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AstraZeneca - Quality Assurance Specialist, through KellyOCG
KellyOCG Sweden AB
Ingenjörer och tekniker inom kemi och kemiteknik

Are you ready to make an impact on the future of medicine? KellyOCG, a global talent solutions provider, is seeking a Quality Advisor (QA Specialist) on behalf of our partner, AstraZeneca. The 12-months long contract position (with possibility for extension) is based onsite in Gothenburg/Mölndal, Sweden, where you will be completely integrated with the AstraZeneca team, reporting directly to the onsite manager. The arena Are you interested in a challenging opportunity within the Development Quality function in one of the world’s leading pharmaceutical companies? The Development Quality function is responsible for quality oversight of the pharmaceutical development activities within AstraZeneca. We are now looking for a Quality Advisor with GMP focus to our Gothenburg team. AstraZeneca’s pharmaceutical development organizations manage all facets of the process of turning a molecule into a medicine which can be safely and effectively used by patients. The Quality Advisor role has a broad range of responsibilities to ensure all internal and external requirements are fulfilled for the AstraZeneca projects in the development phase We have an exciting opportunity for a 12 months temporary assignment as Quality Advisor, in the Site Quality Gothenburg team, who’ll be the prime source for quality & compliance advice and providing quality support to the science functions and throughout the drug development process chains. This is a great opportunity for you who are strong in quality and like to work close to development, Good Manufacturing Practice and making sure quality is assured when delivering new products. The role Working in the Site Quality team means you will work closely with the internal assets/facilities, teaming up with the pharmaceutical development functions and be involved in cross business processes. To build strong relationships with these functions knowing their business is key, to give support to projects and develop ways of working that builds for success. The ability to interpret and trend compliance data to measure and improve quality standards is key. You will develop and maintain a knowledge of the quality regulations and guidelines applicable to your area and a deep scientific understanding of the products that you are supporting. Whilst taking on your own specialist areas and making good quality decisions, you will be encouraged to think strategically and use your problem solving skills to resolve any quality issues. You will participate and contribute to continuous improvement projects with the aim to standardize and simplify our internal processes. Typical Accountabilities: • Responsible for quality release of manufactured Drug Product, Investigational Medicinal Product for clinical trials • Support the pharmaceutical development functions with investigations of deviations, changes and other quality and compliance decisions in the development projects related to drug product • Providing proactive quality advice to support the development, implementation and continuous improvement of GMP quality systems across the Clinical Supply functions and support implementation of agreed global standards • Operate as part of a global organisation with an integrated mindset to create an organisation with common processes and ways of working 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 • Demonstrates understanding of international quality systems regulations, concepts, industry practices to adopt best in class processes • A comprehensive understanding of GMP regulations, the pharmaceutical development process and supply chain process would be advantageous • Experience of interacting effectively across interfaces collaborating internally in a good communicative way • Fluent in written and spoken English Required soft skills: • Ability to work in a fast-paced environment, meet deadlines, and balance multiple priorities. Independently motivated, detail-oriented, and "can-do" attitude • Excellent team working and networking skills and encourages team effectiveness • A good communicator with experience of interacting effectively across interfaces collaborating internally Latest application date is February 13th, but we review applications continuously, and could proceed with candidates before the last application date. About AstraZeneca Gothenburg Hub Our stunning campus in Gothenburg is one of AstraZeneca’s three strategic science centers. The site is home to over 2,500 employees, from 50 different nationalities. Gothenburg includes the complete range of functions, and as such offers plenty of development opportunities for a wide range of professionals. Our science teams in Gothenburg collaborate with academic and industry partners in Sweden and globally. And the site itself has been designed with collaboration in mind. From the Coffee Lab to exercise areas, we’ve built a series of environments where innovation can happen.

