If you are a current Jazz employee please apply via the Internal Career site Jazz Pharmaceuticals ... The Associate Director of Drug Product Development is responsible for providing scientific and ...
If you are a current Jazz employee please apply via the Internal Career site Jazz Pharmaceuticals ... The Associate Director of Drug Product Development is responsible for providing scientific and ...
Staff Scientist, Pharmaceutical Development
South San Francisco, CA · On-site
$160K - $180K/yr
This position reports to the Director of Pharmaceutical Development is an onsite position requiring in-person collaboration with cross-functional teams. Responsibilities * Develop early formulation ...
Staff Scientist, Pharmaceutical Development
South San Francisco, CA · On-site
$160K - $180K/yr
This position reports to the Director of Pharmaceutical Development is an onsite position requiring in-person collaboration with cross-functional teams. Responsibilities * Develop early formulation ...
This position reports to the Director of Pharmaceutical Development is an onsite position requiring in-person collaboration with cross-functional teams. Responsibilities * Develop early formulation ...
This position reports to the Director of Pharmaceutical Development is an onsite position requiring in-person collaboration with cross-functional teams. Responsibilities * Develop early formulation ...
Pharmaceutical Development Principal Scientist I Position Summary * Work Schedule: Monday to Friday 8am-5pm * 100% based on-site in Kansas City Catalent's Kansas City (KCM) facility is a premier site ...
Pharmaceutical Development Principal Scientist I Position Summary * Work Schedule: Monday to Friday 8am-5pm * 100% based on-site in Kansas City Catalent's Kansas City (KCM) facility is a premier site ...
Serve as a senior technical leader within Pharmaceutical Development, representing CMC project teams across the product lifecycle from early discovery through commercialization and lifecycle ...
Serve as a senior technical leader within Pharmaceutical Development, representing CMC project teams across the product lifecycle from early discovery through commercialization and lifecycle ...
Pharmaceutical Development Principal Scientist I Position Summary * Work Schedule: Monday to Friday 8am-5pm * 100% based on-site in Kansas City Catalent's Kansas City (KCM) facility is a premier site ...
Pharmaceutical Development Principal Scientist I Position Summary * Work Schedule: Monday to Friday 8am-5pm * 100% based on-site in Kansas City Catalent's Kansas City (KCM) facility is a premier site ...
Serve as a senior technical leader within Pharmaceutical Development, representing CMC project teams across the product lifecycle from early discovery through commercialization and lifecycle ...
Serve as a senior technical leader within Pharmaceutical Development, representing CMC project teams across the product lifecycle from early discovery through commercialization and lifecycle ...
New Business Development Manager
Dallas, TX · On-site
The right candidate must have expertise in pharmaceutical development, analytical chemistry, microbiology testing, and regulatory compliance consulting , and a proven ability to partner with clients ...
New Business Development Manager
Dallas, TX · On-site
The right candidate must have expertise in pharmaceutical development, analytical chemistry, microbiology testing, and regulatory compliance consulting , and a proven ability to partner with clients ...
This position reports to the Director of Pharmaceutical Development is an onsite position requiring in-person collaboration with cross-functional teams. Responsibilities * Develop early formulation ...
Quick apply
This position reports to the Director of Pharmaceutical Development is an onsite position requiring in-person collaboration with cross-functional teams. Responsibilities * Develop early formulation ...
The right candidate must have expertise in pharmaceutical development, analytical chemistry, microbiology testing, and regulatory compliance consulting , and a proven ability to partner with clients ...
The right candidate must have expertise in pharmaceutical development, analytical chemistry, microbiology testing, and regulatory compliance consulting , and a proven ability to partner with clients ...
New Business Development Manager
Dallas, TX · On-site
The right candidate must have expertise in pharmaceutical development, analytical chemistry, microbiology testing, and regulatory compliance consulting , and a proven ability to partner with clients ...
Quick apply
New Business Development Manager
Dallas, TX · On-site
The right candidate must have expertise in pharmaceutical development, analytical chemistry, microbiology testing, and regulatory compliance consulting , and a proven ability to partner with clients ...
Ionis Pharmaceuticals seeks an experienced pharmaceutical development scientist to support laboratory experiments, review development data, and author and standardize technical reports for injectable ...
Ionis Pharmaceuticals seeks an experienced pharmaceutical development scientist to support laboratory experiments, review development data, and author and standardize technical reports for injectable ...
Ionis Pharmaceuticals seeks an experienced pharmaceutical development scientist to support laboratory experiments, review development data, and author and standardize technical reports for injectable ...
Ionis Pharmaceuticals seeks an experienced pharmaceutical development scientist to support laboratory experiments, review development data, and author and standardize technical reports for injectable ...
Development Scientist II
Greenville, NC · On-site
Development Scientist II The Development Scientist II serves as a primary point of contact with the client regarding pharmaceutical development and clinical manufacturing project related activities.
