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Quality Control Lab Technology Jobs in Massachusetts

Mativ

Quality Control Technician

Greenfield, MA · On-site

$17.50 - $22.25/hr

Review production schedules in order to plan for QC Lab Test work and testing requirements needed ... Our broad portfolio of technologies combines polymers, fibers, and resins to optimize the ...

Integrated Resources INC

Quality Control Analyst

Lexington, MA · On-site

$27 - $36.25/hr

Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing. This position ... QC analyst and Lab Testing experience Feel free to forward my email to your friends/colleagues who ...

Artech Information System LLC

QC Analyst

Devens, MA · On-site

$26.75 - $36/hr

Company Description Artech is the 10th Largest IT Staffing Company in the US, according to Staffing ... lab. Proficiency (or mastery) of Cell passaging techniques preferable with automation (1 year)

LGC Group

Quality Control Analyst I

Milford, MA

$26.25 - $35.25/hr

... advanced technologies that collectively improve patient outcomes - from the widely adopted and ... Maintain the appearance of the QC lab on a daily basis for audit readiness. * Follow Operational ...

Integrated Resources INC

QC Microbiologist

Andover, MA · On-site

$25.75 - $34/hr

Known lab errors investigation for root cause and impact Requirements for role will include ... technology related science discipline with equivalent experience Knowledge of SOP preferred ...

LGC Group

Quality Control Analyst I

Milford, MA · On-site

$26/hr

... advanced technologies that collectively improve patient outcomes - from the widely adopted and ... Maintain the appearance of the QC lab on a daily basis for audit readiness. * Follow Operational ...

LGC Group

Quality Control Analyst I

Milford, MA · On-site

$26 - $39/hr

... advanced technologies that collectively improve patient outcomes - from the widely adopted and ... Maintain the appearance of the QC lab on a daily basis for audit readiness. * Follow Operational ...

LGC Group

Quality Control Analyst I

Milford, MA · On-site

$26.25 - $35.25/hr

... advanced technologies that collectively improve patient outcomes - from the widely adopted and ... Maintain the appearance of the QC lab on a daily basis for audit readiness. * Follow Operational ...

LGC Group

Quality Control Analyst I

Milford, MA · On-site

$26.25 - $35.25/hr

... advanced technologies that collectively improve patient outcomes - from the widely adopted and ... Maintain the appearance of the QC lab on a daily basis for audit readiness. * Follow Operational ...

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Showing results 21-40

All JobsQuality Control Lab Technology JobsQuality Control Lab Technology Jobs in Massachusetts

Quality Control Lab Technology information

What is the difference between Quality Control Lab Technology vs Quality Control Analyst?

AspectQuality Control Lab TechnologyQuality Control Analyst
CredentialsAssociate's or Bachelor's in Science, certifications in lab techniquesAssociate's or Bachelor's in Science, certifications in testing methods
Work EnvironmentLaboratory setting, equipment operationLaboratory testing, data analysis
Industry UsageManufacturing, pharmaceuticals, food productionPharmaceuticals, biotech, manufacturing

Both roles work in laboratory environments within manufacturing or pharmaceutical industries. Quality Control Lab Technicians often focus on operating equipment and supporting testing processes, while Quality Control Analysts primarily perform testing and data analysis. Understanding these differences helps clarify career paths and employer expectations.

How to become a quality control lab technician?

To become a quality control lab technician, candidates typically need a high school diploma or equivalent, with some roles requiring an associate degree or certification in laboratory techniques or quality assurance. Relevant skills include attention to detail, knowledge of laboratory equipment and testing procedures, and familiarity with safety protocols. Gaining experience through internships or entry-level positions can also improve job prospects.

What is the role of a quality control lab technology?

A quality control lab technician is responsible for testing and analyzing products, raw materials, and processes to ensure they meet quality standards and regulatory requirements. They use laboratory instruments and techniques, such as spectroscopy or chromatography, and often follow standard operating procedures and safety protocols. Their work helps maintain product consistency, safety, and compliance in manufacturing environments.

What cities in Massachusetts are hiring for Quality Control Lab Technology jobs?

Cities in Massachusetts with the most Quality Control Lab Technology job openings:

Quality Control Lab Technology jobs near you

Associate Director, Quality Control (56861)

Boston, MA • On-site, Remote

Praxis Precision Medicines, Inc
Biotechnology Research and Development • 51 - 200 employees
Learn more about Praxis Precision Medicines, Incexternal

$150K - $169K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 12 days ago

Key responsibilities

  • Manage and oversee Quality Control activities related to product testing, release, and stability.

  • Support the establishment and review of QC systems, including product specifications, documentation, and stability programs.

  • Perform data review and trending analysis for in-process testing, release, and stability to ensure regulatory compliance.

