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Form of workJob Description
Benefits:
DESCRIPTION:
Primary responsibilities include ensuring the quality of all products. You will also be required to review/maintain quality system documents and records; be involved in new mold/product validation, cross qualifications, and continuous improvement activities; and be assigned daily 5S and/or process audits.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
Participate in product design reviews.
Resolve internal product quality issues to reduce defects/scrap.
Be on the CAPA team.
Participate in resolving customer on-site quality issues and/or quality reviews.
Perform part specific quality training.
Perform daily 5S and process audits.
Verify and validate reports after mold repair, including capability studies, gauge R & Rs, first article reports, etc.
Develop and maintain statistical process control database for new medical components.
Perform daily inspection of product on the production floor.
Support Internal Audits, Customer Audits, and ISO/QS Audits
Assist in procedure development and/or maintenance.
Responsible for MRB disposition of nonconforming products in the absence of the Quality Manager
QUALIFICATIONS:
Degree in engineering or related discipline.
Plastics experience.
Manufacturing experience with excellent problem-solving skills and the ability to perform root cause analyses.
Must have experience in CMM, GD&T, Vision Systems and Minitab.
Demonstrated teaching skills, with a desire and the ability to train and mentor others.
Previous quality control experience to include data collection and quality analytics.
Knowledge of data collection and some Statistical Quality/Process Control.
Excellent written/verbal communications and organizational skills.
Flexibility to work additional hours when necessary.
Must be able to lift to 50 lbs.
This position is at our clients Vermont manufacturing facility. Compensation based on experience.
- STLTD
- Pet Insurance
- Life Insurance
- FSA
- 401(k)
- Competitive salary
- Dental insurance
- Health insurance
- Paid time off
- Vision insurance
DESCRIPTION:
Primary responsibilities include ensuring the quality of all products. You will also be required to review/maintain quality system documents and records; be involved in new mold/product validation, cross qualifications, and continuous improvement activities; and be assigned daily 5S and/or process audits.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
Participate in product design reviews.
Resolve internal product quality issues to reduce defects/scrap.
Be on the CAPA team.
Participate in resolving customer on-site quality issues and/or quality reviews.
Perform part specific quality training.
Perform daily 5S and process audits.
Verify and validate reports after mold repair, including capability studies, gauge R & Rs, first article reports, etc.
Develop and maintain statistical process control database for new medical components.
Perform daily inspection of product on the production floor.
Support Internal Audits, Customer Audits, and ISO/QS Audits
Assist in procedure development and/or maintenance.
Responsible for MRB disposition of nonconforming products in the absence of the Quality Manager
QUALIFICATIONS:
Degree in engineering or related discipline.
Plastics experience.
Manufacturing experience with excellent problem-solving skills and the ability to perform root cause analyses.
Must have experience in CMM, GD&T, Vision Systems and Minitab.
Demonstrated teaching skills, with a desire and the ability to train and mentor others.
Previous quality control experience to include data collection and quality analytics.
Knowledge of data collection and some Statistical Quality/Process Control.
Excellent written/verbal communications and organizational skills.
Flexibility to work additional hours when necessary.
Must be able to lift to 50 lbs.
This position is at our clients Vermont manufacturing facility. Compensation based on experience.
