handel jobs

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10 Jobs gefunden für handel jobs

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Alliance & Project Manager

Randstad Schweiz AG

Basel, BS
Heute
Basel, BS
Heute
Our client, a pharmaceutical company in Basel, is looking for an Alliance & Project Manager
  • Start date: April 1st
  • End date: 1 year duration with possibility of extension
  • Remote/Home Office: Home Office now. After COVID on site
Background:
The Senior Alliance & Project Manager will be responsible for preparation and management of complex master project plans and for all reporting obligations for a global, cross-divisional project funded by a government grant. Deliverables will include budget oversight, project milestone tracking and risk management, conflict resolution and responsibility for all reporting requirements and communication to internal and external key stakeholders.
Perfect Candidate:The perfect candidate is someone with a scientific background and minimum 5 years (8 years would be the most appreciated but no more than 12 years of experience) in a similar position. This person should have strong experience with alliance and project management: driving projects with external partners (government and funding initiatives)
Tasks & Responsibilities:
  • Management of the relationship with the partner to ensure partnership progress and resolution of key challenges
  • Creates, prepares and manages integrated master project plans and revises them as needed
  • Facilitates and coordinates project setup, planning, implementation and progress
  • Manages project deliverables, costs, work schedules, scope and resource requirements throughout the projects
  • Fulfils all reporting requirements in alignment and compliance with contractual obligations, managing all issue and conflict actively to the benefit of the partnership
  • Manages the preparation of reports to document project progress, financial status and ensures project documents are complete, current, and stored appropriately
  • Motivates project team for the delivery of all contract related project deliverables
  • Implements contractual amendments in coordination with Legal, Finance and all relevant internal stakeholders
  • Single point of contact to collect project-related data from various team functions to compile reports. Tactical coordination of timelines/budgets for all projects and functions within an area
  • Delivers informative, well-organized reports and presentations on project status and selected project topics
  • Monitor and report on project issues, risks, changes, progress and deviations from plan and escalate to functional management in a timely fashion and propose mitigation strategies
  • Drives project management excellence through best-in-class project management methodologies, systems and tools. Set-up and adapt relevant project management processes and structure in alignment with stakeholders and ensure process implementation within project team
  • Effectively facilitates and leads project team meetings (set agenda, organize meetings, edit minutes). Participates as a member of the project team. Holds regular status meetings with project team to ensure milestones are being met
  • Prepares and leads joint governance committee meetings working with internal and external senior leadership
  • Conducts post-project debrief to identify and communicate learnt lessons
  • Collaborates to establish a working relationship with Pharma and Diagnostics development and supporting functions. Works within global cross-functional teams to build strong business relationships
  • Effectively manages communications, expectations, and interactions with all departments and internal and external stakeholders. Identify and assess impact on all stakeholders and manage the communication accordingly

Must haves:
  • Minimum Bachelor’s Degree in Life Science or Healthcare (****)
  • Minimum 5 years of experience in relevant similar role (****)
  • Scientific background and sound knowledge of drug development from early discovery to end of life cycle (pharma or biotech experience) (****)
  • Extensive alliance or project management experience, preferably in pharmaceutical product development or other healthcare-related field (****)
  • Experience with project management disciplines, methodology, tools and project management reporting elements for projects funded by external grants and contracts (****)
  • Excellent stakeholder management (C-level) and ability to effectively collaborate across global organizations, build consensus, and manage conflict in challenging or difficult situations
  • Strong experience in the preparation of master project plans and the preparation of complex project reports
  • Outstanding strategic and operational management skills with the ability to develop and present sound proposals and recommendations with high-quality
  • • Ability to successfully manage multiple projects simultaneously
  • Exceptional organizational & time management skills: proven ability to manage complex objectives and goals to an effective and efficient conclusion
  • Excellent interpersonal and communication skills with a proven ability to lead and develop project teams of diverse expertise on both a direct and matrix basis to achieve organisational objectives
  • Able to work effectively across cultures
  • Strong oral and written communication skills, including fluency in written and verbal English
Nice to haves:
  • Advanced degree (PhD, MBA and/or MD)
  • Experience in managing projects funded by government grants such as BARDA contracts
  • Experience in the infectious diseases healthcare landscape

