Under direct supervision, is responsible for development and execution of analytical test methods that facilitate drug product development / manufacturing and regulatory submissions for clinical ...
Under direct supervision, is responsible for development and execution of analytical test methods that facilitate drug product development / manufacturing and regulatory submissions for clinical ...
Under direct supervision, is responsible for development and execution of analytical test methods that facilitate drug product development / manufacturing and regulatory submissions for clinical ...
Under direct supervision, is responsible for development and execution of analytical test methods that facilitate drug product development / manufacturing and regulatory submissions for clinical ...
Senior Scientist Analytical Development & Quality Control
Newark, CA · On-site
$140K - $160K/yr
Senior Scientist Analytical Development & Quality Control Protagonist Therapeutics is seeking a ... This position reports to the Senior Director of ADQC. Responsibilities * Develop, optimize, and ...
Senior Scientist Analytical Development & Quality Control
Newark, CA · On-site
$140K - $160K/yr
Senior Scientist Analytical Development & Quality Control Protagonist Therapeutics is seeking a ... This position reports to the Senior Director of ADQC. Responsibilities * Develop, optimize, and ...
Senior Scientist Analytical Development & Quality Control
Newark, CA · On-site
$140K - $160K/yr
Senior Scientist Analytical Development amp; Quality Control Protagonist Therapeutics is seeking a ... This position reports to the Senior Director of ADQC. Responsibilities * Develop, optimize, and ...
Senior Scientist Analytical Development & Quality Control
Newark, CA · On-site
$140K - $160K/yr
Senior Scientist Analytical Development amp; Quality Control Protagonist Therapeutics is seeking a ... This position reports to the Senior Director of ADQC. Responsibilities * Develop, optimize, and ...
Senior Scientist, Analytical Development, Manager About Site Catalent's San Diego, CA site is an ... This position offers the chance to make a direct impact on patient outcomes by improving the ...
Senior Scientist, Analytical Development, Manager About Site Catalent's San Diego, CA site is an ... This position offers the chance to make a direct impact on patient outcomes by improving the ...
Associate Director, Technical Operations (Analytical Development-Biologics)
San Diego, CA · On-site
$150 - $195/hr
... analytical development of biologics, preferably in late-stage drug development. * Direct knowledge of HPLC, CE-SDS, cIEF, potency bioassays, peptide map, ELISA, LC-MS and other relevant analytical ...
Associate Director, Technical Operations (Analytical Development-Biologics)
San Diego, CA · On-site
$150 - $195/hr
... analytical development of biologics, preferably in late-stage drug development. * Direct knowledge of HPLC, CE-SDS, cIEF, potency bioassays, peptide map, ELISA, LC-MS and other relevant analytical ...
... analytical development of biologics, preferably in late-stage drug development. * Direct knowledge of HPLC, CE-SDS, cIEF, potency bioassays, peptide map, ELISA, LC-MS and other relevant analytical ...
... analytical development of biologics, preferably in late-stage drug development. * Direct knowledge of HPLC, CE-SDS, cIEF, potency bioassays, peptide map, ELISA, LC-MS and other relevant analytical ...
Senior Scientist, Analytical Development, Manager
San Diego, CA · On-site
$97K - $132K/yr
Senior Scientist, Analytical Development, Manager About Site Catalent's San Diego, CA site is an ... This position offers the chance to make a direct impact on patient outcomes by improving the ...
Senior Scientist, Analytical Development, Manager
San Diego, CA · On-site
$97K - $132K/yr
Senior Scientist, Analytical Development, Manager About Site Catalent's San Diego, CA site is an ... This position offers the chance to make a direct impact on patient outcomes by improving the ...
Associate Director, Technical Operations (Analytical Development-Biologics)
San Diego, CA · On-site +1
... analytical development of biologics, preferably in late-stage drug development. * Direct knowledge of HPLC, CE-SDS, cIEF, potency bioassays, peptide map, ELISA, LC-MS and other relevant analytical ...
