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Quality Assurance Senior Quality Assurance Officer Full-time Leiden Quality Specialist Full-time Leiden Production Biotechnician Full-time Oss Animal Care Taker Full-time Oss Senior Biotechnician Full-time Oss Senior Biotechnician Full-time Oss Animal Caretaker Full-time Eindhoven Biotechnician Full-time Eindhoven Marketing Senior Director Market Access Full-time Flexible Europe Director of Commercial Analytics Full-time USA Marketing Director Full-time USA Finance Finance Officer Full-time Leiden Financial Accountant Full-time Leiden Financial Reporting Manager Full-time Leiden Clinical and Medical Clinical Trial Assistant Full-time Warren, New Jersey USA R&D Senior Scientist Non-Clinical Development, Pharmacology Full-time Leiden Scientist Formulation Development Full-time Leiden Technical Operations & QC CQV Engineer Full-time Oss (Sr) Director Manufacturing, Science & Technology Full-time Leiden Supply Chain Logistics Specialist Full-time Leiden Regulatory Affairs Medical Writer Full-time Leiden ICT Servicedesk Engineer Full-time Leiden Bijgekomen; ICT Servicedesk Engineer Full-time Leiden Afgenomen: Aantal openstaand: 22 Totaal vacatures toe of afname vanaf 29 sept 2020 Bijgekomen: 37 Afgenomen 26
ICT Servicedesk Engineer Full-time Leiden Pharming is a global, commercial stage biopharmaceutical company developing innovative protein replacement therapies and precision medicines for the treatment of rare diseases and unmet medical needs. The company is poised for further scientific, technological and new product development and additional commercial roll-outs. The company is based internationally and growing quickly. As a result of this growth, we are looking for a Servicedesk Engineer. About the role: The Servicedesk Engineer provides outstanding ICT customer support on all inquiries from corporate users from start to finish. He/she responds to user ICT inquiries and resolves or escalates issues relating to hardware, software and network to ensure that the most important problems are resolved promptly. He/she understands user questions, provides technical support and solves technology problems remote or on site. Areas of responsibilities: Install, upgrade, support and resolve issues related to PC’s or laptops, printers, scanners, phones. LAN and WAN, hardware and software from start to finish, all the while keeping the user informed of the process. Maintain security, anti-virus solutions, configure and maintain operating systems and software applications, backup devices. Suggest ideas for improving service desk functions, service delivery and overall customer service, helping to develop and improve the servicedesk Testing and evaluating new hardware or software applications as upgrades or enhancements to the production environment Diagnose hardware, software, and operator problems and take appropriate remedial actions and document installation and configuration procedures Ensure IT Operations complies with all the IT defined policies and procedures Ensure all systems are managed and tracked in the asset management system Communicate with vendors to resolve issues related to software, hardware and network Provide IT support in projects (e.g. data collection/hardware installation) Required skills and qualifications in order to be successful in this role: Strong customer focus Excellent communication skills in English and Dutch Problem analysis skills Agile Teamplayer Eager to learn and develop Knowledge: MBO 4 ICT / A+ Certification or equivalent MCSE certification preferred MOS certification preferred ITIL certification preferred Experience: Minimum of 2 years experience in a similar role Proven ability to complete tasks independently and under pressure TOPdesk Microsoft 365 Azure Windows 10 Office 365
Quality Assurance Senior Quality Assurance Officer Full-time Leiden Quality Specialist Full-time Leiden Production Biotechnician Full-time Oss Animal Care Taker Full-time Oss Senior Biotechnician Full-time Oss Senior Biotechnician Full-time Oss Animal Caretaker Full-time Eindhoven Biotechnician Full-time Eindhoven Marketing Senior Director Market Access Full-time Flexible Europe Director of Commercial Analytics Full-time USA Marketing Director Full-time USA Finance Finance Officer Full-time Leiden Financial Accountant Full-time Leiden Financial Reporting Manager Full-time Leiden Clinical and Medical Clinical Trial Assistant Full-time Warren, New Jersey USA R&D Senior Scientist Non-Clinical Development, Pharmacology Full-time Leiden Scientist Formulation Development Full-time Leiden Technical Operations & QC CQV Engineer Full-time Oss (Sr) Director Manufacturing, Science & Technology Full-time Leiden Supply Chain Logistics Specialist Full-time Leiden Master Data & Artwork Specialist Full-time Leiden Regulatory Affairs Medical Writer Full-time Leiden ICT Servicedesk Engineer Full-time Leiden Bijgekomen; Master Data & Artwork Specialist Full-time Leiden Afgenomen: Aantal openstaand: 23 Totaal vacatures toe of afname vanaf 29 sept 2020 Bijgekomen: 38 Afgenomen 26
