Scientist – Early Product Development and Manufacturing

Publiceringsdatum: 2025-05-20

Letar du efter anställning inom hälso- och sjukvård? Ett spännande jobb som apotekare hos Randstad AB väntar på dig - varför inte söka idag? Intresserade sökes för heltid-jobb hos Randstad AB - är du intresserad? De letar efter någon som vill jobba 6 månader eller längre.

Mölndal är platsen där detta jobb har sin tjänsteort. Om du tycker att det låter intressant att börja jobba hos Randstad AB i rollen som apotekare så har de just nu en ledig tjänst som skulle kunna vara en perfekt match för dig! Du har fortfarande tid att söka jobbet som apotekare hos Randstad AB om du sickar in din ansökan senast sista ansökningsdag som är fredag den trettionde maj 2025.

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Jobbannons

Job description

Are you ready to make a significant impact on the development of new medicines? Join us at AstraZeneca's Early Product Development and Manufacture (EPDM) unit in Gothenburg, Sweden. We are accountable for delivering a vast portfolio of early investigational medicinal products, supplying different types of clinical trial material to studies across the globe. This is your chance to explore and innovate in our dynamic environment!

This is an exciting opportunity to join our Pharmaceutical Sciences department which is accountable 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 role will be offered at Scientist level.

What you will do:

As part of the EPDM manufacturing unit, you will work in a GMP (Good Manufacturing Practice) environment, contributing to the delivery of clinical results. Your role will focus on the manufacturing of drug product, with responsibilities including timely manufacture of various drug products, working with practical hands-on processes in our GMP facilities, monitoring regulatory requirements, supporting documentation activities, and driving initiatives to improve flexibility and productivity. As we are investing in innovative technology, among others within Continuous manufacture, we need to expand knowledge and competence in this area. Depending on prior experience and interest this role could be more adapted to this area.

This is a consultant assignment starting in August with Randstad Life Sciences. Randstad Life Sciences is specialized in competences within Life Science. As a consultant you get a competitive salary, benefits and collective agreements. Your consultant manager 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 social activities.

Deadline 2024-05-30 - the selection process and interviews will be ongoing, so please apply as soon as possible!

Responsibilities

• Work with practical hands-on processes in our GMP facilities following manufacturing batch records and perform transactions in material management systems.
• Assume responsibilities toward timely manufacture of various drug products in line with the plans agreed within EPDM and surrounding stakeholders.
• 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.

Why AstraZeneca?

At AstraZeneca, we follow the science to explore and innovate. We are unlocking the power of what science can do, working towards treating, preventing, modifying and even curing some of the world's most complex diseases. If you're driven by curiosity and courage, inspired by the possibility of doing things that have never been done before, this is the place for you.

Qualifications

Essential for the role:

• MSc or BSc in pharmacy/engineering or extensive GMP-manufacturing experience from the pharmaceutical industry
• Excellent collaboration, communication, and planning skills
• Strong sense of responsibility, teamwork and delivery focus
• Strong verbal and documentation skills in English
• Experience from pharmaceutical development or working in a manufacturing or supply chain organisation and knowledge of GMP is a merit for this role.
• Keen interest to learn and operate complex manufacturing equipment

About the company

Randstad

At Randstad, we see the possible in people. With business all over Sweden and in all areas of expertise, we help people find work that feels good, where they get the opportunity to develop and realize their true potential.

With close to 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry. Our mission is to become the world’s most valued working life partner. By combining our passion for people with the power of today’s technology, we support people and organizations in realizing their true potential. We call it Human Forward.