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QC Analyst I – Production Testing

Watchmaker Genomics

This is a Full-time position in Boulder, CO posted July 22, 2021.

Job Description

Position: QC Analyst I
– Production Testing

Position Type: Full-Time Employee

Location: Boulder, CO

Experience: 3+ Years

Introduction:

Watchmaker Genomics is an early-stage life science company based in Boulder, Colorado.

Our team is passionate about innovation and values collaboration, creativity and scientific rigor.

We believe the intersection of biology, engineering and computer science presents exciting opportunities for developing novel technologies that promote research and improve human health.

Watchmaker Genomics specializes in the design, development and production of DNA
– and RNA-modifying enzymes that enable high-growth applications in genomics, molecular diagnostics and personalized medicine.

Watchmaker Genomics is inviting applications for the full-time position of Quality Control Analyst.

The ideal candidate is passionate about life sciences, and is detail oriented with excellent organizational skills.

This position provides great opportunities for growth for candidates with a strong background in molecular biology and biochemistry.

There are a variety of methods the QC Analyst will use to support the characterization of enzymes and reagents across our product portfolio.

In addition to executing on core QC processes, the individual will be increasingly responsible for the implementation and validation of new methods.

This position reports to the QC Manager and will interface closely with many aspects of quality control, manufacturing, and logistics.

The successful candidate will thrive in a dynamic, fast-paced working environment and contribute directly to our company culture and success.

The position provides an opportunity to gain valuable experience spanning many business facets.

Responsibilities:
Core testing for the characterization of a broad range of enzymes and reagents Manufacturing and qualification of intermediate reagents and parts used in core QC processes Maintenance of raw material and intermediate material stocks used in core QC processes Maintaining and improving procedures and instructions to generate records and reports within the Quality Management System (QMS) and/or Records Management System (RMS) Operating within defined business processes for the usage and maintenance of instrumentation, equipment, and chemicals Analysis of scientific data and QC method troubleshooting as required Prompt notification of completed records and reports to the QC Manager

Skills and Requirements:
3+ years of molecular biology laboratory experience Excellent organizational skills and attention to detail The ability to multitask, and perform consistently under pressure
● Strong interpersonal skills and ability to work as an effective member of a goal-oriented team Strong written and verbal communication skills Receptive, communicative, and collaborative High standards for integrity and scientific rigor Additionally, experience in the following areas is considered highly desirable: Gel electrophoresis PCR, qPCR Colorimetric and fluorescent assays Next-Generation Sequencing ISO’s, QMS, GLP

Education:
BS in molecular biology or related field

Application Procedure:

To apply for the position, please submit the following in MS Word or PDF format by email to :
Letter of motivation ( applications submitted without a letter of motivation will NOT be considered ) Curriculum vitae, highlighting relevant qualifications and experience, and containing: A current email address and mobile phone number The names and contact information of two references who are able to assess your suitability for the position in terms of the specified requirements