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Quality Assurance Technician

Bentec Medical Opco LLC

Woodland, CA

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JOB DETAILS
JOB TYPE
Full-time
SKILLS
Analysis Skills, Business Writing, Calibration, Change Control, Coaching, Code of Federal Regulations, Communication Skills, Corrective Action, Cross-Functional, Current Good Manufacturing Practice (cGMP), Customer Relations, Customer Support/Service, Data Collection, Educational Technology, External Audit, FDA (Food and Drug Administration), Government Regulations, ISO (International Organization for Standardization), Information Technology/Systems Audit, Internal Audit, Inventory Management, Leadership, Maintain Compliance, Mathematics, Medical Equipment, Microsoft Office, Plane Geometry, Presentation/Verbal Skills, Process Management, Product Safety, Purchase Orders, Purchasing/Procurement, Quality Assurance, Quality Assurance Methodology, Quality System Requirements (QSR), Regulations, Regulatory Requirements, Reporting Skills, Root Cause Analysis, Solid Geometry, Systems Analysis, Team Player, Technical Writing, Theater Production, Trigonometry, Vendor/Supplier Evaluation, Writing Skills
LOCATION
Woodland, CA
POSTED
8 days ago
Job Description

Job Title:            Quality Assurance Technician

Summary
Coordinate the quality assurance systems in accordance with all applicable regulations.  Provide leadership and support for customer focused quality and quality system improvement initiatives by performing the following duties personally or through responsible process owners/supervisors/managers.

Essential Duties and Responsibilities
Duties include, but not limited to the following.  Other duties may be assigned.
  • Coordinate quality assurance processes (NCR, Corrective and Preventative Action, Complaint Handling, Product Safety, Change Control, validation programs, Supplier Qualification and Monitoring, Calibration Program, Internal Audit Program, etc.) in compliance with Medical Device industry requirements (ISO 13485, FDA CFR Title 21 Part 820, etc.).
  • Coordinate/assist during various quality system audits:  Internal Audits and External (Customer/Third Party) audits for Supplier Qualification and for Quality System certifications.   Assess improvement initiatives resulting from all quality audits.
  • Perform QA Final Release activities for all stages of production (incoming, in-process, and finished goods).
  • Interprets specifications, drawings and requirements.
  • Manage area inventories using Purchase Requisitions and Material Transfers.
  • Works with cross functional team members to ensure compliance with FDA/cGMP, ISO and other regulatory requirements.
  • Perform training to support team and foster team environment.  Coach and guide employees to support departmental priorities in a positive way.


Qualifications
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.  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.

Education and/or Experience
Bachelors degrees (BA) from four-year college or university or one to two years related experience and/or training; or equivalent combination of education and experience.

Language Skills
Ability to read, analyze and interpret general business periodicals, professional journals, technical procedures or governmental regulations.  Ability to write reports, business correspondence and procedure manuals.  Ability to effectively present information and respond to questions from groups of managers, clients, customers and the general public.

Mathematical Skills
Ability to work with mathematical concepts such as probability and statistical inference and fundamentals of plane and solid geometry and trigonometry.  Ability to apply concepts such as fractions, percentages, ratios and proportions to practical situations.

Reasoning Ability
Ability to define problems, collect data, establish facts and draw valid conclusions.  Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables.

Other Skills and Abilities
Working knowledge of cGMP (QSR), ISO 13485 and Medical Device Directives.  Knowledge of Microsoft Office computer programs and previous technical writing experience with clear written and verbal communication skills.  Basic knowledge of quality tools (flow diagramming, histograms, root cause analysis and pareto charts) is desirable. 
 

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About the Company

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Bentec Medical Opco LLC