Wir verwenden Cookies, um die Benutzererfahrung zu verbessern, den Verkehr zu analysieren und relevante Anzeigen anzuzeigen.
Mehr Annehmen
Position eingeben

Gehaltsübersicht für Quality Process Manager in Aargau

Erhalten Sie Statistikinformationen per E-Mail

Gehaltsübersicht für Quality Process Manager in Aargau

16 000 ₣ Durchschnittliches Monatsgehalt

Durchschnittliches Gehaltsniveau in den letzten 12 Monaten: "Quality Process Manager in Aargau"

Währung: CHF USD Jahr: 2021
Das Balkendiagramm zeigt die Änderung des Gehaltsniveaus in der Quality Process Manager Branche in Aargau

Verteilung des Stellenangebots "Quality Process Manager" in Aargau

Währung: CHF
Wie die Grafik zeigt, in Aargau gilt Gränichen als die Region mit der größten Zahl der offenen Stellen in und an zweiter Stelle folgt Oberentfelden. Den dritten Platz nimmt Kaiseraugst ein.

Ranking der Kantone in Aargau gemäß dem Gehaltsniveau für den Beruf "Quality Process Manager"

Währung: CHF
Wie die Grafik zeigt, in Aargau gilt Gränichen als die Region mit der größten Zahl der offenen Stellen in und an zweiter Stelle folgt Oberentfelden. Den dritten Platz nimmt Kaiseraugst ein.

Ranking der ähnlichen Stellenangebote gemäß dem Gehaltsniveau in Aargau

Währung: CHF
Unter den ähnlichen Berufen in Aargau gilt Directeur als der bestbezahlte Beruf. Laut unserer Webseite beträgt das Durchschnittseinkommen 32000 CHF. An zweiter Stelle folgt Director Business Development mit dem Gehalt von 32000 CHF und den dritten Platz nimmt Disposition mit dem Gehalt von 32000 CHF ein.

