Pharmaceutical Manufacturing Documentation Specialist – PMDS 25-22542 Position Available In Guilford, North Carolina

Pharmaceutical Manufacturing Documentation Specialist – PMDS 25-22542 NavitsPartners Greensboro, NC Job Details Contract $29 an hour 1 day ago Qualifications Microsoft Powerpoint Microsoft Word CGMP Microsoft Excel Engineering GMP Mid-level High school diploma or GED Bachelor’s degree Manufacturing 2 years

Full Job Description Job Title:

Pharmaceutical Manufacturing Documentation Specialist Location:

Durham, NC (Onsite)

Duration:

6-

Month Contract Rate:

$29.00/hour (W2)

Job Description:

Provide documentation support for vaccine manufacturing processes. Review batch records, logbooks, and electronic records for errors; collaborate with Production, Quality, and other departments to resolve discrepancies. Support updates and improvements to batch records and standard operating procedures (SOPs). Maintain and utilize metrics to track performance of manufacturing documentation processes. Assist in deviation investigations by contributing meaningful corrective and preventive actions aimed at reducing deviation frequency. Use standard business software tools including MS Word, Excel, PowerPoint, Outlook, and Teams. This role is part of the Manufacturing Support Team, interacting closely with shop floor production, Technical Support, and Quality Operations. The ideal candidate thrives in a fast-paced environment, is hands-on when needed, and has a strong attention to detail, with a solid grasp of Good Documentation Practices (GDP).

Qualifications:

Education:

Bachelor’s degree in Science, Engineering, English, Business, or a related discipline OR High School Diploma with at least two years of GMP Biopharmaceutical industry experience

Required Skills:

Strong independent work ethic and collaborative team player Demonstrated values of Integrity, Precision, Accomplishment, Ambition, Respect, and Inclusion Excellent critical thinking and problem-solving capabilities Working knowledge of current Good Manufacturing Practices (cGMPs) and industry regulations Experience with document creation, review, and approval in a GMP environment Must complete and pass BCG medical clearance, including questionnaire, blood test, and chest X-ray