Gehaltsübersicht für Chemistry in Schweiz

Im Auftrag unserer Kunden - ein renommiertes Pharma Unternehmen aus der Region Basel - suchen wir derzeit eine(n):Rohrschlosser (m/w) Hauptaufgaben:Herstellen, montieren und schweissen von Rohrleitungen nach IsometrieMassenaufnahme vor Ort beim KundenDrehscheibe zwischen Projektleiter und KundeErstellen der Dokumentationen Teilweise Ausseneinsätze im Raum BaselGesuchtes Profil: Abgeschlossene Berufsausbildung als Rohrschlosser oder Anlagen- und ApparatebauerFundierte Schweisskenntnisse mit TIG, WIG und Elektroden)Aktuelle Schweisszertifikate von VorteilKenntnisse im Lesen von R&I'sSehr gute Deutschkenntnisse Führerschein Kat. B und flexibelTeamfähigkeit und Bereitschaft Neues zu lernenDie Vorteile: WeiterbildungsmöglichkeitenRegelmässige Arbeitszeiten Moderne Infrastruktur Kollegiales und kompetentes TeamEin job für dein Talent: querdenker, exakt, selbständig, leidenschaftlich und kontaktfreudigInteressiert? Dann freuen wir uns auf deine online Bewerbung inklusive Upload sämtlicher benötigten Unterlagen (Lebenslauf, Qualifikationen, Arbeitszeugnisse etc.).Dein Randstad Team

PhD Student Positions in Bioinorganic Chemistry 60 %Department of Chemistry PhD Student Positions in Bioinorganic Chemistry60 % The research of the group of Prof. Dr. Eva Freisinger is focused on the investigation of metallothioneins from different organisms. MTs are rather small cysteine-rich proteins with the ability to coordinate a number of transition metal ions. The positions are standard full-time PhD positions, formally designated 60% based on the officially assigned salary class. Your responsibilities Your research will span the entire area from identifying new and exciting protein sequences, cloning and recombinant protein production, purification and initial spectroscopic and spectrometric characterisation (UV, CD, AAS, ESI-MS, MALDI, etc), followed by structural studies with NMR and X-ray or functional analyses in collaboration with groups from the biological field. Your profile Applications must have a Master's Degree in Natural Sciences, a Master's Degree in Chemistry is preferred but not strictly required. However, profound knowledge in coordination chemistry is essential. Applicants must have excellent oral and written communication skills in English, and also the soft skills to be a good team player and foster the collaborative and collegial environment in our Lab and the entire department. You must enjoy working in a scientific environment, mastering challenges and be always open to find and investigate the unexpected. What we offer We offer varied and interesting work in an inspiring international environment with access to state-of-the art scientific infrastructure. Diversity and inclusion are important to us.All PhD students of the Department are part of the Graduate School of Chemical and Molecular Sciences Zurich CMSZH, which thrives to interlink its members and fosters interactions and exchange. The CMSZH also offers a variety of courses, excursions, travel awards and financial support for visiting conferences and courses. Place of work University of Zurich, Winterthurerstrasse 190, 8057 Zürich, Switzerland Start of employment Earliest April 1, 2022 or by agreement.Please send your application materials including short motivation letter, CV, transcripts of records and the names and contact details of three referees in a single PDF file. Applications that do not follow these instructions will not be considered.Deadline for Application: Evaluations will continue until the positions are filled.

