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C&Q Engineer Long term contract Switzerland A fantastic opportunity has become available for several C&Q Engineers to join a leading Pharmaceutical Manufacturer in Swtizerland. Role related Activities * The Commissioning & Qualification Engineer is responsible for commissioning, Installation Qualification (IQ) and operational qualification (OQ) of applicable projects / changes may also provide production support during Performance Qualification (PQ) activities. Specific Tasks, Responsibilities * Commissioning of Upstream, Downstream Units and Utilities, both clean and black. * Final parameter tuning of units. * Execution of process commissioning & qualification tests in adherence with project schedule. * Accepts turnover of equipment / system from construction group.Ensures Commissioning & Qualificatio execution is in accordance with GEP cGMP. * Co-ordination of adaptions (mainly automation and schedule). * Organisation of Qualification execution. * Co-ordination of Operations shift resource during C&Q phase. * Punch list generation and closeout. * Change request. Specific Tasks, Responsibilitie * Work within a cGMP environment. * Work within the safety and environmental regulations as they apply to this industry. * Work outside normal hours may apply occasionally
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Jocelyn Blackham is recruiting for a Laboratory Technician to join a rapidly growing pharmaceutical company at their site based in Basel on a contract basis for 12 months, with the possibility of extension. The main purpose of the role will be to: · Develop, optimize and implement analytical methods, e.g., for purity-, stability-, content-, potential genotoxic impurity determinations. · Write-up of analytical methods for implementation. · Conduct of release, retest, stability studies, transfer and validation analyses. · Prepare documentation of all analytical activities according to Good Documentation Practices through compilation of all analytical testing records (e.g., notebooks, raw data hardcopies). · Interpret and document analytical data including results from method development, release, retest, validation, stability, and transfer. · Write-up of analytical protocols and reports, e.g., for validation and stability studies. Further responsibilities will include: · Assurance of adequate maintenance and operation of analytical equipment according to GMP. · Drafting and review of CoAs and/or Analytical results sheet. · Drafting of SOPs, GUIs, TPLs, FRMs. · Training of Laboratory personnel. · Ensuring of cleanliness of laboratory and work space. In order to be considered for this role, you will be required to have the following qualifications, skills and experience: · Apprenticeship-, College-, or university-degree or equivalent education in the field of chemistry, biology, biochemistry, pharmacy, or chemical engineering with 2-4 years BS or 1-3 years MS. · Ability to efficiently plan and effectively execute and document analytical experiments in a GMP-compliant pharmaceutical environment. · Previous laboratory experience is essential · Basic knowledge of GMP. · Good knowledge of sample preparation, HPLC instrumentation and techniques. · Basic knowledge of spectroscopic methods, e.g., UV/VIS, IR. · Basic trouble-shooting skills for analytical analyses. · Flexibility, good communication, time management and team-working skills. · Ability to work independently and to take initiative. · Life-long learning mindset. · Proficient in English. This is an excellent opportunity to join innovative biopharmaceutical company. Please could you send any correspondence in English. Please quote reference 46966 in all correspondence
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Jocelyn Blackham is recruiting for a Regulatory and Compliance Consultant to join a leading company in the medical device industry at their site based in Zuchwil on a contract basis until July 2020. The main purpose of the role will be to: - Ensure effective business wide compliance program that meets requirements for the medical device business - Partner with Compliance leaders from the EU region to ensure overall compliance through internal audit process. - Collaborate with the Source compliance team and EU Compliance team and all levels building partnerships to further the company's compliance organization in its goals and objective - Maintain Source strategic collaborator and company quality system processes in compliance with ISO13485, FDA QSRs and the EU MDR and other applicable regulations and standards. Further responsibilities will include: - Conducting and leading Internal Audit as per company Internal Audit schedule and assess compliance with local, national, international and company regulations, policies and procedures - Supporting inspection readiness plan within EU region against EU MDR in high collaboration with site compliance partners and business partners. - Collecting metrics data from sites. - Use of tracking and trending tools in order to share proactive trends/signal to the compliance leader. - Supporting Compliance improvements, which result from audits, Quality Board Issues and other system indicators - Working effectively with the Source Compliance