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Director, Regulatory CMC (Remote)
Director, Regulatory CMC (Remote)IMMUNEERING CORPORATION • Cambridge, MA, US
Director, Regulatory CMC (Remote)

Director, Regulatory CMC (Remote)

IMMUNEERING CORPORATION • Cambridge, MA, US
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Job Description

Job Description

About Immuneering : Immuneering is a clinical-stage oncology company outpacing cancer to help patients outlive their disease. Our lead product candidate, atebimetinib (IMM-1-104) is currently in a Phase 2a trial in patients with advanced solid tumors including pancreatic cancer. Immuneering’s R&D team is based in a ~38,000 square foot lab and office facility in San Diego. The company also has offices in New York City and Cambridge MA. Immuneering has grown to more than 50+ employees, all working to apply their expertise, passion and creativity to improve the lives of people with serious diseases. Immuneering’s team works collaboratively and relentlessly, thinking across traditional boundaries to help shape the frontiers of drug development.

General Summary of Duties :

The Director, Regulatory, CMC (Chemistry, Manufacturing, and Controls) is a pivotal regulatory role responsible for developing and executing regulatory strategies for CMC activities across the company’s clinical product portfolio. This position ensures compliance with all applicable regulatory requirements and works cross-functionally to support product development, registration, and lifecycle management.

A successful candidate will be a highly collaborative individual with strong interpersonal skills and will be an exceptional team player.

Specific Duties , may include but not be limited to the following :

  • Develop and lead global CMC regulatory strategies for investigational and commercial products to ensure timely submissions and approvals.
  • Prepare, review, and submit CMC sections of regulatory documents including INDs, IMPDs, NDAs, BLAs, ANDAs, and supplements to FDA, and other regulatory authorities including the EMA.
  • Provide regulatory guidance on CMC matters to project teams, including manufacturing changes, process development, and technology transfers.
  • Monitor and interpret current and emerging CMC regulatory requirements, guidelines, and trends to proactively address potential impacts.
  • Represent Regulatory CMC in cross-functional teams and meetings, providing expertise and input on regulatory implications of manufacturing and quality changes.
  • Lead interactions and communications with regulatory agencies regarding CMC topics, e.g. pre-IND, end-of-phase, and pre-submission meetings.
  • Work with a sense of purpose to get work done using influence and good project management skills, fostering alignment with organizational goals.
  • Collaborate with Quality, CMC, R&D, Finance, Legal, Clinical and other internal departments to ensure regulatory compliance and readiness. Partner effectively and smoothly with CRO’s and consultants.

Desired Skills and Qualifications

  • Bachelor’s degree in Chemistry, Pharmacy, Life Sciences, or related field required; advanced degree (PhD, PharmD, MS) highly preferred.
  • Minimum of 8+ years of experience in CMC regulatory affairs within the biopharmaceutical or pharmaceutical industry, including experience with small molecule development in oncology. More experience is a plus.
  • Proven track record of successful CMC submissions and approvals in the US and internationally.
  • In-depth knowledge of FDA, EMA, and ICH guidelines, regulations, and processes related to CMC.
  • Strong leadership, communication, and project management skills.
  • Must be focused on working collaboratively and within our values of : Data rules, All-in, Own it (Accountable), Caring and Humble.
  • Ability to work effectively in a collaborative, fast-paced environment.
  • Location : Remote or Hybrid, if you live near an Immuneering office, regular Meet Ups are available.

    Physical Demands / Working Conditions

    The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of the job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

    Requires prolonged sitting, some bending, stooping, and stretching. Requires eye-hand coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator, and other office equipment. Requires the ability to perform essential job functions with or without reasonable accommodation. No significant lifting is associated with the role.

    While extensive travel is not anticipated with this role, it is possible to perhaps up to [X]% at times. Requires prolonged sitting, some bending, stooping, and stretching. Requires eye-hand coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator, and other office equipment. Requires normal range of hearing and eyesight to record, prepare and communicate appropriate reports. No significant lifting is associated with the role.

    Immuneering is an equal opportunity employer. We are committed to creating a diverse and inclusive workplace where all employees are treated with fairness and respect. We do not discriminate on the basis of race, ethnicity, color, religion, gender, sexual orientation, age, disability, or any other legally protected status. Our hiring decisions and employment practices are based solely on qualifications, merit, and business needs. We encourage individuals from all backgrounds to apply and join us in our mission.

    Job Offers : Immuneering uses the Immuneering.com domain and email addresses for all official communications. If you received communication from any other domain, please consider it spam.

    Note to Recruitment Agencies : We appreciate your interest in finding talent for Immuneering but please be advised that we do not accept unsolicited resumes from recruitment agencies. All resumes submitted to Immuneering without a prior written agreement in place will be considered property of Immuneering, and no fee will be paid in the event of a hire. Thank you for your understanding.

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    Director Regulatory • Cambridge, MA, US

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