Minimum 10 years in pharmaceutical/biotech facilities engineering with at least 5 years in a network, multi-site, or above-site role; direct experience with celltherapy, biologics, or ATMP ...
Minimum 10 years in pharmaceutical/biotech facilities engineering with at least 5 years in a network, multi-site, or above-site role; direct experience with celltherapy, biologics, or ATMP ...
Senior Director, Cell Therapy Manufacturing Network F&E Lead
Los Angeles, CA · On-site
$185K - $278K/yr
Minimum 10 years in pharmaceutical/biotech facilities engineering with at least 5 years in a network, multi-site, or above-site role; direct experience with cell therapy, biologics, or ATMP ...
Senior Director, Cell Therapy Manufacturing Network F&E Lead
Los Angeles, CA · On-site
$185K - $278K/yr
Minimum 10 years in pharmaceutical/biotech facilities engineering with at least 5 years in a network, multi-site, or above-site role; direct experience with cell therapy, biologics, or ATMP ...
If interested in expanding your therapeutic area expertise, Medpace also offers Certificate Programs in medical device, rare disease, infectious disease, advanced therapeutic medicinal products (ATMP ...
If interested in expanding your therapeutic area expertise, Medpace also offers Certificate Programs in medical device, rare disease, infectious disease, advanced therapeutic medicinal products (ATMP ...
If interested in expanding your therapeutic area expertise, Medpace also offers Certificate Programs in medical device, rare disease, infectious disease, advanced therapeutic medicinal products (ATMP ...
If interested in expanding your therapeutic area expertise, Medpace also offers Certificate Programs in medical device, rare disease, infectious disease, advanced therapeutic medicinal products (ATMP ...
If interested in expanding your therapeutic area expertise, Medpace also offers Certificate Programs in medical device, rare disease, infectious disease, advanced therapeutic medicinal products (ATMP ...
If interested in expanding your therapeutic area expertise, Medpace also offers Certificate Programs in medical device, rare disease, infectious disease, advanced therapeutic medicinal products (ATMP ...
If interested in expanding your therapeutic area expertise, Medpace also offers Certificate Programs in medical device, rare disease, infectious disease, advanced therapeutic medicinal products (ATMP ...
If interested in expanding your therapeutic area expertise, Medpace also offers Certificate Programs in medical device, rare disease, infectious disease, advanced therapeutic medicinal products (ATMP ...
Author and revise batch records, SOPs, and technical reports;protocols,manufacturing summary reports,ensure adherence to cGMP/ATMP requirements and data integrity principles (ALCOA+). * Training ...
Author and revise batch records, SOPs, and technical reports;protocols,manufacturing summary reports,ensure adherence to cGMP/ATMP requirements and data integrity principles (ALCOA+). * Training ...
If interested in expanding your therapeutic area expertise, Medpace also offers Certificate Programs in medical device, rare disease, infectious disease, advanced therapeutic medicinal products (ATMP ...
If interested in expanding your therapeutic area expertise, Medpace also offers Certificate Programs in medical device, rare disease, infectious disease, advanced therapeutic medicinal products (ATMP ...
This position is a team member in the Large Molecule & Advance Therapy Medicinal Products (ATMP) Services in a Good Manufacturing Practices (GMP) laboratory environment. Critical Performance Areas
This position is a team member in the Large Molecule & Advance Therapy Medicinal Products (ATMP) Services in a Good Manufacturing Practices (GMP) laboratory environment. Critical Performance Areas
This position is a team member in the Large Molecule & Advance Therapy Medicinal Products (ATMP) Services in a Good Manufacturing Practices (GMP) laboratory environment. Critical Performance Areas
This position is a team member in the Large Molecule & Advance Therapy Medicinal Products (ATMP) Services in a Good Manufacturing Practices (GMP) laboratory environment. Critical Performance Areas
If interested in expanding your therapeutic area expertise, Medpace also offers Certificate Programs in medical device, rare disease, infectious disease, advanced therapeutic medicinal products (ATMP ...
If interested in expanding your therapeutic area expertise, Medpace also offers Certificate Programs in medical device, rare disease, infectious disease, advanced therapeutic medicinal products (ATMP ...
