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

Quality Assurance Specialist - Document Control

$85k - $95k
Full-time

Carlsmed

About Carlsmed

Our mission is to improve outcomes and decrease the cost of healthcare for spine surgery and beyond. The Carlsmed aprevo® personalized surgery platform is designed to improve the standard of care for spine surgery one patient at a time.

Position Description

The Quality Assurance Specialist administers document control and related quality records within the Quality Management System (QMS). This individual contributor supports QA’s mission to define, maintain, and improve the QMS by keeping approved information current, changes traceable, and records complete and retrievable. The role focuses on controlled documents, Arena administration, training records, and documentation support for QA activities. The Specialist works with process owners and designated approvers and performs reviews or approvals within documented training and delegated authority.

Responsibilities

Controlled documents and change orders

  • Process document and engineering change orders, verifying document details, supporting records, and approvals before release.
  • Coordinate document creation, revision, approval, distribution, and archival, including effective dates and required implementation and training actions.
  • Review documents for format, completeness, consistency, and cross-references. Resolve discrepancies with owners responsible for technical content and impact assessments.
  • Maintain controlled documents and records, ensuring current revisions are available at points of use and superseded versions are controlled.

Arena administration and data integrity

  • Administer Arena templates, workflows, attributes, and authorized user access under approved change controls; provide user support.
  • Import and verify approved master data, resolve discrepancies, and maintain traceability of corrections.
  • Support change assessments and validation through assigned checks, documented results, and evidence approved before implementation.

Training administration and user support

  • Onboard employees into the QMS and assign training using approved role requirements and curricula, coordinating with managers responsible for role-specific competence.
  • Maintain training records, track completion, follow up on overdue assignments, and escalate gaps to managers.
  • Report training status and guide employees on document control procedures.

Quality records and audit support

  • Maintain quality records under approved access, confidentiality, and retention requirements; retrieve documents and evidence for audits and inspections.
  • Check assigned QA records for completeness and required approvals, return deficiencies to owners, and archive approved records, including patient-specific preproduction files and DHRs.
  • Maintain supplier and other QMS files, track documentation due dates, and follow up with owners.
  • Support controlled label templates, approved label data, assigned BarTender administration, and device identifier records under approved procedures.
  • Identify recurring errors and recommend improvements to document control workflows and user guidance.

Qualifications

  • 7+ years in document control or QA within a regulated industry, preferably medical devices.
  • Working knowledge of controlled documents, change control, training records, and good documentation practices; familiarity with ISO 13485, applicable FDA quality system requirements, and MDSAP.
  • Experience with an electronic QMS or product lifecycle management system; Arena experience preferred.
  • Proficiency with Microsoft Office and accurate data entry and record retrieval.
  • Strong attention to detail, organization, written communication, and follow-through; ability to coordinate with multiple functions and escalate missing evidence or overdue work.
  • Experience supporting audits and electronic system changes preferred; BarTender or other controlled labeling system experience is beneficial.

Equal Opportunity Employer

Carlsmed is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. Carlsmed is committed to providing reasonable accommodations for candidates with disabilities in our recruiting process. If you need any assistance or accommodations due to a disability, please let us know.

Compensation

The anticipated annual base salary range for this position is $85,000 - $95,000. Individual compensation is determined based on factors such as experience, skills, education, certifications, and geographic location.

In addition to base salary, eligible employees may participate in incentive compensation programs and receive a comprehensive benefits package. Our benefits reflect our commitment to the health and well-being of our employees and their families and include 100% employer-paid medical, dental, and vision insurance premiums, a 401(k) plan with employer matching, and unlimited paid time off (PTO). Your recruiter can provide additional details about our total rewards package during the hiring process.

Vacancy posted 1 day ago
Similar jobs that could be interesting for youBased on the Quality Assurance Specialist - Document Control in Carlsbad, CA vacancy
  •  ...Job Summary: Quality Assurance Specialist II will provide hands-on support for production and...  ...production activities, inspections, audits, documentation, and continuous compliance...  ...QA oversight and approval of Quality Control activities, including method transfers... 
    Suggested
    Work at office

    Katalyst Healthcares and Life Sciences

    Oceanside, CA
    15 hours ago
  • $97.17k - $133.61k

    A brief overviewThe Sr. Quality Assurance Specialist fulfills a critical role in Quality Assurance. This...  ...GMP system improvements, technical documents, and review of GMP documentation and...  ...6 years experience with GMP document control, validation, qualification and calibration... 
    Suggested

    Bachem

    Vista, CA
    2 days ago
  •  ...sciences, is seeking a " QA Specialist (Biotech / Pharmaceutical manufacturing...  ...with regulatory and site quality standards. Key...  ...Manage deviations, CAPAs, change controls, investigations, and hold events...  ...compliance •Perform walkthroughs, document control tasks, and update... 
    Suggested
    Long term contract

