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Qa Supervisor Jobs

Company

Integra LifeSciences

Address , Añasco, Pr
Employment type FULL_TIME
Salary
Expires 2023-10-06
Posted at 9 months ago
Job Description
Changing lives. Building Careers.

Joining us is a chance for you 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, more than 4,000 of us are challenging what’s possible and making headway to help improve outcomes.
Responsible for assuring that raw materials purchased by Integra meet specifications. Develop and implements systems, procedures and policies to assure the area operates effectively, manage human resources in accordance with company goals and regulatory requirement. Ensure the efficacy, the quality and reliability of the Incoming Inspection of the facility. Knowledge in EN’s, ISO Standards, FDA QSR., Canadian Regulation and ISO 10993. This job description is designed to outline the primary functions and qualifications of this position. This definition does not limit the employee or Integra to just the areas described. It does not identify all tasks that may be required or address performance exceptions, nor does it limit Integra from changing the content. The job description does not constitute an employment agreement between the employer and employee. Assure the performance of the Incoming Inspection area through chemical and physical tests required for raw materials and other components in order to approve their release for use in manufacturing operations. Conducts laboratory/supplier research when necessary to help in the solution of raw material related problems.
1. Directly supervises/manages the incoming inspectors and product release area assuring compliance to company policies.
2. Monitor Incoming raw material testing to procedures, CGMP's, QSR, GLP's and ISO Series.
3. Implements projects/programs that lead to better efficiency at lower costs.
4. Participates in supplier audits.
5.Coordination of workload for incoming inspection, 1st articles, and other test requirements.
6. The investigation of raw material non-conformances.
7. Evaluate and approve inspection test results.
8. Assures maintenance of skip-lot log books. Verifies each has a rationale.
9. Coordinates finger-lift/heavy truck license renewals; calibration of equipment.
10. Train subordinates and direct them to achieve company goals. Help develop professional capabilities in subordinates.
11. Assures all areas of responsibility are in full compliance with ISO QSR Series, GMP, OSHA, company and other legal requirements.
12. Other responsibilities as assigned by Quality Management.
Qualification:
Education and Experience:
  • One to three years of experience supervising or coordination of a work group in an FDA regulated industry.
  • Knowledgeable in the use of statistical sampling required.
  • Fully bilingual English/Spanish
  • B.S. in Engineering, Science or Business Administration
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
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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 [email protected] or call us at 855-936-2666.
Integra - Employer Branding from Integra LifeSciences on Vimeo