Lediga jobb som Forskare, IT i Mölndal

Job description
At AstraZeneca we turn ideas into life changing medicines and strive to continuously meet the unmet needs of patients worldwide. Working here means being entrepreneurial, thinking big and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you’re our kind of person.


Human Biological Samples (HBS) are fundamental to medical research in the discovery, development and implementation of new treatments and diagnostics. HBS are ethically sensitive materials and the collection, handling and access to HBS are subject to strict regulations, principles and ethical guidelines.
 
The HBS Compliance Associate Director is responsible for ensuring the compliant use of samples for research.
They are experienced in the review of informed consent and able to ensure samples are used in accordance with patient wishes, protecting our License to Operate.
They will ensure HBS Compliance procedures are followed with regard to HBS specific policies and standards, and can advise stakeholders on use of samples, including decision making on approval of requests for their use in research.


This is a consulting assignment with Randstad Life Sciences. Randstad Life Sciences is specialized in competences 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 social activities.

Responsibilities
Typical accountabilities:
Review and advise on use of HBS in accordance with patient consent.
Lead the identification and establishment of effective HBS compliance procedures to support review of samples as part of US inventories.
Manage HBS processes to ensure standards are adhered to and compliance requirements are consistently applied for use of HBS in research for samples in the US for the Amnesty project.
Support the business with compliant use of HBS through expert advice and decision making
Ensure risks arising from HBS due diligence activities for US Inventory are identified and recorded.
Maintain the documentation/SOPs associated with HBS due diligence activities for the US Amnesty project.
Monitor the effectiveness of HBS due diligence processes and identify opportunities for improvement.
Perform HBS due diligence reviews for AZ clinical sample use and re-use requests for HBS in the biobank to support delivery of timely and effective decisions.
Act as subject matter expert, reviewing informed consents and making recommendations on HBS use

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.


Deadline: 2024-02-23, selection and interviews will be ongoing. For more information: Please contact Katan Ali, [email protected]

Qualifications
Required Skills/ Experience/ Education/ Qualifications:
Bsc. degree
Experience in pharmaceuticals, a healthcare related industry or academia/hospital environment related to HBS
Experience in the review of ICFs regarding use of HBS and knowledge of HBS regulations, laws and standards
Experience of working with multiple stakeholders while maintaining ethical standards and willingness to challenge inappropriate proposals/actions of senior leaders
Experience in collection and use of HBS as part of ongoing clinical trials is desirable
Previous experience as a process owner and process improvement is desirable
Excellent analytical, written and oral communications skills
Strong collaborative, partnering, and interpersonal skills
Strong ability to work independently
Willingness to take decisions
Excellent knowledge of English, both written and spoken

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.

About the company

Kelly Services (UK) Limited Visa mindre

Job description
Analytical scientists Oral Product Development


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. In AstraZeneca we set pride to drive the development in a sustainable way, in all areas of our business from influencing our suppliers through development to commercial products.


The arena: We now have the opportunity for two consultants to join our team in the roles as Analytical Scientists (Career Level C) within the Analytical Science Unit in the department Oral Product Development at AstraZeneca Gothenburg. The assignment is to 31 Dec 2024.


This is a consulting assignment with Randstad Life Sciences. Randstad Life Sciences is specialized in competences 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 social activities.

Responsibilities
Tasks and responsibilities/The role: We are looking for a scientist in Analytical Chemistry who can provide input in the area of analytical science during the development of drug products, and can work together with us determining the quality attributes during the development of the formulations. The work includes analytical testing , documentation, and attending and presenting in project team meetings. The role is primarily laboratory based.


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.


Deadline: 2024-02-08, selection and interviews will be ongoing.
For more information: Please contact Katan Ali, [email protected]

Qualifications
Essential for the role:
-BSc or MSc typically from pharmaceutics, chemistry or analytical science, but also other disciplines with relevant skills.
-Scientific knowledge within analytical science, laboratory experience including working with computerized systems and chromatography techniques (e.g. UPLC) for detection of small molecules.
-Experience from working within the pharmaceutical industry is an advantage.
-If you have experience from working in a GMP environment or worked in AstraZeneca or pharmaceutical industry, this will be an advantage.
-Good knowledge in written and spoken Swedish and/or English is necessary


As a person, you should be well organized, analytical, flexible and accurate.
Good team working skills are also important, together with the ability to operate independently.
Good communication skills linked to the ability to work to tight timelines are highly valued.

About the company

Kelly Services (UK) Limited Visa mindre

Job description
Analytical scientists Oral Product Development


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. In AstraZeneca we set pride to drive the development in a sustainable way, in all areas of our business from influencing our suppliers through development to commercial products.