Reference:15553
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Manager Commercial Packaging Operations

Seagen

Zug, ZG
Vor 4 Tagen
Zug, ZG
Vor 4 Tagen

Seagen is seeking a highly motivated Packaging professional to join our team and drive EU commercial packaging and labelling in close collaboration with the Sr Mgr. of Commercial Supply Operations in the US – to whom this role reports. This role will manage the planning and execution of commercial label and packaging operations for global supply in the EU. The incoming candidate is expected to have extensive knowledge across many functional areas and resources related to CMC and commercialization activities.  You must also be able to build and maintain exceptional partnerships with all internal and external stakeholders and lead discussions, problem-solving efforts, and process improvements to ensure supply goals are met or exceeded.

Principal Responsibilities

Manage relationships with CMO partners focused on commercial packaging in Europe
Streamline tech transfer of packaging activities from US to EU CMOs
Drive issue resolutions for technical and compliance issues pertaining to packaging and labelling in Europe
Collaborate closely with Technical Operations colleagues in Europe – in Quality and Manufacturing – in order to address and resolve issues
Act as the information nexus between the US Packaging team, Supply Chain & Tech Ops colleagues in the US and in Europe, and external partners with regards to commercial labelling and packaging operations
Lead and participates in various projects with both internal and external teams related to Commercial Packaging Operations,
Execute on program deliverables, ensure follow-up of any action items and other administrative responsibilities as required.
Provide support and collaboration on packaging and labeling related themes in for products in   This includes validation projects, qualification protocols, specification and GMP documents.

Qualifications

5+ years of relevant experience in Manufacturing or Supply Ops with a focus on Packaging Operations
Labelling experience is a plus
Excellent organizational, verbal and technical written communication skills, as well as interpersonal, and negotiation skills are essential.
Skilled commercial packaging and labeling (primary and secondary) operations/project management of small molecules.
Working knowledge of packaging and labeling operations of biologics, and other compounds.
Blister packaging experience is a plus
Proficient in MS Word, Excel, Outlook, Powerpoint, Project and other project management tools
Working knowledge of cGMP and 21 CFR Part 11 is required
Ability to travel ~10%

Education

BS/BA Degree in a business or life science field
PMP credential and experience with latest PM tools, software and processes highly valued

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Director Operations

Ametek

Reinach, BS
Vor 4 Tagen
Reinach, BS
Vor 4 Tagen

AMETEK Compliance Test Solutions (CTS) is a leading provider of test and measurement instrumentation solutions for electromagnetic compatibility (EMC) testing, with manufacturing sites in Switzerland, Germany and the United Kingdom and a worldwide sales and service network. The product portfolio comprises testing systems for conducted and radiated disturbances as well as amplifiers in the RF and microwave range. AMETEK CTS is uniquely positioned to serve the EMC community. Under AMETEK CTS, the renowned EMC and RF product brands - EM TEST, TESEQ, MILMEGA and IFI - are united into a single global business offering innovative customer solutions and services to almost all industries.

The Director of Operations is responsible to lead all Operations through the next business cycle, which is expected to be a period of significant rebuilding, consolidation and organic growth. Broadly speaking, near term deliverables include:

• Lead and manage all operations for CTS including supply chain warehouse, manufacturing, test and calibration
• Successfully deliver each Plant’s performance targets consistent with the corporate culture which emphasizes accountability and results;
• Successfully manage a proactive growth agenda with a focus on new markets and new product development;
• Ensure that the right people are in place to allow the business to perform to its full potential; including objective evaluation and development of team members, and enhancing the team;
• Accountable directly and through others, to create and implement business operations practices, procedures, metrics, systems and structures to align with the location business plan and to meet customer requirements. Identify and implement operating changes to improve productivity and reduce cost.
• Directly and through others, accountable for the effective and efficient allocation and use of all location resources, capital and inventory. Works with Department Managers to establish ongoing capacity analysis for the various operating departments and to match resources to this capacity.
• Accountable to establish plans to guide and drive future operations activities to include but not be limited to safety, customer needs, business profitability, resource allocation and inventory control; Where applicable, work with internal and external experts to establish optimum workflow, systems, facilities, equipment and resource requirements;
• Prepare weekly, monthly, quarterly and annual manufacturing Forecasts, Activity Reports, Budgets, Project Management documents, etc.

