What are the responsibilities and job description for the Lead Biotech Production Coordinator position at Regeneron?
REGENERON PHARMACEUTICALS, INC.
Job Description
GLOBAL
Job Title: Lead Biotech Production Coordinator I-IV
Department: Manufacturing
Prepared on: 17OCT2024
Summary: Facilitate and coordinate inventory, documentation and perform record- related
activities for manufacturing. Maintain and coordinate inventory, scheduling, sampling, and
documentation requirements for manufacturing.
Essential Duties and Responsibilities include, but are not limited to, the following:
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 (hourly)
$24.04 - $37.60
Job Description
GLOBAL
Job Title: Lead Biotech Production Coordinator I-IV
Department: Manufacturing
Prepared on: 17OCT2024
Summary: Facilitate and coordinate inventory, documentation and perform record- related
activities for manufacturing. Maintain and coordinate inventory, scheduling, sampling, and
documentation requirements for manufacturing.
Essential Duties and Responsibilities include, but are not limited to, the following:
- Coordinate, review, and catalogue various types of manufacturing documentation.
- Prepare routine progress reports and tracking on various KPIs.
- Responsible for lifecycle management of documentation
- Maintain inventory systems through investigations, weekly reviews, reconciliations, and
- Serves as a liaison between manufacturing and other functional areas as needed.
- Ability to decipher and navigate a variety of different systems, data, calculations, and
- Performing analysis of GMP and GxP data.
- Coordinate appropriate material needs using varying systems and forms to ensure
- Ensuring systematic bill of materials are created and maintained for production needs.
- Evaluate, initiate, and monitor deviations and other compliance events.
- Create and review sampling intake for all manufacturing unit operations and protocols
- Can provide hands on leadership to employees.
- Ensure employee timesheets are completed on time.
- Participate with employee training to ensure that all requirements are met.
- Perform, minimally, monthly performance feedback meetings with reports.
- Raise all performance issues to Manager and/or Directors and/or HR.
- Requires BS/BA Degree with 0-2 years of related experience or equivalent combination
- Experience in a cGMP environment, quality assurance, project management, or inventory
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 (hourly)
$24.04 - $37.60
Salary : $24 - $38