The arena: We now have the opportunity for two consultants to join our team in the roles as Analytical Scientists (Career Level C) within the Analytical Science Unit in the department Oral Product Development at AstraZeneca Gothenburg. The assignment is to 31 Dec 2024.


This is a consulting assignment with Randstad Life Sciences. Randstad Life Sciences is specialized in competences 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 social activities.

Responsibilities
Tasks and responsibilities/The role: We are looking for a scientist in Analytical Chemistry who can provide input in the area of analytical science during the development of drug products, and can work together with us determining the quality attributes during the development of the formulations. The work includes analytical testing , documentation, and attending and presenting in project team meetings. The role is primarily laboratory based.


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.


Deadline: 2024-02-08, selection and interviews will be ongoing.
For more information: Please contact Katan Ali, [email protected]

Qualifications
Essential for the role:
-BSc or MSc typically from pharmaceutics, chemistry or analytical science, but also other disciplines with relevant skills.
-Scientific knowledge within analytical science, laboratory experience including working with computerized systems and chromatography techniques (e.g. UPLC) for detection of small molecules.
-Experience from working within the pharmaceutical industry is an advantage.
-If you have experience from working in a GMP environment or worked in AstraZeneca or pharmaceutical industry, this will be an advantage.
-Good knowledge in written and spoken Swedish and/or English is necessary


As a person, you should be well organized, analytical, flexible and accurate.
Good team working skills are also important, together with the ability to operate independently.
Good communication skills linked to the ability to work to tight timelines are highly valued.

About the company

Kelly Services (UK) Limited Visa mindre

Job description
Analytical Scientist, Advanced Drug Delivery


At AstraZeneca, we turn ideas into life changing medicines and strive to continuously meet the unmet needs of patients worldwide. Working here means being entrepreneurial, thinking big, and working together to make the impossible a reality. If you are swift to action, confident to lead, willing to collaborate, and curious about what science can do, then you’re our kind of person.


We continually push the boundaries of science to deliver medicines that treat diseases across our main therapy areas. Through our integration with Alexion, this now includes expanding the limits of scientific research to better understand rare diseases and to discover new life-changing treatments for them.


Pharmaceutical Sciences is a department within AstraZeneca Biopharmaceutical R&D. The Pharmaceutical Sciences’ mission is to transform molecules into investigational medicines, meeting the unmet needs of future patients. Advanced Drug Delivery is a department in Pharmaceutical Sciences. Our portfolio of projects spans traditional small molecules, proteins, oligonucleotides to RNA based therapeutics across AstraZeneca’s therapy areas and our mission is to transform diverse modalities into investigational medicines.
We are now recruiting a hardworking and motivated Scientist to join our GMP Analytics team within the Advanced Drug Delivery (ADD) function in Gothenburg, Sweden. The role sits within the ADD group at our vibrant R&D site in Gothenburg, Sweden. With more than 2 800 employees from over 70 different countries, our vibrant Gothenburg site is a truly inspiring place to work.


This is a consulting assignment with Randstad Life Sciences. Randstad Life Sciences is specialized in competences 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 social activities.

Responsibilities
Essential for the role
MSc in a relevant scientific field (such as Analytical Chemistry, Biochemistry or Biotechnology)
In-depth knowledge of analytical methodologies such as chromatography, mass spectrometry and other biophysical/chemical characterization techniques
Understanding of principles and applications of GMP
An interest in exploratory analytical work related to complex molecules, delivery systems and new technologies
Ability to communicate in English both orally and in writing
Thorough understanding of principles, applications and management of Safety Health and Environment (SHE)

Why AstraZeneca?
At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognizing their potential. Join us on our journey of building a new kind of organization to reset expectations of what a bio-pharmaceutical company can be. This means we’re opening new ways to work, pioneering cutting edge methods and bringing unexpected teams together. Interested? Come and join our journey.


Deadline: 2023-12-08, selection and interviews will be ongoing. 
The position may be filled before the last day of application, therefore, apply as soon as possible.

Qualifications
What you will do
As a scientist, you will be part of the development of analytical methods, stability assessments as well as exploratory scientific initiatives. Additionally, you will perform analytical work to support the clinical phase development, such as validation of analytical methods, release analysis and stability studies. Part of the work is performed according to Good Manufacturing Practice (GMP).


You will be a member of different drug development project teams, representing your skill and scientific area. You will work in close collaboration with formulation scientists, analytical chemists as well as biopharmaceutics experts at AstraZeneca in Sweden, UK and US. Profound knowledge of the discovery and development phase as well as awareness of clinical drug development are central for being successful in this role.


We are looking for you, who together with your team will make a difference for patients' lives every day. This through your ability to independently lead and achieve set goals within budget, time and to the right quality.


AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.

