Quality Engineer, Medical Devices – Wilmington, DE – Katalyst HLS


identify, document & implement V&V process improvements and inter-departmental coordination to more efficiently conduct end to end development/test/to market cycle.
https://www1.jobdiva.com/candidates/myjobs/openjob_outside.jsp?a=irjdnw4aqkb0a5bhkjucv8p00hyqhk05031z6ahtakm0pgjg8f34dc29wtyqerjr&from=COMP&id=11385731&SearchString=&StatesString=&jobseq=2&rowsperpage=30&divisions=&divisions2=

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Quality Control job – Katalyst HealthCares & Life Sciences – Boston, MA |


July 16, 2018 – Quality Control – p b Responsibilities: /b /p ul li The Contractor, Quality Control is responsible for the day-to-day oversight of analytical testing at contract
https://www.indeed.com/viewjob?t=quality+control&jk=784e2730d916f27c&_ga=2.226626910.252329648.1531907807-1408033885.1530798869

Quality Control job – Katalyst HealthCares & Life Sciences – Boston, MA | Indeed.com


July 16, 2018 – Quality Control – p b Responsibilities: /b /p ul li The Contractor, Quality Control is responsible for the day-to-day oversight of analytical testing at contract
https://www.indeed.com/viewjob?t=quality+control&jk=784e2730d916f27c&_ga=2.145052980.141253053.1531760607-366033881.1528839132

Quality Engineer, Medical Devices, Wilmington, DE – Katalyst HLS


Medical Device Testing Analyst responsible for testing background and experience to identify, document & implement V&V process improvements and inter-departmental coordination to more efficiently conduct end to end development/test/to market cycle.
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Senior Quality Engineer job – Katalyst HealthCares & Life Sciences – Warsaw, IN


April 16, 2018 – Senior Quality Engineer – p b Job Description: /b /p ul li Coordinate design Assurance activities in support of product development and life cycle processes between
https://www.indeed.com/viewjob?t=senior+quality+engineer&jk=d9574fa57fab03fc&_ga=2.164653564.21866735.1523909483-251423520.1515107595

Senior Quality Engineer Katalyst HLS


Job Description:
The Principal Pharma Quality Engineer will provide quality assurance expertise for the development, site transfer, manufacturing and testing of combination medical device/drug products for the Fridley CRHF (Rice Creek) Pharmaceutical Operations business.
In this role, you would provide quality engineering support in sterilization management, environmental control, and cGMP pharmaceutical manufacturing of combination products including analytical lab activities. Provide support to internal and external customers, perform root cause analysis and implement corrective action. May manage projects for new or revised products or quality system changes in cGMP pharmaceutical requirement of combination products. Provides coaching on cGMP regulations and all relevant standards to Quality and Manufacturing Engineering staff. to staff.
CRHF seeks candidates who will meet our customer expectations by striving without reserve for the greatest possible reliability and quality in o
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