15 Jobs für Product Strategy in Schweiz
Product Development Intern

Vor 15 Tagen gepostet
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**Eligibility Requirements:**
+ **EU / EEA citizenship**
+ **Degree obtains later than December 2025**
These requirements are related to local legislation hence there is no flexibility in the application.
**Let's talk about the role**
You as Product developer intern will work in close partnership with the Product developer associate, Designer and PM on the designated category and drive the review and the development of new styles, supporting the team to deliver cost targets aligned with style details and related construction.
**Get ready to make an impact! Here's what you'll be responsible for joining our team as product developer Intern**
. Translating designs into full specification packages with accurate technical details, bill of materials, construction details, size specs and grade rules, proactively offering suggestions for improved construction, aesthetics and manufacturing enhancements.
. Building efficient interaction with the Fit and Tech specialist to improve level of execution and alignment across product categories.
. Monitor style FOB targets, ensuring Timberland quality and fit standards are executed while adopting structured methods and processes to improve workflow.
. Supporting the Product developer associate to plan and track development schedule of all assigned products to ensure timely completion.
. Developing a strong relation with Regional Sourcing teams and work together with vendors to ensure all products meet required standards.
**What you Bring**
The ideal candidate for this role is a detail-oriented team player with basic technical knowledge, interest in textile and apparel industry, strong organizational skills and effective communication abilities.
We are looking for someone who has demonstrated:
+ The ability to quickly adapts to new tools, environments and tasks.
+ The capability to collaborate with teams and that contributes positively to group objectives
+ An understanding of time management, prioritizes tasks efficiently to meet deadlines and maintain productivity
+ A good technical knowledge and proficiency in Microsoft office (Excel, Powerpoint)
+ Good communication skills to interact with team members and stakeholders
+ Willingness and proactive attitude
**What's in it For You**
The VF EMEA Internship Program is a 12-month journey designed to develop and empower emerging talent at the start of their careers. As a company committed to unleashing human potential-fuelled by the ideas, energy, and dedication of our people-you can expect a structured learning path and rich hands-on experience, including:
+ Participate in dedicated skill-building workshops
+ Collaborate on an internal consulting group project
+ Gain on-the-ground insight about our brands during a store visit day
+ Connect through networking opportunities with peers and senior leadership
In the role of Product developer you will work with an international team, discovering all secrets about apparel. We will support you with ad hoc trainings and networking opportunities across other functions and brands.
We want you to focus on what matters, that's why we offer comprehensive benefits that encourage mental, physical, and financial well-being. You will enjoy:
+ A supportive feedback-based culture where respect and integrity guide us
+ An inclusive international environment where people of diverse backgrounds, lifestyles and nationalities work together
+ Being part of an iconic lifestyle brand in a multi-brand, multi country organization
+ On-site gym offering health and well-being initiatives, break out areas with complimentary drinks
+ A discount card with 50% on all VF brands
**Free to Be, Inclusion & Diversity**
As an equal opportunity employer, we strive to foster a culture of belonging based on respect, connection, openness and authenticity.
We are committed to building and maintaining a workplace that celebrates the diversity of our associates, allowing them to bring their authentic selves to work every day.
If you like what you have read and want to join our team then we would like to hear from you!
ARE YOU IN? Apply now - early application increases your chances!
R-
VF Diversity Vision Statement
VF is committed to creating an inclusive environment that welcomes and values the differences among all of our associates, customers, suppliers and the communities in which we live and conduct business. The continued success and growth of VF is enhanced through initiatives that promote diversity throughout VF around the world.VF is an equal employment opportunity/ affirmative action employer of minorities, females, protected veterans and the disabled. VF is committed to providing equal opportunities in employment, and treating our VF associates and VF applicants without discrimination on the basis of their race, color, gender, age, national origin, religion, sexual orientation, gender identity or expression, marital status, citizenship, disability, protected veteran status, HIV/AIDS status, or any other legally protected factor.
Product Development Director
Heute
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Jewelry Watches Product Development
Gestern
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**YOUR MISSION**
Your cross-functional role will be to oversee the entire product development process for your projects, from marketing brief to delivery of the first series.
You are responsible for the transversal management of internal and external stakeholders in the development and launch of new watches.
