- Participate in New Product Development Risk Analysis including FMEA and PFMEA.
- Assist in supplier qualification develop receiving inspection and Ship to Stock (SOS) program.
- Work with different departments to develop and review processes ensuring product quality such as inspection techniques raw material inspections and inprocess checks.
- Investigate customer concerns perform evaluations and prepare CAPAs for nonconforming products.
- Lead process validation for equipment and processes.
- Prepare documentation for UL IEC and FDA submissions as required by Regulatory Affairs.
Qualifications :
- Bachelors degree with at least 5 years of experience manufacturing operations.
- ASQ CQE preferred.
- Experience with or knowledge of FDA regulated industries is a plus.
- Ability to make recommendations to effectively solve problems using judgment consistent with standards practices and company capabilities.
- Proficient in Microsoft word and excel and able to learn other software packages easily.
- Strong independent work ethic and ability to multitask.
Additional Information :
The Rewards:
Comprehensive Benefit Package
- 401(k) with Company Match
- Competitive Health Dental and Vision insurance plans
- Paid Vacation Holidays and Personal Days
- Paid Life Insurance Employee Assistance Program and ShortTerm Disability
All qualified applicants will receive consideration for employment without regard to race color gender identity or expression age religion intellectual disability mental disability physical disability including but not limited to blindness unless it is shown that such disability prevents performance of the work involved medical condition handicap national origin ancestry sexual orientation marital status domestic partnership status parental status military status veteran or military discharge status or housing status or any other status protected by applicable law. GF Health Products Inc. is a drug free workplace.
Remote Work :
No
Employment Type :
Fulltime