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synergy

CRDMO offering full product lifecycle services

Organic Synthesis Chemist

Translational Research & Bench BiologyUpdated on Nov 7
Full-timeDallas, TX, USANo salary listedIn-person

About the Job

Requirements

  • A Master’s degree or PhD in Organic Chemistry or a related field is required.
  • At least 7 years of hands-on experience in the organic synthesis of enantiomeric compounds is required.
  • Experience with multi-step organic synthesis and route optimization is required.
  • Deep knowledge of stereochemistry, enantiomeric synthesis, reaction mechanisms, synthetic methodologies, and analytical techniques is required.
  • Hands-on experience documenting work in GMP-compliant laboratory environments is required.
  • Experience working closely with analytical scientists, including interpreting characterization data, coordinating method support, and partnering on project timelines, is required.
  • Hands-on experience with HPLC, GC-MS, and LC-MS is required.

Responsibilities

  • Design and perform multi-step organic syntheses to produce enantiomeric chemical entities.
  • Develop and optimize synthetic routes to improve yield, purity, and scalability of enantiomeric chemicals.
  • Document experimental procedures, data, and results accurately in lab notebooks and reports, following good documentation practices.
  • Collaborate with analytical scientists to support project goals and timelines.
  • Ensure compliance with safety, GMP, and regulatory requirements in all laboratory activities.
  • Troubleshoot synthetic scheme challenges, characterization data, and reaction conditions, and propose solutions.

Desired Qualifications

  • Experience with chiral chromatography and NMR is a plus.

About the Company

synergy

CRDMO offering full product lifecycle services

Synergy Bioscience provides CRDMO/CDMO services for pharma, biotech, and medical devices. It supports the product lifecycle with fee-for-service work, including method development and validation, analytical testing, biocompatibility studies, residual solvent analysis, and clinical research to move products from concept to market. The firm differentiates itself by serving small-to-mid-sized companies with cost-effective, high-quality, end-to-end laboratory and regulatory support across USP/EP/ISO standards. Its goal is to be a dependable technical partner that helps clients navigate regulatory requirements and bring products to market.

Company size
1-10
Company stage
Not listed
Total funding
Not listed
Headquarters
Dallas, TX
Founded
2016

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