC ...
Associate I, QC Microbiology (Contract)
Waltham, MA · On-site
$33 - $48/hr
The Associate I, QC Microbiology is responsible for performing routine activities at our Waltham facility. This role will be responsible for ensuring daily functions and responsibilities of the QC ...
Associate I, QC Microbiology (Contract)
Waltham, MA · On-site
$33 - $48/hr
The Associate I, QC Microbiology is responsible for performing routine activities at our Waltham facility. This role will be responsible for ensuring daily functions and responsibilities of the QC ...
QC Analyst
$26.75 - $36/hr
Quality Control Analyst Location: Devens, MA Duration: 6 Months(extension up to 3 year) QC ... Additional Information For more information, Please contact Pankhuri Razada Associate Recruiter ...
QC Analyst
$26.75 - $36/hr
Quality Control Analyst Location: Devens, MA Duration: 6 Months(extension up to 3 year) QC ... Additional Information For more information, Please contact Pankhuri Razada Associate Recruiter ...
Director, Quality Control
Waltham, MA · On-site
$210K - $220K/yr
Reporting to the Associate Vice President of QC and AD, the ideal candidate should have relevant experience in compendial, cellular, molecular, and environmental monitoring in a cGMP facility, and ...
Director, Quality Control
Waltham, MA · On-site
$210K - $220K/yr
Reporting to the Associate Vice President of QC and AD, the ideal candidate should have relevant experience in compendial, cellular, molecular, and environmental monitoring in a cGMP facility, and ...
Associate, QC Microbiology, B1 shift, Cell Therapy
Devens, MA · On-site
$35.82 - $43.41/hr
Associate, QC Microbiology, B1 shift, Cell Therapy
Associate, QC Microbiology, B1 shift, Cell Therapy
Devens, MA · On-site
$35.82 - $43.41/hr
Associate, QC Microbiology, B1 shift, Cell Therapy
Director, Quality Control
Waltham, MA · On-site
$210K - $220K/yr
Reporting to the Associate Vice President of QC and AD, the ideal candidate should have relevant experience in compendial, cellular, molecular, and environmental monitoring in a cGMP facility, and ...
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Director, Quality Control
Waltham, MA · On-site
$210K - $220K/yr
Reporting to the Associate Vice President of QC and AD, the ideal candidate should have relevant experience in compendial, cellular, molecular, and environmental monitoring in a cGMP facility, and ...
Director, Quality Control
$210K - $220K/yr
Reporting to the Associate Vice President of QC and AD, the ideal candidate should have relevant experience in compendial, cellular, molecular, and environmental monitoring in a cGMP facility, and ...
Director, Quality Control
$210K - $220K/yr
Reporting to the Associate Vice President of QC and AD, the ideal candidate should have relevant experience in compendial, cellular, molecular, and environmental monitoring in a cGMP facility, and ...
Associate, QC Analytical, B2 Shift, Cell Therapy
$35.82 - $43.41/hr
Associate, QC Analytical, B2 Shift, Cell Therapy
Associate, QC Analytical, B2 Shift, Cell Therapy
$35.82 - $43.41/hr
Associate, QC Analytical, B2 Shift, Cell Therapy
Associate, QC Analytical, B2 Shift, Cell Therapy
Devens, MA · On-site
$35.82 - $43.41/hr
Associate, QC Analytical, B2 Shift, Cell Therapy
Associate, QC Analytical, B2 Shift, Cell Therapy
Devens, MA · On-site
$35.82 - $43.41/hr
Associate, QC Analytical, B2 Shift, Cell Therapy
Quality Control Specialist
$73K - $125K/yr
Quality Control Specialist Job Code: 34801 Job Location: Northampton, MA Schedule: 9/80 The Quality ... Training of lower-level associates on Quality policies and procedures. * Collaborate with ...
Quality Control Specialist
$73K - $125K/yr
Quality Control Specialist Job Code: 34801 Job Location: Northampton, MA Schedule: 9/80 The Quality ... Training of lower-level associates on Quality policies and procedures. * Collaborate with ...
Associate, QC Microbiology, B1 shift Cell Therapy - Devens MA
Devens, MA · On-site
$75K - $100K/yr
Position Summary Responsible for supporting QC testing for in-process, final product, stability ... Associate degree with equivalent combination of education and work experience may be considered.
Associate, QC Microbiology, B1 shift Cell Therapy - Devens MA
Devens, MA · On-site
$75K - $100K/yr
Position Summary Responsible for supporting QC testing for in-process, final product, stability ... Associate degree with equivalent combination of education and work experience may be considered.
