Job Detail

Manufacturing Associate I / II Job Openings by IGM Biosciences in Mountain View

IGM Biosciences Jobs 2020 - IGM Biosciences call a new employee to fill Manufacturing Associate I / II that will be placed in Mountain View.

IGM Biosciences Job Vacancies 2020

Detail of : Manufacturing Associate I / II Job Openings in Mountain View

(Nasdaq: IGMS) is a clinical-stage biotechnology company focused on creating and developing engineered IgM antibodies. IgM antibodies have inherent properties that we believe may enable them to improve upon the efficacy and safety of IgG antibodies in multiple therapeutic applications. We have created a proprietary IgM antibody technology platform that we believe is particularly well suited for developing T cell engagers, receptor cross-linking agonists, and targeted cytokines. Our lead product candidate, IGM-2323, is a bispecific T cell engaging IgM antibody targeting CD20 and CD3, and we a Phase 1 clinical trial for the treatment of relapsed/refractory B cell Non-Hodgkin's lymphoma (NHL) patients in 2019. Our second product candidate is expected to be an IgM antibody targeting Death Receptor 5 (DR5), which we plan to have a Phase I clinical trial initiated in late 2020.
We are looking for energetic and talented team players to join our growing Manufacturing site in Mountain View. The Manufacturing Associate will follow GMP and best practices to streamline operations within the manufacturing department. You will work in support of the daily manufacturing operations. In this role you’ll execute process recipes across a variety of production activities such as Cell Expansion, Fermentation and/or Purification, follow written procedures (SOPs), monitor equipment and processes, independently perform laboratory tasks, including pH, conductivity testing, product sampling, and conduct routine sanitization tasks to maintain facility and equipment. You should have a strong understanding of current Good Manufacturing Practices (cGMP), compliance while operating under supervision, and aseptic technique in handling of products and materials. You may troubleshoot equipment events, initiate deviations, and review batch records and logbooks.
In this role, you will report to the USP/DSP Manager or Supervisor.
Responsibilities: Set up, operate equipment, and monitor production processes, and report production in written and electronic documents in accordance with good documentation procedures (GDPs), review documentation as appropriate.
Attain qualification for all assigned tasks and maintain individual training plan
Perform basic laboratory tasks, such as monitor pH, conductivity, test product samples, etc.
Perform material movements, transfer raw materials, and chemicals into, out of, through the production areas.
Maintain facility and equipment through routine cleaning and sanitization, support continuous improvement programs.
Understand and follow job safety procedures, attend required health and safety training, proactively promote safety at work, and promptly report actual and potential accidents and injuries. Must comply with safety policies of the company and site.
Provide training to others, as necessary.
Use sophisticated laboratory instrumentation and computer systems to collect and record data.
Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, QSR and cGMP regulations.
The normal working environment is: Production Floor setting, requiring PPE, gowning, safety shoes and glasses.

Qualifications: High School diploma or equivalent. AS/BS degree preferred in a science related discipline
For Manufacturing I: 1-2 years of experience in manufacturing setting.
For Manufacturing II: 2-3 years of experience in manufacturing setting.
Proven logic and decision-making abilities, critical thinking skills.
Must be able to read and follow defined SOPs and policies.
Must be able to use automated process equipment and tools.
Able to work in a cleanroom environment, and foster safe work practices
Must be a strong team player.
Must be able to lift and/or move up to 40lbs.
Strong written and verbal communication skills are required.
Flexible and adaptable to changing business priorities.
Open to and actively seek out feedback performance and able to translate that feedback into action.

We offer a fast-paced, collaborative, team-based and family-like work environment. It is one of our biggest goals to maintain our company culture.
One of our top priorities is to maintain the health and wellbeing of our employees and their families. To achieve this goal, we are offering robust and comprehensive benefits with a variety of options:
Medical, dental and vision insurance. The full premium amount for our employees and their dependents is covered by IGM
STD, LTD, Basic Life and AD&D Insurance, Supplemental Life and AD&D Insurance
401(k) Plan
120 hours of Paid Time Off, 5 sick days per year, 10 holidays
Cell phone & internet subsidy
Employee Referral Bonus Program
Annual training budget for professional development
Commuter Benefit
Annual bonus program
New hire stock options

IGM is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity or expression, national origin or ancestry, age, disability, marital status, and veteran status. All qualified applicants will receive consideration for employment.

For further information, please refer official source from IGM Biosciences Career Center on following link below. If you meet the requirement and are interested in building a future career with IGM Biosciences, please register yourself at :

Notes :
  • Only qualified candidates that meet with the above requirements would be processed in this recruitment.
  • Only qualified, short-listed applicants will be invited for furthers process.

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