Associate Medical Safety Director

Offer
  • a diverse job at a pharmaceutical company
  • an interesting job because of the international contacts
  • a temporary contract for 12 months, with the possibility to extent
Organisation

Our client manufactures and markets high-quality drugs in a diversity of fields. The organisation has been undergoing substantial growth and expects to be a global top ten player. In Europe, our client produces, develops and markets products through a network of affiliated companies. The European R&D and manufacturing activities are concentrated in The Netherlands. The European organisation is located in Leiden but has tight lines all around the world. The organisation is looking for support for the Pharmacovigilance department Urology & Nephrology. They would like to come in contact with an experienced Associate Medical Safety Director.

Position

As a Medical Safety Director, you are responsible and accountable for the coordination and medical-scientific monitoring and assessment of the safety profile of one or more specific products assigned to the Global TA. In this case you act as a Product Responsible person (PRP). As this position may require more hands on oversight from the Group Lead or (Medical) Director, assigned products may include high priority marketed products, including those which are marketed in multiple regions, and those with multiple license partners; typical, straightforward global development products. You lead GPV Product Responsible Teams for assigned products, co-chairs Global Development Safety Management Teams, and participate in Global Development Core Teams and Global Medical Affairs Core Medical Teams as the pharmacovigilance specialist. Therefore, you ensure the medical safety of products for the assigned Global TA and contributing to an optimal benefit-risk profile. You will also be responsible and accountable for the timely identification and communication of emerging safety issues and safety updates of the Company Core Data Sheet, Investigator’s Brochure and local product labelling. This also includes responsibility for effective and regular communication with the Global TA Group Lead and with the applicable QPPV. Furthermore, you will be responsible and accountable for the design of safety surveillance strategies, management of safety signals for drug products, both in development and marketed products. You will also be responsible and accountable for the risk management of assigned drug products, both in development and marketed products. You will also contribute periodic and ad hoc (e.g. health authority requests) safety reports for assigned products in terms of authoring and review of medical sections, the overall medical-scientific analyses and conclusions.

Profile
  • at least a master’s degree, preferable MD, DO, PharmD or PhD
  • over 6 years of experience in Pharmacovigilance/Medical Safety
  • experience in pharmaceutical industry
  • experience in project management
  • working experience as a PRP
  • good communication skills in English
  • living in Europe is a preference
Response

Interested? Please send your resume and motivational letter by e-mail, with reference to DT/20-043-DD, to Sandra van Putten: info@derksenderks.nl. For further information, please call and discuss the opportunity with Sandra van Putten at number +31 (0)33 472 80 87.

Our client has chosen Derks & Derks B.V. as recruitment agency for this assignment. We request therefore to send any application or other response to Derks & Derks.

vacature sales-marketing

Global Business Development Director

Offer
  • challenging international business management position
  • ability to explore the market and seize the opportunities
  • international traveling required
  • member of the Management Team of the organization
Organisation

Or client, Pivot Park Screening Centre, is an organization specialized in the scientific research. They provide highly regarded screening assessments and research programs. Their long-standing experience in an early drug discovery and state-of-art High Troughput Screening infrastructure provides their partners with the best confirmed leads. The High Troughput Screening (HTS) is a widely applied approach to find starting points for the development of new medicines. The organization are continuously expending their knowledge and experiences, which benefits both in the scientific community and their partners. The organization is growing fast and to reach their future goals, they are searching for someone who can utilize the international opportunities within Asia and the United States.

Position

The purpose of this position is to develop and implement an international growth strategy for the organization. Based on facts, data and analyses, you formulate a strategic plan in which you are not only responsible for the drafting, but also for implementation. The Global Business Development Director will also segment the market and focus in particular on the opportunities offered by Asia (Japan) and United States. The Global Business Development Director is responsible for managing and developing European relations.

Furthermore, the Global Business Development Director is responsible for sales and marketing and will also conduct a competitive analysis to identify the (EU, Asia and U.S.) market and therefore the opportunities. The Global Business Development Director will focus on the growth markets, where the Business Development Manager will focus on Europe. The aim is to add and acquire new customers who will use the services of Pivot Park Screening Centre.

The Global Business Development Director is expected to be mostly abroad to engage in a dialogue with the target group (40% -60% traveling). The ideal candidate enjoys and is experienced in entering into and developing relationships abroad and is experienced. The Global Business Development Director is a commercial sparring partner for the client and its own organization and also strong in terms of content. Keeping in touch with the Pivot Park Screening Centre and involving its project managers in his / her plans and results is crucial. Together they come to a planning, objectives are formulated, and a budget plan is drawn up.

Profile
  • university degree or higher with a preference for a Phd, Pharmacy, biology or chemical background
  • a minimum of 7 years of experience within an international sales position
  • knowledge off, affinity with and understanding of the pharmaceutical R&D field
  • a network in the Asian or American pharmaceutical market is recommended
  • demonstratable acquisition results, excellent negotiation skills, data-driven and market-oriented
  • strong conceptual capacity to translate organizational developments into commercial results
  • business economic knowledge and experience with managing results
  • living in the Netherlands and willingness to travel (40%-60%)
Response

Interested? Please send your resume and motivational letter by e-mail, with reference to WS/20-031, to Toon Fleminks : info@derksenderks.nl.

For further information, please call Toon at number +31 (0)33 472 80 87.

An individual assessment is part of the selection procedure.

Our Client has chosen Derks & Derks B.V. as recruitment agency for this assignment. We request therefore to send any application or other response to Derks & Derks.

vacature techniek

Benelux Lead Project Manager Serialization

Offer
  • a challenging Benelux position as Lead Project Manager
  • an organization where you can use your skills and experience to improve
  • clear focus on serialization project in an international context
  • a permanent place in the organization
  • the change to growth and develop your knowledge
Organisation

Our client is active worldwide in the development and production of commercial and clinical packaging materials. They have multiple offices and production locations around the world, employing around 1,800 people every day. For the Benelux locations in Belgium and the Netherlands they are looking to replace an interim manager for a permanent employee to keep building. They are looking for an experienced and enthusiastic Lead Project Manager.

Position

In the position as Lead Project Management you will be responsible to manage the sites to the continuously improvement process of Serialization as well as implementing and evaluating the process. Together with the team you lead, coach and guide the assigned projects. You will also lead the creation, implementation and monitoring of the serialization vision and architecture for the European organization. Therefor you need to oversee the complete serialization portfolio in the Benelux and Europe. You need to guard and report the project process and make sure that you have project ownership to ensure the progress, budgets and invoicing over the projects. Therefore you need to coordinate, monitor and report serialization packaging projects within timelines, budget, resource consumption and scope included changes. You will also identify the project risks in an early stage and mitigate, control or escalate them appropriately. Your reporting line is directly to the Site Leader of the plant in Belgium.

Profile
  • a bachelor or master degree
  • at least 2 years of experience as a Leading Project Manager
  • experience in a complex organization within a multidisciplinary team
  • experience in the pharmaceutical or packaging industry and familiar with serialization
  • familiar and practical knowledge with GMP guidelines
  • affinity with IT systems
  • excellent communication skills spoken and written
  • fluent in both Dutch and English
  • willing to travel within Europe
Response

Interested? Please send your resume and motivational letter by e-mail, with reference to WL/20-034-DD, to Sandra van Putten: info@derksenderks.nl.

For further information, please call Sandra van Putten at number +31 (0)33 472 80 87.

An individual assessment may be part of the selection procedure.

Our Client has chosen Derks & Derks B.V. as recruitment agency for this assignment. We request therefore to send any application or other response to Derks & Derks.