Associate Director, Technical Operations (Analytical Development-Biologics)
San Diego, CA · On-site +1
... analytical development of biologics, preferably in late-stage drug development. * Direct knowledge of HPLC, CE-SDS, cIEF, potency bioassays, peptide map, ELISA, LC-MS and other relevant analytical ...
As a Principal Scientist, Potency, you will report to the Sr. Director, Head of Molecular and ... Follow ICH and internal Method Development Guidance Document to develop robust analytical methods ...
As a Principal Scientist, Potency, you will report to the Sr. Director, Head of Molecular and ... Follow ICH and internal Method Development Guidance Document to develop robust analytical methods ...
Summary: Vaxcyte is seeking an accomplished Director, Immunoassay Development to join the CMC ... Strengthen immunoassay analytical control strategies, including critical reagent strategy ...
Summary: Vaxcyte is seeking an accomplished Director, Immunoassay Development to join the CMC ... Strengthen immunoassay analytical control strategies, including critical reagent strategy ...
As a Principal Scientist, Potency, you will report to the Sr. Director, Head of Molecular and ... Follow ICH and internal Method Development Guidance Document to develop robust analytical methods ...
As a Principal Scientist, Potency, you will report to the Sr. Director, Head of Molecular and ... Follow ICH and internal Method Development Guidance Document to develop robust analytical methods ...
Director, Pharmaceutical Development
Brisbane, CA · On-site
$218 - $260/hr
Director, Pharmaceutical Development Nurix Therapeutics is a clinical stage biopharmaceutical ... analysis and implement corrective actions. Late‑Stage Development & Regulatory * Drive ...
New
Director, Pharmaceutical Development
Brisbane, CA · On-site
$218 - $260/hr
Director, Pharmaceutical Development Nurix Therapeutics is a clinical stage biopharmaceutical ... analysis and implement corrective actions. Late‑Stage Development & Regulatory * Drive ...
New
Vaxcyte is seeking an accomplished Associate Director, Immunoassay Development to join the CMC ... Perform and oversee routine analytical testing within the CMC Immunoassay group, including ...
Vaxcyte is seeking an accomplished Associate Director, Immunoassay Development to join the CMC ... Perform and oversee routine analytical testing within the CMC Immunoassay group, including ...
Senior Scientist 1, Analytical Development
San Diego, CA · On-site
$97K - $132K/yr
Significant and direct work experience with analytical instruments and techniques such as HPLC/UPLC ... Well-developed organizational skills and the ability to thrive under pressure. * Intermediate to ...
Senior Scientist 1, Analytical Development
San Diego, CA · On-site
$97K - $132K/yr
Significant and direct work experience with analytical instruments and techniques such as HPLC/UPLC ... Well-developed organizational skills and the ability to thrive under pressure. * Intermediate to ...
Position Summary The Director/Senior Director, Analytical Methods will serve as a domain expert and ... adaptation, or development of novel approaches. * Develop and deploy cutting-edge analytical ...
Position Summary The Director/Senior Director, Analytical Methods will serve as a domain expert and ... adaptation, or development of novel approaches. * Develop and deploy cutting-edge analytical ...
The Senior Director, CMC Lead is a unique opportunity to transform CMC product development into ... Representing CMC (DS, DP, Analytical) in applicable governance forums serving as spokesperson and ...
The Senior Director, CMC Lead is a unique opportunity to transform CMC product development into ... Representing CMC (DS, DP, Analytical) in applicable governance forums serving as spokesperson and ...
Position Summary The Director/Senior Director, Analytical Methods will serve as a domain expert and ... adaptation, or development of novel approaches. * Develop and deploy cutting-edge analytical ...
Position Summary The Director/Senior Director, Analytical Methods will serve as a domain expert and ... adaptation, or development of novel approaches. * Develop and deploy cutting-edge analytical ...
