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• Atlanta
• Negotiable
• Posted about 9 hours ago

Director of Quality - Med Device Location: Raleigh, NC Working situation: Hybrid Level: Director Our client, a large, successful med device company and is looking to add to their Quality team! The Director - Quality Assurance will help lead the Quality department and oversee all aspects of Qualit...

• Morristown
• Negotiable
• Posted about 9 hours ago

Quality Systems Manager As the Quality Systems Manager, you will play a pivotal role in championing daily activities for quality excellence. You will develop, implement, and enforce quality systems that meet the highest standards, including FDA Drug and Medical Device regulations, customer requir...

• Burlington
• Negotiable
• Posted about 9 hours ago

Overview: QA Leader to support the quality management systems and processes for a CRO based in Burlington. Working within pharma in both biologic development and cell and gene therapy and reporting directly to the Senior Director of Global Compliance. Role Responsibilities: Shape and expand our U...

• Boston
• US$120001 - US$170000 per year
• Posted about 10 hours ago

SUMMARY This clinical-stage biopharmaceutical company is looking for an innovative scientist with a strong background in Upstream Process Development to oversee the development of all upstream technical activities for their lead vaccine program. They will also be expected to oversee CRO/CDMOs to ...

• Boston
• US$150000 - US$170000 per annum
• Posted about 15 hours ago

Manager, Analytical Development - Medical Devices Location: Boston Working situation: On-Site Level: Manager Our client is a medical device company pursuing research into exciting combination products and therapies looking for a Manager Analytical Development with a passion for curing and enhanci...

• California
• Negotiable
• Posted 1 day ago

Title: Regulatory Affairs Manager Location: San Jose, CA Base Salary: $140,000-$190,000 About: Currently working with a medical device company dedicated to developing and commercializing breakthrough catheter devices that revolutionize patient care on a Regulatory Manager position. In this critic...

• Raleigh
• US$110000 - US$125000 per annum
• Posted 1 day ago

Validation Lead Location: Raleigh, NC Working Situation: Hybrid A global speciality pharmaceutical company is looking to bring on a Validation Lead to support the global quality organization. You will be supporting tech transfer and validation activities while also working cross-functionally to s...

• Cambridge
• Negotiable
• Posted 2 days ago

Senior Compliance Auditor Role Description: Oversee and participate in audits, reporting on findings. Manage Quality Technical Agreements with critical suppliers. Conduct internal audits to meet GMPs, 820 standards, and company requirements. Lead and support supplier audits (onsite and remote) fo...

• Minneapolis
• US$70000 - US$75000 per year
• Posted 3 days ago

Summary: The Quality Systems Specialist II is tasked with implementing Quality System requirements for designated processes, encompassing Change Control, Post Market Quality, Nonconforming Material Handling, CAR/CAPA, Equipment/Gage Calibration & Preventive Maintenance, Environmental Controls, Re...

• United States of America
• Negotiable
• Posted 3 days ago

Senior Clinical Trial Manager San Diego, CA (Hybrid) $160,000 - $180,000 Job Description EPM is partnered with a trailblazing biotech nestled in sunny San Diego, dedicated to pioneering breakthroughs at the intersection of oncology and immunology. Leveraging cutting-edge research and innovative t...