225 Jobs in Brüttelen

Du bist Pflegeprofi mit Herz und Humor? Dann bist du hier richtig – wir suchen dich als Verstärkung im Pflegedienst!

Pflegefachperson HF 40–50%

Aufgaben

Du gestaltest aktiv den Aufbau einer Inhouse-Spitex.

Du verantwortest Pflegeprozesse mit interRAI Schweiz.

Du stellst die pflegerische und medizinische Versorgung sicher.

Du unterstützt Teams bei pflegerischen Fragen und Herausforderungen.

Du koordinierst ärztliche Verordnungen und Dokumentationen mit easyDOK.

Profil

Ausbildung als Dipl. Pflegefachperson HF/FA/AKP/DNII

Erfahrung in Spitex und interRAI HC

Kenntnisse in Akut- und/oder Langzeitpflege

Sozialkompetenz, Organisationstalent und klare Kommunikation

Belastbar, flexibel, humorvoll und teamorientiert

PW-Ausweis sowie sichere EDV-Kenntnisse

Vorteile

Abwechslungsreiche Aufgaben mit einem motivierten Team.
Regelmässige Arbeitszeiten im Tagesbetrieb.
Attraktive Bedingungen nach kantonalen Richtlinien.
Kostenloser Parkplatz und ÖV-Anschluss.

Klingt spannend? Dann freuen wir uns, dich kennenzulernen!

Kontaktinformationen

Falls du weitere Fragen zu diesem Stellenangebot (Referenz: JN - ) hast, kontaktiere bitte Fabienne Zbinden unter .

Über uns

Adecco ist Marktführer für Personallösungen in der Schweiz und weltweit. Jeden Tag sorgen unsere Teams in unseren rund 50 Standorten schweizweit für den besten Match zwischen Kandidat:innen und Kunden in unterschiedlichen Berufsfeldern und Branchen.

Adecco Schweiz ist ein Unternehmen der Adecco Gruppe, dem weltweit führenden Unternehmen für Talent Advisory und Solutions. Wir glauben daran, jeden für die Zukunft fit zu machen und beschäftigen täglich über 3,5 Millionen Menschen. Wir rekrutieren, entwickeln und bilden Talente in 60 Ländern aus, und ermöglichen es Organisationen, die Zukunft der Arbeit mitzugestalten.

