About Aerogen Pharma Aerogen Pharma is a US based clinical-stage specialty pharmaceutical company with a mission to develop inhaled drug/biologic and device combination that will transform the ...
About Aerogen Pharma Aerogen Pharma is a US based clinical-stage specialty pharmaceutical company with a mission to develop inhaled drug/biologic and device combination that will transform the ...
Aerogen information
See California salary details
$12.81 - $13.98
1% of jobs
$13.98 - $15.14
1% of jobs
$15.14 - $16.30
7% of jobs
$17.26 is the 25th percentile. Wages below this are outliers.
$16.30 - $17.47
19% of jobs
The median wage is $18.42 / hr.
$17.47 - $18.63
26% of jobs
$18.63 - $19.80
14% of jobs
$20.53 is the 75th percentile. Wages above this are outliers.
$19.80 - $20.96
11% of jobs
$20.96 - $22.13
7% of jobs
$22.13 - $23.29
6% of jobs
$23.29 - $24.46
5% of jobs
$24.46 - $25.62
2% of jobs
$12
$19
$25
How much do aerogen jobs pay per hour?
As of Sep 3, 2026, the average hourly pay for aerogen in California is $19.36, according to ZipRecruiter salary data. Most workers in this role earn between $17.07 and $20.87 per hour, depending on experience, location, and employer.
What is an Aerogen?
Aerogen jobs refer to positions at Aerogen, a medical device company specializing in aerosol drug delivery systems, particularly for respiratory care. Employees at Aerogen may work in various roles such as research and development, engineering, quality assurance, sales, or customer support, all focused on improving patient outcomes through innovative inhalation therapies. Team members contribute to designing, manufacturing, and supporting devices used in hospitals and healthcare settings worldwide. Working at Aerogen often involves collaborating with healthcare professionals, ensuring regulatory compliance, and staying at the forefront of medical technology.
What are the key skills and qualifications needed to thrive as an Aerogen?
To thrive as an Aerospace Engineer, you need a solid background in physics, mathematics, and engineering principles, typically supported by a bachelor's degree in aerospace engineering or a related field. Familiarity with CAD software, computational fluid dynamics (CFD) tools, and industry standards such as FAA regulations is important. Strong problem-solving abilities, attention to detail, and effective teamwork skills set candidates apart in this role. These competencies are crucial for ensuring the safety, efficiency, and innovation required in designing and developing aircraft and spacecraft systems.
What are some common challenges faced by professionals working at Aerogen, and how can they be addressed?
Professionals at Aerogen, particularly those in engineering, product development, or sales roles, often encounter challenges such as keeping pace with rapid technological advancements in medical devices and meeting strict regulatory requirements. Collaboration across multidisciplinary teams—engineering, clinical, and regulatory affairs—is essential to ensure products meet both innovation goals and compliance standards. Employees can address these challenges by actively participating in ongoing training, leveraging robust internal communication channels, and seeking mentorship from experienced colleagues. Aerogen also fosters a collaborative work environment that supports knowledge sharing and continuous improvement.
What is the difference between Aerogen vs Respiratory Therapist?
| Aspect | Aerogen | Respiratory Therapist |
|---|---|---|
| Credentials | Typically requires certification in medical device operation or related training | Requires state licensure and certification (e.g., RRT) |
| Work Environment | Manufacturing, medical device companies, clinical settings | Hospitals, clinics, respiratory care centers |
| Industry Usage | Medical device manufacturing and sales | Patient care and respiratory therapy services |
| Job Focus | Design, production, and support of aerosol delivery devices | Assessing, treating, and managing patients with respiratory issues |
While Aerogen professionals focus on medical device development and support, Respiratory Therapists provide direct patient care. Both roles are essential in respiratory health but differ in responsibilities, work environments, and required credentials.
What are popular job titles related to Aerogen jobs in California?
For Aerogen jobs in California, the most frequently searched job titles are:
- Respiratory Therapist Government
- Respiratory Therapist Ecmo
- Respiratory Therapist Travel
- Respiratory Therapy Associate
- Work From Home Respiratory Therapist Rt
- Contract Flight Respiratory Therapist
- Respiratory Care Therapist
- Dme Respiratory Therapist
- Overnight Agency Respiratory Therapist
- Respiratory Equipment
What job categories do people searching Aerogen jobs in California look for?
The top searched job categories for Aerogen jobs in California are:
- Per Diem Remote Respiratory Therapy
- International Respiratory Therapist
- Respiratory Year
- Contractual Respiratory Therapy Manager
- Kaiser Respiratory Therapist
- Volunteer Respiratory Therapy Intern
- Traveling Respiratory
- Overnight Respiratory Therapist Sign On Bonus
- Volunteer Respiratory Therapy
- Respiratory Therapy Manager
What cities in California are hiring for Aerogen jobs?
