CRISPR Therapeutics AG

Quality Control Analyst (Multiple Openings)

CRISPR Therapeutics AG$93K — $103K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in a relevant scientific area with 3-5 years of industry experience.
  • Hands-on experience with techniques like flow cytometry, PCR, or UPLC Chromatography.
  • Strong communication skills and detail-oriented technical writing ability.
  • Proficient in managing time and adapting to evolving priorities in a dynamic environment.

Responsibilities

  • Support the implementation and validation of analytical methods at the Framingham facility.
  • Conduct routine in-process, final release, stability, and microbiological testing of CRISPR-based products.
  • Write and revise SOPs, test methods, protocols, and reports as needed.
  • Assist in QC investigations, including OOS and change control processes.
  • Utilize Laboratory Information Management System for data packet completion and review.
  • Perform additional duties as dictated by business needs.

Benefits

  • Comprehensive health benefits including medical, dental, and vision coverage.
  • Discretionary bonus structure to reward performance.
  • Equity opportunities to participate in the company's growth.
  • Supportive team environment fostering collaboration and innovation.
Full Job Description
Job Description:

Position Summary

Our QC team is looking for enthusiastic individuals to work full time at our state-of-the-art manufacturing facility in Framingham, MA. QC Analyst is a lab based role that is a valuable member of the Quality Control team that will perform in-process, final product, raw material, stability, environmental monitoring, and microbiological testing of novel drug therapies. The successful candidate will perform various biochemical, biophysical, molecular biology, chromatographic, environmental and compendial tests in a GMP environment. In addition, the QC Analyst will support analytical method implementation, transfer and validation projects to support business and clinical needs.

Responsibilities
  • Support the implementation and validation of analytical methods to the Framingham facility.
  • Performs routine in-process, final release, stability, raw material, environmental monitoring, and microbiological testing of CRISPR based products.
  • Write and/or revise SOPs, test methods, protocols, and reports.
  • Support QC investigations, OOS, deviations, CAPA implementation, and change controls.
  • Utilize Laboratory Information Management System to complete the data packets for review by senior members.
  • Perform other related duties based on business needs.


Minimum Qualifications
  • Minimum of bachelor's degree in a relevant scientific area with 3-5 years of relevant industry experience.
  • Hands-on experience with at least one of the following techniques: flow cytometry, PCR, UPLC Chromatography.
  • Excellent communication skills, technical writing, and detail oriented.
  • Good at managing time and evolving priorities in a flexible manner in dynamic environment.


Preferred Qualifications
  • Experience with cell culture, aseptic techniques, raw material testing, and/or chromatography preferred.


Competencies
  • Collaborative - Openness, One Team
  • Undaunted - Fearless, Can-do attitude
  • Results Orientation - Delivering progress toward our mission. Sense of urgency in solving problems.
  • Entrepreneurial Spirit - Proactive. Ownership mindset.


Due to the nature of their work, our manufacturing and lab-based positions are located fully on-site.

QC Analyst: Base pay range of $93,000 to $103,000 + discretionary bonus, equity and benefits.

The range provided is CRISPR Therapeutics' reasonable estimate of the base compensation for this role. The actual amount will be based on job-related and non-discriminatory factors such as experience, training, skills, and abilities.

About CRISPR Therapeutics AG

CRISPR Therapeutics AG, a gene editing company, focuses on developing transformative gene-based medicines for serious diseases using its proprietary CRISPR/Cas9 gene-editing platform. The company develops its products through in-house research programs and partnerships with biopharmaceutical companies and academic researchers. Its lead product candidate is CTX001, an ex vivo CRISPR gene-edited therapy for treating patients suffering from transfusion-dependent beta thalassemia or severe sickle cell disease in which a patient's hematopoietic stem cells are engineered to produce high levels of fetal hemoglobin in red blood cells. The company was formerly known as Inception Genomics AG and changed its name to CRISPR Therapeutics AG in April 2014. CRISPR Therapeutics AG was founded in 2013 and is headquartered in Zug, Switzerland.
Learn more about CRISPR Therapeutics AG
Size
473 employees
Market Cap
$3.3 billion
Industry
Net Income
-$348.8 million
Founded
2013
5 Year Trend
+181.6%
Revenue
$720,000
NASDAQ

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