PhD Student position in Organofluorine chemistry and Catalysis 60 %Department of Chemistry PhD Student position in Organofluorine chemistry and Catalysis60 % Dr. David Rombach is seeking an outstanding candidate for a PhD position in organofluorine chemistry. Our group focuses on the development of methods to chart unknown chemical space through two strategies: (I) unlocking unknown reactivity modes of known small molecules or (II) developing new reagents for the preparation of unknown compounds. For more information, please see our group's website and the following publications: Activation of SF6 (see ChemCatChem 2018, 10, 2955., Angew. Chem. Int. Ed. 2020, 59, 300. and Chem. Eur. J. 2021, 27, 8088.) Hydroelementation of Triisopropyl silyl acetylene sulfur pentafluoride (TASP) (see ChemRXiv 2022, DOIs: 10.26434/chemrxiv-2022-brg1w and 10.26434/chemrxiv-2022-01jhn.) Your responsibilities You will be responsible for developing new synthesis methods and reagents, synthesizing the required substrates, optimizing reactions, and elucidating the underlying reaction mechanisms using spectroscopic, electrochemical, and mass spectrometric methods. Additionally you will also be involved in teaching by supervising practical laboratory courses and bachelor/master theses. Your profile We are looking for an enthusiastic, dedicated and creative individual. The successful candidate will be driven by curiosity and be a strong and proactive team player. You must have a Bachelor's/Master's degree in organic or inorganic chemistry. Basic communication skills in English are required. What we offer We are a dynamic young research group led by Dr. David Rombach. We strive to treat each other with respect and to create an encouraging and motivating work atmosphere that values the individual, whoever that may be. Our research combines aspects of synthetic inorganic, organic, radio and photochemistry with mechanistic studies using an integrated spectroscopic approach as well as computational chemistry. This project is embedded in a strong European collaborative network. Place of work University of Zurich, Winterthurerstrasse 190, Zürich, Switzerland Start of employment We are committed to diversity in all its forms and welcome students from all countries. We encourage to apply excellent candidates regardless of their nationality, race, skin color, gender or any other personal identities. We are looking forward to receiving your application as a single PDF document including your letter of motivation, quickly describing what drives you to join our team, a short research summary (BSc, MSc etc.), your CV, your transcripts of records and certificates as well as the details of one reference.

Open PhD Student position in theoretical chemistry 60 %Department of Chemistry Open PhD Student position in theoretical chemistry60 % A 4-year PhD student position is available in the Luber group at the Department of Chemistry at University of Zurich (Switzerland). Our group focuses on forefront computational methods at the interface of chemistry, biology, physics, and materials science and has broad experience in modelling of reactions using DFT-MD, catalysis (such as water splitting), spectroscopy, excited states, and development of various other methodologies (e.g. in the CP2K package). For more details, see our group's website. Your responsibilities The PhD project will deal with development and application of novel, accurate approaches for the study of functional compounds. A possible direction of the project is the development of advanced dynamic approaches for detailed and realistic study of reaction mechanisms and reaction networks considering in a sophisticated manner environmental effects (also under catalytic conditions). This can include the development of advanced enhanced sampling approaches and embedding techniques for highly accurate description beyond the DFT level / at catalytic conditions (possibly also combined with machine learning). Additionally, the project(s) may be carried out in close collaboration with experimental or other computational groups. Your profile The candidate must hold an excellent Master's degree in chemistry, interdisciplinary natural sciences, physics, or related, and have profound English and autonomous learning ability skills. The successful candidate will be highly creative, ambitious, and motivated. Strong programming skills and very good knowledge about electronic structure theory, (ab initio) molecular dynamics and/or catalysis are an advantage. What we offer We offer a vibrant, inspiring environment in a brand-new building with cutting-edge resources and research, access to world-leading supercomputers, and high-profile interdisciplinary collaborations. Funding for the participation at summer schools, conferences etc. is also available. Place of work University of Zurich, Winterthurerstrasse 190, Zürich, Switzerland Start of employment Employment starts by arrangement. Interested applicants are encouraged to submit their application documents (cover letter, CV, diplomas, description of research experience and motivation, names of at least two academic references) as one pdf document. The pdf can also include a one-page statement discussing one or two publications of the group with respect to what the applicant finds particularly interesting and what could be possible future improvements of the research described in the publication(s).