Position Requirements:
AMETEK seeks a proven, highly-motivated operations leader, with the future potential to assume greater responsibility. Specific experiences required or desired include:

• An undergraduate degree in engineering (highly desired) and an MBA or Masters degree in engineering (highly desired);
• At least 15 years of total business experience, including a minimum of three successful years in the same/similar role;
• Expertise in plant management and multi-site operations;
• Experience in working for a globally managed company in matrix organizations.
• Expertise in Lean Manufacturing /Operational Excellence is a must (Preferably Lean Six Sigma Black belt)
• Business and financial acumen, including a solid understanding of budgeting and forecasting are essential; Sound analytic skills and decision-making capabilities;
• Excellent written and verbal communication skills; able to communicate as effectively on the shop floor as in the executive suite. Should be bilingual: German and English.
• Sound MS Office and ERP knowledge (Navision as an advantage)

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Associate Director, External Quality Operations

Seattle Genetics, Inc.

Zug, ZG
Vor 4 Tagen
Zug, ZG
Vor 4 Tagen

Description
The Associate Director of External Quality Operations is responsible for all quality aspects associated with the manufacturing operations across a portfolio of Contract Manufacturing Operations (CMO) network. You will lead a team of seasoned quality professionals responsible to establishing and maintaining the Quality oversight of third-party suppliers of both commercial and clinical intermediates, BDS, and DP to ensure an uninterrupted supply of product distributed globally.  This role will serve as the primary quality Point of Contact for all matters pertaining to commercial and clinical manufacturing, including establishment of a CMC network and expertise in the regional regulatory and quality landscape.

Principal Responsibilities:

Manages and leads the ESO Quality team in Zug responsible for all aspects of manufacturing, packaging, and testing, including technical batch release as applicable
Accountable for the quality oversight of third-party suppliers of commercial intermediates, BDS, and DP, ensuring on-time delivery of products in compliance with all applicable international policies and regulations
Facilitates disputes pertaining to quality or compliance to reach swift resolution
Manages regular quality meetings at CMOs to discuss performance, risks, and opportunities to drive continuous improvement
Serves as the quality single point of contact (SPOC) and Subject Matter Expert (SME) for all quality matters pertaining to commercial manufacturing at CMO including regulatory inspection support at third-party suppliers or at HQ
Coordinate cross-functional activities between the CMOs, partners, and stakeholders to enable execution and efficient disposition of batches
Serves as an advocate for the organization while maintaining good relationships with external teams and responsible for escalation of problems, disputes or questions
Develop, monitor, and maintain positive business relationships with CMOs and partners to encourage collaboration, improvements, transparency, and accountability
Establishes a CMC network, understands and shares the regional regulatory and quality landscape. Participates and presents in key industry meetings, is an influential Quality voice
Strategically scales resources to maintain an efficient and flexible operation according to commercial demands
Provides leadership to local Quality staff. Is able to recruit, develop and retain first class self-driven talent into their function. Is a collaborative partner with other Quality and TOPS leaders
Is able to foster cooperation across multiple organizational functions, sites and levels. Responsible for communicating quality issues to the External Quality management and driving their resolution successfully
Responsible for leading strategic initiatives to continuously improve and adapt the External Quality business processes within Quality
Manage the periodic management reviews with CMO and internal Seagen stakeholders, ensuring the reviews are documented and that appropriate corrective and preventive actions are identified and implemented for each CMO
Recruit, retain and develop QA/QC talent responsible for the management of quality operations to ensure the compliance of all products.
Develop performance goals and objectives for the assigned team; drive and monitor performance against objectives
Sustain employee engagement by creating a culture of excellence and an environment in which individuals and teams can excel and continuously improve in a diverse environment
Manages the utilization of Quality resources to ensure on-time supply of products and adherence to financial targets
Qualifications:

