• Valais
• Posted about 16 hours ago

QA/Deviation Expert – 3-Month Contract   We’re looking for a reliable QA/Deviation Expert for a 3-month contract — 3 days/week on-site, 2 days home office.   This would be well suited to someone with experience in closing technical deviations for releasing batches related to drug substance.   You...

• Zurich
• Posted 2 days ago

Our global client is looking for a Medical Affairs consultant to join for an initial 6 month contract, working fully remote, 4-5 days a week, based in either the UK, Switzerland or New York. After the 6 month contract the role will either be extended or you would be offered a permanent contract. ...

• Posted 3 days ago

General Job Duties:   Quality Management & Compliance: Operates under the direction of the Director of Quality Operations to ensure compliance with our client's GMP Quality Management System program. Leadership & Communication: Serves as the backup for the Director of Quality Operations and maint...

• Feltham
• £60,000
• Posted 3 days ago

BioTalent is supporting a global cold chain logistics organisation seeking an International Business Development Manager to drive growth across pharma logistics, airfreight, and ocean freight. This role combines strategic account management with new business development, offering strong long-term...

• Switzerland
• Posted 7 days ago

QA Batch Record Reviewer – Pharmaceuticals  9 month contract - Valais. Open to Swiss residents + EU Citizens who can relocate.  Onsite (2 days home office possible)  BioTalent looking for a detail-oriented Batch Record Reviewer to join our team and help ensure every batch meets strict GMP and reg...

• United States of America
• Posted 13 days ago

A fast-growing healthtech organisation building AI-driven clinical tools to expand global healthcare capacity. Backed by $35M+ in funding, the team combines medical, engineering, and AI expertise to deliver scalable, patient-centric solutions.   At this role you will be offered A founding Data En...

• San Francisco
• Posted 14 days ago

Introduction Join a fast-growing HealthTech company building an AI-driven data platform designed to eliminate waste and inefficiency across the U.S. healthcare system. This is a rare opportunity to contribute to technology that directly improves care outcomes and transforms how health plans and p...

• Switzerland
• Posted 15 days ago

English Version QC Microbiology Laboratory Technician – Valais Join our QC Microbiology team in Visp! We’re looking for a Laboratory Technician (m/f/d) to support microbial identification (PCR, mass spectrometry) and endotoxin testing within our analytical group. What you’ll do: Perform and docum...

• Switzerland
• Posted 15 days ago

SME - QC Microbiology – Valais  Join our team in Visp as a SME - QC Microbiology Specialist, representing the department both internally and externally in customer meetings, audits, and inspections. Your responsibilities: Act as the technical and scientific SME for QC Microbiology within assigned...

• San Diego
• Posted 15 days ago

Join a mission-driven team building secure, innovative medical diagnostic technologies that improve lives every day. Our Diagnostics Software Engineering (R&D) team is seeking a Lead Product Security Engineer with strong medical device or instrument security experience to serve as the cybersecuri...

• New York
• Posted 21 days ago

Introduction Join a rapidly growing HealthTech organisation at the forefront of AI-driven communication in healthcare. This company is reimagining how clinics and providers engage with patients—using cutting-edge voice, language, and automation technologies to eliminate administrative bottlenecks...

• Santa Ana
• Posted 21 days ago

Position Summary We are seeking an experienced and strategic Regulatory Affairs Manager to support global regulatory submissions and compliance activities for our medical device portfolio. This role will be instrumental in driving regulatory strategies for both new product development and lifecyc...

• Westlake Village
• Posted 23 days ago

Position: R&D Sustaining Engineer Overview The R&D Sustaining Engineer will lead projects and provide technical expertise to ensure the continued reliability, compliance, and cost-effectiveness of existing medical device products. This role plays a vital part in supporting products throughout the...

• Ireland
• €80,000-95,000
• Posted 27 days ago

A high-growth pharmaceutical company is creating a new AI function to accelerate rare-disease drug commercialization. This is a greenfield role—you will design, build, and deploy AI automations from scratch, directly impacting regulatory, commercial, and operational workflows.   This Role Offers ...

• Holly Springs
• Posted 27 days ago

Job Title: Lockout/Tagout (LOTO) Technician Introduction Join a world-class biopharmaceutical manufacturing organization dedicated to safety, precision, and operational excellence. As a Lockout/Tagout (LOTO) Technician, you will play a critical role in ensuring the safety of personnel and complia...

• Holly Springs
• Posted 27 days ago

Job Title: Technician 3, Maintenance Introduction Join an innovative biopharmaceutical organization dedicated to operational excellence, safety, and reliability. As a Maintenance Technician 3, you will take a leadership role in maintaining, troubleshooting, and improving critical process equipmen...

• Holly Springs
• Posted 27 days ago

Job Title: Technician 2, Maintenance Introduction Join a world-class biopharmaceutical manufacturing organization committed to excellence, innovation, and patient safety. As a Maintenance Technician 2, you will play a vital role in ensuring that all process-related systems and equipment operate s...

• United States of America
• 250000
• Posted 28 days ago

About the Role Our client, a leading global medical communications agency, is seeking a dynamic and strategic Vice President or Senior Vice President of Client Services to join their expanding US leadership team. This is a newly created role driven by growth, offering the opportunity to lead majo...

• Visp
• Posted 29 days ago

Deutsch 12-Monats-Vertrag: Batch Record Reviewer (m/w/d) Standort: [Ort einfügen] Wir suchen eine engagierte Person, die als Batch Record Reviewer eigenverantwortlich Produktions- und Reinigungsprotokolle im pharmazeutischen Umfeld überprüft und Daten in Kontrollsysteme überträgt. Sie arbeiten en...

• San Diego
• Posted about 1 month ago

BioTalent is conducting a confidential search on behalf of a leading global CDMO who have been supporting top pharmaceutical and biotech companies for over 25 years. The organization operates multiple R&D and manufacturing sites globally and is known for its technical excellence and regulatory st...