Empfohlene Stellenangebote

Senior Test Manager
ITech Consult AG, Kaiseraugst, Rheinfelden
Project: For our customer a big pharmaceutical company situated in Kaiseraugst we are searching for a highly qualified Senior Test Manager (f/m/d) Background: The company has initiated a global Business Process and ERP Program, which will define, implement and deploy the Future ERP solutions based on SAP S/4HANA and other cloud and on premise systems, supporting simplified, standardized and automated global business processes by leveraging SAP industry best practices. To support us on this journey, specifically in the area of a global procurement cloud-based solution, we are looking for an experienced and strategic test professional with relevant experience in the Life Science industry. The ideal candidate will support our implementation and deployment efforts regarding a sustainable test strategy and solution quality approach. Tasks & Responsibilities: Define the approach for the test preparation, planning, execution and coordination in close collaboration with Test Manager / Coordinators, Project and Deployment Leads Drive continuous improvements and efficiencies of the test management strategy, approaches, tools and foster integrated ways of working (e.g. with scrum and deployment teams) in close alignment with Project Leads, Program Test Lead and Implementation Partner Enabling a team of Test Managers and Coordinators who execute the testing and report progress. Define appropriate education needs / prerequisites for all teams involved in the testing, Advocating the appropriate level of quality by defining and implementing a holistic test strategy incorporating all aspect of the solution and implementation (e.g. product development/enhancement, data and configuration, localization, regression and E2E Testing) Define KPIs & SLAs for the test preparation, execution and defect management across all areas involved in the myBuy Program. (scrum and deployment teams) Define template(s) to track the test readiness & progress (E2E) Plan & Forecast testing activities across the mid-level and deployment plans aligned with our partner systems. Analyse and implement management improvement processes in alignment with the project leads. Must haves: . 5 years of experience as a Test Manager, including definition and implementation of a test strategy for a global solution Experience in a regulated environment, preferred in the pharmaceutical or medical device industry 10 years of relevant experience in global and complex system implementation projects as a core team member Strong Project management and Planning skills in waterfall and agile approaches Experience in working with SAP Solution Manager and JIRA Familiar with CSV practices (no certification required) Business level fluency in English both written and verbal, German is an advantage Strong communication skills is a must Strategic and system thinking with a view to long-term sustainability Strong listening, facilitation and collaboration skills Requires excellent problem solving and analytical skills to resolve a variety of routine and complex issues and challenges Proven capability in negotiation, conflict resolution and stakeholder management Flexibility to work outside of normal working hours to support global projects Should you find yourself suitable for this position then please send us your complete CV using the link in this advert. If the position is not a perfect match and you wish to receive other opportunities directly, you can send us your CV anyway via this advert or to jobs[at]itcag[dot]com. Contact us for further information regarding our company, our positions or our attractive payroll-only-program: 41 41 760 77 01. About us: ITech Consult is a certified ISO 9001:2015 Swiss company with offices also located in Germany and Ireland. ITech Consult is specialised in delivering IT and Life Science candidates for contract work. We were founded in 1997 by IT professionals; hence we well understand what it means to be professionally supported in your search for a new project and being employed. ITech Consult Recruitment The Old Station House 15a Main Street Blackrock Co. Dublin A94 T8P8 Ireland Type Duration Description cookielawinfo-checkbox-necessary session 1 year Records the default button state of the corresponding category. It works only in coordination with the primary cookie. cookielawinfo-checkbox-non-necessary session 1 year viewed_cookie_policy session 1 year Is the primary cookie that records the user consent for the usage of the cookies upon accept and reject. It doesn't track any personal data and is set only upon user action (accept/reject). _ga third party 2 years This cookie is installed by Google Analytics and collects information on how users interact with the website. The cookies store information anonymously and assigns a randomly generated number to identify unique visitors. It is used to distinguish users. _gat third party 1 minute Google Analytics cookies to track users as they navigate the website and help improve the website's usability. _gid third party 24 hours This cookie is installed by Google Analytics and collects information on how users interact with the website. The cookies store information anonymously and assigns a randomly generated number to identify unique visitors. It is used to distinguish users.
Senior Test Manager
Global IT Recruitment, Kaiseraugst, Rheinfelden
