Compliance Specialist 2

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Posted 21 hours ago  •  10 applicants •  Be one of the first to apply!
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Compliance Specialist 2

Our Client - Hospital & Health Care company

  • Sunnyvale, CA
$22.22 - $29.33/hour
Exact compensation may vary based on skills, experience, and location.
40 hrs/wk
Contract (w2)
Remote work no
Travel not required
Start date
August 17, 2026
End date
August 17, 2027
Superpower
Finance
Capabilities
Compliance
Preferred skills
Communication
ISO 14971 Standard
Quality Management Systems
Customer Service
International Standards
Audit Management
Diagnostic Tools
Medical Devices
Critical Thinking
Regulatory Compliance
Verbal Communication Skills
Notified Body
ISO 13485 Standard
Process Improvement
Management
Product Recall
Title 21 Of The Code Of Federal Regulations
Innovation
Microsoft Teams
Median
Preferred industry experience
Hospital & Health Care
Experience level
5 - 8 years of experience

Job description

***Please note that our customer is currently not considering applicants from the following locations: Alabama, Arkansas, Delaware, Florida, Indiana, Iowa, Louisiana, Maryland, Mississippi, Missouri, Oklahoma, Pennsylvania, South Carolina, and Tennessee.***


Our Customer is a corporation that develops, manufactures, and markets robotic products designed to improve clinical outcomes of patients through minimally invasive surgery. Founded in 1995, their goal was to create innovative, robotic-assisted systems that help empower doctors and hospitals to make surgery less invasive than an open approach. Working with the top medical professionals, they continue to develop new, minimally invasive surgical platforms and future diagnostic tools to help solve complex healthcare challenges around the world.


We are seeking a Compliance Specialist 2 on a contract basis to support our Customer's business needs. This role is onsite in Sunnyvale, CA.


Role Overview:

  • The primary function of this position is to coordinate and assist field action team related activities.
  • They are to possess a general understanding of the field action process.
  • They will work closely with field action team to ensure that appropriate processing of customer acknowledgement forms and inquiries related to field actions.
  • Collaboration with business partners, field action team, and management to address customer escalation, concerns as it related to field action.
  • They will have strong organization and communications skills to support established customer-focused quality initiatives.
  • The specialist will also be expected to assist the team in record retention based on company and regulatory standards
  • Onsite 3 days a week.


Responsibilities:

  • Processing and reconciling customer returned acknowledgement forms per regulations and internal procedures.
  • Provides guidance to customers for product recall related questions.
  • Help provide updates on effectiveness levels for each field action.
  • Assist in preparing monthly regulatory reports on field action effectiveness status.
  • Manage the recalls inbox and complete requests as needed.
  • Assist in providing status updates to cross-functional teams when needed.
  • Assists with providing information to Audit Management on maintaining audit, readiness for internal and external audits.
  • Performs assessments, develops action plans, and drives plan to effectively, manage recall inbox and address any urgent communication appropriately.
  • Collaborate in development, maintenance, and improve processes and procedures for various processes within the quality management system and where necessary.


Qualifications:

  • Minimum Bachelor Degree – BS degree in Engineering, Physical or Biological Science or other technical field
  • Minimum 4 plus years’ experience in product quality or regulatory compliance (or combined experience) in the medical device or other regulated industry.
  • Has general understanding of applicable US medical device regulations (e.g., 21 CFR Part 820, 21 CFR Part 11), international standards (e.g., ISO 13485, ISO 14971), and international regulations (e.g., CMDR – Canada, European, RDC – Brazil)
  • Experience with computer regulations/standards and methodologies
  • Strong organizational, written, and verbal communication skills; plus critical thinking skills and proficient in constructive dialogue
  • Effective at prioritizing tasks and responsibilities within a fast-paced, dynamic environment
  • Effective in collaborating and partnering with field action team and displaying an appropriate level of assertiveness
  • • Experience working directly with the FDA, Notified Body, or other governmental agencies (preferred).


We offer a competitive salary range for this position. Most candidates who join our team are hired at the median of this range, ensuring fair and equitable compensation based on experience and qualifications.


Contractor benefits are available through our 3rd Party Employer of Record (Available upon completion of waiting period for eligible engagements) Benefits include: Medical, Dental, Vision, 401k.

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

All applicants applying for U.S. job openings must be legally authorized to work in the United States and are required to have U.S. residency at the time of application.

If you are a person with a disability needing assistance with the application, or at any point in the hiring process, please contact us at support@themomproject.com.