#yournextjob

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
Are you set for an outstanding opportunity in Switzerland with a top-notch team? As a Program Manager at Thermo Fisher Scientific Inc., you'll be crucial in ensuring flawless project execution while maintaining exceptional standards.
**Responsibilities:**
+ Manage programs allocated to the Lengnau site, guaranteeing that project achievements are met as per the plan/contract.
+ Raise issues to site leadership and uphold effective communication with clients and program owners.
+ Lead all aspects of Project Charters for each project, clearly defining objectives, timelines, communication channels, and meeting regimes.
+ Act as a role model and main driver of the execution of the Project Charter, encouraging effective communication with clients, ThermoFisher senior management, Subject Matter Experts, and project teams.
Budget Control
+ Maintain accurate financial records with the assistance of ThermoFisher's financial team.
+ Ensure timely invoicing to generate revenue for ThermoFisher.
+ Communicate with the finance department to offer detailed financial reporting of the program internally.
Expertise and Compliance
+ Provide extensive knowledge of the pharmaceutical industry to ensure safe product availability to patients.
+ Ensure ThermoFisher's Safety Standards are maintained throughout the project execution.
+ Document program activities to meet regulatory authorities' mentorship and expectations.
+ Maintain a strong network of Subject Matter Experts within the ThermoFisher team to bolster a range of skills.
**Position Qualifications:**
+ Master degree in science/engineering or other similar education
+ >7 years experience in the pharmaceutical industry, within CMC/technical development
+ >5 years in project management or related
+ Proficiency in project management methodologies, including managing project plans, schedules, and budgets
+ Understanding of the technical aspects relevant to the projects being managed
+ Ability to identify, assess, and mitigate risks throughout the project lifecycle
+ Leadership: Ability to inspire and motivate the team. Strong decision-making skills and confidence in leading the project
+ Communication: Excellent verbal and written communication skills. Ability to communicate effectively with stakeholders, team members, and management
+ Adaptability: Flexibility to adapt to changing project requirements and environments. Ability to handle unexpected challenges and changes effectively
Embark on our journey to improve global health, cleanliness, and safety. Your role at Thermo Fisher Scientific will significantly impact international health and safety benchmarks. We are looking forward to having you on board with our team!
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards
**Job Description**
**Job Purpose:**
The Manufacturing Planner is responsible for the day-to-day scheduling and coordination of manufacturing activities to support continuous and efficient production. This includes planning campaign sequences, issuing daily schedules, monitoring progress on the shop floor, and adjusting plans in real time to ensure seamless operations. The role acts as the link between Production, Quality, Maintenance, and Supply Chain to maintain smooth campaign execution under GMP conditions.
**Key Responsibilities:**
**Daily Scheduling and Execution**
+ Prepare and issue daily and weekly production schedules for all manufacturing areas.
+ Ensure the availability of equipment, materials, and documentation before batch start.
+ Track progress of ongoing batches and update plans in real time based on operational status.
+ Communicate daily priorities and updates to Production Manager, Supervisors and Operators.
+ Adjust schedules promptly in response to deviations, equipment issues, or material delays.
**2. Campaign Planning**
+ Support the setup and coordination of manufacturing campaigns.
+ Define batch sequence, cleaning intervals, and equipment allocation to optimize efficiency.
+ Ensure readiness of all required tools, parts, and utilities prior to campaign start.
+ Maintain an overview of campaign progress and escalate delays or risks to the Production Manager.
**3. Cross-Functional Coordination**
+ Coordinate with Supply Chain and Warehouse to confirm raw material and component availability.
+ Work closely with Maintenance to plan interventions and avoid production interruptions.
+ Support communication between shifts to ensure continuity of production activities.
**4. Documentation and Systems**
+ Maintain up-to-date information in planning and tracking tools.
+ Record production plan changes, reasons for delays, and corrective actions in compliance with GMP documentation standards.
+ Prepare short-term capacity and utilization reports as needed.
**5. Continuous Improvement**
+ Propose and implement improvements to scheduling processes and coordination routines.
+ Participate in daily tier meetings and performance reviews to identify efficiency gains.
+ Support Production in troubleshooting and reducing downtime related to planning or coordination gaps.
**Education & Experience:**
+ Bachelor/Master/PhD in Chemistry, Biochemistry, Biotechnology, Biology, or Food Science.
+ Proficiency in English; German is a plus.
+ Minimum of 5 years in pharmaceutical operations within a GMP environment.
+ Strong experience in biotech processes, sterile processes, and production equipment handling.
+ Ability to thrive in a matrix environment with cross-functional teams.
+ Availability for remote on-call duties.
**Benefits:**
+ Competitive remuneration and comprehensive benefits package.
+ Work with an innovative, forward-thinking organization that values integrity, intensity, involvement, and innovation.
+ Outstanding career and development prospects.
+ A company culture that embraces diversity and values individual contributions.
Join us! At Thermo Fisher Scientific, you'll be part of a global team of over 100,000 colleagues dedicated to making the world healthier, cleaner, and safer. Start your story with us, where diverse experiences, backgrounds, and perspectives are valued. Together, we're accelerating research, solving complex scientific challenges, and supporting patients in need
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

