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Per Diem Analytical Method Development Jobs (NOW HIRING)

Labcorp

Method Development Scientist I

Madison, WI · On-site

$70/hr

Develops routine and complex analytical methods for quantitation of pharmaceuticals from biological ... Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive ...

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Per Diem Analytical Method Development information

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$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 Chemist

Analytical Development Chemist

Pegasus Laboratories, Inc.

Pensacola, FL • On-site

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 14 days ago

Job description

Location: Pensacola, FL

Position Summary

The Analytical Development Chemist will develop and validate analytical methods, provide analytical support for product development, and design, write, and execute technical documents such as protocols and reports. This role will serve as a subject matter expert for analytical methods and technical writing. 

Compensation & Benefits 

  • Employee Ownership (ESOP):Company-funded retirement contribution of approximately 18% of pay, plus 401(k) 
  • Competitive base salary with performance-based bonus opportunity 
  • Comprehensive benefits package: Medical, Dental, Vision, Life, Disability, FSA, and Pet Insurance 
  • Generous paid time off, paid holidays, and parental leave 
  • Fitness and tuition reimbursement programs 

Essential Duties & Responsibilities

  • Responsible for development and validation of analytical methods (Assay, Impurities, Dissolution, Cleaning, and Residual Solvents). 
  • Designs, writes, and executes method validation protocols, reports, and other technical documents in accordance with current industry standards as well as regulatory requirements, i.e. FDA, USP, EP. 
  • Coordinate validation projects and ensure all validation documentation is finalized, current and archived as required. 
  • Oversee development of analytical services projects including formulations support to stability and validation. 
  • Must be able to understand and interpret data from formulation design to in-vitro/in-vivo performance and design experiments to support product development. 
  • Must be able to understand the purpose and objective of the studies to appropriately design laboratory experiments and protocols 
  • Coordinates analytical method transfer and training of testing with the Quality Control Laboratory and serves as a technical resource for investigations. 
  • All other tasks as requested or assigned. 

Required Qualifications

  • Bachelor's or master's degree in chemistry or related field.  PhD preferred. 
  • Experience: 3+ years required with advanced degree (research or work experience) work experience with BS degree experience in pharmaceutical analytical method development and validations.  
  • Proficient in data analysis including raw data review and interpreting results.  
  • Strong writing and documentation skills (cGMP, protocols, reports, OOS investigations, lab notebooks) 
  • Proficient with Microsoft Office Suite (Word, Excel, Outlook) 
  • Familiar with using QMS systems (i.e., Empower, Master Control) 

Preferred Qualifications

  • Experience: prefer 5+ years' work experience with BS degree experience in pharmaceutical analytical method development and validations.  
  • Experience in HPLC, Dissolution, UV-Vis, GC, Cleaning Validations, Empower, and compendial (USP, FCC, EP) testing preferred. 

Work Environment & Culture 

PBI-Gordon Companies offers a collaborative, employee-owned environment where accountability, partnership, and continuous improvement are valued. Team members are encouraged to contribute ideas, develop professionally, and grow their careers alongside the business. 

Equal Opportunity Employer 

PBI-Gordon Companies is an Equal Opportunity Employer. We value diversity and are committed to creating an inclusive environment for all employees. 

Ready to Apply? 

If you're passionate about pharmaceutical analytical method development and validation, data analysis and technical writing, and working in a cGMP-regulated environment, we'd love to hear from you.
Apply today to join an employee-owned company committed to scientific excellence, collaboration, and shared success.

Apply