    Dawar Consulting

    Oceanside, CA
    2 days ago
  • Quality Assurance Associate IPM Shift: Monday - Friday 7:00AM - 3:30PMPay: $25.00 - $27.00 an hour depending on experienceSafety...  ...Associate I, you will:Conduct internal audits, documentation, data analysis, control of non-conforming material, authorization of customer... 
    Suggested
    For contractors
    Monday to Friday
    Flexible hours
    Shift work

    Senior plc

    Oceanside, CA
    3 days ago
  • $80k - $90k

     ....   Position Description   As a QA Specialist, you will work on projects related to proprietary...  ...to enable personalized surgery.  The Quality Assurance department encompasses activities related to Documentation Control, Change Control, Corrective Action and Preventive... 
    Suggested

    Carlsmed

    Carlsbad, CA
    10 days ago
  •  ...Under general guidance, the Senior Quality Systems Specialist will collaborate with leadership to champion, sustain and continually improve...  ...organization on requirements of the QMS. # Manages the document control program, including the creation, revision, distribution... 
    Full time
    Work at office

    KINOVATE LIFE SCIENCES, INC

    Carlsbad, CA
    4 days ago
  •  ...SUMMARY: Under supervision, the Quality Assurance Associate supports and upholds quality...  ...identity and labeling. Issues applicable controlled Quality Control (QC) test records. # Issues controlled batch record documentation to the Production department. Attends... 
    Work at office
    Immediate start

    Kinovate Life Sciences Inc

    Carlsbad, CA
    4 days ago
  • $43.08 - $80 per hour

     ...cancer care by ensuring the quality and compliance behind...  .... As a QA Operations Specialist at Novartis, you will...  ...Responsibilities ~ Provide Quality Assurance support for manufacturing, quality control, engineering, and...  ...reviewing quality documentation and supporting... 
    Hourly pay
    Shift work
    Rotating shift

    Production / Manufacturing

    Carlsbad, CA
    more than 2 months ago
  • $159.43k

     ...implement, and maintain the project-specific Quality Assurance Surveillance Plan (QASP) in compliance...  ...Perform daily quality inspections and document work progress to ensure materials,...  ...Oversee construction contractor’s Quality Control meetings (Preparatory, Initial, and... 
    Contract work
    For contractors
    Work experience placement
    For subcontractor
    H1b
    Immediate start
    Flexible hours

    CDM Smith

    Carlsbad, CA
    1 day ago
  • $130k - $140k

     ...manufacturing, with a focus on product quality, yield optimization, and...  ...to the Director, Quality Control. This role is an on-site...  ..., Tech Transfer, Quality Assurance, and Senior Management An...  ...affinity for precise and detailed documentation skills. The ability to... 
    Contract work
    Temporary work
    Local area
    Monday to Friday
    Flexible hours
    Weekend work

    Argonaut Manufacturing Services

    Carlsbad, CA
    29 days ago
  • $27 - $35 per hour

     ...is looking to hire aQuality Control Associate, Microbiology for a...  ...We are seeking a Microbiology Specialist to support aseptic fill/finish...  ...Author, revise, and review Quality Control (QC) standard operating...  ...-task, prioritize workload, document properly and interpret data accurately... 
    Hourly pay
    Contract work
    Temporary work
    Work at office

    Johnson Service Group

    Carlsbad, CA
    2 days ago
  • $27 - $32 per hour

     ...manufacturing, with a focus on product quality, yield optimization, and reliable delivery...  ...with aseptic filling operations and controls and drug product process validation is highly...  ...QC Multi-task, prioritize workload, document properly and interpret data accurately... 
    Hourly pay
    Contract work
    Temporary work
    Work at office
    Local area
    Monday to Friday
    Flexible hours
    Weekend work

    Argonaut Manufacturing Services

    Carlsbad, CA
    29 days ago
  • Bachem Americas is seeking a Sr. Quality Assurance Specialist to strengthen GMP compliance across manufacturing and QC operations in Vista, CA. You will review GMP documents, support real-time batch record review, lead audits, and drive LEAN GMP improvements with cross... 

    Bachem Holding AG

    Vista, CA
    4 days ago
  •  ...Quality Control Inspector Location: San Marcos, CA Pay: DOE Shift:...  ...detail, and the ability to accurately document inspection results. Responsibilities...  ...Previous quality control, quality assurance, or manufacturing experience preferred.... 
    Shift work
    Day shift

    Partners Personnel Management

    San Marcos, CA
    1 day ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to Quality Assurance Specialist - Document Control. Be the first to apply!