Bayer HealthCare jobs Whippany NJ - Regulatory Affairs Specialist
90000.00 $
Published date: 2025/06/01
- Location: Wharton, New Jersey, United States
Location: Wharton, New Jersey
Company: Bayer HealthCare
Salary: $75,000 – $90,000 per year, based on experience
Working Hours: Full-Time | Monday – Friday | Hybrid Option
Job Description:
Bayer HealthCare is hiring a Regulatory Affairs Specialist to support U.S. and global regulatory submissions and compliance for pharmaceutical products. This position is based at Bayer’s U.S. headquarters in Whippany, NJ, and offers a hybrid work arrangement.
Key Responsibilities:
Prepare and maintain regulatory documentation and submissions (e.g., INDs, NDAs)
Ensure compliance with FDA and international health authority requirements
Support regulatory strategies and product lifecycle activities
Coordinate with cross-functional teams including R&D, QA, and clinical affairs
Monitor changes in regulations and update internal teams
Requirements:
Bachelor’s degree in life sciences, pharmacy, or related field (Master’s preferred)
2–4 years of regulatory affairs experience in the pharmaceutical industry
Knowledge of FDA regulations and global submission formats (eCTD)
Strong written and verbal communication skills
Attention to detail and ability to manage multiple projects
Benefits:
Competitive base salary and annual bonus
Comprehensive health and wellness coverage
401(k) with generous company match
Employee development and continuing education programs
Hybrid work flexibility and career growth at a global company
Keywords: Bayer HealthCare jobs Whippany NJ, regulatory affairs jobs NJ, pharmaceutical compliance roles, Bayer regulatory specialist, FDA submission careers
Company: Bayer HealthCare
Salary: $75,000 – $90,000 per year, based on experience
Working Hours: Full-Time | Monday – Friday | Hybrid Option
Job Description:
Bayer HealthCare is hiring a Regulatory Affairs Specialist to support U.S. and global regulatory submissions and compliance for pharmaceutical products. This position is based at Bayer’s U.S. headquarters in Whippany, NJ, and offers a hybrid work arrangement.
Key Responsibilities:
Prepare and maintain regulatory documentation and submissions (e.g., INDs, NDAs)
Ensure compliance with FDA and international health authority requirements
Support regulatory strategies and product lifecycle activities
Coordinate with cross-functional teams including R&D, QA, and clinical affairs
Monitor changes in regulations and update internal teams
Requirements:
Bachelor’s degree in life sciences, pharmacy, or related field (Master’s preferred)
2–4 years of regulatory affairs experience in the pharmaceutical industry
Knowledge of FDA regulations and global submission formats (eCTD)
Strong written and verbal communication skills
Attention to detail and ability to manage multiple projects
Benefits:
Competitive base salary and annual bonus
Comprehensive health and wellness coverage
401(k) with generous company match
Employee development and continuing education programs
Hybrid work flexibility and career growth at a global company
Keywords: Bayer HealthCare jobs Whippany NJ, regulatory affairs jobs NJ, pharmaceutical compliance roles, Bayer regulatory specialist, FDA submission careers
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