
BioTalent: Life Sciences Recruitment Specialists
BioTalent stands as a premier life sciences recruitment specialist, connecting talented professionals with transformative career opportunities across the biotechnology and pharmaceutical industries. Founded in 2018 and headquartered in London, this rapidly growing company has strategically expanded its global footprint with offices in New York, Boston, San Diego, Miami, and Zug, Switzerland, positioning itself as a trusted partner for life sciences professionals seeking opportunities in dynamic US markets.
Specialized Expertise Across Life Sciences
As part of The IN Group-a collection of specialist talent brands including Investigo, InX, Definia, Caraffi, and Sigma Labs-BioTalent leverages extensive industry expertise to address complex talent challenges across North America and Europe. The company's specialized focus areas encompass:
- Research & Development and Data Science & AI
- Clinical Operations and Regulatory Affairs
- Medical & Drug Safety and Medical Communications
- Engineering & CQV and Manufacturing & Operations
- Quality Assurance and Commercial functions
Culture of Excellence and Continuous Improvement
BioTalent cultivates a supportive work environment that values professional growth and team collaboration. The company's culture emphasizes:
- High-impact leadership opportunities with dynamic, collaborative teams
- Focus on excellence in safety, quality, cost optimization, and delivery
- Commitment to development through structured training programs and succession planning
- Work-life balance with sustainable working practices
- Career advancement through annual talent reviews and clear promotion paths
- Global perspective with access to innovative biotech startups and established pharmaceutical leaders
Strategic Market Presence
With a team of 51-200 dedicated professionals and a 4.3-star Glassdoor rating, BioTalent has cultivated a strong reputation in the staffing sector. The company's substantial LinkedIn following of over 310,000 life sciences professionals reflects its influence and credibility. Strategic presence in major US life sciences hubs-including San Diego's biotech corridor, Boston's pharmaceutical cluster, and New York's growing life sciences sector-enables identification of regional market opportunities and emerging trends in AI-driven drug discovery, personalized medicine, and biotechnology innovation.
Expert Guidance and Meaningful Connections
BioTalent's expert consultants provide personalized guidance and deep industry knowledge, ensuring meaningful connections that drive both career growth and organizational success. Whether you're seeking your next opportunity or building your team, BioTalent's consultants understand the nuances of the life sciences landscape and are committed to finding the right fit for your career trajectory.
Frequently Asked Questions
Offices
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Jobs for BioTalent in United States


Orange County, CA
91361 Westlake Village, CA
92002 Carlsbad, CA
33483 Delray Beach, FL
02298 Boston, MA
92189 San Diego, CA










91361 Westlake Village, CA

Senior Quality Engineer Contract Position
Description
***********************NO C2C OR THIRD PARTIES***********************
- Duration: 6-months with potential for extension
- Location: on-site 4x per week in Carlsbad, CA
- Hourly rate: $40-55/hr DOE
Join an innovative medical-device team focused on improving patient outcomes through engineering excellence and regulatory precision. The Quality Engineer/Senior Quality Engineer will play a key role in ensuring compliance, reliability, and performance of life-changing technologies - supporting both product development and ongoing manufacturing operations.
What You'll Do
- Develop and maintain quality controls, processes, and analytical methods to ensure conformance to product specifications.
- Lead verification and validation (V&V) testing, including protocol design, execution, data analysis, and reporting.
- Support design control activities and cross-functional reviews for new product development and significant design changes.
- Drive statistical analysis and data-driven decision making for process stability and product quality.
- Collaborate with manufacturing and suppliers to maintain conformance and improve assembly, testing, and documentation practices.
- Support supplier qualification, incoming inspection, and process improvement initiatives.
- Participate in risk management activities (ISO 14971) and ensure compliance with QMS and regulatory standards.
- Support internal and external audits (FDA, ISO), nonconformance investigations, and CAPA initiatives.
- Analyze field issues and deviations, perform root cause analysis, and implement effective corrective actions.
What You'll Bring
- Bachelor's degree in Biomedical, Mechanical, Chemical, or related Engineering field.
- 3-5+ years of experience in a medical device quality engineering role.
- Working knowledge of FDA QSR, ISO 13485, ISO 14971, and risk-based quality systems.
- Hands-on experience with verification testing, statistical analysis, and process validation.
- Strong communication skills - able to produce clear reports, present findings, and collaborate across disciplines.
- Proficiency with Excel, Minitab, MATLAB, or equivalent analytical tools.
- Detail-oriented, organized, and proactive in driving continuous improvement.

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