Buyer (Livingston, Scotland)

  • Position: Full time
  • Open Date: Apr 14, 2021 8:42 AM
  • Location: Livingston, Scotland

Valneva is a specialty vaccine company focused on the development and commercialization of prophylactic vaccines for infectious diseases with significant unmet medical needValneva has leveraged its expertise and capabilities both to successfully commercialize two vaccines and to rapidly advance a broad range of vaccine candidates into and through the clinic, including candidates against Lyme disease, the chikungunya virus and COVID-19. 

Valneva has operations in Austria, Sweden, the United Kingdom, France, Canada and the U.S. with over 600 employees.

An opportunity has arisen at Valneva Scotland for Buyer within the SCM Procurement Department.

Job Summary

The Buyer will work in association with their team in ensuring that all materials, equipment and services is procured in line with quality and regulatory expectations, with the most favourable commercial terms and in line with the Company procedures.

Responsibilities

  • End to end procurement, including contract & supplier management
  • Purchase goods, materials and services from approved suppliers and in line with defined Company SOPs and protocols
  • Secure the most favourable terms in regards to cost, quality, guarantee of delivery and continuity of supply
  • Negotiate and improve prices and terms of business with suppliers continuously reviewing opportunities to make tangible savings and improve on commercial terms
  • Manage purchase orders on the company ERP system.
  • Contact suppliers to resolve price, delivery timelines, quality or invoice issues
  • Communicate and monitor any supply and/or service issues which may impact the business operations in a timely manner
  • Work cross functionally and collaboratively to improve the performance of existing suppliers and escalate as appropriate poor performance and alternative routes of supply
  • Ensure that a professional and consistent approach is taken with all internal and external relationships
  • Communicate in a consistent and professional manner
  • Compile data and reports relating to supplier performance and to enable evaluation
  • Ensure training and QMS are up to date in a timely manner.
  • Actively contribute to the development and maintenance of an enthusiastic, supportive and collaborative environment within the team setting
  • To undertake any other duties as requested by the line manager in accordance with company requirements

Experience

  • Relevant work experience in a procurement role within a manufacturing environment; experience of working in a GMP environment would be advantageous but not essential
  • Knowledge and experience of working with a quality management system
  • Experience working within a procurement team managing a supply chain with a portfolio of complex products identifying and mitigating areas of risk
  • CIPS knowledge and understanding would be beneficial but not essential
  • Experience of working closely and collaboratively with suppliers
  • Computer literate (Microsoft Office)

Required Skills

  • Team player
  • Able to build and maintain effective a collaborative relationships with internal and external stakeholders
  • Good communication and written skills
  • Commercial awareness with an understanding of how failure impacts the business operation
  • Able to manage time effectively, focus and prioritise critical tasks and to achieve set targets
  • Able to work well under pressure
  • Familiarity with an integrated Enterprise Resource Planning (ERP) system would be beneficial
  • Self-motivated, energetic and value driven
  • Desire to develop and grow as the company expands
Apply Now

Procurement Assistant (Livingston, Scotland)

  • Position: Full time
  • Open Date: Apr 13, 2021 10:39 AM
  • Location: Livingston, Scotland

Valneva is a specialty vaccine company focused on the development and commercialization of prophylactic vaccines for infectious diseases with significant unmet medical needValneva has leveraged its expertise and capabilities both to successfully commercialize two vaccines and to rapidly advance a broad range of vaccine candidates into and through the clinic, including candidates against Lyme disease, the chikungunya virus and COVID-19. 

Valneva has operations in Austria, Sweden, the United Kingdom, France, Canada and the U.S. with over 600 employees.

An opportunity has arisen at Valneva Scotland for a Procurement Administrator within our SCM Procurement Department, working on a 12 month Fixed Term Contract.

Job Summary

The Procurement Administrator will work in association with the Procurement Co-ordinator by supporting the Buyers in our busy Procurement Department undertaking general administration duties in line with departmental and organisational Standard Operating Procedures (SOPs).

