Scientist Pharmaceutical Sci, Gothenburg, AstraZeneca

Job description
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 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/Senior Scientist starting as soon as possible with the location Gothenburg, Sweden.

Responsibilities
The role
Within the EPDM manufacturing unit, in the GMP arena, you will make an important contribution in delivering clinical results in the development of new medicines. 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.




Qualifications
Requirements / desired requirements for the matrix:
MSc in pharmacy/engineering
GMP-manufacturing experience from the pharmaceutical industry.
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.

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.

Do you have the essential qualifications for these roles?
We are looking for a Scientist/Senior 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 a MSc in pharmacy/engineering and/or extensive GMP-manufacturing experience from the pharmaceutical industry.







Application
Deadline: 2022-09-23, selection and interviews will be ongoing. The position may be filled before the last day of application, therefore, apply as soon as possible.

For more information:
Please contact Yonis Ismail,
Yonis.Ismail@randstad.se

About the company
About randstad life sciences.
Randstad Life Sciences is specialized in competencies within Life Science. As a consultant with us, you get a competitive salary, benefits, and collective agreements. Your consultant manager is always there for you and ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many activities.

With more than 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry and offers staffing, consulting and recruitment solutions in all areas of expertise. We also offer interim management, executive search and outplacement services. We have a broad network of clients and candidates, which means we convey hundreds of jobs within different industries all over Sweden. Our ambition is to be the best employer in the market.

By combining our passion for people with the power of today’s technology, we help people and organizations to reach their true potential. We call it Human Forward.