**Work Schedule**
Rotational days/weekends
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed, Cold Room/Freezers -22degreesF/-6degrees C, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
**Job Description**
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. We strive to support our customers in promoting a healthier, cleaner, and safer global environment. Whether our customers are advancing life sciences research, solving sophisticated analytical challenges, improving efficiency in their laboratories, promoting patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to assist them. Our distributed team of over 100,000 colleagues collaborates across various locations to provide a ground-breaking mix of brand-new technologies, convenient purchasing options, and pharmaceutical services. Our industry-leading brands include Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
The state-of-the-art multi-purpose manufacturing facility is crafted for large-scale production of biologics and has high expansion potential. After completion of construction activities, our site in Lengnau will offer highly flexible biomanufacturing technologies, from development to large-scale production including stainless steel equipment to meet our customer needs.
**Purpose**
+ This position leads a manufacturing team (shift in upstream, downstream, solution preparation and support) to ensure the operational activities for the production of recombinant products
+ This position supports project teams in the design, commissioning, qualification and validation of new production lines for recombinant products
**Responsibilities**
+ Is responsible for the daily operations of their shift in manufacturing suites, including daily schedule,
+ Is responsible for the daily execution of manufacturing activities in USP or DSP
+ Owns Work Instructions and SOP in their area
+ Support Manufacturing Excellence in order to run robustly and smoothly
+ Participates in defining robust process parameters during routine manufacturing campaigns
+ Participate in New Product Introduction activities
+ Ensure training and compliance records are in date
+ Commits to Thermo Fisher Scientific values and adherence to ethics and legal compliance standards.
+ Takes personal accountability for their presence, performance, and productivity for the achievement of defined objectives.
+ Adheres to EHSS legal requirements, rules, policies, procedures and instructions for their area of responsibility.
+ Contributes to EHSS initiatives and issues as well as near miss reporting and follow-up.
**Qualifications**
+ Bachelor's degree in pharmaceutical, food or chemistry
+ Language: English or German
+ 1-3 years successful experience in pharmaceuticals operations in a GMP relevant environment
+ The function requires a first experience in pharmaceutical industry
+ Willingness to learn
+ Can-do attitude
+ Work on a shift rotation model, this includes regular weekend, and public holiday work
+ On-call duties is expected according to respective planning
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

**Date Posted:**

**Country:**
Switzerland
**Location:**
Route de Moncor 12, CP 1136, 1701 Fribourg
**Votre rôle :**
**Véritable pilier de l'accueil et du bon fonctionnement du bureau, vous assurez une présence professionnelle, chaleureuse et efficace, tout en apportant un soutien administratif polyvalent à l'ensemble de l'organisation.**
**Responsabilités :**
**Accueil & communication**
+ Gérer les appels téléphoniques et les courriels entrants avec professionnalisme.
+ Accueillir les visiteurs avec courtoisie et les orienter vers les bons interlocuteurs.
**Gestion administrative & logistique**
+ Réception, tri, distribution et envoi du courrier, colis, etc.
+ Suivi des fournitures de bureau, des cartes de parking, etc.
+ Coordination de la maintenance des locaux et des prestataires externes.
+ Organisation de réunions, réservation de salles et coordination des déplacements.
**Soutien opérationnel & événementiel**
+ Appui à l'équipe de direction pour la gestion de correspondances confidentielles et la coordination d'événements.
+ Organisation d'activités internes (conférences, team building, etc.).
+ Rédaction de comptes rendus de réunions clairs et synthétiques.
**Support RH & juridique**
+ Participation à l'intégration des nouveaux collaborateurs au siège.
+ Préparation de documents administratifs et juridiques simples.
+ Veille au respect des procédures internes et des normes réglementaires.
**Compétences clés**
+ **Relationnelles :** Sens de l'accueil, écoute active, diplomatie, discrétion.
+ **Organisationnelles :** Rigueur, ponctualité, gestion des priorités et des imprévus.
+ **Linguistiques :** Maîtrise du français, de l'allemand et de l'anglais (oral et écrit). L'italien est un atout.
+ **Techniques :** Bonne maîtrise des outils bureautiques (Word, Excel, Outlook).
**Indicateurs de performance**
+ **Qualité de l'accueil :** Satisfaction des visiteurs et interlocuteurs.
+ **Efficacité administrative :** Respect des délais et fiabilité des livrables.
+ **Polyvalence :** Capacité à gérer plusieurs missions simultanément avec calme et méthode.
If you live in a city, chances are we will give you a lift or play a role in keeping you moving every day.
Otis is the world's leading elevator and escalator manufacturing, installation, and service company. We move 2 billion people every day and maintain approximately 2.2 million customer units worldwide, the industry's largest Service portfolio.
You may recognize our products in some of the world's most famous landmarks including the Eiffel Tower, Empire State Building, Burj Khalifa and the Petronas Twin Towers! We are 69,000 people strong, including engineers, digital technology experts, sales, and functional specialists, as well as factory and field technicians, all committed to meeting the diverse needs of our customers and passengers in more than 200 countries and territories worldwide. We are proud to be a diverse, global team with a proven legacy of innovation that continues to be the bedrock of a fast-moving, high-performance company.
When you join Otis, you become part of an innovative global industry leader with a resilient business model. You'll belong to a diverse, trusted, and caring community where your contributions, and the skills and capabilities you'll gain working alongside the best and brightest, keep us connected and on the cutting edge. 
We provide opportunities, training, and resources, that build leadership and capabilities in Sales, Field, Engineering and Major Projects and our Employee Scholar Program is a notable point of pride, through which Otis sponsors colleagues to pursue degrees or certification programs.
Today, our focus more than ever is on people. As a global, people-powered company, we put people - passengers, customers, and colleagues - at the center of everything we do. We are guided by our values that we call our Three Absolutes - prioritizing Safety, Ethics, Quality in all that we do. If you would like to learn more about environmental, social and governance (ESG) at Otis click here ( .
Become a part of the Otis team and help us #Buildwhatsnext!
_Otis is An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status, age, or any other protected class according to applicable law. To request an accommodation in completing an employment application due to a special need or a disability, please contact us at
**Privacy Policy and Terms:**
Click on this link ( to read the Policy and Terms
We go to great lengths to hire and develop the best people, and offer a supportive environment where employees are motivated and empowered to perform at their full potential. Today, we continue pushing the boundaries of what's possible to thrive in a taller, faster, smarter world.

