Quality Assurance Advisor, AstraZeneca
Poolia Väst AB / Apotekarjobb / Mölndal
Observera att sista ansökningsdag har passerat.
Visa alla apotekarjobb i Mölndal,
Göteborg,
Partille,
Härryda,
Kungsbacka eller i
hela Sverige Visa alla jobb hos Poolia Väst AB i Mölndal,
Göteborg,
Partille,
Härryda,
Kungsbacka eller i
hela Sverige Presentation
Are you interested in a challenging opportunity within Quality Assurance, for one of the world's leading pharmaceutical companies? We are happy to announce that we are now hiring a Quality Assurance Advisor to AstraZeneca within the function of Pharmaceutical Development.
You will have a broad range of responsibilities, the possibility to influence and to contribute to the pharmaceutical development function, and the delivery of our pipeline of exciting new medicines.
AstraZeneca is a global, innovation-driven pharmaceutical company focusing on the discovery, development and commercialization of novel medicines. At AstraZeneca, we are proud to have a unique culture that inspires innovation and collaboration both within the company and with external partners. 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 in the beginning of June and go on for 12 months.
Are you the one we are looking for? Apply now - The recruitment process is already ongoing.
Arbetsuppgifter
The arena:
Pharmaceutical Development is the function within AstraZeneca that designs and delivers the active drug product required to support new medicines. The Quality Assurance group within Pharmaceutical development now wants to take in Quality Assurance contractors with a Good Manufacturing Practice (GMP) focus. AstraZeneca's Pharmaceutical Development organization deals with all facets of the process of turning a new chemical entity (NCE) into a medicine which can be safely and effectively used by patients. The Quality Advisor role has a broad range of responsibilities to ensure internal and external requirements are fulfilled for AstraZeneca projects in the development phase. Interactions occur among various internal functions and sites, but also with vendors and suppliers.
The role:
In your work as a Quality Advisor at AstraZeneca you will have a broad range of responsibilities, the possibility to influence and to contribute to the pharmaceutical development function, and the delivery of our pipeline of exciting new medicines.
• Provide QA advise into Pharmaceutical Development internal/external manufacturing activities for Drug Product
• QA release of internally/externally manufactured and packed Drug Product as part of the Supply Chain to clinical trials
• Support the Pharmaceutical Development functions with investigations of deviations and other quality and compliance decisions having a major impact on AstraZeneca development projects
• Provide Pharmaceutical Development projects with QA support, such as GMP risk assessment and interpretation of GMP regulations
• Provide appropriate QA input to business improvement projects
• Close collaboration with AstraZeneca QA colleagues globally
The role may also include:
• Responsible for QA approval of documentation related to manufacturing equipment and facilities to ensure compliance, including maintenance, calibration, validation and change control
• Interpret, trend and report compliance data, to measure and improve quality standards within Pharmaceutical Development.
• Developing QA Agreements with suppliers or contractors delivering services or products to the Pharmaceutical Development Supply Chain.
Utbildning/erfarenhet
Minimum requirements - Education and Experience:
• MSc in pharmacy or engineering (specializing in Pharmaceuticals) with at least 3 years' experience of working within a pharmaceutical GMP environment
• Broad understanding of Quality Systems and GMP
• Comprehensive understanding of the pharmaceutical/drug development process
• Good communicator with experience of interacting effectively across interfaces
• Fluent in written and spoken English
Preferred requirements:
• Experience preferably within a pharmaceutical manufacturing organization
• Good team working and networking skills
• Capable of making effective decisions
• Demonstrate a high degree of personal credibility
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.se Sluttext
Are you the one we are looking for? Apply now - The recruitment process is already ongoing.
Language
en-GB
Varaktighet, arbetstid
Heltid Visstid, mer än 6 månader
Publiceringsdatum2017-05-19ErsättningFast lön
Så ansöker duSista dag att ansöka är 2017-05-26
Ange följande referens när du ansöker: 46812
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 3511011
Observera att sista ansökningsdag har passerat.