• Vista
• 130,000
• Posted about 1 hour ago

Looking for an experienced Regulatory & Quality Assurance Supervisor to help us maintain compliance and drive excellence in our QMS. This role is perfect for someone who thrives in dynamic environments and wants to make a direct impact on patient safety and product quality.   What you’ll do: Serv...

• Posted about 4 hours ago

Radiochemist I/II Department: Isotrak Production Location: Atlanta General Job Duties In this role, you will be responsible for a variety of tasks related to the production of radiochemical materials. Your duties will include: Manufacturing calibration standards, check sources, and PE samples. Pr...

• Vista
• $80.00-$95.00/hr
• Posted about 6 hours ago

Key Responsibilities Serve as the designated Management Representative for quality and regulatory compliance matters. Lead preparation for, host, and directly interface with FDA, ISO, and Notified Body audits; manage corrective actions and close-outs. Assess, streamline, and optimize the company’...

• Oberdorf
• Posted about 8 hours ago

Quality Inspector Summary Ensure products meet internal and external specifications through inspections, testing, batch release, and records management. Responsible for first article inspection, 3D CMM programming/use, and calibration activities. Key Responsibilities Perform inspections on finish...

• Huntington Beach
• Posted 1 day ago

Manufacturing Engineer II Our client is seeking a highly motivated Manufacturing Engineer II to drive manufacturing process analysis, improvement, and validation, with a focus on implantable devices. This role will collaborate closely with management, internal engineers, and external vendors to e...

• Huntington Beach
• Posted 1 day ago

IT Manager Our client is seeking an IT Manager to serve in a multidisciplinary role, collaborating across the business to plan, design, implement, and maintain a secure, scalable, and compliant IT infrastructure. This is a critical position responsible for safeguarding sensitive data, protecting ...

• Pompey
• Posted 1 day ago

About the Role We are seeking a mid-level Computer System Validation (CSV) Engineer to join our project team on a 6-month contract. The successful candidate will be heavily involved in the execution phase of the project, delivering validation of GxP computerized systems in line with regulatory an...

• Pompey
• Posted 1 day ago

About the Role We are seeking a mid-level Commissioning, Qualification & Validation (CQV) Engineer to join our project team for a 6-month contract. The successful candidate will be focused on the execution phase of a large-scale project, with heavy involvement in IQ, OQ, and PQ activities. This i...

• Belgium
• Posted 6 days ago

Overview: Our client, a leading pharmaceutical manufacturer, is seeking an experienced CQV/CSV Engineer with a strong background in Automated Visual Inspection (AVI) systems for parenteral vials in a fill-finish environment. The successful candidate will be responsible for delivering full lifecyc...

• United States of America
• Posted 7 days ago

We are partnering with a leading global biopharmaceutical organisation committed to developing life-changing medicines for patients with serious diseases. Their mission is to innovate through science, delivering solutions where limited or no therapeutic options exist. With a diverse portfolio spa...

• Visp
• Posted 8 days ago

BioTalent are uniting with a progressive and patient-focused partner of organisations within the pharmaceutical and biotech spaces! They are searching for a Lead Warehouse & Logistics to join their world-class team in Visp, Switzerland.   This role will offer you The opportunity to play a key rol...

• United Kingdom
• Posted 9 days ago

We are partnered with a global biopharmaceutical organisation dedicated to transforming the lives of patients and their families. With a strong commitment to delivering life-changing medicines for serious conditions — often where limited or no therapeutic options exist — this company combines a d...

• United Kingdom
• 60,000-95,000
• Posted 9 days ago

We are working with a global biopharmaceutical organisation dedicated to transforming patient outcomes through pioneering research and development. With a strong focus on serious and complex conditions, this company combines advanced science, innovative technologies, and a patient-first approach ...

• Irvine
• Posted 12 days ago

PROJECT MANAGER We're seeking a Project Manager to join our team at a small, innovative Class III medical device company specializing in breakthrough MedTech products. The ideal candidate is a mid-level professional with a proven track record of managing projects through design verification (DV) ...

• Irvine
• Posted 13 days ago

Principal Design Quality Engineer   Our client is seeking an experienced Principal Design Quality Engineer to join their team in Irvine, CA. This client is a team of passionate engineers and visionaries dedicated to incubating breakthrough ideas into medtech startup companies. They focus on impro...

• San Diego
• 180,000
• Posted 14 days ago

Join a dynamic team focused on advancing cardiac arrhythmia therapy. You’ll work at the system level, integrating hardware and software for cath lab environments and collaborating across R&D, QA, and regulatory teams.   What You’ll Do: Engineer integrated hardware/software systems targeted for ca...

• United States of America
• 180,000
• Posted 14 days ago

We’re seeking a motivated Electrical Engineer to join our growing team and contribute to the development of innovative medical technologies. This is an exciting opportunity to work on a dynamic project already in motion, where your contributions will have an immediate and meaningful impact.   💡 W...

• Posted 18 days ago

About the Job   Location: 100% ONSITE - Westlake Village, CA Our client's mission: To improve the quality of life for women! A message from the hiring manager: We are looking for a recent MBA graduate (within 2 years) with a strategic and analytical mindset to support our client's M&A integration...

• Denmark
• Posted 18 days ago

Product Owner – Drug Product Tech Transfer Hillerød, Denmark Full-time | On-site A global CDMO is hiring a Product Owner to join their newly formed Drug Product & Finished Goods Tech Transfer team. This is a key role supporting strategic and timely tech transfers related to formulation, sterile f...

• Braine-l'Alleud
• Posted 20 days ago

A global life science organisation at the forefront of scientific innovation is seeking a proactive and solution-oriented Digital Technology Expert to join its Digital Technology team. This is a unique opportunity to lead the implementation and management of digital solutions that support Researc...