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As well as applications for jobs within the Napp Pharmaceutical Group, which includes Bard Pharmaceuticals Limited, we also handle applications on behalf of our independent associates who are based on our Cambridge site, Mundipharma International (MINT) and Mundipharma Research Limited (MRL). New career opportunities regularly become available within all three of these organisations. Whilst Napp, MINT and MRL actively encourage development and appointment from within, it is always their objective to recruit the best person for the job.

Below are the vacancies for which Napp, MINT or MRL are currently looking to recruit. If you wish to apply for any of these positions, unless stated otherwise in the individual vacancy details, please click on the "apply online" link against the relevant vacancy.

If you prefer to apply by post, please download an Application Form and send the completed form along with a copy of your CV to the Personnel Department, Napp Pharmaceutical Holdings Limited, Cambridge Science Park, Milton Road, Cambridge, CB4 0AB.

If you would be interested in a career at Napp, MINT or MRL, but not specifically in the vacancies listed below, please send your current CV, along with a covering letter including your contact details, to vacancies@napp.co.uk .

 
Job DescriptionFilter
Expand/Collapse Company : Napp Pharmaceuticals ‎(9)
Expand/Collapse Department : Information Technology, Procurement, Finance ‎(2)
EC SBSenior Buyer 

To complement an existing team of Procurement professionals. Implement sourcing plans for assigned materials & services at the lowest possible long term cost, thus allowing maximisation of profits to those functions for which the materials / services are procured. Contribute at strategic level to both department and stakeholders.  Interact with all levels of management both inside the company and outside in supplier company organisations representing the function in a thoroughly professional manner.  Support the overall departmental objectives of exploiting commercial opportunities, risk management and business process improvement. Set departmental objectives and drive function aims forward. Click here to view the job description

EC ITJAJunior Analyst - ITTo work within the Support Services team of the IT Department supporting the continued operations of the IT facilities and infrastructure at the Cambridge site.    This position is a 1 Year Short Term Contract.  To view the job description, please click here.  CLOSING DATE FOR APPLICATIONS:  FRIDAY 18 DECEMBER 2009
Expand/Collapse Department : Medical ‎(4)
VM MLAMedical Liaison Advisor x2

Predominantly field based, the primary role is to develop and maintain relationships with Key Opinion Leaders as well as providing non-promotional scientific information related to Napp products and related therapeutic areas to healthcare professionals in accordance with relevant legal, regulatory and ethical guidelines.  Please click here to view the job description.

VM MLMMedical Liaison Manager

Predominantly field based, the role is to lead, coach, and develop the medical liaison team to realise its full potential. Develop and maintain relationships with Key Opinion Leaders as well as providing non-promotional scientific information related to Napp products and related therapeutic areas to healthcare professionals in accordance with relevant legal, regulatory and ethical guidelines. To view the job description, please click here.

VM SA RESPScientific Advisor - Respiratory

The role of the Scientific Advisor is to work at the interface between Medical Information, Medical, Sales and Marketing to scientifically develop each brand to its full potential. To view the job description please click here.

EC SMASenior Medical Advisor x2To provide medical support activities covering marketed and pipeline products by participating in cross-functional working across the business, especially the Medical/Marketing interface, to optimise growth consistent with company strategy.  To provide support to Company to ensure medical and scientific credibility and high corporate ethical standards.  To view the job description, please click here.
Expand/Collapse Department : Production and Supply Chain ‎(2)
DL PE (RP)Project Engineer (Engineering & Facilities)The Project Engineer is responsible for the effective delivery, implementation and handover of all allocated multi discipline engineering projects. To support and deliver Company, departmental and individual objectives.    This role covers FACILITIES and UTILITIES .  To view the job description, please click here.  CLOSING DATE FOR APPLICATIONS: 19 FEBRUARY 2010
DL PE (SW)Project Engineer (Processes and Equipment)The Project Engineer is responsible for the effective delivery, implementation and handover of all allocated multi discipline engineering projects. To support and deliver Company, departmental and individual objectives.  this position covers PROCESSES AND EQUIPMENT.  To view the job description, please click here.  CLOSING DATE FOR APPLICATIONS: 19 FEBRUARY 2010
Expand/Collapse Department : Sales and Marketing ‎(1)
VMSales ForceIf you are interested in a career in sales with Napp, you can view the Company profile here. 
Expand/Collapse Company : Mundipharma Research Limited ‎(14)
Expand/Collapse Department : Information Technology, Procurement, Finance ‎(1)
SWProTraSysProcess & Training Systems Coordinator, UKTo assist process development to ensure harmonisation across groups within European Research & Development (Eu R&D), to develop and maintain quality systems used for document control and the tracking of training requirements within Eu R&D.  For further information on this vacancy, please click here.
Expand/Collapse Department : Medical ‎(13)
HGRegOncSpeRegulatory Oncology Specialist, UK or Germany

