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Full Time Biocompatibility Jobs (NOW HIRING)

Working knowledge of biocompatibility requirements * The ability to execute plans/strategies to ... Full-Time Annual Salary Please Note: At this time, we are unable to sponsor employment visas.

Working knowledge of biocompatibility requirements * The ability to execute plans/strategies to ... Full-Time Annual Salary Please Note: At this time, we are unable to sponsor employment visas.

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Full Time Biocompatibility information

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$41K

$115.4K

$214K

How much do full time biocompatibility jobs pay per year?

As of May 30, 2026, the average yearly pay for full time biocompatibility in the United States is $115,369.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,000.00 and $135,500.00 per year, depending on experience, location, and employer.

What is the difference between Full Time Biocompatibility vs Full Time Regulatory Affairs Specialist?

AspectFull Time BiocompatibilityFull Time Regulatory Affairs Specialist
Required CredentialsBiocompatibility certifications, scientific degreesRegulatory certifications, science or law degrees
Work EnvironmentLaboratories, manufacturing plantsRegulatory agencies, corporate offices
Industry UsageMedical devices, implantsMedical devices, pharmaceuticals
Common Search IntentBiocompatibility testing, safety assessmentRegulatory compliance, submissions

Full Time Biocompatibility roles focus on testing and assessing the safety of medical materials, often requiring scientific certifications and laboratory work. In contrast, Full Time Regulatory Affairs Specialists handle compliance documentation and submissions to regulatory bodies, working more in office settings. Both roles are essential in the medical device industry but serve different functions related to product safety and approval processes.

More about Full Time Biocompatibility jobs
What cities are hiring for Full Time Biocompatibility jobs? Cities with the most Full Time Biocompatibility job openings:
What are the most commonly searched types of Biocompatibility jobs? The most popular types of Biocompatibility jobs are:
What states have the most Full Time Biocompatibility jobs? States with the most job openings for Full Time Biocompatibility jobs include:
What job categories do people searching Full Time Biocompatibility jobs look for? The top searched job categories for Full Time Biocompatibility jobs are:
Infographic showing various Full Time Biocompatibility job openings in the United States as of May 2026, with employment types broken down into 100% Full Time. Highlights an 86% In-person, and 14% Remote job distribution, with an average salary of $115,369 per year, or $55.5 per hour.
Quality Engineer, Sustaining

Quality Engineer, Sustaining

Alphatec Spine

Carlsbad, CA • On-site

$75K - $90K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 11 days ago


Job description

The Quality Engineer will join our Quality Engineering team, focusing on product sustaining. This role is responsible for supporting the manufacture of high quality implantable and non-implantable spine surgery medical devices by ensuring compliance with contractual and regulatory requirements. Working closely with our NPI QE team, contract manufacturers and quality control, you will ensure only good product goes on shelve. Activities involves assessing incoming inspection methods and sampling, process controls at the contract manufacturers, facilitating nonconforming material report investigation and closure, failure investigations, CAPA and SCAR ownership, and change control activities. This role liaisons with R&D, Quality NPI, Supplier Quality, Supply Chain and Regulatory and includes continuous improvement projects

Essential Duties and Responsibilities

  • Support Material Review Board (MRB).
  • Develop and revise inspection methods, gages and associated drawings and procedures.
  • Support Engineering Change Order Review.
  • Perform Design For Manufacturing activities (DFM).
  • Technical interface with contract manufacturing
  • Support suppliers in performing IQ, OQ and PQ processes
  • Provide statistical support to analyze manufacturing processes and to recommend appropriate process controls for ensuring product conformance to specification.
  • Lead Risk Management efforts in accordance with ISO 14971.
  • Lead continuous improvement projects
  • Participate in FDA, ISO, and other regulatory audits.
  • Other duties as assigned.

Requirements

The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Technical:

  • Knowledge of both US and International medical device quality system requirements (e.g. 21 CFR Part 820, ISO 13485), and other applicable standards.
  • Experience supporting on-market / commercialized product
  • Knowledge of mechanical inspection methods and equipment
  • Knowledge of SPC, DOE, probability, and statistics
  • Ability to read, analyze, and interpret blueprints and GD&T
  • Ability to solve complex problems to root cause and prevent re-occurrence (CAPA)
  • Proficient in Technical Writing (Protocols, Reports)
  • Knowledge of Solid Works or other CAD software
  • Working knowledge of biocompatibility requirements
  • The ability to execute plans/strategies to completion
  • Project management and communication with internal and external customers

Personal Attributes:

  • Self-starter, works independently and maintains positive, enthusiastic attitude with a high-level of attention to detail/quality.
  • Ability to handle competing priorities and a broad variety of tasks simultaneously under high pressure and ambiguity.
  • Strong facilitation skills, confident communicator (both verbally and written) with all levels of organization and diverse audiences.
  • Ability to develop and maintain strong working relationships with internal and external customers and suppliers.
  • Ability to have good decision-making skills and judgment.

Must be able to travel up to 10% of the time to Alphatec Spine, Inc. facilities and suppliers.

Education and Experience

  • Minimum Bachelor’s degree (BS) from a four-Year College or university in Mechanical, Industrial and Systems, Biomedical, or Manufacturing Engineering.
  • 3+ years related experience and/ or training; or equivalent combination of education and experience.

Certificates, Licenses, registrations

Six Sigma Black Belt, ASQ CQE/OE (Certified Quality Engineer/Operational Excellence), preferred.

For roles based in the United States that require access to hospital facilities, must be eligible for and maintain credentials at all required hospitals, including meeting any applicable physical requirements or vaccination requirements (including the COVID-19 vaccine, as applicable).

ATEC is committed to providing equal employment opportunities to its employees and applicants without regard to race, color, religion, national origin, age, sex, sexual orientation, gender identity, gender expression, or any other protected status in accordance with all applicable federal, state or local laws. Further, ATEC will make reasonable accommodations that are necessary to comply with disability discrimination laws.

Salary Range

Alphatec Spine, Inc. complies with state and federal wage and hour laws and compensation depends upon candidate’s qualifications, education, skill set, years of experience, and internal equity. $75,000 to $90,000 Full-Time Annual Salary

Please Note: At this time, we are unable to sponsor employment visas.

Benefits

  • Health Care Plan (Medical, Dental & Vision)
  • Retirement Plan (401k, IRA)
  • Life Insurance (Basic, Voluntary & AD&D)
  • Paid Time Off (Vacation, Sick & Public Holidays)
  • Family Leave (Maternity, Paternity)
  • Short Term & Long Term Disability
  • Free Food & Snacks
  • Stock Option Plan