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Hologic, Inc.

Corporate Document Control Analyst

Hologic, Inc. - Marlborough, MA

Corporate Document Control Analyst','170952','!*!Hologic, Inc. is a leading developer, manufacturer and supplier of premium diagnostic products, medical imaging systems and surgical products. The Company's core business units focus on diagnostics, breast health, GYN surgical, and skeletal health. With a unified suite of technologies and a robust research and development program, Hologic is dedicated to The Science of Sure.

There has never been a more exciting time to join us. Bright people, working together to pioneer advances in human health care, have created Hologic's success. Our company believes that people are our greatest asset and only by recruiting, hiring, developing and retaining the most talented employees can we continue to be successful.  Our work atmosphere is stimulating, innovative and customer focused. We provide employees with state-of-the art tools and technology, a collaborative and passionate work environment and the ability to make a dramatic difference in the world of healthcare.

We are rapidly growing and yet we have never been more focused – on our people, on our growth, on our future.','!*!Job Summary

Responsible to review, route and approve company Quality System related documents to ensure these are managed according to all internal and external requirements as applicable.  Facilitates and coordinates the interaction between multiple cross functional groups to ensure appropriate changes are documented.  Provides Document Control Guidance, support, and troubleshooting to the user community as needed.  Gathers data and generate document control related reports to provide visibility and signal to management on the document control process performance according to established goals and objectives.  Manages and executes storage of quality system related documentation per established retention schedules.

Essential Duties & Responsibilities

Duties are listed in order of greatest importance.  The incumbent may be asked to perform other function-related activities in addition to the below mentioned responsibilities as reasonably required by business needs. 

Reviews, routes and approves Quality system related documents according to established policies and procedures.

Effectively manage global projects assuring timely completion of all document control deliverables.

Communicate efficiently and effectively with project teams, management and various cross-functional contacts on documentation progress.

Manage the storage of quality system related documentation, as appropriate, per established schedules.

Interface with appropriate cross functional contacts - R&D, Manufacturing, Advanced Engineering, Marketing, Regulatory, Quality etc. - to expedite documents timely and support business needs.

Create and provide training on document control processes including Agile to all levels within the organization.

Develops and executes to key performance indicator metrics for documentation control and other Quality System elements including preparation and distribution of reports as needed.

Provides support and documentation to support internal and external audits.

Assists with providing resolution and/or addressing root cause of issues related to document control.

Works with outside vendors, as appropriate, to develop part and component documentation.

Manages Document Control projects and initiatives, as necessary.

Document Control subject matter expert and represents the documentation control department as required.

Provides input and support in the development and improvement of document control related procedures and work instructions.

Provides guidance to users to ensure compliance and accurate document generation and revision.

Develop custom dashboards in the PLM system that will be used for reporting, work lists and monitoring quality systems.

Ensures Quality System related documents are maintained in a secure and organized manner and ensures documentation is retrievable and accurate.

Monitors and tracks the review, approval, and distribution of documents to ensure timely completion to meet established timelines.

Resolves and provides guidance on complex Document Control issues.','!*!Qualifications  

Education  

Bachelor’s Degree in Engineering, Technology, Document Management preferred or an equivalent combination of education and experience

Experience 

3-5 years’ experience in document control in an FDA regulated environment

Understanding of documentation control regulations as well as ISO and FDA requirements

Skills

Excels in the use of quality data management tools such as Agile.

Strong computer skills with a working knowledge of Microsoft Office suite

Strong attention to detail and excellent organization skills

English Language: Knowledge of the meaning, spelling, and use of the English language.

Working Knowledge of ORACLE and Agile application preferred.

Agency and Third Party Recruiter Notice:

Agencies that submit a resume to Hologic must have a current executed Hologic Agency Agreement executed by a member of the Human Resource Department. In addition Agencies may only submit candidates to positions for which they have been invited to do so by a Hologic Recruiter.  All resumes must be sent to the Hologic Recruiter under these terms or they will not be considered.

Hologic, Inc. is proud to be an Equal Opportunity Employer & VEVRAA Federal Contractor','United States-Massachusetts-Marlborough','','','','Quality Management Systems','Full-time','Day Job','','Aug 29, 2017','Corporate Document Control Analyst

9 days 9 hours ago

Hologic, Inc.

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Corporate Document Control Analyst Hologic, Inc. - Marlborough, MA, United States

   

Location: Marlborough, MA

Company Profile:
Hologic, Inc. (Nasdaq: HOLX) is a leading developer, manufacturer and supplier of premium diagnostic products, medical imaging systems, and surgical products, with an emphasis on serving the healthcare needs of women throughout the world