Principal Process Engineer, Manufacturing Sciences & Technology, Cell Therapy
Los Angeles, CA · On-site
Author and revise batch records, SOPs, and technical reports; protocols, manufacturing summary reports, ensure adherence to cGMP/ATMP requirements and data integrity principles (ALCOA+). * Training ...
Principal Process Engineer, Manufacturing Sciences & Technology, Cell Therapy
Los Angeles, CA · On-site
Author and revise batch records, SOPs, and technical reports; protocols, manufacturing summary reports, ensure adherence to cGMP/ATMP requirements and data integrity principles (ALCOA+). * Training ...
Author and revise batch records, SOPs, and technical reports;protocols,manufacturing summary reports,ensure adherence to cGMP/ATMP requirements and data integrity principles (ALCOA+). * Training ...
Author and revise batch records, SOPs, and technical reports;protocols,manufacturing summary reports,ensure adherence to cGMP/ATMP requirements and data integrity principles (ALCOA+). * Training ...
Senior Engineer II, Applied Technologies
Norwood, MA · On-site
$118K - $162K/yr
Familiarity with expedited regulatory pathways, EU GMP Annex 1, ATMP/CGT guidances, and relevant ICH (e.g. Q8, Q9, Q10, Q12, Q13). * Expertise with mRNA, lipid nanoparticle formulation, or other ...
Senior Engineer II, Applied Technologies
Norwood, MA · On-site
$118K - $162K/yr
Familiarity with expedited regulatory pathways, EU GMP Annex 1, ATMP/CGT guidances, and relevant ICH (e.g. Q8, Q9, Q10, Q12, Q13). * Expertise with mRNA, lipid nanoparticle formulation, or other ...
HDR is providing PM/CM services for the Los Angeles World Airports ATMP Landside Improvements Project. The project will deliver critical improvements to the roadways, streets, and thoroughfares in ...
HDR is providing PM/CM services for the Los Angeles World Airports ATMP Landside Improvements Project. The project will deliver critical improvements to the roadways, streets, and thoroughfares in ...
Experience with stem cell or iPSC-based therapies or other ATMP modalities * Experience supporting or participating in FDA inspections * Experience working with global health authorities, such as EMA ...
Experience with stem cell or iPSC-based therapies or other ATMP modalities * Experience supporting or participating in FDA inspections * Experience working with global health authorities, such as EMA ...
... ATMP) including 21 CFR Part 11. * Project management experience; may include leading teams or projects with demonstrated leadership skills in team building and accomplishing complex projects. * Must ...
... ATMP) including 21 CFR Part 11. * Project management experience; may include leading teams or projects with demonstrated leadership skills in team building and accomplishing complex projects. * Must ...
LUH- 72A Lakota Simulator Instructor Operator
Marana, AZ · On-site
$24.25 - $30.50/hr
Coordinate daily with WFFC/ATMP simulator maintenance teams to track system status and service requests. * Work with course managers to allocate simulation time for formal training. * Coordinate with ...
LUH- 72A Lakota Simulator Instructor Operator
Marana, AZ · On-site
$24.25 - $30.50/hr
Coordinate daily with WFFC/ATMP simulator maintenance teams to track system status and service requests. * Work with course managers to allocate simulation time for formal training. * Coordinate with ...
Manager, Regulatory Affairs CMC
$133K - $172K/yr
Experience with cell therapy / CAR-T / ATMP programs * Experience supporting regulatory submissions and lifecycle management * Familiarity with GMP and manufacturing processes * Basic understanding ...
Manager, Regulatory Affairs CMC
$133K - $172K/yr
Experience with cell therapy / CAR-T / ATMP programs * Experience supporting regulatory submissions and lifecycle management * Familiarity with GMP and manufacturing processes * Basic understanding ...
Vice President, Regulatory Affairs *PC 884
$163K - $215K/yr
ATMP experience is a plus. * Ability to analyze and interpret scientific and technical information, as well as regulatory documents. * Stays abreast of current and evolving regulatory requirements ...
Vice President, Regulatory Affairs *PC 884
$163K - $215K/yr
ATMP experience is a plus. * Ability to analyze and interpret scientific and technical information, as well as regulatory documents. * Stays abreast of current and evolving regulatory requirements ...
Atmp information
See salary details
$8.89 - $13.70
16% of jobs
$15.17 is the 25th percentile. Wages below this are outliers.
$13.70 - $18.51
29% of jobs
The median wage is $19.71 / hr.
