Veelzijdige kwaliteitsrol bij een ondernemende, creatieve, ambachtelijke en toegewijde organisatie (Flevoland) ...

Onze relatie ontwikkelt en produceert een breed assortiment aan voedingssupplementen, cosmetica en farmaceutische producten. De producten zijn te koop bij drogisterij- en supermarktketens binnen en buiten Europa. Het assortiment omvat meer dan duizend producten, varierend van A-merken tot private label producten. ...

Als QA Manager ben je verantwoordelijk voor de kwaliteit van de producten die onze opdrachtgever produceert. Samen met je team van 4 fte draag je zorg dat de producten voldoen aan wettelijke richtlijnen, wensen en eisen van de klant en de kwaliteitseisen van de organisatie. Om dit te kunnen garanderen, houd je de ontwikkeling betreffende wetgeving en internationale richtlijnen over de productcategorieën nauwlettend in de gaten en ben je verantwoordelijk voor de incorporatie van deze ontwikkeling...

Onze relatie ontwikkelt en produceert een breed assortiment aan voedingssupplementen, cosmetica en farmaceutische producten. De producten zijn te koop bij drogisterij- en supermarktketens binnen en buiten Europa. Het assortiment omvat meer dan duizend producten, varierend van A-merken tot private label producten. ...

A temporary position for the period of at least five months at a global pharmaceutical company ...

Our client is a global pharmaceutical leader and the world’s largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Their employees are at the core of their success, with colleagues in over 80 countries, delivering the world’s largest medicine cabinet to 200 million people every day. They offer a uniquely diverse portfolio of products and solutions for patients and they have built a promising pipeline centred around their co...

As an Administration Coordinator you will assist the departmental secretary in all services provided to the department and the sales force. You will directly report to the Business Unit Manager, but you will collaborate on daily basis with the National Sales Manager, finance department and sales reps. In this position, you manage all existing and new contracts for wholesalers, hospitals, healthcare insurers, buying groups, drugstore chains and individual agreements with pharmacies. You will be r...

• Preferably a Bachelor’s degree. • At least 2 years of experience in a similar role. • Experience in working within an international environment. • Experience in working with SAP & Ariba is preferred. • Good communication skills. • Good common in both Dutch and English. ...

Product Specialist Allergie Midden-West Nederland (Rotterdam - Den Bosch - Utrecht)...

Allergy Therapeutics Nederland is een jong en innovatief bedrijf gevestigd in Amersfoort. Het hoofdkantoor van Allergy Therapeutics is gevestigd in Worthing UK en houdt zich bezig met diagnostiek en de behandeling van allergie bij patiënten met hooikoorts en overgevoeligheid voor antibiotica. Om onze sterke groei te continueren en uit te breiden zijn we op zoek naar een gedreven energieke zelfstarter met een goed netwerk bij huisartsen en voornaamste medisch specialisten op het gebied van all...

Als Product Specialist Allergie ben je binnen jouw regio verantwoordelijk voor het adviseren van huisartsen en de belangrijkste medisch specialisten (Allergologen, KNO artsen, Dermatologen, Longartsen en Kinderartsen) over allergie en de behandeling van hooikoorts. Aan de hand van een zelf opgesteld regioplan probeer je jouw doelstellingen voor de regio te behalen. Actie gerichtheid en constructief denken in mogelijkheden is zeer gewenst. Verantwoordelijkheden Product Specialist Allergie -...

Functie eisen Product Specialist Allergie - Energieke zelfstarter die denkt in mogelijkheden! - Minimaal 1 jaar buitendienstervaring in een farmaceutische omgeving - Ervaring binnen de het indicatie gebied Allergie en/of Astma/COPD is een duidelijke pré - Gedreven persoonlijkheid met groot verantwoordelijkheid gevoel en discipline voor zijn/haar werk! - Hands-on, gedreven en gewend in een commerciële, dynamische omgeving te werken - Enige kennis van de farmaceutische industrie en de mark...

A temporary position for the period of at least five months at a global pharmaceutical company ...

Our client is a global pharmaceutical leader and the world’s largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Their employees are at the core of their success, with colleagues in over 80 countries, delivering the world’s largest medicine cabinet to 200 million people every day. They offer a uniquely diverse portfolio of products and solutions for patients and they have built a promising pipeline centred around their co...

As a Group Leader Quality Control it is your responsibility to manage the team in establishing and maintaining quality at the lab in accordance with site SOPs, regulatory guidelines and cGxP compliance requirements. You will manage up to 12 team members and your main focus is to maintain a culture of enhancing quality throughout the entire laboratory. You are responsible for delivering a sustainable planning for release testing and parental & inhalation drug products. You manage your own team th...

