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How much do remote pharmaceutical inspector jobs pay per hour?

As of Jun 10, 2026, the average hourly pay for remote pharmaceutical inspector in the United States is $27.36, according to ZipRecruiter salary data. Most workers in this role earn between $18.51 and $31.49 per hour, depending on experience, location, and employer.
What are the most commonly searched types of Pharmaceutical Inspector jobs? The most popular types of Pharmaceutical Inspector jobs are:
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Infographic showing various Remote Pharmaceutical Inspector job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 82% Full Time, 15% Part Time, and 2% Contract. Highlights an 90% Physical, 2% Hybrid, and 8% Remote job distribution, with an average salary of $56,905 per year, or $27.4 per hour.
Manager, Quality Computerized System Validation (CSV)

Manager, Quality Computerized System Validation (CSV)

Nuvalent, Inc.

Cambridge, MA • Remote

Other

Posted 22 days ago

Job description

The Role:

Reporting to the Director, Quality Systems, the Manager, Quality Computerized System Validation (CSV) is responsible for maintaining the validation lifecycle of GxP-regulated computerized systems across the organization in a remote pharmaceutical operating model. The ideal candidate is a strategic thinker with strong hands-on validation experience, excellent cross-functional communication skills, and understanding of compliance in a cloud-based and SaaS environment.

Responsibilities:

  • Partner with IT, Quality, Regulatory, Clinical, TechOps, Pharmacovigilance, and vendors to support GxP system implementations, enhancements, and upgrades.
  • Develop, maintain, and continuously improve CSV policies, SOPs, and forms aligned with regulatory expectations and industry best practices.
  • Ensure application of risk-based validation approaches and data integrity principles (ALCOA++).
  • Act as CSV subject during internal audits, vendor audits, and regulatory inspections.
  • Review and approve GxP system validation deliverables, change controls, deviation investigations, and periodic reviews.
  • Assess inspection trends and proactively update validation practices accordingly.
  • Evaluate vendor documentation for GxP system validation and SDLC for suitability and leverage where appropriate.

 Competencies:

  • Risk-based decision making
  • Strategic thinking with practical execution
  • Strong written and verbal communication
  • Attention to detail with business mindset

 Qualifications:

  • Bachelor's degree or related experience
  • 3-5 years' experience in GxP computerized system validation within the pharmaceutical, biotech, or medical device industry.
  • Veeva QualityDocs experience required.
  • Deep knowledge of CSV, SDLC, Part 11, Annex 11, ICH E6(R3) Data Governance, and data integrity principles.
  • Experience validating cloud-based and SaaS systems.
  • Strong understanding of change management and system lifecycle management.
  • Ability to work Eastern Time Zone and across time zones as needed 

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