Chez Nespresso Suisse nous pensons qu'il est possible d'élever l'univers du café et nous voulons contribuer positivement à changer les vies et les paysages pour le mieux. Élu meilleur employeur 2025, nous plaçons chacun de nos 14 000 collaborateurs, sans exception, au cœur de notre réussite. Pour y parvenir, nous adoptons quatre comportements essentiels : « We Inspire, we Care, we Act, and we iNnovate ». Et vous ? Voulez-vous nous accompagner dans cette aventure passionnante ? Rejoignez l'équipe Nespresso ! Et réimaginez la nature du café. Réimaginez votre avenir.
**Le poste en un coup d'œil**
Lieu : Avenches, Switzerland
Entité : Centre de Production Nespresso
Taux : Temps plein 100%
Type de contrat : Contrat indéterminé
**Ce que nous offrons chez Nespresso**
De réelles opportunités d'évolution de carrière et de développement personnel
Un cadre de travail flexible facilitant la créativité et la collaboration
Une culture fondée sur la bienveillance et l'inclusivité, où chacun peut être soi-même
La qualité et la durabilité au cœur de notre identité et une vision essentielle pour favoriser le changement positif L'opportunité de travailler pour une entreprise certifiée B Corp, et l'une des marques les plus fiables et appréciées à l'échelle mondiale.
Au cours du processus de recrutement, n'hésitez pas à nous en parler pour en savoir plus !
Découvrez notre page Linkedin : Nespresso Centres de production ( n
Découvrez nos métiers : Métiers Nespresso - YouTube ( e
**Résumé du poste**
En tant que **Technicien de maintenance en horaire d'équipe 4x8 (H/F/D)** , vous serez en charge d'assurer le fonctionnement et la maintenance de nos lignes de production. Vous effectuerez les interventions techniques correctives et participerez activement à l'amélioration continue. Découvrez le métier de Technicien Vidéo Métier ( .
**Une journée dans la vie d'un(e) Technicien de maintenance en horaire d'équipe 4x8 (H/F/D)**
- Assurer le bon fonctionnement et le dépannage mécanique, électrique et automatique de nos installations de production
- Participer aux divers travaux de maintenance préventive, corrective et maintenance conditionnelle dans les différentes zones de l'usine
- Participer aux projets d'amélioration continue
- Suivre et respecter les directives de sécurité, de santé, d'environnement et d'hygiène.
**Vos atouts pour réussir**
- CFC d'Automaticien ou formation jugée équivalente
- OIBT15, un atout
- Expérience de minimum 2 ans dans la maintenance industrielle
- Bonne capacité d'analyse et de résolution de problèmes.
**Avantages**
- 5 semaines de vacances
- Possibilité de formation et de développement internes
- Caisse de pension avec excellentes contributions de l'employeur
- Participation financière à l'assurance maladie
- Politique parentalité avantageuse
- Restaurant d'entreprise sur place avec menus à prix subventionnés
- Parking gratuit et bornes de recharge pour voitures électriques
- Nombreux avantages auprès du Club Nespresso
Chez Nespresso, nous avons bâti une culture fondée sur la bienveillance et l'inclusion, où chacun peut être soi-même, tout en grandissant aux côtés de l'entreprise. Nous innovons, osons essayer, apprenons et grandissons dans un environnement numérique et connecté où tout va très vite. Au sein d'une équipe diverse regroupant plus de 90 nationalités dans 58 pays, vous pouvez prendre part à une culture innovante, dans laquelle les personnes n'hésitent pas à s'entraider. Une culture dans laquelle chacun est encouragé à remettre en question le statu quo et à définir l'avenir d'une des plus grandes entreprises durables. Quel que soit le rôle que vous jouerez, vous découvrirez que vous pouvez réellement changer les choses et partager votre enthousiasme. Rejoignez ce lieu où vous pourrez vous épanouir, trouver une appartenance et l'inspiration pour devenir le meilleur de vous-même et vous surpasser.