You will work closely with the Operations and Design teams, as well as with external partners, to ensure that customer and company expectations are met in terms of quality, deadlines and costs.
**YOUR ROLE IN DETAIL**
+ Manage and coordinate new product development projects, ensuring delivery on time and on budget, while guaranteeing product quality.
+ Draw up and manage project schedules to ensure successful completion, identifying potential risks and deviations as early as possible.
+ Supervise and coordinate the actions of the various internal and external teams involved in the project.
+ Collaborate with internal and external teams to identify technical and aesthetic solutions in the design/prototyping phase.
+ Monitor project progress, identify risks and implement appropriate corrective measures
+ Regularly present status reports and progress reports to stakeholders and management.
+ Manage the budget allocated to projects, monitoring costs and identifying any discrepancies.
**PROFILE**
You have a Master degree in a relevant field such as industrial management, mechanical engineering or equivalent, **with a watchmaking background highly desirable.**
You have significant experience (+5 years) in **managing development projects within the luxury watchmaking OR jewelry sector** . You have an in-depth understanding of the manufacturing process and techniques used in the creation of watches.
Your personal attributes include excellent organizational skills, including time management and effective prioritization. You have natural leadership skills, enabling you to drive a multidisciplinary team towards a common goal. You are able to summarize complex information and solve issues effectively. Dynamism, rigor and proactivity are essential, as is technical curiosity.
You're bilingual in French and English, with excellent oral and writing skills.
You have a perfect mastery of the Office Pack (PowerPoint), MS Project, and any other tool.
_We make it a priority to hire those who have a commitment to people and service, a real interest in watches, and a passion to continuously improve. If you are ready to make your mark, let's connect!_
**Job Identification** : 61422
**Job Category:** : Manufacturing
**Assignment Category** : Regular Full-time
**Remote Positions** : No
**Professional Experience** : Minimum 5 Years
Equal Opportunity Employer
R&D Product Development Engineer
Heute
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Adecco
Hai pregressa esperienza in un ruolo di gestione progetti e/o in un ruolo d'ingegnere di ricerca e sviluppo ed un'ottima conoscenza della lingua inglese?
Se si', approfondisci quest'opportunità!
Responsabilità
Lo scopo del ruolo è quello di una gestione efficiente della progettazione e dello sviluppo di nuovi prodotti così come il perfezionamento dei prodotti esistenti
- Responsabilità dello sviluppo della parte meccanica del prodotto e responsabilità dell'intero progetto nei casi in cui si é nominati Project Leader
- Studio e sviluppo dei prodotti nel rispetto delle specifiche di prodotto richieste, del budget di progetto e delle tempistiche definite nella Roadmap
- Modellazione 3D del prodotto, disegni tecnici di fabbricazione con aggiornamento documentazione tecnica e BOM
- Design meccanico del prodotto e relative valutazioni tecniche (Design for Manufacturing e Design to Cost, dimensionamento e analisi di catene di tolleranza, assemblaggi, selezione dei materiali e calcolo della loro resistenza - statica e a fatica), simulazioni e valutazioni delle condizioni operative e ambientali di lavoro dei prodotti, valutazioni termiche, analisi di test in laboratorio)
- Ottimizzazione dei prodotti dal punto di vista tecnico e logistico con orientamento all'ottimizzazione dei processi produttivi e di controllo
- Valutazione ed ottimizzazione degli aspetti ambientali e di sostenibilità associati all'intero ciclo di vita di un prodotto
- Monitoraggio costante dello stato d'avanzamento dei progetti (project leader) e presentazione dei risultati durante le review di progetto (project engineer)
- Contatto con fornitori per la definizione della parte tecnica dei componenti
- Supporto tecnico ai diversi reparti aziendali: alle vendite durante meeting con clienti; a product managers, vendita e clienti per la definizione tecnica di specifiche per nuovi progetti; ad altri reparti nell'ambito di richieste tecniche, valutazione proposte di miglioramento, richieste di modifica, ritorni cliente, problemi di qualità, blocchi di produzione e altro
Profilo
- Formazione universitaria conclusa nell'ambito della meccanica, microtecnica, meccatronica, robotica, aerospace (Master)
- Ottima conoscenza della lingua inglese; preferibile la conoscenza di tedesco e/o francese
- Pregressa esperienza in un ruolo di gestione progetti e/o in un ruolo di ingegnere di ricerca e sviluppo (minimo 3 anni)
- Preferibile l'esperienza in un settore affine, ovvero la progettazione di micromotori elettrici o la realizzazione di sistemi in ambito microtecnico
- Conoscenza di CAD NX Siemens
- Piacere al contatto interpersonale, carattere aperto e comunicativo, predisposizione al lavoro in squadra
- Orientamento all'obiettivo
- Spiccato senso organizzativo e di gestione delle priorità
- Approccio analitico e di problem solving
- Flessibilità e capacità di lavoro su più progetti contemporaneamente
Vantaggi
Inserimento in una realtà del Canton Ticino a tempo indeterminato.
