2,526 Pharmaceutical Development jobs in the United States

Our client, a dynamic and innovative pharmaceutical company, is seeking a highly accomplished Senior Formulation Scientist to join their Research and Development department in Grand Rapids, Michigan, US . This role is integral to the discovery and development of novel drug delivery systems and advanced pharmaceutical formulations. The ideal candidate will possess a deep understanding of pharmaceutics, pre-formulation studies, formulation development, and manufacturing scale-up for various dosage forms. You will lead projects focused on creating stable, effective, and bioavailable drug products. Responsibilities include designing and executing formulation studies, characterizing active pharmaceutical ingredients (APIs), and developing various dosage forms such as oral solids, injectables, or topicals. You will collaborate closely with analytical chemists, process engineers, and regulatory affairs teams to ensure all development activities are robust and compliant with GMP standards. The ability to troubleshoot formulation challenges, optimize processes, and conduct pre-clinical and clinical trial material manufacturing is essential. We are looking for a scientifically driven individual with excellent analytical skills, a thorough understanding of regulatory guidelines (e.g., FDA, EMA), and a passion for bringing life-changing therapies to patients. This position offers a stimulating environment with opportunities for professional growth and contribution to significant advancements in pharmaceutical science.

Qualifications:

• Ph.D. or Master's degree in Pharmaceutics, Pharmaceutical Sciences, Chemistry, or a related field.
• Minimum of 7 years of experience in pharmaceutical formulation development.
• Proven expertise in designing, developing, and optimizing various dosage forms (e.g., tablets, capsules, sterile injectables, topical formulations).
• Strong knowledge of pre-formulation, excipient selection, and drug delivery technologies.
• Experience with analytical techniques for formulation characterization (e.g., HPLC, dissolution testing, particle size analysis).
• Familiarity with Good Manufacturing Practices (GMP) and relevant regulatory guidelines.
• Experience in process development and scale-up of pharmaceutical manufacturing.
• Excellent problem-solving, critical thinking, and experimental design skills.
• Strong written and verbal communication skills, with the ability to present complex data clearly.
• Ability to work effectively in a cross-functional team environment.

**Director of Pharmaceutical Development**
Science & Research
Minneapolis , MN, US
Pay Rate Low: 150,000 | Pay Rate High: 200,000
+ Added - 21/08/2025
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We are excited to partner with a leading CDMO in pharmaceutical development and manufacturing to hire a **Director of Pharmaceutical Development** . This key leadership role will guide end-to-end drug development efforts-from early-stage research through commercial production-accelerating therapies to market.
Onsite: Minnesota
Salary: Starting at $150k **Key Responsibilities**
+ Lead site-based product development, ensuring scalable processes, high-quality outcomes, and on-time client delivery.
+ Oversee small-scale synthesis and formulation of small molecules, peptides, and antibodies.
+ Prepare and manage CMC documentation to support regulatory filings and clinical/commercial readiness.
+ Champion innovation in compounds, delivery technologies, and development strategies.
+ Mentor and develop a high-performing, collaborative team.
+ Partner with leadership to define project plans, timelines, budgets, and deliverables.
+ Support deviation investigations and ensure full compliance with GMP and regulatory standards.
**Qualifications**
+ Ph.D. in Chemistry, Biochemistry, or related field.
+ 5+ years of experience in pharmaceutical/biotech product development (small molecules, peptides, or antibodies).
+ Proven leadership in team management and mentorship.
+ Experience preparing CMC documentation for IND, NDA, or equivalent submissions.
+ Strong understanding of GMP requirements and pharmaceutical manufacturing.
+ Track record of success in dynamic, fast-paced environments.
+ Flexible, adaptable, and willing to work extended hours as needed.
+ Driven by innovation and continuous improvement.
This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