**Work Schedule**
Rotational days/weekends
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed, Cold Room/Freezers -22degreesF/-6degrees C, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
**Job Description**
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. We strive to support our customers in promoting a healthier, cleaner, and safer global environment. Whether our customers are advancing life sciences research, solving sophisticated analytical challenges, improving efficiency in their laboratories, promoting patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to assist them. Our distributed team of over 100,000 colleagues collaborates across various locations to provide a ground-breaking mix of brand-new technologies, convenient purchasing options, and pharmaceutical services. Our industry-leading brands include Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
The state-of-the-art multi-purpose manufacturing facility is crafted for large-scale production of biologics and has high expansion potential. After completion of construction activities, our site in Lengnau will offer highly flexible biomanufacturing technologies, from development to large-scale production including stainless steel equipment to meet our customer needs.
**Purpose**
+ This position conducts the production of recombinant products by operating automated production equipment
+ The holder supports compliance, scheduling, material management, change controls, investigation, CAPA, operational excellence, etc
+ This position supports project teams in the design, commissioning, qualification and validation of new production lines for recombinant products
+ This position supports the start-up of new production lines
**Responsibilities**
+ Is responsible for the daily execution of manufacturing activities in USP, DSP or support area (media and buffer preparation, equipment cleaning and preparation)
+ Act as first point of contact and reference within manufacturing team regarding training and troubleshooting
+ Owns Work Instructions and SOP in their area
+ Investigate Manufacturing Excellence initiatives in order to run robustly and smoothly
+ Participates in defining robust process parameters during routine manufacturing campaigns
+ Participate in New Product Introduction activities
+ Ensure training and compliance records are in date
+ Commits to Thermo Fisher Scientific values and adherence to ethics and legal compliance standards
+ Takes personal accountability for their presence, performance, and productivity for the achievement of defined objectives
+ Adheres to EHSS legal requirements, rules, policies, procedures and instructions for their area of responsibility
+ Actively contributes to EHSS initiatives and issues as well as near miss reporting and follow-up
**Qualifications**
+ Bachelor/Master in Chemistry / Biochemistry / Biology / Food Science
+ 3-5 years successful experience in pharmaceuticals operations in a GMP relevant environment
+ The function requires experience in biotech or pharma processes, either in sterile processes, USP, DSP, solution preparation, single use, CIP/SIP processes
+ Willingness to learn
+ Can-do attitude
+ Language: English and German preferred
+ Work on a shift rotation mode, this includes regular weekend and public holiday work as well as night work
+ On-call duties is expected according to respective planning
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