Lösungen für den sta Ɵonären Netzspeichermarkt zu bieten. Wir sind bestrebt, Innova Ɵon und Nachhal Ɵgkeit imEnergiespeichersektor voranzutreiben.Seit der Gründung im Jahr 2008 ist die Ba Ʃery Consult AG ein vertrauenswürdiger Partner in na Ɵonalen undinternaƟonalen Forschungsprojekten und hat zahlreiche Technologietransfers abgeschlossen. UnsereEnergiespeicherzellen vom Typ STC-140 und STC-250 sind unter der Patentnummer PCT/EP 2020-073992 registriert.Mit Sitz in der Energie-Stadt Meiringen, Berner Oberland, Schweiz, setzen wir Maßstäbe bei fortschri ƩlichenEnergiespeicherlösungen.www.baƩeryconsult.ch(3) BaƩery Consult AG: Company Page Admin | LinkedInAnnouncement: Dr. Rebecca Busch Joins Ba Ʃery Consult AG as Head of ChemistryBaƩery Consult AG is happy to announce the addi Ɵon of Dr. Rebecca Busch toour team as Head of Chemistry, effec Ɵve from January 2024. With a Ph.D. fromKIT, Karlsruhe in Germany, Dr. Busch brings extensive exper Ɵse in baƩerysystems, specializing in the development of inorganic electrolyte systems.Driven by passion for the energy transi Ɵon, Dr. Busch firmly believes in providingsustainable energy storage solu Ɵons, like our groundbreaking SaltBa Ʃeries, forindustrial applica Ɵons. Joining us during this cri Ɵcal period, she will play a vitalrole in bringing our innova Ɵve soluƟons to the market.We would like to express our hear ƞelt graƟtude to Dr. Akane Hartenbach, whohas played an important role in our journey so far. Dr. Hartenbach has diligently driven chemicaldevelopments for many years and has been instrumental in the establishment and management of thechemical opera Ɵons at BaƩery Consult AG. Ms. Hartenbach will soon transi Ɵon into a professional sabba Ɵcal,handing over the reins to Ms. Busch.In Dr. Busch's own words, "I'm thrilled to join Ba Ʃery Consult AG and be part of this dynamic, innova Ɵveteam. As we drive change and contribute to the energy transi Ɵon, this is a pivotal Ɵme for thecommercializa Ɵon of sustainable energy storage solu Ɵons. I firmly believe in the tremendous poten Ɵal ofSaltBaƩeries for industrial applica Ɵons, and I'm excited to shape the future of energy storage with a strongfocus on sustainability and the environment."We are delighted to welcome Dr. Rebecca Busch, a competent, visionary team player. Together, we willrevoluƟonize the energy storage industry and have a sustainable impact on the world. The en Ɵre team atBaƩery Consult AG, as well as the board of directors, would like to thank the previous posi Ɵon holder, Dr.Hartenbach, for the trus ƞul collabora Ɵon over the past years and wish her all the best for the future.For more informa Ɵon or media inquiries, please contact:BaƩery Consult AGContact Person: Elisabeth Mostofi, CEOEmail: elisabeth.mostofi@ba Ʃeryconsult.chPhone: +41 33 972 1308About Ba Ʃery Consult AGBaƩery Consult AG, the global competence center for SaltBa Ʃeries, is a leading research and development companyspecializing in SaltBa Ʃery technology. Ba Ʃery Consult is commi Ʃed to driving innova Ɵon and sustainability in the energystorage sector.With a focus on op Ɵmizing NaNiCl2-cell and ba Ʃery designs, the company aims to achieve sustainable and cost-effec ƟvesoluƟons for the sta Ɵonary grid storage markets. Since its establishment in 2008, Ba Ʃery Consult AG has been a trustedpartner in na Ɵonal and interna Ɵonal research projects and has completed numerous interna Ɵonal technology transfers.Energy cells type STC-140 and STC-250 are registered for patent under the number PCT/EP 2020-073992.BaƩery Consult AG is based in the Energy city of Meiringen, Berner Oberland, Switzerland.www.baƩeryconsult.ch(3) BaƩery Consult AG: Company Page Admin | LinkedInBattery Consult AGVeröffentlicht:18 Januar 2024Pensum:100%Vertrag:FestanstellungArbeitsort:MeiringenHead of ChemistryFrau Dr. Rebecca Busch übernimmt die Leitung der Chemie bei derBaƩery Consult AGBaƩery Consult AG freut sich, die Aufnahme von Dr. Rebecca Busch als Leiterinder Chemie ab Januar 2024 bekannt zu geben. Mit einem abgeschlossenenDoktoratsstudium am KIT, Karlsruhe in Deutschland, bringt Frau Dr. Buschumfangreiches Fachwissen im Bereich Ba Ʃeriesysteme mit, insbesondere in derEntwicklung anorganischer Elektrolyt-Systeme.Mit Leidenscha Ō für die Energiewende, freut sich Dr. Busch, nachhal ƟgeEnergiespeicherlösungen wie unsere bahnbrechenden SalzBa Ʃerien fürindustrielle Anwendungen anzubieten. Ihr Eintri Ʃ in dieser kri Ɵschen