Informazioni di Contatto
Invia ora la tua candidatura tramite il nostro sito web.
JN -
Chi siamo
Adecco è leader di mercato per le soluzioni di staffing in Svizzera e nel mondo. Ogni giorno, i nostri team nelle nostre circa 50 sedi in tutta la Svizzera assicurano il miglior incontro tra candidati e clienti in diversi ambiti professionali e settori. Il Adecco Svizzera è una società del Gruppo Adecco, leader a livello globale per Talent Advisory e Solutions. Siamo profondamente convinti di poter far sì che tutti siano in forma per il futuro e impieghiamo più di 3,5 milioni di persone quotidianamente. Reclutiamo, sviluppiamo e creiamo talenti in 60 Paesi, permettendo alle organizzazioni di contribuire a plasmare il futuro del lavoro.
PERM
Technik und Fertigung
Branche: Anderes
Funktion: Anderes
Lead Medical Director, Product Development, Ophthalmology
Heute
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We advance science so that we all have more time with the people we love.
**The Opportunity**
Roche's Clinical Development organization is structured by therapeutic area and is responsible for developing and executing the late development (Phase II - III) clinical strategies and plans that deliver medically-differentiated therapies that provide meaningful improvement to patients. The Lead Medical Director makes major contributions to development of the Clinical Development (CD) strategy and plan and is responsible for effective and efficient execution for the assigned molecule(s)/indication(s).
+ You will support the development and implementation of the Clinical Development Plan (CDP) for assigned molecule(s)/indication(s); gathering and analyzing data and information necessary to create the CD plan.
+ You will collaborate with a variety of internal/external partners & stakeholders, as well as multidisciplinary internal groups, including business development, research, commercial, legal, etc.
+ You may participate in meetings, reviews, discussions and other interactions regarding early development/Phase I studies to provide clinical science input & guidance; including reviewing and providing late stage input to Phase I & II protocols.
+ You have a demonstrated understanding of Phase II - III drug development.
+ You will take an active role with other CST members, regulatory and other internal partners/stakeholders in the completion and submission of regulatory filings and other regulatory documentation. Provides clinical science information and input for regulatory submissions and other regulatory processes. Includes developing label and packaging language, etc.
+ You will be responsible to ensure strategic and operational alignment of the CD plan with the relevant CD strategy, strategic and annual LCP; you will work with other CST members and relevant sub-teams to develop CD plan components (e.g., analytics/data strategy, KOL development, publications strategy, etc.)
This position is based in South San Francisco, CA, (USA), Boston, MA (USA), Welwyn, UK or Basel, Switzerland.
Relocation benefits are not being offered for this position.
**Who You Are:**
**(Required)**
+ You have an MD/MBBS, MD/PhD, 3+ years clinical experience; Board Certified training in Ophthalmology
+ You have significant experience working with the principles and techniques of data analysis, interpretation and clinical relevance.
+ You have 4+ years of pharma/biotech late stage clinical development experience.
**Preferred:**
+ You have demonstrated late stage development experience in retina-related diseases.
+ You have demonstrated experience as a clinical development lead; you have the proven ability to use sophisticated analytical thought, identify innovative approaches and act a mentor.
+ You have demonstrated experience working with various clinical trial designs, (e.g. accelerated approval, pivotal, breakthrough etc)
+ You have sound knowledge of the pharma/biotech industry, the multiple functions and roles involved in the drug development process.