Minimum Bachelor’s degree in a scientific discipline (Biotechnology, Chemistry, Microbiology, Pharmacy ) – 10+ years experience in the pharmaceutical industry, with 5-10 years in QA and 3+ years of people management
Experience with the production and testing of biologics/sterile injectable preferred
Should have demonstrated knowledge and experience in the interpretation and application of cGMPs and ICH requirements for both domestic and international territories
Must possess strong skills in leadership, motivation and mentorship
Able to carry out difficult decisions in a logical, rational manner, and demonstrated ability to work as a senior team member and to engage and influence team members in a matrixed environment
Ability to work well in both internal and external teams, including experience in virtual teams
Should possess a flexible risk-based approach to problem solving and be an adept negotiator
Excellent communicator both verbally and in writing with all levels of staff, both inside and outside of the organization
Ability to work in a fast-paced environment
Ability to prioritize work and handle multiple assignments, while maintaining a high level of quality
Ability to travel frequently within Europe as well as occasional travel to the Corporate HQ in Seattle

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Psychiatrisch Verpleegkundige in Bazel, Zwitserland

TMI

Bazel, GE
Vor 1 Tag
Bazel, GE
Vor 1 Tag

Heb jij wel eens nagedacht over werken in Zwitserland? Niet te ver van huis (ruim een uur vliegen) en toch in een hele andere omgeving? In een moderne stad of juist in de prachtige natuur? En dit alles tegen zeer aantrekkelijke arbeidsvoorwaarden? Dan hebben wij goed nieuws voor jou! Wij zijn namelijk per direct op zoek naar een enthousiaste en ervaren psychiatrie verpleegkundige voor een zorginstelling in Bazel (Basel-Stadt) in Zwitserland.

Werken in Zwitserland

Zwitserland telt ruim 300 ziekenhuizen en privéklinieken op 8 miljoen inwoners. In Nederland is de verhouding ongeveer 100 ziekenhuizen op 16 miljoen inwoners. De vraag naar Zorgprofessionals is groot, mede doordat er weinig opgeleid wordt. De Nederlandse Zorgprofessionals worden erg gewaardeerd om hun hoge opleidingsniveau, werkmentaliteit en flexibiliteit. Doordat er zoveel aanvragen zijn, heb je zelf de mogelijkheid om te kiezen in welk gebied je wilt werken. Wil je graag in een moderne privékliniek aan de slag, midden in de prachtige natuur? Of liever werken in een groot ziekenhuis in één van de grote steden? Er is zeer veel mogelijk!

TMI

TMI is sinds 2001 dé detacheerder in de Zorg. Wij detacheren en bemiddelen breed op verpleegkundig en (para)medisch vlak. TMI biedt zorgprofessionals de mogelijkheid om ervaring op te doen bij diverse instellingen in zowel binnen- als buitenland. Wij verlenen jou persoonlijke begeleiding bij het gehele traject, waardoor jij zelf zo min mogelijk moeite hoeft te doen voor de functie die het best matcht met jou wensen! Voor jou dé kans om eens aan de slag te gaan over de grens en verzekerd te zijn van optimale begeleiding en de beste voorwaarden.

Taalniveau

Om te werken in Zwitserland moet je minimaal Duits op B2 niveau beheersen. TMI heeft een beëdigde docent in dienst die jou persoonlijk, vakgericht en in jouw eigen tempo opleidt tot het gewenste taalniveau.

Jouw profiel:

  • Je hebt een afgeronde opleiding tot psychiatrisch verpleegkundige;
  • Je hebt werkervaring in de gerontopsychiatrie, ervaring met acute opname is een pré;
  • Je beheerst de Duitse taal op B2 niveau of bent bereid dit te leren;
  • Je bent minimaal één jaar beschikbaar;
  • Je kunt zowel goed zelfstandig als in teamverband werken.

