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Pharmaceutical Research Associate - R&D \ Manufacturing \ GMP
Eingestellt von Sentinel IT LLP
Gesuchte Skills: Design, Client
Projektbeschreibung
Pharmaceutical Research Associate - R&D/Manufacturing/GMP (Senior)
Leading global pharmaceutical client require a Senior Research Associate with GMP/Manufacturing environment experience for a long-term contract in Belgium.
Responsibilities:
* Contribute to technical feasibility analysis of complex research and design concepts.
* Evaluate results relative to product requirements, definitions and/or program goals.
* Independently plan and execute a series of design and/or technical tasks that may not be well-defined, have multiple variables, and require advanced techniques within negotiated deadlines.
* Play a lead role in the evaluation, selection and adaptation of various techniques, which accomplish business objectives such as quality and cycle-time.
* Manage technical scale-up activities and transfers to plants.
* May provide training and supervision to junior members within the discipline. Routinely provide advice and assistance to team members regarding unique problems.
* Devise new approaches to complex problems through adaptations and modifications of standard technical principles. Incorporate new methods and technologies for improving existing or new products/processes.
* Maintain current knowledge of relevant regulatory requirements related to R&D (product development, process validation, design and safety) to ensulre compliance in all research, data collection and reporting activities.
* Maintain technical knowledge on manufacturing processes for various product families, technical platforms and plants.
* Improve and validate modifications of existing commercialized products. Lead remediation and investigation studies on marketed/new products.
* Develop budgets and activity schedules of limited scope.
* Develop an in-depth knowledge and understanding of GMP and related regulations and guidance.
* Build documentation for new products and changes on existing products in agreement with GMPs and regulations.
* Maintain focus on meeting both external and internal customer expectations.
Required Experience:
* Bachelors degree with 5-7 years experience or 3-5 years experience with Masters and 0-3 years experience with PhD
* GMP/Manufacturing environment experience
* Experience in the pharmaceutical industry
In addition to this, fluent French speaking would be highly desirable but not essential.
Please apply now for more details!
Leading global pharmaceutical client require a Senior Research Associate with GMP/Manufacturing environment experience for a long-term contract in Belgium.
Responsibilities:
* Contribute to technical feasibility analysis of complex research and design concepts.
* Evaluate results relative to product requirements, definitions and/or program goals.
* Independently plan and execute a series of design and/or technical tasks that may not be well-defined, have multiple variables, and require advanced techniques within negotiated deadlines.
* Play a lead role in the evaluation, selection and adaptation of various techniques, which accomplish business objectives such as quality and cycle-time.
* Manage technical scale-up activities and transfers to plants.
* May provide training and supervision to junior members within the discipline. Routinely provide advice and assistance to team members regarding unique problems.
* Devise new approaches to complex problems through adaptations and modifications of standard technical principles. Incorporate new methods and technologies for improving existing or new products/processes.
* Maintain current knowledge of relevant regulatory requirements related to R&D (product development, process validation, design and safety) to ensulre compliance in all research, data collection and reporting activities.
* Maintain technical knowledge on manufacturing processes for various product families, technical platforms and plants.
* Improve and validate modifications of existing commercialized products. Lead remediation and investigation studies on marketed/new products.
* Develop budgets and activity schedules of limited scope.
* Develop an in-depth knowledge and understanding of GMP and related regulations and guidance.
* Build documentation for new products and changes on existing products in agreement with GMPs and regulations.
* Maintain focus on meeting both external and internal customer expectations.
Required Experience:
* Bachelors degree with 5-7 years experience or 3-5 years experience with Masters and 0-3 years experience with PhD
* GMP/Manufacturing environment experience
* Experience in the pharmaceutical industry
In addition to this, fluent French speaking would be highly desirable but not essential.
Please apply now for more details!
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung, Medien/Design