Regulatory Affairs Associate
Location: Clark, NJ (Onsite)
Duration: 12 Months (Extension Possible)
Responsibilities
- Prepare and maintain regulatory registration dossiers.
- Support global product registration and launch activities.
- Track registration requirements, KPIs, and project timelines.
- Coordinate with global affiliates and provide status updates.
- Maintain regulatory documentation with a high level of accuracy.
Qualifications
- Bachelor's degree in Chemistry, Biology, Life Sciences, or a related scientific field.
- Internship or professional experience in Regulatory Affairs or Regulatory Operations.
- Strong attention to detail and organizational skills.
- Proficient in Microsoft Office.
- Strong written and verbal communication skills.
Candidates will be considered ineligible if they:
- Do not have a completed Bachelor's degree in Chemistry, Biology, Life Sciences, or a related scientific discipline.
- Have no internship or professional experience supporting Regulatory Affairs, Regulatory Operations, or product registration activities.
- Have experience limited to laboratory, QA/QC, R&D, formulation, or manufacturing with no regulatory support experience.
- Require current employment sponsorship or No Valid proof of EAD, if applicable to work in the U.S.
- Are unable to work onsite in Clark, NJ.
Eligible & interested candidates, please also share your earliest availability for a recruiter screening call.
Company Description
Buckeye Global IT Inc, one of the fastest-growing IT and Healthcare staffing and services firm in the nation specializing in staff augmentation for an end-to-end Enterprise IT Solutions.