ZipRecruiter

Log In

1

Per Diem Analytical Method Development Jobs (NOW HIRING)

Eurofins

Bioassay Method Development

Indianapolis, IN · On-site

... Development and Manufacturing Organisations. It also has a rapidly developing presence in highly ... Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety ...

Actalent

Analytical Chemist

Hercules, CA

$30 - $35/hr

Analytical Chemist (Method Development & Validation) Overview We are seeking a highly skilled Analytical Chemist to support complex drug substance and drug product programs in a regulated laboratory ...

Granules

Scientist I, AR&D

Chantilly, VA · On-site

This includes performing the Assay Dissolution, analytical method development, and method ... Draft test methods, method validation protocols and reports as per the Company SOPs and regulatory ...

next page

Showing results 1-20

People also search for

All JobsPer Diem Analytical Method Development Jobs

Per Diem Analytical Method Development information

See salary details

$89K

$191.4K

$287.5K

How much do per diem analytical method development jobs pay per year?

As of Jun 6, 2026, the average yearly pay for per diem analytical method development in the United States is $191,412.00, according to ZipRecruiter salary data. Most workers in this role earn between $94,000.00 and $249,000.00 per year, depending on experience, location, and employer.

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 cities are hiring for Per Diem Analytical Method Development jobs? Cities with the most Per Diem Analytical Method Development job openings:
What are the most commonly searched types of Analytical Method Development jobs? The most popular types of Analytical Method Development jobs are:
What states have the most Per Diem Analytical Method Development jobs? States with the most job openings for Per Diem Analytical Method Development jobs include:
Per Diem Analytical Method Development jobs near you
Infographic showing various Per Diem Analytical Method Development job openings in the United States as of May 2026, with employment types broken down into 4% As Needed, 84% Full Time, 8% Part Time, and 4% Temporary. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution, with an average salary of $191,412 per year, or $92 per hour.
Analytical Development Scientist II

Analytical Development Scientist II

Kindeva Drug Delivery

Bridgeton, MO • On-site

Full-time

Posted 7 days ago

Job description

Our Work Matters
At Kindeva, we make products that save lives, ensuring better health and well-being for patients around the world.
The Impact You Will Make
As an Analytical Development Scientist II, you will play a critical role in supporting analytical method transfer, verification, and validation activities for both small molecule and biologic products within a Contract Development and Manufacturing Organization (CDMO) environment. This position contributes to the development and implementation of analytical capabilities while supporting quality control testing, technical investigations, process transfers, and validation activities. You will collaborate closely with the Manufacturing, Quality, Validation, and Technical Operations teams to ensure analytical activities are executed efficiently and in compliance, in support of bringing life-changing therapies to patients around the world.
Responsibilities
Analytical Method Development, Transfer & Validation
  • Execute analytical method transfer, verification, validation, and troubleshooting activities supporting both biologic and small molecule pharmaceutical products.
  • Perform routine and non-routine analytical testing of raw materials, in-process samples, finished products, stability samples, and validation studies.
  • Support technical investigations, specification development, regulatory submissions, and analytical activities associated with cleaning validation and manufacturing support.

Laboratory Operations & Continuous Improvement
  • Support the implementation, qualification, and maintenance of analytical instrumentation and laboratory systems.
  • Identify and implement opportunities to improve analytical methods, laboratory processes, efficiency, compliance, and overall testing capabilities.
  • Maintain technical expertise across a variety of analytical and biochemical techniques while supporting laboratory best practices and data integrity requirements.

Cross-Functional Collaboration & Technical Support
  • Collaborate with Quality Control, Manufacturing, Quality Assurance, Validation, and Technical Operations teams to support routine operations and project activities.
  • Provide technical guidance and training to laboratory personnel as needed.
  • Author and revise analytical methods, protocols, reports, Standard Operating Procedures (SOPs), and other technical documentation while maintaining compliance with current Good Manufacturing Practices (cGMPs) and Good Documentation Practices (GDPs).
  • Support occasional off-shift, weekend, or manufacturing-related activities as business needs require.

Qualifications
  • Bachelor's degree in Chemistry, Biochemistry, or a related scientific field with 5+ years of relevant industry experience; Master's degree with 3+ years of relevant industry experience; or Ph.D. with 2+ years of relevant industry experience. Equivalent combinations of education, training, and experience may be considered.
  • Experience supporting Quality Control or Analytical Development activities within GMP-regulated pharmaceutical, biotechnology, or CDMO environments, including biologics (proteins, peptides, monoclonal antibodies) and small molecule pharmaceutical products.
  • Hands-on experience performing analytical method transfer, method validation, compendial verification, troubleshooting, and analytical testing using techniques such as HPLC, UPLC, LC-MS, GC-MS, FTIR, SDS-PAGE, ELISA, Western Blot, protein concentration assays, Karl Fischer titration, pH analysis, and general wet chemistry methods.
  • Proficiency with chromatography data systems and laboratory software platforms, including Empower and Chromeleon, along with a strong understanding of cGMP regulations, FDA and ICH guidance, method validation principles, data integrity requirements, and laboratory safety standards.
  • Demonstrated ability to troubleshoot analytical issues, critically evaluate data, perform statistical calculations, generate technical reports, protocols, SOPs, and other scientific documentation while providing scientifically sound recommendations and conclusions.
  • Strong verbal and written communication skills with the ability to collaborate effectively across cross-functional teams, manage multiple priorities, and meet deadlines in a fast-paced pharmaceutical manufacturing environment.

Physical Requirements
  • Specific vision requirements include close vision, distance vision, color vision, and the ability to adjust focus.
  • Ability to use computers and laboratory systems for extended periods of time.
  • Ability to follow all cGMP, laboratory, and safety procedures.
  • Must wear required personal protective equipment (PPE) and perform assigned work safely.
  • Ability to use proper lifting techniques and remain aware of workplace hazards.
  • Must occasionally lift and/or move up to 25 pounds.
  • Ability to support occasional weekend, off-shift, or manufacturing support activities as business needs require.

#LI-Onsite
California residents should review our Notice for California Employees and Applicants before applying.
Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employees-regardless of format-without a valid, signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or referral.
Equal Opportunity Employer:
Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.
Do you see yourself as part of the Kindeva mission? Click Apply Now Today!

Apply