Job description

Associate Director, Quality Control
Reports to: Senior Director, Quality Operations, CMC
Location: This position may be performed remotely with travel to the Boston area as needed.
Position Summary
Praxis is seeking a highly experienced, motivated, and innovative quality leader with strong experience in late-stage development and commercialization to join our Quality team as Associate Director, Quality Control to support QC product release and stability activities. Reporting to Senior Director, Quality Operations CMC, this position will be responsible for managing and executing Quality Control activities in support of product testing, release, and stability, and toxicology studies test material inventory support. Ensure GMP activities are conducted in accordance with applicable SOPs, compendia, approved methods, and in accordance with company's and regulatory agencies' policies and procedures.
Primary Responsibilities
  • Quality control oversight of contract lab activities e.g. routine testing, testing results review and approval, generation of Certificate of Analysis, review/approval of technical documents such as method validation and qualification protocols/reports, and regulatory filing documents per project needs as required
  • Manage and lead clinical and commercial quality control compliance for stability, reference standard, and specification programs
  • Support the establishment of QC systems such as product specifications, product expiry, reference standard program, QC documentation including SOP's, material specifications and other quality documents, etc.
  • Support CMC Analytical Development in a QC aspect by review and approval of applicable documents in support of activities such as method development, transfer, characterization, comparability investigations, analytical test method qualification plans/protocols and reports
  • Perform data review of trending for in-process testing, release, and stability and identify data trends, to ensure compliance with regulatory filings and ICH or other global health authority guidance documents, as applicable
  • Support technology transfer and process performance qualification with product characterization/process validation activities
  • QC support in the generation, quality, and compliance review of bioanalytical data from preclinical and clinical projects for proprietary compounds and in some cases support for sample analysis projects
  • Support tox material inventory monitoring process, to ensure no impediments to completing studies
  • Additional responsibilities and ad hoc projects as required

Qualifications and Key Success Factors
  • Bachelors degree strongly preferred, with minimum of 6 years of experience in cGMP Quality Control environment
  • In-depth technical and regulatory understanding of GMP biologics manufacturing and testing including applicable international regulations/standards (GMP and ICH guidelines) in all phases of product development and commercialization
  • Experience managing third party assay laboratories, collaborations, and relevant bioanalytical vendors preferred
  • Extensive knowledge of GMP regulations, ICH guidelines, and stability testing requirements.
  • Proven track record of managing stability programs and COA processes for clinical and commercial products
  • Experience working in QC lab environment with hands-on experience in running, qualifying, and validating analytical methods
  • Ability to work effectively in a fast-paced, dynamic environment
  • Experience managing Contract Test Labs activities
  • Experience with regulatory inspections and interactions with health authorities
  • Excellent communication skills and ability to build key networks and business relationships across all levels of the business

Compensation & Benefits
At Praxis, we're proud to offer an exceptional benefits package that includes:
  • 99% premium cost covered for medical (Blue Cross Blue Shield), dental, and vision plans
  • Bonus program structured to pay on a quarterly basis
  • 401k plan with 100% match up to 6% of employee's contribution (Traditional & Roth)
  • Wellness benefit of $200/month towards incredibly flexible options including travel, fitness equipment & memberships, student loan repayment, sports fees and much more
  • Unlimited PTO, (2) weeklong shutdowns each year, and a generous extended family leave benefit
  • Eligibility for equity awards and Employee Stock Purchase Plan (15% discount)

To round out this world-class total rewards package, we provide base salary compensation in the range of $150,000 to $169,000 annualized. Final salary range may be modified commensurate with job level, education, and experience.
Company Overview
Praxis Precision Medicines is a clinical-stage biopharmaceutical company translating genetic insights into the development of therapies for central nervous system disorders characterized by neuronal imbalance. At Praxis we share a common vision of reshaping the human condition into a more freeing and fulfilled existence by developing high impact medicines for patients and families affected by and living with complex brain disorders. Our core Values of Trust, Ownership, Curiosity and Results are foundational to every aspect of our business and are exemplified by each and every one of our team members.
Diversity, Equity & Inclusion
Guided by our core values, at Praxis Precision Medicines, Inc. we continue to DARE FOR MORE ® to advance, promote, and champion diversity, equity, and inclusion by encouraging individuals to bring their authentic selves and perspectives to work each day. We are an equal opportunity employer and committed to providing opportunities to all qualified applicants without regard to race, religious creed, color, gender identity or expression, age, national origin, sexual orientation, disability, genetics, military service and veteran status, or any other characteristic protected by federal, state, or local laws.
Attention: Job Scam Alert
Praxis has recently become aware of fraudulent job recruitment postings from individuals claiming to represent Praxis. These postings seek financial information in connection with fraudulent opportunities for employment. If you suspect any fraudulent activity or misrepresentation in connection with a Praxis job opportunity, please report it to careers@praxismedicines.com.
Praxis does not accept unsolicited submissions from recruitment agencies for open positions. We ask all recruitment agencies to refrain from contacting any Praxis employee regarding any position. All unsolicited resumes submitted by recruitment agencies to any Praxis employee in any form or method will be deemed to be the property of Praxis, and Praxis explicitly reserves the right to hire those candidate(s) without any financial obligation to the recruitment agency.

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