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Senior Scientist, Process Development

Remote: 
Hybrid
Contract: 
Salary: 
119 - 146K yearly
Experience: 
Senior (5-10 years)
Work from: 
San Francisco (US), Santa Monica (US)

Offer summary

Qualifications:

PhD in Immunology or related field with 3 years experience OR MS with 6 years industry experience OR BS with 8 years industry experience, Knowledge of biology/immunology/biochemistry in cell and gene therapy processes, Experience in autologous T-cell therapy manufacturing, Hands-on experience with automation equipment, Understanding of cGMP manufacturing regulations.

Key responsabilities:

  • Lead process development for T-cell-derived therapies
  • Support technology transfer of therapy processes
  • Implement automated end-to-end manufacturing processes
  • Conduct data analysis and integrate results
  • Oversee associates and mentor staff in career development
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AstraZeneca Pharmaceuticals XLarge http://www.astrazeneca.com/
10001 Employees
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Job description

At AstraZeneca's Oncology R&D division, we follow the science to explore and innovate. We are working towards treating, preventing, modifying, and even curing some of the world's most complex diseases. Here we have the potential to grow our pipeline and positively impact the lives of billions of patients around the world. We are committed to making a difference and have built our business around our passion for science. Now we are fusing data and technology with the latest scientific innovations to achieve the next wave of breakthroughs.

The Senior Scientist, Process Development leads process development activities and ensures the application of well-designed unit operations for use in the clinical manufacture of cell therapy products. You will work with colleagues in Analytical Development, Research, Manufacturing, Quality Control/Assurance, Regulatory, and other areas. This role is based in Santa Monica, CA, and reports to the Senior Director, Process Development.

What you will do:

  • Guide autologous platform and process development efforts focused on T-cell-derived cell therapies.
  • Support technology transfer of autologous T-cell derived cell therapy processes into the development and clinical manufacturing environment.
  • Directly support the implementation of automated end-to-end manufacturing processes, working with equipment vendors and internal resources to ensure successful outcomes.
  • Collaborate with and participate in teams to facilitate IND-enabling, clinical Phase I/II-promoting activities.
  • Perform data analysis, provide interpretation, and integrate results into the context of a project.
  • Independently design strategies for implementation of scalable upstream and downstream manufacturing processes of engineered T cells.
  • Collaborate within the project team to interpret study results and contribute to technical discussions for subsequent study design.
  • Prepare experimental proposals, technical reports, SOPs, and manufacturing batch records.
  • Communicate program progress and issues to management.
  • Work collaboratively within PD group and with other groups to meet Technical Operation organization goals.
  • Other responsibilities as assigned.
  • Oversee associates in the execution of development activities.
  • Potentially oversee laboratory, equipment, and facilities.
  • Mentor staff in career development and managing development plans

Minimum Qualifications:

  • PhD in Immunology, Biological Sciences, Biomedical Engineering, or related field with a minimum of 3 years of experience (academic experience post-graduate also considered) OR MS with a minimum of 6 years of industry experience (relevant academic experience also considered) OR a BS with a minimum of 8 years of industry experience is required.
  • Knowledge of biology/immunology/biochemistry as applied in cell and gene therapy processes is required.
  • Experience in autologous T-cell therapy manufacturing is required.
  • Prior hands-on experience with automation equipment and end-to-end systems is required; expertise in their operations in both process development and manufacturing environments for cell therapies is advantageous.
  • Knowledge of cGMP manufacturing and regulations and practical experience in GMP operations.
  • Knowledge of statistical analysis for process development.
  • Design and complete experiments.

When we put unexpected teams in the same room, we fuel bold thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace, and challenge perceptions. That's why we work, on average, a minimum of three days per week from the office. But that doesn't mean we're not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world.

The annual base salary for this position ranges from $119,110 to $145,578. However, base pay offered may vary depending on multiple individualized factors, including market location, and job-related experience. If hired, the employee will be in an "at-will position" and we reserve the right to modify base salary (and any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.

Benefits

  • Short-term incentive bonus opportunity

  • Equity-based long-term incentive program

  • 401(k) plan

  • Paid vacation and holidays; paid leaves

  • Health benefits including medical, prescription drug, dental, and vision coverage.

Date Posted

22-Sep-2024

Closing Date

06-Oct-2024Our mission is to build an inclusive and equitable environment. We want people to feel they belong at AstraZeneca and Alexion, starting with our recruitment process. We welcome and consider applications from all qualified candidates, regardless of characteristics. We offer reasonable adjustments/accommodations to help all candidates to perform at their best. If you have a need for any adjustments/accommodations, please complete the section in the application form.

AstraZeneca requires all US employees to be fully vaccinated for COVID-19 but will consider requests for reasonable accommodations as required by applicable law.

Required profile

Experience

Level of experience: Senior (5-10 years)
Industry :
Pharmaceuticals
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Other Skills

  • Collaboration
  • Mentorship

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