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SomaLogic, Inc. Senior Quality Control Analyst in Boulder, Colorado

Position Summary:

SomaLogic is a privately-owned bio-information company that developed SomaScan®, a revolutionary proteomics platform technology capable of measuring thousands of different human proteins in a single small blood or other type sample. We are a dedicated team of cross functional professionals now moving towards commercializing the health-related information derived from our platform to help people worldwide proactively manage their health. As a part of our commercialization effort, we are seeking additional Quality Control expertise to join our dedicated team and help us realize that vision.

We are currently looking for a Quality Control Analyst to perform analytical analysis on raw materials, finished product, stability samples, and R&D materials as part of the quality team. This will include understanding the basics of proteomics and DNA, handing sensitive materials, performing statistical analysis on results, and technical writing to report results as part of supporting multiple departments to achieve a common goal. Level commensurate with experience.

Key Job Responsibilities:

· Complying with cGMPs, CLIA regulations, SOPs, safety requirements, and all company policies and procedures

· Perform laboratory tests in the QC laboratory for evaluation of raw materials, components, and finished products

· Generating and maintaining laboratory data and records in accordance with company policies

· Conducting product stability testing and product expiration testing in accordance with defined schedules

· Analytical analysis of material to determine molecular weight, purity, amount, and other parameters as required. Testing may be performed in support of multiple working groups

· Independently performing and adequately documenting basic investigations for out-of-specification or out-of-trend results

· Assisting department management in the execution / implementation of projects or other duties as required

· As appropriate, will cross-train in other departments or job functions to meet production or assay timelines when needed

· Participates in departmental or cross functional process improvement programs or other projects



Bachelor’s Degree – major in chemistry or related science is required.

Skills and experience

Ÿ 5-10 years of experience in a Quality Control work environment, preferably in the pharmaceutical or medical device industries, with knowledge of GMPs or ISO regulations required

Ÿ Attention to detail required

Ÿ Proficient in LC-MS, UPLC, spectroscopy, including operation and maintenance required

Ÿ Demonstrated ability to devise solutions for complex problems

Ÿ Ability to prioritize and meet deadlines, proven ability to multi-task effectively

Ÿ Knowledge and experience using LIMS preferred

Ÿ Strong communication and presentation skills, including technical writing and reporting

Ÿ Ability to build effective relationships across departments and working groups

Ÿ Proficient in MS Word and PowerPoint, highly proficient in Excel

Work Environment:

Ÿ Ability to work in a fast-paced environment.

Ÿ Physical Demands / Surroundings – Works in a laboratory setting. The individual will be required to enter production support areas/laboratories while wearing appropriate PPE (personal protective equipment) such as lab coat, gloves and safety glasses. Note: Potential to work in proximity to patient samples, including blood, plasma, CSF, and other matrices, including known and suspected infectious material.