Hoofd Ziekenhuisapotheek

Aanbod

  • invloedrijke positie met breed pakket aan taken en verantwoordelijkheden;
  • uitdagende veranderopdracht naar een integrale ziekenhuisapotheek;
  • verantwoordelijk voor de aansturing van 250 fte;
  • maakt onderdeel uit van medische staf van top klinisch ziekenhuis;
  • competitieve arbeidsvoorwaarden.

Bedrijf

Het Albert Schweitzer ziekenhuis is een modern en vooruitstrevend ziekenhuis met locaties in Dordrecht, Zwijndrecht en Sliedrecht, en een buitenpolikliniek in Ridderkerk. De organisatie telt 250 medisch specialisten en een kleine 4.000 medewerkers en maakt deel uit van de Samenwerkende Topklinische opleidings Ziekenhuizen(STZ). Dat betekent dat er in het ziekenhuis en de apotheek talent opgeleid wordt en dat de organisatie zich onderscheidt met patiëntgericht wetenschappelijk onderzoek en hoogwaardige zorg. Het ASz werkt intensief samen met zorgverleners en ziekenhuizen in de regio, zoals het Amphiaziekenhuis, Bravis en Rivas.

Het Albert Schweitzer ziekenhuis heeft bij de oprichting een visie ontwikkeld die nog altijd richtinggevend is voor strategie en beleid: “Zorg met hoofd, hart en ziel”. In de ambities van het ziekenhuis wordt integraal gedacht en vormen de wensen en belangen van de patiënt altijd het uitgangspunt. De apotheek vormt een belangrijk onderdeel in de patiëntenzorg van het ASz en er is een substantieel deel van het ziekenhuisbudget mee gemoeid. De ziekenhuisapotheek bestaat uit de klinische ziekenhuisapotheek en de poliklinische apotheek. Daarbij heeft het ASz in samenwerking met het Amphia Ziekenhuis een succesvolle eigen productie apotheek A+ die ook andere zorgverleners bedient.

Besloten is om de ziekenhuis-en poli-apotheek te integreren tot één ziekenhuisapotheek die het totale pallet van farmaceutische zorg levert, onafhankelijk van waar de patiënt zich bevindt. Het gaat om een organisatie ‘in wording’. Een Farmaceutisch Integratie Team, bestaande uit ziekenhuis-en poliapothekers, denkt na over de gewenste toekomstige inrichting, de voordelen in kwaliteit en bedrijfsvoering en de uitdagingen voor integratie. De nieuwe integrale ziekenhuisapotheek wordt geleid door een duaal bestuur, bestaande uit een Hoofd Ziekenhuisapotheek en een Bedrijfskundig Manager.

Functie

Het Hoofd Ziekenhuisapotheek en de Bedrijfskundig Manager zijn als collegiaal bestuur verantwoordelijk voor de integrale ziekenhuisapotheek en haar taken en verantwoordelijkheden. Het Hoofd Ziekenhuisapotheek is eindverantwoordelijk op inhoud voor kwalitatief hoogwaardige farmaceutische zorg en een klantgerichte dienstverlening. Dit gaat om inkoop, bereiding, distributie, poliklinische apotheken, laboratorium en productie. Het Hoofd Ziekenhuisapotheek is direct leidinggevende van de apothekers en tevens meewerkend ziekenhuisapotheker. Hij/zij stuurt in beleid, uitvoering en management op kwaliteit, patiëntveiligheid en patiënttevredenheid. Intensieve samenwerking wordt gevraagd, zowel met de Bedrijfskundig Manager, als met de stakeholders binnen de eigen afdeling, in het ziekenhuis en in de zorgketen. Het Hoofd Ziekenhuisapotheek is samen met de Bedrijfskundig Manager verantwoordelijk voor een voorspoedige implementatie van de nieuwe organisatiestructuur, inclusief bijhorende processen en (samen)werk afspraken.

De unieke kwaliteiten van de poliklinische apotheek en de ziekenhuisapotheek worden hierbij benut en gedeeld. Respect en leren van elkaar staan hoog in het vaandel. Het Hoofd Ziekenhuisapotheek rapporteert direct aan de Raad van bestuur.

