Pharmaceutical Quality Officer Benelux

Our Company: At the Janssen Pharmaceutical Companies of Johnson & Johnson, what matters most is helping people live full and healthy lives. We focus on treating, curing and preventing some of the most devastating and complex diseases of our time. And we pursue the most promising science, wherever it might be found. The Local Operating Company ensures that these innovative medical solutions are launched into the Benelux market in the most optimal way to address important unmet medical needs in oncology, immunology, neuroscience, infectious diseases and vaccines, and cardiovascular and metabolic diseases. We are Janssen. Our mission drives us. Our patients inspire us. We collaborate with the world for the health of everyone in it. The Job in General: Janssen Cilag NV/BV, the Local Operating Company within the Benelux region, is recruiting for a (Senior) Pharmaceutical Quality Officer Benelux/RP. The Pharmaceutical Quality Officer is part of the Business Quality Department Benelux. He/she plays an important role in the implementation and maintenance of Quality Systems, holds ownership of those systems and contributes to the continuous improvement of the Pharmaceutical Quality aspects of our business. As a registered Responsible Person (RP) the Pharmaceutical Quality Officer Benelux jointly holds the responsibility to ensure GDP compliance in parallel with the Head of Quality Benelux and will act as a permanent back-up of the Head of Quality Benelux in this role. Tasks and responsibilities: · Act as local process owner for event and deviation management, CAPA management and change management systems · Act as back-up for the Head of Quality, focussing on product quality complaint handling and product issue handling, recalls and field actions Assist in GxP inspections and audit preparation and provide support during actual inspection /audit execution Implement and lead the quality management review process enabling the company to identify opportunities for, and guarantee continual improvement of various compliance areas (GDP, GMP, RA, PV). Ensuring that new / revised quality management systems are implemented and maintained · Guide the local Product Quality Review process, assuring compliance with the EU GMP guidelines and J&J Business Quality requirements · Ensuring the execution of the JC GxP training program to support company objectives, both internally and externally towards vendors. · Together with QA associate QMS, take leadership in document management processes. · Act as primary contact for the European Distribution Center regarding batch version and batch status management · Coordinating and performing promptly any recall operations · Ensuring that relevant customer complaints are dealt with effectively · Authorizing the return to saleable stock of any returned medicines Profile/ qualifications: Degree in Pharmacy /Chemistry/Medicine or a related scientific discipline. Preferably 2 years experience in pharmaceutical or related industry, ideally with a mix of manufacturing / Distribution / QA operations experience. Understanding of pharmaceutical product development, qualification, manufacturing, packaging, validation, testing, release and distribution processes and their relation to the marketing authorization process. Up-to-date knowledge of relevant pharmaceutical legislation, directives and guidelines, GMP/GDP and Janssen / J&J policies and SOP's. Understanding of the evolutions and trends in the healthcare legislation in general are a plus Ability to work independently, systematically and orderly with great accurateness. Creative and pro-active team player. Strong analytical and problem-solving skills, able to solve new issues in a practical and creative manner. Excellent communication and collaboration skills...
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  • Omschrijving: pharma
  • Plaats: Tilburg
  • Plaatsingsdatum: 13-04-2018

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Pharma Tilburg
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Account Manager Cardiology

