QA Specialist I - Document Control
Company: ADMA BIOMANUFACTURING LLC
Location: Boca Raton
Posted on: June 25, 2022
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Job Description:
Job DetailsJob LocationADMA Biologics - Boca Raton, FLJob
CategoryQA - Quality ControlDescriptionADMA Biologics is a
biopharmaceutical company relentlessly committed to creating
superior products for immunodeficient patients at risk for
infection. It is our devotion to this underserved population that
fuels us and our hands-on approach to production and development
that sets us apart. If you are looking for a dynamic, innovative,
growing company in the biopharmaceutical industry that is committed
to excellence and integrity, then consider ADMA Biologics. The QA
Specialist I - Document Control will create, format, revise and
proofread controlled documents such as Standard Operating
Procedures (SOPs), Forms, Validations, etc. from departments
including but not limited to Quality Assurance, Manufacturing,
Facilities, and Quality Control. Perform general office duties such
as photocopying, word processing, filing, scanning, physical
inventory, ordering supplies.QualificationsCreate, format, revise
and proofread controlled documents such as Standard Operating
Procedures (SOPs), Forms, Validations, etc. from departments
including but not limited to Quality Assurance, Manufacturing,
Facilities, and Quality Control. Enforce limited access
restrictions of secured controlled documents in the electronic and
physical document locations.Process documents for approval
signatures, official distribution, and absolution. Assist with
maintaining inventory of on-site documentationAssist with the
maintenance of document retention and destruction schedules.Perform
general office duties such as photocopying, word processing,
filing, scanning, physical inventory, ordering supplies,
etcProficient in cGMPs.Proficiency in computer systems
requirements, validations, role and training assignments.
Willingness to take on new projects Education Requirements: High
School diploma required. Bachelor's Degree preferred but can be
offset by work experience. Experience Requirements: 1-2 years
experience with in pharmaceutical or biotechnology industry and
document management systems and software.In addition to competitive
compensation, we offer a comprehensive benefits package
including:401K plan with employer match and immediate
vestingMedical, Vision, Life and Dental InsurancePet Insurance
Company paid Short and Long-Term Disability PlansCompany Paid
Holidays 3 Weeks' Paid Time Off (within the first year)Tuition
Assistance (after the first year)Easily accessible to Tri-RailFree
shuttle to the Boca Tri-Rail stationADMA Biologics uses E-Verify to
confirm the employment eligibility of all newly hired employees. To
learn more about E-Verify, including your rights and
responsibilities, please visit www.dhs.gov/E-Verify. ADMA Biologics
is an Equal Opportunity Employer.
Keywords: ADMA BIOMANUFACTURING LLC, Boca Raton , QA Specialist I - Document Control, Other , Boca Raton, Florida
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