As a preferred supplier for Roche Basel in Kaiseraugst, we are looking for an individual as Senior Test Manager (contract for 12 months, with possible extension). The earliest start date is as soon as possible or within 3 months. Define the approach for the test preparation, planning, execution and coordination in close collaboration with Test Manager / Coordinators, Project and Deployment Leads Drive continuous improvements and efficiencies of the test management strategy, approaches, tools and foster integrated ways of working (e.g. with scrum and deployment teams) in close alignment with Project Leads, Program Test Lead and Implementation Partner Enabling a team of Test Managers and Coordinators who execute the testing and report progress. Define appropriate education needs / prerequisites for all teams involved in the testing, Advocating the appropriate level of quality by defining and implementing a holistic test strategy incorporating all aspect of the solution and implementation (e.g. product development/enhancement, data and configuration, localization, regression and E2E Testing) Define KPIs & SLAs for the test preparation, execution and defect management across all areas involved in the myBuy Program. (scrum and deployment teams) Define template(s) to track the test readiness & progress (E2E) Plan & Forecast testing activities across the mid-level and deployment plans aligned with our partner systems. Analyse and implement management improvement processes in alignment with the project leads. Must Have 5 years of experience as a Test Manager, including definition and implementation of a test strategy for a global solution Experience in a regulated environment, preferred in the pharmaceutical or medical device industry 10 years of relevant experience in global and complex system implementation projects as a core team member Strong Project management and Planning skills in waterfall and agile approaches Experience in working with SAP Solution Manager and JIRA Familiar with CSV practices (no certification required) Business level fluency in English both written and verbal, German is an advantage Strong communication skills is a must Strategic and system thinking with a view to long-term sustainability Strong listening, facilitation and collaboration skills Requires excellent problem solving and analytical skills to resolve a variety of routine and complex issues and challenges Proven capability in negotiation, conflict resolution and stakeholder management Flexibility to work outside of normal working hours to support global projects Application process Interested? You can find more information here: Infopackage . Please apply via the "Bewerben" button below and answer all questions, otherwise we will be unable to process your application. Professional Analytics Software Engineer/ Digital Biomarker (Scientific and Manufacturing)
Application Manager Finance & Controlling 80-100% (f/m/d)
Zehnder Group AG, Gränichen, CH
OverviewZehnder stands for energy-efficient products and solutions for a healthy and comfortable indoor climate to help to improve quality of life. The Zehnder Group produces and sells decorative radiators, as well as heating and cooling ceiling systems, comfortable indoor ventilation and air cleaning systems on an international level.As well as working together with our customers as an excellent team, we are dedicated, we radiate passion and we love what we do - all to ensure that we are always the number one choice among customers. As a leading innovator, we employ 3500 people globally.The slogan "always the best climate" also applies to the workplace at the Zehnder Group. The Zehnder Group's thinking is long-term and sustainable. A healthy motivating working environment is the only way to achieve top performance in every area. We therefore want to recruit the best talent and at the same time promote from within and achieve mutual commitment.Zehnder Group International AG, located in Gränichen Switzerland, is looking for a highly motivated and team oriented personality to strengthen the Business Applications Department. Your main tasks:Responsible for the SAP application area of Finance and ControllingResponsible for consistency and functionality including dependencies to other systems and interfaces during rollouts and in daily operations3rd level support of the relevant business application in daily operationsEvaluation of solution concepts of change requests (CRs) in terms of feasibility, risks and process / function standardizationTechnical specification of change requests required for developments / interfacesImplements functional changes based on approved change requests raised by global process ownersCustomizing of the system including documentationTraining and know how transfer to key users Your qualifications:Several years of experience in SAP Finance & Controlling application areaFounded knowledge of business processes related to Finance incl. legal intentions and Controlling aspectsGood knowledge of integrative SAP processes and their impact on Finance / Controlling processes and dataKnowledge of E-Topics (Reporting, Invoicing) and Bank Communications is an advantageWillingness to travel up to 30% especially during rollout projectsFluent in English and German language skills are of advantageTeam spirit and professional communication skillsOpenminded and interested in new topics Our offer:Staff restaurantEmployee profit-sharing schemeCompany health management (Zehnder snow day, Zehnder football tournament)40 hours/ week and flexible working hoursOptional savings plan with the pension fundFree parking spacesPurchase of Zehnder products at reduced pricesREKA card - discount 20% - subscription limit CHF 1,500 per calendar yearFree advice at MOVIS and SIZ Your future:We offer you, as a highly responsible person with good communication skills an interesting employment in a dynamic environment.
