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Quality Control Laboratory Assistant Jobs in Roxbury, MA

Sebela Pharma

QC Chemist

Holbrook, MA · On-site

$55K - $60K/yr

The QC Chemist is a laboratory bench position that performs routine release testing for raw materials, intermediates, and final products within a cGMP environment. PRINCIPAL DUTIES AND ...

Thermo Fisher Scientific

QC Scientist 1

Bedford, MA · On-site

$53K - $79K/yr

Experience in quality control laboratory environment, preferably in pharmaceutical/biotech industry preferred • Preferred Fields of Study: Chemistry, Biochemistry, Biology, Molecular Biology or ...

Thermo Fisher Scientific

QC Scientist 1

Bedford, MA

$53K - $79K/yr

Experience in quality control laboratory environment, preferably in pharmaceutical/biotech industry preferred • Preferred Fields of Study: Chemistry, Biochemistry, Biology, Molecular Biology or ...

Eurofins Scientific

QC Analytical Chemist

Andover, MA · On-site

$27 - $30/hr

In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 ... Maintain, calibrate, and operate instrumentation in the QC laboratory * Document work as required ...

RoslinCT US

Sr. QC Analyst, Microbiology

Hopkinton, MA

$26.25 - $35.50/hr

Experience in a cGMP QC laboratory environment performing environmental monitoring, contamination control and investigation writing. * Excellent/Effective written and verbal communications skills.

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Quality Control Laboratory Assistant information

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How much do quality control laboratory assistant jobs pay per hour?

As of Aug 14, 2026, the average hourly pay for quality control laboratory assistant in Roxbury, MA is $24.78, according to ZipRecruiter salary data. Most workers in this role earn between $17.74 and $25.05 per hour, depending on experience, location, and employer.

How to become a quality control laboratory assistant?

To become a quality control laboratory assistant, candidates typically need a high school diploma or equivalent, along with basic knowledge of laboratory procedures and safety protocols. Relevant skills include attention to detail, familiarity with testing equipment, and the ability to follow strict guidelines; some positions may require on-the-job training or certifications in laboratory safety or quality assurance.

What are some typical challenges faced by quality control laboratory assistants during sample analysis, and how are they managed?

Quality Control Laboratory Assistants often encounter challenges such as handling a high volume of samples, meeting tight deadlines, and ensuring precise adherence to testing protocols. Managing these challenges involves strong organizational skills, meticulous attention to detail, and effective communication with team members and supervisors. Many labs use standard operating procedures and regular training to help assistants maintain accuracy and efficiency, while also fostering a collaborative environment where questions and support are encouraged.

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

To thrive as a Quality Control Laboratory Assistant, you need a solid understanding of laboratory procedures, basic chemistry or biology, and typically an associate's or bachelor's degree in a science-related field. Familiarity with laboratory information management systems (LIMS), analytical instruments like spectrophotometers, and standard operating procedures is important. Attention to detail, strong organizational skills, and effective communication are valuable soft skills in this role. These skills and qualifications ensure accurate testing, compliance with regulations, and the reliability of data in quality assurance processes.

What is the difference between Quality Control Laboratory Assistant vs Quality Control Technician?

AspectQuality Control Laboratory AssistantQuality Control Technician
CredentialsHigh school diploma or equivalent; some roles may require certificationHigh school diploma; technical certification or associate degree often preferred
Work EnvironmentLaboratory setting, assisting with sample preparation and data entryLaboratory or production environment, performing testing and analysis
ResponsibilitiesSupporting testing processes, maintaining lab equipment, recording dataConducting tests, analyzing results, ensuring quality standards

Both roles operate in laboratory environments within manufacturing or pharmaceutical industries. The main difference lies in responsibilities, with the Laboratory Assistant providing support and preparation, while the Technician performs actual testing and analysis. Understanding these distinctions helps in choosing the right career path or job search focus.

What is a quality control laboratory assistant?

Quality Control Laboratory Assistants are professionals who help ensure that products and materials meet established quality standards by conducting laboratory tests and inspections. They prepare samples, operate laboratory equipment, record and analyze data, and report any deviations from quality specifications. Their work supports overall product safety and consistency, making them essential to companies in industries like pharmaceuticals, food production, and manufacturing.

What qualifications do you need to be a quality control laboratory assistant?

A quality control laboratory assistant typically needs a high school diploma or equivalent, with some roles requiring post-secondary education in science or related fields. Basic knowledge of laboratory procedures, attention to detail, and familiarity with testing equipment are important; certifications in quality assurance or laboratory techniques can be advantageous.

What cities near Roxbury, MA are hiring for Quality Control Laboratory Assistant jobs?

Cities near Roxbury, MA with the most Quality Control Laboratory Assistant job openings:

Quality Control Laboratory Assistant jobs near you

Director, Quality Control

Sebela Pharmaceuticals Inc.