Position Summary The Director/Senior Director, Analytical Methods will serve as a domain expert and ... adaptation, or development of novel approaches. * Develop and deploy cutting-edge analytical ...
Position Summary The Director/Senior Director, Analytical Methods will serve as a domain expert and ... adaptation, or development of novel approaches. * Develop and deploy cutting-edge analytical ...
The Senior Director, CMC Lead is a unique opportunity to transform CMC product development into ... Representing CMC (DS, DP, Analytical) in applicable governance forums serving as spokesperson and ...
The Senior Director, CMC Lead is a unique opportunity to transform CMC product development into ... Representing CMC (DS, DP, Analytical) in applicable governance forums serving as spokesperson and ...
Director Analytical Development information
See California salary details
$100.2K is the 25th percentile. Wages below this are outliers.
$87.8K - $105.6K
36% of jobs
$105.6K - $123.5K
0% of jobs
$123.5K - $141.3K
0% of jobs
$141.3K - $159.1K
0% of jobs
$159.1K - $176.9K
0% of jobs
$176.9K - $194.7K
4% of jobs
$194.7K - $212.5K
8% of jobs
The median wage is $214.2K / yr.
$212.5K - $230.3K
16% of jobs
$241.2K is the 75th percentile. Wages above this are outliers.
$230.3K - $248.1K
16% of jobs
$248.1K - $265.9K
11% of jobs
$265.9K - $283.7K
7% of jobs
$87.8K
$188.9K
$283.7K
How much do director analytical development jobs pay per year?
What are the typical daily responsibilities of a director analytical development?
A Director Analytical Development typically oversees the design, implementation, and optimization of analytical methods to support product development and quality control. This involves leading a team of scientists, ensuring projects meet regulatory requirements, troubleshooting technical challenges, and collaborating closely with cross-functional groups such as R&D, quality assurance, and manufacturing. Daily tasks often include reviewing analytical data and reports, planning project timelines, and making strategic decisions to align with organizational objectives. The role requires balancing hands-on scientific guidance with high-level management to drive innovation and efficiency within the analytical function.
What is a director analytical development?
A Director of Analytical Development oversees the strategy, development, and implementation of analytical methods to support product development and manufacturing. They lead a team of scientists, ensure regulatory compliance, and collaborate with cross-functional teams to optimize processes. Their role includes troubleshooting analytical issues, validating methods, and contributing to regulatory submissions. This position is critical in maintaining product quality and ensuring data-driven decision-making in pharmaceutical, biotechnology, or related industries.
What are the key skills and qualifications needed to thrive in the director analytical development position, and why are they important?
To thrive as a Director Analytical Development, you generally need an advanced degree in chemistry, biochemistry, or a related scientific field, along with substantial experience in analytical method development and validation, and team leadership. Familiarity with laboratory information management systems (LIMS), chromatographic and spectroscopic instrumentation, and regulatory guidelines such as ICH, FDA, and GMP is crucial. Excellent project management, strategic thinking, and interpersonal communication are standout soft skills for this position. These competencies enable effective oversight of complex analytical projects, ensure regulatory compliance, and foster team collaboration in a fast-paced R&D environment.
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Full-time
Medical, Dental, Vision, Retirement, PTO
Posted 6 days ago
Job description
Neurocrine Biosciences is a leading biopharmaceutical company with a simple purpose: to relieve suffering for people with great needs. We are dedicated to discovering, developing and commercializing life-changing treatments for patients with under-addressed neurological, psychiatric, endocrine and immunological disorders. The company's diverse portfolio includes FDA-approved treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic congenital adrenal hyperplasia, hyperphagia in Prader-Willi syndrome, endometriosis* and uterine fibroids*, as well as a robust pipeline including multiple compounds in mid- to late-phase clinical development across our core therapeutic areas. For more than three decades, we have applied our unique insight into neuroscience and the interconnections between brain and body systems to treat complex conditions. We relentlessly pursue medicines to ease the burden of debilitating diseases and disorders, because you deserve brave science. For more information, visit neurocrine.com, and follow the company on LinkedIn, X, Facebook and YouTube. (*in collaboration with AbbVie)
About the Role:
Under direct supervision, is responsible for development and execution of analytical test methods that facilitate drug product development / manufacturing and regulatory submissions for clinical study introduction through phase III trials. Activities includes test method development, qualification/validation, transfer and execution. Supports late stage troubleshooting and development of products, processes, and methods in support of product commercialization.
