FU Engineer vacancy requiring profound CQV knowledge for a globally operating Neuchatel based company in the pharmaceutical sector . Your tasks: Supporting current Engineering activities on the project, particularly in sink sanitization and heating loop system Performing technical documentation revision, SAT protocol writing, and coordination of supplier interventions Providing technical oversight and support for project activities Offering process support for engineering, qualification, and validation of new equipment Providing ongoing technical support for change control, deviation investigations, and CAPA management Your experience/knowledge: Experience in executing static and dynamic Site Acceptance Testing SAT, Performance Qualification PQ, and ensuring compliance with cGMP and company standards Hands-on experience in commissioning, qualification, and validation activities Proficiency in revising technical documentation such as Piping and Instrumentation Diagrams P&ID, technical specifications, and spare parts lists Ability to write SAT static, automation, dynamic protocols Strong coordination skills for managing suppliers' interventions according to site requirements Location: Neuchatel, Switzerland Sector: Pharmaceutical Start: ASAP Duration: 03MM+ Ref .Nr.: BH21576 Take the next step and send us your resume along with a daytime phone number where we can reach you. Due to Swiss work permit restrictions, we can only consider applications from Swiss nationals, EU citizens as well as current work-permit holders for Switzerland. Ukrainian refugees are warmly welcomed, we will support you all the way. We welcome applications from individuals of all genders, age groups, sexual orientations, personal expressions, ethnic backgrounds, and religious beliefs. Therefore, there is no requirement to provide gender information or a photo in your application. As per client requirements, we need information about your marital status, nationality, date of birth, and a valid Swiss work permit. For applicants with disabilities, we are happy to explore potential solutions with our end client.
23/04/2024
Project-based
FU Engineer vacancy requiring profound CQV knowledge for a globally operating Neuchatel based company in the pharmaceutical sector . Your tasks: Supporting current Engineering activities on the project, particularly in sink sanitization and heating loop system Performing technical documentation revision, SAT protocol writing, and coordination of supplier interventions Providing technical oversight and support for project activities Offering process support for engineering, qualification, and validation of new equipment Providing ongoing technical support for change control, deviation investigations, and CAPA management Your experience/knowledge: Experience in executing static and dynamic Site Acceptance Testing SAT, Performance Qualification PQ, and ensuring compliance with cGMP and company standards Hands-on experience in commissioning, qualification, and validation activities Proficiency in revising technical documentation such as Piping and Instrumentation Diagrams P&ID, technical specifications, and spare parts lists Ability to write SAT static, automation, dynamic protocols Strong coordination skills for managing suppliers' interventions according to site requirements Location: Neuchatel, Switzerland Sector: Pharmaceutical Start: ASAP Duration: 03MM+ Ref .Nr.: BH21576 Take the next step and send us your resume along with a daytime phone number where we can reach you. Due to Swiss work permit restrictions, we can only consider applications from Swiss nationals, EU citizens as well as current work-permit holders for Switzerland. Ukrainian refugees are warmly welcomed, we will support you all the way. We welcome applications from individuals of all genders, age groups, sexual orientations, personal expressions, ethnic backgrounds, and religious beliefs. Therefore, there is no requirement to provide gender information or a photo in your application. As per client requirements, we need information about your marital status, nationality, date of birth, and a valid Swiss work permit. For applicants with disabilities, we are happy to explore potential solutions with our end client.
On-site 2-3 days (and otherwise remote/off-site) in Måløv, Denmark Duration: Expected duration 12 months. Expected experience: Strong Vue. skills and experience with Python is a must Preferred experience: Hands-on experience with Titian Mosaic or a similar research sample inventory system is considered an advantage but not a must. Knowledge of Oracle DB, SQL or PL/SQL (fundamental understanding). Be able to communicate in English Software Development: We would rather look also for someone with a more workflow/Front End focus. Application Configuration: Titian/Mosaic experience or worked with a COTS system and administered/configured it. Technologies to be used: Python Vue CI/CD Git REST APIs AWS and ADO Cloud Oracle database SQL Responsibilities and skills: Contributes to an agile product team that is onboarding Pharma R&D wet-labs to the Titian Mosaic sample inventory system Development, bug fixing and second line support on our in-house build application for sample management handling (build in Vue). Analyze complex lab workflows and translate the sample management needs of scientists into requirements for the IT solution Implements changes in the configuration (user roles, data model) as well as metadata (dropdowns) in the Mosaic system Be able to work in highly changeable organization. Communicate and collaborate with R&ED scientists (typically lab associates/scientists), Research IT experts, Software Engineers, and Product Owners You will work with our agile Inventory Management System product team together with eight other colleagues. They are working on implementing our new browser-based inventory system, Mosaic, from Titian software company as well as an in-house develop web application for sample management. You will be in touch with different laboratory teams in Denmark, UK and US regularly, to ensure business consistency and continuity. Finally, you will collaborate with business analysts and developers in the team to share knowledge and develop new solutions.