Development Scientist II
Greenville, NC · On-site
Development Scientist II The Development Scientist II serves as a primary point of contact with the client regarding pharmaceutical development and clinical manufacturing project related activities.
Development Scientist II
Greenville, NC · On-site
Development Scientist II The Development Scientist II serves as a primary point of contact with the client regarding pharmaceutical development and clinical manufacturing project related activities.
Development Scientist II
Greenville, NC · On-site
Development Scientist II The Development Scientist II serves as a primary point of contact with the client regarding pharmaceutical development and clinical manufacturing project related activities.
Business Development Manager
Santa Fe Springs, CA · On-site
$120K - $160K/yr
Build and maintain strong relationships with key decision-makers across pharmaceutical, biotech ... Analytical chemistry testing, Method development and validation, Regulatory and compliance testing ...
Business Development Manager
Santa Fe Springs, CA · On-site
$120K - $160K/yr
Build and maintain strong relationships with key decision-makers across pharmaceutical, biotech ... Analytical chemistry testing, Method development and validation, Regulatory and compliance testing ...
Ionis Pharmaceuticals seeks an experienced pharmaceutical development scientist to support laboratory experiments, review development data, and author and standardize technical reports for injectable ...
Ionis Pharmaceuticals seeks an experienced pharmaceutical development scientist to support laboratory experiments, review development data, and author and standardize technical reports for injectable ...
Process Development Scientist St. Louis
Saint Louis, MO · On-site
$89K - $134K/yr
Involve in selection/sizing, process optimization, and tech transfer for purification of new pharmaceuticals, focused on Phase I-III development * Provide customer consultations via email, telephone ...
Process Development Scientist St. Louis
Saint Louis, MO · On-site
$89K - $134K/yr
Involve in selection/sizing, process optimization, and tech transfer for purification of new pharmaceuticals, focused on Phase I-III development * Provide customer consultations via email, telephone ...
Process Development Scientist St. Louis
$89K - $134K/yr
Involve in selection/sizing, process optimization, and tech transfer for purification of new pharmaceuticals, focused on Phase I-III development * Provide customer consultations via email, telephone ...
Process Development Scientist St. Louis
$89K - $134K/yr
Involve in selection/sizing, process optimization, and tech transfer for purification of new pharmaceuticals, focused on Phase I-III development * Provide customer consultations via email, telephone ...
Senior Counsel, Pharmaceutical Development and Manufacturing
Redwood City, CA · Hybrid
$170K - $232K/yr
... development and commercialization. The ideal candidate has deep experience in biotech or pharmaceutical contracting, a strong understanding of GMP and regulatory considerations, and the ability to ...
Senior Counsel, Pharmaceutical Development and Manufacturing
Redwood City, CA · Hybrid
$170K - $232K/yr
... development and commercialization. The ideal candidate has deep experience in biotech or pharmaceutical contracting, a strong understanding of GMP and regulatory considerations, and the ability to ...
Pharmaceutical Development information
See salary details
$23.5K - $33.3K
11% of jobs
$37.5K is the 25th percentile. Wages below this are outliers.
$33.3K - $43K
33% of jobs
$43K - $52.8K
4% of jobs
The median wage is $56.1K / yr.
$52.8K - $62.6K
6% of jobs
$62.6K - $72.4K
15% of jobs
$79.1K is the 75th percentile. Wages above this are outliers.
$72.4K - $82.1K
9% of jobs
$82.1K - $91.9K
4% of jobs
$91.9K - $101.7K
3% of jobs
$101.7K - $111.5K
5% of jobs
$111.5K - $121.2K
4% of jobs
$121.2K - $131K
5% of jobs
$23.5K
$68.4K
$131K
How much do pharmaceutical development jobs pay per year?
What is a Pharmaceutical Development job?
A Pharmaceutical Development job involves researching, formulating, and optimizing new drug products to ensure safety, efficacy, and regulatory compliance. Professionals in this role work on drug formulation, process development, and scale-up for manufacturing. They collaborate with scientists, regulatory teams, and production staff to bring medications from the lab to market. This field requires strong knowledge of chemistry, biology, and regulatory requirements.
What are the key skills and qualifications needed to thrive in the Pharmaceutical Development position, and why are they important?
To thrive in Pharmaceutical Development, you need a strong background in pharmaceutical sciences, chemistry, or related fields, often supported by an advanced degree (MS or PhD) and experience in drug formulation and testing. Proficiency in analytical instrumentation (e.g., HPLC, GC), regulatory compliance systems, and Good Laboratory Practice (GLP) certifications are highly valued. Strong project management, problem-solving abilities, and effective communication skills set top performers apart. These competencies ensure the development of safe, effective pharmaceuticals while navigating complex regulatory requirements and cross-functional team dynamics.
How much do pharmaceutical developers make?
What is the highest paying job in pharmaceuticals?
What does a pharmaceutical developer do?
What is pharmaceutical development?
