Document Control Coordinator

Posted 13 Days Ago
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Raleigh, NC, USA
In-Office
Junior
Healthtech • Pharmaceutical • Telehealth
The Role
The Document Control Coordinator manages controlled document processes, ensures compliance with regulations, and provides administrative support in a pharmaceutical manufacturing environment.
Summary Generated by Built In

Why Us?

At Par Health, we believe great healthcare is built on getting the essentials right. We’re looking for passionate, talented individuals who share our commitment to improving lives. With a global workforce, we lead with pride and purpose—prioritizing quality and safety while fostering a culture of continuous improvement, accountability, and teamwork. Elevating the Essentials isn’t just our tagline, it’s the higher standard we live by every day.

Job Description Summary

SUMMARY OF POSITION:
The Documents Control Coordinator serves as a documentation technical resource to the plant. She/he is the primary point of contact for the controlled document and related processes. Also serves as a back-up to Batch Record Review.

Job Description

ESSENTIAL FUNCTIONS:

  • Oversees and administers the controlled document process for the site, ensuring compliance of the system with FDA regulations and company policies and procedures.
  • Serves as the DMS administrator for the software system used to electronically house the Site’s documents.  Provides training to employees on how to use the system.
  • Coordinates DMS related projects and improvements.
  • Provides timely processing and administration of controlled documents.
  • Provides word processing assistance to departments to ensure controlled documents and batch records are formatted consistently.
  • Monitors completion status of periodic reviews and change control action items to ensure timely documentation of actions and maintain compliance.
  • Periodically audits master copies of documents to ensure issued copies are current.
  • Enters all revised documents into the Learning Management System in a timely manner so training can be conducted.
  • Proofs APAP finished lot labels and batch records.
  • Back-up for label administration including program label changes, adding new codes to labeling computer, and conducting label audit trails.
  • Supports annual DMF updates.

Additional Functions:

  • Provides support to investigations, both exceptions and OOS’s to support product disposition.
  • Provide support to intermediate labeling and tank inspections as needed.

DEPARTMENT SPECIFIC/NON-ESSENTIAL FUNCTIONS:

  • Other duties as assigned, with or without accommodation.
  • Provides administrative duties for the department, such as mail distribution, coordination of supplies, and maintenance for the fax and copy machines.
  • Participates in a certified 5S Workplace System to ensure good housekeeping and organization.

MINIMUM REQUIREMENTS:

Education:

High school diploma, GED, or equivalent required. 

Associate/Technical degree or higher preferred. 

Experience:

Competency in MS Word, Excel, and Adobe is required. 

1-3 years pharmaceutical manufacturing experience is preferred.

Experience using an electronic document system is preferred.

Preferred Skills/Qualifications:

Other Skills/Competencies:

Organization, follow-through, effective communication, and computer literacy.

Action Oriented, Conflict Management, Customer Focus, Functional / Technical Skills, Presentation Skills, Priority Setting, Written Communication

Demand for labels and record retrieval creates interruptions. 

A high degree of concentration is required to prevent mix-up and consequent errors.

RELATIONSHIP WITH OTHERS/ SCOPE:

  • This position will report to the Site Quality Director.
  • This position consults with all levels of plant personnel on issues and projects as required.  This position will also interact with personnel from other locations / positions within Mallinckrodt.
  • No employees directly reporting to this position.
  • This position requires self-motivation and daily execution of tasks with limited supervision interaction.

WORKING CONDITIONS:

  • Generally normal office and meeting room conditions, but must complete some routine assignments in plant and non-air conditioned production environment.
  • Exposure to fugitive emissions of chemicals typical for chemical operations.
  • Position may require some travel.
  • Must be able wear the required Personal Protective Equipment (PPE) as deemed necessary by EH&S, leadership team, corporate, or safety guidelines.

DISCLAIMER:

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification.  They are not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required of employees assigned to this position.

EEO Statement:

We comply with all applicable federal, state, and local laws prohibiting discrimination and harassment, and provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status, or genetic information, or any other classification protected by federal, state or local law. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training. 

Skills Required

  • High school diploma or GED
  • Associate/Technical degree or higher
  • Competency in MS Word, Excel, and Adobe
  • 1-3 years pharmaceutical manufacturing experience
  • Experience using an electronic document system

Endo Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Endo and has not been reviewed or approved by Endo.

  • Fair & Transparent Compensation Pay is considered competitive to good across many roles, with total compensation in commercial positions strengthened by sizable bonus/OTE when targets are met. Subsidiary experiences within the group also point to good compensation, reinforcing a generally positive pay story.
  • Healthcare Strength Core medical, dental, and vision coverage is strong, complemented by virtual care, disease‑management programs, and a health advocate service. Health coverage is described as good, adding perceived value beyond base pay.
  • Retirement Support A 401(k) plan provides a company match up to 4%, supporting employees’ long‑term savings. Current materials outline the matching formula clearly for prospective comparisons.

Endo Insights

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The Company
Montreal, Quebec
1,722 Employees
Year Founded: 1997

What We Do

At Endo, our far-reaching vision is simple: to help everyone we serve live their best life. As a specialty pharmaceutical company, we’re motivated by a strong sense of purpose to find better ways to meet unique medical needs. Our global team of passionate employees understands the importance of their work. We’re dedicated to supporting one another as we connect with communities and foster partnerships that elevate quality-of-life and bring the best treatments forward. Our uncompromising commitment results in the delivery of life-enhancing therapies. From intelligent product selection to commercialization, we strive to make a meaningful, tangible impact to help everyone live their best life. Endo has global headquarters in Malvern, Pennsylvania. Community Guidelines: 1. Be respectful. Everyone who visits our page should feel comfortable and respected. 2. If we see a comment that violates anything in the following list, it may be removed. • Comments that use profanity; personally attack or bully another individual; or are off-topic, misleading, factually inaccurate, political, spam, defamatory, discriminatory or promotional. • Comments that are excessively repetitive and/or disruptive to the community. • Comments that promote illegal activity, use copyrights or trademarks or are related to an ongoing legal matter. • Comments that appear to be medical advice. We reserve the right to remove a reply for any reason at any time. 3. Adverse Event Reporting: If we see a post about an adverse event, an Endo representative will need to contact you to find out more information to comply with regulatory guidelines. If you experience a side effect while using an Endo product, please consult your physician or pharmacist immediately. You may also report to the FDA at fda.gov/medwatch or 800-FDA-1088. Replies from other users do not necessarily reflect the views of Endo. We do not endorse content added by other users.

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