Master Data & Artwork Specialist Full-time Leiden Pharming is a global, commercial stage biopharmaceutical company developing innovative protein replacement therapies and precision medicines for the treatment of rare diseases and unmet medical needs. The company is poised for further scientific, technological and new product development and additional commercial roll-outs. The company is based internationally and growing quickly. As a result of this growth, we are looking for a Master Data & Artwork Specialist. About the role: The Master Data & Artwork Specialist implements and maintains both product and artwork configuration in several quality controlled systems (e.g. SAP, Master Control), including the operational management of 3rd parties involved in the creation thereof. You ensure that current and future products of Pharming (manufactured and/or sold) can be produced and distributed following the GxP guidelines, with the goal to improve quality of live of patients. Areas of responsibilities: Ensuring GxP integrity and quality of master data in key systems (SAP, Master Control) as well as maintaining the processes to support the data quality, and documentation of these processes (if necessary, with other functional data owners); Based on defined release and decommissioning processes in the key systems setup, maintain and decommission, inter alia, item master data, location master data, including machine and work center data, bill of resources, bill of materials, bill of sampling, customers including price lists and suppliers including outline agreements; Assisting in the application and implementation of procedures for data standards and guidelines on data ownership, coding structures, and data replication to ensure access to and integrity of data sets; Artwork Manage the creation of and maintain the process for artwork development for printed packaging components from specification through publishing to external suppliers for artwork globally Ensure appropriate approvals are obtained from other functions where applicable, assure communication is made with third party manufacturer/packager and all necessary proofreading are completed at all stages as per current procedure Responsible and accountable for process execution and adherence to required completion date. Document, submit, monitor the execution of, and closure of change controls related to phasing in and phasing out of, inter alia, markets, dossier changes, products, locations, customers, suppliers, work & machine centers etc; Interaction Setup and maintain proactive interaction with all internal departments (i.e. Clinical, finance, manufacturing, marketing, procurement, quality assurance, quality control, research & development, regulatory affairs, and sales) involved in the creation and decommissioning of master data and its related artwork. Act as SME for end user support and training Participates in cross-departmental projects Required skills and qualifications in order to be successful in this role: Accuracy; Planning and organizing; Independence; Customer orientation (internal and external); Results orientation; Organizational sensitivity ; Problem analysis; Teamwork. Knowledge: MBO degree with preferably HBO level of thinking; Good X Practice (GxP) knowledge of Manufacturing, Distribution, Documentation, Clinical; ERP systems (preferably SAP); Excel knowledge; Pharmaceutical packaging & artwork; Industry standards and regulations in this domain Text verification tools; Project / time management skills; Good analytical and problem-solving skills; Working knowledge of the Dutch and English Language, other languages are beneficial. Experience: 7+ years’ experience in data management and (pharmaceutical) artwork management
Quality Assurance Senior Quality Assurance Officer Full-time Leiden Quality Specialist Full-time Leiden Production Biotechnician Full-time Oss Animal Care Taker Full-time Oss Senior Biotechnician Full-time Oss Animal Caretaker Full-time Eindhoven Biotechnician Full-time Eindhoven Marketing Senior Director Market Access Full-time Flexible Europe Director of Commercial Analytics Full-time USA Marketing Director Full-time USA Finance Finance Officer Full-time Leiden Financial Accountant Full-time Leiden Financial Reporting Manager Full-time Leiden Clinical and Medical Clinical Trial Assistant Full-time Warren, New Jersey USA R&D Senior Scientist Non-Clinical Development, Pharmacology Full-time Leiden Scientist Formulation Development Full-time Leiden Technical Operations & QC CQV Engineer Full-time Oss (Sr) Director Manufacturing, Science & Technology Full-time Leiden Supply Chain Logistics Specialist Full-time Leiden Master Data & Artwork Specialist Full-time Leiden Regulatory Affairs Medical Writer Full-time Leiden ICT Servicedesk Engineer Full-time Leiden Bijgekomen; Afgenomen: Senior Biotechnician Full-time Oss Aantal openstaand: 22 Totaal vacatures toe of afname vanaf 29 sept 2020 Bijgekomen: 38 Afgenomen 27