What are some typical daily responsibilities for professionals in Pharmaceutical Development?
Professionals in Pharmaceutical Development typically oversee the formulation and optimization of new drug products, conduct lab-based experiments, and analyze test data to ensure product efficacy and safety. They frequently collaborate with cross-functional teams such as quality assurance, regulatory affairs, and manufacturing to advance each stage of product development. Regular responsibilities also include drafting technical reports, maintaining detailed laboratory documentation, and supporting regulatory submissions. The role often requires balancing hands-on lab work with strategic planning, ensuring that all processes comply with industry standards and regulations.
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Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 13 days ago
Job description
Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases - often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit www.jazzpharmaceuticals.com for more information.
Job Description
The Associate Director of Drug Product Development is responsible for providing scientific and technical leadership for Jazz Pharmaceuticals' Pharmaceutical Development programs at various stages of the development life-cycle including preformulation, formulation and process development, technical transfer and validation. The Associate Director of Drug Product Development will oversee drug product aspects of development and manufacturing projects from pre-formulation and product feasibility through to clinical trial supply and technology transfer/commercialization. In addition, the Associate Director of Drug Product Development may provide leadership of cross-functional CMC development teams. The Associate Director of Drug Product Development will have broad experience in pharmaceutical product development, demonstrated problem solving ability, module 3 authorship, development of robust manufacturing processes through designed experiments and data analysis, and excellent project management, teamwork and leadership skills.
Essential Functions
- Leads the development of small molecule drug product formulations, appropriate to the phase of pharmaceutical development, with sufficient stability and robustness for clinical and/or commercial manufacturing.
- Responsible for specifying product and process requirements, including manufacturing equipment and methods, performance criteria, materials, test protocols, required analytical methodology, packaging (clinical and commercial); and in developing robust processes for pharmaceutical production.
- Directs projects and leads cross-functional teams (as required) with technical proficiency, scientific creativity, collaboration with others to achieve project goals on time and within budget.
- Create intellectual property covering Jazz Pharmaceuticals products and ensure freedom to operate in the development of new drug products
- Support the identification and selection of suitable drug product development and commercial manufacturing vendors (CMOs).
- Direct technical projects (internally and at CDMOs) including developing detailed technical work plans and managing performance of vendors.
- Work cooperatively with, or lead, internal and external teams as required.
- Author CMC sections of regulatory dossiers for products at all stages to enable acceptance by global regulators.
- Supports asset due diligence and new product introduction and integrations
- Apply current knowledge of cGMP and industry standards for process design and validation to manage vendors and contract development organizations.
Required Knowledge, Skills, and Abilities
- >10 years' experience in drug product development in the pharmaceutical industry required. Direct experience with formulation development, process development, technical transfer and/or process validation.
- Demonstrated technical proficiency, engineering, collaboration with others, and independent thought. Strong teamwork skills.
- Demonstrated troubleshooting and problem-solving skills including the use of designed experiments, statistical process control,
- Development/authorship of CMC regulatory filings for pharmaceutical products.
- Broad exposure to multiple drug delivery technologies and knowledge of standard dosage forms preferred.
- Excellent written and verbal communication skills
- Current knowledge of quality systems and FDA and EU regulations as they relate to pharmaceutical development and validation.
- Experience in intellectual property development desirable.
- Proven project management skills for technical programs.
- Flexibility to travel on company business when required
Required/Preferred Education and Licenses
- Advanced degree in Chemistry, Pharm. Sci., Engineering, or related field, or equivalent combination of education and work-related experience required.
Description of Physical Demands
- Occasional mobility within office environment. Routinely sitting for extended periods of time.
- Constantly operating a computer, printer, telephone and other similar office machinery.
Jazz Pharmaceuticals is an equal opportunity/affirmative action 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 characteristic protected by law.
FOR US BASED CANDIDATES ONLY
Jazz Pharmaceuticals, Inc. is committed to fair and equitable compensation practices and we strive to provide employees with total compensation packages that are market competitive. For this role, the full and complete base pay range is:
$157,600.00 - $236,400.00
Individual compensation paid within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, and other pertinent factors. The goal is to ensure fair and competitive compensation aligned with the candidate's expertise and contributions, within the established pay framework and our Total Compensation philosophy. Internal equity considerations will also influence individual base pay decisions. This range will be reviewed on a regular basis.
At Jazz, your base pay is only one part of your total compensation package. The successful candidate may also be eligible for a discretionary annual cash bonus or incentive compensation (depending on the role), in accordance with the terms of the Company's Global Cash Bonus Plan or Incentive Compensation Plan, as well as discretionary equity grants in accordance with Jazz's Long Term Equity Incentive Plan.
The successful candidate will also be eligible to participate in various benefits offerings, including, but not limited to, medical, dental and vision insurance, 401k retirement savings plan, and flexible paid vacation. For more information on our Benefits offerings please click here: https://careers.jazzpharma.com/benefits.html