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    Principal Quality Compliance Specialist - Troy, United States - Regeneron Pharmaceuticals

    Regeneron Pharmaceuticals
    Regeneron Pharmaceuticals Troy, United States

    3 weeks ago

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    Description
    Regeneron Pharmaceuticals

    Principal Quality Compliance Specialist

    Troy ,

    New York

    Apply Now

    We are currently looking to fill a Principal Quality Compliance Specialist position on the Quality Assurance Change Control Team.

    The Quality Compliance Specialist ensures quality and compliance to cGMPs, internal, external, and international requirements with respect to change control activities.

    This role works within the QA Change Control Team to facilitate process improvements and support the Quality Management System.
    As a Principal Quality Compliance Specialist, a typical day might include the following:

    Partnering with other members of the Quality Assurance team and/or end users of the system to Identify, Develop, and Implement Continuous Improvements to the Change Control System, Process and associated procedures.

    Facilitating cross functional meetings and providing guidance and consultation to change control owners.
    Developing tools to ensure consistent communications with different functional areas regarding change priorities, timelines, and communications.
    Developing and deliver end user training.
    Interpreting compliance and regulatory requirements for incorporation into departmental systems, procedures and documentation.
    Assisting as needed in audits and inspections.
    Review and Approval of Change Proposals as required.
    This role might be for you if:

    Demonstrated ability to perform independent work requiring attention to detail, accuracy and scientific judgment and a consistent record of shifting thought processes quickly from one task to another.

    Demonstrated strong organizational abilities, record of creating structure from different sources.
    Always looking for a better way to do things.

    Aptitude to comprehend, analyze and interpret process and systems information, technical procedures, reports and regulations to make decisions in GMP environment.

    Proven track record of establishing and maintaining effective working relationships with managers and employees as well as influencing individuals of various levels to gain understanding and/or acceptance of an idea, policy, procedure, or plan.

    Possess excellent interpersonal, written and oral communication skills with the ability to utilize active listening skills to understand concerns or reasoning in order to be responsive, gain trust and build strategic relationships.

    Proficient digital literacy in Microsoft (MS) Word, Excel, PowerPoint, and SharePoint required. Experience with Quality Management Systems heavily preferred.

    To be considered for the Quality Compliance Specialist position you must have a Bachelors in a scientific or engineering discipline or related field with the following minimum amounts of relevant experience for each level, in a combination of quality, production, engineering, regulatory (chemistry, manufacturing and control) and/or laboratory, with demonstrated accomplishments in effectively implementing cGMP requirements.

    Senior Specialist 5+ years
    Principal Specialist 8+ years
    Experience in change control function strongly preferred. Level is determined based on qualifications relevant to the role.
    #REGNQA
    Does this sound like you? Apply now to take your first steps toward living the Regeneron Way We have an inclusive and diverse culture that provides comprehensive benefits including health and wellness programs, fitness centers and equity awards, annual bonuses, and paid time off for eligible employees at all levels

    Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations.

    We will ensure that individuals with disabilities are provided reasonable accommodations to participate in the job application process. Please contact us to discuss any accommodations you think you may need.
    The salary ranges provided are shown in accordance with U.S. law and apply to U.S. based positions, where the hired candidate will be located in the U.S. If you are outside the U.S, please speak with your recruiter about salaries and benefits in your location.

    #J-18808-Ljbffr
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