Regulatory Affairs Co-Op: Build Submissions & Records

Haleon

Northern (KY)

Hybrid

USD 28,000 - 41,000

Full time

9 days ago
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Job summary

Haleon in Warren, NJ seeks a Regulatory Affairs Co-Op for 6 months starting January 2027. You will organize FDA submissions, maintain regulatory records, and support knowledge management across R&D, Quality, Safety, and Commercial teams.

As an enrolled student in Life Sciences or related field, you will gain hands-on exposure to consumer healthcare products, including OTC medicines and dietary supplements, while building data management and regulatory documentation skills in an in-office,

Qualifications

  • Enrolled in a Bachelor's program in Life Sciences or related field, graduating between December 2027 and May 2028.
  • Proficient in Microsoft Excel and Word.
  • Strong attention to detail with ability to organize and manage data, records, and documentation.

Responsibilities

  • Support the management and organization of FDA submissions, correspondence, and regulatory records.
  • Maintain regulatory databases, tracking tools, and documentation to ensure data accuracy and accessibility.
  • Review historical regulatory information to identify trends, insights, and key learnings.
  • Prepare summaries and presentations to support Regulatory Affairs projects and knowledge management initiatives.
  • Collaborate with team members on data management and continuous improvement efforts.

Skills

Excel
Word
Data management
Attention to detail
Regulatory knowledge

Education

Bachelor's in Life Sciences or related field

Job description

Haleon in Warren, NJ seeks a Regulatory Affairs Co-Op for 6 months starting January 2027. You will organize FDA submissions, maintain regulatory records, and support knowledge management across R&D, Quality, Safety, and Commercial teams.

As an enrolled student in Life Sciences or related field, you will gain hands-on exposure to consumer healthcare products, including OTC medicines and dietary supplements, while building data management and regulatory documentation skills in an in-office,

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