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Manager Analytical Development Jobs in New York (NOW HIRING)

Neion Bio

Scientist, Analytical Development

New York, NY · On-site

$130/hr

The successful candidate will be responsible for in-house development and managing external programs. Key Responsibilities * Develop and execute analytical strategies for monoclonal antibodies and ...

Neion Bio

Scientist, Analytical Development

New York, NY · On-site

$130/hr

The successful candidate will be responsible for in-house development and managing external programs. Key Responsibilities * Develop and execute analytical strategies for monoclonal antibodies and ...

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Manager Analytical Development information

See New York salary details

$36.1K

$84.7K

$145.5K

How much do manager analytical development jobs pay per year?

As of Aug 5, 2026, the average yearly pay for manager analytical development in New York is $84,720.00, according to ZipRecruiter salary data. Most workers in this role earn between $64,000.00 and $99,000.00 per year, depending on experience, location, and employer.

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 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 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 does a Manager Analytical Development do?

A Manager of Analytical Development oversees the design, validation, and implementation of analytical methods used to test and ensure the quality of pharmaceutical or biotech products. They lead teams of scientists, coordinate method development projects, and ensure compliance with regulatory standards such as GMP and FDA guidelines. The role often requires expertise in analytical techniques, laboratory management, and relevant certifications.
What are the most commonly searched types of Analytical Development jobs in New York? The most popular types of Analytical Development jobs in New York are:
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What cities in New York are hiring for Manager Analytical Development jobs? Cities in New York with the most Manager Analytical Development job openings:
Manager Analytical Development jobs near you
Infographic showing various Manager Analytical Development job openings in New York as of July 2026, with employment types broken down into 89% Full Time, 8% Part Time, and 3% Contract. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $84,720 per year, or $40.7 per hour.

Contract, Analytical Development

Ptc Therapeutics, Inc.

Bridgewater, NJ • On-site

Full-time

Posted 9 days ago

Job description

PTC Therapeutics is a global commercial biopharmaceutical company. For over 25 years our team has been deeply committed to a unified purpose: Extending life's moments for children and adults living with a rare disease.

At PTC, we cultivate an inclusive culture where everyone feels valued, respected, and empowered. We welcome candidates from all backgrounds to join our team, fostering a strong sense of belonging.

Visit our website to learn more about our company and culture!
Site: www.ptcbio.com

Job Description Summary: The Contract, Analytical Development supports and contributes to PTC's analytical development function for early stage and late stage development projects. The incumbent develops, implements, validates, transfers and troubleshoots a variety of analytical methods (e.g. Chromatographic methods) used for in-process evaluation, releases of Active Pharmaceutical Ingredients (API), and bulk and final drug products at Contract Research Organizations (CROs) and Contract Manufacturing Organizations (CMOs/CDMOs). He/she also provides analytical support for clinical formulation development.
The incumbent works cross-functionally with internal departments and external resources on analytical development related issues.
The Contract, Analytical Development supports adherence to relevant regulatory requirements and company Standard Operating Procedures (SOPs) as appropriate.
.Job Description:

ESSENTIAL FUNCTIONS

Primary duties/responsibilities:

  • Conducts analytical method development for New Chemical Entities (NCEs) and drug products using chromatography and other analytical techniques.
  • Coordinates development of analytical and control tests for API, starting materials, process intermediates and drug product at PTC and at CMOs; provides oversight and direction for analytical method transfer and validation at external CMOs.
  • Coordinates requirements and acquisition of analytical documentation/data/reports needed to support, or to be included in, submissions to Investigational New Drug applications (INDs), New Drug Applications (NDAs), Marketing Authorization Applications (MAAs), amendments, supplements, and annual reports; authors and reviews regulatory documents and responses.
  • Perform investigations and unknown impurity identifications in in-house lab using High Pressure Liquid Chromatography (HPLC), Liquid Chromatography/Mass Spectrometry (LC/MS) and Gas Chromatography/Mass Spectrometry (GC/MS).
  • Assists in providing oversight for all stability related work at CROs/CMOs/CDMOs.
  • Represents department as a subject matter expert (SME) in relevant analytical areas, as needed.
  • Complies data from internal and external sources and provides data summaries to management.
  • Conducts a second analyst review of analytical data and work, as needed.
  • Provides analytical support to early and late stage discovery programs, as needed.
  • Coordinates analytical development related activities within the company and external contractors as needed.
  • Purchases required lab supplies, maintains instruments, purchases, installs, qualifies laboratory instrumentation.
  • Performs other tasks and assignments as needed and specified by management.

