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Regulatory Affairs Specialist

Remote: 
Full Remote
Contract: 
Experience: 
Senior (5-10 years)
Work from: 
New Jersey (USA), United States

Offer summary

Qualifications:

Bachelor's or Associate's degree in relevant field and 6-8 years industry experience, Knowledge of Regulatory Affairs, trends, legislation, and product maintenance requirements.

Key responsabilities:

  • Support data maintenance, regulatory submissions, and develop work processes
  • Stay updated on regulations, guidelines, and trends. Provide training and guidance to team members
Katalyst HealthCares & Life Sciences logo
Katalyst HealthCares & Life Sciences Pharmaceuticals SME https://www.katalysthls.com/
51 - 200 Employees
See more Katalyst HealthCares & Life Sciences offers

Job description

Responsibilities:
  • Independently support data maintenance and archival and retrieval of regulatory documentation in computerized systems.
  • Assist with preparing high quality US regulatory submissions required by local and federal agencies for BI products.
  • Ensure that all submissions are prepared per established requirements and submitted within established timelines.
  • Maintain working knowledge of regulations, policies, and guidelines with appropriate agencies.
  • Contribute to the development and implementation of applicable work processes and instructions. Ensure they are kept up to date and implemented.
  • Maintains advanced and current knowledge of relevant regulations, policies, and guidelines and acts as Regulatory Affairs Subject Matter Expert in assigned areas.
  • Understand and monitor regulatory trends; understand and implement regulations and guidance. Interfaces with relevant stakeholder groups as needed to ensure compliance.
  • Provide training for team members in assigned areas of responsibility. Provides guidance/direction within the regulatory department and stakeholder groups relative to regulatory compliance of BIAH products and processes.
  • With minimum guidance and supervision, support systems for product compliance and maintenance and support key user responsibilities as applicable.
Requirements:
  • Bachelor's degree, preferably in science, and 6 years relevant industry experience (OR)
  • Associate's degree and 8 years of relevant industry experience.
  • Knowledge in relevant Regulatory Affairs areas. Ability to understand and anticipate regulatory trends.
  • Knowledge and established understanding of regulatory legislation and requirements for the maintenance of veterinary products.
  • Strong proficiency in supporting data maintenance and archival and retrieval of regulatory documentation in computerized systems.
  • Strong experience creating detailed work instructions that align with Regulatory Authority and Regulations for streamlined processes.
  • Intrapreneurial spirit while being rigorous and disciplined with compliance requirements.
  • Demonstrated ability to successfully collaborate in a global organization and manage a full workload.
  • Effective communicator with good negotiation and interpersonal skills and the ability to form productive working relationships at all levels across disciplines and nationalities.
  • Strong attention to detail.
  • Must exhibit good judgment, and ability to problem-solve issues in daily work.
  • Able to meet stringent time and quality demands.
  • Self-motivated with a high degree of initiative, commitment and persistence.
  • Well developed organizational capabilities.
  • Strong team player who is collaborative with the mission of BI, but able to drive change.
  • AAI Competencies.

Required profile

Experience

Level of experience: Senior (5-10 years)
Industry :
Pharmaceuticals
Spoken language(s):
English
Check out the description to know which languages are mandatory.

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