**Work Schedule**
Rotational days/weekends
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
**Job Description**
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. We strive to support our customers in promoting a healthier, cleaner, and safer global environment. Whether our customers are advancing life sciences research, solving sophisticated analytical challenges, improving efficiency in their laboratories, promoting patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to assist them. Our distributed team of over 100,000 colleagues collaborates across various locations to provide a ground-breaking mix of brand-new technologies, convenient purchasing options, and pharmaceutical services. Our industry-leading brands include Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
The state-of-the-art multi-purpose manufacturing facility is crafted for large-scale production of biologics and has high expansion potential. After completion of construction activities, our site in Lengnau will offer highly flexible biomanufacturing technologies, from development to large-scale production including stainless steel equipment to meet our customer needs.
**Purpose**
+ This position leads a manufacturing team (shift in upstream, downstream, solution preparation and support) to ensure the operational activities for the production of recombinant products
+ This position supports project teams in the design, commissioning, qualification and validation of new production lines for recombinant products
+ This position supports New Product Introduction for recombinant products
**Responsibilities**
+ Is responsible for the daily operations of their shift in manufacturing suites, including daily schedule, shift rotations
+ Lead and develop team members in order to run areas robustly and smoothly, ensuring appropriate succession planning
+ Participates in defining robust process parameters during routine manufacturing campaigns
+ Build cross functional teams and work well with other support functions such as Quality Assurance, Quality Control, Manufacturing Science and Tachnology, Engineering, Validation, and other relevant functional areas
+ Ensures implementation of and adherence to current GMP rules, Quality policies, procedures and instructions for their area of responsibility.
+ Ensures contribution of their interpersonal unit to continuous quality improvement initiatives and deviation reporting and follow-up.
+ Ensures implementation of and adherence to EHSS legal requirements, rules, policies, procedures and instructions for their area of responsibility.
+ Ensures contribution of their interpersonal unit to EHSS initiatives and issues as well as near miss reporting and follow-up.
**Qualifications**
+ Bachelor/Master in Chemistry / Biochemistry / Biology / Food Science
+ 5-7 years successful experience in pharmaceuticals operations in a GMP relevant environment
+ The function requires experience in biotech or pharma processes, either in sterile processes, USP, DSP, solution preparation, single use, CIP/SIP processes
+ Good knowledge and competence in the field of automated processes
+ Experience in leading teams
+ Language: English or German
+ Shift work is expected
+ On-call support
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

**Work Schedule**
Rotational days/weekends
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed, Cold Room/Freezers -22degreesF/-6degrees C, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
**Job Description**
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. We strive to support our customers in promoting a healthier, cleaner, and safer global environment. Whether our customers are advancing life sciences research, solving sophisticated analytical challenges, improving efficiency in their laboratories, promoting patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to assist them. Our distributed team of over 100,000 colleagues collaborates across various locations to provide a ground-breaking mix of brand-new technologies, convenient purchasing options, and pharmaceutical services. Our industry-leading brands include Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.
The state-of-the-art multi-purpose manufacturing facility is crafted for large-scale production of biologics and has high expansion potential. After completion of construction activities, our site in Lengnau will offer highly flexible biomanufacturing technologies, from development to large-scale production including stainless steel equipment to meet our customer needs.
**Purpose**
+ This position leads a manufacturing team (shift in upstream, downstream, solution preparation and support) to ensure the operational activities for the production of recombinant products
+ This position supports project teams in the design, commissioning, qualification and validation of new production lines for recombinant products
+ This position supports New Product Introduction for recombinant products
**Responsibilities**
+ Is responsible for the daily operations of their shift in manufacturing suites, including daily schedule, shift rotations
+ Lead and develop team members in order to run areas robustly and smoothly, ensuring appropriate succession planning
+ Participates in defining robust process parameters during routine manufacturing campaigns
+ Build cross functional teams and work well with other support functions such as Quality Assurance, Quality Control, Manufacturing Science and Tachnology, Engineering, Validation, and other relevant functional areas
+ Ensures implementation of and adherence to current GMP rules, Quality policies, procedures and instructions for their area of responsibility.
+ Ensures contribution of their interpersonal unit to continuous quality improvement initiatives and deviation reporting and follow-up.
+ Ensures implementation of and adherence to EHSS legal requirements, rules, policies, procedures and instructions for their area of responsibility.
+ Ensures contribution of their interpersonal unit to EHSS initiatives and issues as well as near miss reporting and follow-up.
**Qualifications**
+ Bachelor/Master in Chemistry / Biochemistry / Biology / Food Science
+ 5-7 years successful experience in pharmaceuticals operations in a GMP relevant environment
+ The function requires experience in biotech or pharma processes, either in sterile processes, USP, DSP, solution preparation, single use, CIP/SIP processes
+ Good knowledge and competence in the field of automated processes
+ Experience in leading teams
+ Language: English or German
+ Shift work is expected
+ On-call support
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.