Senior Scientist, Regulatory Chemistry, Manufacturing and Control
Organon is a Women’s Health Company that believes in a better and healthier every day for every woman! We are a passionate, global community of thousands dedicated to redefining the future of women’s health. Our mission is to deliver impactful medicines and solutions for a healthier every day. But what really makes it work at Organon is our people.
We’re looking for real, passionate team players, curious innovators, forward thinkers, empowered by the idea of shaping their career, and ready to bring their fire to embrace change and the opportunities it brings for progress.
At Organon, you’ll get to enjoy the best of both worlds: the open, agile, collaborative culture of a start-up, and operating at the scale of a Fortune 500 company with an international footprint that serves people in more than 140 markets.
It’s going to be an exciting future—come be a part of it.
Reporting to the Director or Executive Director in Regulatory Chemistry, Manufacturing & Control (CMC), the Senior Scientist is responsible for implementing Regulatory CMC strategies for assigned products in accordance with global regulations, guidance's, and defined regulatory strategies. The Senior Scientist is responsible for the preparation and review of information required for development of Regulatory CMC dossiers for projects and products including clinical development, original registrations, life-cycle maintenance submissions, and post-approval changes. The candidate may also support project team goals and organizational initiatives on an as needed basis. Primary responsibilities include, but are not limited to:
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 global regulatory strategies by leading the development, authoring and review of CMC submission components and documentation to support global development (IND, IMPD), new registrations (NDA, MAA), post-approval supplements, annual reports, registration renewals and responses to health authority questions per established business processes and systems.
Ensure product compliance through timely and accurate maintenance of CMC submissions in the systems.
Liaise with our Company's 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 our company's Regulatory CMC management, as needed.
Education Minimum Requirements:
Bachelor’s degree, in a science, engineering, or a related scientific field. Fields of study include Chemistry, Biochemistry, Chemical Engineering, Biology, Pharmacy, Microbiology, Virology, or Molecular Biology with at least four years of overall relevant work experience.
Advanced degree (MS, MBA, Ph.D., PharmD) in a science, engineering, or related scientific field. Fields of study include Chemistry, Biochemistry, Chemical Engineering, Biology, Pharmacy, Microbiology, Virology, or Molecular Biology with at least two years of overall relevant work experience.
Required Experience and Skills:
The candidate must be proficient in English; additional language skills are a plus.
Evaluation of Subject Matter Expert (SME) technical documentation for completeness and sufficient details in order to make accurate regulatory assessments through utilization of current global regulatory guidances.
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.
Familiar with regulatory guidelines for product development, new registrations, post-approval change management and data requirement.
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 complex regulatory problems and effectively work with and communicate to key stakeholders.
Demonstrated flexibility in responding to changing priorities or dealing with unexpected events.
Demonstrated effective leadership, communication, interpersonal, and negotiating skills.
Managing multiple projects to ensure on-time deliverables and timely submissions to ensure product supply continuity.
Preferred Experience and Skills:
Direct experience in Regulatory CMC and/or authoring of regulatory documentation for global clinical trial applications (IND, IMPD), new registrations (NDA, MAA) and/or post-approval submissions.
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.
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Organon proudly embraces diversity in all of its manifestations and is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity, or gender expression, national origin, disability, veteran status or any other characteristic protected by state or federal law.
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Organon LLC., does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.
Applicable to United States Positions Only: Under various U.S. state laws, Organon is required to provide a reasonable estimate of the salary range for this job. Final salary determinations take a number of factors into account including, but not limited to, primary work location, relevant skills, education level, and/or prior work experience. The applicable salary range for this position in the U.S. is stated below. Benefits offered in the U.S. include a retirement savings plan, paid vacation and holiday time, paid caregiver/parental and medical leave, and health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans.
Salary Range$100,700.00 - $171,200.00
Travel Requirements: Organon employees must be able to satisfy all applicable travel and credentialing requirements, including associated vaccination prerequisites.10%
Flexible Work Arrangements:Not Specified
Shift:1st - Day
Valid Driving License:No
Number of Openings:1