AstraZeneca
Join to apply for the
Manufacturing Specialist
role at
AstraZeneca Join to apply for the
Manufacturing Specialist
role at
AstraZeneca Get AI-powered advice on this job and more exclusive features. We are looking for a Manufacturing Specialist to support our dynamic Manufacturing team in the production of TCR-T, CAR-T, and allogeneic cell therapy investigational products. This role is based in Santa Monica, CA, with occasional travel to Tarzana, CA. You will report to the Associate Director of Manufacturing, NGF40.
The Manufacturing Specialist role will ensure successful manufacture and release of cell therapy products by following established processes in full compliance with cGMP. You will support manufacturing operational readiness and the successful technology transfer of pipeline products using knowledge of cGMP regulations.
You Will
Use general application of principles, support activities to ensure GMP readiness for clinical manufacturing, including equipment procurement, installation and qualification, facility qualification, and technology transfer. Perform tasks in a manner consistent with safety policies, quality systems, and cGMP requirements. Help develop Standard Operating Procedures (SOPs) and other documents for manufacturing processes. Set up manufacturing areas and equipment, including complex automated cell processing equipment. Follow all cleaning and gowning procedures for the facility. Maintain appropriate inventories of material and supplies within the cleanroom areas to support manufacturing activities. Ensure all materials and equipment are identified and available in time for manufacturing activities. Support Process Development to align manufacturing plans with product development plans. Ensure that all production operations are controlled and performed within cGMP regulatory guidelines. Provide verbal and written updates to Manufacturing leadership. Perform other responsibilities and project-based assignments to support manufacturing operations. Work is reviewed upon completion for adequacy in meeting goals.
You Have
Minimum of five (5) years of experience with a High School Diploma or a BS/BA in a relevant science or engineering discipline. Understanding of cGMP process and knowledge of CMC regulatory framework for biologics. Knowledge of and experience in aseptic techniques for primary human cell cultures, clinical and commercial GMP manufacturing, and supporting tech transfer.
Additional Requirements
Knowledge of industry practices, cell therapy manufacturing experience preferred. Develop solutions to complex problems independently. Refer to established precedents and policies or use original thinking. Help determine goals of assignment. Plan schedules and arranges own activities.
The annual base salary for this position ranges from $81,000 to $122,000. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles).
Our Benefits
Benefits offered include:
A qualified retirement program [401(k) plan] Paid vacation, holidays, and paid leaves Health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment.
#celltherapy
Date Posted
04-Aug-2025
Closing Date
30-Aug-2025
Our 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.
Seniority level
Seniority level Mid-Senior level Employment type
Employment type Full-time Job function
Job function Management and Manufacturing Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at AstraZeneca by 2x Sign in to set job alerts for “Manufacturing Specialist” roles.
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#J-18808-Ljbffr
Manufacturing Specialist
role at
AstraZeneca Join to apply for the
Manufacturing Specialist
role at
AstraZeneca Get AI-powered advice on this job and more exclusive features. We are looking for a Manufacturing Specialist to support our dynamic Manufacturing team in the production of TCR-T, CAR-T, and allogeneic cell therapy investigational products. This role is based in Santa Monica, CA, with occasional travel to Tarzana, CA. You will report to the Associate Director of Manufacturing, NGF40.
The Manufacturing Specialist role will ensure successful manufacture and release of cell therapy products by following established processes in full compliance with cGMP. You will support manufacturing operational readiness and the successful technology transfer of pipeline products using knowledge of cGMP regulations.
You Will
Use general application of principles, support activities to ensure GMP readiness for clinical manufacturing, including equipment procurement, installation and qualification, facility qualification, and technology transfer. Perform tasks in a manner consistent with safety policies, quality systems, and cGMP requirements. Help develop Standard Operating Procedures (SOPs) and other documents for manufacturing processes. Set up manufacturing areas and equipment, including complex automated cell processing equipment. Follow all cleaning and gowning procedures for the facility. Maintain appropriate inventories of material and supplies within the cleanroom areas to support manufacturing activities. Ensure all materials and equipment are identified and available in time for manufacturing activities. Support Process Development to align manufacturing plans with product development plans. Ensure that all production operations are controlled and performed within cGMP regulatory guidelines. Provide verbal and written updates to Manufacturing leadership. Perform other responsibilities and project-based assignments to support manufacturing operations. Work is reviewed upon completion for adequacy in meeting goals.
You Have
Minimum of five (5) years of experience with a High School Diploma or a BS/BA in a relevant science or engineering discipline. Understanding of cGMP process and knowledge of CMC regulatory framework for biologics. Knowledge of and experience in aseptic techniques for primary human cell cultures, clinical and commercial GMP manufacturing, and supporting tech transfer.
Additional Requirements
Knowledge of industry practices, cell therapy manufacturing experience preferred. Develop solutions to complex problems independently. Refer to established precedents and policies or use original thinking. Help determine goals of assignment. Plan schedules and arranges own activities.
The annual base salary for this position ranges from $81,000 to $122,000. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. In addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles).
Our Benefits
Benefits offered include:
A qualified retirement program [401(k) plan] Paid vacation, holidays, and paid leaves Health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment.
#celltherapy
Date Posted
04-Aug-2025
Closing Date
30-Aug-2025
Our 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.
Seniority level
Seniority level Mid-Senior level Employment type
Employment type Full-time Job function
Job function Management and Manufacturing Industries Pharmaceutical Manufacturing Referrals increase your chances of interviewing at AstraZeneca by 2x Sign in to set job alerts for “Manufacturing Specialist” roles.
Manufacturing Engineering – Fasteners, Supply Chain (Dragon & Falcon)
Manufacturing Engineering – Fasteners, Supply Chain (Dragon & Falcon)
Thousand Oaks, CA $40.00-$42.00 21 hours ago Thousand Oaks, CA $35.50-$40.96 10 hours ago Manufacturing Specialist, Additive (Starship)
Internship- Manufacturing Engineering (CNC)
Manufacturing Operations Excellence Lead
Downey, CA $100,295.00-$125,369.00 1 week ago Manufacturing Specialist - (Albumin Purification)
Los Angeles Metropolitan Area 3 weeks ago Process Planner, Materials Lab Operations
Production Manager - Fastener Manufacturing
Los Angeles, CA $99,278.00-$105,000.00 1 month ago Manufacturing Manager (Multi Manufacturing) - 2nd shift
Redondo Beach, CA $165,000.00-$195,000.00 4 weeks ago Part-time Manufacturing Engineering Specialist IV
Avionics Specialist (Harness Manufacturing)
Los Angeles, CA $75,000.00-$85,000.00 5 hours ago Hawthorne, CA $95,000.00-$115,000.00 3 weeks ago Long Beach, CA $80,000.00-$110,000.00 2 days ago We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
#J-18808-Ljbffr