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Full Time Method Validation Jobs (NOW HIRING)

Pharmaceutical Specialties Inc

Chemist II

Rochester, MN · On-site

$70K/yr

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

Author and execute method validation protocols and reports. * Be able to assist with new ... This position is eligible for all full-time benefits including: * Health Insurance greatly ...

Pharmaceutical Specialties Inc

Chemist II

Rochester, MN · On-site

$70K/yr

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

Author and execute method validation protocols and reports. * Be able to assist with new ... This position is eligible for all full-time benefits including: * Health Insurance greatly ...

Sigan America LLC

Analytical Chemist

Ottawa, IL · On-site

$50K - $70K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

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 ...

Codexis Inc

Sr. Scientist, Quality Control

Plano, TX · On-site

$160K - $175K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... 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 ...

Revlon Corporate

Director, Quality Control

Oxford, NC

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

This role requires full-time presence at our North Carolina office. Revlon is seeking a Director ... Oversee analytical method qualification, validation, verification, transfer, and lifecycle ...

System One

Analytical Science Manager

Parsippany, NJ · On-site

$100K - $135K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Direct Hire - Full time permanent Compensation: $100,000.00 - $135,000.00 Work Model: Hybrid - 2 days onsite, 3 days work from home Responsibilities * Lead analytical method transfers and validation ...

System One Holdings, LLC

Analytical Science Manager

Parsippany, NJ · On-site

$100K - $135K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Direct Hire - Full time permanent Compensation: $100,000.00 - $135,000.00 Work Model: Hybrid - 2 days onsite, 3 days work from home Responsibilities * Lead analytical method transfers and validation ...

System One

Analytical Science Manager

Parsippany, NJ · On-site

$100K - $135K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Direct Hire - Full time permanent Compensation: $100,000.00 - $135,000.00 Work Model: Hybrid - 2 days onsite, 3 days work from home Responsibilities * Lead analytical method transfers and validation ...

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 Aug 16, 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.

What cities are hiring for Full Time Method Validation jobs?

Cities with the most Full Time Method Validation job openings:

What are the most commonly searched types of Method Validation jobs?

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Full Time Method Validation jobs near you
Infographic showing various Full Time Method Validation job openings in the United States as of August 2026, with employment types broken down into 90% Full Time, 3% Part Time, and 7% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Scientist, Method Development - Ligand Binding Assays

Celerion

Lincoln, NE • On-site

$30.75 - $38.50/hr

Full-time

Re-posted 18 days ago

Celerion rating

7.0

Company rating: 7.0 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

62nd of 73 rated research

Job description

Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you!
Celerion is seeking a Scientist to join our Ligand Binding Assay Development team. The successful candidate will have strong problem-solving skills, scientific expertise and knowledge in Ligand Binding bioanalytical method development.
This full-time role is located at our Lincoln, NE facility.
As a Scientist, Method Development, you will provide scientific expertise and method development skills to the Ligand Binding Assay Development group at Celerion. A key component of the role is to provide innovation and change management required to remain on the cutting edge of Ligand Binding Bioanalytical Sciences.
Responsibilities:
  • Undertake original and innovative research and techniques that include developing ligand binding assays utilizing state-of-the-art technologies for the rapid and accurate analysis of protein/peptides/ antibodies in biological matrices
  • Perform assays (pharmacokinetics (PK), pharmacodynamics PD)/biomarkers, ADA) according to regulatory and quality systems
  • Analyze and interpret data, generate summary tables, and troubleshoot assay performance, as well as peer-review raw data for accuracy and completeness
  • Work effectively within a team and across teams to meet objectives under time constraints
  • Support the associate director in achieving challenging business objectives for the method development team. Includes innovation, change management, evaluation of new technology, and growth in market share, revenue, profit, and customer loyalty.
  • Develop methods by applying and interpreting scientific theories, concepts, techniques, and regulatory requirements in bioanalytical studies
  • Provide technical/scientific guidance and leadership to study teams, as well as other areas of the company to ensure project completion in a timely manner
  • Author scientific manuscripts for publication in peer-reviewed journals and present research findings through posters and oral presentations at scientific conferences
  • Participate and provide technical expertise during client calls and visits

Requirements:
  • Minimum of a Bachelor's degree in Biochemistry, Chemistry or Biology required. An advanced degree is preferred.
  • 5+ years of related scientific experience preferred; CRO/industry experience is a plus
  • The candidate must have proven proficiency in immunoassay development and be capable of working on multiple projects simultaneously
  • Strong hands-on experience in at least one of the following pharmacokinetics (PK), pharmacodynamics (PD)/biomarkers, ADA assay development
  • Understanding of FDA and ICH guidelines in method validation and sample analysis
  • Prior experience working in a regulated GLP-compliant environment is preferred
  • Experience in one or more immunoassay techniques (Ligand Binding assay: ELISA, MSD, Gyrolab, AlphaLISA)
  • Experience using Watson LIMS is preferred
  • Excellent verbal and technical writing skills and be capable of presenting to an audience of researchers from a variety of disciplines
  • Ability to work well with a team and with staff in other locations effectively

Celerion Values: Integrity Trust Teamwork Respect
Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as "Not Junk" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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