+ You have the ability to collaborate with relevant team members to measure and monitor study progress against objectives and plans, including any variances, and proactively communicate any issues, challenges and potential strategies to resolve such
+ You have strong interpersonal skills: Outstanding interpersonal, verbal, and written communication and influencing skills: has built and cultivated important relationships both inside an organization and externally. Has proven abilities to influence internal partners and stakeholders, thought leaders, national advocacy organizations, national standard-setting bodies, and other relevant external parties. Seamlessly collaborates with colleagues/other parts of the organization.
Relocation benefits are not being offered for this position.
The expected salary range for this position based on the primary location of South San Francisco, CA is $233,500 - $433,600. **Actual pay will be determined based on experience, qualifications, geographic location,** and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance.
This position also qualifies for the benefits detailed at the link provided below.
Benefits ( is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants ( .
Lead Clinical Scientist, Product Development, Rheumatology & Nephrology
Heute
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Arbeitsbeschreibung
We advance science so that we all have more time with the people we love.
The Roche/Genentech Clinical Development organization is structured by therapeutic area and is responsible for developing and executing the late stage development (Phase 2-3) clinical strategies and plans to deliver medically differentiated therapies that provide meaningful improvement to patients.
The Lead Clinical Science position is responsible for the clinical science aspects relative to the study team, Study Leadership Team (SLT) or project team and may lead a clinical study or other project as part of these teams in order to support effective and efficient execution of the Clinical Development Plan (CDP) for the molecule/indication. This includes contributing to the clinical science aspects of the CDP strategy and clinical documentation, representing the CDP on appropriate sub-teams and forums, leading training of study site personnel, acting as a primary point-of-contact for questions and enquiries to the CDP at a study level, conducting ongoing medical/safety data reviews, and providing clinical science inputs into study reporting.
Lead Clinical Scientists will have interactions with external stakeholders, e.g. investigators, Therapy Area Experts (TAEs) and vendors. Alongside CSL, they may participate in external interactions with Health Authorities (HAs). Lead Clinical Scientists perform their responsibilities independently.
This role presents the potential to support two distinct indications within the nephrology therapeutic area, encompassing both study team and filing team functions. It's a highly visible position that offers significant opportunities for leadership and influence across projects.
+ You are able to contribute and develop outlines for internal/external clinical presentations and communications (e.g. investigator meetings, study site interactions, patient information, newsletters); you have the ability to present at internal meetings (e.g. Study Leadership Team, Global Development Team) and external meetings (e.g. investigator meetings, advisory boards), abstracts, posters and content for scientific meetings; in addition, you are able to contribute to manuscripts for submission to peer-reviewed journals.
+ You have demonstrated experience in trial design, protocol writing/ICF, (writing or amendment), constructing appropriate CRFs and coordinating cross-functionally; you understand the integration of individual (pivotal) studies into the broader CDP context, including alignment with the Clinical Science Team (CST).
+ You are experienced in (or have clear ability) contributing to CTA/EC written interactions, briefing packs and responses to HA questions; contribution to the strategic approach and cross-functional coordination.
+ You have experience working in a collaborative environment and demonstrated experience working with external stakeholders; including, guided by the CSL, contribute to TAE interactions (e.g. advisory boards, individual engagements, steering committees) and contribute to building relationships with significant external partnerships/institutions (e.g. business alliance partners, academic institutions) in order to advance clinical studies and programs.
+ You have experience presenting, with guidance by the CSL, the clinical science aspects of the program at non-reference HA interactions (TC/F2F) and contribute to varied aspects of regulatory submissions.
This position is located in San Francisco, CA (US), Boston, MA (US), Welwyn (UK), or Basel (CH).
Relocation benefits will not be provided.
**Who You Are:**
**(Required)**
+ You hold an Advanced Clinical/Science Degree (e.g. PhD, PharmD, MSN, MPH, etc).
+ You have 2+ years of clinical development industry experience, in both early and stage R&D drug development
+ You have demonstrated knowledge with governing laws, regulations, guidelines and Roche SOPs on global clinical trial execution is required and some knowledge of medical aspects of GCP (Good Clinical Practice), ICH (International Conference on Harmonization of Technical Requirements for Registration of Pharmaceuticals for Human Use), FDA, EMA and other relevant guidelines and regulations.