Wat kun je verwachten:

  • Een netto salaris (in Zwitserse Franken, CHF) dat twee tot drie keer hoger ligt dan het netto salaris in Nederland (geen naheffing van belasting)
  • Een vast dienstverband met een verwachte minimale inzet van twaalf maanden
  • Totaalbegeleiding van de gehele sollicitatie- en registratieperiode
  • Een meeloopdag in Zwitserland voor rekening van TMI tot max 300 euro
  • Uitstekende aanvullende voorwaarden zoals een uitstekende pensioenopbouw en riante kinderbijslag.

#tmi

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Partner Manager (Europe)

Yandex

Люцерн
Vor 30+ Tagen
Люцерн
Vor 30+ Tagen
The International Department of the Yandex Commercial Department is looking for a Partner Manager who will build, develop, and maintain long-term relationships with advertising agencies in a number of countries in Europe. The ideal manager is ready to dive into the business processes and tasks of agencies and their advertisers and offer viable solutions, while also seeking ways to expand development of the joint business and increase our company's share.

In this position, you will:

  • build long-term trust-based relationships with foreign advertising agencies;
  • help agencies resolve technical, financial, and legal issues by involving relevant Yandex divisions;
  • train agencies and help them master our products;
  • execute a sales plan and implement internal projects and tasks;
  • increase Yandex's share and role in the agency's business.

You are a good fit if you have:

  • in-depth knowledge of the online advertising ecosystem and the processes used by advertising agencies;
  • negotiation skills that you can apply at the level of decision makers;
  • the ability to multitask and set priorities;
  • public speaking skills;
  • a desire to work as a team and share expertise;
  • a track record that shows you are stress-resistant, independent, and result-oriented;
  • advanced English and Russian skills (at least level C2), with bonus points for skills in other languages.

You will also have the opportunity to:

  • work on a friendly and motivated team;
  • complete interesting and challenging tasks;
  • hold personal meetings with partners and organize training seminars and webinars;
  • participate in conferences and industry events;
  • receive training as a new employee and work with a personal mentor during the first year.
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SEH Verpleegkundige in Bazel, Zwitserland

TMI

Bazel, GE
Vor 1 Tag
Bazel, GE
Vor 1 Tag

Voor een ziekenhuis in kanton Bazel (Basel-Stadt) in het prachtige Zwitserland zoeken wij enthousiaste spoedeisende hulp verpleegkundigen. Het betreft een functie met zeer aantrekkelijke arbeidsvoorwaarden! Je komt te werken in een ziekenhuis in een mooie en levendige omgeving, waar de werkdruk beduidend minder hoog ligt vergeleken bij de werkdruk in Nederland.  Heb je interesse en ontvang je graag aanvullende informatie? Neem dan vandaag nog contact met ons op door te reageren op deze vacature, dan plannen we graag een vrijblijvend kennismakingsgesprek met je in!

Werken in Zwitserland als SEH verpleegkundige

Zwitserland telt ruim 300 ziekenhuizen en privéklinieken op 8 miljoen inwoners. In Nederland is de verhouding ongeveer 100 ziekenhuizen op 16 miljoen inwoners. De vraag naar zorgprofessionals is groot, mede doordat er momenteel (te) weinig verpleegkundigen opgeleid worden in Zwitserland. De Nederlandse zorgverleners worden erg gewaardeerd om hun hoge opleidingsniveau, werkmentaliteit en flexibiliteit. Je komt te werken bij een instelling in een mooie en levendige omgeving, waar de werkdruk beduidend minder hoog ligt vergeleken bij de werkdruk in Nederland.

TMI

TMI is sinds 2001 dé detacheerder in de Zorg. Wij detacheren en bemiddelen breed op verpleegkundig en (para)medisch vlak. TMI biedt zorgprofessionals de mogelijkheid om ervaring op te doen bij diverse instellingen in zowel binnen- als buitenland. Wij verlenen jou persoonlijke begeleiding bij het gehele traject, waardoor jij zelf zo min mogelijk moeite hoeft te doen voor de functie die het best matcht met jou wensen! Voor jou dé kans om eens aan de slag te gaan over de grens en verzekerd te zijn van optimale begeleiding en de beste voorwaarden.