Phase wirdeine entscheidende Rolle bei der Einführung unserer innova Ɵven Lösungen auf dem Markt spielen.Wir möchten Dr. Akane Hartenbach, die bisher eine wich Ɵge Rolle auf unserer Reise gespielt hat, unserengrossen Dank aussprechen. Akane Hartenbach hat über viele Jahre die chemischen Entwicklungen mitgrosser Umsicht vorangetrieben und war federführend beim Au ĩau und der Leitung der Chemie der Ba ƩeryConsult AG. Frau Hartenbach wird in Kürze eine professionelle Auszeit nehmen und das Ruder an Frau Buschübergeben.Frau Dr. Busch mit ihren eigenen Worten: "Ich freue mich sehr, bei der Ba Ʃery Consult AG mitzuarbeiten,und Teil dieses dynamischen Teams zu sein. Dies ist eine entscheidende Zeit für die KommerzialisierungnachhalƟger Energiespeicherlösungen, und ich bin begeistert, Veränderungen voranzutreiben und zurEnergiewende beizutragen. Ich glaube fest an das Potenzial der SalzBa Ʃerie für industrielle Anwendungen,und ich freue mich darauf, die Zukun Ō der Energiespeicherung mit einem starken Fokus auf Nachhal Ɵgkeitund Umwelt zu prägen."Wir freuen uns, mit Dr. Rebecca Busch einen kompetenten, visionären Teamplayer willkommen zu heissen.Gemeinsam werden wir die Energiespeicherbranche revolu Ɵonieren und eine nachhal Ɵge Wirkung auf dieWelt haben. Das gesamte Team der Ba Ʃery Consult AG, sowie der Verwaltungsrat, bedanken sich bei derbisherigen Stelleninhaberin, Frau Dr. Hartenbach für die vertrauensvolle Zusammenarbeit der letzten Jahreund wünschen alles erdenklich Gute für die Zukun Ō.Für weitere Informa Ɵonen oder Presseanfragen wenden Sie sich bi Ʃe an:BaƩery Consult AGAnsprechpartner: Elisabeth Mostofi, CEOE-Mail: elisabeth.mostofi@ba Ʃeryconsult.chTelefon: +41 33 972 1308Näheres zur Ba Ʃery Consult AG:BaƩery Consult AG ist das globale Kompetenzzentrum für SalzBa Ʃerien und spezialisiert auf SalzBa Ʃerie-Technologie.Unser Fokus liegt auf der Op Ɵmierung von NaNiCl2-Zellen- und -Ba Ʃeriedesigns, um nachhal Ɵge und kosteneffek Ɵve

Laboratory Analyst (chemistry) On behalf of our client, a growing company based in Neuchâtel, we are currently looking for a Laboratory Analyst (chemistry) Vos tâches Duties and Responsibilities Performs analytical testing of solid oral drug products for release and stability testing (HPLC / UPLC, GC, UV/VIS, dissolution, etc.). Performs associated laboratory work (preparation of solutions, waste disposal, etc). Supports testing of raw materials according to pharmacopeia requirements. Performs peer review of analytical data. Respects EHS rules at all time. Respects 5S principles and proposes ideas for continuous improvement to lab processes. Can be assigned special tasks and project work. Votre profil Competences The main responsibility of the position of Laboratory Analyst is to perform analytical chemistry testing that is required for release of drug products, stability samples and raw materials. Additional responsibilities may include support to analytical method transfers and validations, stability studies, revision of documents, handling of deviations and implementation of change controls. As a QC team member, the person filling this position supports all activities to continuously maintain the GMP status of the QC Laboratory. Skills/Knowledge Required Federal Certificate of Capacity as Laboratory Technician or similar education 2 - 3 years of work experience in a GMP environment or similar (ISO 17025, ...) Hands-on experience in HPLC and GC techniques Knowledge of dissolution, UV/VIS and IR techniques. Good writing skills. Excellent team spirit. Working knowledge in English and good knowledge of French. Comfortable using common Office software. Langues Working knowledge in English and good knowledge of French. M. Dominique Bréa+41 32 720 20 30Grand-Rue 62000Neuchâtelhttps://www.maffioli.ch