**Director of Pharmaceutical Development**
Clinical
Olmsted county, MN, US
+ Added - 19/08/2025
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We are proud to partner with a leading CDMO specializing in pharmaceutical development and manufacturing to hire a Director of Pharmaceutical Development. In this pivotal role, you'll join a team of experts dedicated to supporting the entire drug development lifecycle from early-stage research to commercial production helping to accelerate the path to market!
**Location:** Olmsted County
**Principal Responsibilities**
+ Drive and oversee product development activities at the site, ensuring robust, scalable processes, high-quality results, and on-time delivery of client commitments.
+ Develop, optimize, and enhance small-scale synthesis and formulation processes for small molecules, peptides, and antibodies.
+ Manage CMC documentation to support regulatory submissions and clinical/commercial readiness.
+ Drive innovation through new compounds, delivery methods, and development strategies.
+ Lead, mentor, and develop staff while encouraging a collaborative, high-performing team environment.
+ Partner with leadership and project teams to establish project plans, timelines, budgets, and key deliverables.
+ Assist in deviation investigations and ensure compliance with GMP and regulatory requirements.
**Qualifications & Requirements**
+ Ph.D. in Chemistry, Biochemistry, or a related scientific discipline.
+ Minimum of 5 years of experience in pharmaceutical/biotech product development involving small molecules, peptides, or antibodies.
+ Proven leadership experience, including team management and mentorship.
+ Experience in preparing CMC documentation for regulatory submissions (e.g., IND, NDA).
+ Strong knowledge of GMP standards and pharmaceutical manufacturing practices.
+ Demonstrated success in delivering projects in fast-paced, innovative environments.
+ Flexible and adaptable, including willingness to work extended hours when needed.
+ Passion for innovation and continuous improvement in product development.#INDBH
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

**Pharmaceutical Development Technician I**
Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually.
**Catalent is committed to a Patient First culture through excellence in quality and compliance, and to the safety of every patient, consumer, and Catalent employee.**
Catalent's Kansas City, MO facility is home to our Oral & Specialty Drug Delivery, Biologics Analytical Services and Clinical Supply Services businesses. The site provides a range of integrated services for oral solid dosage forms, from formulation development and analytical testing to clinical and commercial-scale manufacture. The Kansas City facility is a Center-of-Excellence for our Biologics Analytical Services business. Our talented team has over 25 years of experience providing analytical services for stand-alone and integrated biologics projects.
Our facility in Kansas City, MO is hiring for a **Pharmaceutical Development Technician I** . The **Pharmaceutical Development Technician I** is responsible for performing setup/teardown, manufacturing and cleaning of all equipment and processes associated with manufacturing operations.
**This is a full-time, hourly position and is 100% onsite. The schedule is Monday - Friday, 6:00AM - 2:30PM.**
**The Role**
+ Ensures that all Catalent safety procedures are followed and identifies/communicates the necessary adjustments to address potential safety concerns. Will also ensure the proper use of PPE (Personal Protection Equipment).
+ Focuses on learning all equipment and testing within core group while maintaining high quality standards.
+ Maintain up to date training on equipment and site procedures.
+ Perform daily tasks to ensure that working areas are stocked with proper materials and supplies.
+ Perform physical characterization testing on raw and in-process materials.
+ Support sampling and packaging of in-process and finish product material.
+ Maintain active inventory of excipients and API used for Experimental processing.
+ Other duties, as assigned.
**The Candidate**
+ High School degree or equivalent.
+ Must be able to manage priorities and projects effectively.
+ Must communicate clearly with all levels of management.
+ Capability to work in a matrix organization.
+ Physical Requirements: On an average 8-hour day this position requires the ability to walk, sit and stand, use hands to handle or feel, reach with hands and arms at or above shoulder height and below waist height, climb or balance, stoop, kneel, crouch, or crawl; talk, hear, and smell, and lift to 40 pounds. Specific vision requirements include reading of written documents; visual inspection of materials and frequent use of computer monitor screens.
**Why you should join Catalent**
+ Medical, dental, vision, and wellness benefits are effective on the first day of employment.
+ Potential for career growth on an expanding team and organization.
+ 152 hours of paid time off annually plus 8 paid holidays.
+ Community engagement and green initiatives.
+ Engaging D&I Employee Resource Groups.
+ Tuition reimbursement program.
+ Generous 401K match.
**Catalent offers rewarding opportunities to further your career!** Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.
personal initiative. dynamic pace. meaningful work.
Visit Catalent Careers ( to explore career opportunities.
Catalent is an Equal Opportunity Employer, including disability and veterans.
If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to . This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.
Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.
Important Security Notice to U.S. Job Seekers:
Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond- it is a fraudulent request. Please forward such requests to for us to investigate with local authorities.
California Job Seekers can find our California Job Applicant Notice HERE ( .

