Scientist – Early Product Development and Manufacturing to AstaZeneca

Scientist – Early Product Development and Manufacturing to AstaZeneca

Arbetsbeskrivning

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.

OM TJÄNSTEN
The manufacturing unit within Early Product Development and Manufacture (EPDM) in Gothenburg is accountable for manufacture 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 with the location Gothenburg, Sweden.

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

ARBETSUPPGIFTER
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 responsibilities 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 perform 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 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.


VI SÖKER DIG SOM
- MSc in pharmacy/engineering
- Strong verbal and documentation skills in English is a requirement.
- Desirable with experience from pharmaceutical development or working in a manufacturing or supply chain organization.
- Desirable with knowledge of cGMP.

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Other information


* Start: As soon as possible
* Extent: Full time
* Location: Mölndal


The recruitment process is handled by Academic Work and our client wishes that all quiestions regarding the role is handled by Academic Work. We work with an ongoing selection and the advert might be closed before the role is filled if we have moved forward to the selection and interview phase.

INFORMATION OM FÖRETAGET
View more about AstraZeneca as a company here

Kontaktpersoner på detta företaget

Sara Frykedal

Consultant Manager Fanny Rosén
08-52257636
Fanny Rosén

Mette Risberg
0736448575
Hedvig Svärd

Konsultchef Catrin Laudon

Sara Frykedal
08-52257605
Fredrik Bardon

Konsultchefsassisten Anna Bengtsson
08-12 05 2224
Konsultchef Lisa Nordell
0812052231

Sammanfattning

  • Arbetsplats: Academic Work
  • 1 plats
  • 6 månader eller längre
  • Heltid
  • Fast månads- vecko- eller timlön
  • Publicerat: 5 januari 2023
  • Ansök senast: 5 februari 2023

Besöksadress

Lindstedtsvägen 24
Stockholm

Postadress

Lindstedtsvägen 24
Stockholm, 11428

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