ZipRecruiter

Log In

1

Formulation Drug Delivery Director Jobs (NOW HIRING)

adareps

Senior Formulation Scientist I

Vandalia, OH · On-site

Six years of experience in pharmaceutics, solid dosage formulation development, drug delivery technologies, processing technologies, or a related field. * Experience in pharmaceutical operations ...

Nevakar Pharmaceuticals Inc

Design and conduct pre-formulation, formulation development, process development and process optimization of parenteral and ophthalmic formulations and related alternate drug delivery systems such as ...

UNIVERSITY OF ARIZONA

Design and perform experimentsevaluating formulation performance in cellular and animal models ... Experience with liposomal drug delivery systems. * Experience with lipid nanoparticles (LNPs)

previous pagenext page

Showing results 21-40

All JobsScience JobsResearch JobsScientist JobsFormulation Drug Delivery Director Jobs

Formulation Drug Delivery Director information

See salary details

$14

$22

$42

How much do formulation drug delivery director jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for formulation drug delivery director in the United States is $22.83, according to ZipRecruiter salary data. Most workers in this role earn between $18.27 and $22.84 per hour, depending on experience, location, and employer.

What does a formulation drug delivery director do?

A Formulation Drug Delivery Director is responsible for overseeing the development, optimization, and implementation of drug formulations and delivery systems within a pharmaceutical company. They lead teams of scientists and manage projects focused on creating effective ways to deliver medications, such as oral, injectable, or transdermal systems. This role involves coordinating research, ensuring regulatory compliance, collaborating with cross-functional teams, and guiding the transition of drug products from the laboratory to clinical trials and commercial production. The director also stays updated on the latest advancements in drug delivery technologies and may interact with regulatory agencies to ensure product safety and efficacy.

What are the key skills and qualifications needed to thrive as a formulation drug delivery director?

A Formulation Drug Delivery Director needs deep expertise in pharmaceutical sciences, formulation development, and regulatory compliance, often supported by an advanced degree (PhD or MS) in pharmacy, chemistry, or related fields. Familiarity with industry-standard analytical tools, GMP environments, and drug delivery technologies, along with experience in project management software, is essential. Exceptional leadership, cross-functional collaboration, and strategic problem-solving skills help professionals excel in this role. These competencies ensure innovative, safe, and effective drug products are developed on time and in accordance with regulatory standards.

How does a formulation drug delivery director typically collaborate with cross-functional teams during the drug development process?

A Formulation Drug Delivery Director frequently works alongside R&D scientists, regulatory affairs specialists, quality assurance teams, and manufacturing personnel to ensure that drug formulations are both effective and compliant with industry standards. This role often involves leading discussions during project meetings, troubleshooting formulation challenges, and aligning the team on timelines and deliverables. Effective communication and leadership are essential, as the director must integrate feedback from various departments to optimize formulation strategies and support successful product launches.

What are popular job titles related to Formulation Drug Delivery Director jobs?

For Formulation Drug Delivery Director jobs, the most frequently searched job titles are:

Associate Director/Director, Formulation & Downstream Process Development

San Diego, CA • On-site

Pivotal
See more jobs at Pivotalexternal

$65K - $100K/yr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 23 days ago

Job description

Research Associate, Formulation Development

Location: San Diego, CA

Job Type: Full-Time, Onsite

About Us

We are an innovative, stealth-mode biotech focused on developing best-in-class delivery for in vivo gene editing.

Job Summary

We are seeking a highly motivated and skilled individual to join our team as a Research Associate in Formulation Development. The successful candidate will be responsible for designing, executing, analyzing, and making recommendations on research protocols for lipid nanoparticle (LNP) drug delivery systems aimed at gene editing. Title level and salary will be commensurate with experience.

Responsibilities
  • Develop lipid nanoparticle (LNP) formulations for gene editing applications.
  • Conduct experiments to optimize formulation parameters such as particle size, encapsulation efficiency, and stability.
  • Optimize production processes to improve yields and scalability.
  • Troubleshoot and resolve issues related to formulation processes.
  • Perform analytical characterization of LNPs using techniques such as dynamic light scattering (DLS), zeta potential measurement, and electron microscopy.
  • Support in vitro and in vivo studies to evaluate the efficacy and safety of LNP formulations.
  • Collaborate with preclinical and clinical teams to ensure successful translation of formulations.
  • Maintain accurate and detailed laboratory records.
  • Prepare technical reports and presentations to communicate findings.
  • Stay current with advancements in LNP technologies and methodologies.
Qualifications
  • Bachelor's degree or higher in Chemistry, Pharmaceutics, Biochemistry, Biomedical Engineering, Chemical Engineering, or a related field.
  • 3+ years of experience in pharmaceutical formulation, with a focus on lipid nanoparticle drug delivery systems.
  • Experience with techniques such as DLS, zeta potential measurement, and other analytical tools used in nanoparticle characterization.
  • Strong analytical and problem-solving skills.
  • Excellent communication and teamwork abilities.
  • Ability to work independently and manage multiple tasks effectively.
Preferred Qualifications
  • GMP production experience.
  • Familiarity with regulatory requirements and quality control in bioprocessing.
Benefits
  • Competitive salary, equity, and benefits package.
  • Opportunities for professional growth and development.
  • Fast paced collaborative and innovative work environment.
  • We offer an exceptional benefits package to include Medical, Dental, Vision, Life, Disability, a 401k Match of 4%, Paid Time Off and Equity.
Equal Opportunity Employer

We are an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All employment decisions are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.

Salary Range

$65,000 - $100,000

#J-18808-Ljbffr

Apply