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Contract Method Validation Jobs in Indiana (NOW HIRING)

Astrix Inc

R&D Formulation Scientist

Columbus, IN · On-site

$27 - $30/hr

Pay Rate Low: 27 | Pay Rate High: 30 Our client is a leader in contract manufacturing and ... Lead and support method validation and method transfer activities in accordance with applicable ...

Actalent

Senior Lab Technician - ICP

Noblesville, IN · On-site

$38.46/hr

Develop, optimize, and validate analytical methods for new process matrices or prototype materials ... Job Type & Location This is a Contract to Hire position based out of Noblesville, IN. Pay and ...

Actalent

Senior Lab Technician - ICP

Noblesville, IN · On-site

$38.46/hr

Develop, optimize, and validate analytical methods for new process matrices or prototype materials ... Job Type & Location This is a Contract to Hire position based out of Noblesville, IN. Pay and ...

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All JobsContract Method Validation JobsContract Method Validation Jobs in Indiana

Contract Method Validation information

What is the difference between Contract Method Validation vs Analytical Method Validation?

AspectContract Method ValidationAnalytical Method Validation
PurposeValidates that a contracted method meets specific requirements for a particular project or clientEnsures an analytical method is accurate, reliable, and reproducible for testing purposes
ScopeTypically project-specific, focusing on methods used under contractual agreementsBroader, covering method development, validation, and routine testing
CredentialsOften requires validation expertise, GMP knowledge, and industry-specific certificationsRequires analytical chemistry knowledge, validation experience, and relevant certifications
Work EnvironmentPharmaceutical, biotech, or manufacturing settings with client-specific projectsLaboratories performing routine testing and method development in similar industries

Contract Method Validation focuses on validating methods for specific client projects, while Analytical Method Validation ensures the overall reliability of testing methods used routinely in laboratories. Both roles require similar credentials and work in related environments, but their scope and purpose differ.

What cities in Indiana are hiring for Contract Method Validation jobs?

Cities in Indiana with the most Contract Method Validation job openings:

Contract Method Validation jobs near you

R&D Formulation Scientist

Astrix Inc

Columbus, IN • On-site

$27 - $30/hr

Full-time

Re-posted 18 days ago

Job description

Pay Rate Low: 27 | Pay Rate High: 30
Our client is a leader in contract manufacturing and integrated product development, formulation science, technical operations, packaging expertise, and in-house analytical and stability programs to deliver results-from innovative new systems to modernized legacy brands. Come join the team!
Schedule: Monday-Friday, 8:00 AM - 5:00 PM
Job type: Direct Hire
Pay rate: $27/hr. -$30/hr.
Summary
We are seeking an experienced and detail-oriented Senior Microbiologist / Formulation Scientist to join our Research & Development team. The ideal candidate will have 3-5+ years of industry experience with a strong background in formulation development, microbiology, and analytical method validation. This role will be responsible for developing and optimizing formulations, executing microbiological testing, writing and validating laboratory methods, and supporting product development initiatives from concept through commercialization.
Key Responsibilities
  • Develop, optimize, and evaluate formulations for new and existing products.
  • Design, execute, and document formulation studies and stability testing.
  • Write, review, and execute analytical and microbiological test methods.
  • Lead and support method validation and method transfer activities in accordance with applicable regulatory and quality requirements.
  • Perform microbiological testing including media preparation, culturing, plating, microbial enumeration, and environmental monitoring.
  • Maintain aseptic technique and ensure compliance with laboratory best practices.
  • Analyze experimental data, prepare technical reports, and present findings to cross-functional teams.
  • Accurately document laboratory activities in notebooks, protocols, and electronic systems.
  • Support investigations related to microbiological results, contamination events, and product performance.
  • Maintain laboratory equipment, calibration records, inventory, and overall laboratory organization.
  • Collaborate with R&D, Quality, Manufacturing, and Regulatory teams to support product development and commercialization efforts.
  • Adhere to all safety guidelines, SOPs, and Good Laboratory Practices (GLP).
Qualifications
  • Bachelor's degree in Microbiology, Biology, Chemistry, Pharmaceutical Sciences, or a related scientific field; advanced degree preferred.
  • 3-5+ years of relevant industry experience in microbiology, formulation development, or product development.
  • Strong hands-on experience with formulation development and optimization.
  • Experience writing, executing, and supporting method validation protocols and reports.
  • Solid microbiology background with experience in:
    • Microbiological testing
    • Aseptic techniques
    • Environmental monitoring
    • Microbial identification and enumeration
    • Bioburden and contamination investigations
  • Strong understanding of laboratory documentation requirements and data integrity principles.
  • Experience with stability studies, product testing, and analytical techniques is preferred.
  • Excellent problem-solving, organizational, and communication skills.
  • Ability to work independently while contributing effectively within a collaborative team environment.

Preferred Skills
  • Experience in regulated environments such as pharmaceutical, biotech, personal care, cosmetics, medical device, or consumer products industries.
  • Familiarity with GLP, GMP, USP microbiological methods, and validation requirements.
  • Proficiency with laboratory software, data analysis tools, and technical report writing.
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