Document Control Assistant - 2nd Shift
Quick Summary
Prepare documentation for third party inspection/audits. Assist validation and regulatory department for documentation and for their various
High School or GED - Required Associate Degree - Preferred Experience: 1 year of experience in Manufacturing or Document Control Specialized Knowledge: cGMP, Computer Skills (MS Word, Excel,
The Document Control Assistant is responsible for administering the processes and practices which support documentation compliance. The Specialist will work in a pharmaceutical production facility and in close collaboration with Quality Assurance, Quality Control and Production with a key-focus on documentation accuracy, quality and integrity.
- Manage document control processes thru electronic systems and/ or paper base systems. Distribute approved documentation to appropriate personnel, track receipt of documentation and notebooks.
- Maintaining lists and postings required for both electronic and hard copy; maintain specific databases in Document Control Department and training records.
- Perform data entry and management in systems (Document Compliance and Process Compliance) and maintain the print/soft copies for all documents.
- Collaborate with teams to complete, maintain an up-to-date Document Control Systems.
- Store, archive, and retrieve the version documents such as certificate of analysis of materials and products, specifications, methods, protocols, and report files.
- Prepare and distribute PBRs, Packaging Batch Records, SOPs, methods and protocols, and other controlled documents.
- Distribute approved documentation to appropriate personnel, track receipt of documentation and notebooks. Track document approvals and any related activities and ensure on-line documents are updated and accurate.
- Work with other departments to clarify and correct documentation to ensure compliance.
- Organize and maintain the work area and keep up-to-date files
Responsibilities
~1 min read- →Prepare documentation for third party inspection/audits.
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Assist validation and regulatory department for documentation and for their various requirements.
- High School or GED - Required
- Associate Degree - Preferred
- 1 year of experience in Manufacturing or Document Control
- cGMP, Computer Skills (MS Word, Excel, Access)
The hourly rate for this position ranges from $20-$25.00 per hour. In addition, Amneal offers a short-term incentive opportunity, such as a bonus or performance-based award, as well as a long-term incentive award, such as restricted stock units, with this position within the first 12 months.
Amneal ranges reflect the Company’s good faith estimate of what Amneal reasonably believes that it will pay for said position at the time of the posting. Individual compensation will ultimately be determined based on a variety of relevant factors, including but not limited to, qualifications, experience, geographic location and other relevant skills. At the heart of our Total Rewards commitment is a comprehensive, flexible and competitive benefits program for eligible positions that enables you to choose the plans and coverage that meet your personal needs. This includes above-market, diverse and robust health and insurance benefits to meet the varied needs of our employees as well as a significant 401(k) matching contribution to help our employees save for retirement. We also promote employee well-being with programs that help you enjoy your career alongside life’s many other commitments and opportunities.
Location & Eligibility
Listing Details
- Posted
- July 13, 2026
- First seen
- July 14, 2026
- Last seen
- July 16, 2026
Posting Health
- Days active
- 0
- Repost count
- 0
- Trust Level
- 51%
- Scored at
- July 14, 2026
Signal breakdown
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