Quality Assurance Senior Quality Assurance Officer Full-time Leiden Quality Specialist Full-time Leiden Production Biotechnician Full-time Oss Animal Care Taker Full-time Oss Senior Biotechnician Full-time Oss Animal Caretaker Full-time Eindhoven Biotechnician Full-time Eindhoven Marketing Senior Director Market Access Full-time Flexible Europe Director of Commercial Analytics Full-time USA Marketing Director Full-time USA Finance Finance Officer Full-time Leiden Financial Accountant Full-time Leiden Financial Reporting Manager Full-time Leiden Clinical and Medical Clinical Trial Assistant Full-time Warren, New Jersey USA R&D Senior Scientist Non-Clinical Development, Pharmacology Full-time Leiden Scientist Formulation Development Full-time Leiden Technical Operations & QC CQV Engineer Full-time Oss (Sr) Director Manufacturing, Science & Technology Full-time Leiden Supply Chain Logistics Specialist Full-time Leiden Master Data & Artwork Specialist Full-time Leiden Regulatory Affairs Medical Writer Full-time Leiden Human Resources HR Generalist Full-time Warren, New Jersey USA HR Coordinator Full-time Warren, New Jersey USA ICT Servicedesk Engineer Full-time Leiden Bijgekomen; Human Resources HR Generalist Full-time Warren, New Jersey USA HR Coordinator Full-time Warren, New Jersey USA Afgenomen: Aantal openstaand: 24 Totaal vacatures toe of afname vanaf 29 sept 2020 Bijgekomen: 40 Afgenomen 27
HR Generalist Full-time Warren, New Jersey USA About Pharming: Pharming is a global, commercial stage biopharmaceutical company developing innovative protein replacement therapies and precision medicines for the treatment of rare diseases and unmet medical needs. The company is poised for further scientific, technological and new product development and additional commercial roll-outs. The company is based internationally and growing quickly. As a result of this growth, we are looking for a HR Generalist for our organization in the USA. About the role: The HR Generalist plans, develops, implements, and evaluates our people programs, processes, and solutions spanning across all areas of Human Resources. Working in collaboration with the HR Director and other members of the HR Team, the HR Generalist will help make sure Pharming Healthcare Inc. continues to attract, engage, and retain top talent through the administration, execution, and evaluation our Total Rewards, Talent Development, Compliance, and Culture & Engagement offerings while creating an excellent employee experience as it relates to our overall people services and operations. Areas of responsibilities: Provide project support for overall HR initiatives spanning across a wide-range of areas including Total Rewards, Operations, Succession and Workforce Planning, Learning & Development, and Communication and Engagement Coach and guide Employees and Managers on HR policies, programs, and processes, taking an Employee-centric approach to ensure a high-level of customer service Facilitate the Pharming Connect onboarding program ensuring a smooth transition for our new Employees Maintain employee data and records putting processes and controls in place to ensure a high-level of data integrity. Collaborate with internal and external stakeholders to implement solutions to streamline the processing of HR data while understanding downstream impacts Provide analysis and insights on compensation related issues, leveling of positions, and pay recommendations to support recruitment, promotions, transfers, pay, and other employee changes Administer, explain, and market our Total Reward programs to Employees Maintain knowledge of Federal and State employment and Labor Laws, providing education and guidance to our Employees and Managers and making sure our programs and policies are compliant Oversee the governance and ongoing documentation of our HR operational processes and policies leveraging insights, data, and employee feedback to make continuous improvements Develop employee communications and activities to connect our employees, share information, and engage our Teams Required skills and qualifications in order to be successful in this role: Teamwork Excellent verbal and written communication skills Planning, organizing, and prioritizing work Integrity and Trust Process management with a continuous improvement mindset Flexible in approach; can adjust quickly to changes in direction Results Oriented Customer Focus Personal Development/Self Awareness Knowledge: BA in Human Resource Management, Organizational Development, Business or a related discipline Knowledge of State and Federal Laws and compliance requirements Human Resources Acumen in the following areas: Total rewards administration, HR Operations (technology, systems and analytics), Onboarding and Engagement, Employee Relations Experience: 5+ years of experience in a HR Generalist role of which 2+ years experience with benefits plan administration (incl. 401k) and HR Operations and administration Proficiency in Microsoft Office software Experience in making process improvements to support HR operations and activities