team and other site compliance specialist to ensure consistent systems across the organization. - Ensuring proper internal audit reporting, response review and approvals, communication of issues. - When required assisting given facilities for both external audit preparation and assistance during their external audit In order to be considered for this role, you will be required to have the following qualifications, skills and experience: - Extensive knowledge of Quality Systems (21 CFR 820/ISO 13485/EU MDR) within a regulated environment - Previous working experience in a regulated Medical Device industry - Experience in a quality and/or compliance function as well as leading performing audits is required - Excellent Communication Skills (written & oral) in English - German would be a plus - Excellent Team Player - High Sense of Urgency - Available to travel (mostly within Switzerland) Please quote reference 46974 in all correspondence
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Alex Tosney is recruiting for a Supply Operations Manager to join a company in the pharmaceutical industry at their site based in Basel on a contract basis for 6 months. The main purpose of the role will be to drive detailed planning, scheduling and order management to assure agreed delivery performance level to CPO's. Develop and manage the relationship with External Suppliers and to customers for all supply related matters, such as demand/supply planning and analysis and order management to guarantee high customers service levels including stock management for free of charge customer-supplied components. Further responsibilities will include: • Meeting with CMO's to discuss department and business KPI's to provide performance feedback, root cause analysis and implement improvements • Designing and executing S&OP meetings with Suppliers based on frequencies outlines in the segmentation assessment • Analyzing inventories to determine how to increase inventory turns, reduce waste / write off, or optimize KPI's / CSL • Designing and implementing supply chain models that support business strategies which can adapt to changing market conditions, new business opportunities, or cost reduction strategies • Participating in the coordination of engineering changes, product line extensions, or new product launches to ensure orderly and timely transitions of production flow • Responsible for order fulfillment tasks for a products manufactured at External Suppliers within scope of SRT In order to be considered for this role, you will be required to have the following qualifications, skills and experience: • Education: Medium to high education in a technical, economics or scientific degree that contains supply chain management, logistics and/or planning including an APICS CPIM or APICS CSCP certification • Languages: Good command of English written and spoken - Local language written and spoken • Planning experience in an industrial operations environment. • Experience working in a GMP environment. • Knowledge of pharmaceutical operations principles and supply chain practices. • Extensive knowledge and under-standing of Materials • Knowledge of pharmaceutical operations and industry practices, preferred • Strong knowledge of Good Manufacturing Practices. • Commercial negotiations skills This is an excellent opportunity to join a leading medical device and pharmaceutical industry. Please could you send any correspondence in English. Please quote reference 46968 in all correspondence
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Cell Chain Manager Duration: 12 months Period: 12/01/2019 to 11/30/2020 Good afternoon, I am currently working with a major Pharmaceutical client in Switzerland who is looking for a Cell Chain Manager for a 12 month contract. Requirements: Degree in supply chain management or operations or similar Deep supply chain system experience with ERP and CRM applications. Deep experience with GxP Validated systems. Project Management, Stakeholder Management, Program Management ERP Master Data set-up Experience in a cGMP manufacturing environment. Deep experience in supporting 21CFR Part 11 Computer System Validation and HIPAA regulations. FDA Audit participation experience.My client will be taking interviews in CW46. If you are interested, please send me your up to date cv or refer this opportunity to a colleague in your network. For more information or to apply, please email or call (phone number removed) Best regards Pirmin Stehle g2 Recruitment are committed to equality of opportunity for all applications from individuals are encouraged regardless of age, disability, sex, gender reassignment, sexual orientation, pregnancy and maternity, race, religion or belief and marriage and civil partnerships or any other characteristic protected by law
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Android Developer required on a 6-month contract. One of my clients are looking for an Android Developer for a 6-month contract. Details: LOCATION: Switzerland DURATION: 6 Months START: ASAP REMOTERequired Skills: Android App Development Embedded C/C++ Java Responsibilities: Migration from Embedded C/C++ to Android If you are interested in this role, please give me a call on (phone number removed) or email me on g2 Recruitment are committed to equality of opportunity for all applications from individuals are encouraged regardless of age, disability, sex, gender reassignment, sexual orientation, pregnancy and maternity, race, religion or belief and marriage and civil partnerships or any other characteristic protected by law