Experience
Team-working
Pharmaceuticals
Analytical


About the company

Kelly Services (UK) Limited Visa mindre

Hire location: Cambridge (UK), Gothenburg (SWE) or Gaithersburg (US)
Competitive salary and Benefits
Be empowered to be innovative and creative where difference is valued
Join a place built on innovation and creativity. Where different views and perspectives are encouraged and valued.
An environment that champions inclusion, and teams that reflect the diversity of the communities that we serve.
It propels each of us forward, harnessing our differences to unlock challenges and bring new solutions. Unleash your curiosity and entrepreneurial spirit to uncover new insights that challenge conventions.
Here we are forever pushing the boundaries as we feel comfortable spotting opportunities, making quick decisions and taking sensible risks
The AI and Analytics team within Astrazeneca’s R&D Data Science and AI group is where great things happen in applying sophisticated algorithms and techniques to some of the hardest problems in the discovery and development of new medicines.
The team demonstrates a blend of scientific, problem solving, and quantitative skills to develop and deliver innovative methods addressing critical problems in Astrazeneca’s R&D environment.
Our team of data scientists & informaticians work right next to our other scientists, allowing them to be close to the questions that matter and work on a broad range of the most promising opportunities quickly.
As a Senior Health Data Scientist, you will be part of a rapidly growing team of Healthcare and Visual Analytics expert focusing on analysing and manipulating routinely collected patient-level data from healthcare settings to generate insights that brings innovative medicines to patients faster.
In this role, you will use patient-level databases including claims, EMR, and registry data to develop innovative data science solutions across multiple therapeutic areas (Respiratory, Cardiovascular, Renal and Metabolism) in clinical drug development.
To achieve this, you will scout new technologies/methods/data assets and work in a highly multidisciplinary environment with world leading clinicians, data scientists, biological experts, statisticians and IT professionals.
You will deal with a flexible and varied portfolio of challenges that could include – but are not limited to:
Understanding the patient journey in real world data to optimize patient treatment pathways
Working with drug project teams to find the right sites/investigators in which to run a clinical trial
Researching and developing Machine learning models on multi-modal data to identify digital biomarkers further our understanding of disease
Developing advanced visualisation and visual analytics of routinely collected healthcare data

Accountabilities
Utilises Real World Data (EHR, Claims, Registry & observational data) to support multi-functional projects in R&D and develops advanced data science/informatics solutions across multiple therapeutic areas (Respiratory, Cardiovascular, Renal and Metabolism).
Develops novel analytics solutions where off-the-shelf methodologies do not fit.
Work multi-functionally with multiple partners across R&D to deliver innovative scientific solutions to enable drug projects to optimally utilise large observational datasets and support critical business decisions
Collaborates with the Healthcare and Visual Analytics team to provide technical input to strategic decisions on RWE data strategy, platforms and capability build
Develops working practices to ensure that work is delivered to robust quality standards
Ensures own work is compliant within Clinical Development
Independently keeps own knowledge up to date and learns from senior team members, proposing appropriate training courses for personal development.

Essential
BSc or MSc in a Life Science, Computer Science or equivalent experience
Disease/therapy area and/or biological sciences domain knowledge
Demonstrated experience in method development and application using statistical languages (such as R, Julia or python) and database languages (e.g. )
Experience in EMR/Health IT, disease registries, and insurance claims databases
Knowledge of clinically relevant public and commercial Real world data assets
Superb communication skills with the ability to work with others to achieve objectives
A passion to apply advance analytics/machine learning to tackle difficult problems in drug development using Real world Data

Desirable
PhD in a Life Science or Computer Science preferred
Expertise with clinical data standards, medical terminologies and controlled vocabularies used in healthcare data and ontologies
Use of Machine Learning and Artificial Intelligence in the generation of hypotheses from patient level data
In-depth experience of working in a global organization with complex/geographical context
Strong track record of delivering and managing multi-disciplinary informatics projects
Multiple published papers and/or patents, contribution to external open source projects
Experience in advanced visualisation and visual analytics of routinely collected clinical/healthcare data Visa mindre

Job description
Are you interested in the development of pharmaceuticals and curious about what it is like to work at AstraZeneca? Do you have a summer break and would like to learn new skills in an exciting environment? Welcome with your application for Holiday Work at AstraZeneca in Gothenburg!
 
At AstraZeneca, all of our employees make a difference to patients’ lives every day. We operate in more than 100 countries around the world and are one of Sweden’s most important export companies.
 
With more than 2,400 employees from 50 countries, the vibrant Gothenburg site helps to support the entire life-cycle of AstraZeneca medicines, from drug discovery and clinical trials, to global commercialization and product maintenance. Gothenburg is one of AstraZeneca’s three strategic, global R&D centers, alongside Cambridge and Gaithersburg, and plays a central role in our mission to deliver life-changing medicines to patients.