Responsibilities will include, but not be limited to:

  • Assist the Procurement Co-ordinator in placing all planned purchase orders (POs) with external suppliers via the Company ERP system
  • Assist in placing POs for all other purchases, as and when requested
  • Electronically file all PREQs and associated POs and quotes
  • Support suppliers with PO queries
  • Run reports for outstanding orders, non-confirmed orders etc.
  • General filing & housekeeping
  • Provide monthly KPI reports to management
  • Assist Buyers with data input to contract registers
  • Resolve and respond to any invoice queries received from Finance
  • Any additional tasks requested by line management

Experience

  • Previous experience in an administration role
  • Proven track record of all general administration duties e.g. filing, updating documents and spreadsheets etc.

Required Skills

  • Good MS Office skills
  • Good attention to detail
  • Familiarity with an integrated Enterprise Resource Planning (ERP) system would be beneficial but not essential as training will be given
  • Desire to develop and grow as the company expands
Apply Now

QC Coordinator (Raw Materials) (Livingston, Scotland)

  • Position: Full time
  • Open Date: Apr 8, 2021 3:50 PM
  • Location: Livingston, Scotland

Valneva is a specialty vaccine company focused on the development and commercialization of prophylactic vaccines for infectious diseases with significant unmet medical needValneva has leveraged its expertise and capabilities both to successfully commercialize two vaccines and to rapidly advance a broad range of vaccine candidates into and through the clinic, including candidates against Lyme disease, the chikungunya virus and COVID-19. 

Valneva has operations in Austria, Sweden, the United Kingdom, France, Canada and the U.S. with over 600 employees.

A full-time opportunity has arisen at Valneva Scotland for a QC Coordinator (Raw Materials)

Job Summary 

To execute defined and trained Quality Control department tests for the release of raw materials, intermediate products and final products according to defined procedures and protocols and according to best cGMP work practices, Quality Standards and metrics, as well as assisting in the implementation and maintenance of policies for Quality Control department within Valneva.  Carry out laboratory tasks as identified by QC department.

Responsibilities

  • Execute analytical procedures, for testing of raw materials, intermediate products and final products, according to defined SOPs and protocols
  • Apply best cGMP work practices and techniques to test and release raw materials and product within specification
  • Ensure that all necessary training is complete in the procedures conducted, and operate in compliance with best cGMP working practices at all times
  • Conduct on-time reporting according to the defined and trained document management standards including review and verification of analytical data
  • Immediately escalate and report any deviations to materials, facilities, processes or procedures to the Laboratory Manager
  • Be accountable for the analytical laboratories being clean, tidy and well organised and in a state of continuous inspection readiness
  • Conduct all activities in the most careful and safe manner and in full compliance with HSE requirements
  • Ensure that equipment, facilities and materials used in the QC laboratories comply with defined standards
  • Support change controls, investigations and CAPA’s in the post diligent manner
  • Identify areas for continuous improvement and escalate those to the Head of QC
  • Actively contribute to the development and maintenance of an enthusiastic, supportive and collaborative environment within the team setting
  • Maintain adequate stocks of materials and equipment and laboratory consumables
  • Assist in monitoring and maintaining calibration status of all equipment within the Quality Control department
  • Calibration of pipettes and informing relevant personnel in a timely manner of any failure of calibration
  • Assist in ensuring adequate stocks of material and equipment for effective operation of laboratories
  • Storage of in process and final products samples including for stability and retention purposes
  • Preparation of SOPs (where applicable) in accordance with Valneva Quality systems
  • Perform filing duties and other QC administrative duties as required by the laboratory manager or Head of QC
  • To undertake any other duties as requested by the line manager in accordance with company requirements

Experience includes: 

  • Degree in chemical/biological sciences or relevant experience
  • Knowledge of usage of Pharmacopoeias
  • Knowledge of GMP guidelines and regulatory bodies
  • Experience in method validation / verification is beneficial but not essential
  • Experience of Quality Management Systems
  • Experience in working with Microsoft Excel, and ERP systems
  • Experience of working to deadlines and managing conflicting priorities
  • Experience working effectively in a team, influencing as appropriate

Skills required:

  • Attention to detail
  • Excellent organisational skills
  • Effective communication skills
  • Flexible and adaptable team player
  • Ability to think analytically
Apply Now

Supply Chain Controller (12 month FTC) (Livingston, Scotland)

  • Position: Full time
  • Open Date: Apr 8, 2021 3:47 PM
  • Location: Livingston, Scotland

Valneva is a specialty vaccine company focused on the development and commercialization of prophylactic vaccines for infectious diseases with significant unmet medical needValneva has leveraged its expertise and capabilities both to successfully commercialize two vaccines and to rapidly advance a broad range of vaccine candidates into and through the clinic, including candidates against Lyme disease, the chikungunya virus and COVID-19. 