HR Coordinator Full-time Warren, New Jersey USA About Pharming: Pharming is a global, commercial stage biopharmaceutical company developing innovative protein replacement therapies and precision medicines for the treatment of rare diseases and unmet medical needs. The company is poised for further scientific, technological and new product development and additional commercial roll-outs. The company is based internationally and growing quickly. As a result of this growth, we are looking for a HR Coordinator for our organization in the USA. About the role: The HR Coordinator provides the execution and coordination support for our operational processes spanning across all areas of Human Resources. Working in collaboration with the Sr. HR Generalist and other members of the HR Team, the HR Coordinator creates an excellent employee experience throughout all phases of the employee lifecycle, ensuring the executional excellence of our overall people programs at Pharming Healthcare Inc. Areas of responsibilities: Provide coordination and executional support for overall HR initiatives including Benefits and 401k administration, Interview Coordination, Onboarding/Offboarding, Compliance, and Performance Management and Learning and Development. Coach and guide Employees on HR policies, programs, and processes, taking an Employee-centric approach to ensure a high-level of customer service. Facilitate the onboarding process including pre-employment screening, completion of employee paperwork, I9’s, and the coordination of the Pharming Connect onboarding program. Maintain employee data and records putting processes and controls in place to ensure a high-level of data integrity. Administer our Total Reward programs serving as liaison between our internal partners, external vendors, and Employees. Track Employee questions and issues identifying opportunities for improvements with our vendors, processes, and practices. Provide technical and troubleshooting support for our HR Systems, helping guide our Managers and Employees and providing training as needed. Create monthly payroll, headcount, and ad-hoc reports as needed, providing analysis and periodic audits. Maintain compliance documentation and records ensuring we meet OSHA, Federal, and State requirements. Create documentation, training, and reference materials ensuring information is readily available and updated. Handle the approval and processing of vendor invoices, purchase orders, and new vendor set-up. Required skills and qualifications in order to be successful in this role: Teamwork Excellent verbal and written communication skills Planning, organizing, and prioritizing work Integrity and Trust Process focused with a continuous improvement mindset Flexible in approach; can adjust quickly to changes in direction Results Oriented Customer Focus Personal Development/Self Awareness Knowledge: BA in Human Resource Management, Organizational Development, Business or a related discipline Knowledge of State and Federal Laws and compliance requirements Human Resources Acumen in the following areas: Total rewards administration, HR Technology & Systems, Onboarding Experience: 2+ years of experience in HR in a role covering benefits plan administration (incl. 401k) and HR Operations and administration Proficiency in Microsoft Office software Experience in making process improvements to support HR operations and activities
Quality Assurance Senior Quality Assurance Officer Full-time Leiden Quality Specialist Full-time Leiden Production Biotechnician Full-time Oss Animal Care Taker Full-time Oss Senior Biotechnician Full-time Oss Animal Caretaker Full-time Eindhoven Biotechnician Full-time Eindhoven Marketing Senior Director Market Access Full-time Flexible Europe Director of Commercial Analytics Full-time USA Marketing Director Full-time USA Finance Finance Officer Full-time Leiden Financial Accountant Full-time Leiden Financial Reporting Manager Full-time Leiden Clinical and Medical Clinical Trial Assistant Full-time Warren, New Jersey USA R&D Senior Scientist Non-Clinical Development, Pharmacology Full-time Leiden Scientist Formulation Development Full-time Leiden Technical Operations & QC CQV Engineer Full-time Oss (Sr) Director Manufacturing, Science & Technology Full-time Leiden Supply Chain Master Data & Artwork Specialist Full-time Leiden Regulatory Affairs Medical Writer Full-time Leiden Human Resources HR Generalist Full-time Warren, New Jersey USA HR Coordinator Full-time Warren, New Jersey USA ICT Servicedesk Engineer Full-time Leiden Bijgekomen; Afgenomen: Logistics Specialist Full-time Leiden Aantal openstaand: 23 Totaal vacatures toe of afname vanaf 29 sept 2020 Bijgekomen: 40 Afgenomen 28
