På denna webbsida använder vi Cookies (Kakor) för att du skall få ut mesta möjliga av ditt besök på sidan.
Genom att använda webbsidan godkänner du användningen av Cookies, som beskrivs i vår Integritetspolicy Ok

Laboratorieingenjör inom kemiområdet
Spela filmen

Laboratorieingenjör inom kemiområdet

62 Lediga jobb

Regulatory CMC – Specialist, AstraZeneca Södertälje

Arbetsgivare / Ort: Randstad AB
Omfattning / Varaktighet: Heltid / Tills vidare
Lönetyp: Fast månads- vecko- eller timlön
Ansök senast 26 september (23 dagar kvar)
Publicerad: 2021-09-17
Källa: Arbetsförmedlingen
Kvalifikationer
Arbetslivserfarenhet
Krav
  • Kemist

Om jobbet

Job description

Do you like working cross-functionally in a global environment and have experience from pharma industry? Maybe you’ve also worked with Regulatory CMC submissions and/or product maintenance? Then you’re the one we’re looking for!

Randstad is now looking for a consultant placed at AstraZeneca as a Regulatory CMC – Specialist. 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.

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the discovery, development and commercialization 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.

At Campus Södertälje, we come together in an innovative and high-tech environment to manufacture life-changing medicines. Here we enjoy days filled with healthy choices: from morning workouts in the training room, laughter-filled coffee breaks with colleagues, or walks on the Campus nature trail. Welcome to our world, where we have 42 different nationalities, half of our leaders are women, and we all work actively for a healthier world for our employees and our patients: For us, where there is a drive, there are opportunities. Which path do you choose?

CMC Regulatory Affairs is a global function that manages all Chemistry, Manufacturing and Controls (CMC) regulatory activities across AstraZeneca’s global supply chain. We are curious, creative, and open to new ideas and ways of working. Above all, we are passionate about science and driven to always put patients first. Join us and be part of an extraordinary place to work; an environment that energizes and empowers each of us to support compliant product supply through partnership with other AstraZeneca teams.

Responsibilities

What you’ll do
Our CMC Regulatory Affairs Managers provide CMC regulatory and compliance advice on regulatory post-approval submissions and project manage timely submissions of post approval CMC documentation.

Our new colleague is expected to have broad knowledge of medicinal products, project management, pharmaceutical process engineering, complex Supply Chains in global organizations, and how you contribute to achieving the objectives of the business as well as an understanding of the teams and organization you interact with. The role offers you opportunities to work with global networks.

You will be encouraged to use your regulatory knowledge to deliver to high standards, influence others and ensure the application of global CMC regulations and guidance within AstraZeneca.

Qualifications

Essential for the role
We would like you to hold a degree in a scientific field (for example, Chemistry, Pharmacy or Chemical Engineering). In addition, you need:
• Experience from CMC Regulatory affairs or Regulatory Affairs
• Experience from working in the Pharmaceutical industry preferably Pharmaceutical Production, Process Engineering, Quality Assurance or R&D, or experience from Pharmaceutical Agencies or Associations
• Practice from working with or contributing to Regulatory CMC submissions including medical products
• Project management experience, preferably within CMC Regulatory affairs
• To be proficient in both spoken and written English and Swedish

Desirable for the role
You have excellent communication skills, can build constructive networks with colleagues and work collaboratively with customers to achieve optimum outcomes for the business. Strong project management skills and experience of working within a global environment will be invaluable for planning and controlling your own workload as well as effectively managing the expectations of diverse partners. You are comfortable with the use of electronic information and document management tools, and standard Office programs. Background from a LEAN environment would be advantageous.

Why AstraZeneca?
At AstraZeneca we’re dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There’s no better place to make a difference to medicine, patients and society. An inclusive culture that champions diversity and collaboration, and always committed to lifelong learning, growth and development. We’re on an exciting journey to pioneer the future of healthcare.

