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Full Time Method Validation Jobs (NOW HIRING)

Catalyst Nutraceuticals

Chemist

Buford, GA · On-site

... method development and validation projects. The position will report to the Laboratory Manager. The position is a Full-time onsite role, Monday-Friday, from our headquarters office in Buford, GA.

Codexis Inc

Sr. Scientist, Quality Control

Plano, TX · On-site

$160K - $175K/yr

... Full Time Location: Redwood City, CA Compensation: $160,000 - $175,000 / year Description The Sr. Scientist in Quality Control will be leading analytical method transfer and validation for ...

Sigan America LLC

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Analytical Chemist

Ottawa, IL · On-site

$50K - $70K/yr

Ottawa, IL 61350 Schedule: Full-Time | First Shift Position Summary We are seeking a highly ... This role is responsible for developing, validating, and executing analytical methods that support ...

Silicon Resourcing Solutions, LLC.

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Lab Technician

Ventura, CA · On-site

$21 - $24/hr

... review method validation protocols and validation reports. Full time position, Friday to Monday, 4/10s schedule, 7:00 AM-5:30 PM with possible overtime on occasion. Essential Duties and ...

Artius Solutions

Analytical QA Supervisor

Fall River, MA · On-site

$78K - $99K/wk

Fall River, MA Experience Required: 5 - 15 Years Job Type: Full-time | On-site Shift: General (8:30 ... Oversee and verify method validation reports, comparisons, and study documentation. * Monitor ...

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Full Time Method Validation information

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How much do full time method validation jobs pay per hour?

As of Jul 4, 2026, the average hourly pay for full time method validation in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.
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What are the most commonly searched types of Method Validation jobs? The most popular types of Method Validation jobs are:
Full Time Method Validation jobs near you
Senior Scientist - Biosimilars ARD

Senior Scientist - Biosimilars ARD

Kashiv Biosciences LLC

Piscataway, NJ • On-site

$91K - $125K/yr

Full-time

Posted 18 days ago

Job description

Job Type
Full-time
Description
Summary
A Sr. Scientist I will be a key technical resource responsible for independently developing methods, generating reliable and interpreting data, using analytical instrument that include HPLC, UPLC, GC, UV/Vis, dissolution apparatus and particle analyzer. You will be expected to develop a close working relationship with technical personnel at all levels within the organization to provide technical support needed in meeting R&D milestones and goals.
Conduct instrumenttroubleshooting.or designing experiments, writing method validation protocols, conducting method validation, and processing and interpreting the analytical data.
Essential Duties & Responsibilities
  • Develop and validation analytical method for drug substances, drug products, and excipients
  • Conduct routine and advanced analytical tests in accordance with SOPs and regulatory guidance.
  • Write protocols, reports, methods, standard operation procedure, and submission documents.
  • Provide analytical support for formulation and process development.
  • Perform independent scheduling and coordination of activities
  • Complies with all companypolicies and standards
  • Analyze analytical data, identify trends and provide recommendation.
  • Review laboratory notebooks, raw data and technical documentation (e.g. test method, validation protocol, or validation report) in support of regulatory filings
  • Train and provide technical guidance to junior scientists.
  • Conduct laboratory investigation and prepare laboratory investigation report.
  • Proactively provide Lab management with suggestions on how to improve the methods, lab practice or lab system.
  • Evaluate and improve existing test methods
  • Proactively provide Lab management with suggestions on how to improve the methods, lab practice orlab system.ection.
  • Review and evaluate drug substance supplier's technical documents and provide recommendation in APIvendor selection.
  • Performs other functions asrequired or assigned

Requirements
PREREQUISITES:
Education:
  • Minimum B.S. degree in Analytical Chemistry, Biophysical/biochemical sciences, pharmaceutical sciences with 8 years industry experience
  • Or Master's Degree in Biochemistry, Biotechnology, Biology with 5+ years' experience in protein mass spectrometry
  • Or Ph.D. in Biochemistry, Biotechnology, Biology with 3+ years of experience in protein mass spectrometry

Experience:
  • A strong theoretical understanding and experience in protein chemistry and biochemistry.
  • In-depth hands-on experience with operation of HPLC, GC, dissolution, plate-readers and UV techniques is required.
  • An in-depth understanding of USP requirements, ICH guidelines and USP/EP pharmacopeia requirements
  • Excellent communication and technical writing skills
  • Experience in method development, as well as method qualification/verification/validation in a GLP/GMP environment
  • Strong experience in analytical method development and validation
  • Demonstrated skills as a team-player and team-management.
  • Ability to plan, schedule and work independently in a fast pace environment. Self-motivation, adaptability, and a positive attitude.
  • Working knowledge of applicable safety and standards guidelines, such as SOP, cGMP, GLP, DEA regulations and/or MSDS.
  • Ability to work under pressure and meet deadlines

SPECIALIZED KNOWLEDGE AND SKILLS:
  • Ability to multitask technical responsibilities in a fast-paced, dynamic environment is required
  • Proficiency with the following software is required: Microsoft Word, Excel, PowerPoint, and Outlook.
  • Experience with Mass Spectrophotometer is required.
  • Experience with Empower HPLC software programs is required.

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