 Work Your Magic with us!   Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.   United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe. Stage - QC Chimie Lieu: Corsier-sur-Vevey, SuisseQuand : à déterminer Durée : 1 année En tant que membre du QC, vous aurez comme activités principales : L'implémentation d'un nouvel équipementLa validation des méthodes analytiquesL'Amélioration des méthodes du QC Chimie En parallèle, vous apporterez votre soutien aux activités du QC Chimie :Gestion des échantillons physiques et via notre système de gestion des échantillons GLIMSImplication dans l'EHSNormalisation des méthodesParticipation aux projets du QC ChimieAlignement à la Conformité (ouverture de déviations et collaboration à toute enquête analytique) Vous aurez aussi à participer activement aux activités quotidiennes du QC. Vous effectuerez des analyses de routine conformément au planning et retournerez les rapports de résultats dans les délais impartisEn tant que membre de l'équipe, vous prendrez part aux discussions et participerez activement à l'amélioration continue de l'équipe. Vous contribuerez également à l'élaboration de procédures pertinentes et, le cas échéant, à la mise à jour des documents contrôlés pour répondre aux exigences. TON PROFILConnaissance des méthodes Analytiques du laboratoire de chimieConnaissance des pharmacopées et notion des GMP Connaissance des équipements du laboratoire de ChimieExpérience dans la Gestion de ProjetsUne forte capacité à communiquer et des compétences diplomatiquesFrançais courant, bonnes connaissances en Anglais (oral et écrit) CE QUE NOUS OFFRONSNous offrons un environnement de travail moderne et international pour libérer votre potentiel d’innovation dans des équipes diversifiées et prendre la responsabilité de nos employés, de nos produits, de l’environnement et de la société. Please note that only candidates currently undertaking their studies are eligible for an intern position. An Internship Agreement will have to be issued by your school. Only applicants fulfilling this criterion will be considered. What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!   Apply now and become a part of our diverse team! Über das Unternehmen:Merck KGaA Darmstadt, GermanyBranche:QC, Chemistry, Environmental Health & Safety, Neurology, Oncology, Quality, Science, Healthcare

Bei der nemensis ag haben wir bereits tausende Bewerber mit ihrem Traumjob verbunden und ihnen die Möglichkeit gegeben, sich weiterzuentwickeln oder wieder in den Arbeitsmarkt einzusteigen. Für unseren Kunden, ein internationales Unternehmen in der Region Schachen LU, suchen wir eine/n Laborant Mikrobiologie. Vertragsart: Temporär über nemensis ag, 100%ID: 20626Beschäftigungsdauer: 01.03.2024 - 28.02.2025Lohnspanne: CHF 42.- - 51.- / Std. brutto Ihre Hauptaufgaben:Mitarbeit im Team der Qualitätskontrolle Mikrobiologie Review von papierbasierten Rohdaten und Rohdaten innerhalb elektronischer Datenmanagementsystemen, sowie DatenevaluierungLeiten von mikrobiologischen Studien und Projekten Erstellen von Standardarbeitsanweisungen (SOPs) und von Qualifizierungs- und Validierungsprotokollen und Reports Mikrobiologische Laborarbeiten in Unterstützung für aktuelle Projekte Auslösen, Bearbeiten und Abschliessen von Abweichungsdokumentation und Änderungsmanagement Zusätzliche Aufgaben gemäss Erfahrung Ihr Profil:Master Abschluss in Mikrobiologie oder einem verwandten Gebiet mit 1+ Jahr Berufserfahrung in der Pharmaindustrie, abgeschlossene Berufsausbildung (EFZ Fachrichtung Biologie) oder Bachelor in Biologie mit 3+ Jahren Berufserfahrung Stärke für die termingerechte Lieferung von Ergebnissen zur Unterstützung der Pipeline Erfahrung im GMP-Umfeld Teamorientierte und offene Persönlichkeit Wir freuen uns auf Ihre Bewerbung!Annika Schelp, +41 61 205 98 78, [email protected] Branche: Pharma-IndustrieFunktion: Forschung und EntwicklungAnstellungsart: Temporäre ArbeitÜber das Unternehmen:nemensis ag

Working with Us Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible. Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us. In this role you will share oversight of Quality Control (QC) activities related to Drug Product and Incoming Material to ensure compliance with internal policies, procedures, and regulatory requirements. This position will provide support for design, execution, troubleshooting and monitoring of QC process and testing activities pertaining to raw material (including sampling), stability, in-process, and bulk product. You will be responsible for cGMP compliance of the laboratory area and operations under your responsibility as well as for applying and ensuring staff complies with Environmental Health & Safety applicable procedures. This position reports to the Associate Director Quality Control Drug Product and Incoming Material. Key Responsibilities Manage team and ensures cGMP compliance of the laboratory area and operations under responsibility. Create a positive and collaborative team environment and ensure that Bristol Myers Squibb standards are met. Manages performance