Hou je van sales, netwerken en oprechte toegevoegde waarde leveren? Denk je dat je medisch inhoudelijke informatie goed kunt vertalen naar commerciële kansen? Wil je collega's die net zoals jij professioneel gedreven, commercieel, maar - net zo belangrijk - ook erg leuk zijn? Dan zit er maar een ding voor je op, solliciteren op de functie Account Manager Cardiology (regio Brabant) bij Bayer. Hoe ga je bij ons impact hebben als account manager? Oprechte toegevoegde waarde komt voort uit jouw vermogen om relaties te creëren en lange termijn relaties op te bouwen met medisch specialisten (cardiologen/internisten/longartsen), ziekenhuisapothekers en huisartsen. Dat doe je door hen, middels jouw diepgaande kennis, te informeren en adviseren over onze uitstekende producten. Natuurlijk kun je ze alleen adviseren als je ook inhoudelijk verstand hebt van de ziektebeelden en behandelstrategieën waarmee ze te maken hebben. Aan jou dus de taak om daar een expert in te worden én te blijven. Dat doe je zelfstandig door het bezoeken van congressen, onderzoeken van nieuwe medische ontwikkelingen en het analyseren van markttendensen. Wij zullen je daar een handje mee helpen door het faciliteren van trainingen en opleidingen. De kennis die je verwerft zal je vervolgens ook inzetten om lezingen en wetenschappelijke bijeenkomsten te initiëren. Je zet je kennis ook in om bv. de salesstrategie in een accountplan te gieten. Je rapporteert in deze functie aan de National Sales Manager en je kunt rekenen op extra ondersteuning van een Field Coach. Hoe gaan wij impact hebben op jou? We geloven als TOP-employer dat onze medewerkers het verschil maken. Wij voegen de daad bij het woord door o.a. een uitstekend arbeidsvoorwaardenpakket aan te bieden: prima basissalaris met 8% vakantietoeslag, 13e maand en een prestatiebonus vergoeding voor jouw 'home office', je werkt vanuit huis dus maak er wat moois van! auto, laptop & mobiel van de zaak 34 vakantiedagen, waarvan vijf worden vastgesteld voor collectieve sluiting goede pensioenregeling, met slechts 4% eigen bijdrage Internationale carrièremogelijkheden gefaciliteerde periodieke 'Total Body Scan', stomerijservice, stoelmassages en nog veel meer! Daarnaast kun (en moet) je jezelf volop ontwikkelen met ondersteuning van onze interne trainingsafdeling en uitgebreide trainingscatalogus. We snappen dat je staat te popelen om te solliciteren, maar toch zijn er wel een aantal voorwaarden: een afgeronde hbo-opleiding zoals b.v. HEAO, Bedrijfskunde, MER of medisch aantoonbare commerciële drive, ervaring en successen (overtuig ons!) Twee jaar commerciële ervaring zeer goede beheersing van de Engelse en Nederlandse taal uitstekende communicatieve vaardigheden je bent klantgericht en communicatief sterk Verder ben je een netwerker, resultaatgericht, planner en organisator, ondernemer, team player en wil je je graag ontwikkelen je woont bij voorkeur in de regio Brabant Natuurlijk is het een pre als je verstand hebt van cardiology, maar het belangrijkste is dat je het interessant vindt om medische kennis te vergaren, te vertalen naar commerciële kansen en deze door jouw persoonlijkheid te verzilveren. Wil je onze prachtige organisatie leren kennen of vind je dat wij jou moeten leren kennen? Solliciteer dan direct via de 'Solliciteer' button. Wil je eerst meer informatie? Bel dan onze recruiter Iluska Lang en stel haar je vragen via 06-28157703. Een assessment maakt deel uit van de sollicitatieprocedure. Acquisitie naar aanleiding van deze vacature wordt niet op prijs gesteld. Kijk ook op onze website naar onze vacature Account Manager Oogheelkunde: www.career.bayer.nl/en/job/Vacature-Account-Manager-Oogheelkunde-Zuid-Oost-Bayer B.V.Pha...
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  • Omschrijving: pharma
  • Plaats: Eindhoven
  • Plaatsingsdatum: 03-04-2018

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Pharma Eindhoven
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Process Sciences Project Manager

Summary: Acts as a Project Manager within the Process Sciences department to support operational management and optimization. Works as point of contact between various departments within Regeneron and with the external vendors to support manufacturing activities, for timely communication of data and to facilitate internal lab process transfers, process improvements and investigations. The individual should be able to work and effectively communicate with the scientific staff and senior management with ease. Essential Duties and Responsibilities: include, but are not limited to, the following: Help facilitate planning of tasks, resource (people and equipment), criticality assessment, PS analytical sample management etc for late stage process characterization campaign, cross site investigations etc. Act as key point of contact for information transfer to/from Process Sciences department. Handle and analyze large amounts of unstructured information and distill into easy-to-understand communication vehicles, schedules and other documents. Knowledge and Skills: Excellent communication skills and a good understanding of Microsoft Office Suite (especially MS project) are required. Attention to detail while maintaining a high-level view to the processes and activities. Prior experience in leading multi-disciplinary teams is required. Prior experience in building models for optimization, scenario analysis, resource planning, project planning, criticality analysis etc. is required. Working knowledge of biologics manufacturing (cell banking, cell culture and bioreactor operation, purification, and drug formulation) is an advantage. Prior Project Management experience is essential (min 2 years) Education and Experience: MSc in a technical area (Chemical Engineering, Biochemical Engineering, Biotechnology, Pharmaceutical Technology, Biochemistry etc) or MA in business area (General Management, Project Management, Corporate or Operations Strategy). 3 + years' work experience in a Pharmaceutical/Biotechnology industry, other relevant technical industries may be considered (e.g. operations management and operational efficiency, or in strategy consulting with experience with operational strategy projects). A qualification in Project Management or equivalent is an advantage. This is an opportunity to jo...
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  • Omschrijving: pharma
  • Plaats: Limerick
  • Plaatsingsdatum: 22-03-2018

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Pharma Limerick
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Sr Manager QC Support

Summary: Responsible for the oversight of QC equipment maintenance program, and all QC inputs into the Regeneron quality system including investigations, deviations and change controls. Essential Duties and Responsibilities include, but are not limited to, the following: Oversight of QC equipment lifecycle activities (including procurement, installation, qualification, maintenance, and decommissioning). Provide direction to Managers and staff that support the Equipment Ensures Equipment qualification and maintenance programs are compliant with regulatory agencies requirements, qualified and available for QC laboratory usage. Interact with QC partner groups to establish internal requirements for Equipment. Lead QC equipment validation / qualification efforts through partnering and interaction with QA-Validation and IT groups. Oversight of the preventive and corrective maintenance monitoring program. Oversight of the QC compliance process Provide direction to Managers and staff that support the Compliance programs. Ensure that all activities related to the investigation and resolutions of non-conformities are performed in a timely manner and in compliance with Regeneron procedures and regulatory requirements. Assist Quality Control personnel in meeting timelines associated with investigations, deviations, corrective and preventative actions and change controls. Report Quality Control metrics associated with data generated and Regeneron's quality system to regulatory agencies and Quality Control managers. Provide feedback to Quality Control personnel on trends that have been identified within the quality system and promote continuous improvement in this regard. Develop Compliance Specialists to comprehend quality system inputs and provide support to Quality Control personnel in completing tasks. Oversee Quality Control's coordination of subject matter experts during regulatory inspections. Performs personnel management functions including time sheet submissions, scheduling of vacations, personnel development, and performance evaluations. Education and Experience: BS in chemistry, biology or related field with 8+ years relevant experience (pharmaceutical or biotechnology industry) in laboratory man...
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  • Omschrijving: pharma
  • Plaats: Limerick
  • Plaatsingsdatum: 22-03-2018

