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As of Jul 24, 2026, the average hourly pay for atmp in the United States is $26.34, according to ZipRecruiter salary data. Most workers in this role earn between $15.14 and $30.77 per hour, depending on experience, location, and employer.

What are some common challenges faced by ATM (Automated Teller Machine) Technicians and how can they overcome them?

ATM Technicians often face challenges such as troubleshooting complex hardware or software malfunctions, ensuring security protocols are followed, and responding quickly to service calls. Working in various environments and sometimes outside regular hours can also be demanding. To overcome these challenges, technicians should stay updated on the latest ATM technologies, maintain strong problem-solving skills, and communicate effectively with both team members and financial institution clients. Continuous professional development and hands-on experience can further help in managing and resolving technical issues efficiently.

What are the key skills and qualifications needed to thrive as an Advanced Therapy Medicinal Products (ATMP) Specialist, and why are they important?

To thrive as an ATMP Specialist, you need a strong background in biotechnology, cell and gene therapy, and regulatory compliance, typically supported by a degree in life sciences or pharmacy. Familiarity with Good Manufacturing Practices (GMP), quality management systems, and validation tools is essential, along with possible certifications in GMP or ATMP manufacturing. Strong attention to detail, problem-solving abilities, and effective communication skills help ensure product safety and regulatory adherence. These skills are crucial for safeguarding patient health and ensuring the successful development and delivery of advanced therapies.

What are ATMPs?

ATMPs, or Advanced Therapy Medicinal Products, are a class of innovative medicines that are based on genes, cells, or tissue engineering. They are used to treat, diagnose, or prevent diseases and can include gene therapy, somatic cell therapy, and tissue-engineered products. ATMPs are regulated under specific frameworks in regions such as the European Union due to their complexity and potential impact on patient health. These therapies offer new possibilities for treating conditions that currently have limited or no effective treatment options.
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Infographic showing various Atmp job openings in the United States as of July 2026, with employment types broken down into 96% Full Time, and 4% Contract. Highlights an 89% Physical, and 11% Remote job distribution, with an average salary of $54,791 per year, or $26.3 per hour.
Director, Regulatory Affairs

Director, Regulatory Affairs

Sonoma Biotherapeutics

South San Francisco, CA • On-site

Full-time

Posted 15 days ago

Job description

Salary: $210,000 - $275,000

About Sonoma Biotherapeutics

Sonoma Biotherapeutics is a South San Francisco and Seattle-based company leading the development of adoptive T-reg therapies cell for autoimmune and degenerative diseases. Using next generation genome editing and target-specific cell therapy, Sonoma is focused on developing its best-in-class platform across the entire spectrum of T-reg cell therapeutic capabilities. Founded by pioneers in Treg biology and cell therapy, the company brings together leadingexpertiseand proprietary methodologies for the discovery and development of diseasemodifyingand curative therapies. More information atwww.sonomabio.com.


Job Purpose/Summary:

We seek an experienced Regulatory professional to manage regulatory activities associated with pipeline and late phase clinical development, working in partnership with the development R&D team and CMOs. This position reports into the SVP Regulatory Affairs and Quality Assurance.The candidate must be able to interpret biologic/ATMP regulations as they apply to given phases of drug development including preclinical, clinical and commercial. This is an exciting team-building, hands-on leadership role within the Sonoma Biotherapeutics team. The position will be based in the US in the SSF headquarters. Remote US candidates are also considered.


Roles and Responsibilities:

  • Proactively participate in design of global regulatory strategies for the development of cell therapy products
  • Oversee and manage preparation and submissions (including but not limited to protocol amendments, Initial INDs, Pre-IND/EOP meetings, CTAs, BLA/MAA, Fast Track/Breakthrough and PIPs) of high-quality regulatory according to set timelines; this will require, strong regulatory knowledge and experience, cross-functional interactions, excellent project management and writing skills, and a good understanding of the underlying science.
  • Interface with Regulatory counterparts (Reg CMC and Reg Ops) and collaborate with the nonclinical, clinical and CMC teams to ensure seamless strategy and integration of components in all initiatives and submissions
  • Participate in interactions and negotiations with regulatory agencies to clarify and solidify strategy and resolve issues
  • Lead preparation of agency meetings and actively participate in scheduled meetings
  • Drive adherence to regulatory requirements and guidelines
  • Perform regulatory intelligence activities monitor regulation changes and competitor trends/strategy
  • Provide regulatory input regarding budget
  • This position requires 15-20% travel


Qualifications and Education Requirements:

  • BA/BS degree in life sciences preferably in biotechnology, chemistry and/or biology. MS/PhD preferred but not required
  • At least 8-10 years of regulatory pharmaceutical product development experience preferably in biotechnology, ideally in cell & gene therapy
  • Well-versed in regulatory strategy and regulatory science writing
  • Knowledgeable in ICH, FDA, EMA and WHO regulations/guidelines
  • Ability to work independently and thrive in a fast-paced environment
  • Strong attention to detail and well organized and able to multi-task
  • Outstanding communication and time management skills
  • Passionate about patient-focused drug development toward finding cures for patients in need