Senior Quality Engineer I - Validations, Risk Management & Statistics

Changing lives. Building Careers.

Joining us is a chance to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, our colleagues are challenging what's possible and making headway to innovate new treatment pathways to advance patient outcomes and set new standards of care.

The Sr. Q uality Engineer / Quality Operations (Validations, Risk Management & Statistics) will provide Plant Quality compliance support for the following Quality tasks and duties : Assist in the Introduction and launching of new or improved products and processes into the Manufacturing Site. Participate in problem solving teams. Facilitate from a Quality Engineering & Quality Systems and Plant perspective the launching of new or improved products / processes. Provide guidance on the development and implementation of new and updated Quality System procedures for ISO / QSR, such as validation protocols, manufacturing procedures, product & material specifications, design & development documentation, SOPs, development and task force projects. Facilitates the development, implementation and monitoring of quality programs and policies that ensure that the development, manufacture and distribution of medical products is in compliance with corporate policies, U.S. Food and Drug Administration regulations, ISO 9001, ISO 13485, the Medical Device Directive, the Canadian Medical Device Regulations (CMDR), and other applicable regulatory agencies.

Primary responsibilities are :

(Validations, Risk Management and Statistical Process Controls)

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

Assists in the launching of new or improved products / processes, and the transfer of technology from development to commercialization from a Quality and manufacturing perspective.

Providing guidance on the development and implementation of new and updated Quality System procedures for ISO / QSR, such as validation protocols, manufacturing procedures, product & material specifications, design & development documentation, SOPs, development and task force projects.

Participate in the execution of Process FMEA and other applicable risk analysis documentation as deemed appropriate.

Develop statistically based sampling plans for in-process and finished goods testing, inspections, validations and where required. Provide Statistical Analysis of the data to support all Quality Systems documentation such as validations, NCs, Complaints, etc.

Develop, review and approve validations and completion reports for new and existing products, processes and equipment.

Prepare monthly and quarterly trending, including Statistical Process Control documentation, and support the Quality Management Review Process.

Maintains a thorough understanding of the following regulations and guidelines : U.S. Food and Drug Administration (FDA) regulations, ISO 9001, ISO 13485 : 2003, Medical Device Directive (MOD), the Canadian Medical Device Regulations (CMDR), Integra Corporation's policies and procedures, and other applicable regulatory agency requirements.

Participate in FDA inspections, ISO Certification and surveillance audits and customer audits.

Perform other Quality Assurance and Quality Engineering related duties as required.

The requirements listed below are representative of the knowledge, skill and / or ability required for his position.

Education : Bachelor's Degree in engineering preferred (Biomedical, mechanical, chemical, or electrical) or Science (Biology).

Certifications : ASQ CQE preferred

Experience : 6 to 8 years of experience in a Quality Assurance role for medical device or pharmaceutical manufacturing.

Demonstrates knowledge of statistical sampling and analysis.

Demonstrates excellent organizational, communication, and project management skills

Proficient with the MS Office Suite, and statistical software.

Must be able to work independently with minimal supervision.

Able to prioritize projects to meet organizational goals and objectives

Salary Pay Range :

$81,650.00 - $112,700.00 USD Salary

Our salary ranges are determined by role, level, and location. Individual pay is determined by several factors including job-related skills, experience, and relevant education or training . In addition to base pay, employees may be eligible for bonus, commission, equity or other variable compensation . Your recruiter can share more about the specific salary range for your preferred location during the hiring process.

Additional Description for Pay Transparency :

Subject to the terms of their respective plans, employees and / or eligible dependents are eligible to participate in the following Company sponsored employee benefit programs : medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance, and savings plan (401(k)).

Subject to the terms of their respective policies and date of hire, Employees are eligible for the following

Integra LifeSciences is an equal opportunity employer, and is committed to providing equal employment opportunities to all qualified applicants and employees regardless of race, marital status, color, religion, sex, age, national origin, sexual orientation, physical or mental disability, or protected veteran status.

This site is governed solely by applicable U.S. laws and governmental regulations. If you'd like more information on your rights under the law, please see the following notices :

EEO Is the Law () | EOE including Disability / Protected Veterans ()

Integra LifeSciences is committed to provide qualified applicants and employees who are disabled veterans or individuals with disabilities with needed reasonable accommodations in accordance with the ADA () . If you have difficulty using our online system due to a disability and need an accommodation, please email us at careers@integralife.com.

Unsolicited Agency Submission

Integra LifeSciences does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. A formal written agreement is required before engaging any agency, and it must be executed and authorized by the Vice President, Talent Acquisition. Where agency agreements are in place, introductions (the initial sharing of a candidate's name, resume, or background) are position-specific and may only occur within the scope of that approved agreement. Please, no phone calls or emails.

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