(job) Sr QA Auditor - Southbridge, MA
A client of mine in Southbridge, MA is seeking a Senior QA Auditor. They are
the world's leading provider of critical research products and integrated
preclinical support services for the biomedical community to enable
innovative and efficient drug discovery and development.
Reporting to the Director of Quality Assurance/Regulatory Compliance. Senior
position at Southbridge facility, will be the primary individual to
implement GLP compliant systems at the facility. Will be responsible with
the Director of Regulatory to set up key systems for auditing, training,
document control, client and agency inspections. Will work with senior staff
at Southbridge and support person for all regulatory inspections.
REQUIREMENTS: BS in biology or other scientific related field, with 5 or
more years of QA experience working in the pharmaceutical, Biotech or CRO
industry specifically for GLP toxicology programs with large animal species
experience (dogs, NHP, sheep, cattle, etc). Experience in both a CRO and
large Bio/Pharm is preferred. Must have a high level of understanding of
GLP's (domestic and foreign), specific experience with toxicology, computer
validation/part 11 experience. Must have the ability to communicate with all
levels of staff; to manage multiple priorities; independently work on
established goals; and look to move into a leadership role in regulator.
What do you think? If you are interested in pursuing this opportunity,
please forward to workwonders at earthlink.net:
-your resume in word or text format
-your salary requirement
-your citizenship status.
If you aren't interested or feel you are not qualified, do you know anyone
who would be interested? We do offer generous referral fees.
Thanks for your time and have a great day!
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