Associate, QC Microbiology, B1 shift Cell Therapy - Devens MA
Devens, MA · On-site
$75K - $100K/yr
Position Summary Responsible for supporting QC testing for in-process, final product, stability ... Associate degree with equivalent combination of education and work experience may be considered.
Associate, QC Microbiology, B1 shift Cell Therapy - Devens MA
Devens, MA · On-site
$75K - $100K/yr
Position Summary Responsible for supporting QC testing for in-process, final product, stability ... Associate degree with equivalent combination of education and work experience may be considered.
Quality Control Technician - Lead
Westminster, MA · On-site
$20 - $25.50/hr
Ability to lead 3 to 4 QC technicians within the machining plant. * Perform first article, in ... High school diploma or GED; technical school or associate degree preferred. * 3+ years of quality ...
Quality Control Technician - Lead
Westminster, MA · On-site
$20 - $25.50/hr
Ability to lead 3 to 4 QC technicians within the machining plant. * Perform first article, in ... High school diploma or GED; technical school or associate degree preferred. * 3+ years of quality ...
Position Summary Responsible for supporting QC testing for in-process, final product, stability samples and for supporting environmental and facility monitoring. May assist with documentation ...
Position Summary Responsible for supporting QC testing for in-process, final product, stability samples and for supporting environmental and facility monitoring. May assist with documentation ...
Quality Control Technician, Microbiology
Framingham, MA · On-site
$33/hr
Associate Degree/Certificate with 1-3+ years relevant GMP experience or BS in Biology or related ... Quality Control Technician, Microbiology: Base pay range of $33.00 per hour to $35.00 per hour ...
Quality Control Technician, Microbiology
Framingham, MA · On-site
$33/hr
Associate Degree/Certificate with 1-3+ years relevant GMP experience or BS in Biology or related ... Quality Control Technician, Microbiology: Base pay range of $33.00 per hour to $35.00 per hour ...
Quality Control Associate information
See Worcester, MA salary details
$11.51 - $13.93
3% of jobs
$13.93 - $16.35
12% of jobs
$18.50 is the 25th percentile. Wages below this are outliers.
$16.35 - $18.77
12% of jobs
$18.77 - $21.20
14% of jobs
$21.20 - $23.62
8% of jobs
The median wage is $24.22 / hr.
$23.62 - $26.04
6% of jobs
$26.04 - $28.46
7% of jobs
$30.57 is the 75th percentile. Wages above this are outliers.
$28.46 - $30.88
15% of jobs
$30.88 - $33.30
14% of jobs
$33.30 - $35.72
6% of jobs
$35.72 - $38.14
3% of jobs
$11
$25
$38
How much do quality control associate jobs pay per hour?
As of Jun 15, 2026, the average hourly pay for quality control 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 does a Quality Control Associate do?
A Quality Control Associate is responsible for ensuring that products meet established standards of quality, including reliability, usability, and performance. They conduct inspections, perform tests, and document their findings to identify defects or deviations from specifications. Quality Control Associates often work closely with production teams to address issues and help maintain compliance with industry regulations. Their role is critical in maintaining customer satisfaction and upholding the reputation of their company. They may work in a variety of industries, including pharmaceuticals, manufacturing, and food production.
What are the key skills and qualifications needed to thrive as a Quality Control Associate, and why are they important?
To thrive as a Quality Control Associate, you need a solid understanding of quality assurance principles, attention to detail, and often a background in science or manufacturing. Familiarity with inspection tools, laboratory equipment, and quality management systems (such as ISO standards) is typically required, and certifications like Six Sigma or ASQ may be advantageous. Strong analytical thinking, problem-solving abilities, and effective communication skills set exceptional candidates apart. These skills ensure that products consistently meet standards, reduce errors, and support overall operational excellence.
What are some common challenges Quality Control Associates face when ensuring product consistency across different production batches?
Quality Control Associates often encounter challenges such as variations in raw material quality, changes in manufacturing processes, and tight production schedules that can lead to inconsistencies between batches. Addressing these issues requires keen attention to detail, effective communication with production teams, and a strong understanding of standard operating procedures. Staying proactive in identifying potential sources of variation and collaborating closely with other departments helps maintain high product standards and minimizes the risk of defects.
Is a degree needed to be a QC?
A degree is not always required to become a Quality Control Associate, but many employers prefer candidates with a high school diploma or equivalent, along with relevant skills such as attention to detail and knowledge of quality standards. Some positions may require or prefer post-secondary education or certifications in quality management or related fields. Practical experience and familiarity with testing tools can also be valuable for this role.
Which is higher position, QA or QC?
