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

Quality Specialist

NESCO Inc

Quality Assurance Specialist I - Contingent WorkerExecutes day-to-day quality assurance objectives following a varied set of procedures, ensuring adherence to company standards and regulatory requirements. Conducts inspections, drafts and reviews quality related documentation, and monitors production processes to maintain product quality and regulatory compliance. Refines testing protocols to accommodate new product designs, troubleshoots unexpected deviations in quality metrics, or adjusts compliance procedures in response to regulatory updates. Communicates with internal and/or external contacts in- and outside of the quality function on matters that involve obtaining or providing information requiring explanation, such as coordinating corrective actions with manufacturing teams, interpreting compliance guidelines for suppliers, and assisting auditors with documentation reviews during inspections.Job Duties and ResponsibilitiesSupports generation of job packets for ProductionSupports batch record review process.Assist in Label generationSupports certification requestsComplies with company policies, procedures, work instructions, and training requirements focusing on customer service, production, and quality.Ensures documentation and physical product segregation and containment of non-conforming material.Reviews production documentation for accuracy, completeness, and GDP compliance.Communicates issues / concerns to area owner and direct supervisor or manager.Assist with ensuring a state of audit readiness at all times.Follows applicable safety proceduresDocument any deviations or non-conformances, following procedures and Work Instructions, encountered during routine activities.Assist in resolving basic quality issues under supervision.Collect data for quality reports.Order supplies for the quality department when needed.Ensures cleanliness of work areas.Performs other duties as assigned.Knowledge Skills and AbilitiesGood communication, written skills, and interpersonal skillsGood attention to detailAbility to read, understand, and follow proceduresAbility to escalate issues according to established proceduresFamiliarity with Quality Management SystemsGMP knowledge is preferredSelf-motivated and ability to work independently and with a teamKnowledge and experience utilizing Microsoft Outlook, Word, Excel, and Access, or equivalent software packagesGood mathematics skillsBasic understanding of quality standards such as ISO 9001.Documentation skills to accurately record test results and quality issues.Qualifications (Education/Training, Experience and Certifications)High School completion or equivalent (GED) required.Bachelors degree is preferred.A minimum of 1-year related experience and/or training in a regulated industry is preferred.Experience in a Quality role within the medical device, biotech, or pharmaceutical industry is preferred.Skills/Experience: BioTech pharma, GMP regulations, or ISO requirements experience - preferred Required Skills: Must be comfortable with Word and Excel - used heavily in the role. Desired Skills: The ideal candidate is self-driven - 2nd shift is less supervised than 1st shift.Will check behind each other's work. Should have a strong attention to detail as there is a lot of record keeping. Should have the ability to stay on task with routine tasks.Degree Requirement: GED requiredCertification Requirements:Six Sigmas certification is a plus but not required. Power Automate or Power BI programs is a plus but not required.Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services. Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.

Vacancy posted 5 days ago
Similar jobs that could be interesting for youBased on the Quality Specialist in Devens, MA vacancy
  •  ...POSITION SUMMARY: The Quality Specialist will support critical Quality Assurance and Quality Control functions as well as planned process studies/projects/improvements and identify opportunities for continual process improvements for H&V Operations in the MA Mills. The... 
    Suggested
    Flexible hours

    Hollingsworth & Vose

    Groton, MA
    1 day ago
  • $31 - $63 per hour

     ...join us. People who’ll bring new perspectives, solve tough problems, and thrive as part of a team. Join the power movement as a Quality Specialist The quality specialist is an essential role within the quality control team at CFS, responsible for monitoring adherence to... 
    Suggested
    Hourly pay

    Commonwealth Fusion Systems

    Harvard, MA
    14 hours ago
  •  ...Specialist QA (CMO)50% onsite Location of work: Summit West, NJ or Devens, MAThe Specialist QA (CMO) position is an individual contributor...  ...industry experience with a minimum of 3 years experience in quality assurance, quality control, and compliance.Knowledge of... 
    Suggested
    Work experience placement

    Omni Inclusive

    Devens, MA
    1 day ago
  • $89.53k - $108.49k

     ...employees with the resources to pursue their goals, both at work and in their personal lives. Position Summary The Supplier Quality Senior Specialist is responsible for work which supports the GMP/GDP Vendor and Material Management programs at the Devens Biologics site.... 
    Suggested
    Full time
    Work experience placement

    VetJobs

    Harvard, MA
    1 day ago
  • $89.53k - $108.49k

     ...goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us. Position Summary The Supplier Quality Senior Specialist is responsible for work which supports the GMP/GDP Vendor and Material Management programs at the Devens Biologics site.... 
    Suggested
    Hourly pay
    Full time
    Temporary work
    Part time
    For contractors
    Work experience placement
    Summer work
    Live in
    Work at office
    Local area
    Remote work
    Flexible hours
    Shift work

    Bristol Myers Squibb

    Harvard, MA
    2 days ago
  • Bristol Myers Squibb in Devens, MA is seeking a Supplier Quality Senior Specialist to support GMP/GDP vendor and material management programs. The role involves vendor qualification, material qualification, change management, and handling supplier-related non-conformances... 

