Temporary Senior QC Analyst
Mountain View, CA
Process Development & Manufacturing – Quality /
Contract /
On-site
About IGM Biosciences, Inc.
IGM Biosciences (Nasdaq: IGMS) is a clinical-stage biotechnology company committed to developing and delivering a new class of medicines to treat patients with cancer and autoimmune and inflammatory diseases. The Company’s pipeline of clinical and preclinical assets is based on the IgM antibody, which has 10 binding sites, compared to conventional IgG antibodies with only 2 binding sites. We have created unique IgM antibodies with high selectivity, affinity, and avidity that may redefine what is possible for therapeutic antibody medicines. We believe our proprietary IgM antibody technology platform is particularly well suited for developing T cell engagers and receptor cross-linking agonists. The Company also has an exclusive worldwide collaboration agreement with Sanofi to create, develop, manufacture, and commercialize IgM antibody agonists against oncology, immunology, and inflammation targets. For more information, please visit www.igmbio.com.
IgM Antibodies and Autoimmune and Inflammatory Diseases
Antibody treatments have revolutionized outcomes for patients with autoimmune and inflammatory diseases. We are committed to exploring how our IgM antibody platform's unique structure and binding properties can improve outcomes for patients with these serious conditions.
IgM Antibodies and Oncology
The potential of our IgM antibodies drives our focus on oncology. Leveraging the power of avidity and the strong and durable binding of our IgM antibodies, we are developing new treatment options for cancer patients. Our initial efforts in this field are centered around the broad application of IgM antibodies to activate receptors, triggering the programmed death of cancer cells.
Position Summary:
The Temporary Sr. QC Analyst will report to a QC Supervisor or Lab Director. This position will support the quality control-related activities and GMP production for on-site manufacturing.
This is an on-site temporary role based in Mountain View, CA. Training will be provided.
Responsibilities:
- Review raw material and laboratory documentation against established QC requirements.
- Provide administrative and lab support for the QC department to facilitate GMP manufacturing operations.
- Perform data entry of QC data for analyses and metrics.
- Execute GMP experiments for compendial or custom complex assays for in process, release, stability, method qualifications and transfers
- Review QC test results against established requirements and specifications.
- Maintain organization and inventory of the quality control laboratory.
- Write and review documents (e.g., specifications, test methods, protocols, reports and SOPs)
- Participate in staff and cross-functional meetings.
Qualifications:
- Level commensurate with experience.
- BA or BS degree in a scientific discipline required, or comparable experience.
- Familiarity with GMP regulations.
- Experience with USP and Ph. Eur. Compendial assays is preferred.
- Experience with complex biologic assays (e.g., SE-HPLC, RP-HPLC, CE-SDS, SDS-PAGE, icIEF) is preferred.
- Musthaveexcellentverbal,written,interpersonal,organizational,andcommunicationskills.
- Great organizational ability to manage a wide range of tasks.
- Attention to detail and accuracy.
- Adaptability and a high degree of flexibility.
- Must be able to commute to and work onsite in Mountain View, CA.
$30 - $60 an hour
This range reflects the characteristics of the job, such as required skills and qualifications and is based on the office location noted in this job posting. The range may also be adjusted based on applicant's geographic location.
Actual individual pay is determined by demonstrated experience and internal equity alignment.