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Pharma Limerick
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Project Manager, Technology Transfer

Summary: Based at the Raheen, Limerick site, the Project Manager will work with the Manufacturing Sciences and Technology (MSAT) group in Rensselaer, New York to transfer manufacturing processes to Raheen and partner facilities. The position will also focus on ensuring site to site consistency after the processes are successfully transferred. The Project Manager will also provide floor support during operations of manufacturing campaigns, review process data to ensure operational consistency and provide support for investigations. Essential Duties and Responsibilities include, but are not limited to, the following: Work with all relevant departments to coordinate technology transfer activities. Assess manufacturing requirements and capabilities prior to the transfer of new processes into the manufacturing facilities. Review technology transfer protocols and reports, manage document exchange (which includes Regeneron documents such as SOPs, SPECs, validation, raw material and instrument qualification documents, batch records, etc.). Provide process transfer support to external facilities, including generation of process descriptions and facility fit comparisons. Organize and lead meetings to support transfer activities. Track team activities and timelines to ensure that the deliverables within the project plan are met and are on-time. Prepare, distribute & present project status reports to project team members and management. Manage and set priorities for specific projects/programs. Provide technical support and training of manufacturing personnel to improve understanding of both cell culture and purification operations across the manufacturing organization. Assist in the writing and review of manufacturing records, batch sheets and SOPs. Provide manufacturing descriptions and technical evaluations for regulatory filings and inspections. Work effectively and efficiently in a team-oriented environment to ensure maximum and high-quality output. Provide and schedule floor support in the processing areas during manufacturing operations. Lead special projects as assigned. Education and Experience BS in Biological Sciences or Engineering with 7+ years of relevant experience in a cGMP environment; relevant Masters or PhD may be considered in lieu of industry experience. (Level commensurate with experience.) A qualification in Project Management is desirable. Knowledge and Skills: Ability to communicate clearly the timelines and important milestones Ability to adapt to a quickly changing environment. Solid knowledge of cGMP and other applicable regulations. Ability to effectively communicate issues and ideas with peers and with management. Ability to facilitate meetings with cross functional teams. Demonstrated interpersonal, written, and oral communication skills. Ability to build effective working relationships throughout the organization. This is an opportunity to jo...
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  • Omschrijving: pharma
  • Plaats: Limerick
  • Plaatsingsdatum: 22-03-2018

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Pharma Limerick
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Sr Process Scientist Purification

Summary: Supports the Process Sciences Department through small scale laboratory experiments, as well as analysis, troubleshooting, and validation of manufacturing bioprocesses. Essential Duties and Responsibilities may include, but are not limited to, the following: Provides technical support for Technology transfer purification activities. Performs purification investigations in the laboratory and creates associated reports. Develops and writes responses for technical sections of Regulatory documents. Conducts scaled-down production procedures to improve the efficiency and yield of candidate or existing bioprocesses. Develops and writes protocols for small-scale process validation studies. Carries out small-scale purification process validation studies. Assists in the analysis of samples generated from lab scale studies. Tabulates results and writes summary reports of process evaluation and validation studies. Presents findings at group and possibly at interdepartmental meetings. Maintains lab supplies and equipment. Produces and maintains accurate records. Provides coaching and mentoring to junior members of the team. Education and Experience: PhD in Biotechnology, Biochemistry, Chemical Engineering or a related field with 3+ years experience; may consider another discipline with added relevant experience. Candidates with an MSc Biotechnology or related field with 6+ years experience will also be considered. This is an opportunity to jo...
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  • Omschrijving: pharma
  • Plaats: Limerick
  • Plaatsingsdatum: 22-03-2018

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Pharma Limerick
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Senior Manager QC Bioanalytics

Summary: Oversees the laboratory quality control testing of in-process, stability, and final drug products. Has technical responsibility for all bioanalytical aspects of QC testing. Essential Duties and Responsibilities include, but are not limited to, the following: Coordinates with members of Manufacturing, Stability, and Business Ops to provide analytical support. Manages QC Analysts, distributes work load, and monitors progress. Oversees product testing to ensure efficient and compliant operations. Reviews test reports. Ensures QC Analysts receive proper training. Attends meetings to keep informed of manufacturing priorities. Ensures that safety standards are maintained. Ensures compliance with applicable cGMP regulations and SOPs. Investigates atypical and OOS test results as necessary. Manage assay transfer internally from R&D to the QC laboratory or from PAS to the QC Laboratory. Manage assay transfer externally from QC laboratory to contract labs, includes audits if needed. Oversee QC projects including analytical commitments for Regulatory filing, follow-up actions for general GMP inspections and its readiness. Track and coordinate major analytical investigation Track and monitor timeline of analytical validation projects. Monitor the team performance for Compliance events, track, assist and organize continuous improvement event. Interact with Regulatory Agencies as needed to ensure cGMP compliance. Special projects as assigned. Performs personnel management functions including time sheet submissions, scheduling of vacations, personnel development/feedback, and performance evaluations Education and Experience: BS in chemistry, biology or related field with 8+ years' relevant experience (pharmaceutical or biotechnology industry) in laboratory management and analytical sciences and 5+ years' experience in a supervisory/leadership capacity. Thorough understanding of bioanalytical techniques in a cGMP environment. This is an opportunity to jo...
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  • Omschrijving: pharma
  • Plaats: Limerick
  • Plaatsingsdatum: 22-03-2018