Quality Assurance Senior Quality Assurance Officer Full-time Leiden Quality Specialist Full-time Leiden Production Biotechnician Full-time Oss Animal Care Taker Full-time Oss Senior Biotechnician Full-time Oss Animal Caretaker Full-time Eindhoven Biotechnician Full-time Eindhoven Marketing Senior Director Market Access Full-time Flexible Europe Director of Commercial Analytics Full-time USA Marketing Director Full-time USA Finance Finance Officer Full-time Leiden Financial Accountant Full-time Leiden Financial Reporting Manager Full-time Leiden Clinical and Medical Clinical Trial Assistant Full-time Warren, New Jersey USA R&D Senior Scientist Non-Clinical Development, Pharmacology Full-time Leiden Scientist Formulation Development Full-time Leiden Technical Operations & QC CQV Engineer Full-time Oss (Sr) Director Manufacturing, Science & Technology Full-time Leiden PMO Project Manager Full-time Leiden Supply Chain Master Data & Artwork Specialist Full-time Leiden Regulatory Affairs Medical Writer Full-time Leiden Human Resources HR Generalist Full-time Warren, New Jersey USA HR Coordinator Full-time Warren, New Jersey USA ICT Servicedesk Engineer Full-time Leiden Bijgekomen; Project Manager Full-time Leiden Afgenomen: Aantal openstaand: 24 Totaal vacatures toe of afname vanaf 29 sept 2020 Bijgekomen: 41 Afgenomen 28
Project Manager Full-time Leiden Pharming is a global, commercial stage biopharmaceutical company developing innovative protein replacement therapies and precision medicines for the treatment of rare diseases and unmet medical needs. The company is poised for further scientific, technological and new product development and additional commercial roll-outs. The company is based internationally and growing quickly. As a result of this growth, we are looking for a Project Manager. About the role: The Project Manager oversees and monitors all aspects of a multidisciplinary project using planning and control processes. He/she sets deadlines, assigns responsibilities and monitors and summarizes progress of projects to Program Manager. The Project manager coordinates and controls completion of all activities inherent to different disciplines within the agreed timelines, plan and budget, and in compliance with the appropriate quality standards and legislation. Areas of responsibilities: Writes project plans and keeps track of the progress Ensures that the project is on time and on budget with appropriate quality Reviews and approves project deliverables Acts as Single Point of Contact (SPOC) for all project team members and program manager(s) to ensure a close productive relationship between all people involved in the project Reports project status, including resources and risk analysis to Program Manager Documents all relevant project information in a methodical and secure way Required skills and qualifications in order to be successful in this role: Excellent communication skills Leadership skills Problem analysis Planning and organizing Result orientation Behavioral flexibility Persuasiveness Knowledge: (Bio)Pharmaceutical/ Life Science background Academic degree (MSc) Fluent in English (written and spoken) Working knowledge of MS Project and reporting tools (pre) Up-to-date knowledge of GMP and/or GLP and other applicable regulatory requirements (pre) Experience: At least 2 years of experience in the pharmaceutical industry working as a project manager or project lead (drug development expertise is a pre)
Quality Assurance Senior Quality Assurance Officer Full-time Leiden Quality Specialist Full-time Leiden Production Biotechnician Full-time Oss Animal Care Taker Full-time Oss Senior Biotechnician Full-time Oss Animal Caretaker Full-time Eindhoven Biotechnician Full-time Eindhoven Finance Finance Officer Full-time Leiden Financial Accountant Full-time Leiden Financial Reporting Manager Full-time Leiden Clinical and Medical Clinical Trial Assistant Full-time Warren, New Jersey USA R&D Senior Scientist Non-Clinical Development, Pharmacology Full-time Leiden Scientist Formulation Development Full-time Leiden Technical Operations & QC CQV Engineer Full-time Oss (Sr) Director Manufacturing, Science & Technology Full-time Leiden PMO Project Manager Full-time Leiden Supply Chain Master Data & Artwork Specialist Full-time Leiden Regulatory Affairs Medical Writer Full-time Leiden Human Resources HR Generalist Full-time Warren, New Jersey USA HR Coordinator Full-time Warren, New Jersey USA ICT Servicedesk Engineer Full-time Leiden Bijgekomen; Afgenomen: Marketing Senior Director Market Access Full-time Flexible Europe Director of Commercial Analytics Full-time USA Marketing Director Full-time USA Aantal openstaand: 21 Totaal vacatures toe of afname vanaf 29 sept 2020 Bijgekomen: 40 Afgenomen 31