Responsibilities
Your placement will depend on your previous experience, education and what department you will work in. The holiday work experience will provide you with valuable insight into working in an international company within the biopharmaceutical industry.
 
Please note that we have three different advertisements for holiday work at AstraZeneca this year, within IT/technology, Life Science and administrative/facility. Please apply only to the advertisement that suits your qualifications best.

Qualifications
• You are currently a University student within IT, e.g. data science, computer science, software engineering etc.
• You have knowledge in programming, preferably Java, Python, R or similar.
• You have a genuine interest and curiosity to learn new things and would like to gain insight in working in a large international company.
 
If you have already graduated, please visit vacancies at www.careers.astrazeneca.com

Application
To send your application, click “Apply!”. Please attach your CV and personal letter in Swedish or English. Make sure to specify your line of interest, experience and your technical skills. You can apply even if you are not available all summer, please specify which weeks you are available.
 
All complete applications will be registered. During March, the number of summer job opportunities will be compiled, and your application will be matched against the open positions. Randstad is responsible for the recruitment. If you are selected for the next step in the process, you will be contacted in March-April. Randstad will also contact all candidates that are not selected for holiday work via e-mail in the beginning of May. Your employment will be with Randstad and you will have an assignment at AstraZeneca during the summer.
 
All chosen candidates will have to go through a background check and undergo an alcohol and drug test before starting the assignment.
 
We only handle applications sent through www.randstad.se  
 
Welcome to apply latest March 13th.

About the company
Randstad Technologies specializes in the field of IT and is part of Randstad, the world leader in recruitment and consulting with operations in 38 countries. With this global network, in combination with our strong local foundation, we can offer a wide range of varied and developing assignments and jobs for you who are a specialist in IT. Our mission is to help you reach your true potential with your career in focus! Visa mindre

Location: Gothenburg, (Sweden)
Salary: Competitive, with excellent benefits package
Fuel your curiosity, feel valued and follow the science!
If you have a bachelor’s or master’s degree and a desire to explore and develop your skills in data science and artificial intelligence within a global biopharmaceutical organisation, our Data Science and AI Graduate Programme could be the perfect start to your career. You’ll gain invaluable insight, exposure and opportunities across our diverse, Research and Development organisation. We’ll accelerate your learning and help you achieve your potential.
About AstraZeneca
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialisation of prescription medicines for some of the world’s most serious diseases. But we’re more than one of the world’s leading pharmaceutical companies.
A company that genuinely follows the science and values individuals at all levels, you’ll be backed and encouraged to speak up, ask questions, and share ideas to push the boundaries of science and continuously learn and explore.
Embrace the novel opportunity to work at a business that puts patients first. Working with data and an agile mindset in our constantly changing business, we help uncover solutions that power the business to better harness the science and get it to market. It means we play our part in reaching patients in need and influencing outcomes.
Thrive in a place where the brightest and most curious minds seamlessly come together in our inclusive environment. With more than 2,400 employees from over 50 countries, our vibrant Gothenburg site is a truly inspiring place to work. Here, the history and future of scientific breakthrough come together. We believe that the diversity of our people is crucial to bringing new discoveries to life.
What does the programme involve?
The two-year programme will start in September 2022, consisting of three individual eight-month placements. Each placement will provide you with fantastic insights and experience in our use of machine learning, AI and data science to advance drug discovery and development. You’ll work closely with peers, mentors and experts to develop a broad set of skills, knowledge and experience that will help develop your professional capabilities and pave the way for your future.
As a valued member of our team, you’ll discover how we harness the potential of Data Science, Machine Learning and Artificial Intelligence to accelerate our science, and move our research projects forward. You could be contributing to detecting safety risks, designing novel molecules, optimising clinical trial design and processes, or developing new models for use in high profile drug discovery and development projects. As well as helping you broaden your industry and technical knowledge, we’ll help you develop ‘soft’ skills required to fulfil your career potential.
You will gain an invaluable blend of on-the-job experience and coaching. You’ll enjoy guidance and advice from a huge support network, including a mentor and dedicated programme manager. We’ll also encourage you to identify and build collaborative relationships with specialists and leaders across our organisation, and our external networks including leading academic and biotech research institutions.
Together, we’ll help accelerate your development and knowledge!
Essential requirements
A bachelor’s or master’s degree in a quantitative science focused subject including Maths, Physics, Statistics, computer science and software engineering awarded in 2021, or due to be awarded in 2022.
Experience of applying data science, artificial intelligence, machine learning, statistics, computational biology, computational chemistry, bioinformatics or cheminformatics techniques.
Knowledge of the design and application of machine learning or statistical models.
Experience in using multiple data-centric programming languages to enable big data analysis (e.g. Python).
Enthusiastic and passionate advocate for the potential of data science and AI to make an impact.
Proactive problem solving and critical thinking skills.
Planning, organisational and time management skills.
Collaborative, with a partnership approach to achieving success.
Available to start in September 2022.