2 dagar sedan
Sista ansökan:
13 februari 2025
AstraZeneca - Quality Assurance Partner, through KellyOCG
KellyOCG Sweden AB
Ingenjörer och tekniker inom kemi och kemiteknik

Are you ready to make an impact on the future of medicine? KellyOCG, a global talent solutions provider, is seeking a Quality Assurance Partner, on behalf of our partner, AstraZeneca. The 12-months long contract position (with possibility for extension) is based onsite in Gothenburg/Mölndal, Sweden, where you will be completely integrated with the AstraZeneca team, reporting directly to the onsite manager. Quality Assurance Partner- Associate Director Validation Join us in our Site Quality Team! We provide Quality oversight in the development of Investigational products and have the responsibility for Licence to Operate at our development site and play an important part in the commercialisation of new medicines. Development Quality is a Global group, with teams located in Gothenburg (Sweden), Macclesfield, (UK) and Durham (North Carolina, US). With a portfolio encompassing both small and large molecules, combination products and ground breaking technologies you will be a part of providing novel life-changing medicines to our patients around the globe. Are you ready to take the lead in ensuring patient safety and maintaining License to Operate across our Development functions? As an Associate Director in Site Quality, you will be the prime source for quality/compliance advise in validation activities and provide quality leadership to Development functions. You will interpret AZ regulatory and GMP standards into appropriate quality standards and provide guidance to ensure AstraZeneca and Regulatory requirements are met. The role requires independent operation, risk management and lean skills, and decision-making against a background of varying regulations and standards. Your responsibility will extend to internal assets and GMP compliance decisions, having a major impact on AZ’s business. Your role As an Associate Director, you will develop and maintain in-depth knowledge of the quality regulations and guidelines applicable to your area. You will mentor and support junior colleagues, build strong customer relationships, and participate in GxP audits/initiatives. You will also be responsible for developing and approving GMP documentation and QA risk assessments, providing Quality input into business improvement projects, and be part of external Regulatory Authority GMP inspections. You will work closely with the leadership teams of our customers to set strategic direction for quality within that area, maintaining quality oversight and driving continuous improvement. Most appreciated in the role is the ability to lead projects, to improve processes or ways of working and support different functions with your subject matter expert knowledge. Working in a development environment makes your role versified and enables lifelong learning in everyday tasks. Essential for the role: • Appropriate scientific degree with extensive experience (5-10 years) of working with validation, in a pharmaceutical GMP environment, preferably within a pharmaceutical development organization • Extensive experience from working with all types of validation including, equipment, automation and IT system. • A broad and comprehensive understanding of Quality Systems and GMP and good knowledge and reputation in the QA arena and specifically in GMP matters • A comprehensive understanding of the pharmaceutical/drug development process is essential. A detailed scientific understanding of the Product types being supported is desirable • Experienced in leading projects, making decisions, acting courageously and communicating with conviction and inspiration and in building excellent relationships both internally and with external suppliers or service providers • Understanding of Supply Chain processes is desirable Soft skills: •You thrive when you work independently, when leading projects and take pride in structuring your day, knowing that the diverse workload can change the schedule with little notice. • You are a problem solver who can look at solutions in a pragmatic way - coming up with creative solutions whilst still following our strict regulations. • Excellent team working and networking skills • Demonstrates independent judgement and uses risk management in complex situations • Capable of making decisions, acting courageously and communicating with conviction and inspiration • Demands excellence (sets high bar) and delivers • A good communicator with experience of interacting effectively across interfaces Latest application date is February 13th, but we review applications continuously, and could proceed with candidates before the last application date. Why AstraZeneca At AstraZeneca, we take Quality seriously. Our work is important, valued, and at the forefront of discovery, development, and commercialization. We are always innovating, trialing the latest models and technologies to improve reliability and excellence in our processes. We are proactive, science-based, and driven by our ambition to go far. We are a team of ambitious people who want to achieve. We work together as a team, get our pipeline out to patients sustainably, reliably, and safely. We follow evidence to reach outcomes that benefit patients and AstraZeneca. Make a difference! Apply now and join us in our journey to push the boundaries of science and make a real-life difference to patients. About AstraZeneca Gothenburg Hub Our stunning campus in Gothenburg is one of AstraZeneca’s three strategic science centers. The site is home to over 2,500 employees, from 50 different nationalities. Gothenburg includes the complete range of functions, and as such offers plenty of development opportunities for a wide range of professionals. Our science teams in Gothenburg collaborate with academic and industry partners in Sweden and globally. And the site itself has been designed with collaboration in mind. From the Coffee Lab to exercise areas, we’ve built a series of environments where innovation can happen.

