Orion Group
Join Orion Group as a Documentation Coordinator for a Leading Pharmaceutical Client in Branchburg, NJ!
Documentation Coordinator
6-month contract to start M-F 7:30 am-4 pm
$22-26/HR
Are you detail-oriented and passionate about accuracy in the pharmaceutical field?
Orion Group is looking for a
Documentation Coordinator
to support critical documentation processes that ensure product quality and regulatory compliance. This is your opportunity to work with a respected industry leader and grow your career in a dynamic, collaborative environment.
What You'll Do: As a Documentation Coordinator, you'll play an essential role in maintaining compliance and accuracy across all documentation processes. Your responsibilities will include:
Creating PI sheets in the ERP system and obtaining serological test results via email, fax, and tissue portal. Verifying and cross-referencing TRP paperwork and labels against the ERP system and RFID labels. Interpreting test results in compliance with
FDA regulations, state requirements, and AATB standards . Entering and verifying serological and microbiology results, ensuring accuracy for medical review. Managing final disposition decisions and donor chart grading within the ERP system. Assembling complete donor files, performing data entry, reconciling documents, and supporting Tissue Services Portal operations. What We're Looking For:
Education:
High school diploma required; Bachelor's degree preferred. Experience:
1-3 years in GMP environments; medical or pharmaceutical industry experience is a plus. Skills:
Strong attention to detail, accurate data entry, and familiarity with medical terminology. Why Join Us?
Work with an
industry-leading pharmaceutical client
in a regulated, high-impact environment. Gain valuable experience in
compliance, quality control, and ERP systems . Opportunity for
career growth
in the pharmaceutical and biotech industry. Take the next step in your career and apply today!
Our role in supporting
diversity
and
inclusion As an international workforce business, we are committed to sourcing personnel that reflects the diversity and values of our client base but also that of Orion Group. We welcome the wide range of experiences and viewpoints that potential workers bring to our business and our clients, including those based on nationality, gender, culture, educational and professional backgrounds, race, ethnicity, sexual orientation, gender identity and expression, disability, and age differences, job classification and religion. In our inclusive workplace, regardless of your employment status as staff or contract, everyone is assured the right of equitable, fair and respectful treatment.
Documentation Coordinator
6-month contract to start M-F 7:30 am-4 pm
$22-26/HR
Are you detail-oriented and passionate about accuracy in the pharmaceutical field?
Orion Group is looking for a
Documentation Coordinator
to support critical documentation processes that ensure product quality and regulatory compliance. This is your opportunity to work with a respected industry leader and grow your career in a dynamic, collaborative environment.
What You'll Do: As a Documentation Coordinator, you'll play an essential role in maintaining compliance and accuracy across all documentation processes. Your responsibilities will include:
Creating PI sheets in the ERP system and obtaining serological test results via email, fax, and tissue portal. Verifying and cross-referencing TRP paperwork and labels against the ERP system and RFID labels. Interpreting test results in compliance with
FDA regulations, state requirements, and AATB standards . Entering and verifying serological and microbiology results, ensuring accuracy for medical review. Managing final disposition decisions and donor chart grading within the ERP system. Assembling complete donor files, performing data entry, reconciling documents, and supporting Tissue Services Portal operations. What We're Looking For:
Education:
High school diploma required; Bachelor's degree preferred. Experience:
1-3 years in GMP environments; medical or pharmaceutical industry experience is a plus. Skills:
Strong attention to detail, accurate data entry, and familiarity with medical terminology. Why Join Us?
Work with an
industry-leading pharmaceutical client
in a regulated, high-impact environment. Gain valuable experience in
compliance, quality control, and ERP systems . Opportunity for
career growth
in the pharmaceutical and biotech industry. Take the next step in your career and apply today!
Our role in supporting
diversity
and
inclusion As an international workforce business, we are committed to sourcing personnel that reflects the diversity and values of our client base but also that of Orion Group. We welcome the wide range of experiences and viewpoints that potential workers bring to our business and our clients, including those based on nationality, gender, culture, educational and professional backgrounds, race, ethnicity, sexual orientation, gender identity and expression, disability, and age differences, job classification and religion. In our inclusive workplace, regardless of your employment status as staff or contract, everyone is assured the right of equitable, fair and respectful treatment.