Application

So, what’s next? 
Are you already imagining yourself joining our team in Södertälje? Great, because we can’t wait to hear from you.  
Selection and interviews will be ongoing, therefore, apply as soon as possible. Last day for application 2021-09-26

About the company

With more than 600 000 employees in 38 countries, Randstad is the global leader in the HR services industry and offers staffing, consulting and recruitment solutions in all areas of expertise. We also offer interim management, executive search and outplacement services. We have a large network of clients and candidates, which means that we convey hundreds of jobs within different industries all over Sweden. Our ambition is to be the best employer in the market. 
 
By combining our passion for people with the power of today’s technology, we help people and organizations to reach their true potential. We call it Human Forward.
Arbetsgivare
Randstad AB
Ansökan
Ansök senast 26 september (23 dagar kvar)

Ansök här
VISA MINDRE

Tolling Coordinator

Arbetsgivare / Ort: Nouryon Surface Chemistry AB / GÖTEBORG
Omfattning / Varaktighet: Heltid / Tills vidare
Lönetyp: Fast månads- vecko- eller timlön
Ansök senast idag
Publicerad: 2021-10-07
Källa: Arbetsförmedlingen
VISA MER
Om jobbet

Do you want to be part of making everyday life easier for people around the world? Without seeing it, you meet us every day in your everyday life. We are in your soles, in your mobile and in the newspaper you read. With a common commitment to innovation, sustainability and safety, our employees work daily for a sustainable future.

Main responsibilities

As a Tolling (contract manufacturing) Coordinator within Nouryon, you’ll perform work tasks such as production planning, material planning, inventory management and coordination of transfers between production plants. You will generate supply forecasts to our Tollers and follow up on performance with them. You are also expected to work towards continuous improvements to the operational aspects of Tolling. This is a key position where you will represent the company with internal as well as external stakeholders.

Qualifications

To be successful in this position we believe you have strong analytical and interpersonal skills. Further, you are an organized team player with a “can-do” attitude. We also see that you have:

  • B.Sc in Supply Chain or related degree
  • 1-3 years work experience within Supply Chain or a manufacturing facility
  • Strong IT competence/experience regarding
  • Standard Office Software, especially Excel
  • SAP (Production Planning, Materials Management) Ability to troubleshoot SAP transactions highly desirable.
  • Fluent in written and spoken English.

Why join us?

Are you passionate about sustainability, innovation, safety, and collaboration? Do you want to grow together with a company that is forward-looking and continuously improving how they work? Our employees have ideas on how to build a sustainable future and the drive and passion to realize them. They believe that building long-term relationships and integrity are keys to success. If that describes you, we will gladly make way for your ambitions. We offer you countless career opportunities. From day one we support you with your personal growth, through challenging positions and comprehensive learning and development opportunities, in a dynamic, international, diverse, and proactive working environment.

Additional information

This is a permanent position on a full-time basis, reporting to the Tolling Operations Lead and based in Gothenburg, Sweden.

Please apply via our online recruitment system with an uploaded job specific resume and cover letter. We do not accept applications via e-mail, these applications will be disregarded.

For additional information about the vacancy please contact Maria Kovacevic, Tolling Operations Lead [email protected] +46 73 581 63 06

For information about the recruitment process or your application, please contact Wictoria Majstrand, HR Business Partner +46 709 577 646

For unions related questions please contact:

Akademikerklubben, Anna-Lena Palm, +46 733 855 113

Unionen, Magnus Svensson, +46 73 385 58 38

If you have any general questions or need assistance, please contact: [email protected]

About Nouryon

Nouryon is a global, specialty chemicals leader. Markets and consumers worldwide rely on our essential solutions to manufacture everyday products, such as personal care, cleaning goods, paints and coatings, agriculture and food, pharmaceuticals, and building products. Furthermore, the dedication of more than 9,700 employees with a shared commitment to our customers, business growth, safety, sustainability and innovation has resulted in a consistently strong financial performance. We operate in over 80 countries around the world with a portfolio of industry-leading brands. Visit our website and follow us @Nouryon and on LinkedIn.

The application process

After the closing date, we will start the selection process.

