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Mansueto Ventures is home to two of the most iconic and vibrant brands in business publishing: Inc. and Fast Company. Every day, the content, awards, and events produced help entrepreneurs and innovators succeed by providing useful insights, sparking essential conversations, and offering much-needed inspiration.

Inc. is the voice of the American entrepreneur, inspiring and documenting the risk-takers and ultra-driven go-getters who represent the most dynamic force in the American economy.
Fast Company is the world’s leading business media brand, focusing on innovation in technology, leadership, and design to inspire readers to shape the future of business.

","New York, NY","coloredLogo","logoAttachment","thumbnail","thumbnailAttachment","hexCode","#080D0C","headline","Publisher of Inc. and Fast Company, empowering innovators and entrepreneurs.","/companies/mansueto-ventures-careers","hasJobSubmission","isSavedJob","similarJobs",[510,519,527,533,540],{"_429":428,"_434":511,"_452":453,"_444":445,"_243":512,"_441":513,"_427":428,"_111":437,"_431":194,"_433":194,"_454":453,"_442":514,"_425":515,"_455":456,"_430":115,"_476":516,"_460":517,"_478":437,"_479":514,"_481":482,"_483":518,"_485":486},["D",1771088400000],"The Associate Manager – CMC Regulatory Submissions Compliance supports the management of Clinical Trial Application (CTA) pre-submission review processes within CMC Regulatory Affairs. In this role, you will coordinate and review documentation planned for submission to global health authorities, ensuring consistency across CTAs and adherence to country-specific requirements.

A Typical Day

Contribute to and coordinate the CTA pre-submission review process to ensure consistent CMC information across global submissions and prevent clinical lot release issues.

Support regulatory release and QP certification by helping generate regulatory submission forms and related documentation.

Participate in cross‑functional meetings to identify and resolve CMC regulatory issues in clinical trial submission documents.

Facilitate timely communication between IOPS and global development stakeholders.

Represent CMC Regulatory Affairs in meetings with CROs to ensure submission requirements are met; provide consistent metrics and feedback on CTA processes and procedures.

Help develop procedures and systems to enhance tracking of global regulatory submission packages and approval status.

Keep management and stakeholders informed of assessments, strategies, risks, and project status.

Contribute to training programs and knowledge‑sharing across teams.

This Role Might Be for You If You Have

Ability to build collaboration and teamwork across cross‑functional teams.

Comfort working in ambiguity and delivering results with minimal direction.

A track record of positive relationship‑building internally and externally.

Strong communication and negotiation skills.

Openness to change and a continuous improvement mindset.

Understanding of quality principles in a regulated manufacturing environment.

To be considered for this role\nBS/BA in Chemistry, Biology, or a related field (advanced degree preferred). 5+ years of experience in biopharmaceutical manufacturing or a related industry, including regulatory or compliance activities. Strong compliance background preferred; program management experience is a plus.

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.\nPlease be advised that at Regeneron, we believe we are most successful and work best when we are together. For that reason, many of Regeneron’s roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about Regeneron’s on‑site policy and expectations for your role and your location.

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.

