BD (Becton, Dickinson and Company) Advanced Quality Engineer II in Irvine, California
Job Description Summary
BD Interventional’s Surgery business unit is a leading developer, manufacturer, and marketer of innovative, life-enhancing medical technologies. We have stood out as the market leader in providing solutions in soft tissue reconstruction including products for hernia repair, specialized surgical procedures, fixation and biologic implants. In addition to this extensive suite of products, our BioSurgery business is delivering a growing line of enhanced sealants and hemostatic products to complement surgical techniques across, thoracic, cardiovascular and other surgical specialties.
Our company has a strong tradition of developing our employees to learn, grow and excel. We are continually building our team with qualified, team oriented individuals to enhance the success of our company.
The Irvine Plant is situated in in the heart of Orange County with easy access to the expansive coastline, John Wayne Airport, Amtrak and Metrolink. Our office is within a 20 minute drive to local attractions including Laguna, Huntington and Newport beaches, Disneyland, Los Angeles Angels Stadium, the Honda Center of Anaheim, and is just a short distance to San Diego and Los Angeles.
Summary of Position with General Responsibilities:
The Advanced Quality Engineer II (Operations) will lead activities involving product impact assessments for events, product quarantine activities, non-conformance reporting/issue resolution, auditing of production areas, and procedural updates to ensure the process and documentation is compliant with 21CFR820, ISO 13485, and other regulatory requirements as well as internal requirements.
Essential job Functions:
Initiates and leads QA Operations process improvements from start to implementation including creating/revising procedures using the MasterControl Change Control system.
Actively participates in MRB by providing direction and support on the non-conformance process, product impact assessment, root cause analysis, and product quarantine as non-conformances arise. Ensures non-conformance reports are initiated per established requirements and applicable activities are identified and implemented.
Audits personnel and processes in manufacturing areas for practice versus procedures and against current regulatory requirements (FDA, ISO, etc.). Analyze audit results for trends and provide feedback to site management.
Responsible for performing Product Quarantine activities, such as entering product into quarantine, completing quarantine documentation, reviewing/disposition non-conformance records for quarantine release and removal of product from quarantine area.
Leads investigations and corrective action to address out-of-tolerance calibration results, quality events, audit nonconformances, and CAPAs.
Develops or assists in the development of Process Validation documentation such as protocols and reports (IQ, OQ, PQ), executes qualifications, and performs statistical analysis as required.
Creates and executes component qualification protocols and reports
Supports risk management activities including review and development of process FMEAs
Interact in a team environment with Operations, Quality Engineering, Regulatory, and Engineering personnel and participate in project team to help improve the process and increase product quality while keeping within compliance with site Quality Systems procedures.
Lead and/or support other duties as assigned.
B.S. Degree in Engineering or related field with a minimum of 3 years relevant experience or M.S. Degree in Engineering or related field with a minimum of 2 years relevant experience or an equivalent combination of education and experience
Experience in Quality Engineering disciplines including product/process validation, applied statistics and technical problem solving
Strong Compliance understanding especially in post-market activities including complaints, failure investigations, nonconforming material and CAPAs.
Experience in Risk Management activities.
Relevant medical device experience.
Applied Knowledge of the requirements of FDA QSR, ISO13485 and ISO 14971.
ASQ certification preferred.
Experience with metrology and/or calibration instrumentation preferred.
Excellent problem solving and project management skills.
Must have a positive attitude with excellent communication, negotiation and interpersonal skills to maintain a team oriented environment.
Ability to thrive under challenging deadlines and in an energetic environment.
Ability to manage multiple projects, communicate updates, and meet milestones in a timely fashion.
Additional Desirable Qualifications Skills and Knowledge:
- Travel - Approximately 10% of work time may be spent traveling
Physical demand - the physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to stand, walk, and sit for extended periods of time. Occasionally the employee will be required to lift or moved at least 50 pounds.
Mental demand - Moderate to high degree of concentration due to volume, complexity, and/or "pressure" of work. Expected to meet project deliverables that may require significant time commitments and support.
BD Interventional and Becton Dickinson are Affirmative Action/Equal Opportunity Employers, M/F/D/V. VEVRAA Federal Contractor.
Primary Work LocationUSA CA - Irvine Neomend
Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.