In our first selection we thoroughly go through all the applications. If your skills and qualifications match the profile we are looking for, you will be invited to an initial phone interview that takes approximately 30 minutes. If you proceed in our selection process, we invite you to a face-to-face interview that takes about 1,5 hours. There you will meet with the hiring manager.

We look forward to your application!

We kindly ask you as an internal candidate to apply with your Nouryon email.

We have already chosen our sourcing channels for this recruitment and kindly ask not to be contacted by any advertisement agents, recruitment agencies or manning companies.

Arbetsgivare
Nouryon Surface Chemistry AB
Marieholmsgatan 70
41502 GÖTEBORG
Ansökan
Ansök senast idag

Ansök här
VISA MINDRE

Technical Manager - Analytical Sciences

Arbetsgivare / Ort: Astrazeneca AB
Omfattning / Varaktighet: Heltid / 6 månader eller längre
Lönetyp: Fast månads- vecko- eller timlön
Ansök senast 21 oktober (1 dag kvar)
Publicerad: 2021-09-30
Källa: Arbetsförmedlingen
VISA MER
Kvalifikationer
Arbetslivserfarenhet
Krav
  • Kemist

Om jobbet
Type of position: fixed term for 24 months Locations: Gothenburg, Macclesfield, and Bad Homburg Are you an experienced scientist looking for a role where your expertise can make an outstanding impact? Can you envision joining a dynamic and enthusiastic environment, delivering critical support to drug development projects? Then this is the place for you! AstraZeneca is a global, innovative BioPharmaceutical business that focuses on the discovery, development, and commercialisation of prescription medicines for some of the world's most serious disease. We have an exciting opportunity to join as Technical Manager - Analytical Sciences, for a 24-month fixed term role. You will be part of Manufacturing Science and Technology (MS&T), On-market technical function. We're part of the Pharmaceutical Technology & Development (PT&D) organisation, responsible for drug product design, development and technical support for drug substance and products throughout the life cycle. MS&T is a multi-skilled organisation based in 7 locations in 5 countries, and we provide the expert technical support for AstraZeneca commercial oral solid dosage (OSD) products. Our technical support and expertise spans from product formulation, manufacture, process engineering, statistics, modelling to devices and testing. The areas in which we deploy our technical expertise are in the support of drug product improvement projects, changes, technology transfers, investigations, regulatory responses, new submissions, product robustness, validation, risk, and manufacturability. What you'll do As Technical Manager - Analytical Sciences, you will be the responsible specialist for a major commercial product or group of products related to the Analytical Methods subject matter area. Using your knowledge in analytical methods, you will provide expertise and leadership to aid in the resolution of analytical method issues and complaints impacting supply and proactively find opportunities for analytical method improvements. We will also rely on you to train and mentor colleagues and partners in methods used in your expert field. Furthermore, you'll be responsible for the technical support during the transfer of established product analytical methods within sites as well as to external manufacturing partners. Your main accountabilities will include: * Development of suitable corrective and preventive actions in support of investigations * Leading, assess impact and supporting complex technical improvements or change activities, assuring product and methods performance * Responsible for analytical method lifecycle activities to ensure performance and compliance across sites * Providing support for regulatory file authoring, review, license renewals and response to questions Essential for the role You have MSc or PhD degree, complemented with considerable experience in an appropriate subject area such as Chemistry, Pharmacy, Pharmaceutical Sciences or similar. Your knowledge spans all the commercial product requirements in the areas of analytical methods establishment and optimisation, including control of drug products, biopharmaceutics, stability, trace analysis (e.g. elemental impurities, extractables & leachables). You have phenomenal interpersonal skills and proven track record to lead and collaborate across functions and locations. You also have: * Significant experience in analytical methods optimization and transfer, including understanding of equipment and method capability and performance. * Significant experience on issue investigation and change assessment from analytical point of view. Good knowledge of standard tools for root cause analysis (5 whys, PPS, Level 0, etc.) * A detailed understanding of principles, applications and management of SHE and cGMP * Experience in Operations or R&D with a track record of successful project delivery * Understanding of a broad range of Analytical techniques (standard and non-standard) and good direct experience with standard techniques for OSD testing Desired for the role * Experience in or exposure to multiple subject areas in CMC and related functions (e.g. Product Development, Operations, Global Supply, Marketing Companies) * Previous experience and training in Lean, problem solving tools and have experience in data analysis and interpretation * Strong leadership skills and behaviours with demonstration of being able to work across different functions Why AstraZeneca At AstraZeneca we're dedicated to being a Great Place to Work. Where you are empowered to push the boundaries of science and unleash your entrepreneurial spirit. There's no better place to make a difference to medicine, patients, and society. An inclusive culture that champions diversity and collaboration. Always committed to lifelong learning, growth, and development. So, what's next! If you want to be part of a team that makes a bigger impact on patients' lives, then there's no better place to be. We look forward to finding out more about you - make sure you apply no later than October 20th, 2021. Preferred start date: November 2021 Competitive salary and benefits package on offer. Opening date: 28th September, 2021 Closing date: 20th October, 2021
Arbetsgivare
Astrazeneca AB
Ansökan
Ansök senast 21 oktober (1 dag kvar)

