CMC Regulatory Scientist I

Spectraforce Technologies; Rahway (NJ); Hybrid; USD 90,000 - 120,000; Full time

Job summary

Spectraforce Technologies is seeking a CMC Regulatory Scientist I for a 6+ month assignment in Rahway, NJ. The hybrid role combines on‑site and remote work with a focus on developing regulatory submission strategies and drafting CMC dossiers.

The successful candidate will have a BS in a scientific field, at least 2 years of related experience, and strong English communication. You will work with cross‑functional teams to ensure timely registrations and compliance across global markets.

Qualifications

• Bachelor of Science in science, engineering, or related field (advanced degree preferred).
• Minimum 2 years of relevant experience in pharma/CMC or manufacturing/quality.
• Strong English, professional communication, and cross‑functional collaboration.

Responsibilities

• Develop CMC regulatory submission strategies and timelines for projects.
• Prepare and review regulatory CMC dossiers for new and existing products.
• Coordinate with global regulators to manage renewals, variations, and responses to authority questions.
• Assess post‑approval changes and drafting strategies with timelines and risk mitigation.
• Maintain regulatory information to support compliance and registrations.
• Share knowledge of CMC regulations and guidelines (FDA, EMA, VICH).
• Identify regulatory issues early and communicate with management.
• Collaborate with product development teams to meet milestones.

Skills

English proficiency

Leadership

Communication

Prioritization

Problem solving

Attention to detail

Education

Bachelor's degree

Job description

CMC Regulatory Scientist I

Duration: 6+ Months

Location: Rahway, NJ

Work Arrangment: Hybrid (3 days onsite, 2 days WFH) | Tuesday and Wednesday (core onsite days)

Education

• Bachelor of Science degree (minimum) in science, engineering, or other relevant field (advanced degree preferred).

Experience

• At least 2 years of relevant experience (for example: pharmaceutical research, manufacturing, or quality), proficient in English, high level of professionalism, experience reviewing scientific information, demonstrated oral and written communication skills, demonstrated understanding of related fields (manufacturing, testing, and quality assurance), leadership skills (problem solver, ability to deal with multiple priorities, strong interpersonal skills, sound judgement and attentive to details).
• Previous CMC experience is preferred.

Summary of Position

The Senior Specialist is responsible for developing CMC regulatory submission strategies and timelines for assigned pharmaceutical projects/products in accordance with global regulations and guidance.

The Senior Specialist is also responsible for the preparation and review of information required for development of regulatory CMC dossiers for new and existing commercial products.

Major Activities and Responsibilities

• Work independently and effectively with other functions to manage and prepare regulatory CMC dossiers, renewals/annual reports, variations/supplements, and responses to authority questions as required in each country in order to gain new and maintain existing product registrations.
• Assess post approval changes, provide regulatory filing strategies and timelines, identify risks and propose mitigation strategies.
• Ensures important submissions/tasks are completed on a timely basis.
• Actively participate on new product development teams as well as other types of teams and initiatives and deliver on all assigned regulatory milestones.
• Maintain regulatory information in accordance with processes and procedures to support regulatory compliance.
• Continuously build and share knowledge of CMC related regulations and guidelines (including but not limited to FDA-CVM, EMA, and VICH), authority expectations, as well as current industry standards.
• Identify and communicate potential regulatory issues to management, as needed.
• Performs other tasks as requested by management.