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Gc Therapeutics Jobs (NOW HIRING)

Anodyne

Optometrist

Boston, MA · On-site

$140K - $160K/yr

Topical and Oral Therapeutic Pharmaceutical Agents (TPA) Certification. * Glaucoma Certification (GC). * Excellent clinical judgment and communication skills. * Commitment to providing exceptional ...

PHARMALOGIC HOLDINGS

PET Chemist

Salem, VA · On-site

$60K - $75K/yr

... therapeutic agents to patients from bench to bedside. PharmaLogic offers you an exceptional ... Support analytical methods for HPLC, GC and TLC. Quality Control testing of final product. 2.  ...

PHARMALOGIC HOLDINGS

PET Chemist

Pittsburgh, PA · On-site

$65K - $80K/yr

... therapeutic agents to patients from bench to bedside. PharmaLogic offers you an exceptional ... Support analytical methods for HPLC, GC and TLC. Quality Control testing of final product. 2.  ...

PHARMALOGIC HOLDINGS

PET Chemist

Salem, VA · On-site

$60K - $75K/yr

... therapeutic agents to patients from bench to bedside. PharmaLogic offers you an exceptional ... Support analytical methods for HPLC, GC and TLC. Quality Control testing of final product. 2.  ...

PHARMALOGIC HOLDINGS

PET Chemist

Salem, VA · On-site

$60K - $75K/yr

... therapeutic agents to patients from bench to bedside. PharmaLogic offers you an exceptional ... Support analytical methods for HPLC, GC and TLC. Quality Control testing of final product. 2.  ...

Thecentermemphis

$52 - $75/hr

We have established in-house LC-MS- and GC-MS-based metabolomics and isotope-tracing platforms and ... Defining metabolic deficiencies and therapeutic opportunities in metabolic and neurodevelopmental ...

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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.

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Gc Therapeutics jobs near you
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.

Associate Scientist II, Quality Control

Scorpion Therapeutics

Madison, WI • On-site

$70 - $85/hr

Other

Posted 4 days ago

Job description

The Position

This role is within Quality Control (Quality Organization). An Associate Scientist II, Quality Control supports analytical testing of pharmaceutical raw materials, in-process samples, finished drug substances/drug product, and/or stability samples for new drug substances and drug products. The role also supports Environmental Monitoring sample collection, GLP Toxicology and cGMP Clinical Trial material release testing, and stability studies. Performs multiple analytical techniques and makes sound scientific decisions with guidance from management. Reports to the QC-EM Scientist.


Responsibilities

  • Develop understanding of cGMP requirements and meet project timelines/deliverables.

  • Collect Environmental Monitoring samples in a cGMP manufacturing space.

  • Perform routine analytical testing using established methods/procedures.

  • Execute training requirements; ensure SOP compliance and maintain up-to-date training records.

  • Use/become proficient with analytical instrumentation (e.g., HPLC, GC, FT-IR, UV/Vis, KF).

  • Set up instrumentation for testing with little/no supervision; plan/execute tasks with minimal supervision.

  • Perform analyses timely; troubleshoot minor analytical problems and communicate issues to senior staff/management.

  • Maintain accurate laboratory notebook/worksheet records; review others’ test data as applicable.

  • Aid drafting technical documents (OOS/atypical investigations, deviations, CAPAs).

  • Calibrate/maintain/troubleshoot analytical equipment with supervision; remain flexible with changing priorities; additional duties as assigned.


Requirements

  • B.S. in Microbiology, Chemistry, or related field; 1–3 years relevant lab experience.

  • cGMP laboratory requirements/operations experience.

  • Familiarity with analytical instrumentation, test method validation, data acquisition systems, and cGMP policies/practices.


Preferred

  • Environmental Monitoring and/or cleanroom experience.

  • Microbiology experience.

  • Ability to interpret SOPs/test methods and write/present clearly; respond to questions.

  • Mathematical, reasoning, and basic computer skills (Windows, MS Office, chromatography data systems).


Benefits / Pay

  • Wisconsin pay range: $70,000 USD - $85,000 USD.

  • Competitive salaries and an excellent benefit package.


Candidates must have current, valid authorization to work in the country where the role is located.

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