Valneva has operations in Austria, Sweden, the United Kingdom, France, Canada and the U.S. with over 600 employees.

A full-time opportunity has arisen at Valneva Scotland for a Supply Chain Controller based on a 12 month fixed term contract to join our team in Livingston.

Job Summary

To support all Supply Chain activities by controlling and organising the various administrative functions within a busy warehouse setting.  Working hours for this role are working Monday to Friday 9am to 5pm.

Responsibilities

  • Booking in of all Purchase Order Receipts
  • Printing of all status labels from AX system
  • Request Certification and make up Raw Material Receipt packs
  • Support labelling of raw materials as required
  • Control incoming Picking requests and Co-ordinate with team
  • Print off Pick requests
  • Post Picking journals when picks are completed and verified
  • Review of onsite stocks and organise for offsite stocks to be brought in to satisfy requirements
  • Communicate to QC, materials that require release approval and arrange for materials to be moved to the appropriate areas.
  • Run expiry reports weekly and arrange for materials to be cleared from shelves
  • Post expired material journal from AX and update Expiry report tracker on Excel
  • Maintain high standards of housekeeping within the office
  • You will be required to travel between Valneva Scotland sites
  • To undertake any other duties as requested by the line manager in accordance with company requirements and your abilities

Required Skills

  • Strong attention to detail and follow-up skills
  • Competent with using Microsoft Office packages
  • Exceptional interpersonal, organisational and time management skills
Apply Now

Supply Chain Controller (Livingston, Scotland)

  • Position: Full time
  • Open Date: Apr 8, 2021 3:46 PM
  • Location: Livingston, Scotland

Valneva is a specialty vaccine company focused on the development and commercialization of prophylactic vaccines for infectious diseases with significant unmet medical needValneva has leveraged its expertise and capabilities both to successfully commercialize two vaccines and to rapidly advance a broad range of vaccine candidates into and through the clinic, including candidates against Lyme disease, the chikungunya virus and COVID-19. 

Valneva has operations in Austria, Sweden, the United Kingdom, France, Canada and the U.S. with over 600 employees.

A full-time opportunity has arisen at Valneva Scotland for a Supply Chain Controller to join our team in Livingston.

Job Summary

To support all Supply Chain activities by controlling and organising the various administrative functions within a busy warehouse setting.  Working hours for this role are working Monday to Friday 9am to 5pm.

Responsibilities

  • Booking in of all Purchase Order Receipts
  • Printing of all status labels from AX system
  • Request Certification and make up Raw Material Receipt packs
  • Support labelling of raw materials as required
  • Control incoming Picking requests and Co-ordinate with team
  • Print off Pick requests
  • Post Picking journals when picks are completed and verified
  • Review of onsite stocks and organise for offsite stocks to be brought in to satisfy requirements
  • Communicate to QC, materials that require release approval and arrange for materials to be moved to the appropriate areas.
  • Run expiry reports weekly and arrange for materials to be cleared from shelves
  • Post expired material journal from AX and update Expiry report tracker on Excel
  • Maintain high standards of housekeeping within the office
  • You will be required to travel between Valneva Scotland sites
  • To undertake any other duties as requested by the line manager in accordance with company requirements and your abilities

Required Skills

  • Strong attention to detail and follow-up skills
  • Competent with using Microsoft Office packages
  • Exceptional interpersonal, organisational and time management skills
Apply Now

Stores Person (12 month FTC) (Livingston, Scotland)

  • Position: Full time
  • Open Date: Apr 8, 2021 3:43 PM
  • Location: Livingston, Scotland

Valneva is a specialty vaccine company focused on the development and commercialization of prophylactic vaccines for infectious diseases with significant unmet medical needValneva has leveraged its expertise and capabilities both to successfully commercialize two vaccines and to rapidly advance a broad range of vaccine candidates into and through the clinic, including candidates against Lyme disease, the chikungunya virus and COVID-19. 

Valneva has operations in Austria, Sweden, the United Kingdom, France, Canada and the U.S. with over 600 employees.

Due to the increase in business we are currently recruiting for a Stores Person to work on a 12 month fixed term contract to work at our Livingston site.

