Biotech Production Coordinator

Regeneron Pharmaceuticals; Rensselaer (IN); On-site; USD 34,000 - 53,000; Full time

Job summary

Regeneron Pharmaceuticals in Indiana is seeking an inventory and documentation coordinator for manufacturing operations. The role ensures accurate inventory records, prepares reports, and coordinates material needs to sustain production.

You will manage documentation lifecycle, review sampling intake, and liaise across manufacturing and QA to maintain compliance in a cGMP environment. This on-site position follows a Monday–Friday schedule.

Qualifications

• Requires Bs/BA Degree with 0-2+ years of related experience or equivalent combination of education and experience.
• Experience in a cGMP environment, quality assurance, project management, or inventory management desired.

Responsibilities

• Oversees the lifecycle management of documentation
• Prepare both routine and non-routine progress reports and tracking on various KPIs.
• Maintain inventory systems through investigations, weekly reviews, reconciliations, and other related activities to ensure accuracy.
• Performing and interpreting analysis of GMP and GxP data.
• Create and review sampling intake for all manufacturing unit operations and protocols per the appropriate documentation prior to operators going on the floor.
• Coordinate appropriate material needs using varying systems and forms to ensure production continuity.
• Ensuring systematic bill of materials are created and maintained for production needs.
• Evaluate, initiate, and monitor deviations and other compliance events.
• Coordinate, review, and catalogue various types of manufacturing documentation
• Serves as a liaison between manufacturing and other functional areas as needed.

Skills

System navigation

Education

Bs/BA Degree

Job description

Summary

Maintain and coordinate inventory, scheduling, sampling, and documentation requirements for manufacturing. Facilitate and coordinate inventory, documentation and perform record- related activities for manufacturing.

Essential Duties and Responsibilities

• Oversees the lifecycle management of documentation
• Prepare both routine and non-routine progress reports and tracking on various KPIs.
• Maintain inventory systems through investigations, weekly reviews, reconciliations, and other related activities to ensure accuracy.
• Performing and interpreting analysis of GMP and GxP data.
• Create and review sampling intake for all manufacturing unit operations and protocols per the appropriate documentation prior to operators going on the floor.
• Coordinate appropriate material needs using varying systems and forms to ensure production continuity.
• Ensuring systematic bill of materials are created and maintained for production needs.
• Evaluate, initiate, and monitor deviations and other compliance events.
• Coordinate, review, and catalogue various types of manufacturing documentation
• Serves as a liaison between manufacturing and other functional areas as needed.

This position will be 1st, Monday-Friday, 8:00 a.m.-4:30 p.m.

Education and Experience

• Requires Bs/BA Degree with 0-2+ years of related experience or equivalent combination of education and experience.
• Experience in a cGMP environment, quality assurance, project management, or inventory management desired.

Knowledge, Skills, and Abilities

• Ability to decipher and navigate a variety of different systems, data, calculations, and documentation.

Does this sound like you? 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)

$24.76 - $38.70