Quality Assurance Senior Quality Assurance Officer Full-time Leiden Quality Specialist Full-time Leiden Production Biotechnician Full-time Oss Animal Care Taker Full-time Oss Senior Biotechnician Full-time Oss Animal Caretaker Full-time Eindhoven Biotechnician Full-time Eindhoven Finance Financial Accountant Full-time Leiden Financial Reporting Manager Full-time Leiden Clinical and Medical Clinical Trial Assistant Full-time Warren, New Jersey USA R&D Senior Scientist Non-Clinical Development, Pharmacology Full-time Leiden Scientist Formulation Development Full-time Leiden Technical Operations & QC CQV Engineer Full-time Oss (Sr) Director Manufacturing, Science & Technology Full-time Leiden PMO Project Manager Full-time Leiden Supply Chain Master Data & Artwork Specialist Full-time Leiden Regulatory Affairs Medical Writer Full-time Leiden Recruitment Talent Acquisition Specialist Full-time Leiden Human Resources HR Generalist Full-time Warren, New Jersey USA HR Coordinator Full-time Warren, New Jersey USA ICT Servicedesk Engineer Full-time Leiden Bijgekomen; Talent Acquisition Specialist Full-time Leiden Afgenomen: Finance Officer Full-time Leiden Aantal openstaand: 21 Totaal vacatures toe of afname vanaf 29 sept 2020 Bijgekomen: 41 Afgenomen 32
Talent Acquisition Specialist Full-time Leiden Pharming Group N.V. develops innovative therapeutics for the treatment of genetic disorders. The company is poised for further scientific, technological and new product development and additional commercial roll-outs. The company is growing quickly and as a result of this growth we are currently looking for a Talent Acquisition Specialist for in our Leiden office. About the role: As Talent Acquisition Specialist, you will be responsible for attracting and hiring talent for Pharming vacancies, ensuring that Pharming’s mission, vision and culture is incorporated in the recruitment process. The Talent Acquisition Specialist will take part in employer branding projects, ex-and internal recruitment activities and will act as a sparring partner for hiring managers, giving advice on all TA matters. Areas of responsibilities: Effective and timely sourcing of candidates for Pharming vacancies Strategic use of LinkedIn and other candidate sourcing channels Provide an excellent candidate experience that incorporates Pharming’s culture and values Participate in Employer Branding projects Partner with hiring managers to ensure an efficient and smooth talent acquisition process Monitor metrics to help optimize the recruitment process Monitoring of a large volume of vacancies and tight timelines Coordinate and plan talent acquisition activities Advise hiring manager in selection process Required skills & qualifications in order to be successful in this role: Strong communication skills Strong in building relationships/stakeholder management Pro-active Positive attitude Attention to detail Able to prioritize Knowledge and Experience: 3-5 years work experience in a similar position Fluent in both Dutch and English Experience in hiring Medior/Senior/Management level positions (BSc. - PhD level roles)
Quality Assurance Senior Quality Assurance Officer Full-time Leiden Quality Specialist Full-time Leiden Production Biotechnician Full-time Oss Animal Care Taker Full-time Oss Senior Biotechnician Full-time Oss Animal Caretaker Full-time Eindhoven Biotechnician Full-time Eindhoven Finance Financial Accountant Full-time Leiden Financial Reporting Manager Full-time Leiden Clinical and Medical Clinical Trial Assistant Full-time Warren, New Jersey USA R&D Senior Scientist Non-Clinical Development, Pharmacology Full-time Leiden Scientist Formulation Development Full-time Leiden Technical Operations & QC CQV Engineer Full-time Oss (Sr) Director Manufacturing, Science & Technology Full-time Leiden PMO Project Manager Full-time Leiden Supply Chain Master Data & Artwork Specialist Full-time Leiden Regulatory Affairs Medical Writer Full-time Leiden Recruitment Talent Acquisition Specialist Full-time Leiden Human Resources HR Coordinator Full-time Warren, New Jersey USA ICT Servicedesk Engineer Full-time Leiden Bijgekomen; Afgenomen: HR Generalist Full-time Warren, New Jersey USA Aantal openstaand: 20 Totaal vacatures toe of afname vanaf 29 sept 2020 Bijgekomen: 41 Afgenomen 33
Quality Assurance Senior Quality Assurance Officer Full-time Leiden Quality Specialist Full-time Leiden QA Officer Full-time Leiden/Brabant Production Biotechnician Full-time Oss Animal Care Taker Full-time Oss Senior Biotechnician Full-time Oss Animal Caretaker Full-time Eindhoven Biotechnician Full-time Eindhoven Finance Financial Accountant Full-time Leiden Financial Reporting Manager Full-time Leiden Clinical and Medical Clinical Trial Assistant Full-time Warren, New Jersey USA R&D Senior Scientist Non-Clinical Development, Pharmacology Full-time Leiden Scientist Formulation Development Full-time Leiden Technical Operations & QC CQV Engineer Full-time Oss (Sr) Director Manufacturing, Science & Technology Full-time Leiden Junior F&E (Facility & Equipment) Engineer Full-time Oss PMO Project Manager Full-time Leiden Supply Chain Master Data & Artwork Specialist Full-time Leiden Regulatory Affairs Medical Writer Full-time Leiden Recruitment Talent Acquisition Specialist Full-time Leiden Human Resources HR Coordinator Full-time Warren, New Jersey USA ICT Servicedesk Engineer Full-time Leiden Bijgekomen; QA Officer Full-time Leiden/Brabant Junior F&E (Facility & Equipment) Engineer Full-time Oss Afgenomen: Aantal openstaand: 22 Totaal vacatures toe of afname vanaf 29 sept 2020 Bijgekomen: 43 Vervuld: 33
