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Quality Assurance & Validation - Medical Device

​Quality Assurance (QA) is an essential part of the pharmaceutical industry, with responsibility for ensuring that pharma products consistently meet the required standards and regulations and are safe for use. QA is a broad field encompassing any aspect that may affect a drug's quality during its research, development, manufacturing, and sales phases. MSI Pharma recruit for permanent and contract Quality Assurance, Quality Control and Validation jobs for pharmaceutical and life sciences companies across the world.

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Latest jobs in Quality Assurance & Validation - Medical Device

MSI Pharma is engaged globally, placing candidates within the Life Sciences industry.

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Medical Device

Auditors - Medical Device Clinical Research - Medical Device Materiovigilance - Medical Device Medical Communications - Medical Device Pharmacovigilance - Medical Device Quality Assurance & Validation - Medical Device Regulatory Affairs - Medical Device Research & Development - Medical Device Technical Operations - Medical Device Technical Specialists - Medical Device Technical Writers - Medical Device
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Contracts Specialist

Negotiable | United States of America

Commercial Contract Specialist, USA - remote, Contract - Ongoing, Competitive Pay Rate!Key Responsbilities include: First point of contracts triaging and assessmentManaging, organizing, and storing electronic versions of documentsEnsuring that contracts are executed properly and uploaded in a timely manner to contract management systemDraf...

Warehousing Supervisor

Up to US$50 per hour | Illinois

MSI Pharma is currently helping one of our global Pharma clients based in Kankakee look for a Distribution Warehousing Supervisor. The Distribution Specialist will be responsible for daily functions of the department, such as inbound deliveries, associated manufacturing orders, and inventory tasks. The Warehousing Supervisor will supervise activities to ensure a safe, timely and efficient environment of the Warehouse operators which includes shipping, receiving, in...

Veeva Vault

US$50 - US$65 per hour | California

System administration in Veeva Vault: Solution and/or maintain system workflows management of system access and permissions design solutions and manage configuration configure and manage integrations to Vault platform perform change management activities in support of vendor enhancements and customer requirements participate in the development of solutions and manage project/change timelines liaise with users to resolve issues oversee Veeva managed services resources define and o...

Computer System Validation Engineer

€70 - €100 per hour | Switzerland

We are hiring a Computer System Validation Engineer for a leading Pharmaceutical company in Switzerland. The essential responsibilities required are: Assess and lead the CSV package(s) on an assigned project. Taking accountability for the work to be produced by yourself and other colleagues that are under the assigned packages lead by this position.Hands on: Plan, coordinate and execute all phases for computer system validation of production and QC ...

CMC Regulatory Affairs

Negotiable | United States of America

MSI Pharma are looking to hire a CMC Regulatory Affairs Specialist for a US based pharmaceutical firm. This is a contract role and can be worked fully remotely from anywhere in the USA.In this role you will:...

Biomarker Operations Project Manager

Negotiable | United States of America

MSI Pharma are looking to hire a Biomarker Operations Project Manager for a Top US Biotech Organisation based on the West Coast. This is a contract role and can be worked full remotely anywhere in the USA, or on site if you live locally. In this role you will:Provide project management support for Scientists for non c...

Therapeutic Area Strategy Lead

Competitive | United States of America

MSI are working with a well known Global Pharmaceutical company to source an experienced Safety Physician to join their team as a Therapeutic Area Strategy Lead. The main responsibilities of this role are:- Deputize for the TA Head: - In times of absence or unavailability - Matrix Leadership of Global Safety Officers (GSO) - Maintain Therapeutic Area expertise, product portfolio-specific expertise and ongoing assessment of therapeutic areas, competitive drugs an...

Global Labelling Associate

Negotiable | United States of America

We are currently hiring a Global Labelling Associate (GLA) for one of our global Pharmaceutical clinets to support their end-to-end non-US/Central EU (Most of World) labeling development and implementation. This position provides innovation and technical expertise for the creation, maintenance and implementation of labeling to meet country-specific regulatory requirements and effectively manages labeling operations globally. As a GLA, you would:- Ass...

PV Case Management Head

Competitive | United States of America

MSI are working with a globally recognised pharma company to help source a PV Case Management Head. The client are looking for someone with significant global experience and a strong knowledge of the case management and medical safety evaluation in clinical trial and marketed products. Responsibilities for this role include: · To improve and reinforce globally integrated case management standards, procedures, and systems in line with changes in the regulatory environment and best ...

Sr Safety Physician

Competitive | United States of America

We are seeking a Senior Safety Physician for one of our international biotech companies. They are looking for someone with demonstrated experience answering challenging questions from health authorities and someone with in-depth knowledge of scientific data....

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