Profiel

  • brede ervaring en een hoog ambitieniveau op alle onderdelen van de ziekenhuisfarmacie;
  • geregistreerd ziekenhuisapotheker, minimaal 10 jaar ervaring als apotheker;
  • minimaal vijf jaar leidinggevende ervaring;
  • als leidinggevende stevig en verbindend;
  • v.k.-ervaring met inkoop, zorgverzekeraars en leveranciers;
  • v.k.-ervaring in een omgeving waar de klinische en poliklinische farmaceutische zorg geïntegreerd aangeboden wordt;
  • ervaring met afstemming, overleg, onderhandeling en stakeholdermanagement;
  • visie op de toekomst van de ziekenhuisfarmacie;
  • bedrijfsmatig inzicht (personeel, organisatie, financiën).

Reactie

Geïnteresseerd? Stuur je curriculum vitae en motivatie, onder vermelding van referentienummer WS/20-040-DD, naar Alexander Willemse, info@derksenderks.nl.

Voor meer informatie kun je bellen met Alexander Willemse via 033 – 4728087 of 06-12795418

Voor de werving van deze positie werken wij nauw samen met Ebbinge. Een referentieonderzoek en assessment kunnen deel uitmaken van het selectieproces.

Is dit niet helemaal de functie die je zoekt? Kijk dan op http://www.derksenderks.nl/nl/nieuwe-baan/vacatures voor andere interessante vacatures!

vacature sales-marketing

Sr. Market Access Manager (Neuroscience)

Offer
  • challenging role in a biopharmaceutical organisation
  • combined role with Market Access, Stakeholder Management and Corporate Affairs
  • very attractive employment conditions package
Organization

Our client is a leading biotech organisation that discovers, develops and delivers therapies to improve the lives of patients. They offer therapies for neurological diseases, globally, through direct affiliate presence in 30 countries and a network of distribution partners in over 50 additional countries. The atmosphere is very open and accessible. This is also reflected in the mutual cooperation, along with their key focus on professionalism and a drive to accomplish the best results for the society. They are currently searching for a Sr. Market Access Manager because of the growing challenges and interesting pipeline of medicines.

Position

As Sr. Manager Market Access you will lead the payer related activities for the organizationals Neuroscience (Alzheimer and a larger scope within their neuroscience pipeline) products in the Netherlands. You will be working in close collaboration with the local medical team in addition to global Value & Access teams to develop and execute the local market access strategy. Your key responsibilities in this role encompass leading the preparation of the market to enable a successful launch of new products in the Netherlands by evolving the partnership with payers and other strategic stakeholders. You will manage the patient pathway in the Netherlands and ensure the funding pathway for diagnostic tools, treatment and that monitoring is in place and clearly specified. You are responsible for the preparation of the scientific and economic files for reimbursement. Together with the rest of the team you are responsible for the pricing within the Netherlands. Also you prepare the local player related materials needed for Market Access succes. In the role of Sr. Market Access Manager it is important to have experience within the file preparation regarding the external stakeholders (Zorginstituut, Ministry of Health etc.).

Profile
  • Sc. with a strong preference for the field of Health Economics or Pharmacy
  • +5 years or relevant experience required (in market access, governmental affairs management, public affairs)
  • experience in direct interaction with the external stakeholders (Zorginstituut etc.) and proven track record of access succession is a must have
  • experience in a cross-functional position
  • knowledge of NL healthcare legislation
  • used to travelling, working independently and planning of own time and schedule
  • native Dutch speaker with fluent English skills (verbal, reading and writing)
Response

Interested? Please send your resume and motivational letter by e-mail, with reference to WL/20-040-DD, to Toon Fleminks : info@derksenderks.nl.

For further information, please call Toon Fleminks 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.

Associate QMS Manager

Offer

  • a diverse job at a global pharmaceutical company
  • an interesting job because of the international contacts
  • a temporary contract for 6 months, with the possibility to extend

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 an Associate QMS Manager.