2 dagar sedan
Sista ansökan:
13 februari 2025
Scientist in Microphysiological systems (MPS) - KellyOCG
KellyOCG Sweden AB
Farmakologer och biomedicinare

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. AstraZeneca is proud to offer a unique workplace culture that inspires innovation and collaboration. Are you ready to make an impact on the future of medicine? KellyOCG, a global talent solutions provider, is seeking a Scientist in Bioscience, on behalf of our partner, AstraZeneca. The assignment is for 12 months and is based onsite in Gothenburg, Sweden, where you will be completely integrated with the AstraZeneca team, reporting directly to the onsite manager. This role will be based in the MPS team at the Early Cardiovascular, Renal and Metabolism (CVRM) department in our dynamic R&D site in Gothenburg, Sweden. The MPS team establishes and applies state-of-the-art MPS platforms to support the CVRM portfolio with emerging therapeutic area needs and new drug modalities. Our mission is to improve translatability from in vitro models to humans and accelerate drug discovery and development. What you’ll do: You will execute and provide input into the practical delivery of MPS studies and support the development, characterization, and optimization of new models. Responsibilities include: • Take part in the design, conduct, interpretation and reporting of studies with advanced cell models and MPS. • Carry out various downstream analyses from the cell culture samples with versatile in-vitro analytical methods such as, but not limited to, ELISA’s, qPCR, staining and imaging. • Join further model development activities to support drug projects with MPS data for resolving mechanisms of action, target identification, and candidate drug evaluation. • Effectively communicate and collaborate across the Early CVRM and with the key stakeholders in other functions. Latest application date is February 7th, but we review applications continuously, and could proceed with candidates before the last application date. 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.

10 dagar sedan
Sista ansökan:
7 februari 2025
Sr Scientist - Flow cytometry in Microphysiological Systems (MPS) -KellyOCG
KellyOCG Sweden AB
Farmakologer och biomedicinare

Do you have experience in flow cytometry and versatile knowledge in cell culture, and are you eager to apply your expertise in a company that accelerates innovative science to turn ideas into life-changing medicines? Join our Microphysiological Systems (MPS) team and contribute to the discovery of future preclinical models that support the development of new medications for Cardiovascular, Renal, and Metabolic (CVRM) diseases! ​ ​Are you ready to make an impact on the future of medicine? KellyOCG, a global talent solutions provider, is seeking a senior Scientist on behalf of our partner, AstraZeneca. The 12-months long contract position (with possibility for extension) is based onsite in Gothenburg/Mölndal, Sweden, where you will be completely integrated with the AstraZeneca team, reporting directly to the onsite manager. ​ At AstraZeneca, we are harnessing advanced cell models, microfluidic chip technologies, multi-omics screens, flow cytometry, and mathematical modelling to achieve the next wave of breakthroughs – here we do things that have never been done before. Are you excited to contribute? Then you might be the person we are looking for! This role is based in the MPS team at the Early CVRM department in our dynamic R&D site in Gothenburg, Sweden. The MPS team establishes and applies state-of-the-art MPS platforms to support the CVRM portfolio with emerging therapeutic area needs and new drug modalities. Our mission is to improve translatability from in vitro models to humans and accelerate drug discovery and development. What you’ll do: You will execute and provide input into the practical delivery of MPS studies while also serving as a flow cytometry (FACS) scientist. You will support the development, characterization, and optimization of advanced cell models and flow cytometry-based assays. We’ll look to you as an expert in cell and molecular biology techniques, and you will independently carry out various downstream in-vitro analytical methods. Responsibilities include: • Develop and execute flow cytometry-based assays for cell characterisation and functional analysis including panel design. • Take part in the design, conduct, interpretation, and reporting of studies with advanced cell models and MPS. • Carry out various downstream analyses from cell culture samples with versatile in-vitro analytical methods such as, but not limited to, ELISA, qPCR, staining, and imaging. • Join further model development activities to support drug projects with MPS and flow cytometry data for resolving mechanisms of action, target identification, and candidate drug evaluation. • Effectively communicate and collaborate across the Early CVRM department and with key stakeholders in other functions. Essential for the role: • Master’s degree + 4 years of relevant experience. • Background in Pharmacy, Biology, Biotechnology, Biochemistry, Medical Biosciences, Bioengineering, or similar. • Proficiency in flow cytometry, including assay development, troubleshooting, and data interpretation. • Strong hands-on cell culture experience. • Versatile in-vitro analytical methods (e.g., qPCR, staining and high-content imaging, plate-based assays such as ELISAs). • Independent study design, laboratory work, and data analysis. • Data visualization and statistical analysis. • Strong interpersonal and communication skills in English, both verbal and written. • Strong ability to engage and collaborate across boundaries with a problem-solving attitude and focus on delivery. Desired for the role: • Experience in 3D cell culture, i.e., spheroids, organoids, or multicellular co-cultures. • Experience with one or more of the following cell models: liver, kidney, cardiac, pancreas, or adipose tissue. • Experience in culturing immune cells. • Handling microfluidic chips. • Workflow automation, e.g., robotic liquid handling. • Experience from the pharmaceutical industry. Latest application date is February 7th, but we review applications continuously, and could proceed with candidates before the last application date. 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.

