Manufacturing Document Control Specialist

American Regent

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profile Job Location:

New Albany, OH - USA

profile Monthly Salary: Not Disclosed
Posted on: 30+ days ago
Vacancies: 1 Vacancy

Job Summary

Nature and Scope

The Manufacturing Documentation Control Specialist will author edit review evaluate and maintain GMP documentation (Manufacturing SOPs Manufacturing Batch records etc). The individual will co-ordinate with Document Control and Change Request reviewers from the documents initiation to the approval stage.

The Documentation Control Specialist will be responsible for authoring/revising documents in a pharmaceutical environment requiring the ability to digest complicated technical subject matter and work with incomplete information in a fast-paced continually changing environment and ability to effectively communicate between various departments (QA QC DC etc.)

Essential Duties and Responsibilities

  • Draft and revise SOPs and manufacturing batch records.

  • Provide editorial support and ensure quality of all document content; focus on clarity accuracy and consistency while maintaining adherence to proper formats regulatory requirement and company procedures and guidelines.

  • Manage the Change Control process for documents generated or revised within Manufacturing.

  • Initiate and manage document reviews and revision to achieve clear concise and accurate instructional documents.

  • Manage and track the status of documents being drafted or undergoing revision within Manufacturing.

  • Procure and distribute templates from Document Control for the generation of new documents.

  • Ensure all work is performed and documented in accordance with existing Company policies and procedures as well as cGMP requirements.

  • Develop and maintain expertise through interaction with subject matter experts.

  • Perform any other tasks/duties as assigned by management.

Education Requirements and Qualifications

  • High School Diploma or GED equivalent required. Associates or Bachelors Degree preferred.

  • Experience with the fundamentals of document management and the management of the document life cycle preferred.

  • Ability to perform multiple activities at the same time and produce outstanding results to meet required deadlines.

  • Excellent writing and editing skills with a keen attention to detail.

  • Excellent organizational interpersonal and communication skills (oral and written).

  • Proficient in Microsoft Office applications.

  • Ability to work overtime as needed

Physical Environment and Requirements

  • Physically able to wear cleanroom/protective gowning and equipment including but not limited to gowning goggles face shields and protective gloves. PPE is essential for the health and safety of employees.

American Regent celebrates diversity and we are committed to creating an inclusive environment for all employees. We are an Equal Opportunity Employer and all qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin disability status or protected veteran status.

Applicants have rights under Federal Employment Laws.


Required Experience:

IC

Nature and ScopeThe Manufacturing Documentation Control Specialist will author edit review evaluate and maintain GMP documentation (Manufacturing SOPs Manufacturing Batch records etc). The individual will co-ordinate with Document Control and Change Request reviewers from the documents initiation to...
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Key Skills

  • Customer Service
  • Consumer Durables
  • Document Control Management
  • Field
  • Financial Accounting

About Company

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American Regent, Inc, a Daiichi Sankyo Group Company, develops, manufactures, and supplies high quality sterile injectables for healthcare providers, clinics and hospitals across the United States and Canada. We have locations in New York, Ohio, and Pennsylvania and sales territories ... View more

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