Strategy Lead, Planning Systems & Process Optimization
Roche, Switzerland, Aargau, Kaiseraugst
The Clinical Demand & Supply Planning organization’s mission is to cost-effectively ensure the right product is in the right place at the right time every time, such that no patient will go without treatment and no clinical trial will be delayed.The Strategy Lead for Planning Systems and Process Optimization is a member of the Clinical Supply Planning leadership team, which is jointly responsible for all elements of clinical supply chain planning for the global Roche/Genentech portfolio of >500 studies. The Systems and Process Optimization team is accountable to enable the business through optimized planning systems and business process capabilities. The Strategy Lead role defines the strategy and is ultimately accountable to deliver an industry-leading technology and process architecture for global clinical supply chain planning. This includes capabilities for demand planning, supply planning, stochastic simulation, inventory management and optimization, and long-term planning. He/she then leads the global implementation team and realization of the harmonized end-to-end processes and related system capabilities into clinical supply chain planning.The Strategy Lead is a people leader for the Business Capability Owners (BCOs), Analysts and IRT specialists, living our leadership values and prioritizing the development of the team through defining the vision; architecting teams, systems and work-packages; coaching; and catalyzing change through removing roadblocks.Key to success is a strong collaboration within the Clinical Supply (PTDS) Global Planning Team, the wider Pharma Technical (PT) network, the existing PT BCO Community, ASPIRE work-stream leads and members and other Roche Business Partners.Key ResponsibilitiesLead for OMP system implementation across PTD, including both the PTDS scope and leadership of deployment activities across the global PTD drug substance and drug product networkFor the OMP implementation, ensure detailed scope, team structure and resource management; align with PT ASPIRE; ensure a well-defined deployment plan and project milestones; provide functional leadership; ensure effective communication; oversee external vendor and consultant support; and demonstrate quantified business valueOverall owner of PTDS planning systems architecture, including APO/OMP, stochastic simulation, IxRS, Demand Planning, and Study Management including interfaces to other Roche systems (e.g. Veeva RIM, CTMS,…)Drives for best practises, standardization and optimization of planning processes across PTDS, with a focus on ensuring supply chain and inventory optimization for a scope of 500+ clinical studies and CHF 900 Mio in inventoryOwnership for planning team Project Portfolio Management and CoordinationChallenges status quo and targets break-through innovations. Maintains a strong network and benchmarks internally and externally to bring best practices to Roche. Where needed, organizes industry-wide consortiums to align on industry best practices and develop vendor capabilities for clinical supply chain planning.Represents and advocates for the interests of Clinical Supply Chain Planning at PT-wide and Global IT system governance and capability forums.Job Requirements and QualificationsCompetencies:Solid understanding of drug development process, clinical trial design, drug technical development, drug demand forecasting and supply planning techniquesAdvanced knowledge of supply chain planning processes, IT systems and optimization techniquesStrong knowledge of supply chain considerations (manufacturing, quality, analytics, regulatory, finance, clinical operations) for large molecules and small moleculesExemplary project management skills, especially for large and cross-functional IT system deploymentsCross functional / cross cultural experienceWell developed people management skills and strategic leadership, including demonstrated VACC (visionary, architect, catalyst, coach) competenciesRequired Experience:10+ years operational and IT systems experience in Supply Chain / planning and/or manufacturing, including senior leadership rolesSignificant project leadership experience, including projects that are global, multi-year and highly complex in natureDemonstrated delivery focus and executionExperience with OMP preferredEducation:Degree (BA, MS, MBA) in a technical, business or supply chain fieldAPICS and/or SCOR certification, or associated relevant experienceOperational Excellence/Six Sigma/Lean training a plusJob Level:Manager with direct reports
Quality Assurance Manager - temporary position for two years
Roche, Switzerland, Aargau, Kaiseraugst
