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Manufacturing Quality Engineer
REC10018204 | Updated: May 16, 2020
OPENINGS: 1
JOB TYPE: Full Time
LOCATION: Bethel, Vermont, United States
INDUSTRY: Pharmaceutical / Biotech
SALARY: $75,000.00 - $85,000.00 / year
CATEGORY: Engineering
EDUCATION: Professional Degree
EXPERIENCE: 5-7 years
TRAVEL: Never
RELOCATION ASSISTANCE:
WORK ELIGIBILITY: Green Card, US Citizen
FEES: 9% of Salary
CANDIDATE GUARANTEE TERMS: 30 days
PAYABLE TERMS: 90 days
DATE UPDATED: May 16, 2020
DATE POSTED: Feb 11, 2020
JOB DESCRIPTION
The Manufacturing Quality Engineer is responsible for ensuring the quality of all products, quality system documentation, manufacturing process quality, and customer problem resolution.
Specific Responsibilities
Participates in product design reviews and Engineering hand-off approval.
Resolves internal product quality problems to reduce defects/scrap.
Champions product customer complaint cause and submits corrective action plans in the 8D or customer format.
Participates in and assists in resolving customer on-site quality issues and/or quality reviews.
Oversees and supports Quality Technicians.
Performs specific quality training for Quality Technicians, IPIs, and MQTs.
Develops and maintains QARs (part specific work instructions).
Performs daily 5S and process audits of select injection molding machines against the Master Process and Control Plans.
Verifies and validates reports after mold repair, including capability studies, gauge R & Rs, first article reports, etc.
Annually revalidates medical/automotive components per customer requirements.
Develops and maintains SPC database for medical components.
Performs daily inspection of product/process on the production floor.
Supports internal Audits, Customer Audits, and ISO/QS Audits.
Assists in procedure development and/or maintenance.
Responsible for MRB disposition of nonconforming products in the absence of the Quality Manager.
Other duties as assigned.
Qualifications
Engineering or Science degree desired.
Minimum of 5 years quality engineering experience, with specific experience in medical devices/components desirable.
Knowledge/experience with measurement equipment.
Computer literate in programs such as Word, Excel, and PowerPoint.
Solid statistical knowledge and practical experience.
Knowledge and experience in control plan development, product print and specification understanding, and customer interface experience.
Knowledge of molding process and procedures desired.
FDA/ISO/TS system knowledge and experience.
Good communications skills.
Ability to lift up to 50 pounds.
Certified Quality Auditor and/or Quality Engineer highly desirable.
Ability to travel when needed (less than 5% of the time).
BENEFITS
Medical, Vision, Dental
401k plan,
Paid holidays
QUESTIONS FROM THE EMPLOYER
You will be required to answer the following questions when submitting a candidate to this job
Is the candidate a US Citizen or do they have an active VISA or GreenCard?
If your candidate is selected to be submitted to the hiring manager for further consideration, you agree that the Account Manager for Inuson (Partner) for this client may reach out and speak with your candidate prior to an interview to gather more information and/or prep them for the actual interview, and you will make sure your candidate is aware of this call.
IMPORTANT: All resumes must be submitted with a brief summary that outlines the key qualifications required for this position as per the job description. Please be sure to showcase all skills and experience relevant to each requirement for THIS particular job. This write-up will be forwarded to the client along with the resume.
You can confirm that you have disclosed to your candidate that you are working with (link removed) on the position to avoid any confusion with candidates and clients. (required)
How many years you have worked as a Quality Engineer?
Have you worked in plastic injection molding?
ADDITIONAL INFO
Candidate should have Minimum 3 - 5+ years of experience in manufacturing and plastic injection molding.
Candidate should handle customer complaints and be the potential to work with contractors.
Minimum of 5 years quality engineering experience, with specific experience in medical devices/components desirable.
Knowledge/experience with measurement equipment.
Should have experience in plastic injection molding or plastic manufacturing in medical devices, automobile or Plastic Molded Filtration.
Candidate from New England region will be apt and no job hopping
COMPLIANCE
You will need to confirm the following compliance terms when submitting this candidate
You have directly communicated with this candidate
This candidate wants to be considered for this position
This candidate was obtained in a manner that complies with OFCCP regulations at 41 CFR Part 60-1
Additionally, you'll need to write an introductory note about this candidate, telling the employer why this person is a right fit for the job
ESR Healthcare
