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Senior Quality Analyst at Boston Scientific Corporation Malaysia
, , Canada -
Full Time

Start Date

Immediate

Expiry Date

03 Mar, 26

Salary

0.0

Posted On

03 Dec, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Six Sigma Black Belt, Lean-Six Sigma, SPC, FMEA, MSA, DOE, Quality Systems, GMP, Validation Methodology, Computer Systems Validation, Process Capability, Critical To Quality, Change Management, Business Relationships, Manufacturing Systems, Unionized Environment

Industry

Medical Equipment Manufacturing

Description
Minimum Bachelor's Degree in Science or Engineering Six Sigma Black Belt or equivalent certification trainings and/or experience Advanced knowledge and working experience of lean-six sigma related tools, including, but not limited to SPC, FMEA, MSA, DOE and Quality Systems 5+ years' experience in manufacturing or equivalent with direct experience in a GMP regulated environment, preferably in a quality/engineering role Experience in the medical device or pharmaceutical industry is an advantage Working knowledge of validation methodology, including computer systems validations Enhanced understanding of processes and how they impact the quality of a product, including but not limited to, process capability, critical to quality, critical processing parameters and monitoring Ability to travel domestically and/or internationally up to 20% Highly influential individual who has successfully influenced and sustained change in working environments with a wide array of existing challenges Ability to quickly establish business relationships with colleagues and external partners Experience with implementation of computer systems to support manufacturing and testing capabilities Experience influencing and implementing change in a unionized environment
Responsibilities
The Senior Quality Analyst will be responsible for ensuring product quality through the application of quality systems and methodologies. This role involves influencing and implementing changes to improve processes in a GMP regulated environment.