Together, we push the boundaries of science to deliver life-changing medicines to patients around the world!
Where can I find out more?
Data Science and AI Graduate Programme: https://careers.astrazeneca.com/data-sciences-and-ai-graduate-programme
AstraZeneca Gothenburg: https://www.astrazeneca.com/our-company/our-locations/gothenburg.html
Life in Gothenburg: https://www.movetogothenburg.com/
What next?
After you submit your application, you will be asked to complete a gamified test (Pymetrics), as well as an online assessment (SHL). If shortlisted, you will be invited to a virtual technical interview, w/c 4th April, for successful candidates, this will be followed up with a full day virtual assessment day w/c 25th April.
You can find out more about our application process here https://youtu.be/0CuUY9d_WtU
Our virtual assessment days will be held week commencing 25 April 2022. Visa mindre

Late-Stage CVRM Biometrics

Hays Specialist Recruitment is now looking to recruit 2 Statistical Programmers to join the Late-Stage CVRM Biometrics for 1-year contract assignments to work remotely for AstraZeneca in Gothenburg.

Are you interested in becoming part of the group of statistical programming at AstraZeneca R&D Gothenburg? Late-stage Cardiovascular, renal and Metabolism Biometrics is now looking for Statistical Programmers for on-site contract assignments with start as soon as possible.

Join a team of statisticians and statistical programmers to provide programming expertise to the design, conduct, reporting, interpretation, documentation and regulatory submissions of our clinical development programs. Depending on your experience, you may contribute to more strategic planning, quantitative decision making, act as expert in our contact with external providers and collaborators and be a part of the function's adaptation and development of programming tools, standards and praxis.

Required Background

* Minimum educational level is a BSc degree in a relevant subject such as statistics, biostatistics, mathematics, computer science, life science or engineering.
* Expertise in analysis output programming (ADaM, Tables, Figures etc.)
* Expertise in drug development and clinical data standards (CDISC)
* Good collaboration, communication and influencing skills
* Good written and spoken English

Other relevant qualifications

* Higher academic degree
* Expertise in multiple programming software such as R or Python
* Project management experience

Personal Qualities
Candidates should possess good social skills, be strong team player and be able to work effectively in a global organization where teams often are geographically dispersed. You should be able to work independently, take own initiatives and have a positive, goal oriented and problem-solving attitude. It is essential to have good organizational and communication skills and you should be able to analyze and summarize your results and be comfortable in presenting them. Successful candidates will have the ability to communicate subject matter expertise to other experts, as well as an interest in the application of programming in pharmaceutical development. Visa mindre

Remote Work

Hays Specialist Recruitment is now looking to recruit a Drug Substance Tech Transfer Lead to work remotely for a 6 month contract assignment at AstraZeneca.

AstraZeneca (AZ) is developing a vaccine to target Covid-19. As part of this effort, the Biologics Global Technical Operations (GTO) group is working with AZ colleagues in R&D to enable the technology transfer of the drug substance (DS) and drug product (DP) manufacturing process to multiple large scale external manufacturing partners (CMOs) to enable rapid scale-up, process qualification and commercial manufacture.

We are looking to augment the GTO team working on technology transfers with a DS / DP Tech Transfer Engineer. In this role, you will also work with GTO Drug Substance and/or Drug Product technical stewards, R&D process development and quality experts within AstraZeneca and partner CMO sites to support ongoing technology transfers and process performance qualification at the CMO. You will be expected to stay on the program for a minimum of 6 months and up to 12 months.

To succeed in this role, you will need to be self-motivated, well organized, have strong technical and communication skills, and a solid understanding and hands-on experience of biologics DS and/or DP manufacturing and quality/compliance requirements.

The position provides the opportunity to work with a highly motivated and talented global team, working under aggressive timelines to deliver a cutting edge monoclonal antibody manufacturing process to multiple world-class manufacturing facilities and support AZ's efforts in dealing with the Covid-19 pandemic.