Position

As an Associate QMS Manager you will work under limited supervision or completely independent. In this role it will be your responsibility to implement operational plans for your region. You will support global audits and inspections and deliver on process improvement. You will also be involved at process compliance matters as well as KPI management and Metrics. Delivering support to the management and maintenance of controlled safety documents like SOP are also included in your tasks. You will collaborate with relevant GPV and non GPV partners on a global level. Next to that you will participate in projects related to Audit and Inspection management and Process Improvement. As well as Controlled Document management and/or Compliance management. You will be representing QMS and taking ownership for specific tasks and deliverables. You will make sure they are to ensure oversight as well as compliant with all applicable worldwide pharmacovigilance regulations and internal and external KPIs. In this role you report to the Global Lead QMS or Process Improvement Team Lead.

Profile

  • Minimum BA/BS.
  • At least 4 years within a pharmaceutical, biotechnology or related industry.
  • Minimum 2 years’ of experience in Pharmacovigilance (e.g. in case processing), Regulatory affairs or Safety Quality Assurance, preferably experience in support of the safety quality systems.
  • Understanding of safety regulations for both marketed and investigational products, and excellent knowledge of global health authority requirements including ICH, CFR 21, FDAAA, EU GVP module, JP regulations.
  • Experience and understanding of Process Management, Standards, Training & IT function as they apply throughout the entire pharmaceutical compound/product life cycle.
  • Good understanding of PV and Clinical Research processes, and other processes making up the PV system.
  • including the interfaces between these processes.
  • Very good understanding of PV, data management and adverse event reporting and processing.
  • Excellent oral and written communication skills, ability to interact with all levels of personnel.
  • Must be able to communicate in English (active and passive), other languages considered an asset.
  • Computer literacy (including Microsoft Office, Access and Project).

Response

Interested? Please send your resume and motivational letter by e-mail, with reference to DT/20-065-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 Secondment & Interim as recruitment agency for this assignment. We request therefore to send any application or other response to Derks & Derks.

Sales Manager / Key Account Manager

Offer

  • interesting sales management position combined with key account management
  • global organisation with a focus on long term, sustainable solutions based on science
  • a company with great ambitions and space to develop your team and yourself
  • responsible for commercial team in The Netherlands

Organisation

Our client is a global organisation focused on probiotic skincare. Founded by a scientist passionate about both the skin microbiome and sustainable living, they aim to create effective and sustainable skincare products based on science. Their mission is to redefine global skincare and shift the world’s understanding of and view on skincare. They have a wide range of skincare products and aim to provide long term (sustainable) solutions as opposed to a quick-fix. Currently they are searching a Sales Manager / Key Account Manager for their commercial team in The Netherlands.

Position

As Sales Manager / Key Account Manager you are responsible for the sales and market share development of their wide range of probiotic skincare products in the Netherlands. You are at the start of establishing an independent commercial organization in the Netherlands.

You will build on new relations through different activities and find new collaboration partners and beauty salons to increase the sales. You will ensure a consistent approach towards accounts in line with the company strategy to achieve the commercial goals. In addition, you will lead the current team of 2 sales representatives and offer guidance if needed. You will attend daily sales meetings. You have good communication skills, and understand how to approach different accounts. You understand the sales process, like to build and create leads, and at the same time have the ability to lead a team. You are committed and dedicated to build the brand fast, without compromising on quality. In this job you will report to the General Manager Europe.

Profile

  • Bachelor’s degree or higher (commercial related)
  • at least 2 years of successful experience as Key Account Manager and in Sales Management position
  • experience with and examples in strong key account management
  • demonstrated leadership skills
  • experience within cosmetics sector required
  • affinity or experience with beauty salons is a strong preference
  • ability to translate agreed strategy into an operational action plan with clear timelines
  • fluent use of Microsoft Office, Excel, PowerPoint and Outlook
  • representative, committed, proactive, dedicated, commercial, solution-oriented, strong leadership skills
  • fluent in both Dutch and English

Response

Interested? Please send your resume and motivational letter by e-mail, with reference to WS/20-041-DD, to Jamie van der Heijde : info@derksenderks.nl.

For further information, please call Jamie van der Heijde 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.

Apply directly

Drug Safety Officer

Offer

  • a diverse job at a global pharmaceutical company
  • an interesting job because of the international contacts
  • a temporary contract for 7 months, with the possibility to extend

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 a Drug Safety Officer.

