Quality Assurance & Validation - Pharma jobs

• England
• £50 - £65 per hour
• Posted about 18 hours ago

As the Project Manager for IT Clinical Insights projects (External), you will we be responsible for project management activities in projects focusing on delivering advanced analytics and visualisation for teams in clinical domain. The role can be based Globally. Your main responsibilities As the...

• Braine-l'Alleud
• Negotiable
• Posted about 18 hours ago

MSI Pharma is partnering with a global biopharmaceutical company, and one of the world leaders in cutting-edge scientific research on a Cleaning Validation Engineer role. Start date: ASAP Duration: 3 Month Contract (Possibility of Extension) Location: Braine-l'Alleud, Belgium This is a collaborat...

• North Carolina
• Negotiable
• Posted about 18 hours ago

A global biotechnology organisation based in North Carolina is looking for a Quality Control Analyst to join the team on an initial 12-month contract. Responsibilities The primary responsibilities for this position include performing various tasks associated to QC support. Be responsible for ensu...

• Hopewell
• Up to US$50 per hour
• Posted 26 days ago

Job Title:QA Document Coordinator Duties: Assist with site documentation needs ensuring GMP compliance of day-to-day operations. Support Document Control Team with the formatting of procedural and technical documents, MBRs, and other GMP related documents. Process documents through the Veeva Qual...

• Braine-l'Alleud
• Negotiable
• Posted 26 days ago

Well-respected Biotech in Belgium need a VQL for an initial 12-month assignment to Join their dynamic team, driving strategic and operational Quality Assurance activities for Global Vendors in GMP manufacturing. You will Collaborate with internal stakeholders, manage deviations, KPIs, Quality Agr...

• Liverpool
• Negotiable
• Posted 26 days ago

Professional Automation Engineer role within the Liverpool site Automation Team responsible for the delivery of multiple PCS7/HMI/PLC upgrade projects. The role will involve execution of approved projects and development of new project proposals as part of the site's long term sitewide strategy t...

• Switzerland
• Negotiable
• Posted 26 days ago

MSI Pharma are working together with a multinational manufacturing company in Switzerland seeking an experienced Quality Assurance specialist CSV. Key Responsibilities Responsible for Computerized System Validation (CSV) deliverables for new Large Scale Mammalian facilities, equipment and utiliti...