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Director Formulation Development Jobs in Pennsylvania

Lead endโ€‘toโ€‘end CMC strategy (process development, formulation, scaleโ€‘up, and tech transfer) with direct impact on program scientific objectives. * Design technical DOEs to establish and ...

Senior Analytical Scientist

Harleysville, PA ยท On-site

$88K - $120K/yr

Work with Formulation Development, manufacturing, and quality teams to select and apply optimal ... Must be self-directed, motivated, and have a willingness to take the initiative to identify and ...

Senior Analytical Scientist

Harleysville, PA ยท On-site

$88K - $120K/yr

Work with Formulation Development, manufacturing, and quality teams to select and apply optimal ... Must be self-directed, motivated, and have a willingness to take the initiative to identify and ...

Senior Analytical Scientist

Harleysville, PA ยท On-site

$88K - $120K/yr

Work with Formulation Development, manufacturing, and quality teams to select and apply optimal ... Must be self-directed, motivated, and have a willingness to take the initiative to identify and ...

Senior Analytical Scientist

Harleysville, PA ยท On-site

$88K - $120K/yr

Work with Formulation Development, manufacturing, and quality teams to select and apply optimal ... Must be self-directed, motivated, and have a willingness to take the initiative to identify and ...

Be Seen First

... formulation, regulatory requirements, manufacturing needs, and customer expectations. 2. Raw ... Ensure documentation accuracy and consistency with input from the Director of Product Development ...

The Director of Project Delivery is responsible for providing leadership, oversight, and management ... Analysis, development, formulation, and administration of operating and project budgets. This ...

Principal Scientist - Device Technical and Engineering Lead - Inhalation Programs (Director ... development activities with the clinical, regulatory, formulation, commercial, human factors ...

Senior Scientist II

Bristol, PA ยท On-site

$99K - $120K/yr

... developments. To define and carry out projects & experimental programs to ensure the transfer of ... direct formulation and position new chemicals in the targeted application fields. * Exchange ...

Senior Scientist II

Bristol, PA ยท On-site

$99K - $120K/yr

... developments. To define and carry out projects & experimental programs to ensure the transfer of ... direct formulation and position new chemicals in the targeted application fields. * Exchange ...

Clinical Director IBHS

PA ยท On-site

$79K - $108K/yr

The Clinical Director oversees the Intensive Behavioral Health Services (IBHS) Individual Services ... Responsibilities also include participation in program development, policy formulation, and other ...

Showing results 21-40

Director Formulation Development information

See Pennsylvania salary details

$89.2K

$191.9K

$288.2K

How much do director formulation development jobs pay per year?

As of Aug 10, 2026, the average yearly pay for director formulation development in Pennsylvania is $191,871.00, according to ZipRecruiter salary data. Most workers in this role earn between $94,200.00 and $249,600.00 per year, depending on experience, location, and employer.

What does a Director Formulation Development do?

As a Director Formulation Development, you will oversee the design and optimization of drug formulations, lead a multidisciplinary team of scientists, and ensure that projects meet quality, budget, and timeline expectations. Your daily activities often include strategic planning, reviewing progress reports, troubleshooting formulation challenges, and collaborating with regulatory, manufacturing, and quality assurance departments. You may also interact with upper management to report on key milestones and contribute to long-term product development strategies. This role offers opportunities to influence project pipelines and play a central part in bringing new therapies to market.

What is a Director Formulation Development?

A Director of Formulation Development leads the design and optimization of pharmaceutical formulations, ensuring they meet quality, regulatory, and performance standards. They oversee research, guide teams in developing new drug delivery systems, and collaborate with regulatory and manufacturing teams. This role requires expertise in chemistry, pharmaceutics, and process development to ensure successful product commercialization. Additionally, they manage project timelines, budgets, and technical challenges to drive innovation in drug formulation.

What are the key skills and qualifications needed to thrive as a Director Formulation Development?

A Director Formulation Development typically requires an advanced degree in pharmaceutical sciences, chemistry, or a related field, along with significant experience in drug formulation and team management. Familiarity with industry-standard formulation software, regulatory compliance systems, and relevant certifications such as PMP or Six Sigma are highly valued. Excellent leadership, communication, and strategic planning skills help set high performers apart in this role. These skills and qualities are critical for driving innovative product development, ensuring regulatory compliance, and effectively leading cross-functional teams.