and provides technical guidance, coaching and support to team members. Assigns training requirements and monitors training status of assigned team members. Create team plans to ensure resources are properly allocated and utilized effectively. Ensures all equipment used for GMP testing is in a qualified state. Authors, reviews, and approves complex GMP documentation such as laboratory procedures, work practices, plans, protocols, and reports. Support and sustains Lean Lab initiatives such as 5S, deviation reduction, Right First Time, and inspection readiness. Actively participates in inspections by Health Authorities. Report metrics to monitor schedule progress and help identify risk areas. Supports budget definition and adherence to budget target. Support purchase requisitions and purchase orders are managed as appropriate to ensure business needs are met in timely manner. Oversee QC incoming material, stability, in-process and bulk product testing activities. Collaborate cross-functionally and interdepartmental to define testing priorities, assign work to team members, and monitor progress against schedule. Ensure timely completion of stability samples in compliant with company procedures. Review and approve documentation as required by laboratory procedures. Perform final approval and disposition of QC results. Provide technical support to QC team members. Ensure compendial compliance of excipients (USP, Ph. Eur., JP and JPE as applicable) and evaluates any non-compendial supplier test methods against in-house methods and specifications. Defines incoming testing requirements of Incoming Materials, including specifications. Oversee sampling plan and testing regimes for all Incoming Materials. Provides oversight of testing contracted to external laboratories. Represents QC in cross-functional teams supporting New Product Introductions, Qualification and Risk Assessments. Support Deviations, Investigations and Change Control Management Ensures Deviations, CAPAs and Change controls are handled appropriately and in a timely manner. Initiates and/or implement changes in controlled documents. Own or lead investigations in collaboration with internal and external functions, as required. Approve laboratory investigations, checklists, and deviations as SME/Area Manager. Work with impacted QC area functions to define appropriate and effective corrective and preventive actions (CAPAs). Ensure timely and compliant closure of QC deviations/investigations and CAPAs according to Bristol Myers Squibb procedures. Promotes safe practices and behaviors. Report immediately incidents to Environmental Health and Safety (EHS) department, participate in investigations and identify measures to prevent similar accidents in the future. Ensures that staff (including short duration and temporary contracts) is properly informed on hazards and trained to act in consequence. Promotes safe practices and behaviors, assure that EHS requirements are implemented and respected. Demonstrate Bristol Myers Squibb values. Performs other tasks as assigned. Qualifications & Experience Education and Experience BS or advanced degree in Chemistry, Biochemistry, Pharmacy, or relevant scientific discipline or equivalent combination of education, training and experience. Minimum 5 years of work experience in a GMP environment (pharmaceutical industry or similar field) 1-3 years of Quality Control Laboratory management experience prefer. Exceptional scientific and practical knowledge of analytical techniques (e.g., chromatography techniques (High-performance liquid chromatography, Ultra-performance liquid chromatography, Gas chromatography), Dissolution, UV/VIS, and IR techniques). Experience in executing quality control testing of solid oral dosage forms and raw materials. Exceptional knowledge of incoming material sampling and inspection. Working knowledge of relevant US, EU. and global regulations and ICH, ISPE, ASTM standards/guidelines and experience in participation of regulatory inspections. Experience with Laboratory Information Management System (LIMS), Learning Management System (LMS) and Enterprise Resource Planning System (ERP). Required Competencies: Knowledge, Skills, and Abilities Subject matter expert of Quality Control activities in the pharmaceutical industry with strong knowledge and interpretation of cGMP and regulations applicable to solid oral dose forms. Knowledge of Data Integrity and Good