Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

QA Compliance Specialist

Anika

What You’ll DoAs the QA Compliance Specialist, you’ll help ensure Anika’s manufacturing operations meet applicable quality, regulatory, and documentation requirements. Working in a regulated medical device and life sciences manufacturing environment, you’ll review production records, support shop-floor quality activities, and help maintain compliance with cGMP and ISO 13485 standards.You’ll partner closely with Production and Quality Assurance to ensure documentation is accurate and complete, support investigations and corrective actions, and assist with internal, customer, and regulatory audits. This role is a great opportunity for an early-career quality professional to build hands-on experience in quality systems, manufacturing compliance, and product release activities.This position is based at Anika’s Bedford, MA facility and is fully on-site.How You’ll ContributeReview batch records and Certificates of Analysis (COAs) for accuracy and completeness prior to final product release.Review and approve supplemental logs, charts, and other documentation supporting cGMP manufacturing operations.Provide shop-floor Quality Assurance support to Production, including line clearances, in-process checks, and assistance with quality-related issues.Support investigations involving nonconformances, CAPAs, root cause analysis, product complaints, out-of-specification events, and environmental excursions.Provide Quality Assurance input and support for change controls and planned deviations.Provide document control support and help ensure quality documentation is maintained in accordance with applicable procedures and requirements.Issue and reconcile batch records to support manufacturing operations.Maintain Device History Records (DHRs) to ensure accurate and complete documentation of manufacturing activities.Support internal and external audits, including customer and regulatory audits, as part of the Audit Team.Assist in maintaining and improving the Quality System to support ongoing compliance with cGMP, ISO 13485, and internal quality requirements.Participate in cross-functional project teams and contribute to quality and compliance initiatives.Perform other related duties as assigned.What It TakesYou’re detail-oriented, organized, and interested in building a career in Quality Assurance within a regulated manufacturing environment. You understand the importance of accurate documentation, following established procedures, and working collaboratively to maintain product quality and regulatory compliance. You’re comfortable managing multiple tasks, communicating with different teams, and learning new quality systems and processes.What You BringBachelor’s degree, preferably in Life Sciences or a related discipline; relevant experience may be considered.0–2 years of industry experience. Internship experience and familiarity with GMP and ISO requirements are considered.Basic computer proficiency, including experience with databases and Microsoft Office applications.Strong organizational skills and attention to detail.Good presentation skills.Excellent written and verbal communication skills.Ability to follow procedures, maintain accurate documentation, and work effectively with cross-functional teams.Nice to HaveInternship or previous experience in Quality Assurance, Quality Control, or another regulated manufacturing environment.Familiarity with cGMP requirements and ISO 13485 quality system standards.Exposure to batch record review, Device History Records, document control, nonconformances, CAPAs, or change controls.Experience supporting manufacturing floor activities, quality investigations, or internal and external audits.The salary range provided is based on the Company’s reasonable estimate of the base salary pay range for this position at the time of posting. Actual base pay is determined by several factors relevant to the position, including skills, competencies, experience, education, and geographic location. Anika also offers a discretionary bonus program for all full-time employees, comprehensive healthcare benefits, health savings account, 401(k) plan with up to 5% company match which includes immediate vesting, employee stock purchase plan at a 15% discount, accrued paid time off, additional long-term incentives including stock awards, and much more. At Anika, we take pride in offering robust Total Rewards, inclusive of market-leading benefits to meet our employees where they are in their career and in life.The compensation and benefits information is provided as of the date of this posting. Anika reserves the right to modify compensation and benefits at any time, subject to applicable law.

Vacancy posted 12 hours ago
Similar jobs that could be interesting for youBased on the QA Compliance Specialist in Bedford, MA vacancy
  • $100k - $115k

     ...operations, the Senior Quality Assurance Specialist champions collaborative day to day floor...  ...Oversee and provide regulatory compliance guidance during on-the-floor manufacturing...  ...Participate in batch disposition activities. QA support of drug product aseptic fill... 
    Suggested
    Live in
    Visa sponsorship
    Shift work

    Genezen

    Lexington, MA
    9 days ago
  • $110k - $130k

     ...to make it easier for everyone to experience the world.KAYAK is seeking a motivated, detail-oriented, and proactive Senior Compliance Specialist to join our dynamic in-house legal and compliance team! This versatile role is essential for the smooth operation of our Compliance... 
    Suggested
    Work at office
    Flexible hours
    3 days per week

    Kayak Europe

    Concord, MA
    2 days ago
  •  ...seeking an experienced Quality Assurance Specialist to help establish and maintain an...  ...developing quality systems, ensuring regulatory compliance, maintaining data integrity, and...  ...readiness. The ideal candidate has hands-on QA experience in a regulated laboratory,... 
    Suggested
    For subcontractor

    MEDICILON USA CORP

    Lexington, MA
    6 days ago
  • $81.15k - $101.96k

     ...Taichung. Position Overview: The Quality Assurance Specialist reports to the senior manager of QA and will play a key role in managing the product...  ...and ensuring DSCSA (Drug Supply Chain Security Act) compliance together with supporting QA activities, such as supplier... 
    Suggested
    Flexible hours
    Shift work
    Afternoon shift

    PharmaEssentia U.S.A.