In the context of a Quality Control Associate role, Quality Assurance (QA) is generally considered a higher-level function that focuses on preventing defects through process improvements, while Quality Control (QC) involves inspecting products to identify defects. QA roles often involve more strategic responsibilities and may require broader skills or certifications, whereas QC roles are more focused on testing and inspection tasks.
What is the difference between Quality Control Associate vs Quality Assurance Technician?
| Aspect | Quality Control Associate | Quality Assurance Technician |
|---|---|---|
| Certifications | Often requires GMP, ISO, or industry-specific quality certifications | Similar certifications, with focus on quality standards and compliance |
| Work Environment | Laboratory, manufacturing, or production settings | Laboratory, manufacturing, or quality compliance environments |
| Primary Focus | Inspecting products, testing samples, identifying defects | Developing and implementing quality systems, audits, and process improvements |
| Employer & Industry Usage | Manufacturing, pharmaceuticals, food production | Manufacturing, pharmaceuticals, food industry |
While both roles focus on quality, the Quality Control Associate primarily inspects and tests products to identify defects, whereas the Quality Assurance Technician develops and maintains quality systems to prevent issues. Both roles are essential in ensuring product quality and compliance within manufacturing and production environments.
Is QC a hard job?
Quality Control Associate roles can be challenging due to the need for attention to detail, adherence to strict standards, and sometimes repetitive tasks. The job often requires good observation skills, knowledge of quality procedures, and sometimes certifications, but the difficulty varies depending on the industry and specific responsibilities.
What does a QC associate do?
A Quality Control (QC) Associate inspects and tests products or materials to ensure they meet quality standards and specifications. They document findings, identify defects, and collaborate with production teams to address issues, often using tools like inspection equipment and quality management systems. Attention to detail and knowledge of industry standards are essential for this role.
What are the most commonly searched types of Quality Control jobs in Worcester, MA? The most popular types of Quality Control jobs in Worcester, MA are:
What are popular job titles related to Quality Control Associate jobs in Worcester, MA? For Quality Control Associate jobs in Worcester, MA, the most frequently searched job titles are:
What job categories do people searching Quality Control Associate jobs in Worcester, MA look for? The top searched job categories for Quality Control Associate jobs in Worcester, MA are:
What cities near Worcester, MA are hiring for Quality Control Associate jobs? Cities near Worcester, MA with the most Quality Control Associate job openings:
$48/hr
Contractor
Medical, Dental, Vision, Life, Retirement, PTO
This job post has expired today. Applications are no longer accepted.
Job description
Job Description
Job Title: QC Associate II
Location: Westborough, MA
Zip Code: 01581
Duration: 12 Months
Pay Rate: $48/hr.
Keyword's: #Westboroughjobs; #QCAssociatejobs;
Start Date: Immediate
We provide a competitive pay and benefits package. This position is offering a pay rate of $48hr. however, Belcan considers several factors when extending an offer, including but not limited to education, experience, geographic location, and discipline. Benefits offered may include health care, dental, vision, life insurance; 401(k); education assistance; paid time off including PTO, holidays, and any other paid leave required by law.
Purpose & Scope:
AIRM is seeking a highly motivated individual with strong organizational skills to join us as a Quality Control Analytical Associate II. This position provides Quality Control compliance, commercial readiness, and testing support for AIRM cell therapy products. Looking for a strong GMP and scientific background and experience with quality control testing of cell based therapies.
Essential Job Responsibilities:
Perform routine in-process and release QC testing of AIRM cell products.
Execute GMP analytical assays such as Immunofluorescence, Flow Cytometry, PCR, Viability, Cell growth and various parenteral assays (Visual Appearance, Content Uniformity, pH, Osmolality).
Perform analytical method qualifications, validations and transfers including drafting technical protocols, reports and assay troubleshooting.
Maintain, calibrate and operate GMP equipment and instruments supporting QC testing.
Track and test products according to stability protocols.
Culture and maintenance of cell lines and stem cells.
Work with internal and external resources to maintain lab in a GMP state.
Monitor and trend QC data.
Complete routine record review of test data and related documents for in-process testing, drug substance and drug product release and stablity.
Perform shipment of materials for QC testing to contract labs and perform data review.
Author, revise and review SOPs, qualification/validation protocols and reports.
Conduct investigations regarding out of specifications (OOS) results. Assist and manage deviations and CAPAs related to analytical procedures.
Monitor the GMP systems currently in place to ensure compliance with documented policies.
Perform QC lab duties and technical projects as required.
Quantitative Dimensions: This position interacts with Quality Control, Analytical Development, Drug Product Development, Manufacturing and Quality Assurance. Will contribute to the development of QC departmental processes.