QA Officer Full-time Leiden/Brabant Pharming is a global, commercial stage biopharmaceutical company developing innovative protein replacement therapies and precision medicines for the treatment of rare diseases and unmet medical needs. The company is poised for further scientific, technological and new product development and additional commercial roll-outs. The company is based internationally and growing quickly. As a result of this growth, we are looking for a Quality Assurance Officer in Oss. About the role: The QA officer ensures that the quality system at Pharming, external partners and contractors is compliant with EU and USA GMP legislation, guidelines and/or Pharming quality expectations. He or she evaluates, analyzes and prepares pharmaceutical related documents needed for batch release and compliance to GMP. Areas of responsibilities: Write, implement, review and maintain SOPs, policies and other QA related documentation. in alignment with applicable GxP guidelines. Identify documents which need to be created or updated and ensure this is organized. Act as co-trainer and expert for other Quality Assurance Officers. Organize meetings with BME and/or Pharming departments to ensure problem resolution and conducting investigations associated with deviations, Change Controls, and CAPA’s. Review, analyze and prepare documentation related to commercial starting material production, including batch records, specifications and certificates to ensure compliance with applicable guidelines and procedures. Identify and communicate areas for improvement. Propose ideas for site improvements. Preparing and supporting internal and external audits in relation to applicable guidelines (like GMP, GLP, ISO, GDP, GCP). Required skills & qualifications in order to be successful in this role: Decisiveness Communicative Responsible Quality oriented Teamwork Problem analysis Behavioral flexibility Knowledge: Education: BSc. Biotechnology, chemistry, biopharmaceutics or equivalent Technical skills: Extensive knowledge of and experience with GMP regulations for EU and US. (like GMP, GLP, ISO, GDP, GCP) Experience: Four years of experience in (bio)pharmaceutical environment with at least one year in Quality Assurance.
Junior F&E (Facility & Equipment) Engineer Full-time Oss Pharming is a global, commercial stage biopharmaceutical company developing innovative protein replacement therapies and precision medicines for the treatment of rare diseases and unmet medical needs. The company is poised for further scientific, technological and new product development and additional commercial roll-outs. The company is based internationally and growing quickly. As a result of this growth, we are looking for a junior F&E Engineer. About the role: Pharming is a growing company and there are several capital projects ongoing related to our animal facilities and downstream processing facility where CQV support is needed. The engineer will provide CQV support for these areas Areas of responsibilities: To write the URS for equipment, systems and facilities to ensure that the intended processes can be executed and are in compliance To write and execute qualification protocols (IOQ /PQ), including identification and resolution of non-conformances/deviations and changes and write summary reports for IOQ / PQ testing To ensure that contractors perform equipment, systems and facilities qualifications adequately To implement preventative and corrective actions related to CAPAs To provide improvement opportunities Support the execution of engineering projects To ensure that qualification activities and/or engineering projects are performed timely and within budget Required skills & qualifications in order to be successful in this role: Problem analysis: connects different aspects of information to gain insight, questions (perceived) certainties in order to come up with solutions Learning ability: applies newly acquired knowledge and insights to his own wok Adaptability: shows interest in change and new ways of working Excellent verbal and technical writing skills both in English and Dutch (French is an advantage), separating main issues from secondary issues and sharing information in a logical order Knowledge: Bachelor’ or Master's degree e.g. Biochemical Engineering, Chemical, Electrical, or Mechanical Engineering, Biotechnology or Life Sciences. Engineering degree is preferred. Knowledgeable of Current Good Manufacturing Practices (cGMPs) and regulatory guidelines (EMA, FDA, ICH) Experience: Minimal 5 years of relevant working experience A minimum of 2 years of cGMP CQV experience in areas like biotechnology orpharmaceutical production Experience with lean manufacturing principles (Green Belt certified is an advantage) Experience with regulatory inspections is an advantage
