Senior Scientist, Regulatory Affairs - Chemistry Manufacturing & Controls (CMC)

Organon Comercializadora S de RL de C.V; Florham Park (NJ); On-site; USD 110,000 - 170,000; Full time

Job summary

Organon is seeking a Senior Scientist to implement Regulatory CMC strategies for small molecules or biologics, ensuring compliance with global regulations. The role involves drafting and reviewing CMC dossiers and coordinating with Manufacturing & Supply and partners to support post-approval activities.

The candidate will lead regulatory assessments, identify risks, and deliver milestones across the product lifecycle, with strong English communication and leadership skills.

Qualifications

• Bachelor’s Degree in science/engineering with at least 4 years in biological/pharmaceutical R&D or manufacturing.
• Advanced degree (MS, MBA, Ph.D., PharmD) with at least 2 years of relevant experience.
• Direct experience in Regulatory CMC preferred
• Proficient in English; strong communication skills

Responsibilities

• Contribute to regulatory CMC strategies for products across the lifecycle.
• Author and review CMC submission components and regulatory documentation.
• Coordinate with Organon Manufacturing & Supply and external partners on change management.
• Assess regulatory risks and propose mitigation strategies.
• Deliver regulatory milestones for assigned products.
• Communicate potential regulatory issues to management when needed.

Skills

Regulatory CMC expertise

English proficiency

Technical writing

Cross-functional collaboration

Project management

Education

Bachelor's degree in science/engineering

Advanced degree (MS, MBA, PhD, PharmD)

Job description

Job Description

The Position

The Senior Scientist is responsible for implementing Regulatory Chemistry, Manufacturing & Controls (CMC) strategies for assigned small molecule or biological products in accordance with global regulations, guidances and defined regulatory strategies. The Senior Scientist is responsible for the preparation and review of information required for development of regulatory CMC dossiers for commercial products.

Responsibilities

• Provide input to global product and project regulatory strategies by performing assessments of CMC changes, identifying global regulatory requirements and critically evaluating supporting documentation to assess acceptability and identify potential risks.
• Execute regulatory strategies by leading the development, authoring and review of CMC submission components and documentation to support post-approval supplements, annual reports, registration renewals and responses to health authority questions per established business processes and systems.
• Liaise with Organon Manufacturing & Supply colleagues and external partners to support compliant execution of change management and conduct all activities with an unwavering focus on regulatory conformance.
• Assess and communicate potential regulatory risks and propose mitigation strategies.
• Deliver all regulatory milestones for assigned products across the product lifecycle.
• Identify and communicate potential regulatory issues to Organon Regulatory CMC management, as needed.

Required Education, Experience & Skills

• Bachelor's Degree, in a science, engineering, or a related field. Fields of study include Pharmacy, Chemical Engineering, Biology, Microbiology, Virology, Molecular Biology, or Biochemistry with at least 4 years of relevant experience including biological/pharmaceutical research, manufacturing, testing or a related field OR
• Advanced degree (MS, MBA, Ph.D., PharmD) with at least 2 years of relevant experience including biological/pharmaceutical research, manufacturing, testing or a related field
• Direct experience in Regulatory CMC is preferred
• The candidate must be proficient in English; additional language skills are a plus.
• Experience in reviewing scientific information to assess technical merits and suitability of scientific rationale to ensure information is presented clearly and conclusions are adequately supported by data.
• Demonstrated oral and written communication skills and the ability to communicate issues in a succinct and logical manner. Strong listening skills.
• Demonstrated understanding of related fields (e.g., pharmaceutical manufacturing, analytical testing, and quality assurance).
• Demonstrated ability to generate innovative solutions to problems and effectively work with and communicate to key stakeholders.
• Demonstrated flexibility in responding to changing priorities or dealing with unexpected events.
• Capability to handle multiple priorities and balance work to achieve business goals.
• Demonstrated effective leadership, communication, and interpersonal skills.

Please note, relocation assistance is not provided for this position.

Who We Are:

Organon delivers ingenious health solutions that enable people to live their best lives. We are a $6.5 billion global healthcare company focused on making a world of difference for women, their families and the communities they care for. We have an important portfolio and are growing it by investing in the unmet needs of Women's Health, expanding access to leading biosimilars and touching lives with a diverse and trusted portfolio of health solutions. Our Vision is clear: A better and healthier every day for every woman.

US and PR Residents Only

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