What are popular job titles related to Director Formulation Development jobs in Pennsylvania? For Director Formulation Development jobs in Pennsylvania, the most frequently searched job titles are:
What job categories do people searching Director Formulation Development jobs in Pennsylvania look for? The top searched job categories for Director Formulation Development jobs in Pennsylvania are:
Infographic showing various Director Formulation Development job openings in Pennsylvania as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 19% Part Time, 2% Contract, and 1% Nights. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $191,871 per year, or $92.2 per hour.

Scientific Director, Discovery Pharmaceutics

Jj

Spring House, PA โ€ข On-site

Full-time

Re-posted 17 days ago


Job description

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

Discovery & Pre-Clinical/Clinical Development

Job Sub Function:

Pharmaceutical Product R&D

Job Category:

People Leader

All Job Posting Locations:

Spring House, Pennsylvania, United States of America

Job Description:

About Innovative Medicine

Our expertise in Innovative Medicine is informed and inspired by patients, whose insights fuel our science-based advancements. Visionaries like you work on teams that save lives by developing the medicines of tomorrow.

Join us in developing treatments, finding cures, and pioneering the path from lab to life while championing patients every step of the way.

Learn more at https://www.jnj.com/innovative-medicine

We are searching for the best talent for a Scientific Director, Discovery Pharmaceutics to be located in Spring House, PA.

Purpose: Global Discovery Pharmaceutics is part of the Pharmaceutical Development & Supply (PPDS) organization within the Discovery, Product Development and Supply (DPDS) division of Johnson & Johnson Innovative Medicine (JJIM). The group supports drug discovery programs from hit-to-lead through candidate selection, with a focus on the Synthetics Modalities portfolio - including small molecules, degraders, peptides, oligonucleotides, and conjugates.

As the Scientific Director, you and your team will provide expert scientific leadership to enable informed molecule design and developability decisions. You will collaborate in close partnership with chemistry, biology, pharmacokinetics and pre-clinical safety.

As head of the team, you will provide scientific, strategic, and people leadership while driving the CMC deliverables for discovery programs. Your responsibilities include physical characterization, biopharmaceutical evaluation, and preclinical formulation support across diverse routes of administration - including oral, parenteral and intra-organ - and may include other advanced drug delivery strategies as required.

You will be responsible for:
  • Leading and developing a multidisciplinary scientific team, building technical depth, mentoring talent, fostering a culture of collaboration, innovation and continuous improvement.
  • Developing innovative screening tools and formulation approaches, with the capability of meeting rapid cycle times and miniaturization, to influence and enable early discovery. Collaborating with academia and industry experts.
  • Enhancing digital tools, data analytics and computational approaches to support developability assessments and improve the quality and speed of decision making in discovery programs.
  • Enabling and overcoming exposure challenges for critical tool compounds or non-optimized leads with enabling formulations in support of PK, PK/PD, translational pharmacology and tolerability studies.
  • Influencing compound design early to ensure lead candidates have the desired properties for specific drug delivery platforms and technologies to ensure patient convenience and compliance.
  • Portfolio delivery and accelerating the transition from discovery to development through collaboration with key development functions to support the GLP toxicology studies, formulation strategy and dosage form design for clinical studies.
  • Influencing risk management and mitigation.

Qualifications / RequirementsEducation:
  • A PhD in Pharmaceutical Sciences, Chemistry, Chemical Engineering or a related field with 12+ years of relevant experience OR a Master's degree with 18+ years of relevant experience is required.
Experience and Skills:
  • Demonstrated people leadership and talent development, including technical and non-technical coaching and mentoring is required.
  • Ability to drive and get results through leading others is required.
  • Strong understanding of Discovery and Pharmaceutical Development including ADME, Preclinical Safety evaluation and Drug Development is required.
  • Proven experience in developability assessments for synthetic modalities in the area of molecular design, interpretation of pharmaceutical properties in relation to exposure and toxicology data, setting formulation strategies is required.
  • Track record of scientific contributions is required.
  • Excellent communication, critical thinking and problem solving skills are required.
  • Strong collaboration and networking capabilities are required.
  • Willingness to take informed risks or leave appropriate knowledge gaps, as needed to maintain speed and program progression.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via https://www.jnj.com/contact-us/careers, internal employees contact AskGS to be directed to your accommodation resource.

#LI-Onsite

Required Skills:

Preferred Skills:

Budget Management, Business Savvy, Chemistry, Manufacturing, and Control (CMC), Clinical Trial Protocols, Cross-Functional Collaboration, Data Governance, Developing Others, Drug Discovery Development, Inclusive Leadership, Industry Analysis, Interdisciplinary Work, Leadership, Market Research, Process Improvements, Product Development, Product Strategies, Risk Management Framework, Scientific Research