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Pharma Limerick
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Senior Manager QC Chemistry

Summary: Oversees the laboratory Quality Control testing of in-process, stability and final drug products. Has technical responsibility for all chemical aspects of QC testing. Essential Duties and Responsibilities include, but are not limited to, the following: Coordinates with members of Manufacturing, Stability, and Business Ops to provide analytical support. Manages QC Analysts, distributes work load, and monitors progress. Oversees product testing to ensure efficient and compliant operations. Reviews test reports. Ensures QC Analysts receive proper training. Attends meetings to keep informed of manufacturing priorities. Ensures that safety standards are maintained. Ensures compliance with applicable cGMP regulations and SOPs. Investigates atypical and OOS test results as necessary. Manage assay transfer internally from R&D to the QC laboratory or from PAS to the QC Laboratory. Manage assay transfer externally from QC laboratory to contract labs, includes audits if needed. Oversee QC projects including analytical commitments for Regulatory filing, follow-up actions for general GMP inspections and its readiness. Track and coordinate major analytical investigation Track and monitor timeline of analytical validation projects. Monitor the team performance for Compliance events, track, assist and organize continuous improvement event. Interact with Regulatory Agencies as needed to ensure cGMP compliance. Special projects as assigned. Performs personnel management functions including time sheet submissions, scheduling of vacations, personnel development/feedback, and performance evaluations Education and Experience: BS in chemistry, biology or related field with 8+ years' relevant experience (pharmaceutical or biotechnology industry) in laboratory management and analytical sciences and 5+ years' experience in a supervisory/leadership capacity. Thorough understanding of Analytical Testing in a cGMP environment for Raw Materials, Wet Chemistry, and HPLC assays This is an opportunity to jo...
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  • Omschrijving: pharma
  • Plaats: Limerick
  • Plaatsingsdatum: 22-03-2018

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Pharma Limerick
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Manager QA

Wij, Alcomed B.V., een veterinair farmaceutisch bedrijf in het midden van Nederland (Woerden), zijn op zoek naar een: Manager QA Organisatie Alcomed B.V. is onderdeel van de Alfasan groep. De Alfasan groep is een Nederlands familiebedrijf dat ruim 30 jaar actief is in het ontwikkelen, registreren, produceren en op de markt brengen van diergeneesmiddelen. Deze middelen worden in Woerden geproduceerd en op voorraad gehouden door de eigen GMP-gecertificeerde productiefaciliteit. Alfasan heeft zich gespecialiseerd in steriele injectievloeistoffen- en suspensies, daarnaast produceert zij ook intramammaire injectoren. De tabletten, poeders en oogdruppels worden door loonfabrikanten geproduceerd en geanalyseerd maar gecontroleerd door de eigen QA/ QC-afdeling. De therapeutische groepen waarin Alfasan actief is zijn: antibiotica, antipyretica, anaesthetica, anthelmintica, hormonen, vitamines en voedingssupplementen. Recent is gestart met het ontwikkelen van een “groene” productlijn. Alfasan bestaat uit ongeveer 45 medewerkers waarvan er 3 werkzaam zijn op de QA-afdeling. De werksfeer kan als prettig en informeel worden omschreven. De volgende werkzaamheden horen o.a. tot jouw takenpakket: Verantwoordelijk voor de afdeling QA; Coachen, begeleiden en aansturen van de afdeling; Professionaliseren/ optimaliseren van de afdeling en het QMS systeem; Borgen dat er gewerkt wordt volgens de geldende procedures/ eisen GMP; Verantwoordelijk voor het verder ontwikkelen, realiseren, evalueren en zo nodig bijsturen van het gehele kwaliteitsbeleid op het gebied van product, proces en verpakking; Initiëren en implementeren van verbeteringen in processen en procedures; Opstellen van Management review, Quality Manual, Policies, SMF, VMP, PQR's; Opstellen, reviewen en autoriseren van Validatie- en kwalificatie protocollen, SOP's, Afwijkingen, CAPA's, Changes (e.a. voorkomende farma documentatie); Delen van informatie en kennis rondom veranderende wet- en regelgeving; zorgdragen voor implementatie hiervan; Plannen, voorbereiden, begeleiden en afhandelen van audits, in de rol van auditor bij leveranciers en als geauditeerde door klanten en certificerende instellingen; Beantwoorden van interne en externe vragen op het gebied van kwaliteit en zorgdragen voor een effectieve klachtenafhandeling; Adviseren van en rapporteren aan de directeur. Jij Hebt een opleiding op HBO/WO niveau met aantoonbare ervaring op het gebied van kwaliteitsmanagement (GMP). Hebt minimaal 5 jaar werkervaring in een vergelijkbare leidinggevende functie in de farmaceutische industrie; Hebt bij voorkeur ervaring met steriele injecties/ aseptische bereiding; Beschikt over de volgende kwaliteiten: motiverend, mensgericht, heldere visie, stevige persoonlijkheid, daadkrachtig, proactief, resultaatgericht, kostenbewust en denken in oplossingen. Hebt een sterk analytisch vermogen en bent met weinig begeleiding in staat om snel resultaten te boeken; Bent bij voorkeur geregistreerd als QP, danwel met de ambitie om door te groeien tot QP; Hebt kennis van GMP/ GDP-regelgeving en farmaceutische wetgeving; Bent een teamplayer die positief bijdraagt aan de onderlinge samenwerking en zorgt voor verbetering, optimalisatie en compliance van de processen; Bent communicatief sterk (qua onderbouwing en formulering voor diverse niveaus). Wij zoeken een gedreven persoon die graag samenwerkt met anderen. Je bent in staat om snel inzicht te hebben in complexe processen, waarbij je een risk based benadering kunt toepassen. Je bent in staat om hoofd- van bijzaken te onderscheiden. Je kunt helder communiceren, en hebt op een natuurlijke wijze overwicht en overtuigingskracht. Alcomed is een kleine organisatie; dat vraagt van al onze medewerkers een flexibele, hands-on mentaliteit. Aanbod Een marktconform salaris Een aanstelling met uitzicht op een vast dienstverband; Een 37,5-urige werkweek; Relevante opleidingen en trainingen; Prima pakket aan primaire en secundaire arbeidsvoorwaarden. Interesse? Herken jij jezelf in bovenstaand profiel en wil je aan de slag bij Alcomed? Verstuur dan jouw motivatiebrief met CV via onze sollicitatiepagina t.a.v. onze HR-Adviseur, Nanda Rijkaart. Voor vragen omtrent deze vacature kun je contact opnemen met onze Qualified Person, mevrouw Anne-Marie Philipsen (aphilipsen@alfasan.nl). Acquisitie naar aanleiding van deze vacature wordt nie...
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  • Omschrijving: pharma
  • Plaats: Woerden
  • Plaatsingsdatum: 16-03-2018