Position

As a Drug Safety Officer you will be managing its related duties and act as a contact person for any safety issues at the responsible country and/or Affiliate. You will lead and, if applicable, provide effective management of PSI. Ensure that safety information (Adverse Events) received from all sources by the Affiliate are collected, translated and forwarded to designated Regional PV HQ, in compliance with required timelines (reporting timelines), quality guidelines and standards. If applicable: Timely ICRS submissions to the Competent Authority. You will also ensure the Affiliate is GPvP inspection and audit ready and support a PV audit or inspection if needed. Another field  of responsibility is to provide input for the PSMF regarding the Affiliate communication to GPV Regional HQ. You will also be responsible and accountable for PV self-assessments, PV audits/inspections at the Affiliate and assist in developing CAPAs (with qualitative/quantative measures and timelines) in response to findings/observations. If the position is not various enough you also serve as a point of contact for the PV Regional HQ functions, PV Affiliate Support Function, the Affiliate MT and M&D functions. You report to the manager of the department and interact with your global and local team.

Profile

  • minimum B.Sc. degree in Life Sciences
  • in depth knowledge of regulatory requirements
  • technical expert or manager with an in-depth understanding of all aspects of pharmacovigilance and related disciplines
  • experience in leading a team, project or process function
  • a strong cultural sensitivity, influencing skills without direct hierarchy
  • good oral and written communication and presentation skills in English
  • willingness to travel up to 50%

Response

Interested? Please send your resume and motivational letter by e-mail, with reference to DT/20-064-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 Secondment & Interim as recruitment agency for this assignment. We request therefore to send any application or other response to Derks & Derks.

Is this not the job you are looking for? Please visit www.derksenderks.nl/nl/nieuwe-baan/vacatures for other challenging positions in pharma, food and medical.

Director Commercial Quality / QP

Offer
  • strategic management position
  • responsible for 8 countries
  • working for a company with a diverse and interesting product portfolio
  • attractive remuneration package
Organisation

Our client manufactures and markets high-quality drugs in a diversity of fields. With a diverse portfolio of products and solutions, they are continuously providing patient healthcare solutions. They have built a promising pipeline centered around their core therapeutic areas. Through continuous investment in their research and development, marketing and business development, they keep growing their medicines business. Innovation is at the core of this company, with the aim of improving health and contributing to better, healthier lives. We are currently looking for a Quality Director to complete their European Quality Team.

Position

As a Director Commercial Quality / QP you are responsible for the overall direction, coordination, implementation and execution of commercial quality activities in the Benelux and Nordics. This needs to be in alignment with business units in order to ensure products are efficientlty distributed into the countries by meeting their regional and local standards and customer needs. In this position, you will support the relevant countries to locally roll out their Quality System. You ensure that all relevant local country suppliers/service providers are under control (including but not limited to: QTAs, Audit Program, PQR). You follow and trend-analyze monthly quality metrics in the countries and identify corresponding action plans. Furthermore, you are responsible for business support by participating in the periodic management meeting organized with other supportive functions (Supply Chain, Regulatory Affairs, Pharmacovigilance). When it comes to Critical Quality Incidents, you escalate to the regional quality issues raised at local level and support local quality departments to elaborate and deploy action plans related to quality incidents raised locally or regionally.

As Quality Director, you are responsible for managing and leading the 8 Quality departments, and you also train and provide professional guidance to teams. You define annual objectives in compliance with annual regional quality objectives. This position has 8 direct reports and a total of approximately 20 reports. You will report to the Sr. Director Quality Europe.

Profile
  • Sc. degree in Pharmacy, Biology, Healthcare or equivalent is required; post-graduate or doctoral degree is preferred
  • minimum of 7 years of experience in a Quality Role within the pharmaceutical field, and a minimum of 7 years of experience as a functional leader within an international environment
  • experience or history of being a Qualified Person is required
  • in-depth knowledge of the pharmaceutical industry as it relates to Quality Compliance
  • in-depth understanding of GMP & GDP regulations
  • experience with development and implementation of Quality Systems and application of risk assessment tools
  • strong problem solving skills, autonomous and independent, strong collaboration, management and leadership skills. Able to inspire and motivate a team.
  • excellent communicative skills in English, Dutch is preferred.
Response

Interested? Please send your resume and motivational letter by e-mail, with reference to WL/20-056-DD, to Anneke Aangeenbrug : info@derksenderks.nl.

