External Manufacturing Specialist

Within this role the External Manufacturing Specialist oversees all aspects of contract manufacturing operations (filling, assembly, packaging) including day-to-day operations, ensuring timely completion of associated operations/documentation and assisting in the monitoring of cGMP compliance.

A typical day might include, but is not limited to, the following:

Serving as a Regeneron operational contact for contract manufacturing and/or business partner sites concerning day-to-day activities

Coordinating external manufacturing activities at contract and/or business partner sites, including but not limited to: scheduling of all batches, supply of materials, providing direction on shipment of bulk or finished product, tracking and monitoring of cycle times, providing supporting documentation for manufacturing activities and enlisting support from others who will provide any required associated reports and technical expertise

Liaising between various departments within Regeneron including, but not limited to Quality Control, Quality Assurance, Supply Chain, Operations/Logistics Departments and contract manufacturers or business partners

Leading a sub-team in continuous process improvements, system/equipment implementation and/or strategy development

Supporting all investigations which concern external manufacturing and associated shipping operations

Ensuring product integrity and company reputation by assisting in the monitoring of cGMP compliance at contract manufacturers and business partners

Performing reviews of pre-production master batch records and executed batch records

This role may be for you if you:

Knowledge of external manufacturing from formulation through the final package

Basic knowledge of regulatory compliance inclusive of cGMP, FDA regulations, familiarity with ICH guidelines and EU regulations

Proficient in Excel, PowerPoint, Visio, Word, etc. in addition to experience working within shared work environments

Strong interpersonal, written and oral communication skills

Exhibits confidence, has a high emotional IQ, and has strong interpersonal, written and oral communication skills for providing team updates

Gains understanding from provided instructions and works towards goals with minimal supervision

Exhibits a degree of ingenuity, creativity and resourcefulness in evolving and ambiguous environments

Shows resiliency and flexibility in the face of challenges and adversarial situations

Understands and listens to team members and stakeholders needs while supporting productive team environments toward a common objective

Experience in collaborating with CMOs/CROs preferred

Competencies in German and/or French (oral and written) preferred

Travels up to 25% (domestic and international), as required

To be considered for this opportunity, you should have a BS/BA in scientific discipline and 2 years of related experience in cGMP manufacturing operations (clinical and/or commercial) or equivalent combination of education and experience.

#REGNIRLTO #IREADV #JOBSIEST #LI-Onsite

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. 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, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate.  The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits.  Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit

https://careers.regeneron.com/en/working-at-regeneron/total-rewards/

. For other locations, additional information will be provided during the recruitment process.  If you have any questions, please speak with your recruiter.

Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.

For jobs in Canada: this posting is for an existing position.

Salary Range (annually)

€46,200.00 - €75,400.00