Documentation Practices. Ability to accurately understand, follow, interpret, and apply European Pharmacopeia and United States Pharmacopeia requirements and cGMP requirements. Exceptional technical writing skills. Work to improve efficiencies through process improvements Independent, adaptable, and highly motivated. Action-oriented and capable of setting priorities, managing timelines, and effectively managing changing priorities. Exceptional communication skills (verbal and written) to all employee levels, executive leadership and external partners, suppliers, third parties, and industry organizations. Ability to navigate through ambiguity and rapid growth and adapt to change the status quo. Ability to be agile and effectively collaborate in a dynamic, cross-functional matrix environment. General computer literacy including MS Office (Word, Excel, PowerPoint, Outlook, Visio) Fluent in English or French and professional command (minimum B2 level) of the second language (written and verbal) If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career. Uniquely Interesting Work, Life-changing Careers With a single vision as inspiring as “Transforming patients’ lives through science ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. On-site Protocol Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture. BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [email protected]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement. BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters. BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area. Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations. Data Privacy Link We’re creating innovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.Über das Unternehmen:1112 Celgene International SaRL

The Research Director will be an integral part of a dedicated secretariat team and collaborate closely with various stakeholders including representatives, facilitators, working groups, project managers, and external partners to ensure the completion of scientific research initiatives. The role involves overseeing the scientific research program, fostering engagement within the academic community, and focusing on issues related to human health and the environment, particularly those associated with the tire life cycle.Key Responsibilities:Cultivating and managing an academic network to gather expert knowledge and ensure fact-based communication.Ensuring the neutrality and scientific integrity of research approaches through collaboration with assurance groups and advisory panels.Supervising the progress of scientific research programs and managing project managers.Collaborating with stakeholders to develop study designs, set objectives, and optimize deliverables.Working with industry stakeholders to align on technical needs and outcomes of research projects.Facilitating reporting and reviews at various levels and synthesizing knowledge for broader dissemination.Representing the organization in scientific forums and engagements.Proactively identifying and planning for emerging research topics.Managing and aligning multiple research co-chairs from different organizations.The ideal candidate will possess advanced knowledge of research governance and demonstrate strong management and communication skills.They will play a pivotal role in driving impactful and relevant scientific research initiatives while ensuring transparency and engagement across stakeholders.A PhD or MD in chemistry, toxicology, materials, chemical engineering, engineering or environmental sciences.Min. 10 years of working experience in management of research projects or scientific communication, in private sector or academia.Experience in managing or coordinating complex research programs either in the private sector or academic world with a wide range of stakholders.Global mindset coupled with hands-on experience working across geographies,Good communicator with a diplomatic approach, good listening skills and ability to find consensus and to gather around a common goalExperience in working and collaborating across time zones, with multiple cultures and languagesEnglish fluent is a must have. Japanese is a clear plus. German, Italian, French is a nice to have.Willingness to travel internationally (20%-30%)Ability to commute 2 to 3 times a week to the office either in Geneva or Amsterdam.Only candidates with EU work permit can be considered.