Taalniveau

Om te werken in Zwitserland moet je minimaal Duits op B2 niveau beheersen. TMI heeft een beëdigde docent in dienst die jou persoonlijk, vakgericht en in jouw eigen tempo opleidt tot het gewenste taalniveau.

Jouw profiel:

  • Jij hebt een afgeronde opleiding tot verpleegkundige met een specialisatie tot Spoedeisende Hulp verpleegkundige;
  • Je beheerst de Duitse taal op B2 niveau of bent bereid dit te leren;
  • Jij beschikt over een geldige BIG registratie;
  • Je hebt bij voorkeur reeds relevante werkervaring opgedaan;
  • Je bent minimaal een jaar beschikbaar;
  • Je hebt een flexibele instelling.

Wat kun je verwachten:

  • Een netto salaris (in Zwitserse Franken, CHF) dat twee tot drie keer hoger ligt dan het netto salaris in Nederland (geen naheffing van belasting);
  • Een vast dienstverband met een verwachte minimale inzet van twaalf maanden;
  • Totaalbegeleiding van de gehele sollicitatie- en registratieperiode;
  • Een meeloopdag in Zwitserland voor rekening van TMI tot max 300 euro;
  • Uitstekende aanvullende voorwaarden zoals een uitstekende pensioenopbouw en riante kinderbijslag.

#tmi

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SEH Verpleegkundige in Bern, Zwitserland

TMI

Bern, ZH
Vor 1 Tag
Bern, ZH
Vor 1 Tag

Unieke kans voor spoedeisende hulp verpleegkundigen! Wij zoeken een SEH verpleegkundige die beschikbaar is om waar te nemen in een kleinschalig ziekenhuis in Zwitserland. Je komt te werken in de toeristische regio Bern. Ben je langer dan drie maanden beschikbaar? Dan is het mogelijk je verblijf te verlengen! We bieden je zeer goede arbeidsvoorwaarden, waaronder een zeer hoog salaris. Daarbij ligt de werkdruk beduidend minder hoog ligt vergeleken bij de werkdruk in Nederland.  Heb je interesse en ontvang je graag aanvullende informatie? Solliciteer dan vandaag nog op de vacature!

Werken in Zwitserland

Zwitserland telt ruim 300 ziekenhuizen en privéklinieken op 8 miljoen inwoners. In Nederland is de verhouding ongeveer 100 ziekenhuizen op 16 miljoen inwoners. De vraag naar zorgprofessionals is groot, mede doordat er momenteel (te) weinig verpleegkundigen opgeleid worden in Zwitserland. De Nederlandse zorgverleners worden erg gewaardeerd om hun hoge opleidingsniveau, werkmentaliteit en flexibiliteit. Je komt te werken bij een kleinschalig ziekenhuis in een mooie en levendige omgeving.

TMI

TMI is sinds 2001 dé detacheerder in de Zorg. Wij detacheren en bemiddelen breed op verpleegkundig en (para)medisch vlak. TMI biedt zorgprofessionals de mogelijkheid om ervaring op te doen bij diverse instellingen in zowel binnen- als buitenland. Wij verlenen jou persoonlijke begeleiding bij het gehele traject, waardoor jij zelf zo min mogelijk moeite hoeft te doen voor de functie die het best matcht met jou wensen! Voor jou dé kans om eens aan de slag te gaan over de grens en verzekerd te zijn van optimale begeleiding en de beste voorwaarden.

Taalniveau

Om te werken in Zwitserland moet je minimaal Duits op B2 niveau beheersen. TMI heeft een beëdigde docent in dienst die jou persoonlijk, vakgericht en in jouw eigen tempo opleidt tot het gewenste taalniveau. In het geval van deze vacature is een spoedcursus Duits beschikbaar.

Jouw profiel:

  • Jij hebt een afgeronde opleiding tot verpleegkundige met een specialisatie tot SEH verpleegkundige;
  • Je beheerst de Duitse taal op B2 niveau of bent bereid dit te leren;
  • Jij beschikt over een geldige BIG registratie;
  • Je hebt een flexibele instelling.