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Pharma Woerden
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Digital Medical Representative

A career at Pfizer offers opportunity, ownership and impact. All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Our colleagues have the opportunity to grow and develop a career that offers both individual and company success; be part of an ownership culture that values diversity and where all colleagues are energized and engaged; and the ability to impact the health and lives of millions of people. Pfizer, a global leader in the biopharmaceutical industry, is continuously seeking top talent who are inspired by our purpose to innovate to bring therapies to patients that significantly improve their lives. Digital Medical Representative - UK Role Purpose : This role covers all customers in Primary Care and Secondary Care and involves the promotion of our growth brands to these customers in the digital arena through the use of non-customer facing technology. It is expected that key functions of this role will include the selling of our brands to customers through the planning of remote customer calls and virtual meetings to engage with customers in this different way. The role requires competence in planning and organising to meet digital objectives and some involvement in project work may be required. The role generates insights and intelligence in country for manager and the DMM & product teams to help shape above & in country PCBU strategies. This role will be Head Office based. Key Accountabilities Digital Capabilities Core digital requirements to allow accelerated performance within role Capability to use digital technology provided by the organisation Confident and competent with digital compliance requirements Experience in using a range of digital platforms Basic understanding of core digital metrics used by the organisation Awareness and integration of digital channels to meet our customer needsProduct Promotion & Sales Promote products to designated target customers, who in the first instance will be HCP's; in order to achieve specific customer and sales related objectives (see measures) Effective selling skills in a virtual setting. Achievement of message recall & sales targets. Market Share growth Achievement of activity objectives. Effective selling skills - ICE minimum standards. Achievement of National Sales Targets. Achievement of customer activity metrics. Running effective virtual promotional meetings. Value added programmes are effectively implemented with field and demonstrate return.Customer Relations Skills, Knowledge; QUALIFICATIONS & Experience A' Level or 'Higher' in science subjects and ideally a Life Science Degree. Promoted product knowledge. Up to date knowledge of relevant therapeutic areas. Company information systems. ABPI qualification. Effective selling skills - to standard required Strong presentation skills Advanced Computer ability - e.g. Email /WORD/ Excel e.g. ability to operate digital multimedia & teleconference facility in multitasking mode Effective working knowledge of all primary care structures and customer types. Excellent Communication Skills (verbal and non verbal) Functional/Technical Skills -has the functional & technical knowledge and skills to do the job at a high level of accomplishment Acts Decisively - makes good decisions in a timely manner based on analysis, experience and judgment even with incomplete information or under time pressure Seizes Accountability - Take personal responsibility for own work, pushing self and others to exceed goals and deliver results Grows Self - Takes accountability for own career development, regularly updating and acting on development plan. Change Agile - Demonstrates perspective and poise in the face of uncertainty and effectively gets things done amidst organisational change Self-awareness - Understands own strengths and limitations and seeks and receives feedback in a non-defensive manner Commits to 'One Pfizer' - Models a personal alignment with Pfizer's mission & vision & behaves consistently within culture and values Peer Relationships - Establishes positive colleague relationships which furthers collaboration and cooperativeness The core digital capabilities identified are as follows: Capability to use digital technology provided by the organisation Confident and competent with digital compliance requirements Experience in using a range of digital platforms Basic understanding of core digital metrics used by the organisation Awareness and integrati...
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  • Omschrijving: pharma
  • Plaats: Tadworth
  • Plaatsingsdatum: 13-03-2018

