Manager, Document Control

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Apply Job Description Description:

Document Control Manager oversees the organizational management of electronic and/or paper based system including but not limited to: Batch Record Issuance, Maintenance and Retention, including Protocols, reports, log books and other GMP documents . The Manager will lead the Document Control activities in regulatory inspections by reviewing documents for accuracy and compliance.

Schedule:

1st Shift 8:00am - 4:30pm Monday to

Friday Essential Functions:

Manage document control processes thru electronic systems and/ or paper base systems. Maintaining lists and postings required for both electronic and hard copy; maintain specific databases in Document Control Department. Oversee distribution of all Controlled Documents, printing of SOPs, Methods, Specifications, Issuing Logbooks, and coordinate Biennial SOP review. 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, logbooks, laboratory notebooks, specifications, methods, protocols, and report files. Prepare and distribute PBRs, Packaging Batch Records, SOPs, methods and protocols, and other controlled documents. Track document approvals and any related activities and ensure on-line documents are updated and accurate. Solve issues concerning documentation and/or change controls as required.

Additional Responsibilities:

Manage daily performance of staff. Ensures projects, goals and deadlines are being met. Adhere to all budget requirements. Maintain high-level of confidentiality, in regards to Company and employee information. Additional responsibilities as assigned.

Qualifications Education:

Bachelors Degree (BA/BS) -

Required Experience:

5 years or more in

Quality or Document Control Experience Specialized Knowledge:

cGMP, Microsoft Office (MS Word, Excel, Access, PowerPoint) The base salary for this position ranges from $120,000 to $135,000 per hour. Amneal ranges reflect the Company's good faith estimate of base salary that 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, 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 helps you enjoy your career alongside life's many other commitments and opportunities. Required Skills Change Control Document Review Interpersonal Communications Quality Assurance Quality Management Systems Troubleshooting (Problem Solving) Workflow Management Writing About Us Amneal is an Equal Opportunity Employer that does not discriminate on the basis of sex, age, race, color, creed, religion, national origin, sexual orientation, gender identity, genetic information, disability, veteran status, liability for service in the U.S. Armed Forces or any other characteristic protected by applicable federal, state, or local laws. Apply Now Job Info Job Identification 7844 Job Category Document Control Posting Date 05/05/2026, 11:37 AM Locations 50 Horseblock Road, Brookhaven, NY, 11719, US Job Schedule Full time © MapTiler © OpenStreetMap contributors Legend Jobs at a location Group of locations © MapTiler © OpenStreetMap contributors | © Oracle Corporation Terms Legal Notices Use control and scroll to zoom the map Use two fingers to move the map 50 Horseblock Road, Brookhaven, NY, 11719, US Copy to Clipboard Similar Jobs Data Reviewer-Senior Scientist, Quality Control Piscataway, NJ, United States Posted on 04/15/2026 Trending The Scientist 3 - QC is responsible to perform testing of raw materials, in-process and finished pharmaceutical dosage forms, products on stability, cleaning verification samples following written procedures and applicable SOPs, calculate and report results on applicable specification documents, participate in method transfer activities within departments or between facilities or organizations. This role will also provide feedback on systems and analytical procedures to promote continuous improvement and enhancement of compliance posture. Scientist, Quality Control Piscataway, NJ, United States Posted on 03/27/2026 Trending The Scientist II - QC is responsible for performing chemical testing on raw materials, in-process and finished pharmaceutical products, including stability and cleaning verification samples, while ensuring compliance with SOPs and applicable specifications. This role also involves preparing samples, executing analytical techniques (e.g., IR, UV-Vis, chromatography), documenting results accurately, and supporting method transfers and continuous improvement initiatives. Manager, Quality - Sterile Operations Brookhaven, NY, United States Posted on 04/20/2026 The Sterile

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