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Listed below are the top 10 out of 57 listings that are in the same industry and location as the job you were looking for. To see more than 10 listings, click here to search similar jobs in Andover, MA
Description One of the world's leading biotechnology companies, Genzyme is dedicated to making a major positive impact on the lives of people with serious diseases. ...
Description One of the world's leading biotechnology companies, Genzyme is dedicated to making a major positive impact on the lives of people with serious diseases. ...
Description One of the world's leading biotechnology companies, Genzyme is dedicated to making a major positive impact on the lives of people with serious diseases. ...
Title: Global QA Compliance Specialist GMP Location: Portsmouth, NH 03801 Contact Person: Tom Hayes Description: A growing, global biotechnology company is ...
Mission: Identification of synthetic lethal metabolic targets based on flux balance analysis modeling Goals Discover synthetic lethal relationships through ...
CANDIDATES WITH AT LEAST 5 YEARS EXPERIENCE IN THIS RELATED AREA > PROCESS ENGINEERING IN THE BIOTECH INDUSTRY.. WORKING WITH BIOTECH EQUIPMENT. MUST BE ABLE ...
Description: This role requires the management of commercial change controls with regulatory impact. The required work involves managing the change records ...
QA team works on healthcare imaging sharing product testing and validation. The goal of the QA team is to... QA process from project planning, balancing QA......
is currently seeking a QA Specialist for a full time... with an emphasis on Validation (Equipment IOPQ, Computer systems, Process Validation etc.), Investigations......
automated testing and validation tools, including... and validation, including white-box and black-box testing.3+ years experience in software QA methodologies......
For your reference, we have included the original job posting below.
QA Validation
Job Number:
42904766
Company Name:
Sunrise Systems Inc
Job Location:
Andover, MA US
Job Category:
Science & Biotech
QA Validation
Description: This role requires the management of commercial change controls with regulatory impact. The required work involves managing the change records through the RCCM work flow and portions of site change control system. The scope of work includes drafting new change records in RCCM and promoting them to GCMC Regulatory for review and approval. Skills: Pharmaceutical/ Clinical Quality Assurance Regulatory Experience. ...