Quality Assurance Manager - temporary position for two yearsAs Quality Assurance Manager within the Quality Unit Kaiseraugst you are ensuring that all process and product related activities in the area of Quality Control and Manufacturing are following legal requirements, GMP guidelines and relevant Roche policies.Your main tasks:Direct activities within the area of responsibility to ensure controlled products meet company quality standards and government regulations.Collaboration with our interfaces to Quality Control (QC) and Manufacturing Value Streams personnel and other departments to ensure a constant state of inspection readiness by identifying, escalating and working to resolve compliance risks in the areaCreation, review and approval of all relevant GMP-documents within area of responsibilityGood knowledge/information sharing to management, interfaces and stakeholders as appropriateQuality oversight in operational area of responsibility: release and stability testing, analytical method transfer/validation, sample management, and, prospectively, drug product or finished goods manufacturingSupport the continuous improvement processes according to “Engrained Quality” and “LPS”Support and collaboration in local and global matrix teams representing QA projectsProvide expertise to local and global stakeholdersOOS, deviation management and CAPA review and approvalAct as subject matter expert during inspections and auditsEvaluation and assessment of change recordsReview and approval of risk assessments in the area of responsibilityQualification:Master degree or PhD in Life Sciences and preferably 2 years of relevant experience in the pharmaceutical industryPreferably, knowledge of cGMP and Quality requirementsResults-oriented, analytical working styleAgile mindset, that is characterized by embracing change and the ability to work in self-organizing teamsAbility to communicate clearly and professionally both verbally and in writing in English as well as in GermanIf you have questions then please check our FAQs and videos on careers.roche.ch/faqJob Level:Individual contributor
Aero Tendering Cost Manager
, Baden
Job Description Summary Lead and implement tender cost management in accordance with customer requirements for Aero proposals. Lead digital and process improvements driving a seamless process from pre-ITO, ITO (Inquiry to Order), until OTR (Order to Requisition) to transform the efficiency, quality, and simplicity of the Aero plant costing process. Possesses technical expertise in process improvement as well as technical disciplines related to the Aero gas power plants and product lines. This role will also include managing costs for GE Aero power plant proposal transactions. Job Description Roles and Responsibilities As Aero Tendering Cost Manager, you will be: * Lead cost process continuou
Quality Engineer
Sika Schweiz AG, Widen, Bremgarten
https://krb-xjobs.brassring.com/TGnewUI/Search/home/HomeWithPreLoad?partnerid30001&siteid5009&PageTypeJobDetails&jobid269545&frmSiteId5011 Sika Automotive is a leading innovator and supplier of automotive bonding, sealing, damping, stiffening and reinforcing solutions for vehicle body structures, interior and exterior components. Our full range of Sika branded technologies provides increased structural performance, help to reduce weight and add acoustic comfort in automobiles, while improving automotive production processes. We are looking for a Quality Engineer, to strengthen our Automotive Quality Team in Widen AG (near Zurich). As Quality Engineer, you will assist the Quality Manager in implementing and updating a quality assurance system according to customer specific requirements. You will be responsible for all quality aspects of the customers’ projects for all stakeholders (incl. suppliers, internal production, and customers) and you will coordinate all customer Advanced Product Quality Planning (AQPQ) aspects You will be the key contact for the analysis and follow-up of Quality Customer Specific Requirements (Quality CSR’s) evolutions You will develop quality tools at supplier and with internal production plants (control plans, Risk analysis, product controls, etc.) You will support the defined projects regarding product and process validation at customer, internally and at supplier You will lead Customers’ project audits at suppliers and internal production plants You will manage all aspects of customer and internal complaints for the defined customers We Need Your Skills Degree in Mechanical Engineering or similar qualification in a technical field At least 1-2 years of experience working Quality Assurance in the automotive sector Motivated, self driven Professional with a strong analytical and structured approach Open minded teamplayer with strong communication and social skills Fluent in English and German Open to travel to customer, suppliers and internal production plants Building Trust Every Day Trust is the most important thing for us. We trust in the capabilities of all our Sika team members and reward them with above average freedom and empowerment – every day The chance to bring new ideas, interesting areas for development, and taking responsibility early on are some of the key factors that drive Sika's pioneering spirit We offer a fair employment package with good social benefits Contact Sika is a great employer - especially for those who work well with people on all levels. For insights into what our colleagues say about working at Sika, please click here . For further information on this Quality Engineer role please contact Julia Bachmann (41 79 194 75 92) or apply online.
Supply Chain Operations Manager (m/w) 100% in Kaiseraugst
Stracon Services AG, Kaiseraugst, Rheinfelden
