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Postdoctoral Position In Peptide Synthesis Jobs in New York

Mount Sinai Hospital

Postdoctoral Fellow-MSH

Manhattan, NY · On-site

$53K - $73K/yr

A postdoctoral position in bioinformatics/Biostatistics/data science is available at the Icahn School of Medicine at Mount Sinai. The successful candidate will be joining the Suarez-Farinas Lab, a ...

Mount Sinai Hospital

Postdoctoral Fellow-MSH

Manhattan, NY · On-site

$53K - $73K/yr

This position is funded through a five-year grant from the National Institutes of Health with additional support available to potentially extend in the longer term. The Postdoctoral Fellow will be ...

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Postdoctoral Position In Peptide Synthesis information

What is a postdoctoral position in peptide synthesis?

A Postdoctoral Position in Peptide Synthesis is a research-focused role for individuals who have recently completed their Ph.D. in chemistry, biochemistry, or a related field. The primary responsibility is to design, synthesize, and characterize peptides for various scientific studies, often in drug discovery or biomedical research. Postdocs in this area may also be involved in developing new synthetic methodologies, analyzing experimental data, and publishing their findings. These roles typically provide training and experience necessary for an academic or industry career in chemical and biological sciences.

What are the key skills and qualifications needed to thrive in a postdoctoral position in peptide synthesis?

To thrive in a Postdoctoral Position in Peptide Synthesis, you need a PhD in chemistry, biochemistry, or a related field with a solid background in peptide synthesis and purification techniques. Experience with analytical tools such as HPLC, mass spectrometry, and peptide synthesizers, as well as familiarity with relevant software, is typically required. Strong problem-solving abilities, attention to detail, and effective collaboration and communication skills help you excel in multidisciplinary research environments. These skills ensure the successful design, synthesis, and analysis of peptides, contributing to impactful research outcomes.

What are some common challenges faced in a postdoctoral position in peptide synthesis, and how can they be addressed?

Postdoctoral researchers in peptide synthesis often encounter challenges such as optimizing synthetic routes for complex peptides, managing the purification of difficult sequences, and troubleshooting low yields or unexpected side reactions. These hurdles can be addressed by staying current with the latest literature, using advanced purification techniques like HPLC, and collaborating closely with other chemists or biochemists in the lab. Open communication with mentors and team members also helps in brainstorming solutions and sharing best practices, fostering a collaborative environment that is essential for overcoming technical obstacles.

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Infographic showing various Postdoctoral Position In Peptide Synthesis job openings in New York as of August 2026, with employment types broken down into 100% Full Time. Highlights an 95% In-person, and 5% Remote job distribution.

Technical Manager - Peptide Development

Perspective Therapeutics, Inc.

Somerset, NJ • On-site

Full-time

Re-posted 3 days ago

Job description

Objective
Reporting to the Senior Director, CMC Operations, the CMC Technical Manager, Peptide Development is responsible for the technical oversight of peptide programs at CDMO manufacturing sites and in-house R&D activities. This role supports phase-appropriate development, disposition, and distribution of Perspective Therapeutics' peptide-based radiopharmaceuticals across Phase I-III clinical and pre-commercial programs. The individual will serve as a key technical lead for late-stage peptide development and commercialization activities, including process scale-up, technology transfer, process validation, regulatory submissions, and commercial readiness efforts. This role will ensure compliance with GMP standards, provide oversight of quality-related activities, and serve as a subject matter expert throughout clinical development and commercialization.
Essential Functions
  • Responsible for overseeing all the peptide programs at CDMO and ensuring the activities are completed in a timely manner to support peptide based radiopharmaceutical drug candidates.
  • Lead peptide CMC activities supporting process scale-up, technology transfer, process validation, and commercial readiness at internal and external manufacturing sites.
  • Responsible for review and approval of master batch records, method validation protocols and reports, test methods, specifications, etc. for early phase clinical, late phase clinical and commercial peptide products.
  • Manage the technical and quality aspects of peptide development programs from raw materials through manufacturing, packaging, distribution release and stability, ensuring phase-appropriate GMP compliance and inspection readiness.
  • Provide technical leadership for batch record as review, deviation investigations, CAPAs, change controls, product impact assessments, and disposition activities in partnership with Quality Assurance (QA).
  • Work closely with QA and early Discovery organizations throughout the development and manufacturing processes.
  • Ensure all relevant SOPs are followed to support activities carried out at CDMOs.
  • Acting as SME when needed and in providing or reviewing responses to regulatory agency findings from inspections.
  • Draft and technical review of IND/IMPD CMC sections, briefing packages, and any other regulatory submissions.
Qualifications
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
This is a hybrid position that will require travel to manufacturing sites.Education / Experience
  • Minimum B.S degree in Chemistry, Biochemistry or related field is required.
  • 7+ years' experience in Pharmaceutical Industry in a similar function.
  • Prior experience with peptide synthesis, purification and lyophilization.
  • Demonstrated experience leading peptide CMC programs through late-stage clinical development and/or commercialization, including scale-up, technology transfer, process validation, and regulatory interactions with external manufacturing partners.
  • Experience supporting quality systems and quality-related activities, including deviations, CAPAs, change controls, investigations, and regulatory inspections.
  • Technical writing experience to support CMC module 3.
  • Familiarity with Regulatory and Quality Assurance aspects in manufacturing processes of peptide products.
  • Technical auditing and Radiopharmaceutical experience are a plus.
  • Highly proficient in Microsoft Office (Word, Excel, PowerPoint, Outlook).

Knowledge / Skill / Ability
  • Broad knowledge of risk-based quality systems approaches consistent with ICH Q10 for pharmaceuticals.
  • Full understanding of GMP and peptide manufacturing, methods validations, specifications, and release/stability.
  • Deep understanding of peptide process development, scale-up, manufacturing controls, and commercialization requirements for late-stage clinical and commercial products.
  • Strong project management skills, including contracting, budgeting, and timeline oversight.
  • Must have excellent communication skills (verbal and written).
  • Highly organized with a strong attention to detail, clarity, accuracy and conciseness.
  • Ability to multitask and manage parallel workstreams in a fast-paced drug development environment.
  • Ability to travel up to 15%.
Work Environment
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.
  • Must be willing to work in a facility producing radioactive materials and requiring all employees to participate in safety programs designed to minimize potential and/or actual exposure levels.
  • May be required to sit or stand for long periods of 8+ hours a day while performing duties.
  • Willingness to complete safety training within allotted time limits, and work in a team-based environment.
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.
The annual salary range for this position is $125-160K. For information on Perspective Therapeutics, visit our website at: www.perspectivetherapeutics.com.
Perspective Therapeutics provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.

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