Job Summary

To support all Supply Chain activities including receipt of all raw materials and consumables, stock control and transferring materials between Valneva sites. Adhering to Valneva policies, ensure raw material stocks are available in the right locations at all times.

Responsibilities

  • Receipt and quarantine of supplies
  • Identify and take responsibility for achieving personal training standards required
  • Take personal responsibility for the safe operation within the Warehousing
  • Awareness of the relevant modules of Valneva’s electronic supply management system
  • Support in the implementing of systems, policies and procedures for effective running of the stores, taking into account any relevant regulatory requirements.
  • Receiving deliveries and ensuring that the material conforms to that specified on the purchase order and internal specifications
  • Inform QC of materials that require release approval and move all deliveries to the appropriate areas
  • Operate first in first out (FIFO) policy and first expired (FEFO) for raw materials and consumables
  • Replenish the stock via the inventory management process, ensuring stock is available on time
  • Clear stores of any un-used and expired material as per standard operating procedures
  • Maintain high standards of housekeeping in the warehousing areas
  • You will be required to travel between Valneva Scotland sites
  • You will be required to drive company vehicles including transferring materials between sites
  • You will be required to work different shift patterns between Day shift/Back shift and continental shifts as determined by the business needs.
  • Removal of the waste generated by Goods In
  • To undertake any other duties as requested by the line manager in accordance with company requirements
  • You will also be responsible for your own QMS

Job Requirements

  • Stores experience preferably within a structured (GMP/GLP) environment
  • Current driving licence pre January 1997 to allow driving of company vehicle
  • Forklift, Counter Balance and Reach Truck Experienced preferred

Required Skills

  • Strong attention to detail
  • Good communication skills
Apply Now

Stores Person (Livingston, Scotland)

  • Position: Full time
  • Open Date: Apr 8, 2021 3:42 PM
  • Location: Livingston, Scotland

Valneva is a specialty vaccine company focused on the development and commercialization of prophylactic vaccines for infectious diseases with significant unmet medical needValneva has leveraged its expertise and capabilities both to successfully commercialize two vaccines and to rapidly advance a broad range of vaccine candidates into and through the clinic, including candidates against Lyme disease, the chikungunya virus and COVID-19. 

Valneva has operations in Austria, Sweden, the United Kingdom, France, Canada and the U.S. with over 600 employees.

Due to the increase in business we are currently recruiting for a Stores Person to work at our Livingston site.

Job Summary

To support all Supply Chain activities including receipt of all raw materials and consumables, stock control and transferring materials between Valneva sites. Adhering to Valneva policies, ensure raw material stocks are available in the right locations at all times.

Responsibilities

  • Receipt and quarantine of supplies
  • Identify and take responsibility for achieving personal training standards required
  • Take personal responsibility for the safe operation within the Warehousing
  • Awareness of the relevant modules of Valneva’s electronic supply management system
  • Support in the implementing of systems, policies and procedures for effective running of the stores, taking into account any relevant regulatory requirements.
  • Receiving deliveries and ensuring that the material conforms to that specified on the purchase order and internal specifications
  • Inform QC of materials that require release approval and move all deliveries to the appropriate areas
  • Operate first in first out (FIFO) policy and first expired (FEFO) for raw materials and consumables
  • Replenish the stock via the inventory management process, ensuring stock is available on time
  • Clear stores of any un-used and expired material as per standard operating procedures
  • Maintain high standards of housekeeping in the warehousing areas
  • You will be required to travel between Valneva Scotland sites
  • You will be required to drive company vehicles including transferring materials between sites
  • You will be required to work different shift patterns between Day shift/Back shift and continental shifts as determined by the business needs.
  • Removal of the waste generated by Goods In
  • To undertake any other duties as requested by the line manager in accordance with company requirements
  • You will also be responsible for your own QMS

Job Requirements

  • Stores experience preferably within a structured (GMP/GLP) environment
  • Current driving licence pre January 1997 to allow driving of company vehicle
  • Forklift, Counter Balance and Reach Truck Experienced preferred

Required Skills

  • Strong attention to detail
  • Good communication skills
Apply Now

Project Coordinator (Livingston, Scotland)

  • Position: Full time
  • Open Date: Apr 1, 2021 8:42 AM
  • Location: Livingston, Scotland

Valneva is a specialty vaccine company focused on the development and commercialization of prophylactic vaccines for infectious diseases with significant unmet medical needValneva has leveraged its expertise and capabilities both to successfully commercialize two vaccines and to rapidly advance a broad range of vaccine candidates into and through the clinic, including candidates against Lyme disease, the chikungunya virus and COVID-19. Valneva has operations in Austria, Sweden, the United Kingdom, France, Canada and the U.S. with over 600 employees.