Cities in California with the most Aerogen job openings:
Full-time
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Job description
About Aerogen PharmaAerogen Pharma is a US based clinical-stage specialty pharmaceutical company with a mission to develop inhaled drug/biologic and device combination that will transform the standard of care for acute and critically ill patients. Our goal is to create medically superior, proprietary and commercially differentiated combination products by combining proven therapeutic molecules with a unique, high-performance aerosol delivery system.
We are embarking on an exciting and dynamic stage in our combination product development, moving into phase 3 clinical trial for one of the biggest breakthroughs in Neonatal care. We are a team of passionate industry experts who are leading, shaping, and driving a potentially transformative medical breakthrough for the treatment of neonatal respiratory distress syndrome (RDS) in the developed world.
Join us as we embark on this breakthrough and become inspired to deliver.
What is the role?The person in this role will be responsible for key aspects of pharmaceutical development of AeroFact. A key role will be the regulatory authoring and creating a robust BLA submission.
The role will focus on late stage product development of Aerofact and the biologic / device combination product, inclusive of the data and studies associated with the development or optimization of analytical methods, product characterization of a lipid-peptide formulation, aerosol characterization of the combination product, and management of drug substance/drug product stability studies supporting clinical and BLA registration.
What are the key responsibilities?• Regulatory Authoring and Quality Compliance: Prepare and review documentation for regulatory submissions (INDs, BLAs, NDAs). Ensure adherence to cGMP and regulatory requirements.
• Leadership & Strategy: Manage analytical development projects for biologics, proteins, and peptides, managing projects executed at CDMOs / Contract Laboratories and the data they generate. Develop and execute strategies aligned with Aerogen Pharma's mission and regulatory standards.
• Analytical Methods: Manage method optimization, validation, and transfer for procedures controlling the quality of lipids, proteins, and peptides. Experience with protein and lipid analytical characterization is prefered. Ensure methods are robust and comply with industry standards.
• Stability Management: Design and manage stability studies determining retest date / shelf life of products for late stage clinical development, and primary stability studies defining commercial shelf life for BLA.
• Product Characterization: Design and manage the execution of late stage product characterization studies supporting BLA filing at Contract Laboratories.
• CDMO/CMO Collaboration: Serve as the primary liaison with external manufacturing / analytical partners. Ensure effective communication and coordination to meet project timelines and quality expectations.
• Cross-Functional Collaboration: Work closely with R&D, Manufacturing, Regulatory, and Quality Assurance teams to integrate product development within overall project goals.
• Troubleshooting & Problem Solving: Address and resolve complex analytical issues during development. Implement corrective and preventive actions as needed.
What education and experience are required?• Late-stage product development experience is required.
• Experience authoring CMC dossiers for FDA, EMA and other regulatory agencies is required.
• M.Sc. or Ph.D. in Analytical Chemistry, Chemistry, Biochemistry, or related field.
• 5-10 years of product development experience.
• Experience managing CDMOs / Contract Laboratories is required.
• Knowledge of Good Manufacturing Practices is required.
• Experience with sterile manufacturing is a plus.
• Experience with lipid formulations, liposomes, or related drug delivery technologies, including homogenization and lyophilization is a plus.
• Knowledge and experience in drug-device development, and inhalation drug delivery including aerosol characterization techniques is a plus.
• Excellent written and oral communication skills.
What key skills will make you great at the role?• Communication: Strong written and oral communications skills
• Stability Management: Experience managing stability programs supporting clinical shelf life and primary stability studies for NDA/BLAs.
• Regulatory Knowledge: Deep understanding of regulatory requirements and submission processes for IND and BLA.
• Technical Expertise: Proficiency in lipid and protein quantitation and characterization techniques (e.g. HPLC, LCMS, GCMS). Experience with physical characterization techniques (e.g. Viscosity, Particle Size) and/or aerosol characterization techniques (DDU, aPSD).
• Problem-Solving: Strong analytical skills with a proven track record of overcoming complex scientific challenges. Experience in managing OOS results and analytical investigations.
• Results oriented: Strong initiative, accountability and willingness to take ownership and drive projects to completion. Work independently with CDMOs / Contract Laboratories without close supervision.
