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Manager Analytical Development Jobs in Pennsylvania

Pace

Analytical Chemist- Small Molecule

Norristown, PA · On-site

$75K - $85K/yr

This is a full-time Analytical Chemist / Scientist II Position located in Norristown, PA, Monday ... Serving as a team member and the development and management of projects. * Operating in both a team ...

Altasciences

Senior Analytical Scientist

Harleysville, PA · On-site

$120 - $150/hr

Design and manage analytical approaches to support early drug development projects (R&D, Preclinical and Phase I Clinical) with a focus on chromatographic, dissolution, particle size distribution ...

Merck & Co.

The Vaccine Analytical Research & Development department of our Research & Development Division is ... management. In this role, the individual will work with a team of scientists to develop ...

Altasciences

Senior Analytical Scientist

Harleysville, PA · On-site

$88K - $120K/yr

Design and manage analytical approaches to support early drug development projects (R&D, Preclinical and Phase I Clinical) with a focus on chromatographic, dissolution, particle size distribution ...

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All JobsAnalytical Development JobsManager Analytical Development JobsManager Analytical Development Jobs in Pennsylvania

Manager Analytical Development information

See Pennsylvania salary details

$33.1K

$77.6K

$133.3K

How much do manager analytical development jobs pay per year?

As of Sep 2, 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.

Process & Analytical Development Specialist

Verismo Therapeutics

Philadelphia, PA

Full-time

Re-posted 26 days ago

Job description

Process & Analytical Development Specialist 


Full-Time position
Level: Specialist
Location: On-site in Philadelphia PA
Start date: Open


Why Join Verismo?

Our team is small but driven, with the single focus of bringing life-changing cell therapies to patients with cancer. With a solid pipeline built around a novel KIR-CAR platform, our technology has found a way to circumvent the barriers in solid cancer where other CAR therapies have limited success. KIR-CARs eliminate the artificial chimeric constructs within T cells and instead use a natural NK-cell derived signaling system. This system is potent against both hematologic and solid tumors, and in preclinical models is superior to current CAR-T in conferring long-term sustained anti-tumor function to overcome the challenges posed in solid cancer. We have a strong team for CMC, clinical product manufacture, and clinical investigators already established and moving fast to bring KIR-CARs to patients in need.

Our company is comprised of individuals who each bring something unique to the table and are valued for their contributions. Our culture is based on the concept of 'love what you do' and the dedication that builds a team where people do their best and support one another. Because we believe our people are our greatest asset, career development is an important aspect of our investment in our team and we encourage work/life balance.

About the Position:

We are seeking a passionate and skilled Process & Analytical Development Specialist to join our growing CMC team. In this role, you will play a pivotal role in advancing Verismo's cell therapy products by supporting process and analytical development activities. Reporting directly to the Senior Manager of Process Development, you will contribute hands-on expertise to scale up processes, analyze data, and support tech transfers to external manufacturing partners.

Essential Duties & Responsibilities:
  • Contribute to the setup and organization of Verismo Therapeutics' process and analytical development capabilities.
  • Execute complex development studies (with multiple experiment sets) related to process development and scale-up, ensuring studies balance time and resources.
  • Apply Quality by Design (QBD) principals to process development, characterization, establish process parameters, and contribute to CMC regulatory filings.
  • Support next generation manufacturing processes and analytics for cell therapy and lentiviral vector
  • Author technical and scientific documents including but not limited to SOPs, Master Batch Records, study protocols and reports.
  • Ensure all documentation and reports are accurate, complete, and suitable for support of development, characterization, and regulatory approval of products.

Preferred Experience & Abilities:
  • Experience in a cGMP manufacturing and/or QC setting or process and/or analytical development laboratory
  • Background in cell processing, scale up and tech transfer
  • Working knowledge of analytical tools commonly utilized in cell therapy manufacturing
  • Familiarity with quality by design (QbD) approaches and design of experiment (DoE) based studies
  • Ability to function in a dynamic environment.
  • Knowledge of GMP regulations as it pertains to best practices in cGMP manufacturing
  • Experience with Good Documentation Practices (GDP)

Qualification Requirements:

Bachelor's degree in a scientific field with at least 2 years of relevant experience.

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