
Leading Life Sciences Innovation and Expertise
Astrix stands as the unrivaled market leader in delivering innovative strategies, solutions, and world-class talent to the life sciences community. Founded in 1995 by scientists who understood the unique challenges facing the industry, this privately held company has grown into a powerhouse with over 1,000 employees dedicated to transforming how life science organizations operate, innovate, and succeed.
Comprehensive Life Sciences Solutions
Headquartered in Red Bank, New Jersey, with offices spanning Chicago, New York, Richmond, and Philadelphia, Astrix serves as a strategic partner across the entire life sciences ecosystem. The company specializes in laboratory operations, clinical and regulatory affairs, pharmacovigilance, research and development, and manufacturing solutions that drive measurable business and scientific outcomes through world-class people, process, and technology.
Technical Excellence Meets Client Partnership
What sets Astrix apart is its comprehensive approach to solving complex technical and staffing challenges. The company combines hands-on technical expertise with exceptional client interaction, offering services spanning:
- Strategic consulting and innovative solution design
- Application and platform development
- Data transformation and advanced analytics
- Change management and organizational support
- Specialized staffing and talent solutions
Career Growth In a Mission Driven Environment
Astrix attracts professionals passionate about advancing scientific discovery and improving patient outcomes. The company's deep understanding of regulatory requirements, scientific processes, and technological innovations creates an environment where employees combine technical expertise with meaningful client engagement.
Career Opportunities Include
- Over 111 active positions across diverse technical and consulting roles
- Career paths spanning data science, regulatory affairs, project management, and software development
- Comprehensive benefits including 401(k) and travel expense coverage
- Opportunity to work on cutting-edge projects with real-world impact in biotechnology, pharmaceuticals, and medical devices
- Collaborative culture emphasizing innovation, continuous learning, and professional development
- Hands-on training and mentorship from industry experts
Making a Difference In Life Sciences
Working at Astrix means joining a team of professionals committed to solving the most complex technical and staffing challenges in life sciences. The company's scientist-founded heritage ensures that every solution is grounded in deep industry knowledge, regulatory expertise, and a genuine commitment to improving business and scientific outcomes that ultimately benefit patients and advance human health.
Frequently Asked Questions
Jobs for Astrix in United States
Astrix$140K/yr - $160K/yr46262 Indianapolis, IN
Astrix$35/hr - $42/hr27560 Morrisville, NC
Astrix$95K/yr - $115K/yrCincinnati Metropolitan Area, OH
Astrix$37/hr - $39/hrVentura County, CA

Associate Director Quality Assurance
Description
Looking for a Pharmaceutical leadership role where you can shape quality operations, build strong teams, and influence the direction of a fast-growing organization? This opportunity is ideal for someone who thrives in startup or scale-up environments and enjoys creating structure, elevating standards, and driving continuous improvement.
Pay: $140k-$160k
Schedule: 1st shift
Type of Job: Direct Hire
Location: 100% On-site (Indianapolis area)
At this time, Astrix cannot transfer nor sponsor a work Visa for this position.
Relocation assistance is not available for this position.
Associate Director, Quality & Compliance: Daily Tasks: What you will do:
- Responsible for the oversight of the QA teams responsible for supporting all production/processing areas.
- Leads investigations of product complaints and manufacturing discrepancies for manufactured products and ensures completion of appropriate documentation.
- Responsible for QA review and approval of Investigations, CAPAs, SOPs, Change Controls, and protocols/reports.
- Contributes in Regulatory/FDA inspections and audits by providing information or obtaining information required by the auditors.
- Performs review of root-cause analysis and ensures completeness, accuracy and compliance of all documentation.
- Develops and observes appropriate KPI's for batch documentation review and support of timely batch release.
- Accountable for the QA department planning, talent development, and budget administration.
Associate Director, Quality & Compliance Qualifications/Requirements:
- Bachelor's Degree is required
- 6+ Years of progressive QA/QC experience
- 3+ years in a managerial role in a pharmaceutical or regulated industry
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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