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Pharma Tadworth
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Account Manager Benelux

The opportunity to work for a market leading International temperature controlled packaging manufacturer SALARY: Basic Salary -55,000 - 65,000, OTE -65,000 - -75,000 BENEFITS: Company Car, Contributory Pension, 25 Days Holiday + Stats, Laptop and Mobile LOCATION: Amsterdam COMMUTABLE LOCATIONS: Rotterdam, The Hague, Dordrecht, Eindhoven, Utrecht, Maastricht THE COMPANY: Established over 100 years ago we are the leading designer and manufacturer of specialist temperature controlled packaging and shipping solutions, to the Pharmaceutical and Bio-Tech industries globally. This is a fantastic opportunity for a Sales Manager to develop new business across the Benelux region. The group have manufacturing plants in the UK, Europe and the US, employing over of 19,000 people and turning over in excess of $4.9 million. The product range is sold direct and through distributors all around the world. We combine high quality products, expert technical support, outstanding customer service and innovative approaches to meet our customers specific needs. Our expertise and experience have helped some of the most well- known global organisations around the world. This role has been created due to current company growth, projected growth plans, and the number of opportunities that have arisen in new markets. JOB SPECIFICATION: Reporting to the Sales Director, the successful candidate will be required to achieve annual sales targets and to maintain, grow and record revenues and profit contributions from allocated accounts and markets. Locate, identify and develop new long term business opportunities within existing accounts and new prospects Manage, understand and interpret customer requirements and offer products to meet their needs Expand business intelligence by being aware of all opportunities to further increase the market share Develop new business within existing accounts and new prospects This role is based in the Netherlands and requires regular travel within the Benelux region as well as some attendance to the Regional Head Office in the UK REQUIREMENTS: Experience in new business development and Account management within the healthcare sector is a must, as well as a proven track record of solution selling and experience of managing long sales cycles You will have knowledge of multi layered/multi -tiered and multi-site customers as well as a structured sale approach. Any experience of packaging/temperature controlled sales into the Pharma/Biotech sectors would be of particular interest as well as selling into a highly regulated environment. Excellent communication skills and a high level of flexibility and drive are essential. You will need to be a natural forward planner who critically assesses your own performance as well as being credible and comfortable in dealing with both internal and external contacts. You will also be reliable, tolerant and determined and an empathic communicator, well-presented and business-like. We are interested in receiving applications from career-minded individuals who have a proven track record of success in sales, account management and new business development, experience of international sales, project management experience as well as knowledge of selling complex technical products and solutions. You must speak English to a high business level PROSPECTS: The opportunity to join a leading brand name and worldwide manufacturer, experiencing a period of expansion and growth and seeking to bolster its international talent pool. A group of companies with a structured UK, European and worldwide sales forces. We have an active policy of promotion from within and offer the genuine opportunity to develop your career locally or internationally. A first class remuneration package including a highly competitive salary, bonus, pension, and other benefits normally associated with an international group. It is highly likely you will have worked in any of the following roles and/or markets, and worked with the following products and/or services You could have or be currently holding one of these roles: Sales Manager, Regional Sales Manager, European Sales Manager, Business Development Manager, Account Manager, National Account Manager International Sales Manager, National Acco...
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  • Omschrijving: pharma
  • Plaats: Rotterdam;Den Haag;Dordrecht;Eindhoven;Utrecht;Maastricht
  • Plaatsingsdatum: 13-03-2018

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Pharma Rotterdam Den Haag Dordrecht Eindhoven Utrecht Maastric
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Supervisor QC Microbiology