Why Aerogen PharmaAs a key member of Aerogen Group, the global market leader in high performance aerosol drug delivery, Aerogen Pharma is at a pivotal point in the company's life cycle. With plans to expand and centralize our US hubs over the next two years, we offer an environment where you can thrive professionally and learn from driven industry leaders in drug development and commercialization, inhaled devices, and neonatology.
We foster an inclusive culture that empowers you to contribute to the transformation of Neonatal care, where potential is recognized, and professional development is encouraged.
We are embarking on an exciting and dynamic stage in our combination product development, moving into phase 3 clinical trial for one of the biggest breakthroughs in Neonatal care. We are a team of passionate industry experts who are leading, shaping, and driving a potentially transformative medical breakthrough for the treatment of neonatal respiratory distress syndrome (RDS) in the developed world.
Join us as we embark on this breakthrough and become inspired to deliver.
What is the role?The person in this role will be responsible for key aspects of pharmaceutical development of AeroFact. A key role will be the regulatory authoring and creating a robust BLA submission.
The role will focus on late stage product development of Aerofact and the biologic / device combination product, inclusive of the data and studies associated with the development or optimization of analytical methods, product characterization of a lipid-peptide formulation, aerosol characterization of the combination product, and management of drug substance/drug product stability studies supporting clinical and BLA registration.
What are the key responsibilities?• Regulatory Authoring and Quality Compliance: Prepare and review documentation for regulatory submissions (INDs, BLAs, NDAs). Ensure adherence to cGMP and regulatory requirements.
• Leadership & Strategy: Manage analytical development projects for biologics, proteins, and peptides, managing projects executed at CDMOs / Contract Laboratories and the data they generate. Develop and execute strategies aligned with Aerogen Pharma's mission and regulatory standards.
• Analytical Methods: Manage method optimization, validation, and transfer for procedures controlling the quality of lipids, proteins, and peptides. Experience with protein and lipid analytical characterization is prefered. Ensure methods are robust and comply with industry standards.
• Stability Management: Design and manage stability studies determining retest date / shelf life of products for late stage clinical development, and primary stability studies defining commercial shelf life for BLA.
• Product Characterization: Design and manage the execution of late stage product characterization studies supporting BLA filing at Contract Laboratories.
• CDMO/CMO Collaboration: Serve as the primary liaison with external manufacturing / analytical partners. Ensure effective communication and coordination to meet project timelines and quality expectations.
• Cross-Functional Collaboration: Work closely with R&D, Manufacturing, Regulatory, and Quality Assurance teams to integrate product development within overall project goals.
• Troubleshooting & Problem Solving: Address and resolve complex analytical issues during development. Implement corrective and preventive actions as needed.
What education and experience are required?• Late-stage product development experience is required.
• Experience authoring CMC dossiers for FDA, EMA and other regulatory agencies is required.
• M.Sc. or Ph.D. in Analytical Chemistry, Chemistry, Biochemistry, or related field.
• 5-10 years of product development experience.
• Experience managing CDMOs / Contract Laboratories is required.
• Knowledge of Good Manufacturing Practices is required.
• Experience with sterile manufacturing is a plus.
• Experience with lipid formulations, liposomes, or related drug delivery technologies, including homogenization and lyophilization is a plus.
• Knowledge and experience in drug-device development, and inhalation drug delivery including aerosol characterization techniques is a plus.
• Excellent written and oral communication skills.
What key skills will make you great at the role?• Communication: Strong written and oral communications skills
• Stability Management: Experience managing stability programs supporting clinical shelf life and primary stability studies for NDA/BLAs.
• Regulatory Knowledge: Deep understanding of regulatory requirements and submission processes for IND and BLA.
• Technical Expertise: Proficiency in lipid and protein quantitation and characterization techniques (e.g. HPLC, LCMS, GCMS). Experience with physical characterization techniques (e.g. Viscosity, Particle Size) and/or aerosol characterization techniques (DDU, aPSD).
• Problem-Solving: Strong analytical skills with a proven track record of overcoming complex scientific challenges. Experience in managing OOS results and analytical investigations.
• Results oriented: Strong initiative, accountability and willingness to take ownership and drive projects to completion. Work independently with CDMOs / Contract Laboratories without close supervision.
Why Aerogen PharmaAs a key member of Aerogen Group, the global market leader in high performance aerosol drug delivery, Aerogen Pharma is at a pivotal point in the company's life cycle. With plans to expand and centralize our US hubs over the next two years, we offer an environment where you can thrive professionally and learn from driven industry leaders in drug development and commercialization, inhaled devices, and neonatology.
We foster an inclusive culture that empowers you to contribute to the transformation of Neonatal care, where potential is recognized, and professional development is encouraged.