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Gc Therapeutics Jobs (NOW HIRING)

Material Scientist

Quincy, IL ยท On-site

$65 - $75/hr

ICP-OES, ICP-MS, XRD, XRF, UV-VIS, FT-IR, GC-MS, HPLC, near IR; statistical software; coding knowledge. * Strong project management, data analysis, and technical writing; collaboration; independent ...

Senior Scientist

Princeton, NJ ยท On-site

$110 - $160/hr

Knowledge of bioanalytical sciences including LC-MS/MS, GC-MS, biotransformation, and physical organic chemistry. * Experience with cell-based or biochemical assays. * Excellent oral and written ...

$125 - $140/hr

Join us on our mission to enable current and next-generation therapeutics to improve and save the ... Primary analytical techniques include chromatography (HPLC/UPLC, GC, and IC), Spectroscopy (LC-MS ...

$115 - $125/hr

Join us on our mission to enable current and next-generation therapeutics to improve and save the ... Primary analytical techniques include chromatography (HPLC/UPLC, GC, and IC), Spectroscopy (LC-MS ...

Showing results 21-40

Gc Therapeutics information

What is GC Therapeutics?

GC Therapeutics refers to professionals or organizations specializing in gene and cell (GC) therapy. These experts develop, test, and manufacture advanced therapies that use genetic engineering or cellular manipulation to treat a range of diseases, including genetic disorders and cancers. GC Therapeutics may involve roles in research, clinical trials, regulatory affairs, and biomanufacturing. Their work is critical for advancing innovative treatments that go beyond traditional pharmaceuticals. The field is rapidly growing and requires a strong background in biology, biotechnology, and regulatory compliance.

What skills and qualifications are needed to thrive as a Cell Therapy Scientist at GC Therapeutics?

To thrive as a Cell Therapy Scientist at GC Therapeutics, you need a strong background in cell biology, molecular biology, or a related field, typically supported by an advanced degree (MS or PhD) and relevant laboratory experience. Familiarity with cell culture techniques, flow cytometry, gene editing tools like CRISPR, and regulatory compliance systems such as GMP is essential. Strong analytical thinking, attention to detail, and effective teamwork and communication skills distinguish top performers in this role. These competencies ensure the safe, efficient, and innovative development of cell-based therapies for clinical applications.

What are common challenges faced by professionals working at GC Therapeutics, and how can they be addressed?

Professionals in GC Therapeutics often encounter challenges such as staying current with rapidly evolving gene and cell therapy technologies, navigating complex regulatory requirements, and coordinating multidisciplinary teams. To address these, it's important to engage in continuous professional development, maintain open communication across research, clinical, and regulatory departments, and participate in industry forums or workshops. Collaboration and adaptability are key, as projects frequently require input from scientists, clinicians, and regulatory experts to ensure successful therapeutic development.

What is the difference between Gc Therapeutics vs Clinical Research Associate?

AspectGc TherapeuticsClinical Research Associate
Required CredentialsBachelor's degree in life sciences, relevant certificationsBachelor's degree, often with clinical research certifications
Work EnvironmentPharmaceutical or biotech company, laboratory settingClinical trial sites, hospitals, research organizations
Employer & IndustryBiotech firms, pharmaceutical companiesResearch organizations, CROs, pharmaceutical companies
Common Search & ComparisonYesYes

Gc Therapeutics professionals focus on developing and testing new therapies within biotech or pharmaceutical companies, often working in labs. Clinical Research Associates (CRAs) oversee clinical trials at research sites, ensuring compliance and data accuracy. While both roles require scientific backgrounds and industry experience, Gc Therapeutics roles are more research and development-oriented, whereas CRAs are more involved in trial management and site coordination.

More about Gc Therapeutics jobs

What cities are hiring for Gc Therapeutics jobs?

Cities with the most Gc Therapeutics job openings:

What states have the most Gc Therapeutics jobs?

States with the most job openings for Gc Therapeutics jobs include:

Infographic showing various Gc Therapeutics job openings in the United States as of August 2026, with employment types broken down into 86% Full Time, 5% Part Time, and 9% Contract. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution.

Analytical Chemist

Initial Therapeutics, Inc.

Indianapolis, IN โ€ข On-site

$65 - $169/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 4 days ago


Key responsibilities

  • Develop and optimize analytical methods to measure purity, potency, and other critical quality attributes of small molecule drug substances and intermediates.

  • Select and implement analytical techniques (HPLC, GC, NMR, MS) to support chemical process development and generate data to elucidate reaction mechanisms, characterize kinetic behavior, and identify impurities.

  • Collaborate with synthetic chemists and process engineers to ensure analytical methods are suitable for guiding development activities and can be transferred to GMP laboratories for routine testing and manufacturing support.


Job description

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work - but it's work worth doing. If you're driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.

Overview

Synthetic Molecule Design and Development have an exciting opportunity for an analytical chemist to join our development group. In this hands-on laboratory role (>70% bench work), you will develop analytical methods and characterize chemical processes to advance drug candidates from early development through manufacturing readiness. You will expand and apply your expertise in chromatographic method development and leverage complementary techniques (mass spectrometry, NMR) while partnering closely with synthetic chemists and process engineers to solve critical process development challenges. The ideal candidate brings practical chromatography experience, strong problem-solving skills, and the ability to translate analytical data into actionable insights for project teams.

Position Responsibilities:
  • Develop and optimize analytical methods to accurately measure purity, potency, and other critical quality attributes of small molecule drug substances and synthetic intermediates.
  • Select and implement appropriate analytical techniques (HPLC, GC, NMR, MS) to support chemical process development - independently generating data that elucidates reaction mechanisms, characterizes kinetic behavior, and identifies process-related impurities.
  • Assess stability of development materials under stressed conditions to evaluate potential degradation using chromatographic techniques.
  • Collaborate with synthetic chemists and process engineers to ensure analytical methods are suitable for guiding development activities and can be successfully transferred to GMP laboratories for routine testing and manufacturing support.
  • Perform laboratory activities with a strong emphasis on safety and technical rigor, while adhering to local policies and procedures.
  • Identify and apply new scientific concepts, exhibit strong problem-solving skills, and be self-motivated to contribute across multiple projects.
  • Demonstrate strong written and verbal communication skills to represent both the technical aspects and business-related implications of your work.
Basic Qualifications:
  • Bachelor or Master of Science degree in Analytical Chemistry, Biochemistry, Chemistry, or a related field.
  • Experience with chromatographic (LC, GC, IC) method development or validation in pharmaceutical, chemical, or regulated industry setting
  • Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.
Additional Skills/Preferences:
  • Working knowledge of mass spectrometry (LC-MS, GC-MS) and NMR spectroscopy
  • Familiarity with chemical process development, synthetic organic chemistry, and rationales for establishing material specifications and testing plans.
  • Experience troubleshooting and maintaining analytical instrumentation.
  • Demonstration of scientific leadership and the ability to influence others.
  • Ability to balance multiple responsibilities, prioritize activities, and navigate ambiguity.
Additional Information:
  • Travel: 0 to 10%
  • Potential exposure to chemicals, allergens, and loud noises
  • Lilly is an EEO/Affirmative Action Employer and does not discriminate based on race, gender, protected veteran status, disability, or any other legally protected status
  • Position Local: Onsite Monday through Friday, Indianapolis, IN; Lilly Technology Center-North (LTC-N)

Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.

Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Womenโ€™s Initiative for Leading at Lilly (WILL).

Actual compensation will depend on a candidateโ€™s education, experience, skills, and geographic location.

$65,250 - $169,400

Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities). Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

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