Holbrook, MA

Full-time

Re-posted 4 days ago

Job description

Sebela Pharmaceuticals is a U.S. pharmaceutical company with a market-leading position in Gastroenterology and a focus on innovation in Women’s Health. Our Vision is to build the leading Gastroenterology company in the U.S., with a complementary
focus on innovation in Women’s Health, premised on our expertise in pharmaceutical development and commercialization. Braintree Laboratories, Inc., a part of Sebela Pharmaceuticals, has its contract development and manufacturing organization (CDMO) in Holbrook, MA, offering pharmaceutical-development and in-house manufacturing services for specialty gastroenterology products.
We value dedication, energy, and enthusiasm, and we focus on innovation and results while striving to achieve our corporate mission and vision. Sebela Pharmaceuticals is committed to cultivating an inclusive environment where all employees are treated with respect. We accomplish this by fostering a culture of diversity, equity and inclusion, which is essential to innovation and continuous improvement. Sebela operates from three locations in Roswell, Georgia, Braintree and Holbrook, MA and headquarters in Dublin, Ireland.
This position is responsible for leading Quality Controls Laboratory operations at the Holbrook site including the development, implementation and maintenance of quality control systems and activities to support commercial manufacturing and new product introductions.
PRINCIPAL DUTIES AND RESPONSIBILITIES:
  • Provide strategic leadership and oversight of QC operations, ensuring alignment with company objectives for product quality, regulatory compliance, and business performance.
  • Direct all QC laboratory activities, in support of GMP Testing, release, and stability programs, including laboratory safety, testing operations, resource allocation, and performance management.
  • Review and approve QC specifications, procedures, protocols, validation documents, and analytical methods related to raw materials, intermediates, and commercial products.
  • Ensure all testing is performed in accordance with internal procedures and cGMP requirements.
  • Lead investigations into Out-of-Specification (OOS) results and laboratory deviations ensuring timely root cause identification and implementation of effective corrective and preventive actions (CAPAs).
  • Maintain inspection readiness across QC operations, supporting regulatory inspections, customer audits, and internal quality audits.
  • Oversee laboratory change control processes, risk assessments, equipment qualification activities, and implementation of compliant operational improvements.
  • Ensure critical laboratory equipment is appropriately qualified, calibrated, maintained, and operated to support reliable testing and maintain data integrity.
  • Ensure laboratory data integrity, documentation accuracy, and adherence to ALCOA principles
  • Partner with Quality Assurance, Manufacturing, and external stakeholders to investigate product quality issues and drive continuous improvement initiatives.
  • Lead supplier quality support activities, including supplier qualification, performance monitoring, and resolution of supplier-related quality issues.
  • Monitor and analyze QC performance metrics and quality system trends to identify risks, drive operational excellence, and strengthen compliance.
  • Develop, mentor, and retain a high-performing QC organization, fostering a culture of accountability, collaboration, and continuous professional development.
  • Manage departmental budgets, capital planning, and resource requirements to ensure effective execution of business and quality objectives.
  • Other duties as assigned.
KEY COMPETENCIES:
  • Leadership and teamwork
  • Regulatory Compliance, cGMP, Statistical Process Control
  • Extensive analytical chemistry experience
  • Project management
  • Data collection, management and analysis
  • Ability to direct and be resilient and focused under pressure
  • Planning and time management
  • Strong decision-making skills
  • Ability to manage multiple priorities
  • Ability to foster excellent working relationships across all levels, internal/external customers and suppliers
QUALIFICATIONS:
To perform this job successfully, an individual must be able to perform each essential function satisfactorily, be flexible in terms of work hours, and have strong knowledge and experience in cGMPs and Oral Dose Pharmaceutical Production Processes. The requirements listed below are representative of the knowledge, skills and/or abilities required.
  • BS or master’s degree in chemistry, biology, or other pharmaceutical science related field.
  • Minimum of 8-10 years QC management experience working in pharmaceutical finished product manufacturing with experience in compliance, quality control, and regulatory development.
  • Direct experience interacting with FDA and other regulatory agencies.
  • Strong knowledge and understanding of FDA cGMP regulations.
  • Experienced in GMP audits, including drug product manufacturing and analytical testing sites.
  • Ability to build collaborative relationships and lead effectively in a cross-functional environment.
  • Self-motivated and results-driven leader with a proactive, hands-on approach.
  • Strong organizational, prioritization, and time management skills, coupled with strong critical-thinking abilities to evaluate complex challenges, solve problems effectively, and drive continuous improvement.
  • Strong project management skills.
  • Excellent written and oral communication / presentation skills.
  • Adept at and comfortable with statistical analysis.
Pay Range: $150-190K base (this reflects our reasonable and good faith estimate of what will be paid at the time of posting). Competitive benefits package included.

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