Provide input into the regulatory strategy for Oncology products and regulatory advice on potential Oncology projects for both internal projects and in-licensed products. Liaise with MINT/3rd party companies during all phases of development for Oncology products. Provide advice on EU and international regulatory requirements. For further information on this vacancy, please click here.

KWResResPhyRespiratory Research Physician, UKTo provide specialist medical expertise during all phases of clinical trial processes and specialist advice related to respiratory regulatory submissions. For further information on this vacancy, please click here.
KWOutAssOutsourcing Associate, GermanyWorking with Colleagues from the UK and Germany, support clinical trials outsourcing for European Medical Research Operations, manage Contract Research Organisation contracts, handle negotiations and vendor relationships, and provide input to study cost forecasting.  Ensure use of processes and tools to achieve Company objectives and deliver service excellence according to agreed quality, cost and time parameters.  For futher information on this vacancy, please click here. 
KWProManGerProject Manager, GermanyTo be accountable for managing and executing product development projects.  For further information on this vacancy, please click here.
HGFunDirRegFunctional Director, Regulatory CMC & Manufacturing Compliance, UK or GermanyLead and manage the Regulatory CMC & Manufacturing Compliance function for EU and all additional International countries within scope.  For further information on this vacancy, please click here.
KWClinSupProjClinical Supplies Projects Manager, UK

Working as part of the Clinical Supplies Management Team, manage the projects and staff responsible for preparing supplies for clinical studies. Liaise closely with the Clinical Supplies Management team to ensure projects are delivered according to current timelines and meet the required legislative and quality standards Manage staff within the Clinical Supplies department in respect of their day to day activities, training, development and progression.  For further information on this vacancy, please click here.

KWEurMedScieEuropean R&D Medical/Scientific Adviser, GermanyWe are searching for a suitable person to start, as soon as possible, in our European Pharmacological Intelligence Department as a European R&D Medical/Scientific Adviser.  For further information on this vacancy, please click here.
JSCliSupProClinical Supplies Project Co-ordinator

Co-ordinate supply of clinical trial supplies for phase I to IV clinical trial projects as assigned by management.  Ensure the design, manufacturing, packaging, distribution and reconciliation of all study supplies are completed accurately and to agreed timelines and key project milestones.  Ensure work is carried out to quality standards according to current legislation, guidelines and MRL procedures.  Assist with the supply of clinical trial supplies for Investigator Initiated Trials and Early Access Programmes.  For further information on this vacancy, please click here. 

JSSecManPhaSection Manager - Pharmaceutical DevelopmentTo supervise and manage a team of scientists, undertaking the development of pharmaceutical products from conception to commercial launch.  For further information on this vacancy, please click here.
SWSenStaSenior Statistician, UKTo provide statistical support for nominated studies/projets to include statistical input to protocol, analysis and reporting.  For further information on this vacancy, please click here.
SWSenStaSTCSenior Statistician (8 Month STC), UKTo provide statistical support for nominated studies/projects to include statistical input protocol, analysis and reporting.  For further information on this vacancy, please click here.
HGSenRegAffSenior Regulatory Affairs Officer - LabellingTake responsibility for Regulatory activities associated with the creation and management of Labelling across Europe including Summary of Product Characteristics (SPCs), Patient Information Leaflet (PIL) text and Company Core Data Sheets (CCDs).  Provide regulatory support for the production and submission of Global Periodic Safety Update Reports (GPSURs).  For further information on this vacancy, please click here.
HGPharOffPharmacovigilance Officer (9 Month STC), UKTo conduct all aspects of drug safety operations including receipt, assessment, processing and submission of adverse event information from clinical trials and spontaneous reports to ensure that the EU DSP department can safeguard patient's health and remains compliant with regulatory obligations.  For further information on this vacancy, please click here.

 

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