Wij bieden jou:

  • Een netto salaris (in Zwitserse Franken, CHF) dat twee tot drie keer hoger ligt dan het netto salaris in Nederland (geen naheffing van belasting);
  • Totaalbegeleiding van de gehele sollicitatie- en registratieperiode;
  • Een dienstverband voor twee maanden of indien gewenst langer (kan zelfs voor onbepaalde tijd);
  • Een spoedcursus Duits indien nodig;
  • Een woning wordt voor je geregeld;
  • Uitstekende aanvullende voorwaarden zoals een uitstekende pensioenopbouw en riante kinderbijslag.

#tmi

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Head of Global Maintenance Program (m/w/d)

CH12 Lonza AG

Visp, VS
Vor 28 Tagen
Visp, VS
Vor 28 Tagen

 

Head of Global Maintenance Program (m/w/d)

Today Lonza is a global leader in life sciences. We are more than 15,000 employees in more than 100 locations around the world. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.

As Lonza is successfully and continuously growing we’re looking for a motivated and adaptable individual to lead and further develop our global maintenance program. The purpose of this role is to achieve a high reliability of maintenance disciplines across Lonza’s Pharma and Biotech network at competitive cost. The incumbent defines and implements Lonza’s Asset Management Program (LAMP) including related digitalization & automation activities in collaboration with global and site stakeholders based on evaluation of Lonza’s engineering and maintenance processes, system controls, effectiveness etc. and benchmarking to industry-standards/best-practices.

Key responsibilities:

  • Further develop Lonza’s asset management program, define and lead related work streams which address harmonization, efficiency, reliability, digitalization and asset life cycle management.

  • Provide leadership to a matrix organization, also ensuring good information exchange between upper management and the team

  • Ensure a culture of mutual accountability and full collaboration with customers and diverse Lonza sites as well as departments for effective implementation and sustainable endorsement of standards

  • Implement a vision as service provider in his organization providing hands-on support as well as visionary roadmaps for future opportunities

Key requirements:

  • Master’s Degree in Engineering or equivalent with substantial experience in pharmaceutical industry

  • Experience in new technologies, automation, digitalization

  • Ability to work strategically, hands-on and collaboratively across departments

  • Proven, excellent leadership and communication skills

  • Project management skills, experienced in working in a matrix organization

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

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Head of Global Maintenance Program (m/w/d)

Lonza Ltd.