• Bachelor or Master degree in analytical chemistry/pharmacy or equivalent experience. • Able to act as an excellent liaison between Quality Control & other departments. • Good Knowledge with the use of ICH guidelines and Pharmacopoeia methods. • Excellent organizational skills and a strong analytical oriented mindset. • Experience in working within a pharmaceutical environment. • Experience with compiling planning schedules for analytical testing. • Good knowledge of Pharmaceutical qualit...

Temporary position for 9 months at a pharmaceutical company...

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 motivated...

As an Regulatory Operations Associate you will be responsible to ensure timely preparation and submission of correspondence and applications to regulatory agencies, tracking and planning of such and document conformance to global publishing standards and style manuals. You will also be responsible for timelines and own resource management. You will participate in extended teams/projects/teams and ensure timely internal communication regarding regulatory filing status. In the position you will be...

• at least a Bachelor degree • Bachelor 1-2 years’ experience and Master 0-2 years’ experience • proven ability to prioritize and multi-task with minimal supervision based on interactions with project team members • good written and oral communication skills in English • high integrity with respect to maintenance of proprietary, confidential information • highly accurate and organized, oversees support activities • affinity to work with IT systems and a problem solving mentality • comes u...

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Senior Director of S&OP is required by CareerWise Recruitment for our Cork based Pharma client operating at a global level. This role is a global head of Integrated Planning and is accountable for developing and directing the overall strategy of the S&OP process. ...

• The Senior Director (SD) of S&OP will work in close collaboration with regional Commercial leadership and key stakeholders to tailor the process to meet management objectives. • The SD of S&OP will be responsible for maintaining rigor in the monthly process and ensuring a seamless and efficient generation and handoff of information to global and site supply chain functions. • This role will also be accountable to establish the governance and performance management for S&OP. • This role will...

• Expert leader at a Global level with a proven track record of building and managing high performing teams • Experienced people manager with a strong reputation for mentoring and developing people • Expertise and track record in manufacturing and supply chain execution and oversight, previous ERP implementation experience • Expert in a formal S&OP process • 15+ years of relevant experience in related field and a BS or BA...

This is your opportunity for a change in scenery to the best of what Australia has to offer!...

Our client is a specialized Bioanalytical laboratory which offers services for a range of clients across the pharmaceutical and biotechnology industry. They have an ever-expanding range of services within their specialized laboratories, including Immunoassays, Biomarkers and LC-MS Bioanalysis. Continued year on year growth underpinned by a government R&D Tax initiative. Their facilities operate to FDA and GLP standards, as well being NATA and ISO accredited. Their facilities are based in Adelai...

As a Study Director you ensure timelines are firstly set appropriately considering, company and external stakeholder requirements and once set, ensure timelines are achieved. You are the communication line between internal and external stakeholders. Also, you ensure the scientific, integrity and regulatory compliance of study date by the review of all runs. Troubleshoot scientific issues by liaising with appropriate groups including Research & Development (R&D), Operations and Management. Furthe...

• Bachelor’s degree in life sciences • Minimum 5 years of experience in a regulated Bioanalytical position, ideally in a pharmaceutical or CRO environment. • Preferably at least 2 years work experience as a Study Director. • Proven ability to review SOPs and ALMs. • Experience with immunoassay development or Immunobiology. • Ambitious, entrepreneurial and communicative....

Become part of an expert group which explores new biopharmaceutical modalities...

Our client, a leading, international biopharmaceutical company with site in southern Germany, is looking for an Advanced Therapy Medicinal Product (ATMP) Quality Manager. Would you like to become part of an expert group which explores new biopharmaceutical modalities, Advanced Therapy Medicinal Products and extends our client’s manufacturing expertise within the Biopharma Contract Manufacturing Business Unit? Then show us your strong understanding of existing and leading-edge analytical test met...

As ATMP Quality Manager you provide expertise and guidance to internal functions as well as to external clients in the broad range of quality test methods for viral vectors and therapeutic viruses. Also, you are going to implement robust CMC Compliance Programs covering all aspects of the manufacturing processes, analytical test methods, specifications and shelf live maintenance. You will support technical based discussions during scientific advice with regulatory agencies, drive interactions on...

• Masters/Diploma degree or Doctoral degree (PhD) in virology/biologics, biotechnology, pharmacy, or equivalent • minimum of three years of professional experience in the field of ATMPs/new biopharmaceutical modalities, preferably in analytical development of cells or viruses for new therapies • demonstratable expertise in quality control and/or quality systems required for the manufacturing of viral vectors and therapeutic viruses-based therapeutics • in-depth knowledge in the analytical cha...

Challenging position within a dynamic and challenging environment...

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 ca...

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. T...

• 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 ...

Temporary position for 6 months at a pharmaceutical company...

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 Associat...

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 ...

• 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 regulation...