Rocket Pharmaceuticals, Inc.

Senior Director, Process Development & MS&T

Rocket Pharmaceuticals, Inc.$220K — $293K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • PhD in a relevant field with 10+ years of industry experience, M.S. with 12 years, or BS with 15 years of leadership experience.
  • Hands-on experience in viral vector process development, specifically AAV processing preferred.
  • Proven track record in optimizing processes across PD/MS&T areas.
  • Direct experience with process tech transfer and related methodologies.
  • Excellent communication skills to deliver complex information clearly.
  • Proficient with statistical analysis tools like JMP or Minitab.
  • Strong MS Office skills for technical reporting.

Responsibilities

  • Lead Process Development and Manufacturing Science & Technology across projects.
  • Collaborate with cross-functional teams including Manufacturing and Quality.
  • Oversee scale-up and scale-down model development for process characterization.
  • Author and review vital regulatory and process documentation.
  • Guide and mentor a team of scientists in research activities.
  • Evaluate and implement innovative technologies to enhance processes.

Benefits

  • Medical, dental, and vision insurance
  • 401(k) with company match and generous vesting
  • Paid vacation and holidays
  • Global shutdown days between Christmas and New Year
  • Access to wellness resources and employee support programs
  • Eligibility for short-term bonus incentives and long-term equity awards.
Full Job Description
Overview

Position Summary

The CMC group at Rocket Pharma is seeking an experienced Sr. Director of Process Development (PD) and Manufacturing Science and Technology (MS&T) to join our Technical Development team. The ideal candidate will have extensive experience and knowledge in process development and manufacturing technical support with a passion for tackling new challenges in a fast-paced, dynamic environment. This role will involve overseeing new and existing platform process development activities to support early- and late-stage pipeline products, as well as providing leadership to a team of scientists.

 

We are looking for someone who is deeply curious about science and gene therapy and is motivated to translate innovative research into impactful therapies.

Responsibilities
  • Serve as Head of Process Development (Upstream, Downstream) and Manufacturing Science and Technology to represent the functional area on cross-functional and cross-divisional teams working with Analytical, Manufacturing, Supply Chain, Quality and Regulatory functions.
  • Strategically position PD/MS&T to execute on both supporting current Manufacturing campaigns and establishing/optimizing new platforms
  • Lead scale-up and scale-down model establishment and qualification activities to enable process characterization and manufacturing investigations.
  • Author and review regulatory and process development documentation.
  • Provide hands-on leadership and guidance to scientific staff.
  • Foster the development, coaching, and mentoring of a growing team of scientists.
Qualifications
  • PhD in chemical engineering, biochemical engineering, bioprocessing, bioengineering, biochemistry, biological sciences, or relevant field of study with 10 years of experience in a biotech/biopharmaceutical industrial setting, M.S. with 12 years of relevant experience, or an equivalent combination of education and experience or BS with 15 years of leadership experience.
  • Viral vector process development experience required, hands-on experience with AAV processing preferred
  • Proven success in developing/optimizing processes while leading end-to-end PD/MS&T functional areas
  • Direct experience with process tech transfer, viral clearance, comparability, control strategies, process characterization and process validations/PPQ
  • Excellent communication and presentation skills, capable of conveying complex technical information in a clear, thorough, and influential manner is required.
  • Experience with statistical analysis tools (e.g., JMP, Minitab) is required.
  • Eager to work with highly skilled and dynamic teams in a fast-paced, entrepreneurial, and technical environment.
  • Motivated to drive functional initiatives to evaluate novel technologies and develop templates, platform, and technical standards to support organization growth.
  • Excellent MS Office skills with a specific focus on word, excel and power point applications to author technical reports and presentations.
Compensation

The expected salary range for this position is $220,000 to $293,000.

 

At Rocket, our compensation philosophy and ranges are built upon data and insights collected from validated world-class providers. We are committed to compensating employees equitably based on several factors, including responsibilities and level of the position, depth and types of the employee27s experience, location of the position and availability of similar talent in a competitive market.

 

For U.S.-based candidates, this is an at-will position, and Rocket reserves the right to adjust the range at hire or during the year due to market shifts.

 

In addition to base salary, Rocket offers a competitive total rewards package that may include bonuses (short-term incentives), medical, dental, and vision insurance, life insurance, 401(k) with company match and generous vesting, paid vacation and holidays, global shutdown days between Christmas and New Year27s, and a variety of wellness resources and employee support programs. Also, certain positions are eligible for added forms of compensation, such equity awards (long-term incentives).

About Rocket Pharmaceuticals, Inc.

Rocket Pharmaceuticals, Inc. is a clinical-stage biotechnology company that develops gene therapies for rare and devastating diseases. The company's pipeline includes gene therapies for Fanconi Anemia, Leukocyte Adhesion Deficiency-I, Pyruvate Kinase Deficiency, and Infantile Malignant Osteopetrosis. Rocket Pharmaceuticals' gene therapy platform is based on lentiviral vectors, which are designed to deliver genes to cells to correct genetic defects. The company was founded in 2015 and is headquartered in New York, New York.
Learn more about Rocket Pharmaceuticals, Inc.
Size
151 employees
Market Cap
$1.4 billion
Industry
Net Income
-$139.7 million
Founded
2015
NASDAQ

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