Som miljökemist forskar du på frågeställningar som har stor miljö- och samhällsrelevans. Exempel på intresseområde för en miljökemist är forskning om organiska miljögifters transport och öde i miljön samt om miljöteknik för rening av mark och vatten.
Det är ett akademiskt yrke, högskolestudier i kemi och miljökunskap krävs.
Exempel på en lämplig utbildning för miljökemist är en kandidatexamen i kemi och en kandidatexamen i miljö- och hälsoskydd.
Vidarestudier på masterprogrammet i miljökemi med efterföljande doktorandtjänst kan leda till en forskarkarriär och du kan t ex bli professor vid kemiska institutionen på ett universitet.
Grundläggande gymnasieutbildning finns på Naturvetenskapsprogrammet.
Försurning av haven är ett stort miljöproblem, som mest beror på ökad mängd koldioxid-gaser som finns i luften. Koldioxid löser sig upp i vattnet och försurar det. Koldioxid löser sig snabbare upp i vattnet när det är varmt, men "går ur" vattnet också snabbare i det varma klimatet. På de kallare breddgrader har dioxid svårare att lösa upp sig i vattnet, men stannar också i vattnet under längre tid.
- europarc.org - Europas natur- och kulturarv
- ki.se - masters programme in global health
- kemi.se - Kemikalieinspektionen
- smhi.se/ - beskrivningar av fenomen och händelser kopplade till meteorologi, hydrologi, oceanografi och klimat
- Svenska Kemisamfundets hemsida
- gymnasieguiden.se/ - Sveriges vassaste gymnasiearbete
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.
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.
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.
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.
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
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.
Are you an entrepreneurial project manager with a solid experience within applications of bacterial nanocellulose(BNC)?
You might be what we are looking for. We are looking for you who:
- Have at least five years’ experience with developing applications from BNC.
- Have experience with starting new businesses. Preferably within the applications of BNC area.
- Should have at least two viable applications that are either patented by you or in other ways have a clear freedom to operate status.
- Should be a person who works well with others and can work independently in projects with our customers.
- Have a flexible mindset with regards to achieving the goal of building new businesses focusing on commercialization of BNC based products. This might include: openness to running startup companies within the area, collaborate closely with regional incubators and R&D partners.
- Are able to relocate to Västernorrland, Sweden during the period of hiring.
About the job
We are working with customers that develop processes for producing BNC from Swedish forest feedstocks. We have an opportunity to intensify this work by hiring someone who can contribute towards the product end of the BNC development. You will be working with our customers and regional incubators towards building business cases based on BNC. You will be responsible for suggesting viable products, develop necessary processes to achieve the qualities needed and together with our partners build business cases around these new products. We would prefer that you are also interested in building businesses outside of the hiring at Labservice. During the six months of your hiring period we expect at least one viable application of BNC to have been investigated technically together with two of our partners within this area.
Lab.Service i Sundsvall AB
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Polypeptide Laboratories (Sweden) AB