Document Control Assistant - 2nd Shift

Merck & Co.

Piscataway Township (NJ)

On-site

USD 42,000 - 52,000

Full time

14 days+

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Benefits offered by this job

Bonus potential
401(k) matching
Health benefits

Job summary

Merck & Co. is seeking a Document Control Assistant to administer documentation processes in a pharmaceutical production facility, collaborating with QA, QC and Production to ensure accuracy and integrity.

You will manage electronic and paper systems, distribute approved documentation, track receipts, maintain databases and training records, and archive documents such as COAs, specs, SOPs and protocols.

Qualifications

  • High School diploma or GED required.
  • Associate Degree preferred.
  • 1 year of experience in Manufacturing or Document Control.
  • cGMP knowledge and basic computer skills required.

Responsibilities

  • Manage document control processes through electronic systems and/or paper-based systems.
  • Distribute approved documentation to appropriate personnel and track receipt of documentation and notebooks.
  • Maintain lists and postings for electronic and hard copies; manage databases in Document Control and training records.
  • Collaborate with teams to keep Document Control Systems up to date and compliant.
  • Store, archive and retrieve documents such as COAs, specifications, methods, protocols and reports.

Skills

Document control
Data entry
cGMP knowledge
Quality documentation

Education

High School or GED - Required
Associate Degree - Preferred

Tools

MS Word
Excel
Access

Job description

Description

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.

Essential Functions
  • 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
Additional Responsibilities
  • Prepare documentation for third party inspection/audits.
  • Assist validation and regulatory department for documentation and for their various requirements.
Education
  • 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, Access)
Compensation and Benefits

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.

Equal Employment Opportunity

Amneal is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, national origin, age, disability, genetic information, protected veteran status, or any other characteristic protected by applicable federal, state, or local laws. If you require a reasonable accommodation to complete the application process or to participate in any part of the hiring process, please contact us at accommodations@amneal.com. Requests will be handled confidentially and in accordance with applicable laws.

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