Essential Job Functions:

* Work with Drug Substance/Drug Product Technical Stewards and SMEs from R&D, Quality, Validation with AZ and external partner sites to support technology transfer of drug substance processes (upstream and downstream) to external manufacturing sites.
* Support drafting, review and approval of tech transfer and manufacturing documentation such as risk assessments, gap analyses, batch records, standard operating procedures and sample plans.
* Serve as Manufacturing /Technical point of contact on specific workstreams/sub-projects, attending teleconferences with CMOS and internal teams, following up with stakeholders on action items etc.
* Update project dashboards/presentations with project status to provide timely communication of status to internal team. Proactively identify risks, and develop / implement work plans to manage / mitigate / communicate risk to senior technical transfer leads.
* Work with CMOs to compile and trend DS/DP manufacturing process data during manufacturing campaigns.
* Note: The AZ team will be based in the US East Coast, CMOs receiving technology transfers are located in EU, and Far East. Will require ability to work flexible hours to support multiple global time zones.

Minimum Requirements:
Education/Experience

* Degree in an engineering or scientific discipline with experience in biopharmaceutical Manufacturing Science& Technology/ Manufacturing/ Process Engineering/ Quality. Prior experience in Drug Substance tech transfers preferred.
* B.S with 10+ years of experience
* M.S. with 6+ years of experience
* PhD with 4+ years of experience

Knowledge/Skills

* Strong knowledge of biologics manufacturing operations and equipment, with prior experience in Manufacturing, Technical Operations, MFG Science and Technology, or Quality.
* Ability to work on multiple projects and meet deadlines as needed; emphasis on results-oriented, strong planning and execution skills
* Strong communication skills, with the ability to collaborate in cross functional teams across multiple organizations
* Ability to work in a complex, dynamic, global environment Visa mindre

Statistical programmer, senior statistical programmer, astrazeneca, consultant

Hays Specialist Recruitment is now looking for three Statistical Programmers (Senior) for a one (1) year contract assignment at AstraZeneca in Gothenburg. Possibilities for an assignment extension. Don't hesitate to send in your application now!


Statistical Programmers, Late-Stage CVRM Biometrics, AstraZeneca Gothenburg
Are you interested in becoming part of the group of statistical programming at AstraZeneca R&D Gothenburg? Late-stage Cardiovascular, renal and Metabolism Biometrics is now looking for Statistical Programmers for on-site contract assignments with start as soon as possible.
Join a team of statisticians and statistical programmers to provide programming expertise to the design, conduct, reporting, interpretation, documentation and regulatory submissions of our clinical development programs. Depending on your experience, you may contribute to more strategic planning, quantitative decision making, act as expert in our contact with external providers and collaborators and be a part of the function's adaptation and development of programming tools, standards and praxis.

Required Background

* Minimum educational level is a BSc degree in a relevant subject such as statistics, biostatistics, mathematics, computer science, life science or engineering.
* Experience from drug development clinical and data standards (CDISC)
* Experience in using programming to structure and analyze data in SAS
* Good collaboration, communication and influencing skills
* Good written and spoken English

Other relevant qualifications

* Higher academic degree
* Expertise in multiple programming software such as R, or Python
* Project management experience

Personal Qualities
Candidates should possess good social skills, be strong team player and be able to work effectively in a global organization where teams often are geographically dispersed. You should be able to work independently, take own initiatives and have a positive, goal oriented and problem-solving attitude. It is essential to have good organizational and communication skills and you should be able to analyze and summarize your results and be comfortable in presenting them. Successful candidates will have the ability to communicate subject matter expertise to other experts, as well as an interest in the application of programming in pharmaceutical development. Visa mindre