An opportunity has arisen within Valneva Scotland’s for a Project Co-ordinator to join the team on a 12 month FTC.

Job Requirements

Experience:

  • Experienced in managing / delivering projects.
  • Ideally experienced working within a pharmaceutical environment, understanding and using GMP processes.
  • Proficient in the use of Microsoft systems; MS project, Excel, Word & PowerPoint.
  • An effective team player who is able to establish and build strong business relationships
  • Communicate to all levels of the business/share holders
  • Ability to manage conflicting priorities, workloads and capable of influencing team members to achieve required project goals and milestones
  • Proactive while being able to work to own initiative

Responsibilities 

  • Provide project management support and drive for projects as determined and assigned by the Head of Operational Planning
  • Support project managers to create and deliver project plans, revise as appropriate to meet changing needs and requirements in alignment and agreement with the project sponsor and Head of Operational Planning
  • Set up and manage regular project team meetings with internal and external team members
  • Generate and distribute meeting minutes to the team and relevant stakeholders
  • Using the appropriate project management tools maintain and track project performance
  • Identify and manage project risks by escalating issues to the project team, sponsor and Head of Operational Planning
  • Manage all project activities in accordance and consideration of GMP requirements
  • Maintain project related documentation; ensuring project documents are complete, current, and stored appropriately
  • Support the review of completed projects, ensuring that learning points are captured and actioned in order to drive continual improvement
  • Provide administrative support for project meetings, generating minutes / trackers and following up on actions
  • Provide administrative support for site audit and inspections

Required Skills:

  • Excellent planning and organisational skills
  • Excellent interpersonal skills, ability to influence and motivate at all levels
  • Possess excellent communication skills both verbal and written
  • Multitasking / Prioritisation
  • Time management
  • Meeting management
  • Active listener
  • Positive thinker
  • Possess good IT skills
Apply Now

Principal Regulatory Affairs Specialist (Livingston, Scotland)

  • Position: Full time
  • Open Date: Mar 29, 2021 12:57 PM
  • Location: Livingston, Scotland

Valneva is a specialty vaccine company focused on the development and commercialization of prophylactic vaccines for infectious diseases with significant unmet medical needValneva has leveraged its expertise and capabilities both to successfully commercialize two vaccines and to rapidly advance a broad range of vaccine candidates into and through the clinic, including candidates against Lyme disease, the chikungunya virus and COVID-19.  Valneva has operations in Austria, Sweden, the United Kingdom, France, Canada and the U.S. with over 600 employees.

Job Summary

To ensure that regulatory activities and regulatory strategies concerning CMC (Chemistry, Manufacturing and Controls) are effectively executed to meet the business objectives and regulatory requirements, by acting as main support to the Regulatory Affairs Manager.

Responsibilities

  • To monitor and maintain all the required regulatory documents pertaining to CMC Modules 2+3, at Valneva Scotland Ltd
  • To prepare, compile and interpret the information necessary for regulatory submissions associated with CMC Modules 2+3 for successful granting, maintenance of and variation to such licenses
  • Ensure that quality standards are met and that the deliverables meet deadlines and fulfil regulatory and quality standards.
  • Progress and track on time delivery of department owned Quality Management System actions and documentation.
  • Perform and track the regulatory review of cross-functional owned documents (i.e QMS, Assay/Process Plans/Protocols and Reports).
  • Provide general regulatory advice/strategy on quality related issues and determine whether change requests are compliant with the terms of all applicable license documentation within field of responsibility
  • Provide strategic advice on licensing options and data requirements in order to facilitate process/product modifications and developments.
  • Advise on compliance / regulatory requirements and strategy for process and assay development and technology transfer activities to ensure that regulatory requirements are incorporated into the planning of development work (i.e. validated, set-up and compliant with regulatory guidelines)
  • Provide regulatory support and leadership in the implementation of site project activities
  • Participate in Valneva teams involved with development and clinical trial of new Valneva products and ensure that these are developed in a manner consistent with future regulatory approval
  • Responsible for keeping up to date with regulatory guidelines, regulations and monographs and advising key staff accordingly so that they may review and assess any implications
  • As required, to support the preparation for and to participate in meetings with regulatory authorities and site GMP inspections.
  • Ensure required training status is kept up to date and maintained and procedures performed are in compliance with cGMP at all times
  • To align with other functions to ensure harmonisation of cross-functional and cross-site information
  • To escalate any regulatory matters to the Regulatory Affairs Manager
  • To deliver occasional training briefing sessions related to emerging regulatory trends and guidelines to key personnel
  • Actively contribute to the development, maintenance, support and collaboration of an effective working environment within the team, across the site and between sites.
  • Provide guidance to regulatory team colleagues
  • Deputise for the Regulatory Affairs Manager and team colleagues as required and ensure owned tasks are assigned to deputies in their absence
  • To undertake any reasonable duties as requested by the Regulatory Affairs Manager in accordance with company requirements.

