Facilities Compliance Specialist (CMMS) - Rensselaer, NY | Biospace
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Facilities Compliance Specialist (CMMS)

Regeneron Pharmaceuticals, Inc.

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Location:
Rensselaer, NY
Posted Date:
5/28/2017
Position Type:
Full time
Job Code:
8862BR
Salary:
Required Education:
Associates Degree
Areas of Expertise Desired:

Job Description

Known for its scientific and operational excellence, Regeneron is a leading science-based biopharmaceutical company that discovers, invents, develops, manufactures, and commercializes medicines for the treatment of serious medical conditions. Regeneron commercializes medicines for eye diseases, high LDL-cholesterol, and a rare inflammatory condition and has product candidates in development in other areas of high unmet medical need, including oncology, rheumatoid arthritis, asthma, atopic dermatitis, pain, and infectious diseases.

Summary: Perform tasks in support of Computerized Maintenance Management System (CMMS) compliance for the Rensselaer Facilities Department.

Essential Duties and Responsibilities include, but are not limited to, the following:
* Maintains program for tracking and trending of Work Requests and Records to ensure Requests are prioritized and processed appropriately.
* Acts as primary liaison between the Facilities Department and individuals in other departments who utilize the CMMS system, providing support, information, and assistance as required.
* Ensures records are closed within required timeframes.
* Identifies and addresses trends.
* Ensures integrity of data, i.e. complete, accurate, and consistent.
* Manages program for Compliance Review of Work Records.
* Responds to CMMS related requests for internal and regulatory audits.
* Coordinates/supports training for CMMS users.
* Manages/supports revision of CMMS related Standard Operating Procedures, Work Instructions, Risk Assessments, and OJT Task Evaluations.
* Supports or leads CMMS related Change Controls for upgrades, service releases, configuration improvements, integration projects, etc.
* Identify and lead CMMS improvement projects.
* Oversees activities of contractors who work with the CMMS system, including: request processing, tracking and trending activities, and Compliance Review of Records.
* Follows current good manufacturing practices (cGMPs).

Requirements

Education and Experience:

Title level (Associate, Mid, or Senior) will be determined based on skills and experience:
* Associate Level- BA/BS required, preferably in an engineering or scientific related field, with 0-2 years of relevant experience.
* Mid-Level - BA/BS required, preferably in an engineering or scientific related field, with 2+ years of relevant experience.
* Senior Level - BA/BS required, preferably in an engineering or scientific related field, with 5+ years of relevant experience.

*Will substitute relevant experience in lieu of educational requirements.

This is an opportunity to join our select team that is already leading the way in the Pharmaceutical/Biotech industry. Apply today and learn more about Regeneron's unwavering commitment to combining good science & good business.

To all agencies: Please, no phone calls or emails to any employee of Regeneron about this opening. All resumes submitted by search firms/employment agencies to any employee at Regeneron via-email, the internet or in any form and/or method will be deemed the sole property of Regeneron, unless such search firms/employment agencies were engaged by Regeneron for this position and a valid agreement with Regeneron is in place. In the event a candidate who was submitted outside of the Regeneron agency engagement process is hired, no fee or payment of any kind will be paid.

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.