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How much do rna process development associate director jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for rna process development associate director in the United States is $33.68, according to ZipRecruiter salary data. Most workers in this role earn between $27.64 and $41.35 per hour, depending on experience, location, and employer.

What does an RNA Process Development Associate Director do?

An RNA Process Development Associate Director oversees the design, optimization, and scale-up of RNA manufacturing processes within a biotechnology or pharmaceutical company. They lead teams to develop robust and efficient production methods for RNA molecules, such as mRNA for vaccines or therapeutics. This role involves collaborating with research, quality, and regulatory teams to ensure that processes meet compliance and industry standards. Additionally, they are responsible for troubleshooting technical challenges, implementing new technologies, and guiding projects from development through to large-scale production.

What are the key skills and qualifications needed to thrive as an RNA Process Development Associate Director?

To thrive as an RNA Process Development Associate Director, you need advanced expertise in molecular biology, bioprocess engineering, and RNA therapeutics, usually supported by a PhD or relevant master's degree with significant industry experience. Familiarity with bioprocessing platforms, analytical tools like HPLC and qPCR, and regulatory compliance systems such as GMP is essential. Strong leadership, project management, and cross-functional communication skills set top performers apart. These competencies are critical for driving innovative RNA process development, ensuring regulatory compliance, and leading high-performing teams in a fast-evolving biotech landscape.

What are some common challenges faced by an RNA Process Development Associate Director, and how can candidates prepare to address them?

An RNA Process Development Associate Director often faces challenges such as rapidly evolving regulatory requirements, scaling up laboratory processes for commercial manufacturing, and ensuring cross-functional alignment between R&D, quality, and manufacturing teams. Candidates can prepare by developing strong project management skills, staying updated on regulatory guidelines, and gaining experience in both upstream and downstream RNA manufacturing processes. Additionally, effective communication and leadership abilities are crucial for guiding teams through technical and logistical hurdles while maintaining timelines and quality standards.

What are popular job titles related to Rna Process Development Associate Director jobs?

For Rna Process Development Associate Director jobs, the most frequently searched job titles are:

Infographic showing various Rna Process Development Associate Director job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 82% Full Time, 14% Part Time, and 2% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $70,060 per year, or $33.7 per hour.

Senior Director, Product Development, RNA Therapies

Bedford, MA • On-site

Sarepta Therapeutics, Inc.
Biotechnology Research and Development • 1 - 5K employees
Learn more about Sarepta Therapeutics, Inc.external

$222K - $278K/yr

Full-time

Re-posted 22 hours ago

Key responsibilities

  • Establish a product development laboratory for oligonucleotide manufacture and oversee process development strategies from early development through commercialization.

  • Lead teams responsible for process development, scale-up, tech transfer, regulatory support, and validation readiness, ensuring compliance with regulatory expectations.

  • Develop platform approaches and operational strategies to improve efficiency and effectiveness of RNA therapeutic portfolio advancement.

Job description

Why Sarepta? Why Now?
The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold a leadership position in Duchenne muscular dystrophy (Duchenne) and are building a robust portfolio of programs across muscle, central nervous system, and cardiac diseases. In 2023, we launched our fourth therapy and the first ever gene therapy to treat Duchenne.
We're looking for people who see unlimited potential in themselves and who are motivated by an unwavering commitment to patients.
What Sarepta Offers
At Sarepta, we care deeply about all the people in our community and believe in the importance of supporting them in all aspects of their lives. We aspire to maintain a culture that acknowledges people bring their whole selves to work, and we will strive to help everyone in our community integrate their work and personal lives while maintaining productivity. We are committed to offering a range of benefits and work-life resources designed to support people in the following areas:
  • Physical and Emotional Wellness
  • Financial Wellness
  • Support for Caregivers

For a full list of our comprehensive benefits, see our website: https://www.sarepta.com/join-us
The Importance of the Role
The Senior Director, Product Development is a strategic and operational leader accountable for establishing a product development laboratory and delivering robust, scalable, and compliant RNA manufacturing processes across Sarepta's expanding portfolio of oligonucleotide therapeutics and siRNA modalities.
This role defines and executes phase-appropriate process development strategies from early development through commercialization, ensuring alignment with regulatory expectations, technical excellence, and business objectives for RNA based therapeutic modalities.
The Opportunity to Make a Difference
  • Establish a state of the art flexible product development laboratory for oligonucleotide manufacture using standard and novel amidites.
  • Establish a team capable of producing various modification to attach ligands, peptides, lipids and antibodies to oligonucleotides.
  • Develop and oversee relationships with commercial grade manufacturers for linkers, novel ligands and peptides.
  • Own and execute end-to-end process development strategies across modalities from preclinical through commercialization.
  • Lead teams covering process development, scale-up, tech transfer, regulatory support and validation readiness.
  • Develop platform approaches and operational strategies to improve efficiency and effectiveness of advancing Sarepta's portfolio.
  • Provide technical oversight and support in monitoring performance and in resolving investigations.
  • Ensure QbD-aligned control strategies (CPPs, CMAs).
  • Support CDMO selection and oversight.
  • Drive applicable CMC documentation and regulatory submissions.
  • Collaborate with leadership across the organization to continue to advance Sarepta's mission in advancing valuable therapies to patients in need.

More about You
  • PhD in Chemistry, Chemical Engineering, or related field with 12+ years of experience or MS in Chemistry, Chemical Engineering, or a related discipline with 15+ years of relevant industrial experience in RNA manufacturing and process development oversight.
  • Demonstrated experience in RNA based therapeutics that has led to clinical products. Demonstrated knowledge of chemical linking strategies used in manufacturing processes.
  • Strong expertise in scale-up, GMP manufacturing, tech transfer and health agency interactions.
  • Proven leadership in advancing therapies through clinical development and into commercialization.
  • Exceptional written and verbal communication skills, with the ability to clearly convey complex scientific and regulatory concepts.
  • Strong collaboration and teamwork skills, with the ability to support cross-functional peers and maintain a safe, efficient, and compliant laboratory environment.
  • Deep knowledge of process characterization and control strategies.
  • Ability to travel approximately 15%.

What Now?
We're always looking for solution-oriented, critical thinkers.
So, if you're comfortable with ambiguity and candor, relish challenging yourself, and place kindness and integrity at the forefront of how you approach your peers and work, then we encourage you to apply.
#LI-Hybrid
This position is hybrid, you will be expected to work on site at one of Sarepta's facilities in the United States and/or attend Company-sponsored in-person events from time to time.
The targeted salary range for this position is $222,400 - $278,000 per year. Sarepta is making a good faith effort to be transparent and accurate around our hiring ranges. The salary offer is commensurate with Sarepta's compensation philosophy and considers factors including, but not limited to, education, training, experience, external market conditions, criticality of role, and internal equity.
Candidates must be authorized to work in the U.S.
Sarepta Therapeutics offers a competitive compensation and benefit package.
Sarepta Therapeutics is an Equal Opportunity/Affirmative Action employer and participates in e-Verify.

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