Ansök här
VISA MINDRE

Produktionsingenjör / ingenjör Life Science / Cytvia

Arbetsgivare / Ort: Bravura Sverige AB
Omfattning / Varaktighet: Heltid / Tills vidare
Lönetyp: Fast månads- vecko- eller timlön
Ansök senast 22 oktober (2 dagar kvar)
Publicerad: 2021-09-29
Källa: Arbetsförmedlingen
VISA MER
Kvalifikationer
Arbetslivserfarenhet
Krav
  • Civilingenjör
  • kemiteknik

Om jobbet
Om Bravura: Bravura är ett bemannings- och rekryteringsföretag för organisationer som vill hitta Next Gen Professionals. Hos oss finns massor av jobbmöjligheter, framförallt för dig i början av karriären med 0-8 års erfarenhet. Via oss kan du jobba som konsult eller bli rekryterad. Hitta ditt drömjobb - vi hjälper dig att lyckas! Om tjänsten: Den här tjänsten är en direktrekrytering vilket innebär att rekryteringsprocessen sker genom Bravura och du anställs direkt hos Cytiva. Om företaget: Cytiva är ett bolag inom Life Science-industrin och är i framkant när det gäller att utveckla nya lösningar för att förbättra människors hälsa. Cytivas kunders verksamhet är livsavgörande och inkluderar allt från grundläggande biologisk forskning till utveckling av innovativa vacciner, nya läkemedel samt cell- och genterapier. På Cytiva kommer du att ständigt kunna utveckla dig själv och bolaget - genom att arbeta med utmaningar som verkligen spelar roll tillsammans med människor som bryr sig om varandra, Cytivas kunder och deras patienter. Med medarbetare i 40 länder är Cytiva en plats där varje dag är en möjlighet att lära så att du kan få fart på din karriär och förbättra dina färdigheter på lång sikt. Cytiva arbetar tillsammans med en grupp av nio andra Life Sciences-företag inom Danaher-koncernen. Tillsammans är de pionjärer inom vetenskap och medicin och utvecklar produkter som hjälper forskare i kampen att rädda liv. Arbetsuppgifter: I den här tjänsten planerar, utformar och genomför du förändringar och kapacitetsökningar både i linjen och i större projekt. Du deltar i och driver utveckling och förbättringar av instruktioner och arbetssätt inom ansvarsområdet. Därtill bedömmer du valideringskrav för nya produkter och utrustningar samt vid förändringar. Du presenterar och förklarar processen vid interninspektioner och audit samt supportar produktionen i den dagliga driften. Du följer upp och optimerar processen i förhållande till olika mätetal. I rollen arbetar du nära andra ingenjörer samt operatörer i teamet för att optimera driften. Utbildning, Erfarenhet och personliga egenskaper: • Civilingenjör eller högskoleingenjör med inriktning mot kemi/kemiteknik/maskinteknik eller liknande • Alternativt har du en kandidatexamen inom kemi med 1-2 års erfarenhet som exempelvis operatör inom industri eller liknande roll • Goda kunskaper i svenska och engelska i tal och skrift • Intresse för tillverkningsprocesser/produktionsutrustning och styrsystem • En fallenhet för datorer, IT, automation och förståelse för teknik är meriterande Du motiveras av att få sätta igång projekt och driver dessa av egen kraft samt har ett framgångsrikt tillvägagångssätt för att lösa problem. Du kan arbeta utanför ramen av din arbetsbeskrivning och trivs med att hjälpa och stödja kollegor i de områden som behövs. Vidare får du energi av att umgås och föra dialoger med människor och är bekväm i sociala sammanhang samt har en naturlig fallenhet för att bygga en relation till andra. Du har en noggrannhet och ett säkerhetstänk vad gäller ditt arbete. Övrig information: Start: Omgående Plats: Uppsala Lön: Enligt överrenskommelse Funderingar kring Bravuras rekryteringsprocess? Du finner svar på de vanligast förekommande frågorna här Är du nyfiken på hur vår rekryteringsprocess är upplagd? Du hittar mer information här: https://www.bravura.se/din-karriar. Har du frågor om tjänsten eller kring din registrering är du välkommen att kontakta vår kandidatsupport på vår chatt, [email protected] eller 08-400 240 50 så hjälper vi dig. Ange vilken tjänst det gäller. Vi rekommenderar att du skickar in din ansökan omgående då vi gör ett löpande urval. Välkommen med din ansökan! Sökord: Civilingenjör, ingenjör, produktion, produktioningenjör, kemi, industri, life science, Uppsala, heltid
Arbetsgivare
Bravura Sverige AB
Hemsida: www.bravura.se
Ansökan
Ansök senast 22 oktober (2 dagar kvar)