Supply Chain Operations Manager (m/w) 100% in Kaiseraugst Temporary » Full time Industry / Production » Chemistry / Pharma modern classical Background: We deliver medicines that have a positive impact on patients’ lives - The Supply Chain Operations team ensures on time and in-full delivery of products, documents and data along the global end-to-end supply chain network of Pharma. We provide right first time order, inventory and logistics management services by effectively collaborating with different partners, suppliers and customers across the network. The position will be starting as an Order & Distribution Manager but due to a transition, there is a very high possibility, that the tasks and responsibilities of an Order & Supply Manager will also be part of this position of the Supply Chain Operations Manager. As an Order & Distribution Manager, you trade and deliver finished pharmaceutical products to a defined range of customers and countries within the CMA region. This includes the on-time and in-full supply of products worldwide starting with a customer order receipt and ending with goods arrival at the final destination. Moreover, you build and maintain strong relationships with stakeholders and interfaces, lead discussions, root cause analysis, problem solving efforts and process improvements to ensure that reliable and compliant supply is secured and performance targets and customer requirements are met or exceeded. As an Order & Supply Manager you source, trade and deliver a defined portfolio of drug substance, drug product and finished products among internal and external manufacturing sites worldwide by actively managing the respective inventory and associated flow of goods and funds via our stock keeping and decoupling point in Switzerland. The prime responsibility as an Order & Supply Manager is ensuring on time and in-full supply of products from the handover of the supply plan until the delivery to the next supply chain node. The perfect candidate: We have high expectations around end-to-end thinking and cross-functional collaboration in a global network by taking ownership and delegating decisions to the appropriate level. We value an entrepreneurial mindset with the ability to constantly change or adapt in a dynamic environment. We expect you to focus on the most impactful and value adding work by prioritizing your efforts with a clear focus on creating value for the patient. You will be willing to explore new opportunities, be comfortable with ambiguity and taking smart risks, while complying with the latest regulations. Tasks & Responsibilities: Your general accountability is defined by corporate directives, guidelines and operating principles, as well as by the company's core values and behaviors. In the particular role you will have the following major responsibilities: • Trade and delivery of finished pharmaceutical products to define range of customers and countries • Ensure products are delivered in quality, on time and in a compliant way • Administer effective inventory, order and distribution operations • Manage stock replenishment plan to fulfill short- to mid-term supply and avoid obsolescence • Drive performance monitoring and assessment to address key issues • Maintain effective communication and collaboration across functions • Regularly updates plans to reflect changing circumstances Must Haves: • Bachelor degree in a relevant field or commercial diploma, preferably in supply chain field () • Min. 3 years experience in supply chain, preferably in the pharma industry () • Sound knowledge of SAP SD/MM transactions () • Experience of working in matrix organizations; effectively working within cross-functional and multi-location teams () • Good IT skills in MS Office, Google Suite • Excellent verbal and written communication skills in English is a must, good verbal German skills is a plus () • Experience with international stakeholders/customers/suppliers We expect this person to demonstrate the following competencies: • Strategic agility and flexibility • Good analytical skills • Links own responsibilities with the mission of the whole organization • Focuses on activities that provide the most value • Achieving Results • Goal-directed, persistent; driven to achieve objectives • Self accountable for meeting commitments • Recognizes the contributions of peers • Feedback and Coaching • Seeks candidate feedback on his or her performance • Gives appropriate feedback to others • Actively manages her or his career to pursue personal goals and priorities General Information: • End date: 1 year after start • Extension: Is an option, depending on request and performance Beginning of appointment by arrangement Job Area Canton of Aargau Place of work We can only accept complete ducuments, see Your Candidature for further information. Send the documents to the contact details below or use the form Online Candidature (see below). Contact Personal Contact Basel AG Cristina Diaz Phone 061 666 61 44 Reference Supply Chain Operations Manager (m/w) 100% in Kaiseraugst
Manager RA/PRQ&PS 2
Koninklijke DSM N.V., Kaiseraugst, Rheinfelden
Royal DSM is a global, purpose-led, science-based company active in Nutrition, Health and Sustainable Living. DSM’s purpose is to create brighter lives for all. DSM addresses with its products and solutions some of the world’s biggest challenges while simultaneously creating economic, environmental and societal value for all its stakeholders – customers, employees, shareholders, and society at large. DSM delivers innovative solutions for human nutrition, animal nutrition, personal care and aroma, medical devices, green products and applications, and new mobility and connectivity. DSM and its associated companies deliver annual net sales of about €10 billion with approximately 23,000 employees. The company was founded in 1902 and is listed on Euronext Amsterdam. Responsible for the product approval and maintenance of compliance in the different markets for the entire nutrition cluster. Advices/recommends to Innovation, Marketing and Sales, Product Management, Operations and Purchasing in all regulatory and quality related topics/issues Support of marketing and sales in customer contacts to