Visp, VS
Vor 26 Tagen
Visp, VS
Vor 26 Tagen
Head of Global Maintenance Program (m/w/d) Schweiz - CH – Visp Head of Global Maintenance Program (m/w/d) Today Lonza is a global leader in life sciences. We are more than 15,000 employees in more than 100 locations around the world. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of. As Lonza is successfully and continuously growing we’re looking for a motivated and adaptable individual to lead and further develop our global maintenance program. The purpose of this role is to achieve a high reliability of maintenance disciplines across Lonza’s Pharma and Biotech network at competitive cost. The incumbent defines and implements Lonza’s Asset Management Program (LAMP) including related digitalization & automation activities in collaboration with global and site stakeholders based on evaluation of Lonza’s engineering and maintenance processes, system controls, effectiveness etc. and benchmarking to industry-standards/best-practices. Key responsibilities: Further develop Lonza’s asset management program, define and lead related work streams which address harmonization, efficiency, reliability, digitalization and asset life cycle management. Provide leadership to a matrix organization, also ensuring good information exchange between upper management and the team Ensure a culture of mutual accountability and full collaboration with customers and diverse Lonza sites as well as departments for effective implementation and sustainable endorsement of standards Implement a vision as service provider in his organization providing hands-on support as well as visionary roadmaps for future opportunities Key requirements: Master’s Degree in Engineering or equivalent with substantial experience in pharmaceutical industry Experience in new technologies, automation, digitalization Ability to work strategically, hands-on and collaboratively across departments Proven, excellent leadership and communication skills Project management skills, experienced in working in a matrix organization Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. Posted: 04.02.2021
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Our client, a pharmaceutical company in Basel, is looking for an Alliance & Project Manager
  • Start date: April 1st
  • End date: 1 year duration with possibility of extension
  • Remote/Home Office: Home Office now. After COVID on site
Background:
The Senior Alliance & Project Manager will be responsible for preparation and management of complex master project plans and for all reporting obligations for a global, cross-divisional project funded by a government grant. Deliverables will include budget oversight, project milestone tracking and risk management, conflict resolution and responsibility for all reporting requirements and communication to internal and external key stakeholders.
Perfect Candidate:The perfect candidate is someone with a scientific background and minimum 5 years (8 years would be the most appreciated but no more than 12 years of experience) in a similar position. This person should have strong experience with alliance and project management: driving projects with external partners (government and funding initiatives)
Tasks & Responsibilities:
  • Management of the relationship with the partner to ensure partnership progress and resolution of key challenges
  • Creates, prepares and manages integrated master project plans and revises them as needed
  • Facilitates and coordinates project setup, planning, implementation and progress
  • Manages project deliverables, costs, work schedules, scope and resource requirements throughout the projects
  • Fulfils all reporting requirements in alignment and compliance with contractual obligations, managing all issue and conflict actively to the benefit of the partnership
  • Manages the preparation of reports to document project progress, financial status and ensures project documents are complete, current, and stored appropriately
  • Motivates project team for the delivery of all contract related project deliverables
  • Implements contractual amendments in coordination with Legal, Finance and all relevant internal stakeholders
  • Single point of contact to collect project-related data from various team functions to compile reports. Tactical coordination of timelines/budgets for all projects and functions within an area
  • Delivers informative, well-organized reports and presentations on project status and selected project topics
  • Monitor and report on project issues, risks, changes, progress and deviations from plan and escalate to functional management in a timely fashion and propose mitigation strategies
  • Drives project management excellence through best-in-class project management methodologies, systems and tools. Set-up and adapt relevant project management processes and structure in alignment with stakeholders and ensure process implementation within project team
  • Effectively facilitates and leads project team meetings (set agenda, organize meetings, edit minutes). Participates as a member of the project team. Holds regular status meetings with project team to ensure milestones are being met
  • Prepares and leads joint governance committee meetings working with internal and external senior leadership
  • Conducts post-project debrief to identify and communicate learnt lessons
  • Collaborates to establish a working relationship with Pharma and Diagnostics development and supporting functions. Works within global cross-functional teams to build strong business relationships
  • Effectively manages communications, expectations, and interactions with all departments and internal and external stakeholders. Identify and assess impact on all stakeholders and manage the communication accordingly

Must haves:
  • Minimum Bachelor’s Degree in Life Science or Healthcare (****)
  • Minimum 5 years of experience in relevant similar role (****)
  • Scientific background and sound knowledge of drug development from early discovery to end of life cycle (pharma or biotech experience) (****)
  • Extensive alliance or project management experience, preferably in pharmaceutical product development or other healthcare-related field (****)
  • Experience with project management disciplines, methodology, tools and project management reporting elements for projects funded by external grants and contracts (****)
  • Excellent stakeholder management (C-level) and ability to effectively collaborate across global organizations, build consensus, and manage conflict in challenging or difficult situations
  • Strong experience in the preparation of master project plans and the preparation of complex project reports
  • Outstanding strategic and operational management skills with the ability to develop and present sound proposals and recommendations with high-quality
  • • Ability to successfully manage multiple projects simultaneously
  • Exceptional organizational & time management skills: proven ability to manage complex objectives and goals to an effective and efficient conclusion
  • Excellent interpersonal and communication skills with a proven ability to lead and develop project teams of diverse expertise on both a direct and matrix basis to achieve organisational objectives
  • Able to work effectively across cultures
  • Strong oral and written communication skills, including fluency in written and verbal English
Nice to haves:
  • Advanced degree (PhD, MBA and/or MD)
  • Experience in managing projects funded by government grants such as BARDA contracts
  • Experience in the infectious diseases healthcare landscape



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