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Per Diem Analytical Method Development Jobs in California

Abbott

Method Development Scientist

Santa Rosa, CA

$90K - $180K/yr

Career development with an international company where you can grow the career you dream of ... Troubleshoot existing analytical methods * Author, review, and verify validation protocols and ...

Abbott

Method Development Scientist

Santa Rosa, CA · On-site

$90K - $180K/yr

Career development with an international company where you can grow the career you dream of ... Troubleshoot existing analytical methods * Author, review, and verify validation protocols and ...

Abbott

Method Development Scientist

Santa Rosa, CA

$90K - $180K/yr

Career development with an international company where you can grow the career you dream of ... Troubleshoot existing analytical methods * Author, review, and verify validation protocols and ...

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Per Diem Analytical Method Development information

What is analytical method development?

Analytical method development is the process of creating and optimizing laboratory procedures to accurately measure specific substances in samples. It involves selecting appropriate techniques, such as chromatography or spectroscopy, and validating the method to ensure reliability and compliance with regulatory standards. This skill is essential for roles like Per Diem Analytical Method Development, which focus on ensuring analytical accuracy in pharmaceutical or chemical testing environments.

Are analytical chemists in demand?

Analytical chemists, including those in per diem analytical method development roles, are in demand due to the ongoing need for quality control, regulatory compliance, and method validation in industries like pharmaceuticals and biotechnology. Skills in chromatography, spectroscopy, and regulatory standards such as GMP increase employability, and demand is expected to grow with advancements in analytical technologies.

What is the difference between Per Diem Analytical Method Development vs Per Diem Quality Control Analyst?

AspectPer Diem Analytical Method DevelopmentPer Diem Quality Control Analyst
Primary RoleDevelops and validates analytical methods for testing pharmaceuticalsPerforms routine testing and analysis of pharmaceutical products
Work EnvironmentLaboratory focused on method creation and validationLaboratory conducting routine quality testing
Required CredentialsBachelor's degree in Chemistry or related field; experience in method developmentBachelor's degree in Chemistry or related field; experience in quality testing

Per Diem Analytical Method Development specialists focus on creating and validating new analytical methods, while Per Diem Quality Control Analysts perform routine testing to ensure product quality. Both roles require similar educational backgrounds but differ in their primary responsibilities and work focus.

What are the 4 types of analytical methods?

In analytical method development, the four main types are qualitative methods, which identify the presence of substances; quantitative methods, which measure the amount of substances; separation methods, such as chromatography, used to isolate components; and detection methods, which identify and quantify analytes. A Per Diem Analytical Method Development role often involves selecting and validating these methods to ensure accuracy and compliance with regulatory standards.

What is the highest salary in analytical method development and validation?

In analytical method development and validation roles, salaries can reach up to $120,000 to $150,000 annually for senior-level positions with extensive experience, advanced skills, and relevant certifications. Factors such as industry, location, and company size influence compensation, with specialized knowledge in techniques like HPLC or mass spectrometry often commanding higher pay.
What are the most commonly searched types of Analytical Method Development jobs in California? The most popular types of Analytical Method Development jobs in California are:
What cities in California are hiring for Per Diem Analytical Method Development jobs? Cities in California with the most Per Diem Analytical Method Development job openings:
Per Diem Analytical Method Development jobs near you

Principal Scientist - Analytical Methods Development

Programmable Medicine Operatin

Redwood City, CA • On-site

$165K - $200K/yr

Full-time

Medical, Dental, Vision

Posted 5 days ago

Job description

Programmable Medicine, a clinical stage biopharmaceutical company located in Redwood City, is seeking a motivated Chemist/Sr. Chemist Analytical Method Development. We are focused on developing novel nanomedicines, HD therapeutics (HDTs), to treat unmet medical needs in ophthalmology, neurology, inflammatory diseases, and neuro-oncology. Our HD platform builds therapeutics that are selectively taken up only by inflamed tissues, allowing us to treat diseases with unprecedented precision.
The successful candidate will provide scientific leadership for the development, qualification, stage-appropriate validation of analytical methods supporting complex large molecule therapeutics, including antibody drug conjugates, polymer-based platforms, and other nanomedicine products. The successful candidate will partner closely with Chemistry, Translational, Process Development, Formulation Development, Quality, Regulatory Affairs, Manufacturing, and external contract laboratories to establish robust analytical strategies that support product characterization, process understanding, product test and release, and regulatory submissions.
  • Subject matter expert in analytical methods development that uses scientific knowledge and experience to independently design, plan and execute studies in support of preclinical through Phase 2 programs
  • Performs analytical development and optimizes methods in support of preclinical studies through Phase 2
  • Creates and implements novel ideas and techniques to support analytical activities
  • Leads analytical technology transfersto GLP laboratories in support of GMP production
  • Writes analytical method development reports, SOPs, and analytical sections of regulatory submissions
  • Supervises laboratory personnel including setting priorities, monitoring work, execution of timelines, training to appropriate SOPs, meeting quality standards, and timely completion of documentation

Job Requirements
  • PhD in Analytical Chemistry or related discipline and 10+ years of relevant experience with at least 6 years of experience in the biotechnology/pharmaceutical or related industry
  • Demonstrated experience supporting complex large molecule therapeutics, including at least one of the following: antibody drug conjugates, dendrimers, polymers, biologics, bioconjugates, nanoparticles, or related products.
  • Extensive experience developing analytical methods supporting products from discovery through clinical development
  • Thorough understanding of analytical chemistry and a well-developed understanding of potential in-process impurities generated in production of antibody drug conjugates or polymer-drug conjugates
  • Strong working knowledge of analytical techniques, including: HPLC, SEC, LC-MS/MS, LC-MS, NMR spectroscopy, UV-Vis spectroscopy, , Dynamic Light Scattering (DLS), Zeta potential analysis, Multi-angle light scattering (MALS),.
  • Experience leading analytical method transfers to GMP manufacturing sites and familiarity with CDMO and CRO management
  • Strong knowledge of FDA, ICH, USP, EMA, and global CMC regulatory requirements and experience supporting regulatory submissions, including IND, NDA, and associated agency responses
  • Demonstrated understanding of cross-functional team membership related to drug development
  • Excellent project management skills with proven ability to meet multiple deadlines across a variety of projects/programs, with a high degree of accuracy and efficiency
  • Previous experience supervising and optimizing the performance of a small scientific team
  • Extensive experience in developing analytical methods using fundamental scientific principles including peer reviewed publications as co-author or lead author

About Programmable Medicine
This is a unique opportunity to join a team focused on the development of a new class of precision medicines that selectively treat diseased cells in regions of inflammation. By making precision medicine even more precise, our nanomedicine technology has the potential to change the standard of care across ophthalmology, neurology, inflammatory diseases and neuro-oncology. You will have the opportunity to learn new skills and gain a better understanding of cutting-edge technology.
We have a comprehensive compensation package including fully paid medical, dental and vision benefits for you and your family. We want our employees to become shareholders and offer new hire stock options. The company also offers participation in the annual bonus program. The salary range for MS candidates located in the Bay Area, with a minimum of 8 years of industry experience is $165,000 - $200,000, depending on years of experience and relevant skill sets.

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