$18.51 - $23.32
19% of jobs
$27.58 is the 75th percentile. Wages above this are outliers.
$23.32 - $28.13
12% of jobs
$28.13 - $32.93
8% of jobs
$32.93 - $37.74
5% of jobs
$37.74 - $42.55
4% of jobs
$42.55 - $47.36
2% of jobs
$47.36 - $52.16
2% of jobs
$52.16 - $56.97
1% of jobs
$56.97 - $61.78
1% of jobs
$8
$26
$61
How much do atmp jobs pay per hour?
What are some common challenges faced by ATM (Automated Teller Machine) Technicians and how can they overcome them?
What are the key skills and qualifications needed to thrive as an Advanced Therapy Medicinal Products (ATMP) Specialist, and why are they important?
What are ATMPs?

$185K - $278K/yr
Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 15 days ago
Key responsibilities
Establish user requirements and facility design standards for cell therapy manufacturing and develop risk-based contamination control approaches.
Collaborate with Global Real Estate and Engineering to evaluate network expansion opportunities and provide cell therapy-specific input on site selection and facility requirements.
Lead identification and assessment of facility-related risks across existing sites and new-build programs and develop mitigation strategies.
AstraZeneca rating
8.6
Based on 43 frontline employees who took The Breakroom Quiz
16th of 73 rated pharmaceutical
Job description
You will
Establish user requirements and facility design standards for cell therapy manufacturing;develop risk-based contamination control approaches that account for open and closed processing, personnel gowning regimes, environmental monitoring, and the unique biological risks inherent in patient-derived cellular materials
Collaborate with Global Real Estate and Engineering to evaluate network expansion opportunities; provide cell therapy-specific input on site selection criteria, facility requirements, infrastructure needs, and operational considerations
Provide input to and/or leadengineeringstudiesto inform capital investment decisions, site master planning,newtechnologyadoptionor platform changes
Provide input to andparticipatein the established capital execution governance framework,planningand reporting
Lead identification and assessment of facility-related risks across existing sites and new-build programs,single points of failure in critical utilities, environmental control gaps,safetyand infrastructurerisksand develop mitigationstrategies that inform capital prioritization and operational decisions
Harmonize F&E operating models across existing supply sites byidentifyingopportunities for standardization, shared processes, common resource models,operatingcostsand aligned ways of working; develop a roadmap to bring consistency without disrupting ongoing operations
Support development and deployment of Digital and AI solutions for Facilities & Engineering across the supply network
Support implementation ofnew technologyfor existing F&E site teams-including training, resource planning, and adoption playbooks
Support SHE management review based on data inputs from the supply sites;identifytrends, compliance gaps, and improvement opportunities across the network;
Provide input tocell therapy specificsustainability initiatives aligned with corporatestrategy
You have
Education:Bachelor's degree in engineering(Mechanical, Chemical, Civil/Structural, or Architectural Engineering);Master'sdegree preferred; professional engineering licensure (PE/CEng) desirable
Experience: Minimum 10 years in pharmaceutical/biotech facilities engineering with at least 5 years in a network, multi-site, or above-site role; direct experience with celltherapy, biologics, or ATMP manufacturing facility design strongly preferred; demonstrated experience developing user requirements and design standards for GMP facilities; involvement in greenfield or major expansion programs from conceptual design through operational handover
Technical Knowledge: Expert knowledge of contamination control strategy for aseptic and cell therapy environments, cleanroom design (ISO classifications), pharmaceutical HVAC systems, GMP facility requirements, Engineering Studies, and commissioning/qualification protocols; familiarity with sustainability frameworks and current regulatory expectations for cell therapy facility design
Skills: Engineering judgment, contamination control risk assessment, ability to develop standards and requirements, cross-functional collaboration, stakeholder influence across sites and the ability to translate manufacturing operational needs into facility design requirements; comfortable operating in a support and input role within matrixed governance structures
Systems: Familiarity with BIM (Building Information Modeling), CMMS (Computerized Maintenance Management Systems), environmental monitoring systems, and energy management platforms.
The annual base pay for this position ranges from $185,000 to $278,000. Our positions offer eligibility for multiple 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 coverage in accordance with the terms of the applicable plans.
Date Posted
15-Jun-2026Closing Date
09-Jul-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.
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