    Burlington, MA
    20 days ago
  •  ...DescriptionDescriptionThe Quality Assurance Professional will work in the US External QA team responsible for Contract Manufacturing (CMO) and Contract...  ...of commercial biologics products. Interfacing CMO for site compliance documentation, quality systems review (deviations, CAPA, Change... 
    Suggested
    Contract work
    Flexible hours

    LanceSoft

    Lexington, MA
    1 day ago
  •  ...Facebook, Instagram, X and YouTube. Job Description This QA Specialist is responsible for reviewing and release of semi-finished,...  ...to support product release schedule, ensuring regulatory compliance, customer satisfaction and delivery of products. •Quarantine... 
    Temporary work
    Local area

    AbbVie

    Waltham, MA
    3 days ago
  •  ...QA Specialist Perform the QA review/approval of analytical documentation: Analytical method validation protocols and reports for in-...  ...preparation for Process Performance Qualification activities Broad compliance knowledge (cGMP, ICH, FDA/EU guidance, WHO) as it applies to... 

    Integrated Resources

    Cambridge, MA
    2 days ago
  •  ...Lancesoft Job Details: Title : Quality Assurance Specialist Location : Lexington, MA Duration: 3 years Contract...  ...• Plan, design, deploy, maintain and troubleshoot related to QA tools like Tricentis TOSCA and Impact Analysis/Live Compare tool... 
    Contract work
    Apprenticeship
    Local area

    LanceSoft

    Lexington, MA
    20 hours ago
  •  ...Description• The Quality Assurance Professional will work in the Internal QA team of company's Human Genetic Therapies Quality Assurance...  ...manufacturing on behalf of company.• Support of Commercial QA Compliance: Deviation Review and Trending, CAPA Review and Trending.•... 

    Careers Integrated Resources Inc

    Lexington, MA
    2 days ago
  •  ...Job Description Job Description Food Safety and Regulatory Compliance Specialist About ColdSnap ColdSnap® is a rapid freezing appliance that produces single servings of frozen confections and frozen beverages in about 120 seconds from shelf-stable, ambient temperature... 
    Full time
    Work at office
    Local area
    Relocation package

    ColdSnap

    Billerica, MA
    23 days ago
  • The Sr. RA Specialist is Responsible for preparation of regulatory submissions (domestic and foreign). Ensure implementation and maintenance of regulatory filing in compliance with applicable regulations and Glaukos internal SOPs.Generous. Innovative. Leadership-driven... 
    Local area

    Glaukos

    Burlington, MA
    2 days ago
  • The Compliance Specialist provides support for projects, manufacturing execution, computer systems (GP, EBR, OpCenter APS), quality systems (deviations...  ...teams. Collaborate with other departments including QA, QC, Engineering, Validation, Material Management and Project... 
    Work at office
    Weekend work
    Afternoon shift

    Cedent Consulting

    Cambridge, MA
    1 day ago
  • $132k - $198k

     ...everyone is counted.Work Protected.OverviewMimecast's Governance and Certification Office (GCO) is looking for a Principal GCO High Compliance Systems Advisor to own its high-compliance certification program, including FedRAMP authorization, lead technical control design... 
    Full time
    Work at office
    Local area

    Mimecast

    Lexington, MA
    12 hours ago
  •  ...Job Description Job Description Manufacturing Compliance Specialist I At Vericel Corporation, we are pioneers in advanced cell therapies for sports medicine and severe burn care, transforming patient lives through cutting-edge regenerative medicine. Our commitment... 
    Work at office
    Immediate start
    Monday to Friday

    Vericel Corporation

    Burlington, MA
    1 day ago
  •  ...Job Description Job Description We are seeking a Quality Assurance Specialist for a manufacturing company in Acton, MA. This position offers the opportunity to support all aspects of quality and continuous improvement in a hands-on manufacturing environment. This... 

    Career Crunch

    Acton, MA
    10 days ago
  • $85.4k - $158.6k

     ...an experienced Senior Quality Assurance Specialist, to join Mariana’s Quality Assurance...  ...and radiopharmaceuticals. The Senior QA Specialist plays a critical role in ensuring...  ..., tested, and released in full compliance with cGMP, radiation safety regulations,... 