Organizational Context: Reporting to QC Scientist I Terrence Tamakloe
Qualifications:
Required:
Bachelors degree in biotechnology or related field with 3+ years of Quality Control experience, or a Master"s degree in biotechnology or related field with 0-2 years of Quality Control experience.
Relevant GMP experience in the quality control department of a biotech and/or pharmaceutical industry.
Ability to work weekends is required; while most of the schedule will be during a standard work week, there will be regular weekend work.
Preferred:
Experience with relevant analytical test methods: including PCR, Flow Cytometry, IFA and cell based assays
Experience with ICH guidelines and parenteral test methods
Experience with 21CFR Part 11 Compliance
Experience with the qualification of Analytical Test Methods
GMP Cell Culture experience and Environmental Monitoring
Experience with data tracking/trending analysis
Belcan is an equal opportunity employer. Your application and candidacy will not be considered based on race, colour, sex, religion, creed, sexual orientation, gender identity, national origin, disability, genetic information, pregnancy, veteran status or any other characteristic protected by federal, state or local laws.
Job Title: QC Associate II
Location: Westborough, MA
Zip Code: 01581
Duration: 12 Months
Pay Rate: $48/hr.
Keyword's: #Westboroughjobs; #QCAssociatejobs;
Start Date: Immediate
We provide a competitive pay and benefits package. This position is offering a pay rate of $48hr. however, Belcan considers several factors when extending an offer, including but not limited to education, experience, geographic location, and discipline. Benefits offered may include health care, dental, vision, life insurance; 401(k); education assistance; paid time off including PTO, holidays, and any other paid leave required by law.
Purpose & Scope:
AIRM is seeking a highly motivated individual with strong organizational skills to join us as a Quality Control Analytical Associate II. This position provides Quality Control compliance, commercial readiness, and testing support for AIRM cell therapy products. Looking for a strong GMP and scientific background and experience with quality control testing of cell based therapies.
Essential Job Responsibilities:
Perform routine in-process and release QC testing of AIRM cell products.
Execute GMP analytical assays such as Immunofluorescence, Flow Cytometry, PCR, Viability, Cell growth and various parenteral assays (Visual Appearance, Content Uniformity, pH, Osmolality).
Perform analytical method qualifications, validations and transfers including drafting technical protocols, reports and assay troubleshooting.
Maintain, calibrate and operate GMP equipment and instruments supporting QC testing.
Track and test products according to stability protocols.
Culture and maintenance of cell lines and stem cells.
Work with internal and external resources to maintain lab in a GMP state.
Monitor and trend QC data.
Complete routine record review of test data and related documents for in-process testing, drug substance and drug product release and stablity.
Perform shipment of materials for QC testing to contract labs and perform data review.
Author, revise and review SOPs, qualification/validation protocols and reports.
Conduct investigations regarding out of specifications (OOS) results. Assist and manage deviations and CAPAs related to analytical procedures.
Monitor the GMP systems currently in place to ensure compliance with documented policies.
Perform QC lab duties and technical projects as required.
Quantitative Dimensions: This position interacts with Quality Control, Analytical Development, Drug Product Development, Manufacturing and Quality Assurance. Will contribute to the development of QC departmental processes.
Organizational Context: Reporting to QC Scientist I Terrence Tamakloe
Qualifications:
Required:
Bachelors degree in biotechnology or related field with 3+ years of Quality Control experience, or a Master"s degree in biotechnology or related field with 0-2 years of Quality Control experience.
Relevant GMP experience in the quality control department of a biotech and/or pharmaceutical industry.
Ability to work weekends is required; while most of the schedule will be during a standard work week, there will be regular weekend work.
Preferred:
Experience with relevant analytical test methods: including PCR, Flow Cytometry, IFA and cell based assays
Experience with ICH guidelines and parenteral test methods
Experience with 21CFR Part 11 Compliance
Experience with the qualification of Analytical Test Methods
GMP Cell Culture experience and Environmental Monitoring
Experience with data tracking/trending analysis
Belcan is an equal opportunity employer. Your application and candidacy will not be considered based on race, colour, sex, religion, creed, sexual orientation, gender identity, national origin, disability, genetic information, pregnancy, veteran status or any other characteristic protected by federal, state or local laws.
About Belcan
Sourced by ZipRecruiter
Belcan is a leading provider of qualified personnel to many of the world's most respected enterprises. We offer excellent opportunities for contract/temporary, temp-to-hire, and direct assignments in the engineering, IT, and professional fields. We are the employer of choice for thousands worldwide. Our overriding goal is to provide quality staffing solutions that help people, organizations, and communities succeed.
Industry
It services
Company size
5,001 - 10,000 Employees
Headquarters location
Cincinnati, OH, US
Year founded
1958