Date Posted: 09/04/2026
Hiring Organization: Rose International
Position Number: 507010
Industry: Medical Equipment & Supplies
Job Title: GMP Document Control Specialist - Part-Time
Job Location: Portage, MI, USA, 49002
Work Model: Onsite
Shift: TBD (20hrs/week)
Employment Type: Temporary
FT/PT: Part-Time
Estimated Duration (In months): 13
Min Hourly Rate($): 30.00
Max Hourly Rate($): 35.00
Must Have Skills/Attributes: Audit, Document Control Procedures, GMP
Experience Desired: Experience in document control, quality documentation, or records management (5 yrs); Managing GMP-controlled documentation, master documents, document revisions, and controlled filing (5 yrs); Hands-on experience reviewing or auditing manufacturing equipment maintenance, repair (3-5 yrs); Experience working in a highly regulated, audit-ready environment (3-5 yrs)
Required Minimum Education: High School Diploma or equivalent
**C2C is not available**
Job Description
Required Education:
• High School Diploma or Equivalent
Required Skills:
• Experience in document control, quality documentation, or records management within a regulated manufacturing environment.
• Managing GMP-controlled documentation, master documents, document revisions, and controlled filing systems.
• Hands-on experience reviewing or auditing manufacturing equipment maintenance, repair, and calibration records for completeness and compliance.
• Proven experience maintaining accurate, current documentation manuals and controlled records with strong attention to version control and traceability.
• Experience supporting quality assurance, GMP, FDA, or other regulated quality-system requirements in pharmaceutical, medical device, biotech, or similar environments.
• Demonstrated ability to independently identify documentation discrepancies, missing records, or outdated materials and resolve them using established procedures.
Job Description:
• Provides clerical and administrative support related to documentation system requirements.
• May audit good manufacturing practices document files relating to the maintenance, repair and calibration of manufacturing equipment in order to ensure compliance with external and internal quality assurance requirements.
• Maintains documentation manuals to ensure they are accurate and up-to-date and available to appropriate personnel.
• Maintains filing of all master documents.
• This position requires knowledge that is acquired through experience, specialized education or training.
• The role has clearly defined procedures and tasks as well as defined guidelines to aid in decision making.
• The job should possess a good knowledge and comprehensive understanding of the range of processes, procedures and systems to be used in carrying out assigned tasks and a basic understanding of the underlying concepts & principles upon which the job is based.
• The knowledge can be acquired through a combination of job-related training and considerable on-the-job experience.
• The job requires the ability to make judgements based on practice and previous experience.
• This job typically requires a minimum of 5 or more years experience.
- **Only those lawfully authorized to work in the designated country associated with the position will be considered.**
- **Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client’s business needs and requirements.**
Benefits:
For information and details on employment benefits offered with this position, please visit here. Should you have any questions/concerns, please contact our HR Department via our secure website.
California Pay Equity:
For information and details on pay equity laws in California, please visit the State of California Department of Industrial Relations' website here.
Rose International is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender (expression or identity), national origin, arrest and conviction records, disability, veteran status or any other characteristic protected by law. Positions located in San Francisco and Los Angeles, California will be administered in accordance with their respective Fair Chance Ordinances.
If you need assistance in completing this application, or during any phase of the application, interview, hiring, or employment process, whether due to a disability or otherwise, please contact our HR Department.
Rose International has an official agreement (ID #132522), effective June 30, 2008, with the U.S. Department of Homeland Security, U.S. Citizenship and Immigration Services, Employment Verification Program (E-Verify). (Posting required by OCGA 13/10-91.).
As a contractor, I have to say that Rose International was by far the best agency I have worked for.
Q'testdalir, Consultant
Rose International was not only attentive and responsive, but they were very professional and helpful whenever I called or needed any assistance.
Diane, Consultant
Rose is an assembly of people grounded in honesty, truth and dignity for all of its employees and contractors.
Samba, Consultant
The interactions that I have had with your representatives have always been prompt and very professional. I am very pleased and impressed with your company and services.
Sioe, Consultant
Rose International maintained good communication during assignments and are very informative through email and phone calls.
Sade, Consultant
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