10 dagar sedan
Sista ansökan:
7 februari 2025
Future Opportunities as an Formulation Scientist in Gothenburg

Are you an formulation scientist looking to make an impact in pharmaceutical development? While we don’t currently have open roles, we’re building a talent pool for future opportunities in Gothenburg and would love to connect with skilled professionals like you! About Future Roles As a Formulation Scientist, you’ll play a key role in developing and delivering innovative formulations to support drug development projects. You’ll focus on creating high-quality solutions and conducting essential experimental work to advance our pipeline. Collaboration, problem-solving, and scientific expertise are central to the role. Key Responsibilities Perform lab-based experimental work to deliver high-quality formulation solutions. Develop and characterize formulations to meet project needs. Collaborate closely with formulators, analysts, and other experts to meet project timelines. Support projects by providing technical expertise and problem-solving. Carefully document experimental work with a focus on quality and detail. Engage with internal teams and external partners to strengthen drug delivery capabilities. Essential Requirements MSc degree in a relevant field: formulation science, pharmaceutical technology, chemical engineering, or equivalent. Experience in formulation development or related laboratory work. Familiarity with quality standards and regulatory frameworks (desirable). Why Join Our Community? By joining our talent pool, you’ll be the first to hear about new opportunities as they arise. This is a great chance to connect, share expertise, and stay informed about roles that could match your skills and aspirations. Interested? Submit your details and stay connected with us for future formulation scientist opportunities in Gothenburg! Let’s build something impactful together – your expertise could help shape the future of pharmaceutical development!

50 dagar sedan
Sista ansökan:
28 februari 2025
Future Opportunities as an Analytical Chemist in Gothenburg

Are you an analytical chemist looking to make an impact in pharmaceutical development? While we don’t currently have open roles, we’re building a talent pool for future opportunities in Gothenburg and would love to connect with skilled professionals like you! About Future Roles In these potential positions, you would: Provide scientific input in analytical science to support drug product development. Perform analytical testing using chromatography techniques (e.g., UPLC) and other relevant methods for small molecules. Ensure accurate documentation of experiments and results. Attend and present findings in project team meetings. Collaborate across teams to determine quality attributes during formulation development. Essential Requirements: BSc or MSc in pharmaceutics, chemistry, analytical science, or a related field. Strong scientific knowledge in analytical science. Hands-on laboratory experience, including familiarity with computerized systems and chromatography techniques for small molecules. Desirable Skills and Attributes: Previous experience in the pharmaceutical industry, ideally within a GMP environment. Well-organized, analytical, flexible, and accurate with strong attention to detail. Excellent teamwork skills and the ability to work independently. Effective communication skills and the ability to meet tight deadlines. Why Join Our Community? By joining our talent pool, you’ll be the first to hear about new opportunities as they arise. This is a great chance to connect, share expertise, and stay informed about roles that could match your skills and aspirations. Interested? Submit your details and stay connected with us for future analytical chemist opportunities in Gothenburg! Let’s build something impactful together – your expertise could help shape the future of pharmaceutical development!

50 dagar sedan
Sista ansökan:
28 februari 2025