qPCR Scientist - Gene Therapy in cGMP Lab

Artech LLC.; Chesterfield (MO); On-site; USD 65,000 - 90,000; Full time

Job summary

A leading workforce solutions provider is seeking a scientist in Chesterfield, MO for a contract role in gene therapy. The candidate will conduct analytical testing by qPCR in a cGMP environment and maintain documentation of results. Proficiency in qPCR and Microsoft Office is required, with cGMP experience preferred. Join a dynamic team focused on advancing biotherapeutic development through innovative analytical methodologies.

Qualifications

• Experience with DNA techniques (qPCR) is required.
• Intermediate proficiency in Microsoft Office (Excel, Word, Outlook) is required.
• Must be able to understand and follow standard operating procedures.

Responsibilities

• Perform analytical testing by qPCR in a cGMP environment.
• Analyze and document results.
• Conduct routine lab duties including reagent preparation and consumable stocking.

Skills

qPCR

Microsoft Office (Excel, Word)

cGMP experience

LIMS experience

Job description

LanceSoft is a nationally certified Minority Business Enterprise (MBE) that has established itself as a pioneer in providing highly scalable, cost-effective workforce solutions to a diverse set of customers across various industries in the United States. Headquartered in Virginia, LanceSoft currently operates out of several locations in the US and Canada.

Job Description

Location: Chesterfield, MO

Duration: 18 Months

Job Description:

• The scientist filling this position will work within a highly-matrixed team setting on gene therapy modalities. The contractor will work in a cGMP environment performing sample testing by qPCR. Experience with DNA techniques (qPCR) is required. Intermediate proficiency in Microsoft Office (Excel, Word, and Outlook) is required. Must be able to understand and follow standard operating procedures.

Responsibilities:
• Analytical testing by qPCR in a cGMP environment
• Analysis and documentation of results
• Routine lab duties (ex. reagent preparation, consumable stocking)

The qualified candidate will join the Bioassay and Impurities Testing group, which is part of the Analytical R&D organization located to enable the development of biological therapeutics at Pfizer. The position will be part of a highly matrixed team responsible for developing analytical methodologies (qPCR, ELISA) and strategies needed to progress biotherapeutic products through the pipeline.

Tech Skills Required:
• qPCR (required)
• Proficiency in Microsoft Office (Excel and Word) required
• cGMP experience (preferred)
• LIMS experience (preferred)

Additional Information

Regards,

703-889-6624

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