Scientist - Early Product Development & Manufacturing
Hays AB / Biomedicinjobb / Mölndal
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hela Sverige Hays Life Science / Scientist - Early Product Development & Manufacturing / 6-month / AstraZeneca, Gothenburg
Hays Life Science is now looking for a Scientist - Early Product Development & Manufacturing for a 6-month consultant assignment at our client AstraZeneca in Gothenburg.
About AstraZeneca
At AstraZeneca, we unlock the power of What Science Can Do. Empowered to explore, every day we work towards our ultimate aim - treating, preventing, modifying and even curing complex diseases. Be part of the team where you are empowered to follow the science!
Pharmaceutical Sciences (PharmSci) is responsible for the design and development of synthetic routes, preclinical and phase I/II formulations, encompassing both small molecules and new modalities such as mRNA and oligonucleotides, across the whole range of AstraZeneca's therapeutic areas.
The manufacturing unit within Early Product Development and Manufacture (EPDM) in Gothenburg is accountable for manufacturing of a large and variable portfolio of early investigational medicinal products (oral solution/suspension, parenteral solutions, capsules, tablets and inhalers), mainly for Phases I and II. We supply drug product to AZ clinical studies globally and are a vital part to enable early phase clinical trials, delivering a critical step on the path from idea to patient. In short, we are the first in line to manufacture what could improve the lives of patients around the globe.
We are now looking for a Scientist starting as soon as possible, based in Gothenburg, Sweden.
Your new role
Within the EPDM manufacturing unit, in the GMP (Good Manufacturing Practice) arena, you will make an important contribution in delivering clinical results in the development of new medicines. This role revolves around the manufacturing of drug product where all activities below will have a significant impact on the speed, quality and cost of the AZ development portfolio.
We expect the successful candidate to:
• Assume responsibility toward timely manufacture of various drug products in line with the plans agreed within EPDM and surrounding stakeholders.
• Work with practical hands-on processes in our GMP facilities following manufacturing batch records and performing transactions in material management systems.
• Monitor, secure and follow up on other regulatory requirements according to GMP through associated IT-systems.
• Rapidly develop strong competence within relevant process technologies and build credibility and the ability to drive and secure product establishment, scale-up and clinical manufactures.
• Support documentation activities, e.g. by authoring manufacturing batch records, taking part in deviation investigations, authoring SOPs, and other guidance documents, change control processes etc.
• Assess records and report manufacturing and validation data accurately according to GMP.
• Ensure that SHE (Safety Health and Environment) and GMP standards are upheld and ensure AZ Policies and Standards are understood and followed.
• Be entrepreneurial and drive initiatives to further improve flexibility and productivity, resulting in shorter lead times or increased value for our customers and patients.
In joining EPDM and PharmSci, you will be part of an amazing group of skilled and driven colleagues who truly embrace team spirit, who you will exchange knowledge and collaborate with on many levels in various contexts. This provides excellent opportunities for your professional development, and possibilities to take on further accountabilities in line with your personal growth.
What you'll need to succeed
Do you have the essential qualifications for these roles?
We are looking for a Scientist with excellent collaboration, communication, and planning skills with a strong sense of responsibility, team work and delivery focus.
Strong verbal and documentation skills in English is a requirement. We expect you to have a keen interest to learn and operate complex manufacturing equipment and develop your expertise in pharmaceutical process technology. Experience from pharmaceutical development or working in a manufacturing or supply chain organisation and knowledge of cGMP is a merit for this role.
To be considered for this role, you need to have an M.Sc. in pharmacy/engineering and/or extensive GMP-manufacturing experience from the pharmaceutical industry.
What you need to do now
Are you already imagining yourself joining us? Good, because we can't wait to hear from you!
Welcome with your application; CV and cover letter.
If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now.
If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.
Additional information
BioPharmaceuticals R&D:
https://www.youtube.com/watch?v=pmFx_jr2eFoOur Gothenburg site:
https://www.astrazeneca.com/our-science/gothenburg.htmlCulture and atmosphere of the Gothenburg site:
https://www.linkedin.com/feed/update/urn:li:activity:6496327311678410752/ Ersättning Not Specified
Så ansöker du Sista dag att ansöka är 2023-11-03
E-post:
Hays.72702.3101@haysse.aplitrak.com Arbetsgivarens referens Arbetsgivarens referens för detta jobb är "900615".
Omfattning Detta är ett heltidsjobb.
Arbetsgivare Hays AB (org.nr 556640-6103)
Kontakt Linus Norrbom
Linus.Norrbom@hays.com +46706000967 Jobbnummer 8215044
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