Job Description

Job Description

Job Description

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.

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.

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.

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