Our client, a rapidly growing biopharmaceutical company, is seeking a highly skilled Senior Pharmaceutical Development Scientist to join their innovative research and development team in Seattle, Washington . This role is crucial for advancing the formulation and manufacturing processes of novel drug candidates. You will lead the development of robust, scalable, and regulatory-compliant drug product formulations, overseeing all stages from pre-formulation studies through to technology transfer and clinical batch manufacturing. Responsibilities include designing and conducting formulation experiments, characterizing drug products, developing analytical methods, and collaborating with cross-functional teams, including regulatory affairs, quality assurance, and manufacturing. This position demands a deep understanding of pharmaceutics, drug delivery systems, and CMC (Chemistry, Manufacturing, and Controls) requirements.

Key responsibilities include:

• Leading the formulation development of small molecule and/or biologic drug products.
• Designing and executing pre-formulation studies, solubility enhancement, and stability assessment.
• Developing and optimizing drug product dosage forms (e.g., oral solids, injectables, topical).
• Establishing and validating analytical methods for drug product characterization and quality control.
• Managing technology transfer of formulations to manufacturing sites for clinical and commercial production.
• Writing and reviewing regulatory submission documents (e.g., IND, NDA, ANDA).
• Collaborating with CMC regulatory affairs to ensure compliance with FDA and other health authority guidelines.
• Troubleshooting formulation and manufacturing issues, providing scientific expertise.
• Mentoring junior scientists and contributing to the strategic direction of the R&D department.
• Staying current with advancements in pharmaceutical sciences and drug delivery technologies.

The ideal candidate will possess a Ph.D. or Master's degree in Pharmaceutical Sciences, Pharmaceutics, Chemistry, Chemical Engineering, or a related field. A minimum of 7 years of experience in pharmaceutical product development, with a focus on formulation and process development, is required. Proven experience with CMC aspects of drug development and regulatory submissions is essential. Hands-on experience with various analytical techniques (e.g., HPLC, GC, dissolution, particle size analysis) is crucial. Familiarity with Good Manufacturing Practices (GMP) and drug development lifecycle is a must. Excellent leadership, project management, scientific writing, and communication skills are necessary. This is an outstanding opportunity to contribute to the development of life-changing medicines and advance your career within a dynamic and innovative company.

Our client, a pioneering pharmaceutical company, is seeking a highly accomplished Senior Pharmaceutical Development Scientist to join their fully remote research and development team. This critical role will be instrumental in advancing the company's pipeline of innovative therapeutics from early-stage development through to clinical trials. The ideal candidate will possess a Ph.D. in Pharmaceutical Sciences, Chemistry, or a related field, coupled with extensive experience in drug formulation, product development, and analytical characterization. You will lead complex development projects, collaborate with interdisciplinary teams, and contribute to the scientific and strategic direction of new drug products. This position offers a unique opportunity to work remotely and make a significant impact on patient health.

Key Responsibilities:

• Lead the formulation development of novel drug candidates, including small molecules, biologics, or other therapeutic modalities.
• Design and execute experiments to characterize drug substances and drug products, including stability studies, dissolution testing, and impurity profiling.
• Develop and validate analytical methods for raw materials, in-process controls, and finished products.
• Prepare comprehensive technical reports, regulatory submission documents (e.g., IND, NDA), and patent applications.
• Collaborate closely with preclinical, clinical, manufacturing, and regulatory affairs teams to ensure seamless project progression.
• Troubleshoot formulation and process-related issues, identifying and implementing effective solutions.
• Stay current with advancements in pharmaceutical sciences, regulatory guidelines, and industry best practices.
• Mentor and guide junior scientists and technicians, fostering a culture of scientific excellence and collaboration.
• Manage project timelines and resources effectively to meet development milestones.

Qualifications:

• Ph.D. in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or a related discipline.
• Minimum of 7 years of relevant experience in pharmaceutical R&D, with a focus on drug product development.
• Demonstrated expertise in formulation design, process development, and scale-up of various dosage forms.
• Proficiency in analytical techniques such as HPLC, GC, MS, KF, and DSC.
• Strong understanding of GMP regulations and ICH guidelines.
• Excellent problem-solving, critical thinking, and decision-making skills.
• Exceptional written and verbal communication skills, with the ability to effectively present scientific data and strategies.
• Proven ability to manage multiple projects simultaneously and work effectively in a remote, collaborative environment.
• Experience with biologics formulation and analytical characterization is a plus.