Introductie Ben jij HLO of WO afgestudeerd in Microbiologie, Biotechnologie, Farmaceutische wetenschappen, of een andere vergelijkbare richting? Heb je de ambitie jezelf breed te ontwikkelen als Supervisor in een internationaal biotechnologisch bedrijf? Dan biedt deze baan bij Microbiology Janssen Biologics jou een prachtige kans! De afdeling QC Microbiology is verantwoordelijk voor het analyseren van grondstoffen, tussen- en eindproducten. De afdeling geeft tevens advies op kwaliteitsgebied aan de verschillende productie- en productie ondersteunende afdelingen. Daarnaast voert men het Environmental Monitoring programma uit voor de microbiologische controle van de productieruimten. Op de afdeling worden verschillende technieken gebruikt zoals: Bioburden, EM monitoring, viable- en nonviable particles counting, Sterility tests, gebruik Maldi-Tof voor determinatie, etc. De verkregen resultaten zijn cruciaal voor de voortgang van het productieproces, zowel binnen JBV Leiden als voor andere sites. De subafdeling Microbiology bestaat uit circa 15 personen met een MLO en HLO achtergrond. Van jou wordt verwacht dat je zowel inhoudelijk kennis hebt als aantoonbare kwaliteiten in het aansturen van mensen. Werkzaamheden en verantwoordelijkheden: Als supervisor ben jij er verantwoordelijk voor dat de afdeling de doelstellingen, vastgelegd in Key Performance Indicators (KPI's) haalt. Deze KPI's bevatten doelstellingen op het gebied van tijdig leveren van testresultaten, first time right, procesverbeteringen, etc. Vanzelfsprekend stel je samen met je medewerkers jaarlijks individuele doelstellingen vast. Je volgt de ontwikkeling van jouw medewerkers door op regelmatige basis 1 op 1 gesprekken, functionerings- en beoordelingsgesprekken te houden (5 Conversations). Indien nodig stel je prioriteiten voor de werkzaamheden van de operators. Door de aard van het werk is het van belang om een goede communicatie met de productieafdelingen en andere partijen te onderhouden. Als supervisor wordt van je verwacht dat je, door jouw voorbeeldfunctie, het team weet te motiveren tot continue verbeteringen, zowel op het gebied van het uitvoeren van de testen, als in hun persoonlijke ontwikkeling. Je moet dan ook veel affiniteit hebben met Lean en Process Excellence. Je maakt deel uit van het Microbiology Management Team. In dit team werk je met de andere leidinggevenden, Senior Analyst en Scientist mee aan het vormgeven en realiseren van de algemene Microbiology doelstellingen. Functie-eisen (opleiding, ervaring, kennis, vaardigheden) Afgeronde HLO of universitaire opleiding in Microbiologie, Biotechnologie, Farmaceutische Wetenschappen of vergelijkbaar. Zelfstarter, initiatiefrijk, teamspeler, beslissingen durven nemen. Zich uitstekend kunnen uitdrukken in het Nederlands en Engels, zowel mondeling als schriftelijk. Je hebt oog voor diversiteit en inclusie, je weet het beste te halen uit mensen met verschillende achtergronden, kennis en kunde. Je kunt goed omgaan met wisselende prioriteiten onder tijdsdruk. Je beschikt over minimum 5 jaar werkervaring in QC, waarvan 2 jaar in een leidinggevende rol. Begindatum: 01JAN18 Band: 25 “Caring for the world, one person at a time…” As an employee we consider you as our most valuable asset. We take your career seriously. As part of a global team in an innovative environment your development is key and our day-to-day...
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  • Omschrijving: pharma
  • Plaats: Leiden
  • Plaatsingsdatum: 02-03-2018

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Pharma Leiden
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Senior Financial Analyst

Introduction The position of Sr. Financial Analyst is a key member of the Leiden Supply Chain Finance Team of the Janssen Biologics BV entity. The manufacturing plant in Leiden is one of the largest plants in the global Manufacturing & Technical Operations (MTO) network of the Janssen Supply Chain (JSC). The Sr. Financial Analyst operates within a team of 3 Financial Analysts, reports to the Sr. Finance Manager and is actively involved in a variety of local and international finance (optimization & standardization) initiatives. He/she has close interaction with all local departments and business partners as well as with his/her peers at the other manufacturing sites across the globe. Key responsibilities include but are not limited to Daily financial support and business partnering for the total JSC site P&L as well as departmental expenses and headcount of assigned areas within JSC Leiden: Analysis, review and consolidation of monthly and quarterly results: preparation and review of budget versus actual analyses. Responsibility for the financial closing procedures (in accordance with the Sarbanes-Oxley guidelines). Ensures timely and accurate completion of financial reporting requirements and submissions in financial systems. Responsibility to challenge business assumptions, implement corrective actions, develop business cases, create new or innovative reports for business needs and identify and implement process improvements (Cost improvement Projects, Kaizen, Yellow or Green Belt, etc.). Educate business partners on financial issues and concepts, ranging from daily operations up to long term capital investments. Coordinate and support the yearly Business Planning Process and periodic budget updates: Preparation of templates, detailed calculations, consolidation of input, challenge results, prepare reporting. Understand linkages to strategic plan. Actively cooperate with business partners during budget preparation, apply business knowledge to challenge business partners on assumptions, identify cost savings and influence decision making. Engage business partners using fact-based data and advanced analytics to achieve mutually agreeable business objectives Works with management to complete business plan action items. Prepare business cases for projects, capital investments and new product introduction costing analysis in close cooperation with project managers. Recommend and implement new ideas to reduce current processes cycle time, identify non-value-added activities and leverage systems. Benchmark best practices within J&J network. Active involvement in and/or leading national and international ad-hoc projects. Qualifications A university degree in Finance & Economics. 4 to 6 years of relevant business experience is preferred. Fluency in English is required; fluency in Dutch is a pré. Ability to work pro-actively, independently and taking ownership. Good team player. Open communication, both verbally and in writing. Customer focused, build relations and take into account the needs of business partners. Strong analytical and conceptual skills. Continuous improvement mindset. Ability to handle multiple tasks and deadlines; also under time pressure, while sustaining a high accuracy of business results. Working knowledge of J&J WW-procedures is an asset Sound knowledge of SAP R/3 and MS-Office (Excel, Word, Powerpoint) What's in it for you…? “Caring for the world, one person at a time…” As an employee we consider you as our most valuable asset. We take your career seriously. As part of a global team in an innovative environment your development is key and our day-to-day...
Extra gegevens:

  • Omschrijving: pharma
  • Plaats: Leiden
  • Plaatsingsdatum: 02-03-2018

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Pharma Leiden
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Secretaresse Janssen Vaccines Prevention

At Janssen Vaccines & Prevention we are looking for a Management Assistant who provides general organizational and administrative support to a group of professionals under direct supervision. Key tasks & responsibilities General administrative support Agenda/calendar management Arrange internal meetings Organize departmental meetings Make travel arrangements Make training and conference subscriptions Draw up expense notes Follow-up on vacation management system Arrange external meetings Coordinate visits of external/J&J guests Make departmental meeting minutes & follow-up on action items Contract administration: follow-up on departmental contracts/payments Initiate & follow-up on departmental purchase orders Follow-up on departmental budget Participate, as a team member, in process optimization projects within the administrative group Act as backup for colleagues Qualifications Years of experience and education: Generally requires a minimum of 2 years experience (an international environment is a pre) Key competencies and skills: Accuracy Collaboration / Teamwork Knowledge of applicable processes and systems Monitoring progress in general Initiative and pro-active Good written communication Takes ownership of own development and training plan Knowledge: Good written and spoken knowledge of Dutch and English. Advanced knowledge of Word, Excel, Powerpoint and Outlook. Bachelor degree What's in it for you…? “Caring for the world, one person at a time…” As an employee we consider you as our most valuable asset. We take your career seriously. As part of a global team in an innovative environment your development is key and our day-to-day...
Extra gegevens:

  • Omschrijving: pharma
  • Plaats: Leiden
  • Plaatsingsdatum: 02-03-2018

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Pharma Leiden
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2 Operators voor de Liquid Retort Verpakkingslijn

Abbott Laboratories Zwolle produceert en ontwikkelt een volledig pakket aan medische voedingen, afgestemd op de specifieke voedingsbehoeften van de patiënt. Het assortiment bestaat uit drink- en sondevoedingen zoals EnsureTM Plus en Jevity®, uit ziektespecifieke voeding waaronder Prosure®, en uit drink- en sondevoeding voor kinderen. Om onze missie te blijven omzetten in daden zijn wij voor onze vestiging Abbott Laboratories op zoek naar: De afdeling Liquid Retort Verpakken vult batchgewijs blikken met vloeibare producten. Vervolgens worden de blikken verpakt en verscheept naar onze klanten. De afdeling Liquid Retort Verpakken is het laatste proces van halffabrikaat naar finished product. De werkzaamheden bestaan o.a. uit het bewaken en controleren van het productieproces en de specificiates, zonodig ingrijpen en/of bijsturen, uitvoer van eerste lijn onderhoud en het schoonhouden van de apparatuur en de werkplek, volgens de geldende voorschriften. Voor de afdeling Liquid Retort Verpakken zoeken wij een collega Operators die bereid zijn in een 3-ploegendienst te werken. WAT WORDEN JOUW TAKEN EN VERANTWOORDELIJKHEDEN? Je ziet als Liquid Retort Verpakkingsoperator toe op het optimaal en efficiënt functioneren van het gehele verpakkingsproces. Je komt met verbeteringsvoorstellen om de prestaties van de apparatuur en omgevingsfactoren te verbeteren. Je verricht ook kwaliteitscontroles. Naast deze taken ben je ook verantwoordelijk voor het beheer van voorraden en het coördineren van preventief onderhoud. Daarnaast bewaak je de hygiëne en veiligheid volgens de geldende GMP-, veiligheids- en bedrijfsvoorschriften. WAT ZOEKEN WIJ? Minimaal een afgeronde opleiding op MBO 3 niveau bij voorkeur levenmiddelentechnologie. Ook staan wij open voor jonge starters met een MBO- niveau 4 opleiding bij voorkeur richting levensmiddelentechnologie, verpakkingstechnologie of procestechniek. Sterke affiniteit en kennis van met PLC en beeldscherm gestuurde productiesystemen. Je kunt goed samenwerken met anderen en je communiceert op een open en duidelijke wijze met je collega's. Je hebt een groot verantwoordelijkheidsgevoel, aandacht voor de kwaliteit van het product en een scherp oog voor veiligheid en hygiëne. Je bent inventief en voelt je betrokken bij de gang van zaken binnen de afdeling en Abbott Zwolle, maar ook medeverantwoordelijk voor het resultaat. Competenties waarover je beschikt: Resultaatgericht, Bouwen, Anticiperen, Innovatief, Visie en Strategie. Wat hebben wij jou te bieden? Wij bieden jou een goed salaris. Ook krijg je van ons een Individueel Keuzebudget (IKB) met daarin een vakantietoeslag, 13e maand, bijzonder verlof en extra vakantiedagen. Hoe solliciteer je? Graag ontvangen wij je reactie als je interesse hebt in deze vacature, in werken bij Abbott en je herkent je zelf in het bovenstaande profiel. Je kunt solliciteren met je CV en motivatie via de ''Solliciteer'' button. Graag ontvangen wij je reactie zo spoedig mogelijk. Voor meer informatie...
Extra gegevens:

  • Omschrijving: pharma
  • Plaats: Zwolle
  • Plaatsingsdatum: 27-02-2018

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Pharma Zwolle
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woensdag 25 april 2018 12:27