Change Control Specialist

Posted 23 Hours Ago
Be an Early Applicant
Rensselaer, IN
58K-124K Annually
Junior
Biotech • Pharmaceutical
The Role
The Change Control Specialist is responsible for developing strategic plans for change control, preparing and coordinating documentation, leading cross-functional meetings, and mentoring teams to implement effective change controls in a quality-driven environment.
Summary Generated by Built In

We are currently looking to fill multiple Change Control Specialist positions. These positions develop strategic plans related to change control and the implementation of robust corrective actions to support manufacturing operations by applying function expertise.

Current Department with Openings:

  • Manufacturing

In this role, a typical day might include the following:

  • Craft business plans to independently advances change control initiatives to implement Corrective and Preventative Actions (CAPA’s) and process improvements in support of manufacturing operations

  • Assess sophisticated proposed change controls to evaluate if proposal satisfies company standards

  • Coordinate and prepare change control documentation that assesses and defines the scope, impact, risk, and regulatory impact associated with the change

  • Review, edit, and revise controlled documentation in accordance with cGMP standards

  • Coordinate and/or lead cross-functional meetings with multiple departments to drive change control implementation

  • Provide advice and mentorship to cross-functional teams to enable successful and GMP compliant change controls

  • Independently monitor and progress multiple projects concurrently – identifying, addressing, and/or raising potential obstacles in a timely manner

  • Present business critical and regulatory impactful change controls to senior leadership

  • Document all training

  • Assist with the training of new employees

  • May manage direct reports

This role might be for you if you:

  • Excel in a quality driven organization.

  • Can manage multiple assignments and changing priorities through robust organizational, planning, and project management skills.

  • Have a strong attention to detail.

  • Have strong technical writing and interpersonal communication skills.

  • Enjoy working in a fast-paced environment.

  • Have experience navigating a controlled quality system (preferred but not required).

To be considered for this role you must hold a Bachelor’s degree in Life Sciences, Engineering or related field and following minimum amounts of relevant experience for each level:

  • Associate Specialist – 0-2 years

  • Specialist – 2+ years

  • Sr Specialist – 5+ years

May substitute proven experience for education requirement. Level is determined based on qualifications relevant to the role.

#REGNEC

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, 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. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.

For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.

Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.

Salary Range (annually)

$58,480.40 - $124,300.00

The Company
HQ: New York, New York
15,000 Employees
Hybrid Workplace
Year Founded: 1988

What We Do

At Regeneron we believe that when the right idea finds the right team, powerful change is possible. As we work across our expanding global network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization. And new ways to think about health. Connect with us so we can learn more about you, and you can learn more about our biopharmaceutical medicines. And join us, as we build a future we believe in.

Please visit www.regeneron.com/social-media-terms for information on how to engage with us on social media.

An important note about privacy: Regeneron is committed to your privacy and will not ask for sensitive personal information such as social security number, date of birth or bank account details via email or social media.

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