    VetJobs

    Harvard, MA
    1 day ago
  • $33 - $37 per hour

     ...Quality Control Analyst II Discover Veranova: At Veranova, we believe people are our most important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence... 
    Full time
    Local area
    Shift work

    Veranova

    Devens, MA
    2 days ago
  • $23 - $38 per hour

    VulcanForms Inc. is seeking a Quality Inspector to join our Quality Inspection team, ensuring parts meet precise standards. You will apply GD&T, perform FAI inspections, and support audits and continuous improvement in a fast-paced metal additive manufacturing environment... 
    Hourly pay
    Shift work
    Weekend work

    VulcanForms Inc.

    Harvard, MA
    1 day ago
  •  ...Overview Job Title: QASF (Quality Assurance Specialist, Floor) 2nd Shift/Overnight Training The first three weeks will be training (Monday-Thursday Normal Hours) Topics include gowning, MES, SAP, Label QA, GPS, and Polestry. Responsibilities Execution of label control... 
    Shift work
    Night shift
    Afternoon shift

    SPECTRAFORCE

    Harvard, MA
    2 days ago
  • Marathon Staffing seeks a detail-oriented Quality Inspection Associate to support light industrial clients by inspecting products and materials for defects, accuracy, and compliance with standards. In this on-site role, you’ll perform visual and dimensional checks, document... 

    Marathon Staffing

    Sterling, MA
    6 days ago
  •  ...Quality Assurance Associate Start your career in quality control with ultimate flexibility! We have immediate openings for quality assurance associates to support production on short-term mandates. This role is perfect for detail-oriented individuals who are comfortable... 
    Temporary work
    Immediate start
    Remote work
    Shift work

    Randstad

    Leominster, MA
    3 days ago
  • National Quality Assurance, USA (NQA) is seeking experienced auditors for fulltime and contractor positions across the United States. The role involves conducting audits to AS9100, AS9110, and AS9120, issuing precise audit reports, and coordinating with clients before,... 
    Full time
    For contractors

    NQA

    Acton, MA
    2 days ago
  • Start your career in quality control with ultimate flexibility! We have immediate openings for quality assurance associates to support production on short-term mandates. This role is perfect for detail-oriented individuals who are comfortable with visual checks and documentation... 
    Hourly pay
    Temporary work
    Work experience placement
    Immediate start
    Shift work
    Leominster, MA
    12 days ago
  •  ...Quality InspectorWe're seeking a detail-oriented Quality Inspector to join a fast-paced manufacturing team. This role is ideal for someone with quality or manufacturing experience who takes pride in accuracy and ensuring products meet required standards.What You'll DoPerform... 
    Full time
    Immediate start

    HW Staffing

    Lancaster, MA
    4 days ago
  • Bristol Myers Squibb is seeking a Specialist, Quality Assurance Shop Floor for Devens, MA. You will own quality decisions on the production floor, including deviation triage, review of batch records, and cross-functional triage meetings to ensure cGMP compliance. The role... 
    Night shift

    Biopharma Careers

    Harvard, MA
    5 days ago
  • Bristol Myers Squibb seeks a QA Manufacturing Shop Floor Specialist to oversee 24x7 quality collaboration across Manufacturing, QC laboratories and Warehouse Operations. You will ensure compliance with cGMP and company policies, triage events on the floor, and support... 

    Biopharma Careers

    Harvard, MA
    5 days ago
  • The Senior Specialist, QA Investigations at Bristol Myers Squibb leads quality oversight of deviation investigations and CAPA records at the Devens Cell Therapy Facility. You ensure product quality in compliance with regulations, supporting internal and external inspections... 

    VetJobs

    Harvard, MA
    1 day ago
  • $90k - $105k

     ...important asset, and we are dedicated to building the most talented workforce in our industry. Our commitment to uncompromising focus on quality, compliance, safety, and excellence in delivery shapes everything we do. We are not just looking for skills; we are seeking... 
    Full time
    Local area

    Veranova L P

    Devens, MA
    18 days ago
  • Bristol Myers Squibb in Devens, MA is seeking an Associate, QC Analytical (Cell Therapy) to support in-process, final product and stability testing. You will review GMP documentation, assist with deviations and CAPA, and may train analysts. The role emphasizes attention...
    Night shift

    Bristol-Myers Squibb

    Harvard, MA
    1 day ago
  • A global manufacturing partner is seeking an Administrative Specialist in Pepperell, MA. The candidate will support production and quality operations using the ERP system and ensure compliance with AS9100 standards. Key responsibilities include tracking labor transactions... 

    Prince Industries

    Pepperell, MA
    1 day ago
  • $23 - $38 per hour

    VulcanForms in Harvard, MA is seeking a Quality Inspector for the weekday evening shift. You will ensure the highest standards of quality and safety for our products through detailed inspections and continuous improvements. The ideal candidate will have over 3 years of... 
    Hourly pay
    Afternoon shift
    Weekday work

    VulcanForms

    Harvard, MA
    2 days ago
  • Bristol Myers Squibb is seeking a QC Analytical professional to support testing for in-process, final product, and stability samples in a cell therapy context. The role includes documentation review, data verification, and participation in CAPA and deviation investigations...

    Biopharma Careers

    Harvard, MA
    5 days ago

Do you want to receive more vacancies?

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