Vill du vara med och utveckla framtidens industri? Vill du att det du arbetar med ska göra verklig skillnad? Har du ett stort engagemang för och erfarenhet av forskning inom digitalisering? Har du erfarenhet av rådgivning och coaching? Då är du vår nästa medarbetare!
Vi söker nu en industrinära forskare/coach med placering i Mölndal eller Stockholm.
RISE är en stark partner till svenska företag när det gäller att ta till sig ny teknik och nya arbetssätt. Vi bedriver industrinära forskning och utveckling inom bland annat produktionssystem, digitalisering/automation och industriell arbetsmiljö. Vi driver såväl företagsfinansierade uppdrag och rådgivning som offentligt finansierade forskningsprojekt. Produktionslyftet (se www.produktionslyftet.se) är vårt största utvecklingsprogram, men vi genomför varje år ett stort antal andra projekt, alla med samarbete med industri och/eller universitet och högskola. Vi har ett brett kontaktnät inom svensk industri och forskningsaktörer både inom och utanför RISE.
Om rollen
Som industrinära forskare och coach hos oss kommer du tillsammans med kollegor att arbeta med att utveckla kunskap inom forsknings- och utvecklingsprojekt. Du kommer även att stödja företag i strategiska förändringar gällande digitalisering med ett helhetsperspektiv på ekonomisk, ekologisk och social hållbarhet. Det kan handla om att ta till sig nya arbetssätt, utveckla företagens digitala förmåga och att ta till sig nya teknologier, som kopplar till företagens övergripande vision och strategi. En huvuduppgift för vår grupp är att bidra till en ökad förmåga hos företagen till förnyelse och utveckling, där delaktighet och goda effekter för företagens alla intressenter är centralt. Du kommer vidare arbeta med industrinära metodutveckling och projektledning. Det är en spännande och utmanande tjänst för dig som vill vara med och utveckla svensk industri.
Vem är du?
Vi söker dig som har en stark bas i industriell digitalisering, vilja och förmåga att se teknikens applikationer i praktisk tillämpning. Du drivs av viljan att se ny kunskap, utvecklad av dig och andra, i verklig användning i företag. Du har kunskaper inom exempelvis Industri 4.0, digitaliserade värdeflöden, flexibel automation, digitaliserat underhåll, digitala beslutsstöd och övervakningssystem eller visualisering och användarinterface. Men det centrala är att du har förståelse för kopplingen mellan teknik, människa och organisation.
Du talar och skriver svenska och engelska flytande med god stilistisk förmåga. Vi vill att du har teknisk utbildning på högskolenivå (civilingenjör eller motsvarande) med god teoretisk och praktisk erfarenhet. Forskarutbildning och erfarenhet av ansökningsarbete är meriterande, liksom av förändringsarbete på ledningsnivå. Du har också vilja och förmåga att arbeta tillsammans med såväl företag som akademi. Körkort är ett krav.
Är vi rätt för varandra? 
Vi kan inte lova dig ett enkelt jobb, men vad vi kan lova dig är ett gäng engagerade kollegor och några riktigt spännande samhällsutmaningar att ta i tu med. Du kommer att arbeta i en dynamisk miljö som ger dig utvecklingsmöjligheter både professionellt och personligt. Hos RISE vill att du ska lyckas och må bra, för när du lyckas så bidrar du till en hållbar framtid och till att säkra ett försprång i den globala konkurrensen.
Välkommen med din ansökan!
Vill du veta mer är du välkommen att kontakta Dan Carlsson, gruppchef Produktion och arbetsmiljö, 070-780 61 82. Sista ansökningsdag är den 19 november 2019. Intervjuer kommer att ske löpande under ansökningsperioden.
Våra fackliga representanter är Melina da Silva, Sveriges Ingenjörer, tel: 010-228 46 96 och Simonetta Granello, Unionen, tel: 010-228 48 01.
Samtal från externa rekryteringsföretag och säljare undanbedes vänligen.
RISE Research Institutes of Sweden är Sveriges forskningsinstitut och innovationspartner. I internationell samverkan med företag, akademi och offentlig sektor bidrar vi till ett konkurrenskraftigt näringsliv och ett hållbart samhälle. Våra 2 800 medarbetare driver och stöder alla typer av innovationsprocesser. RISE är ett oberoende, statligt forskningsinstitut som erbjuder unik expertis och ett 100 tal test- och demonstrationsmiljöer för framtidssäkra teknologier, produkter och tjänster. Inom division Material och produktion samlas kompetens inom korrosion, kemi, biologi, medicinteknik och mekanik. Vi är verksamma inom produkt-, produktions- och materialutveckling för textil, polymer, komposit, metall och keram. www.ri.se
Industrinära forskare, Coach, Metodutvecklare, Industriell digitalisering, Stockholm, Mölndal, RISE Visa mindre

Job Description
At AstraZeneca we win through science, it’s at the heart of our every success. That science is only possible when we all work together – we’ll always make sure you’re clear about how your role is connected to our wider mission to really show what science can do.
We are looking to recruit Data Scientists in Computational ADME & Safety to join the Computational ADME & Safety team within the Clinical Pharmacology & Safety Sciences (CPSS) function at AstraZeneca’s vibrant R&D sites in Gothenburg, Sweden or Cambridge, UK.
Clinical Pharmacology & Safety Sciences (CPSS) is a function within our Biopharmaceuticals R&D Unit. The role of CPSS is to characterize absorption, disposition, metabolism and elimination (ADME) properties of compounds, non-clinical toxicology and off-target pharmacology. Working in disease-focused project teams we help to discover efficacious molecules with good safety profiles. CPSS is committed to be an industry leader in supporting the discovery and non-clinical development of safe medicines that improve patients’ lives. Within CPSS, the Computational ADME & Safety team is dedicated towards developing computational models to aid projects to design and select molecules with the right safety and ADME profiles.
As a Data Scientist in Computational ADME & Safety, you will work with cutting edge technology in an open and collaborative environment nursing novel ideas. The group has strong focus on method development within the computational area, acknowledging the need to in depth understanding of the safety or ADME properties of interest. Collaboration within and outside CPSS is essential.
Main Duties and Responsibilities:
As a Data Scientist in Computational ADME & Safety, your main responsibilities will involve:


You will have the opportunity to apply Machine Learning / Artificial Intelligence and mechanistic modeling approaches to ADME and safety endpoints assuring delivery of appropriate tools and in silico models to projects for virtual screening, compound selection and experimental prioritization.
Analyze data and model quality ensuring high performance of models and tools
You’ll provide specialist support for development, interpretation and application of machine learning models along with knowledge of common database query languages e.g.
Support analyses to provide mechanistic and translational insight into compound ADME and Safety profiles
Method development to improve models and enhance model value and generated knowledge

Requirements:
BSc degree (or equivalent) in life science, statistics or computer science, preferably with industry experience
Demonstrated knowledge in one or more of the following areas
Expertise in a variety of machine learning methods (e.g. Deep Learning, SVM, Random Forrest)
Computational chemistry, Computational toxicology or Cheminformatics
Expertise in high-performance computing and programming (e.g. Python, C++, Java). Experience using cloud platforms are beneficial.
Excellent communication skills and ability to work in a multidisciplinary research environment
Innovative thinking, with enthusiasm, energy and drive.
Open-minded, and ready to embrace new ideas and different perspectives.
Strong critical thinking, planning, organizational and time management skills.

Desirable:
PhD (or equivalent) in life science, statistics or computer science
Biological understanding of toxicology and/or drug metabolism and pharmacokinetics (DMPK) and modeling of ADME or safety endpoints



Closing date: Thursday 19 January 2020
If you are interested, apply now


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, protected veteran status (if applicable) or any other characteristic protected by law. Visa mindre

Vill du utveckla framgångsrika organisationer och arbetsplatser? Och göra det tillsammans med svensk industri och vår grupp inom Produktutveckling och småföretagsstöd på RISE IVF? Gruppen bedriver forskning och utveckling i frågan om hur industriell datahantering bäst tillämpas i såväl större som mindre företag med syfte att stärka kundupplevelser och att effektivisera värdeflöden.Vi söker dig som har en vilja och erfarenhet av att bedriva FoU inom big data, machine learning och artificiell intelligens, gärna i flervetenskapliga team, i nära samverkan med företag och universitet/högskolor. Det är en spännande och utmanande tjänst för dig som vill vara med och utveckla svensk industri. Du kommer att arbeta med FoU som leder till verklig förändring, som forskare, projektledare och coach/rådgivare mot företag. Tjänsten avser heltid och placering är i Mölndal.RISE IVF har ett helhetsperspektiv på industriell digitalisering där vi utvecklar lösningar som bidrar till att samtidigt främja goda arbetsförhållanden, konkurrenskraft och förnyelseförmåga. Det kan handla om organisatorisk utveckling, ledarskap, företagskultur och förändringsprocesser, samspelet människa - maskin vid automatisering och/eller utformning av framtidens digitaliserade arbetsplatser. Vi belyser interaktionen mellan människa, teknik och organisation i olika situationer, likväl som kompetens- och samarbetsbehov. Vår FoU syftar till industriell tillämpning.Vem är du?Vi vill att du har utbildning på högskolenivå, gärna forskarutbildning, med god teoretisk och praktisk erfarenhet inom områdena optimering, systemering och datahantering. Tidigare arbete med optimering och med metoder och algoritmer för bildanalys och djupinlärning är meriterande. Du kan Python och gärna Hadoop-miljö. Du har vilja och förmåga att arbeta tillsammans med såväl företag som akademi. Du talar och skriver svenska och engelska.Välkommen med din ansökan redan idag!Låter detta spännande och du vill veta mer så är du välkommen att kontakta Maria Gröndahl, gruppchef, 031-706 61 89 och Peter Bökmark, avdelningschef, 031-706 61 73. Sista ansökningsdag är den 30 augusti 2019. Intervjuer sker löpande under ansökningsperioden.Vi följer Teknikavtalet Unionen/Sveriges Ingenjörer/Ledarna och alla medarbetare har månadslön. Överenskommelse om lön och övriga villkor görs i samband med anställningen.Våra fackliga representanter är Melina da Silva (Sveriges Ingenjörer) 031-706 60 26 och Carina Egeman (Unionen) 031-706 60 09.RISE är Sveriges forskningsinstitut och innovationspartner. I internationell samverkan med företag, akademi och offentlig sektor bidrar vi till ett konkurrenskraftigt näringsliv och ett hållbart samhälle. Våra 2 700 medarbetare driver och stöder alla typer av innovationsprocesser. RISE är ett oberoende, statligt forskningsinstitut som erbjuder unik expertis och ett 100-tal test- och demonstrationsmiljöer för framtidssäkra teknologier, produkter och tjänster. www.ri.se Visa mindre