For further information, please call Anneke Aangeenbrug 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.

vacature regulatory-affairs

Senior Manager CMC-RA

Offer
  • a diverse job at a global pharmaceutical company
  • an interesting job because of the international contacts
  • a temporary contract for 1 year, with the possibility to extend
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 a highly experienced Sr. Manager CMC-RA.

Position

As a Sr. Manager CMC-RA you will support the preparation of variation packages, renewals, new MAA (non-ICH), and response documents concerning both EU and non-EU (i.e. EMEA region) submissions. It concerns both CTD module 3 (and QOS) and Normative Document for small molecules. You will also support the preparation of baseline submissions. In addition, it is your responsibility to contribute to the assessment/comparison of updated ICH/non-ICH file as part of a global compliance project. Furthermore, you will create overviews of available quality modules in order to prepare for migration to another document management system. Finally, you will contribute to the compliance check of CMC-RA information in the applicable systems.

Profile
  • at least 3 years of experience with CMC-RA related preparations for variation packages, renewals, new MAA (non-ICH), and response documents. Preferably, also experience with Normative Document preparation/updates
  • experience with IT systems (like Trackwise, document management system), Excel, Word
  • strong organizational skills, accurate, being able to work independently
  • good communication skills;
  • fluent in English (both written and spoken)
Response

Interested? Please send your resume and motivational letter by e-mail, with reference to DT/20-060-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 Secondment & Interim as recruitment agency for this assignment. We request therefore to send any application or other response to Derks & Derks.

Is this not the job you are looking for? Please visit www.derksenderks.nl/nl/nieuwe-baan/vacatures for other challenging positions in pharma, food and medical.

Associate Director Regulatory Affairs

Offer

  • a diverse job at a global pharmaceutical company
  • an interesting job because of the international contacts
  • a temporary contract for 6 months, with the possibility to extend

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 a highly experienced Associate Director Regulatory Affairs Manager.

Position

As an Associate Director Regulatory Affairs you will be responsible to ensure strategic and operational alignment of RA activities with other functional departments in AP-MENA/SSA and ensure adequate planning and resources to adhere to the targets defined in the Business (Review) Meetings. You will make sure that Regulatory Affairs Managers in AP-MENA/SSA prepare (tailoring for local submission), dispatch to agents and business partners and ensure submission to local authorities and maintain as directed by RAE. You will make sure that Marketing Authorization Applications (MAA) are made according to current legislation, in order to obtain and maintain marketing authorizations in the geographical business area of AP MENA/SSA. This is directly linked to the strategic business obligations of the affiliate to the European objective. You will support the Regulatory Affairs and Quality Director in overall quality improvement and assurance and management of the regulatory group. Together with the Manager you will also have specific regional and product responsibilities and tasks (RAM responsibility). In this position you will work in a small team and report to the director of RA of the MENA/SSA.

Profile

  • Master degree in pharmacy, chemistry of (medical) Biology preferred
  • at least 5 years‘ experience with international RA activities in the pharmaceutical industry
  • preferable additional team leader or project leader experience
  • experience in working in multidisciplinary teams
  • ability to work with well-organized project management, result oriented and working under pressure
  • excellent communication and writing skills (advise, convince, negotiate, listen, coach, present and edit)
  • coaching skills and capability to lead an experts team, with experts working at various levels & experience
  • relatively high abstraction level, to be able to switch to required levels and stand-points
  • ability to generate a realistic work-planning, derived from a vast number of data and information
  • good communication skills (positive & constructive attitude, desire and ability to work in multidisciplinary / international teams)
  • good knowledge of the regulatory rules, guidance and institutes in MENA/SSA territory
  • adequate knowledge to work with information technology systems (e.g. Windows, MS Office and Dbases)
  • Fluent in English language, both spoken and written

Response

Interested? Please send your resume and motivational letter by e-mail, with reference to DT/20-059-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 Secondment & Interim as recruitment agency for this assignment. We request therefore to send any application or other response to Derks & Derks.

