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MEIRxRS Corporate Services

LIFE SCIENCE RECRUITMENT SOLUTIONS

Staffing

PERMANENT STAFFING

Including medical directors, drug safety, biostatisticians, clinical research associates, regulatory and quality professionals.

Executive Search

EXECUTIVE SEARCH

Finding experienced leaders with a history of bringing drugs or medical devices like yours to market.

Temporary Staffing

TEMPORARY STAFFING

When you need capable workers on a project basis or to fill in while a critical staff member is away, experts are available.

Apprenticeships

APPRENTICESHIPS

Through our Foundation, a unique model to on-board and properly train new hires in the life sciences industries

GxP Auditing

GxP AUDITING SOLUTIONS

Senior-level auditors for pharmacovigilance, data management, quality systems, GMP, GCP and GLP audits

Regulatory and Clinical Consultanting

REGULATORY & CLINICAL CONSULTANTING

Ensure your team generates high-quality data and stays on track toward meeting your next regulatory milestone.

Specialist Recruiters in your Sector

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PHARMA

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BIOTECH

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MEDICAL DEVICES

MEIRxRS Blog and News

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HR Generalist Needed, Glendale, CA

HR Generalist Needed, Glendale, CA We are in need of an HR Generalist to manage on boarding (and off boarding) of staff and temps placed with our clients. This is an internal position working directly for MEIRxRS family of companies at our office on 100 N Brand Blvd, Glendale, CA (check your commute). Qualifications 3 or […]

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Clinical Trial Manager Needed in Irvine, CA

Clinical Trial Manager Needed in Irvine, CA Our large pharma client in Irvine needs a temporary Clinical Trial Manager for 6-10 months. Qualifications • B.S. degree. • Minimum of 3 to 5 years of pharmaceuticals/biotech experience. • Minimum of 3 to 5 years drug development experience in the pharmaceutical industry/CRO or commensurate clinical/medical research experience […]

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Clinical Research Project Manager Needed RemoteWork

Clinical Research Project Manager Needed – Remote Work Clinical Research Project Manager needed by our client to manage clinical trials and to ensure on time regulatory submission. Requirements Bachelor’s-level degree required in science/health related field. Nine years of clinical research and/or clinical project management experience (roles such as CRA, CTA, Project manager, CRC etc..) at pharmaceutical […]

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Top 20 Skills You Need To Become An Effective Leader

Top 20 Skills You Need To Become An Effective Leader Do you aspire to become a Executive Leader of Regulatory Affairs, Quality Assurance, Clinical Research, or Medical Affairs? Leadership skills for  are increasingly crucial given that you will have to set a course for an entire team, keep them all on track and keep them unified […]

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Free Professional Development Opportunities in Biotech and Medical Devices

Free Professional Development Opportunities Are you looking for a professional growth opportunity? Our Foundation has received funding to pay for certifications for individuals in California in Biotech, Pharma and Medical Device industries. The funding will cover for free: Certified Quality Improvement Associate (CQIA) primer and exam fees Second approved certification study materials and exam fees […]

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Learn About MDSAP - Free Lunch and Learn by Interek

Learn About MDSAP – a Free Lunch and Learn November 27, 2017 at 11:30 AM Menlo Park, CA November 28, 2017 at 11:30 AM Lake Forest, CA Intertek is hosting a complimentary lunch and learn session on the Medical Device Single Audit Program (MDSAP) and ISO 13485:2016. With ISO 13485:2003 and CMDCAS expiring, MDSAP is […]

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