Lediga jobb KellyOCG Sweden AB i Mölndal

Är du intresserad av att arbeta inom kvalitetssäkring (QA) eller kvalitetskontroll (QC) i en internationell läkemedelsorganisation? För vår partner AstraZeneca söker vi på KellyOCG kontinuerligt efter engagerade konsulter som vill vara med och säkerställa att läkemedel håller högsta kvalitet och säkerhet för patienter världen över.
Om uppdragen
Som konsult via KellyOCG blir du en del av AstraZenecas organisation och arbetar nära verksamheten i Göteborg. Uppdragen varierar i omfattning och inriktning, men har gemensamt att de innebär en central roll i att stödja tillverkning, utveckling eller kvalitetssystem – alltid med fokus på GMP och regulatoriska krav.
Exempel på arbetsuppgifter
Granskning, frisläppning och kvalitetssäkring av tillverkade produkter eller råvaror
Deltagande i utredningar av avvikelser, ändringar och förbättringsarbete
Kvalitetskontroll av läkemedelssubstanser och färdiga produkter
Bidra i tvärfunktionella projekt kring processer, valideringar eller inspektioner

Krav
Naturvetenskaplig universitets- eller högskoleexamen (t.ex. apotekare, civilingenjör, bioteknik, kemi eller liknande)
Erfarenhet av arbete inom läkemedelsindustri, QA eller QC
Kunskap om läkemedelstillverkning enligt gällande regelverk och GMP
Goda kunskaper i svenska och engelska, både i tal och skrift

Meriterande
Erfarenhet från tillverkning, laboratoriearbete, kvalitetsgranskning eller myndighetsinspektioner
Kunskap inom LEAN, validering/kvalificering eller förbättringsarbete
Intresse för digitala processer och system



Om KellyOCG
Som konsult via KellyOCG blir du en viktig del av vår verksamhet samtidigt som du är fullt integrerad i AstraZenecas team. Vi erbjuder trygga anställningsvillkor, kollektivavtal och möjligheten att utvecklas i en global miljö där ditt arbete gör skillnad för patienter världen över.
Är du intresserad av framtida uppdrag inom QA eller QC hos AstraZeneca? Skicka gärna in din ansökan redan idag! Visa mindre

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. Co-workers are empowered to express diverse perspectives—and are made to feel valued, energized, and rewarded for their ideas and creativity.
AstraZeneca is also a leading pharmaceutical company focused on developing Active Pharmaceutical Ingredients (API) with advanced technologies. The Gothenburg facility employs digital solutions and automation to enhance production efficiencies.
As part of our commitment to innovation and collaboration, we are now offering a 6-month consultancy assignment through KellyOCG, with the possibility of extension. You will be fully integrated into AstraZeneca and report directly to your manager at AstraZeneca.
The arena:
The IT/OT Engineer will bridge the gap between IT and Operational Technology (equipment) in the manufacturing facility. Key responsibilities include maintaining IT systems that support business operations and manufacturing, ensuring system integrity and security, troubleshooting IT-related issues, and collaborating with various stakeholders to ensure compliance with industry standards.
Tasks and responsibilities / The role:
IT Infrastructure Management:
Ensure the performance and availability of IT systems.
OT System Support:
Align IT support with production needs.
Proactively address IT-related issues affecting manufacturing.
Cybersecurity Management:
Implement cybersecurity measures for IT and OT systems.
Staff training on security.
Data Integration & Management:
Ensure smooth data flow between IT and OT systems.
Develop interfaces for real-time data exchange.
System Administration & Troubleshooting:
Resolve IT incidents impacting operational efficiency.
Collaborate with vendors for advanced issues.
Vendor and Stakeholder Management:
Manage vendor relationships and service compliance.
Coordinate IT/OT project goals with internal teams.
Compliance and Best Practices:
Maintain GxP compliance and thorough documentation.
Lead system audits and validations.
Continuous Improvement & Innovation:
Evaluate and implement new IT/OT technologies.
Mentor junior staff and lead innovation projects.



Benefits:
• Opportunities for continuous professional development and training.
Performance Indicators:
• Maintain 99.9% uptime of IT/OT critical systems.
• Ensure rapid incident response and 100% compliance with regulations.
• Achieve high satisfaction ratings from stakeholders.
Core systems and equipment:
• High Bay Warehouse system – LAGE
• Clinical supply planning and execution System – SmartSupplies
• Building Monitor System – EMIL
• Scanners and container label printers
• Decommissioning system – Verilite
• Label Printers with servers
• GMP Lab Computers
Essential requirements:
Education: Bachelor’s in Computer Science or related field; OT/Cybersecurity certifications preferred.
Experience: 5+ years in IT with 2+ years in OT, especially in pharmaceutical manufacturing; experience with systems like SAP S4/HANA. Experienced in Power BI, Power Automate, MS Lists.
Skills: Strong knowledge of IT/OT convergence, excellent problem-solving abilities, and understanding of cybersecurity best practices. GMP knowledge.
Soft skills / Personal Attributes:
Effective communication, multitasking, attention to detail, and commitment to excellence.
AstraZeneca is one of the world’s most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we’re on a mission to turn ideas into life-changing medicines that improve patients’ lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world.
Last day to apply for this position is 15 May. Visa mindre

