Pharma jobs

• Japan
• £36000 - £60000 per annum + plus annual bonus
• Posted 5 days ago

Medical Device Auditor / 医療機器品質マネジメントシステム監査人 Japan (home based) 医療サービス・IVDに関する知識と経験を活かして、日本の医療の安全を守る道を歩みませんか？ 私たちのクライアントは、クライアントが直面する潜在的な課題に精通している専門家になるために、最高の審査員の採用とトレーニングに多額の投資をしています。当社の監査人はまた、グローバル顧客満足度調査で非常に高いスコアを獲得しており、最高品質の監査を提供しています。 Do you want to build on the experience you have and lear...

• Île-de-France
• €50000 - €60000 per annum
• Posted 5 days ago

Medical Device Auditor France (home based) Do you want to build on the experience you have and learn what it really takes to get a device on to the market? Have you ever considered working for a notified body? MSI Pharma are representing a market leading MDR/ IVDR designated notified body who con...

• Colorado Springs
• Up to US$95000 per annum
• Posted 5 days ago

Medical Device Auditor Colorado, USA Do you want to build on the experience you have and learn what it really takes to get a device on to the market? Have you ever considered working for a notified body? MSI Pharma are representing a market leading MDR/ IVDR designated notified body who continues...

• California City
• Up to US$95000 per annum
• Posted 5 days ago

Job Title: Medical Device Auditor Location: California, USA Do you want to build on the experience you have and learn what it really takes to get a device on to the market? Have you ever considered working for a notified body? MSI Pharma are representing a market leading MDR/ IVDR designated noti...

• Union
• Negotiable
• Posted 18 days ago

MSI Pharma are working with a growing oncology focused bio tech to hire 2 freelance safety physicians - one US based & one European based. We are looking for candidates with the following profile; MD/MBBS with clinical experience 8+ years global safety experience in a clinical development The rol...

• England
• £100 - £120 per hour
• Posted 18 days ago

MSI Pharma are working with a global bio-pharma to source a global safety physician for a 6 month project in the UK The role will be working on a Phase III Rare disease study so Clinical development safety experience is a must. You will: Be required to be a key contributor and assessor of the ben...

• Bristol
• Negotiable
• Posted 18 days ago

My client in the South-East of England, urgently require an experienced SCADA Automation engineer with Wonderware (Archestra) and some Siemens experience, to join a team working on their new state of the art manufacturing plant. The role will be to interrogate the CIP and SKID / SCADA package to ...

• England
• £65 - £80 per hour + Home working
• Posted 18 days ago

(REMOTE WORKING) Life science consulting company based in London require a Lead design ICSR consultant with 5+ years ICSR process management experience. Within this role you will own the end to end ICSR (Individual Case Safety Reports) process from a technical implementation viewpoint. (REMOTE WO...

• England
• £65 - £80 per hour + Home working
• Posted 20 days ago

(REMOTE WORKING) Life science consulting company based in London require a Lead design ICSR consultant with 5+ years ICSR process management experience. Within this role you will own the end to end ICSR (Individual Case Safety Reports) process from a technical implementation viewpoint. (REMOTE WO...

• East London
• £350 - £500 per day
• Posted 21 days ago

Life science consulting company based in London require a remote ICSR consultant with previous Case processing, Data entry and ICSR process management experience of a minimum of 5 years' experience. You will also require Knowledge of Regulations around PV and you would need an appreciation of Aut...

• East London
• £350 - £500 per day
• Posted 21 days ago

Life science consulting company based in London require a remote ICSR consultant with previous Case processing, Data entry+ ICSR process management experience of a minimum of 5 years. You will also require Knowledge of Regulations around PV and you would need an appreciation of Automation and und...

• East London
• £350 - £500 per day
• Posted 21 days ago

Life science consulting company based in London require a remote ICSR consultant with previous Case processing, Data entry+ ICSR process management experience of a minimum of 5 years You will also require Knowledge of Regulations around PV and you would need an appreciation of Automation and unde...