Ansök här
VISA MINDRE

Material Engineer

Arbetsgivare / Ort: Northvolt AB / Stockholm
Omfattning / Varaktighet: Heltid / Tills vidare
Lönetyp: Fast månads- vecko- eller timlön
Ansök senast 22 oktober (2 dagar kvar)
Publicerad: 2021-09-22
Källa: Arbetsförmedlingen
VISA MER
Kvalifikationer
Arbetslivserfarenhet
Meriterande
  • Kemiingenjör

Om jobbet









  • Basic cell fabrication and evaluation: especially coincell fabrication and evaluation will be essential, even though part of the work could be outsourced as needed. Still it should be followed up and summarized by anode engineers.
  • Electro chemical tests including swelling, EIS, Li plating, rate capability, cyclability, high temperature and low temperature characteristics: Even though some part of the evaluation can be outsourced, data organization and analysis will be very important part since it will give a clue to the selection of materials and also direction of improvement.


The person we are looking for is strongly goal oriented, curious and eager to learn. You will get the chance to have a real impact on our success story in Sweden (to start with) and see the results of your work. Our organization requires and values great self-discipline and a natural talent to make things happen. The anode engineer is a vital member of the cell design team and key to Northvolt's mission to enable the future of energy.

Apply with CV and your complete LinkedIn profile. Full-time employment, fixed salary. Planned starting date is asap.

Education/Experience

  • A degree in BS/MSc or PhD in material, chemical or related engineering is a must
  • Track record of successful achievements
  • Curious, technically educated and with a strong business background


Specific Skills/Abilities

  • Good English is written and oral skills, Swedish is a plus









Arbetsgivare
Northvolt AB
Alströmergatan 20
11247 Stockholm
Ansökan
Ansök senast 22 oktober (2 dagar kvar)

Ansök här
VISA MINDRE
VISA FLER LEDIGA JOBB


MINA ÅSIKTER OM DETTA YRKE

Jobbar du inom detta yrke och tycker att något saknas eller inte stämmer i vår beskrivning?
Fyll i formuläret så lyssnar vi gärna på dina åsikter.
OBS! Vi erbjuder inga jobb eller vägledning via detta formulär.