Job Requirements

  • Degree level education or equivalent experience
  • Working knowledge of EU and FDA regulatory requirements for the manufacturing and testing of biopharmaceutical products in a commercial environment
  • Working experience in the application of regulatory guidelines/regulations to successful dossier preparation, submission and maintenance (CMC)
  • Comprehensive understanding and working knowledge of the Biopharmaceutical industry
  • Strong GxP understanding and experience

Required Skills

  • Excellent scientific writing skills and oral communication skills
  • Strong analytical skill and technical/scientific competence
  • Attention to detail
  • Organisational skills
  • Negotiation skills
Apply Now

QA Specialist (Livingston, Scotland)

  • Position: Full time
  • Open Date: Mar 17, 2021 7:19 AM
  • Location: Livingston, Scotland

These are exciting times at Valneva!  As we continue to expand our business in Livingston, we are looking for a number of experienced QA Specialists.

The Role:

You will be assisting in developing and maintaining a comprehensive quality management system to achieve inspection readiness for Japanese Encephalitis Virus Vaccine (JEV), Coronavirus Vaccine (SARS-CoV-2) and other new products as required.  Additionally, you will act as Quality Assurance support for Valneva’s distribution network.

Your responsibilities will include:

  • Developing, monitoring, improving and maintaining procedures to ensure compliance with EU/FDA Good Manufacturing Practice for the manufacture and testing of pharmaceuticals.
  • Performing activities and reviews in accordance with relevant Standard Operating Procedures, including but not limited to:
    • Risk assessments
    • Externally prepared documents
    • CAPA
    • Change requests
    • Deviations (including Quality Investigations, EME’s and OOS)
    • Complaints (customer / supplier)
    • Development Studies / Reports
    • QMS data logs
    • Room release documentation
    • Batch record review (including PPRs, PTRs, MPRs and SPRs)
    • Fill / Finish documentation
    • Product defect reporting and Quality Investigations
    • Technical and Quality Agreements
    • Validation
  • Performing batch review duties in accordance with relevant procedures, including issuing Certificates of Non-Conformance for bulk drug product and review of QC batch test folders
  • Identifying, investigating and reporting quality issues, escalating to management as required
  • Participating in cross-functional projects
  • Developing, implementing and monitoring Continuous Improvement activities
  • Providing QA coaching / guidance for cross-functional groups to ensure compliance with KPI targets including functional QA if required
  • Co-ordinating and providing training across functional groups in Quality Procedures, cGMP requirements and QA concepts
  • Trend and report batch reviews and QMS data
  • Providing support to management during third-party audits
  • Performing internal housekeeping, in-process visits and quality audits
  • Performing external quality audits, supporting Livingston and other Valneva sites
  • Implementing and maintaining Quality Standard Operating Procedures, as required
  • Training staff in QA related procedures and concepts as directed by line manager
  • Undertaking any other duties as requested by the line manager in accordance with company requirements

What experience will you need?

  • Educated to degree level in relevant qualification or relevant experience
  • Proven and logical approach to problem solving
  • Previous QA experience
  • Experience of working effectively in a team, influencing as appropriate
  • Experience of working within a GMP manufacturing environment
  • Knowledge / experience of the requirements for distribution of pharmaceutical products

Your key skills will include:

  • Attention to detail
  • Excellent organisational skills
  • Effective communication skills
  • Flexible and adaptable team player
Apply Now