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Manager Analytical Development information

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$33.1K

$77.6K

$133.3K

How much do manager analytical development jobs pay per year?

As of Sep 3, 2026, the average yearly pay for manager analytical development in Pennsylvania is $77,624.00, according to ZipRecruiter salary data. Most workers in this role earn between $58,600.00 and $90,700.00 per year, depending on experience, location, and employer.

What is a manager analytical development?

A Manager Analytical Development oversees the development, validation, and implementation of analytical methods to support product development and manufacturing. They ensure compliance with regulatory standards, manage a team of scientists, and collaborate with cross-functional departments to drive innovation and efficiency. Their role is critical in ensuring product quality, consistency, and regulatory approval.

What are the typical day-to-day responsibilities for a manager analytical development?

As a Manager Analytical Development, your typical day involves overseeing laboratory teams, managing analytical method development and validation projects, and ensuring compliance with relevant quality standards. You’ll often collaborate with R&D, quality assurance, and production departments to support product development timelines and troubleshoot analytical challenges. Additionally, you may conduct data reviews, prepare regulatory documentation, and participate in meetings to drive project progress. Your role also includes mentoring team members and optimizing lab workflows for productivity and accuracy.

What are the key skills and qualifications needed to thrive in the manager analytical development position, and why are they important?

To excel as a Manager Analytical Development, you typically need an advanced degree in chemistry, biochemistry, or a related field, along with experience in analytical method development and leadership. Familiarity with laboratory information management systems (LIMS), chromatographic software (HPLC/UPLC), and regulatory standards such as ICH and FDA guidelines is common. Outstanding project management, team leadership, and communication skills help you effectively coordinate cross-functional projects and mentor staff. These competencies enable delivery of high-quality analytical solutions, ensure regulatory compliance, and drive successful product development.

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

The most popular types of Analytical Development jobs in Pennsylvania are:

What are popular job titles related to Manager Analytical Development jobs in Pennsylvania?

For Manager Analytical Development jobs in Pennsylvania, the most frequently searched job titles are:

What job categories do people searching Manager Analytical Development jobs in Pennsylvania look for?

The top searched job categories for Manager Analytical Development jobs in Pennsylvania are:

What cities in Pennsylvania are hiring for Manager Analytical Development jobs?

Cities in Pennsylvania with the most Manager Analytical Development job openings:

Manager Analytical Development jobs near you
Infographic showing various Manager Analytical Development job openings in Pennsylvania as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 19% Part Time, 2% Contract, and 1% Nights. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $77,624 per year, or $37.3 per hour.

(Associate) Scientist, Upstream Viral Process Development

Dispatch Bio

Philadelphia, PA • On-site

Full-time

Re-posted 13 days ago

Job description

The role:

Reporting to the Director, Upstream Process Development, the (Associate) Scientist will contribute to upstream viral process development to bring the company's pipeline of T cell and viral vector-based products to the clinic. Responsibilities will include, but are not limited to, performing the day-to-day activities of the viral process development lab, building the company's viral manufacturing capabilities, and executing experiments to support viral process development/characterization. This role will collaborate significantly with research and analytical development teams. 

Key responsibilities:

  • Contribute to the setup and organization of the company's vector process development capabilities. 
  • Perform day-to-day activities in the vector process development lab including maintaining equipment, ordering materials, managing inventory, and preparing buffers and process aids. 
  • Serve as a PD subject matter expert on both internal and external teams (CDMO, material & equipment suppliers, etc.). 
  • Develop bench scale suspension culture processes for viral vector generation within shake flasks and bioreactors. 
  • Design and execute experiments to support process characterization, and process transfer activities between the research team, TechOps, and external partners. 
  • Provide experimental execution, data review and analysis, and maintenance of accurate and detailed lab notebooks. 
  • Author and review technical documents, including but not limited to batch records, SOPs, development reports and process specific sections of regulatory documents. 
  • Represent the company externally at meetings (professional associations, with regulatory bodies, etc.) 

Required experience & skills:

  • Bachelor's Degree in chemical engineering, biochemical engineering/bioengineering, biotechnology or related discipline with at least 2 years of relevant experience- OR- Master's Degree in relevant discipline 
  • Hands-on experience with viral vector upstream processes, particularly experimentation in and operation of stirred-tank bioreactors 
  • Working knowledge of GMP guidelines for clinical manufacturing 
  • Strong scientific reasoning, problem-solving, and applied mathematics and statistics skills, including the ability to break down complex problems into manageable hypotheses 
  • Proficiency in using Microsoft Word, Excel, Power Point and data analysis/presentation software such as JMP and/or GraphPad 
  • Excellent interpersonal, verbal and written communication skills 
  • Strong organizational & problem-solving skills, with excellent attention-to-detail and the proven ability to collaborate in a dynamic team environment 

Preferred experience & skills:

  • Experience implementing processes in clinical and commercial manufacturing of cell and gene therapy products 
  • Demonstrated ability to apply knowledge of cell biology, chemical engineering, or bioengineering toward process development, scale-up /scale-down and troubleshooting 
  • Detailed understanding of bioreactor operation and control loops 
  • Experience drafting CMC sections for INDs 
  • Proven experience collaborating with internal and external partners 

 

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