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Part Time Pharma Consulting Jobs in California (NOW HIRING)

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Part Time Pharma Consulting information

What is part-time pharma consulting?

Part-time pharma consulting involves providing expert advice and support to pharmaceutical companies or related organizations on a flexible, less-than-full-time basis. Consultants may assist with regulatory compliance, drug development, clinical trials, market analysis, or process optimization. This role allows professionals to use their industry expertise to solve specific problems or guide projects while maintaining a more flexible work schedule. Part-time consultants may work independently or as part of a consulting firm, and often handle multiple clients or projects concurrently.

What are the key skills and qualifications needed to thrive as a part time pharma consultant, and why are they important?

To excel as a Part Time Pharma Consultant, you typically need a background in pharmacy, pharmaceuticals, or life sciences, often supported by relevant degrees or certifications. Familiarity with regulatory guidelines, pharmaceutical software, and data analysis tools is commonly required. Strong communication, analytical thinking, and adaptability are standout soft skills in this field. These competencies ensure effective client support, compliance with industry standards, and the ability to provide valuable strategic insights on a flexible schedule.

What are some common challenges faced by professionals in part-time pharma consulting roles?

Professionals in part-time pharma consulting often encounter challenges related to balancing multiple clients or projects simultaneously, as well as staying up-to-date with rapidly changing industry regulations and standards. Additionally, they must quickly adapt to diverse company cultures and project scopes, often with limited onboarding time. Effective communication and time management skills are essential, as consultants frequently collaborate with cross-functional teams, including regulatory affairs, R&D, and marketing, to deliver actionable insights within tight deadlines.

What are the most commonly searched types of Pharma Consulting jobs in California?

The most popular types of Pharma Consulting jobs in California are:

What are popular job titles related to Part Time Pharma Consulting jobs in California?

For Part Time Pharma Consulting jobs in California, the most frequently searched job titles are:

What job categories do people searching Part Time Pharma Consulting jobs in California look for?

The top searched job categories for Part Time Pharma Consulting jobs in California are:

Part Time Pharma Consulting jobs near you
Infographic showing various Part Time Pharma Consulting job openings in California as of August 2026, with employment types broken down into 100% Part Time. Highlights an 67% In-person, and 33% Remote job distribution.

Sr. Manager, Quality Risk Management

Astrix Inc

South San Francisco, CA • On-site

$90 - $120/hr

Part-time

Re-posted 6 days ago

Job description

Sr Manager, Quality Risk Management - PART TIME
We're hiring a Senior Manager, Quality Risk Management to join a rapidly-growing, well-funded biotech building innovative life sciences solutions and scaling its quality systems. This is a hands-on role working in Veeva to build compliant processes from the ground up. Previous GCP experience is required!
Location: Must be local to South San Francisco, CA or Princeton, NJ
Schedule: Part - Time (20-30 hours)
Pay: $90-$120/hr
Role Overview
We are seeking a Senior Manager, Quality Risk Management (QRM) contractor to support the implementation and maturation of risk-based quality management across GxP activities. This role partners closely with Quality, Clinical, CMC, and functional teams to embed practical, inspection-ready QRM and RBQM practices aligned with ICH Q9 (R1) and ICH E6 (R3).
Key Responsibilities
  • Support implementation of a pharma-focused QRM framework aligned with ICH Q9 (R1) and integrated into the QMS
  • Facilitate and support risk assessments across:
    • Clinical development (RBQM per ICH E6 (R3))
    • Tech Ops (CMC)
    • Quality
    • Vendors and outsourced activities
  • Help identify critical-to-quality (CtQ) factors, define risk controls, and ensure traceability to quality processes
  • Coach and guide cross-functional teams in applying risk-based thinking to decision-making
  • Support inspection and audit readiness by helping teams clearly articulate risk rationales and controls
  • Contribute to risk metrics, trending, and continuous improvement activities

Required Qualifications
  • Bachelor's degree in life sciences, pharmacy, engineering, or related field
  • 7+ years of experience in Pharmaceutical Quality, Compliance, Clinical Operations, or related GxP roles
  • Previous coaching or leadership experience within GCP
  • Practical experience supporting Quality Risk Management and/or RBQM activities aligned with ICH Q9 and/or ICH E6 (R3)

Nice to Have
  • Experience spanning clinical development through manufacturing
  • Familiarity with ICH Q10, ISO 31000, or ISO 14971
  • Prior inspection or audit support experience (FDA, EMA)
  • Consulting or contractor experience in pharma

***This job description is a complete list of all desired skills but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!***
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