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Analytical Method Validation Scientist I Jobs (NOW HIRING)

... AR&D Scientist I Bachelors degree in Chemistry or related science field and minimum 3 years ... in analytical/method development or method validation in the pharmaceutical or biotechnology ...

Scientist I, AR&D

Chantilly, VA ยท On-site

$65K - $75K/yr

As a Scientist I on our Analytical R&D team, you would be responsible for testing the product ... Conduct analytical method development, method optimization, method validation, method verification ...

Scientist I, AR&D

Chantilly, VA ยท On-site

$65K - $75K/yr

As a Scientist I on our Analytical R&D team, you would be responsible for testing the product ... Conduct analytical method development, method optimization, method validation, method verification ...

Scientist I, AR&D

Chantilly, VA ยท On-site

$65K - $75K/yr

As a Scientist I on our Analytical R&D team, you would be responsible for testing the product ... Conduct analytical method development, method optimization, method validation, method verification ...

Analytical Method Development Scientist (Pharma) Eurofins 7 months ago * Ability to work in a GLP ... Development and execution of method validation protocols. * Development of dissolution methodology ...

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Analytical Method Validation Scientist I information

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How much do analytical method validation scientist i jobs pay per hour?

As of Sep 14, 2026, the average hourly pay for analytical method validation scientist i in the United States is $42.08, according to ZipRecruiter salary data. Most workers in this role earn between $31.49 and $48.56 per hour, depending on experience, location, and employer.

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Infographic showing various Analytical Method Validation Scientist I job openings in the United States as of August 2026, with employment types broken down into 93% Full Time, 5% Part Time, and 2% Contract. Highlights an 84% Physical, 5% Hybrid, and 11% Remote job distribution, with an average salary of $87,519 per year, or $42.1 per hour.

QC Scientist, I - Method Validation(W)

Forest, TX โ€ข On-site

Other

Medical, Retirement, PTO

Posted 13 days ago


Key responsibilities

  • Execute analytical method qualification and validation studies supporting release, stability, characterization and in process testing of cell therapy products in a GMP environment.

  • Independently perform cell-based assays, including potency, flow cytometry, viability, proliferation, cytotoxicity, ELISA, and molecular PCR testing methods.

  • Support transfer of commercial methods and method validation into QC in compliance with regulatory requirements.


Job description

Job Summary

Cellipont Bioservices is growing, and we are looking for a QC Scientist I, who believes in the potential of bridging clients discoveries to patient cures and who wants to challenge the status quo and take Cellipont and its clients to the next level.


The QC Scientist I works in a fast-paced environment supporting the quality control department cell therapy analytical method qualifications and validations. The QC Scientist I will be responsible for independent execution of complex laboratory/experiment work with a high degree of technical proficiency focused on method qualification and/or validation within a GMP environment, QC document preparation and revision (SOPs/Protocols/Reports), as well as technical support for QC lab investigations.


The QC Scientist I is also responsible for ensuring all activities are executed timely and cost effectively to ensure customer and stakeholder satisfaction. This role will require the individual to demonstrate strong ability to work cross-functionally and possess strong leadership skills.


The Role

  • Execute analytical method qualification and validation studies supporting release, stability, characterization and in process testing of cell therapy products in a GMP environment.

  • Independently perform cell-based assays, including potency, flow cytometry, viability, proliferation, cytotoxicity, ELISA, and molecular PCR testing methods, among others.

  • Support transfer of commercial methods and method validation into QC in compliance with regulatory requirements.

  • Generate, review, and document analytical data following GMP, GDP, ALCOA+, and regulatory compliance requirements.

  • Present experimental findings and support preparation of technical reports and presentations to clients.

  • Provide technical expertise on bioassay, flow cytometry and/or molecular biology methods in support of QC lab investigations, to identify root cause and provide corrective and preventative actions, if needed.

  • Prepare and revise method qualification/validation protocols, technical reports, SOPs, and laboratory documentation supporting analytical method lifecycle management.

  • Evaluate assay performance characteristics including accuracy, precision, specificity, robustness, and suitability for intended analytical applications.

  • Collaborate with QA, Analytical Development (AD), Manufacturing and Process Development (PD) teams to support compliant analytical testing programs.

  • Work independently in a high-paced team environment, meet deadlines, and prioritize work from multiple projects.

  • Communicate effectively with cross-functional peers, department management, and other partners as needed.


The Candidate

  • B.S. in Biology, Biochemistry, Biotechnology, Immunology, Microbiology, or related scientific discipline, or Master's Degree preferred

  • Minimum 4 years of experience in biotechnology, pharmaceutical or cell therapy experience required. Previous experiment in analytical method qualification/validation is a must.

  • Hands-on experience with mammalian cell culture and aseptic techniques in a laboratory and/or GMP environment.

  • Experience performing analytical methods including flow cytometry, cell-based potency, viability, proliferation, cytotoxicity, ELISA or molecular assays preferred.

  • Self-starter with the ability to produce results in a fast-paced environment to meet client deadlines under minimal supervision.

  • Hands-on experience with analytical method transfers/qualifications/validations is a plus.

  • Technical background and expertise in flow cytometry is a plus.

  • Knowledge of cGMP/ICH/FDA regulations.

  • Excellent oral and written communication skills.


Position Benefits

  • Opportunities for career growth within an expanding team

  • Defined career path and annual performance review & feedback process

  • Cross-functional exposure to other areas of within the organization

  • Robust benefit package designed for unique Health & Wellness needs, including coverage for your furry family members

  • 401K strong employer match
  • Tuition Reimbursement

  • Employee Referral Bonuses

  • Flexible work schedules and PTO based on role/level, increasing 1 PTO day each year and paid holidays

  • Gain experience in the cutting-edge cell therapy space


\"At Cellipont Bioservices, we look for candidates with an innate desire to serve. Our \"family\" approach ensures you will get the mentorship you need to develop a satisfying career here!\"

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