Is this not the job you are looking for? Please visit www.derksenderks.nl/nl/nieuwe-baan/vacatures for other challenging positions in pharma, food and medical.

vacature kwaliteit

Quality Assurance Officer

Offer
  • challenging positions within a dynamic and challenging environment
  • part of a motivated and driven team
  • positions full of possibilities to extend your personal skills and knowledge
Organisation

The organisation produces and exports a broad range of pharmaceuticals for patients throughout the world. At their production site in Amsterdam, they prepare a broad range of medicines derived from blood plasma. These products are used for a large number of disorders, many of which life-threatening. In addition, the organisation makes their knowledge and infrastructure available to their partners. For example, for the contract manufacturing of medicines under their own labels. This client has capabilities and extensive experience in fractionation, formulation, filling and packaging of plasma products. Their facilities are well equipped and all processes are GMP-compliant and meet the regulations of FDA, EMA, and local authorities. Within the organisation there are two Quality Assurance departments: QA Compliance Systems and QA Operations. Both teams are looking for a new, enthusiastic QA Officer.

Position

Our client is looking for an experienced Quality Assurance Officer to become part of the QA Compliance Systems Team or the QA Operations Team. The content of the role depends on the specific role you will be fulfilling. The QA Compliance Systems Team ensures the maintenance, support and the improvement of the quality management systems of the procedures and documentation. The team ensures that strict compliance of the international regulations of the countries where the products are delivered. This role is towards the role of (Lead) Auditor, which is mainly focussed on setting up, leading and conducting internal and external audits in the Netherlands and abroad.

The QA Operations Team monitors the quality of operational activities within the organisation. They focus on the areas of batch review, routine support and release. The team ensures that products and processes are compliant with the internal and external requirement and applicable laws and regulations. This role is towards the role of (Senior) Operations Officer. In this role you will be responsible for the quality and compliance with the area of batch review, routine support and release. Both QA teams are constantly active looking for opportunities to improve. These positions are versatile and challenging and full of possibilities to extend your personal skills and knowledge.

Profile
  • a Bachelor or Master degree in a relevant field
  • broad experience within the pharmaceutical industry, preferably within a QA position
  • experience with cGMP
  • good team player, stress resistant, proactive and the ability to be flexible
  • good communication skills and fluent in both Dutch and English
Response

Interested? Please send your resume and motivational letter by e-mail, with reference to WL/020-058-DD, to Tim van Loon: info@derksenderks.nl.

For further information, please call Tim van Loon 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 kwaliteit

Quality Control Officer

Offer
  • challenging position within an inspiring, inclusive and respectful working environment
  • working on your personal development, ambitions and personal choices
  • positions full of variation and possibilities to extend your validation skills and knowledge
Organisation

The organisation produces and exports a broad range of pharmaceuticals for patients throughout the world. At their production site in Amsterdam, they prepare a broad range of medicines derived from blood plasma. These products are used for a large number of disorders, many of which life-threatening. As a Quality Control Officer you will be part of the QC Support Team, which is one of the two QC departments within the organisation. The QC Support Team helps QC operations with several services. This includes validation, maintenance and calibration of equipment, management of the LIMS system, environmental monitoring and utility monitoring. Also, these teams are responsible for all QC related changes, quality agreements and external contact management. You will be part of a motivated team, where you can work on your personal development, ambitions and personal choices.

Position

Our client is looking for experienced Quality Control Officer to become part of the QC Support Team. As a QC Officer you have a challenging and versatile position. The content of the role depends on the specific role you will be fulfilling. This can be towards the role of Systems Officer, which is mainly focussed on building or improving different parts of the LIMS system. This can also be towards the role of Equipment Officer, which is focussed on validation, maintenance and calibration of equipment. These positions are full of variation and possibilities to extend your validation skills and knowledge!

Profile
  • preferably a Bachelor degree with at least 3 years of experience in a Pharmaceutical laboratory and cGMP environment (QC or R&D)
  • broad experience as a Quality Control Officer or Quality Control Engineer
  • experience with cGMP, LIMS and Validation
  • good communication and negotiation skills to operate in multidisciplinary teams
  • stress resistant, flexible, independent, proactive and hands-on mentality
  • fluent in English both written and spoken
Response

Interested? Please send your resume and motivational letter by e-mail, with reference to WL/20-057-DD, to Tim van Loon: info@derksenderks.nl.

For further information, please call Tim van Loon 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.