    Mariana Oncology

    Watertown, MA
    23 days ago
  • $20 - $25 per hour

     ...Job Description Overview Now Hiring: Quality Assurance Specialist – Food Manufacturing ???? Lowell, MA ???? $20.00–$25.00/hour...  ...potential issues before they affect production Help maintain compliance with food safety, quality, and manufacturing programs... 
    Full time
    Immediate start
    Day shift

    PGI Foods

    Lowell, MA
    19 days ago
  •  ...Job Description Our client is seeking a Quality Assurance Specialist to support quality inspection, continuous improvement, and product...  ...calipers, micrometers, gauges, etc.) ~3–5 years of experience in a QA or Quality Engineering role within a mechanical or electro‑... 
    Relocation
    Visa sponsorship

    Confidential Recruiting Partners

    Acton, MA
    29 days ago
  • Job Description Job Description Massachusetts (Acton), 01720 - Quality Assurance Specialist - Negotiable Salary - On-Site - (3yrs experience + HS diploma or equivalent) Send resume via bkoutlooks.com

    BKOutlooks

    Acton, MA
    26 days ago
  •  ...Regulatory Affairs Specialist II The Regulatory Affairs Specialist II supports regulatory submissions and regulatory authority interactions...  ...regulatory guidance to cross-functional teams to ensure compliance with applicable requirements. • Prepares regulatory... 

    Anika Corporation

    Bedford, MA
    1 day ago
  • $115k - $130k

     ...seeking a skilled and self-motivated Senior Regulatory Affairs Specialist to support the BrioVAD® Left Ventricular Assist System. This...  ...potential effects on CE marking, technical documentation, GSPR compliance, UDI/EUDAMED data, and Notified Body notification requirements... 

    BrioHealth Solutions, Inc.

    Burlington, MA
    1 day ago
  • $150k - $180k

    Job Information Number ICIMS-2026-11080 Job function QA&RA Job type Full-time Location Werfen - Bedford - 180...  ...documents for agile/iterative development environments, and promoting compliance with global digital health requirements. Responsibilities... 
    Full time
    Worldwide
    Shift work

    Werfen

    Bedford, MA
    3 days ago
  •  ...Responsibilities: Determine and document change assessments for US Class II devices to ensure compliance with the US regulation. Plan and prepare submissions for US Class II devices, including creating, translating, revising, reviewing, and compiling documents, as... 
    Worldwide

    Cedent

    Bedford, MA
    3 days ago
  •  ...Quality assurance specialist responsible for reviewing and releasing semi-finished and finished pharmaceutical products while ensuring compliance with manufacturing standards and regulations. Role involves batch record analysis, documentation preparation, and product disposition... 

    AbbVie

    Waltham, MA
    1 day ago
  • $58.66k - $103.5k

     ...Facebook, Instagram, X and YouTube. Job Description This QA Specialist is responsible for reviewing and release of semi-finished,...  ...records to support product release schedule, ensuring regulatory compliance, customer satisfaction and delivery of products. •... 
    Full time
    Temporary work
    Local area

    AbbVie

    Waltham, MA
    3 days ago
  • $110k - $120k

     ...decisions behind it. About the Role As a Senior Quality Systems Specialist at Lexington Medical, you will be the hands-on owner of our...  ...Regulatory, and Manufacturing to keep product quality and QMS compliance on track as processes and products change. Keep the... 

    Lexington Medical, Inc.

    Bedford, MA
    17 days ago
  • $80k - $140k

     ...and strengthen the team’s ability to test intelligent features with speed, rigor, and confidence. This role is ideal for a mid-level QA professional who combines strong software testing fundamentals with hands-on experience applying AI in the test process and testing AI... 
    Full time
    Temporary work
    Flexible hours

    State Street Bank

    Burlington, MA
    4 days ago
  • $135.3k - $202.9k

     ...with cross-functional team, and execution to plan for both development submissions and maintenance submissions to ensure ongoing compliance. Partner with Regulatory Project Management and Submission Management.May act as direct contact to a local HA (e.g. FDA or EMA).... 
    Local area
    Remote work
    Monday to Friday
    Flexible hours

    Merck

    Billerica, MA
    3 days ago
  •  ...oriented and analytical Quality Assurance Specialist to maintain and elevate our product and...  ...internal teams on quality protocols, compliance standards, and document control best practices...  ...: 3–5 years of experience in a QA or Quality Engineering role, ideally within... 
    Permanent employment
    Summer work

    Sparx Hockey

    Acton, MA
    4 days ago
  • Associate Director Of Regulatory Affairs Cmc Hybrid Role The Associate Director of Regulatory Affairs CMC will support development CMC team activities for an emerging portfolio of biologics products. This position will oversee CMC Health Authority submissions, collaborating...

    Accede Solutions Inc.

    Lexington, MA
    3 days ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to QA Compliance Specialist. Be the first to apply!