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  • £600 - £800/day
12-month initial Contract Java Developer Vacancy based in Zurich We are currently recruiting for a Java Developer to be based in Zurich, Switzerland to work for a global organisation on a 12-month initial contract. Mandatory Skills and Experience for the Java Developer * Bachelor's degree in Computer Science, Mathematics or related discipline * 5+ years Core Java (ideally version 8+) and Spring (ideally version 4+) * 5+ years SQL development (preferably Oracle) and query optimization * Microservices * Architectural and Design Patterns * Proven experience in operational stability and technical hygiene strategies and techniques * Should possess strong problem solving, analytical, and debugging skills. * Should be self-starter and proactive in identify and fixing issues. * Agile development using continuous integration and TDD * DevOps practices * Proven experience of adopting cutting-edge technologies to render a system more effective * Good interpersonal and communication (both written and verbal) skills. * Ability to work on multiple tasks in parallel. * Expertise in at least one unit testing framework * Deep knowledge of coding governance and industry practices Desirable Skills and Experience * Previous experience with Financial Regulations and/or Investment Banking * Restful web services * Cloud Technologies (ideally Azure) * Web technologies (HTML5, AngularJS) * JIRA/Confluence * Experience with Kafka
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Position: HVAC Commissioning Engineer Hourly Rate: Negotiable Location: Switzerland Type: Contract (12 Months) A Fantastic new role has just opened at one of our Pharmaceutical clients based in Switzerland. As an HVAC engineer, you will have the technical knowledge and technical support for cleanroom HVAC systems. The role will be based across contract manufacturing, Lab Systems and Research Products. Responsibilities include: * Investigation of technical problems and deviations of HVAC systems * Optimization of existing plants, as well as the project management of these optimization projects across all project phases (feasibility studies to acceptance and documentation test) * GAP analysis with assessment of risks and development of improvement measures * Development of maintenance concepts and maintenance plans * Review and implement regulatory requirements, internal policies, and customer guidelines for HVAC systems * Checking the basic data for the CMMS (Computerized Maintenance Management System) * Participation in departmental and site overlapping engineering, benchmarking and improvement programs Requirements: * BS / MS Degree as Engineer HVAC or Mechanical Engineering with preferably several years of industry experience; or a combination of education, training, and experience. * First experience in a pharmaceutical / GMP-regulated production facility and in commissioning and qualification
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Lead Developer required to join a Global client based in Geneva, Switzerland Deliverables/Services * Coordinate and manage development teams. * Ensure all developments are fully documented, meet high level design requirements e.g. data, customer experience, architecture, security, quality & operations, as well as regulatory & industry standards so projects are fit for purpose leaving testing & transitioning to live. * Ensure all new developments go through an appropriate testing process and have solid release plans for hand-over to live operations and promotion. * Develop applications or scripts when needed * Maintain the technical infrastructure and set up a devops methodology. * Ensure migration to AWS Profile * First level university degree in computer science, information science or other closely related discipline. * Proficiency in English and knowledge of French would be an asset. * At least 6 years’ experience of software development within challenging and changeable environments comprising diverse technologies. * At least 2 years of software quality assurance. * Experience in business analysis, experience in IT project management. Mandatory skills and competencies : * Excellent knowledge of Java language, SQL and databases (ideally Mysql), and web technologies (Javascript, CSS, HTML) * Good knowledge of software quality processes and tools (Jira, Jenkins, Maven, SonarQube) * Project management skills, especially working with different teams abroad * Good knowledge of business analysis methodologies * Interpersonal skills and ability to work in a multicultural environment * Working with Agile approach (Scrum, Kanban) Desirable skills and competencies: * Rest architecture * Project certification (Prince2) * AWS experience * Knowledge of copyright or related rights management Please apply to be considered for the is excellent contract opportunity in Geneva, Switzerland
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