regulatory and product-quality related topics. Representation of DSM in industry associations working groups and supporting the local production sites in contact with local authorities. Job context Globally the use of and the market approval for Food, Feed, pharma ingredients and Personal Care products is highly regulated and the requirements are very diverse between regions. To ensure that the DSM products are in compliance with these complex regulations, Global RA advices / defines or compiles the internal requirements for new products to ensure efficient market clearances and compliance. This encompasses but is not limited to stability testing, heavy metal, residual solvent limits and other aspects. Global Regulatory Affairs further provides guidance and support for new product developments and for existing products in the context of production improvements, product changes or line extensions, new applications and changing regulatory requirements. Global Regulatory Affairs is the interface between external authorities and/or Regional Regulatory Affairs and internal R&D and Innovation, Safety, Marketing Units and Production sites. In the interaction with the DSM customers Global Regulatory Affairs provides a high standard consultation in areas of expertise and as such adds value to the business process. Key areas of accountability/responsibility Lead the joint efforts for the development of the global product approval strategy in a timely and accurate manner. Manage the Dossiers preparation (e.g. DMFs, CEPs, Core Dossiers) for Product approval in collaboration with R&D, Product and Project Management based on the global regulatory affairs strategies of F&B, HNC and ANH. Adapt and submit the dossiers to the Regional authorities or Regional RA, and follow up on the approval process Work with Product Management and production sites to ensure regulatory compliance of DSM products. Responsible for global (e.g. JECFA) or regional (e.g. CRN, FEFANA, EFCI, APIC, FEBEA) representation, networking and shaping activities. Provide input on changing regulatory environments and the related impacts on DSM nutrition and health business Contribute to the development of DSM opinions in the area of Regulatory Affairs Support Customer Requests Serve as Regulatory Expert for business segments (e.g. HNH Food & Beverages), as agreed and appropriate Support TQM for the product-quality-specific aspects (e.g. specifications) in customer Quality agreements, as needed Support TQM for the product specific aspects (e.g. specifications) in customer Quality agreements, as needed Support issue management related to product-quality aspects e.g. impurity complaints in close cooperation with all internal function (e.g QA, Marketing & Sales, DSCM, PM) Representation of Regulatory in regulatory and product-quality related aspects in internal meetings Complexity of the role Global Regulatory Affairs is a cross functional activity with a high level of complexity based on the dynamics of global markets, different and changing global regulatory environments, public awareness and science focus of authorities and customers. Internally Global Regulatory Affairs has to integrate input from Innovation, Marketing and Sales (various industries and BU), SHE, Toxicology, R&D on a global level. To support the organization, Global Regulatory Affairs has to provide easy understandable correct product information with regard to regulatory compliance and approval status of the portfolio. Provide guidance towards external customers concerning the interpretation of regulations / standards and implication on their business. Facing increasing requirements for the approval process, Global Regulatory Affairs has to develop efficient, reliable and effective long-term strategies to achieve approval from relevant Regulatory bodies for the portfolio. Knowledge and educational level University Master’s degree in natural sciences or life sciences Knowledge on regulations and standards for DSM nutrition and health business Good language skills (English, local language where necessary, others appreciated). Solution- and business-oriented The Procedure The DSM Recruitment and Selection Process is in line with the general procedure outlined elsewhere on our Career World. Please apply online including your CV & cover letter. A Reference procedure is part of the DSM Recruitment & Selection Process. You will be contacted when these checks are required. For additional queries, please contact our Recruiter:james.callanddsm.com DSM in 3 minutes Do you know that DSM has the broadest portfolio of nutritional ingredients - that millions of people already have our biomaterials in their body - and that our innovations make materials lighter, healthier, safer, stronger, more durable and have a lower environmental footprint? This short 3 minute video shares our portfolio in Nutrition, Health and Sustainable Living
Business Project Manager in Cross Border & Market Management #194448
, Aarau
  Svizzera-Switzerland - Region Zurich-Zürich |   Tempo pieno | Wealth Management |  ID annuncio  194448Project / Program / Change ManagementEnglish Per saperne di più su Credit Suisse Scoprite di più sulla vita in Credit Suisse Your field of responsibility   In this challenging role you will collaborate with front office, product manufacturing, trading, legal & compliance, operations, IT and risk management to make sure you deliver high quality. In this multifaceted working environment where learning opportunities and professional development is guaranteed you will have high visibility as business partner to internal