+ You have a demonstrated understanding of the multidisciplinary functions involved in drug development; including therapeutic area relevant clinical trial experience or clear potential to assimilate with some support.
**Preferred:**
+ You the ability to independently carry out the majority of the study conduct responsibilities
+ You have experience in the Nephrology, Rheumatology and/or Immunology space
+ You have the ability to effectively integrate and contribute to a cross-functional study team in order to support the global study strategy
+ You have proven ability to work effectively and efficiently within cross-functional teams, e.g. Study Leadership Team/CSL with therapeutic area-relevant clinical trial experience or clear ability to adapt with transferable skills
+ Interpersonal skills: Strong interpersonal, verbal communication and influencing skills: can influence without authority and has proven experience building and cultivating relationships with key partners and stakeholders, both internally and externally
The expected salary range for this position based on the primary location San Francisco, CA is $141,000 - $262,000 . **Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law.** A discretionary annual bonus may be available based on individual and Company performance.
This position also qualifies for the benefits detailed at the link provided below.
Benefits ( is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.
If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this form Accommodations for Applicants ( .
Marketing Strategy & Operations Leader, Europe, Middle East & Africa
Heute
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**Responsibilities:**
+ **Member of the Marketing Leadership Team:** Collaborate closely with other members of the leadership team to drive to the team's winning aspiration.
+ **Strategic Planning:** Collaborate with the marketing team to develop and execute comprehensive marketing strategies to drive business growth and achieve organizational objectives.
+ **Operational Excellence:** Optimize marketing operations to improve efficiency, scalability, and ROI across all initiatives.
+ **Performance Analysis:** Establish metrics to track progress against strategic goals and provide regular updates to the leadership team.
+ **Marketing Leader Support:** Provide high-level business support to the marketing leader, including preparing presentations, providing summary of performance analysis, and managing communications.
+ **Cross-functional Collaboration:** Work closely with internal teams to align marketing efforts with overall business goals and objectives.
+ **Change Management:** Lead change management initiatives to drive organizational transformation and ensure successful implementation of strategic initiatives.
+ **Budget Management:** Manage marketing budgets effectively, ensuring resources are allocated strategically to maximize impact and ROI.
+ **Team Leadership:** Lead and mentor a team of marketing professionals, fostering a culture of innovation, collaboration, and continuous improvement.
+ **Stakeholder Management:** Build strong relationships with key stakeholders, including senior leadership, external partners, and vendors.
+ **Adaptability:** Stay abreast of industry trends, emerging technologies, and best practices in marketing strategy and operations.
**Qualifications:**
+ University Degree with a post-graduate qualification
+ 15+ years proven agriculture experience in marketing strategy, operations management, and leadership roles.
+ Strong analytical and strategic thinking skills, with the ability to translate data into actionable insights.
+ Excellent communication, presentation, and interpersonal skills.
+ Demonstrated ability to lead cross-functional teams and drive results in a fast-paced environment.
+ Proficiency in marketing analytics, digital systems, and marketing communications.
+ Creative problem-solving abilities and a passion for innovation.
+ Ability to thrive in a dynamic, rapidly evolving industry.
If you are a strategic leader with a passion for driving business growth through innovative marketing strategies and operational excellence, we encourage you to apply for this exciting opportunity.
#LI-OB1
To know more about Corteva please watch this video: Agriscience is an equal opportunity employer. We are committed to boldly embracing the power of inclusion, diversity, and equity to enrich the lives of our employees and strengthen the performance of our company, while advancing equity in agriculture. Qualified applicants will be considered without regard to race, color, religion, creed, sex, sexual orientation, gender identity, marital status, national origin, age, veteran status, disability or any other protected class. Discrimination, harassment and retaliation are inconsistent with our values and will not be tolerated. If you require a reasonable accommodation to search or apply for a position, please visit:Accessibility Page for Contact Information
For US Applicants: See the 'Equal Employment Opportunity is the Law' poster. To all recruitment agencies: Corteva does not accept unsolicited third party resumes and is not responsible for any fees related to unsolicited resumes.
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