KNOWLEDGE/SKILLS/ABILITIES REQUIRED

* Minimum level of education and years of relevant work experience.

  • Master's degree in a Chemistry, Biochemistry or Pharmacy related discipline and a minimum of 6 years of analytical development experience in a pharmaceutical, biotechnology or other related industries OR a PhD in a Chemistry, Biochemistry or Pharmacy related discipline and a minimum of 2 years of analytical development experience in a pharmaceutical, biotechnology or other related industries.

* Special knowledge or skills needed and/or licenses or certificates required.

  • Extensive experience in the development, validation, and implementation of analytical Standard Operating Procedures (SOPs) that employ a range of analytical methods (e.g., High Pressure Liquid Chromatography (HPLC), Liquid Chromatography/Mass Spectrometry (LC/MS), Gas Chromatography/Mass Spectrometry (GC/MS), dissolution, particle size, moisture content, etc.).
  • Hands-on experience with the identification, sourcing, and maintenance of analytical instruments.
  • Demonstrated experience in troubleshooting of analytical methods.
  • Working knowledge of US and international Chemistry, Manufacturing and Control (CMC) regulations and guidance, including Good Manufacturing Practice (GMP), the US Code of Federal Regulations (21CFR) and International Conference of Harmonization (ICH) guidelines is desirable.
  • Working knowledge of Laboratory Information Management Systems (LIMS) and Chromatographic data systems (e.g. Empower).
  • Management of reference standards for internal and external needs, as necessary.
  • Experience reviewing analytical data (at release and stability).
  • Experience with designing and executing forced degradation studies for NCEs.
  • Hands-on experience collaborating with the Formulations and Medicinal Chemistry groups in developing analytical methods such as HPLC-UV for early phase formulation development.
  • Proficiency with Microsoft Office.
  • Excellent verbal and written communication and skills.
  • Ability to work independently and collaboratively, as required, in a fast-paced, matrixed, team environment consisting of internal and external team members.
  • Analytical thinker with excellent problem-solving skills and the ability to adapt to changing priorities and deadlines.
  • Excellent planning, organization and time management skills including the ability to manage, support and prioritize multiple projects.

*Special knowledge or skills and/or licenses or certificates preferred.

  • Experience using electronic lab notebook.
  • Track record of authorship of pertinent sections of successful regulatory submissions (INDs, NDAs, Abbreviated New Drug Applications (ANDAs), MAAs, Investigational Medicinal Product Dossiers (IMPDs)) leading to the commercialization of drug products.
  • Experience providing responses to questions from health authorities with respect to regulatory submissions.
  • Experience with statistical data analysis.

* Travel requirements

  • 0-10%
  • Office /Laboratory based position

Expected Hourly Range:

$60 - $85/hour. The hourly salary offered will be contingent on assessment of candidate education level, background, and experience relative to the requirements of the position they are being considered for, as well as review of internal equity.

EEO Statement:

PTC Therapeutics is an equal opportunity employer. We welcome applications from all individuals, regardless of race, color, national origin, gender, age, physical characteristics, social origin, disability, religion, family status, pregnancy, sexual orientation, gender identity, gender expression, disability, veteran status or any unlawful criterion under applicable law. We are committed to treating all applicants fairly and avoiding discrimination.

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