Research Scientist - NGS based Proteomics
At AstraZeneca, our achievements stem from scientific excellence. Our innovative work thrives on collaboration, ensuring that every member of our team understands how their role contributes to our broader mission of showcasing the power of science.
The NGS/Transcriptomics team is a dynamic group dedicated to advancing “omics” technologies and methodologies. Our goal is to generate insightful data that enhances our understanding of drug pharmacology, target mechanisms, model systems, patients, and diseases, aligning closely with AstraZeneca’s strategy for Growth through Innovation.
We are seeking a Research Scientist with a background in molecular biology laboratory practices. The ideal candidate will possess exceptional teamwork skills and a history of collaborative success to drive scientific excellence and deliver robust results for our research projects.
This is a 12-month consultancy assignment through KellyOCG, where you be fully integrated with AstraZeneca and report directly to your manager at AstraZeneca.
Are you driven to push the boundaries of science? Do you want to contribute directly to AZ’s innovative growth strategy? If yes, we invite you to join us at our R&D facility in Gothenburg, Sweden!
Main Duties and Responsibilities:
This role is for a lab-based Research Scientist with knowledge and experience in transcriptomics / proteomics. This is a hands-on laboratory-based role with focus on effective delivery to support various clinical and preclinical projects across multiple diseases, species and drug modalities.
In this role you will:
Utilize prior practical laboratory experience in molecular biology.
Contribute to planning and execution of projects involving new omics technologies.
Implement innovative processes developed by the NGS Tx team.
Maintain laboratory processes and equipment rigorously.
Provide experimental support to fellow team members, fostering a collaborative environment.
Ensure compliance with Safety, Health, and Environmental regulations as well as AstraZeneca’s corporate responsibility policies.
Develop a comprehensive understanding of the pharmaceutical industry and identify opportunities for new business initiatives.
Be collaborative with a wide range of scientists of different backgrounds to ensure the highest quality of research.
Implement cutting edge protocols for the simplification and dissection of multiomic environment.



If you are interested, apply now!
Last day to apply is April 30.
AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status or any other characteristic protected by law. AstraZeneca only employs individuals with the right to work in the country where the role is advertised. Visa mindre

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 March 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. Visa mindre

AstraZeneca is a major international healthcare business engaged in the research, development, manufacture and marketing of prescription pharmaceuticals and the supply of healthcare services. However, as a company they are more than one of the world's leading pharmaceutical companies, they are also proud to have a unique workplace culture that inspires innovation and collaboration.
KellyOCG are now searching for two "Research Scientists - Biosamples, Biobank" for contracts at AstraZeneca through KellyOCG. There is one longer contract (a full year), and one shorter (around 7 months long). Both have opportunities of extension and further future collaborations.

The arena:
Biobank scientists are responsible for the storage and timely supply of human biological samples (HBS) to AZ research projects. HBS are received from e.g. clinical studies or academic collaborations, stored in local biobanks and distributed to projects. The group primarily supports the Sweden Region but partners with other Biobank groups within AZ globally to provide efficient support across AZ and our partner organizations.
The Biobank group works collaboratively to provide support within agreed service levels with a strong focus on our customers. We strive hard to understand what fits their needs best and to add value through our services. With an increased focus on the value and use of biobank samples we actively seek ways to improve our process or exploit new technology to build a cutting-edge facility.

Tasks and responsibilities/The role:
We are currently recruiting for a Biobank Scientist in the AZ Gothenburg Biobank group within the global Precision Medicine and Biosamples organization. This position will provide the opportunity to work in a dynamic and enthusiastic environment whilst supplying a critical service to drug discovery projects. The work is highly collaborative with the team having a collective responsibility for the overall delivery.
The role is focused on supporting drug discovery projects within R&D Gothenburg by maintaining high quality handling and storage of HBS and support projects with requested samples in a timely manner.

As a Biobank Research Scientist you will be expected to:
• Receive and register incoming HBS
• Process requests for HBS to customers, including using automated liquid handler
• Manage customer orders using specialized informatics systems as well as databases and respond to customer queries via mail or telephone
• Partner with Biobank groups globally as well as internal and external customers
• Act upon day-to-day issues that occur whilst processing HBS samples to ensure continuous improvement
The group has a strong emphasis on continuous improvement which takes the form of individual and group projects within the team, the department and across Biobank groups within AZ.

Requirements:
Essential for the role:
• University degree in a Bioscience discipline and previous experience of laboratory work handling biological samples.
• Previous knowledge and experience (1 year) of biobanking is highly desirable.
• Experience of working with various IT solutions, including extensive knowledge of Excel, LIMS systems and database usage, is also a clear advantage.
• Experience of automated liquid handling is advantageous.
• Good analytical and problem-solving skills involving large and complex datasets is desirable.
• Excellent English, both spoken and written

Desirable:
• Knowledge of the regulatory framework of biological samples.
• Interest in logistics and developing processes through customer interactions and technology awareness.
• Drive and enthusiasm to solve the root cause of problems and not only overcome the presenting problem.
• Thrive on working in a committed team and gain satisfaction from the overall performance of the group
The biobank team is a highly collaborative group working to tight delivery schedules so the ability to be comfortable working at a fast pace with a goal orientated and team focused attitude is essential. Excellent communication skills with a proactive and service minded approach is key.

Final date to apply is September 5th. We utilize a continuous selection and interviews, and the positions might be filled before the deadline. So should you find the positions interesting, don't wait to send in your application!
AstraZeneca is one of the world’s most exciting bio-pharmaceutical companies. From scientists to sales, lab techs to legal, we’re on a mission to turn ideas into life-changing medicines that improve patients’ lives and benefit society. We need great people who share our passion for science and have the drive and determination to meet the unmet needs of patients around the world. Visa mindre