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Transdermal Jobs (NOW HIRING)

kindeva

Manufacturing Engineer

Northridge, CA · On-site

$78K - $101K/yr

Lead real-time troubleshooting for inhalation and transdermal drug product processes. * Partner with operators and supervisors to rapidly resolve equipment issues and process deviations. * Ensure ...

Kindeva Drug Delivery

Manufacturing Engineer

Van Nuys, CA · On-site

$76K - $98K/yr

Lead real-time troubleshooting for inhalation and transdermal drug product processes. * Partner with operators and supervisors to rapidly resolve equipment issues and process deviations. * Ensure ...

kindeva

Manufacturing Engineer

Northridge, CA

$78K - $101K/yr

Lead real-time troubleshooting for inhalation and transdermal drug product processes. * Partner with operators and supervisors to rapidly resolve equipment issues and process deviations. * Ensure ...

kindeva

Manufacturing Engineer

Northridge, CA

$78K - $101K/yr

Lead real-time troubleshooting for inhalation and transdermal drug product processes. * Partner with operators and supervisors to rapidly resolve equipment issues and process deviations. * Ensure ...

kindeva

Manufacturing Engineer

Northridge, CA · On-site

$78K - $101K/yr

Lead real-time troubleshooting for inhalation and transdermal drug product processes. * Partner with operators and supervisors to rapidly resolve equipment issues and process deviations. * Ensure ...

kindeva

Senior Process Engineer I

Northridge, CA

$112K - $144K/yr

Lead real-time troubleshooting for inhalation and transdermal drug product processes. * Partner with operators and supervisors to rapidly resolve equipment issues and process deviations. * Ensure ...

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How much do transdermal jobs pay per hour?

As of Jun 7, 2026, the average hourly pay for transdermal 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 transdermal formulation scientists, and how can they be addressed in a team setting?

Transdermal formulation scientists often face challenges such as ensuring drug stability, optimizing skin permeability, and achieving consistent drug delivery rates. Collaboration with analytical chemists, process engineers, and regulatory specialists is crucial to address these issues effectively. Regular team meetings and open communication help identify formulation problems early and foster innovative solutions. Additionally, sharing knowledge on the latest skin permeation technologies and regulatory updates ensures the development process remains efficient and compliant.

What are transdermal jobs?

Transdermal jobs typically refer to roles involved in the research, development, manufacturing, or application of transdermal drug delivery systems. These systems administer medication through the skin, such as in the form of patches, allowing the drug to be absorbed into the bloodstream over time. Professionals in this field may work in pharmaceutical companies, research labs, or healthcare settings, focusing on tasks like formulation, quality control, regulatory compliance, or patient education. Such jobs require knowledge of pharmacology, skin physiology, and drug delivery technologies.

What are the key skills and qualifications needed to thrive as a Transdermal Pharmaceutical Specialist, and why are they important?

To excel as a Transdermal Pharmaceutical Specialist, a strong background in pharmaceutical sciences, drug delivery systems, and often an advanced degree such as a PharmD or PhD is essential. Experience with formulation software, laboratory equipment, and compliance with regulatory standards like FDA or EMA guidelines is typically required. Analytical thinking, attention to detail, and effective teamwork are critical soft skills in this field. These competencies ensure the safe and effective development of transdermal therapies, adherence to regulations, and successful collaboration across multidisciplinary teams.

What is the difference between Transdermal vs Pharmacist?

AspectTransdermalPharmacist
Required CredentialsCertification in medication administration, often with specialized trainingDoctor of Pharmacy (PharmD) degree, licensure required
Work EnvironmentHealthcare settings, clinics, or pharmacies focusing on topical medication applicationPharmacies, hospitals, healthcare facilities, often involving patient counseling
Industry UsagePharmaceutical manufacturing, healthcare, medical device companiesHealthcare, pharmacy services, medication management

Transdermal professionals focus on applying or developing topical medication delivery systems, while pharmacists dispense medications and provide patient counseling. Both roles require healthcare knowledge but differ in scope and responsibilities within the industry.

More about Transdermal jobs
What states have the most Transdermal jobs? States with the most job openings for Transdermal jobs include:
What job categories do people searching Transdermal jobs look for? The top searched job categories for Transdermal jobs are:
Transdermal jobs near you
Infographic showing various Transdermal job openings in the United States as of May 2026, with employment types broken down into 1% As Needed, 66% Full Time, 25% Part Time, 1% Temporary, and 7% Contract. Highlights an 97% Physical, and 3% Remote job distribution, with an average salary of $54,791 per year, or $26.3 per hour.

