Associate Manufacturing Specialist
Associate Manufacturing Specialist
Location:Santa Monica CAand Tarzana, CA
Shift:Wed-Sat0700 to 1730 (1st3 months will be Mon-Fri0800-1630), with flexibility to work a varied schedule.
Position Summary
AstraZenecaisseekinga highly motivated individual for the role ofAssociateManufacturing Specialist, to join our Manufacturing team, to work in an exciting new area of cell therapy atAstraZeneca.This position is based out of Santa Monica, CAas well asoccasionaltravel toTarzana, CA. This role reports directly to theAssociate Director, Manufacturing.
The Manufacturing Specialist role willbe responsible forensuring successful manufacture and release of cell therapy products following all processes and procedures related to operations in full compliance with cGMP. This role will be driving and supporting the manufacturing operational readiness and successful tech transfer using knowledge of cGMP regulations.
Responsibilities (include but not limited to):
Usinggeneral applicationof concepts and principles supports activities to enable GMP readiness for clinical manufacturing including equipment procurement, installation and qualification, facilityqualificationand technology transfer.
Perform tasks in a manner consistent with safety policies, quality systems, and cGMP requirements.
Assistin thedevelopment of Standard Operating Procedures (SOPs) for manufacturing processes.
Assistin setting up manufacturing areas and equipment, including complex automated cell processing equipment.
Follow all cleaning and gowning procedures for the facility.
Maintainappropriate inventoriesof material and supplies within the cleanroom areas to support manufacturing activities.
Ensureall materials and equipment are identified and available in time for manufacturing activities.
Support Process Developmentand MSATto align manufacturing plans with overall product development plans.
Ensure that all production operations are controlled and executed within cGMP regulatory guidelines.
Providetimelyverbal and written updates to Manufacturing leadership.
Support all new product/process introductions on site
Interact with vendors and outside resources
Complete assigned projects
Be the shift lead ifrequired, providing instruction to the team
Troubleshoot and resolve operational problems during processing
Represent Manufacturing in cross-functional initiatives and meetings
Monitor and evaluate process trends and recommend and implement continuous improvement strategies as appropriate
Manage multiple projects independently
Plan and implement complex changes
Perform Environmental monitoring asrequired
Technical expert for entire area(s)
Interact independently with regulatory agencies
Develop and provide training on complex manufacturing processes
Perform Manufacturing review and approval of critical documents
Develop process validation protocols
Maintain good housekeeping and clean andsanitizeclassified areas asrequired
Analyzecomplex problems anddetermineand implement solutions
Other duties andprojectsassignedto meet business needs.
Education & Experience Requirements:
Education: Bachelor’s or Master’s degree in life sciences, engineering, or a related field
Experience: Bachelor’s degree and 0-3 years of general cGMP manufacturing experience | Master’s degree and 0-2 years of general cGMP manufacturing experience
Required Skills:
Basic knowledge in biologics manufacturing process, cell culture and/or vector products.
Technical proficiency in aseptic technique and working with manufacturing equipment in open and closed systems.
Working knowledge of automated manufacturing equipment and/or process analytical technologies.
Proficiency in Microsoft Word, Excel and data analysis.
Desired Skills:
Previous manufacturing or process development experience with cell therapy or vector products.
Dynamic individual with the ability to communicate and engage others.
Independent and self-starting. Ability to work with minimal supervision.
Demonstrate flexibility and willingness to change ways of working/identify opportunities to improve processes within cGMP clinical manufacturing environment.
The annual base pay (or hourly rate of compensation) for this position ranges from $65,000 to$97,000. Ourpositions offer eligibility for various incentives—an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coveragein accordance withthe terms of the applicable plans.
Date Posted
15-Apr-2026Closing Date
21-Apr-2026Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.
AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorisation and employment eligibility verification requirements.
Rejoignez notre réseau de talents
Inscrivez-vous pour recevoir des alertes emplois AstraZeneca.
S'inscrire
