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Boston Scientific · 2 months ago

Quality Tech II - 1st Shift

Arden Hills, MN

Full-time

Onsite

Entry Level

$42K/yr - $72K/yr

2+ years exp

Boston Scientific is a leader in medical science, committed to solving important health industry challenges. The Quality Tech II role involves providing technical assistance to engineering to support manufacturing efforts by implementing corrective and preventative actions, as well as assisting in process improvements and compliance audits.

Health CareMedicalMedical Device

No H1B

Responsibilities

Assists engineering in providing manufacturing support by learning to analyze data and identify manufacturing issues and trends. May also train operators on basic processes and engineering changes and perform operator certification on-the-job training and testing

Assists in identifying Manufacturing issues by working with Engineering to determine root cause and implement corrective and preventative action

Learns process to disposition non-conforming material by utilizing quality tools and by developing knowledge of manufacturing practices and procedures

Helps to develop and implement process improvements by assisting Engineering in researching and validating changes in processes/equipment and test methods to improve yield and/or reduce cycle time per established procedures

Assists Engineering in supporting process development during new product introduction by providing input to traceability and inspection requirements, providing input for statistical process control criteria, developing manufacturing instructions, and creating training sheets and certifications. May also train operators on processes and engineering changes and perform operator certification on-the-job training and testing

Assists Engineering with qualification and validation studies & reports by collecting, compiling, measuring, organizing/recording data, and by writing procedures. May keep lab notebook

Conducts audits of manufacturing and related areas to assess compliance with internal procedures; reviews finding to determine compliance risk and systems issues. Prepare and administer reports of audit findings and participate in post audit conference to discuss them

Evaluates corrective action plans for applicability and effectiveness

Responsible for the final Process Monitor Release for products prior to distribution

Assists Engineers in developing or changing manufacturing instructions

Assists Engineers in monitoring traceability and inspection requirements, statistical process control criteria, and manufacturing practices and procedures

Assist engineers in failure analysis

Lead and participate in continuous improvement projects

Proactively audit the line to identify and escalate Quality opportunities

Own and/or participate in NCEPs