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Assistant Method Validation Jobs (NOW HIRING)

Novartis

Manager, QA Method Validation

Carlsbad, NM

$114K - $211K/yr

Lead review and approval of method validation protocols, reports, and supporting data for accuracy ... Lead and/or support audits and inspections including preparation and follow-up * Assist with ...

Quality Agents

Validation Engineer IV

Rockville, MD · On-site

Review and approve documented test results and maintain records for later analysis. * Assist with ... method validation, or cleaning validation. * Current drivers license and auto insurance Quality ...

Quality Agents

Validation Engineer II

Rockville, MD · On-site

Review and approve documented test results and maintain records for later analysis. * Assist with ... method validation, or cleaning validation. * Current drivers license and auto insurance Quality ...

Quality Agents, LLC

Validation Engineer I

Rockville, MD · On-site

Review and approve documented test results and maintain records for later analysis. * Assist with ... method validation, or cleaning validation. * Current driver's license and auto insurance Quality ...

Abbott

Validation Engineer III

Centre, AL · On-site

... method validation and process validation. * Writes and/or revises IQ, OQ, PQ related documents ... compliance. * Assist with internal and external audits. * Manages validation metrics. * Manages ...

Actalent

Scientist - Microbiology

Cumnock, NC

$30 - $45/hr

Lead and support the validation and qualification of microbiological methods to ensure compliance with GMP and regulatory requirements. * Assist with the development, execution, and documentation of ...

Kellton Tech

QA Validation Technician I

Tampa, FL · On-site

This individual will contribute to method development, validation, troubleshooting, and support ... and reporting procedures. * Assist in maintaining electronic lab systems (e.g., LIMS, CDS ...

Integrated Resources INC

Scientist

Lititz, PA · On-site

Collaborate with R&D and QC personnel to develop and validate complex assay methods for raw material and finished product. Assist in the development of new and optimize existing methods for raw ...

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How much do assistant method validation jobs pay per hour?

As of Jul 26, 2026, the average hourly pay for assistant method validation in the United States is $19.55, according to ZipRecruiter salary data. Most workers in this role earn between $15.14 and $21.39 per hour, depending on experience, location, and employer.
What are the most commonly searched types of Method Validation jobs? The most popular types of Method Validation jobs are:
Assistant Method Validation jobs near you
Infographic showing various Assistant Method Validation job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 76% Full Time, 20% Part Time, 1% Temporary, and 2% Contract. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $40,672 per year, or $19.6 per hour.
Manager, QA Method Validation

Manager, QA Method Validation

Novartis

Carlsbad, NM

$114K - $211K/yr

Full-time

Medical, Life, Retirement, PTO

Posted 2 days ago

Novartis rating

7.4

Company rating: 7.4 out of 10

Based on 16 frontline employees who took The Breakroom Quiz

65th of 86 rated pharmaceutical

Job description

Job Description Summary

Location: Carlsbad, United States
You'll play a critical role at the intersection of quality, innovation, and patient impact-leading laboratory method validation for assays and devices used in clinical and GMP laboratory settings. As a trusted quality leader, you will shape how analytical methods are brought to life in a highly regulated environment, partnering closely with scientific and cross-functional teams to solve complex challenges, strengthen compliance, and enable the delivery of high-quality data that supports breakthrough therapies.
Relocation Support: This role is based in Carlsbad, California. Novartis is unable to offer relocation support: please only apply if accessible.


Job Description

Key Responsibilities

  • Lead review and approval of method validation protocols, reports, and supporting data for accuracy and compliance
  • Providequality guidance on analytical method validations/verifications, troubleshooting, and impact assessments
  • Serve as Quality representative on in vitro diagnostic design teams
  • Evaluate and provide guidance on risk assessments, impact assessment, deviations, and corrective actions
  • Ensure adherence to regulatory and company requirements
  • Lead and/or support audits and inspections including preparation and follow-up
  • Assist with quality management of technology transfer
  • Maintain oversight of documentation, procedures, and training compliance

Essential Requirements

  • Bachelor's degree in engineering, medical technology, biological sciences, or related fieldand a minimum of 8years' experiencein clinical and/or GMP laboratory environments. With an advanced degree, fewer years of experience may be required.
  • At least 3years experiencesupporting in vitro diagnostic development
  • Experience, understanding, and familiarity with regulatory requirements and other compliance requirements and guidelines (such as GxP, Part 11, ICH, ISO, CLIA/CAP, IVDR, QSR)
  • Basic understanding of molecular biology, immunology, immunohistochemistry, flow cytometry, fluorescent in situ hybridization
  • Familiarity with statistical analysis
  • Strong communication, collaboration,and presentation skills

Desirable Requirements

  • Experience with ligand binding assays, flow cytometry, and digital pathology
  • Proven track record of identifying and executing on continuous improvement

The salary for this position is expected to range between $114,100 - $211,900 year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.

To learn more about the culture, rewards and benefits we offer our people click here.

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EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.


Accessibility and reasonable accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.


Salary Range

$114,100.00 - $211,900.00


Skills Desired

Collaboration, Communication Skills (Inactive), Data Integrity, Decision Making, Digital saviness (Inactive), Leadership, Managing Ambiguity, Organizational Saviness (Inactive), Regulatory Requirements knowledge (Inactive), Risk Management

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