Your Contributions (include, but are not limited to):
- With direct supervision, develops and executes chemical and instrumental methods (e.g. HPLC, GC, TGA, DSC, MS, FTIR, Water Content) of analyses of drug product development compounds
- Accurately follows established test methods, procedures, and pharmacopeia chapters (e.g. Dissolution, Content Uniformity) to generate data essential for strategic decision making
- With direct supervision, plans and executes forced degradation, informal stability, and excipient compatibility studies
- With direct supervision and as appropriate, assists/leads the development of analytical methods, investigations for out of specification, out of trend, and/or anomalous results
- With direct supervision, collaboratively plans and executes cross functional studies for formulation development
- Recognizes and responds to unexpected or anomalous observations in all activities
- Maintains complete and accurate records of laboratory work in conformance with company SOPs and training
- Provides detailed reviews of peer generated data as well as that generated from contracted service providers
- Other duties as assigned
Requirements:
- BS/BA degree in chemistry or closely related field and some relevant industry experience preferred; Experience with Empower a plus
- Working knowledge of data systems for computer-controlled instrumentation
- Familiarity with performing analytical testing of solid oral drug products; Hands-on knowledge preferred
- Knowledge of conducting HPLC analysis and troubleshooting. Working knowledge of performing stability indicating method development a plus
- Familiarity with performing dissolution analysis and troubleshooting. Hands-on knowledge performing dissolution method development a plus
- Understanding of analytical data evaluation and ability to draw meaningful conclusions
- Ability to present analytical data clearly and demonstrate knowledge of the testing and the product
- Knowledge of cGMP expectations for laboratory records and quality systems
- Knowledge of ICH guidance and common testing per USP chapters
- Knowledge of statistical analysis a plus
- Ability to provide ideas for process improvements
- Able to execute experiments efficiently and suggest small process improvements
- Able to recognize patterns or inconsistencies in data results
- Able to deduce meaningful results while conducting routine analyses or troubleshoot minor issues. Good knowledge of one scientific discipline
- Developing knowledge of scientific principles, methods and techniques
- Good knowledge and some experience working with discipline specific laboratory equipment/tools
- Ability to work as part of a team
- Good computer skills
- Developing communications, problem-solving, analytical thinking, planning and organization skills
- Detail oriented
- Understands importance of meeting deadlines
- Proficient using MS-Excel, MS-Word
- Ability to work with a team of individuals to meet goals
- Ability to accomplish tasks in a timeline driven setting
#LI-LS1
Neurocrine Biosciences is an EEO/Disability/Vets employer.
We are committed to building a workplace of belonging, respect, and empowerment, and we recognize there are a variety of ways to meet our requirements. We are looking for the best candidate for the job and encourage you to apply even if your experience or qualifications don't line up to exactly what we have outlined in the job description.
The hourly rate we reasonably expect to pay is $35.35-$47.34. Individual pay decisions depend on various factors, such as primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience and skills. In addition, this position offers an annual bonus with a target of 15% of the earned base salary and eligibility to participate in our equity based long term incentive program. Benefits offered include a retirement savings plan (with company match), paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage in accordance with the terms and conditions of the applicable plans.
About Neurocrine Biosciences
Sourced by ZipRecruiter
Industry
Biotechnology research and development
Company size
1,001 - 5,000 Employees
Headquarters location
San Diego, CA, US
Year founded
1992