All jobs everywhere

• Atlanta
• Negotiable
• Posted 2 days 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...

• Burlington
• Negotiable
• Posted 2 days 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 2 days 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 3 days 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 3 days 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 3 days 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 4 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...

• Tokyo
• Negotiable
• Posted 5 days ago

Join a forward-thinking and revolutionary company that is changing the landscape of the biotech sector! Our partner, a prominent biomedical firm, is committed to making a significant difference in the realms of biological research and healthcare. Job Title: Field Engineer Location: Tokyo, Japan R...

• Osaka
• Negotiable
• Posted 5 days ago

Become part of an inventive and trailblazing organization that is transforming the biotech industry! Our client, a top-tier medical device company, is dedicated to making a substantial impact on biological research and medicine. Job Title: Field Engineer Location: Osaka, Japan Responsibilities: P...

• Tokyo
• Negotiable
• Posted 5 days ago

Join a forward-thinking and revolutionary company that is changing the landscape of the biotech sector! Our partner, a prominent biomedical firm, is committed to making a significant difference in the realms of biological research and healthcare. Job Title: Field Engineer Location: Tokyo, Japan R...