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Commission Director Analytical Development Jobs (NOW HIRING)

Otsuka Pharmaceutical Co., Ltd

$169 - $253/hr

Position Summary The Associate Director, Analytical Development (Small Molecules) will lead the strategy, execution and portfolio level of analytical development activities supporting small molecule ...

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How much do commission director analytical development jobs pay per year?

As of Sep 7, 2026, the average yearly pay for commission director analytical development in the United States is $191,412.00, according to ZipRecruiter salary data. Most workers in this role earn between $94,000.00 and $249,000.00 per year, depending on experience, location, and employer.

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Commission Director Analytical Development jobs near you
Infographic showing various Commission Director Analytical Development job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution, with an average salary of $191,412 per year, or $92 per hour.

Associate Director - Analytical Development (Oligonucleotide)

Scorpion Therapeutics

Bridgewater, MA • On-site

$155 - $202/hr

Other

Medical, Dental, Vision, Life, Retirement

Posted 8 days ago

Job description

About The Role

Associate Director, Analytical Development (oligonucleotide-based therapeutics). Provide scientific and strategic leadership for analytical method development, characterization, qualification, validation, and lifecycle management. Lead scientists and collaborate with cross-functional teams (Process Development, Manufacturing, Quality, Regulatory Affairs, and external partners) to execute analytical strategies from early-stage research through commercialization.

What You’ll Do
  • Lead analytical development, characterization, qualification, validation, transfer, and lifecycle management of methods
  • Define analytical control strategies, specifications, stability programs, and impurity characterization approaches
  • Serve as SME in chromatographic and mass spectrometry-based characterization, impurity profiling, degradation pathways, structural characterization, and specification development
  • Oversee internal and external (CRO/CDMO) analytical work for quality, compliance, and on-time delivery
  • Review/approve protocols, reports, regulatory documentation, and data packages for scientific rigor and data integrityAuthor/review analytical sections of IND/CTA/BLA/NDA; support regulatory agency responses
  • Drive innovative analytical technologies and continuous improvement; build and mentor talent; define long-term analytical development strategy
Qualifications
  • BS/MS plus 6+ years biopharma experience OR PhD plus 2 years
  • 3+ years managing direct reports; experience training/mentoring
  • Expertise in chromatography (IP-RP-UPLC, AEX, HILIC) and mass spectrometry-based characterization
  • Knowledge of oligonucleotide impurity profiling, stability assessment, and specification setting
Nice to Have
  • Chemistry/Biochemistry degree; problem-solving skills
  • FDA/EMA/ICH/GMP knowledge; regulatory submission/health authority experience
  • CRO/CDMO relationship management; comfortable in diverse environments
Where/Travel

Bridgewater, NJ; full-time, in-person. Occasional travel ~10%.

Pay Range

$155,000–$201,500 annual.

U.S. Offerings (Highlights)
  • Medical/dental/vision, mental health support, EAP
  • 401(k) match, annual equity awards, ESPP; company-paid life/disability
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