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Senior Regulatory Affairs Manager (Relocation Package Available)

Remote: 
Full Remote
Contract: 
Experience: 
Mid-level (2-5 years)
Work from: 

Offer summary

Qualifications:

Bachelor's degree in a scientific field, Proven experience with CVM, E-Submitter, GLP, Advanced degrees preferred (DVM, PhD, MS), Strong written and verbal communication skills, Results-driven with analytical skills.

Key responsabilities:

  • Support and guide regulatory needs for clients
  • Manage expectations with timely communications
  • Develop regulatory strategies for complex issues
  • Provide expert regulatory advice on product development
  • Identify networking opportunities and contribute to publications
Global Life Science Hub logo
Global Life Science Hub Human Resources, Staffing & Recruiting TPE https://glshub.com/
2 - 10 Employees
See more Global Life Science Hub offers

Job description

Global Life Science Hub has partnered with a one-of-a-kind, global CDMO that specializes in providing comprehensive development and manufacturing services. With an additional 50% growth expected in the Kansas site before the end of Q1 2025, we’re searching for an experienced Regulatory Manager to support their next growth stage.

This is a 100% on-site role with relocation assistance available in Kansas. This is an exceptional opportunity to relocate out of any major busy cities to join one of America’s most affordable states in the Heartland of America. As the Senior Regulatory Manager, your role involves managing client and stakeholder expectations, navigating regulatory processes, and creating solutions for complex regulatory challenges that contribute to producing high-quality pharmaceutical products.

Role: Senior Regulatory Affairs Manager

Location: Kansas City, KS

Responsibilities:

  • Supports and guides regulatory and drug development needs for both external clients and internal initiatives.
  • Manages expectations of clients and stakeholders by delivering timely, precise, and relevant documents, assessments, and communications.
  • Demonstrates a solid understanding of current regulations, guidance documents, regulatory processes, and the animal drug development lifecycle, while maintaining a flexible approach to address regulatory challenges.
  • Develops regulatory strategies for complex issues.
  • Provides expert regulatory advice to clients on animal health product development.
  • Represents Argenta in industry groups (e.g., GADA, AHI, SQA).
  • Identifies and pursues new opportunities for regulatory consulting, including networking with potential clients, attending and presenting at industry events, and contributing to industry publications.

Experience/Qualifications:

  • Bachelor’s degree in a scientific field or equivalent experience; advanced degrees (DVM, PhD, MS) preferred.
  • Proven experience in one or more of the following: CVM, E-Submitter, GLP, GCP, GMP, USDA, EPA, EMA.
  • Strong written and verbal communication skills, with the ability to work effectively within and across teams.
  • Results-driven with strong analytical skills and attention to detail.
  • Demonstrated ability to influence, negotiate, and persuade.
  • Strong organizational skills with the ability to prioritize and adapt to shifting business needs.

Apply:

The Global Life Science Hub is a niche Life Science headhunting firm. We place professionals across Europe and the US for a variety of pharmaceutical, CDMO, and CRO companies ranging from small start-ups to large global organizations.

If you’re interested, please apply below. If this position doesn’t interest you, please visit our website for a list of more vacancies – www.glshub.com

Required profile

Experience

Level of experience: Mid-level (2-5 years)
Industry :
Human Resources, Staffing & Recruiting
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Influencing Skills
  • Analytical Skills
  • Negotiation
  • Organizational Skills
  • Detail Oriented
  • Verbal Communication Skills

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