This fully remote role offers a highly competitive salary, comprehensive benefits, and the chance to contribute to life-changing pharmaceutical innovations from the comfort of your home.

Our client, a rapidly expanding biopharmaceutical company in Provo, Utah, US , is seeking a highly motivated and experienced Principal Pharmaceutical Development Scientist to lead critical drug development programs. This senior role will be instrumental in advancing novel therapeutic candidates from preclinical stages through to clinical trials and potential market approval. The ideal candidate will possess extensive knowledge of pharmaceutical formulation, drug delivery systems, and solid-state chemistry, coupled with a proven track record in IND and NDA preparation. Responsibilities will encompass leading formulation development, designing and executing stability studies, characterizing drug products using advanced analytical techniques (e.g., HPLC, GC, DSC, XRD), and overseeing the technology transfer of processes to manufacturing sites. You will also be responsible for guiding junior scientists, managing external research collaborations, and ensuring adherence to regulatory guidelines (FDA, EMA). This position demands a proactive approach to problem-solving, strong scientific rigor, and exceptional leadership capabilities. A Ph.D. in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or a related field, with a minimum of 8 years of experience in pharmaceutical R&D, is required. Expertise in parenteral formulations, lyophilization, and small molecule drug development is highly desirable. The ability to critically evaluate scientific data, develop creative solutions to complex challenges, and communicate effectively with internal teams and regulatory agencies is paramount. This role presents an exceptional opportunity to make a significant impact on patient lives by contributing to the development of life-changing medicines, offering a competitive compensation package, equity options, and a full suite of benefits.

Our client, a rapidly growing biopharmaceutical company, is seeking a strategic Director of Pharmaceutical Development to lead their drug development pipeline in Denver, Colorado, US . This critical role will oversee all aspects of formulation development, process optimization, and analytical method development for both small molecule and biologic therapeutics. You will be responsible for managing a team of scientists and technicians, ensuring the successful transition of drug candidates from pre-clinical to clinical stages. Key responsibilities include designing and executing development plans, authoring CMC sections for regulatory submissions (IND, NDA), and managing external contract manufacturing organizations (CMOs). You will also ensure compliance with Good Manufacturing Practices (GMP) and all relevant regulatory guidelines. The ideal candidate will possess a Ph.D. in Pharmaceutical Sciences, Chemistry, Chemical Engineering, or a related discipline, with a minimum of 10 years of experience in pharmaceutical R&D, including at least 5 years in a leadership position. Extensive experience in solid-state chemistry, formulation science, analytical development, and regulatory affairs is required. Proficiency with various drug delivery technologies and dosage forms is essential. Strong project management, communication, and team leadership skills are crucial. This is an exciting opportunity to make a significant impact on bringing life-changing medicines to patients and advance your career in the vibrant biotech ecosystem of Denver.

Our client, a rapidly growing pharmaceutical company, is seeking an experienced and strategic Director of Pharmaceutical Development to lead their drug development efforts in **Omaha, Nebraska, US**. This senior leadership role is responsible for overseeing all aspects of preclinical and clinical development, from concept to regulatory submission. The ideal candidate will possess a Ph.D. in a relevant scientific field (e.g., pharmacology, pharmaceutical sciences, biochemistry) and a minimum of ten years of progressive experience in pharmaceutical R&D, with a strong track record of successfully managing drug development programs. Demonstrated experience in regulatory affairs, CMC (Chemistry, Manufacturing, and Controls), and IND (Investigational New Drug) filings is essential. Responsibilities include developing and executing comprehensive development strategies, managing project teams, overseeing budget and resource allocation, ensuring adherence to regulatory guidelines (e.g., FDA, EMA), identifying and mitigating development risks, and collaborating with internal and external stakeholders, including CROs and regulatory agencies. You will also be instrumental in building and mentoring a high-performing development team. This is a critical leadership opportunity to shape the future of our client's therapeutic pipeline. Our client offers a competitive compensation package, extensive benefits, and a stimulating work environment in **Omaha, Nebraska, US**, with opportunities for significant professional impact and growth. We are looking for a visionary leader with exceptional scientific acumen, strategic thinking, and strong project management skills. The ability to navigate the complexities of pharmaceutical development and lead teams effectively is paramount. Join us in **Omaha, Nebraska, US** and drive the advancement of life-changing medicines.