Director, Peptide Process R&D and Scale-Up

Posted Yesterday
Be an Early Applicant
Fishers, IN, USA
In-Office
Senior level
Biotech • Consulting • Pharmaceutical • Manufacturing
The Role
Lead end-to-end peptide process development and scale-up from R&D through first cGMP batches. Define technical direction, select equipment, establish process controls and analytical strategies, drive CMC content for regulatory filings, partner on facility design and commissioning, and build the process development/CMC organization post-Series A. Hands-on leadership with floor-level manufacturing involvement during scale-up and PPQ.
Summary Generated by Built In

Pinnaql is a trusted consulting partner to regulated life sciences companies, providing deep technical, validation, and quality expertise across every stage of the product lifecycle. We partner with pharmaceutical, biotech, and medical device organizations to navigate complexity, accelerate project timelines, and maintain a strong state of compliance and audit readiness.

We are seeking a Director, Peptide Process R&D and Scale-Up to serve as a founding technical leader for an emerging peptide therapeutics company establishing next-generation manufacturing and drug development capabilities in Fishers, IN.

This is a high-impact, hands-on leadership role where you will own peptide process development from early-stage R&D through first cGMP batch production. You will define the technical direction, make critical scale-up decisions, and establish the foundation for the company’s future CMC and process development organization.

This is not a purely strategic role—you will be deeply involved in execution, working directly on the manufacturing floor and influencing real-time decisions.

Candidates must be legally authorized to work in the United States and able to maintain that authorization independently throughout employment. The company is unable to provide employment visa sponsorship for this position. Relocation assistance is available for qualified U.S. based candidates.

Key Responsibilities:

  • Own end-to-end peptide process development and scale-up strategy and execution
  • Design, develop, and scale Fmoc SPPS processes for commercial manufacturing
  • Serve as the technical authority on process development, scale-up, and manufacturing readiness
  • Translate uncertainty into clear, actionable decisions across:
    • Equipment selection
    • Process parameters
    • Purification strategy
    • Cleaning and validation approaches
  • Lead technical CMC content development supporting DMF/ANDA filings
  • Drive equipment URS definition and selection (SPPS reactors, prep HPLC, lyophilization systems)
  • Partner with engineering firms and vendors to enable facility design, build, and commissioning
  • Establish process controls, analytical strategies, and GMP readiness
  • Lead and support scale-up campaigns, PPQ, and first cGMP batch execution
  • Build and scale the process development and CMC function post-Series A

Minimum Qualifications:

  • Extensive hands-on experience scaling Fmoc SPPS processes to commercial or near-commercial scale
  • Direct kilo-scale manufacturing / reactor experience (on the floor, not just in the lab)
  • Proven participation in GMP campaigns or late-stage scale-up programs
  • Demonstrated ability to own development through GMP execution
  • Strong decision-making ability in ambiguous, early-stage environments

Preferred Qualifications:

  • Experience authoring technical CMC sections for DMF or ANDA submissions
  • Experience with facility startup, tech transfer, and equipment qualification (CQV)
  • Deep expertise in:
    • Lipidation and complex peptide chemistries
    • Disulfide bond formation
    • Impurity control strategies
    • Cleaning validation
  • Experience with prep HPLC, lyophilization, and solvent systems at scale
  • PhD preferred; strong MS candidates considered

Leadership & Technical Expectations:

  • Ability to design and size:
    • SPPS reactor trains
    • Purification systems
    • Lyophilization capacity
  • Deep understanding of scale-up risks, tradeoffs, and failure modes
  • Operates with an owner mindset, balancing speed and technical rigor
  • Comfortable challenging vendors, consultants, and assumptions when needed

At Pinnaql, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

Excited to build something meaningful together? We look forward to hearing from you.

Pinnaql is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

#LI-ONSITE

#LI-LN1

Skills Required

  • Extensive hands-on experience scaling Fmoc SPPS processes to commercial or near-commercial scale
  • Direct kilo-scale manufacturing / reactor experience (on the floor, not just in the lab)
  • Proven participation in GMP campaigns or late-stage scale-up programs
  • Demonstrated ability to own development through GMP execution
  • Strong decision-making ability in ambiguous, early-stage environments
  • Experience authoring technical CMC sections for DMF or ANDA submissions
  • Experience with facility startup, tech transfer, and equipment qualification (CQV)
  • Deep expertise in lipidation and complex peptide chemistries
  • Deep expertise in disulfide bond formation
  • Expertise in impurity control strategies
  • Experience with cleaning validation
  • Experience with prep HPLC, lyophilization, and solvent systems at scale
  • PhD preferred; strong MS candidates considered
  • Ability to design and size SPPS reactor trains, purification systems, and lyophilization capacity
Am I A Good Fit?
beta
Get Personalized Job Insights.
Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.

The Company
154 Employees
Year Founded: 2019

What We Do

Pinnaql, Inc. is a professional services consulting firm providing quality, regulatory, and operational excellence solutions to biopharmaceutical, medical device, and CDMO companies worldwide. The company specializes in laboratory validation, engineering, and compliance, helping regulated life sciences organizations navigate manufacturing challenges, reduce execution risks, and accelerate the transition from lab innovation to commercial market readiness.

Similar Jobs

PwC Logo PwC

Senior Manager, Internal Investigations

Artificial Intelligence • Professional Services • Business Intelligence • Consulting • Cybersecurity • Generative AI
Remote or Hybrid
67 Locations
370000 Employees
91K-322K Annually

PwC Logo PwC

US Tech - AI Engineering Senior Associate

Artificial Intelligence • Professional Services • Business Intelligence • Consulting • Cybersecurity • Generative AI
Remote or Hybrid
68 Locations
370000 Employees
151K-187K Annually

PwC Logo PwC

Engineering Manager

Artificial Intelligence • Professional Services • Business Intelligence • Consulting • Cybersecurity • Generative AI
Remote or Hybrid
68 Locations
370000 Employees
212K-244K Annually

General Motors Logo General Motors

Sales Manager

Automotive • Big Data • Information Technology • Robotics • Software • Transportation • Manufacturing
Remote or Hybrid
United States
165000 Employees
81K-109K Annually

Similar Companies Hiring

Amplify Platform Thumbnail
Fintech • Financial Services • Consulting • Cloud • Business Intelligence • Big Data Analytics
Scottsdale, AZ
62 Employees
Fortune Brands Innovations Thumbnail
Manufacturing
Deerfield, IL
2450 Employees
Amalgamated Sugar Thumbnail
Food • Greentech • Agriculture • Industrial • Manufacturing
Boise, Idaho
768 Employees

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account