×
Register Here to Apply for Jobs or Post Jobs. X

Principal Engineer, Technical Development

Remote / Online - Candidates ideally in
Waltham, Middlesex County, Massachusetts, 02254, USA
Listing for: Dyne Tx
Remote/Work from Home position
Listed on 2026-02-27
Job specializations:
  • Engineering
    Process Engineer, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 147000 - 180000 USD Yearly USD 147000.00 180000.00 YEAR
Job Description & How to Apply Below

Our commitment to people with neuromuscular diseases

is our greatest strength

Principal Engineer, Technical Development

Department: 1110GL - Technical Development

Location:
Waltham, MA

Company Overview:

Dyne Therapeutics is focused on delivering functional improvement for people living with genetically driven neuromuscular diseases. We are developing therapeutics that target muscle and the central nervous system (CNS) to address the root cause of disease. The company is advancing clinical programs for Duchenne muscular dystrophy (DMD) and myotonic dystrophy type 1 (DM1) as well as preclinical programs for facioscapulohumeral muscular dystrophy (FSHD) and Pompe disease.

At Dyne, we are on a mission to deliver functional improvement for individuals, families and communities. Learn more at , and follow us on X, Linked In and Facebook.

Role

Summary:

The Principal Engineer, Technical Development serves as a technical engineering lead and driver for strategy, conception, optimization, and implementation of innovative manufacturing technologies within the Technical Development organization. This leader blends deep engineering expertise with cross‑functional influence to implement innovative manufacturing systems for bioprocess and bioconjugation at clinical and commercial scales and accelerates time to market. The role is ideal for someone who thrives at the intersection of innovation, operations, and process development strategy.

This is a full‑time position based in Waltham, MA with no option for remote work.

Primary Responsibilities:

Technical Leadership

  • Design, optimize and implement engineering for manufacturing processes for new and existing products under current Good Manufacturing Practices (cGMP)
  • Lead engineering technology selection, process modeling, equipment specification, and system integration and provide guidance and oversight of outsourced activities at CDMOs.
  • Develop and validate process control strategies, including PAT, automation, and real time monitoring.
  • Serve as the subject matter expert for engineering across manufacturing, operations, and R&D.

Strategic Impact

  • Build and execute the long‑term engineering roadmap for manufacturing capabilities across all relevant modalities (biologics, oligonucleotides, and bioconjugates).
  • Identify opportunities to transition batch processes to innovative platforms, improving throughput and cost‑of‑goods, while preserving product quality.
  • Partner with senior leadership to align manufacturing strategy with business goals and regulatory expectations.

Cross Functional Collaboration

  • Work closely with Quality, Supply Chain, and Manufacturing Operations to ensure seamless technology transfer and scaleup.
  • Guide technical teams through engineering design reviews, process risk assessments, and regulatory submissions, fostering a culture of innovation and technical excellence.

Operational Excellence

  • Drive continuous improvement initiatives using Lean, Six Sigma, and advanced process analytics.
  • Troubleshoot complex manufacturing challenges and implement robust, sustainable solutions.
  • Ensure compliance with cGMP, safety standards, and global regulatory requirements.
Education, Experience, and Skills Requirements:
  • Bachelor’s degree in chemical or similar engineering discipline with minimum of 7 years relevant experience; advanced degree MS or PhD preferred
  • Proven track record designing, implementing, and scaling manufacturing systems
  • Hands‑on approach for operation of and troubleshooting manufacturing skids
  • Development and implementation of PAT technologies
  • Experience overseeing outsourced activities at CDMOs
  • Expertise in process modeling, control systems, automation, and PAT.
  • Experience in Biologics Downstream Purification Process Development and/or Bioconjugation Development preferred
  • Familiar with the concepts of Scale‑Down Model Qualification (SDMQ), Process Characterization, and defining Process Control Strategy (PCS)
  • Strong understanding of current Good Manufacturing Practices (cGMP) and regulatory frameworks (FDA, EMA, ICH) relevant to continuous manufacturing of biologics.
  • Attention to detail, exceptional communication skills, and the ability to influence all levels of the…
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
 
 
 
Search for further Jobs Here:
(Try combinations for better Results! Or enter less keywords for broader Results)
Location
Increase/decrease your Search Radius (miles)

Job Posting Language
Employment Category
Education (minimum level)
Filters
Education Level
Experience Level (years)
Posted in last:
Salary