#J-18808-Ljbffr\n","The Associate Manager – CMC Regulatory Submissions Compliance supports the management of Clinical Trial Application (CTA) pre-submission review pro...","Ireland, West Virginia, United States, 26376",["B","2569271115"],"4 days ago","/jobs/2569271115-associate-manager-cmc-regulatory-affairs","/jobs?location=Ireland%2C+West+Virginia%2C+United+States%2C+26376",{"_429":428,"_434":520,"_452":453,"_444":445,"_243":521,"_441":522,"_427":428,"_111":523,"_431":194,"_433":194,"_454":453,"_442":514,"_425":524,"_455":456,"_430":115,"_476":516,"_460":525,"_478":523,"_479":514,"_481":482,"_483":518,"_485":526},["D",1771088400000],"A leading biopharmaceutical company is looking for an Associate Manager for CMC Regulatory Submissions Compliance. In this role, you will coordinate Clinical Trial Applications and ensure compliance with global health authority submissions. The ideal candidate has over 5 years of experience in the biopharmaceutical industry, strong communication and leadership skills, and a solid understanding of compliance processes. This position emphasizes teamwork and connection between cross-functional teams in navigating regulatory requirements.\n#J-18808-Ljbffr\n","A leading biopharmaceutical company is looking for an Associate Manager for CMC Regulatory Submissions Compliance. In this role, you will coordinat...","Associate Manager, CMC Regulatory Submissions & Compliance",["B","2569288542"],"/jobs/2569288542-associate-manager-cmc-regulatory-submissions-compliance","/jobs?keyword=Associate+Manager%2C+CMC+Regulatory+Submissions+%26+Compliance",{"_429":428,"_434":528,"_452":453,"_444":445,"_243":512,"_441":513,"_427":428,"_111":437,"_431":194,"_433":194,"_454":453,"_442":529,"_425":530,"_455":456,"_430":115,"_476":516,"_460":531,"_478":437,"_479":529,"_481":482,"_483":532,"_485":486},["D",1771088400000],"Rensselaer, Indiana, United States, 47978",["B","2569283436"],"/jobs/2569283436-associate-manager-cmc-regulatory-affairs","/jobs?location=Rensselaer%2C+Indiana%2C+United+States%2C+47978",{"_429":428,"_434":534,"_452":453,"_444":445,"_243":512,"_441":513,"_427":428,"_111":437,"_431":194,"_433":194,"_454":453,"_442":535,"_425":536,"_455":456,"_430":115,"_476":537,"_460":538,"_478":437,"_479":535,"_481":482,"_483":539,"_485":486},["D",1771174800000],"Crosby, Mississippi, United States, 39633",["B","2583200746"],"3 days ago","/jobs/2583200746-associate-manager-cmc-regulatory-affairs","/jobs?location=Crosby%2C+Mississippi%2C+United+States%2C+39633",{"_429":428,"_434":541,"_452":453,"_444":542,"_243":543,"_441":544,"_427":428,"_111":545,"_431":194,"_433":194,"_454":453,"_442":546,"_425":547,"_455":548,"_430":115,"_476":477,"_460":549,"_478":545,"_479":546,"_481":550,"_483":551,"_485":552},["D",1771246800000],"Regeneron Pharmaceuticals, Inc","As an Associate Director you will lead the development and execution of global CMC regulatory strategies for our Obesity portfolio. You will guide regulatory activities across development stages, mentor CMC Regulatory Affairs (RA) staff, supporting cross-functional and external partners, and serving as a key liaison in regulatory authority interactions.

This position is onsite 4 days/week at either our Tarrytown or Rensselaer, NY or Warren, NJ offices. We cannot offer a remote work option. If eligible, we can offer relocation benefits.

A Typical Day

Lead product development activities from a CMC regulatory standpoint with input from senior management.

Represent CMC RA at program meetings and independently provide regulatory interpretation, position, and covering clinical development, initial market applications, and approval/post‑approval activities.

Identify program issues and develop appropriate regulatory strategies to mitigate risks to filings, independently find alternative solutions/work‑arounds, and obtain consensus.

Critically review and provide meaningful and strategic input on regulatory filing documents (e.g., INDs, IMPDs, meeting packages, scientific advice, BLAs, MAAs, BPDRs, annual reports, DSUR, amendments, supplements) to facilitate and expedite the development, licensure, and marketing of drugs and/or biologics.

Lead and facilitate interactions with global regulatory authorities (e.g., meetings, IR responses, inspections).

Perform final review and approval of the compliance activities of the portfolios to confirm regulatory impact and associated submission requirements for clinical and commercial regulatory filings in accordance with country‑specific regulatory guidance documents.

Mentor colleagues in difficult compliance assessment discussions with SMEs or Senior Management; find opportunities for improvement of processes for compliance tasks.

Develop and create working instructions, SOPs, and/or templates to facilitate consistent and efficient practice across the CMC RA groups.

Identify gaps in the IOPS and global RA processes, bring up to higher management, and help to improve business efficiency.

Support establishing, managing, and maintaining a knowledge base of current and emerging regulatory requirements and guidelines in the CMC field.

Find opportunities to initiate operational changes and policy modifications.

Manage and coach team member(s).

Potential Fit

Have a strong grasp of CMC worldwide regulations and guidelines.

Have been successful in building collaboration and teamwork across cross‑functional teams.

Proven track record managing and mentoring people.

Demonstrated skill in managing multiple priorities.

To be considered a bachelor’s degree with a minimum of 10 years of pharmaceutical/biotech industry experience, including 5+ years of relevant CMC experience. An advanced degree is preferred. Proven track record supporting small molecule drugs and/or biological products through development and approval is a distinct advantage. It is required to have a good understanding of current CMC worldwide regulations and guidelines. Experience in interacting with the US FDA and other regulatory authorities. Experience with device regulatory requirements and development processes for combination products is a plus.

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive culture that provides comprehensive benefits, which vary by location. In the U.S., benefits may include health and wellness programs (including medical, dental, vision, life, and disability insurance), fitness centers, 401(k) company match, family support benefits, equity awards, annual bonuses, paid time off, and paid leaves (e.g., military and parental leave) for eligible employees at all levels! For additional information about Regeneron benefits in the US, please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other countries’ specific benefits, please speak to your recruiter.

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

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)

$157,200.00 - $256,600.00

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