QA Documentation Specialist (GMP)
Company: Vale Group
Location: Hillside
Posted on: May 4, 2024
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Job Description:
Be sure to follow our LinkedIn company page for the latest
updates on all our open jobs!We are seeking a qualified QA
Documentation Specialist to work onsite for an opportunity paying
up to $70K salary based on experience, which is located in
Hillside, NJ. This role is crucial for maintaining the integrity
and accuracy of documentation within the Quality Assurance
department. The ideal candidate will ensure that all documentation
processes meet regulatory standards and help maintain a consistent
workflow for quality assurance across the company.Benefits of the
QA Documentation Specialist include: Excellent career growth
opportunity as well as highly competitive benefits.Requirements of
the QA Documentation Specialist: At least 2 years of experience in
documentation management or quality assurance Bachelors degree in a
relevant field Knowledge of cGMP guidelines and regulatory
compliance Exceptional attention to detail and strong
organizational skills Proficiency in documentation software and
systems Skills in managing large datasets and complex information
structures Experience in the pharmaceutical or manufacturing sector
is a plusResponsibilities of the QA Documentation Specialist:
Develop, review, and maintain documents and manuals according to
regulatory standards Manage the document lifecycle from creation to
archiving Ensure documentation clarity, accuracy, and accessibility
Assist in training staff on document control processes and
compliance Collaborate with various departments to ensure
documentation requirements are met Conduct regular reviews and
audits of documents to ensure compliance with industry standards
Support the team as neededInterested or know of someone qualified
who might be? Click Apply or share the job today!Disclaimer: By
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Keywords: Vale Group, North Bergen , QA Documentation Specialist (GMP), Other , Hillside, New Jersey
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here to apply!
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