Manufacturing Engineer

kindeva

Northridge, CA • On-site

$78K - $101K/yr

Other

Posted 19 days ago

Kindeva rating

6.8

Company rating: 6.8 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

Job description

Our Work Matters

At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.

The Impact You Will Make

This Manufacturing Engineer  role will lead critical, high impact technical initiatives that support inhalation and transdermal drug product manufacturing within a 24/7 commercial facility in Northridge, CA. These initiatives may include process robustness improvements, complex root cause investigations, new product introductions, capacity and yield enhancements, compliance-driven process modifications, and strategic manufacturing optimization efforts.

ROLE RESPONSIBILITIES

Manufacturing Support (24/7 Facility)

  • Provide on-call and on-site technical support for commercial production lines.
  • Lead real-time troubleshooting for inhalation and transdermal drug product processes.
  • Partner with operators and supervisors to rapidly resolve equipment issues and process deviations.
  • Ensure uninterrupted supply by proactively identifying and mitigating process risks.
  • Collect and examine basic equipment maintenance problems, facilitating failure analysis for critical equipment (RCA, RCI, FMECA, REM) together with Technical Leaders, generating actions that improve reliability based on field experience and information obtained, considering impact and cost.
  • Reviews the installation and maintenance plans for new equipment, as well as the necessary basic spare parts

Process Ownership & Optimization

  • Serve as process owner and technical subject matter experts (SME) for assigned unit operations.
  • Develop and maintain process control strategies and critical parameter limits.
  • Drive continuous improvement initiatives (OEE, waste reduction, cycle-time improvements).
  • Lead scale-up, tech transfers, and validation activities aligned with regulatory guidelines.
  • Work with our internal clients to modify and/or develop new processes to support new products or improvements to existing products.
  • Use first principles and process optimization knowledge (DOE) to define scientific approaches to support process improvement. Utilize in depth understanding of materials, process and equipment to improve process robustness and reduce variability.
  • Identify and drive improvement opportunities.
  • Support capital projects to create assets and meeting the internal Quality Management System requirements
  • Author URS, DQR, FAT, Commissioning, SAT, IQ, OQ, and PQ 

CAPA, Quality, and Compliance

  • Lead root cause investigations (OOS, deviations, nonconformances).
  • Author or approve CAPAs with strong technical justification.
  • Ensure compliance with cGMP, ISO, and quality system requirements.
  • Support audits, regulatory inspections, and documentation readiness.
  • Lead and support Engineering Change Control activities in accordance with FDA regulations and current Good Manufacturing Practices (cGMP)

Technical Leadership

  • Mentor junior engineers and provide site-wide subject matter guidance.
  • Represent Process Engineering in cross-functional forums.
  • Create a safe and encouraging environment for colleagues to share ideas, contribute and thrive.
  • Drive innovation in manufacturing methods and analytics.
  • Stay current with industry trends in inhalation and transdermal technologies

Required Experience

  • Bachelor's degree in chemical, mechanical, electrical, manufacturing, systems engineering, or other engineering discipline from an accredited institution or a bachelor's degree with manufacturing experience.
  • 8+ years in pharma/biotech/medical device manufacturing is preferred.
  • Expertise in inhalation or transdermal manufacturing is preferred.
  • Strong familiarity with pharmaceutical industrial process equipment and automated assembly, labeling, and packaging machinery is preferred.
  • Strong understanding of cGMP, validation, and process controls.
  • Proven ability to lead investigations and CAPA development.
  • Experience supporting or leading operations in a 24/7 environment.
  • Demonstrated ability to successfully execute medium to large and complex projects in support of manufacturing operations.
  • Ability to successfully lead cross functional teams to achieve project objectives.

Preferred Experience

  • Master’s degree in technical discipline.
  • Experience with Lean Six Sigma, SPC, DOE.
  • Familiarity with automated systems and MES.
  • Experience with P&IDs (Piping and Instrumentation Diagrams) and PHA (Process Hazard Analysis) or equivalent.
  • Experience with high-volume commercial manufacturing or tech transfer.
  • High speed automated product manufacturing experience 

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