Quality Assurance Senior Quality Assurance Officer Full-time Leiden Quality Specialist Full-time Leiden QA Officer Full-time Leiden/Brabant Production Biotechnician Full-time Oss Animal Care Taker Full-time Oss Senior Biotechnician Full-time Oss Animal Caretaker Full-time Eindhoven Biotechnician Full-time Eindhoven Finance Financial Accountant Full-time Leiden Financial Reporting Manager Full-time Leiden Clinical and Medical Clinical Trial Assistant Full-time Warren, New Jersey USA R&D Senior Scientist Non-Clinical Development, Pharmacology Full-time Leiden Scientist Formulation Development Full-time Leiden Technical Operations & QC CQV Engineer Full-time Oss (Sr) Director Manufacturing, Science & Technology Full-time Leiden Junior F&E (Facility & Equipment) Engineer Full-time Oss PMO Project Manager Full-time Leiden Regulatory Affairs Medical Writer Full-time Leiden Recruitment Talent Acquisition Specialist Full-time Leiden Human Resources HR Coordinator Full-time Warren, New Jersey USA ICT Servicedesk Engineer Full-time Leiden Bijgekomen; Afgenomen: Master Data & Artwork Specialist Full-time Leiden Aantal openstaand: 21 Totaal vacatures toe of afname vanaf 29 sept 2020 Bijgekomen: 43 Vervuld: 34
Quality Assurance Senior Quality Assurance Officer Full-time Leiden Quality Specialist Full-time Leiden QA Officer Full-time Oss QA Officer Full-time Leiden Production Biotechnician Full-time Oss Animal Care Taker Full-time Oss Senior Biotechnician Full-time Oss Animal Caretaker Full-time Eindhoven Biotechnician Full-time Eindhoven Finance Financial Accountant Full-time Leiden Financial Reporting Manager Full-time Leiden Clinical and Medical Clinical Trial Assistant Full-time Warren, New Jersey USA R&D Senior Scientist Non-Clinical Development, Pharmacology Full-time Leiden Scientist Formulation Development Full-time Leiden Technical Operations & QC CQV Engineer Full-time Oss (Sr) Director Manufacturing, Science & Technology Full-time Leiden Junior F&E (Facility & Equipment) Engineer Full-time Oss PMO Project Manager Full-time Leiden Regulatory Affairs Medical Writer Full-time Leiden Recruitment Talent Acquisition Specialist Full-time Leiden Human Resources HR Coordinator Full-time Warren, New Jersey USA ICT Servicedesk Engineer Full-time Leiden Bijgekomen; QA Officer Full-time Oss QA Officer Full-time Leiden Afgenomen: QA Officer Full-time Leiden/Brabant Aantal openstaand: 22 Totaal vacatures toe of afname vanaf 29 sept 2020 Bijgekomen: 45 Vervuld: 35
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Atrium European Real Estate
Auplata
Avantium
Axsome Therapeutics
Azelis Group
Azerion
B&S Group
Baan
Ballast Nedam
BALTA GROUP N.V.
BAM Groep
Banco de Sabadell
Banimmo A
Barco
Barrick Gold
BASF SE
Basic-Fit
Basilix
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BE Semiconductor
Beaulieulaan
Befimmo
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Beluga
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Bever
Binck
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Bitcoin en andere cryptocurrencies
bluebird bio
Blydenstijn-Willink
BMW
BNP Paribas S.A.
Boeing Company
Bols (Lucas Bols N.V.)
Bone Therapeutics
Borr Drilling
Boskalis
BP PLC
bpost
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Brederode
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Brunel
C/Tac
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Connect Group
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Crown van Gelder
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Deceuninck
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HAL
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Heijmans
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Hunter Douglas
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HyGear (NPEX effectenbeurs)
HYLORIS
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IBA
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IEX Group
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IMCD
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ING Groep
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IntegraGen
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Johnson & Johnson
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Technicolor
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Telenet Groep Holding
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TITAN CEMENT INTERNATIONAL
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Weibo Corp
Wereldhave
Wereldhave Belgium
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Zalando
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Ziggo
Zilver - Silver World Spot (USD)