Scientist/Senior Scientist to Drug Product Manufacture at AstraZ
Poolia Väst AB / Kemiingenjörsjobb / Göteborg
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Are you a scientist with good team working skills and the ability to operate independently to drive delivery of projects?
We are now looking to hire a Scientist/Senior Scientist to Drug Product Manufacture within Pharmaceutical Technology and Development for a consultant assignment. This role significantly contributes to the manufacturing of drug product in development phase for clinical studies. All below activities will have a significant impact on the speed, quality and cost of the AZ development portfolio.
AstraZeneca (AZ) is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. But we're more than one of the world's leading pharmaceutical companies. At AstraZeneca, we're proud to have a unique workplace culture that inspires innovation and collaboration. Here, employees are empowered to express diverse perspectives - and are made to feel valued, energized and rewarded for their ideas and creativity.
The consulting assignment will start 2017-09-01 or after agreement and go on to 2018-08-31.
Are you the one we are looking for? Apply now - The recruitment process is already ongoing!
Arbetsuppgifter
Pharmaceutical Technology and Development (PT&D) is accountable for delivering the design, innovative, efficient and robust processes for the manufacture of drug substance and product, the supply chain of products for safety and clinical trials and the generation of information and knowledge to ensure regulatory approval of new products.
Drug Product Manufacture (DPM) in Gothenburg manufactures investigational products (oral solution/suspension, parenteral solutions, capsules, tablets and inhalers) to AZ clinical studies mainly in phase I/II around the globe and is a vital part of the Pharmaceutical Supply Chain organization. At DPM in the GMP (Good Manufacturing Practice) arena you will make an important contribution in delivering clinical results and new medicines.
Main Duties and Responsibilities
This role significantly contributes to the manufacturing of drug product in development phase for clinical studies. All below activities will have a significant impact on the speed, quality and cost of the AZ development portfolio.
• Responsible for the timely and cost effective manufacture of drug product in line with the plans agreed within DPM, with focus on practical hands-on work in our pilot plant GMP facilities.
• Strong technical competence, credibility and ability to give assured technical direction.
• Set up Master Manufacturing Records and Batch Records and perform transactions in Warehouse Management System through the Supply Chain IT-systems.
• Assess record and report manufacturing and validation data accurately according to GMP.
• Ensure SHE (Safety Health and Environment) and GMP standards are upheld and ensure AZ Policies and Standards are understood and followed.
• Establish and recommend ways to improve flexibility and productivity, including new ways of working, resulting in shorter lead times.
• Monitor and track relevant Key Performance Indicators (KPIs).
Utbildning/erfarenhet
Essential Requirements
We are looking for a professional scientist with good team working skills and the ability to operate independently to drive delivery of projects.
MSc in pharmacy or engineering (specializing in Pharmaceuticals) or equivalent. Experience from pharmaceutical development or working in a manufacturing or supply chain organization is desired. You will have knowledge of cGMP and SHE and excellent documentation skills, both in English and Swedish. You will also have good understanding and interest in manufacturing equipment.
Förmåner
We take good care of our consultants and we offer social activities, as well as help in planning your future career. Your consultant manager is well experienced from your field, and knows how to get the most out of your assignment.
As a Poolia employee, you are included in the requirements concerning agreements on terms of employment by Unionen. Moreover, you get a grant for working out at your choice of place. You are also covered by a health insurance.
Företagsbeskrivning
Poolia Life Science can offer several opportunities for skilled people with a background in biochemistry, chemical engineering or science. We work with Sweden's leading pharmaceutical and life science companies. So whether you're interested in research, regulatory affairs, quality assurance, environmental and quality control, sales and marketing, or just want a career change, we have the job for you.
Working as a consultant suits whoever wants to get a lot of experience in a short period of time. We offer you the chance to work with well-known brands at renowned companies where you can develop your skills. If you're looking for a world of exciting assignments and new contacts, you'll like being a consultant.
Vår kunds hemsida
www.astrazeneca.com Sluttext
Does the consulting assignment sound interesting for you? Please apply even if you do not meet all minimum requirements and key factor requirements. In this recruitment, we will prioritize your personal qualities: social, earthy, team player, and curious together with your true passion for AstraZeneca and their medical products.
Language
en-GB
Varaktighet, arbetstid
Heltid Visstid, mer än 6 månader
Publiceringsdatum2017-06-15ErsättningFast lön
Så ansöker duSista dag att ansöka är 2017-06-25
Ange följande referens när du ansöker: 47061
Klicka på denna länk för att göra din ansökanKontaktJenny Lundkvist
jenny.lundkvist@poolia.seFöretagPoolia Väst AB
AdressPoolia Väst AB
Kungsgatan 42
41115 Göteborg
KontorsadressKungsgatan 42
Jobbnummer 3559610
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