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Executive Manager Analytical Development Jobs (NOW HIRING)

$134K - $201K/yr

Provide analytical data to support drug substance and drug product development, including purity analysis, chiral purity, and structure elucidation using mass spectrometry. Manage pharmaceutical ...

Lead, develop, and manage a multidisciplinary technical team, including resource planning ... Collaborate with Analytical Development leaders and cross-functional partners to ensure analytical ...

Lead, develop, and manage a multidisciplinary technical team, including resource planning ... Collaborate with Analytical Development leaders and cross-functional partners to ensure analytical ...

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Executive Manager Analytical Development information

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$59.9K

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How much do executive manager analytical development jobs pay per year?

As of Sep 11, 2026, the average yearly pay for executive manager analytical development in the United States is $59,924.00, according to ZipRecruiter salary data. Most workers in this role earn between $52,500.00 and $66,000.00 per year, depending on experience, location, and employer.

What are the most commonly searched types of Manager Analytical Development jobs?

The most popular types of Manager Analytical Development jobs are:

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Infographic showing various Executive Manager Analytical Development job openings in the United States as of July 2026, with employment types broken down into 1% Internship, 92% Full Time, 5% Part Time, and 2% Contract. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $59,924 per year, or $28.8 per hour.

Sr. Manager, Analytical Development

San Francisco, CA • On-site

Scorpion Therapeutics
51 - 200 employees

$175K - $185K/yr

Other

Posted 6 days ago


Job description

What You'll Do
  • Manage analytical development, QC, and stability activities at contract manufacturing sites and contribute to the development of clinical assets and regulatory submissions.
  • Collaborate closely with Drug Substance, Drug Product, and Quality Assurance.
Responsibilities
  • Manage contract drug substance and drug product analytical development and QC activities and timelines.
  • Author and review analytical method transfer and validation protocols and reports.
  • Support batch release by reviewing/approving sampling plans and analytical data; generate/maintain CoAs, CoTs, and product specifications.
  • Review stability protocols and monitor stability programs.
  • Author, review, and adjudicate relevant CMC sections for US and ex-US regulatory filings.
  • Partner with QA on change controls; lead OOS/OOT and deviation investigations, identify root causes, and implement CAPAs.
  • Develop, revise, and approve SOPs and QC processes.
Qualifications
  • At least 10 years of experience in Analytical Development and/or Quality Control in a pharmaceutical setting.
  • Familiarity with CMC analytical regulatory requirements; authoring IND/IMPD/BLA/NDA/MAA filings and responses to regulatory inquiries.
  • Independent proficiency in analytical techniques for biologics and small molecules.
  • Thorough understanding of cGMPs, USP, and ICH guidelines.
  • Stability program management expertise (protocol design, data trending/analysis such as JMP, shelf-life assignment/extension).
  • Proficiency with Veeva Vault, TrackWise, and LIMS.
Skills/Requirements
  • Excellent verbal and written communication; ability to communicate with vendors and prioritize to meet timelines.
  • Ability to adapt to changing priorities and make independent decisions under tight timelines.
  • 5–15% travel; ability to travel internationally.
Where You'll Work
  • Hybrid role; in-office collaboration 2x per week in San Francisco.
Compensation/Benefits (if included)
  • Salary range (California): $175,000–$185,000 USD.
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