Sr. Scientist Protein & Gene Therapy

Great Pharma company in Irvine - benefits are attractive, and a commitment to work-life balance

  • Irvine, CA
  • $100,000 - $130,000
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A bit about us:

We are your single source for high-quality chemistry, manufacturing and control (CMC) services for the pharma, biotech, and medical device industries. Our comprehensive suite of services streamlines processes to accelerate time-to-market. With more than 30 years’ experience, we have deep scientific expertise across a range of products, with a special focus on oligonucleotides.

Why join us?

You’ll partner with the thinkers who have laid the foundation for next-generation therapies and the doers who are changing the world. You’ll work in a diverse, respectful, and safe environment where our teams are empowered to create wonders. The work is rewarding, the benefits are attractive, and our commitment to work-life balance is refreshing.

Job Details

Support the daily operations of the Biopharmaceutical Development Department by performing assigned large molecule-based method development, validation and characterization studies in accordance with cGMP requirements, company policies and procedures as directed by laboratory management.

Responsibilities:

Perform complex method feasibility, development, verification, transfer, qualification, validation and/or characterization testing of biopharmaceutical raw materials, intermediates, API, and/or drug product samples in accordance with cGMP requirements.

Work on routine tasks where analysis of situations or data requires review and evaluation of limited factors, limited judgment is required in resolving problems and making routine recommendations. Exercise judgment within defined practices and policies in selecting methods, techniques, and evaluation criteria for obtaining results.

Assist technical project lead in communicating effectively with internal and external stakeholders during project related discussions or in written communications, including, but not limited to, schedule updates, presentation of technical data, interpretation of results, and/or collaborations on quality exceptions. Work closely with the team to resolve technical issues.

Prepare quality technical documentation, such as protocols, test methods, investigation summaries and other technical reports working closely with relevant laboratory and/or Quality Assurance management.

This list of duties and responsibilities is not all inclusive and may be expanded to include other duties and responsibilities, as management may deem necessary.

Qualifications - Experience and Education:

Bachelor's degree in Biochemistry or equivalent in scientific discipline required. A minimum of 4+ years cGMP pharma work experience required.
Experience with cell and gene therapy
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Job Details
Managed by Jobot Pro
Location
Irvine, CA
Job Type
Permanent
Compensation
$100,000 - $130,000