22/04/2024
Project-based
On-site 2-3 days (and otherwise remote/off-site) in Måløv, Denmark Duration: Expected duration 12 months. Expected experience: Strong Vue. skills and experience with Python is a must Preferred experience: Hands-on experience with Titian Mosaic or a similar research sample inventory system is considered an advantage but not a must. Knowledge of Oracle DB, SQL or PL/SQL (fundamental understanding). Be able to communicate in English Software Development: We would rather look also for someone with a more workflow/Front End focus. Application Configuration: Titian/Mosaic experience or worked with a COTS system and administered/configured it. Technologies to be used: Python Vue CI/CD Git REST APIs AWS and ADO Cloud Oracle database SQL Responsibilities and skills: Contributes to an agile product team that is onboarding Pharma R&D wet-labs to the Titian Mosaic sample inventory system Development, bug fixing and second line support on our in-house build application for sample management handling (build in Vue). Analyze complex lab workflows and translate the sample management needs of scientists into requirements for the IT solution Implements changes in the configuration (user roles, data model) as well as metadata (dropdowns) in the Mosaic system Be able to work in highly changeable organization. Communicate and collaborate with R&ED scientists (typically lab associates/scientists), Research IT experts, Software Engineers, and Product Owners You will work with our agile Inventory Management System product team together with eight other colleagues. They are working on implementing our new browser-based inventory system, Mosaic, from Titian software company as well as an in-house develop web application for sample management. You will be in touch with different laboratory teams in Denmark, UK and US regularly, to ensure business consistency and continuity. Finally, you will collaborate with business analysts and developers in the team to share knowledge and develop new solutions.
Quality System Specialist (m/f/d) - systems administration/support of laboratory systems/Windows Server/Active Directory/Client operating systems/Computerized System Validation/Network topology/English & German Project : For our customer a big pharmaceutical company in Basel we are looking for a highly qualified Quality System Specialist (m/f/d). Background : Are you passionate about Information (IT) and Automation Technology (OT) and aspiring to make a meaningful impact? You are a customer focused individual with aspiration to deliver high quality support in a GMP Lab environment. We Make Medicines! Behind every product sold by Roche is Pharma Global Technical Operations (PT). Starting with Phase I of the development process and continuing through to product maturity, PT makes lifesaving medicines at 11 locations, with the support of partners from around the world. Information (IT) and Automation Technology (OT) teams are key in producing and delivering medicine to patients. The organization is currently undergoing a transformation towards digitalization, advancing fundamental elements to meet future needs, such as leveraging new technologies. You as a System Process Specialist (SPS) will be acting in the 1-Stop-Shop and are part of the support and continuous improvement structure. The System Process Specialist has a profound process understanding and is collaborating with the Business Community to continuously improve business processes and underlying IT Assess & Release applications. By this, he/she acts as a trusted adviser of the end-user/key-user as well as a bridge between the end user and other roles in the Informatics support layers. The SPS can raise incidents on behalf of the user area or work with Process Owner & other local business roles to train (key-)users. In projects, the System Process Specialist can also represent the interests of the systems user group and has the responsibility of coordinating and bringing input from the area of responsibility to the project and communicating project goals, information and progress back to the business areas. The perfect candidate: The perfect candidate is familiar with ITSM processes and support tools for incident and change management. Also we are looking for someone who works independently within guidelines while receiving minimal guidance. Tasks & Responsibilities: * End-User-Support Laboratory Systems * End to End accountability for Assess & Release System support * Responsible for Assess & Release System support * Responsible for 24/7 on-call, nights and weekends on a rotational basis * Personal contact person for Key and End User out of the business department * Log incident/requests into a ticket system for further processing * Triages, prioritizes incidents/requests and performs root cause analysis in problem management (handling issue, data issue, authorization issue, IT issue). * Resolves or forwards incidents/requests based on individual knowledge or knowledge articles * Coordination of End User groups and escalation management as required * Distributes application issues and non-application issues that cannot be solved by him/her, or based on catalog to the 2nd level support * Supports issue clarification on request of 2nd level support * Validate the resolution proposals and performs the necessary test in case tests are required on request of the 2nd level support * Cooperate with 2nd level support team during analysis of reported incidents * Communicating and coordination of End User activities if there is a major incident. Interface Monitoring (Business Errors) * Support Execution of system actions * Support Implementation of new Systems and Equipment * Continuous Improvement of Laboratory Systems * Regular exchange with the Support network and or Business Process Experts (BPE) on support cases, best practices and process improvement proposals with network relevance * Helps the End User to submit new ideas for process improvements, allowing a comprehensive approach for assessing both the process interdependencies as well impact to all underlying * systems. * Describes the full life cycle of an integrated Change process to Business Process with System impact. This Framework combines the Assessment of the requirement, build and test work as well as deployment and possibly delivery of the added value to the End User. * Support Processes & Tools for Laboratory Systems * Local Labsystem and Lab Equipment Bundle, Application Support for eg Cedex Bio, Cedex HiRes, SoloVPE, Cary WinUV * Local Support of Informatics Products eg Central Label Management Software, Nextlab, Labx, Labware, Smartline Data Cockpit, Unicorn * Use of Service Now for incident, problem, request and change management Must Haves: * Relevant completed apprenticeship in IT area or equivalent and/or ideally an advanced degree in the IT or automation field * 3+ years professional experience in complex business environments * Knowledge and experience in systems administration and support of laboratory systems * Knowledge and experience in Windows Server, Active Directory and Client operating systems * Knowledge and experience in Computerized System Validation * Knowledge and experience in Network topology * Fluency German and English is a must (spoken and written) * Good communication skills * Service oriented attitude, being able to communicate with our customers, also in emergency situations * Teamplayer Nice to Have: * Knowledge and experience in systems administration in the manufacturing area (eg MES, PI, SCADA, PCS) * Trainer skills, methodology skills to perform trainings for end-users in specific area (refresh and new) Reference Nr. : 923283SDA Role : Quality System Specialist (m/f/d) Industrie : Pharma Workplace : Basel Pensum : 100% onsite Start: 01.05.2024 (latest Start Date: 1.6.2024) Duration : 12 Deadline : 25.04.2024 If you are interested in this position, please send us your complete dossier via the link in this advertisement. About us: ITech Consult is an ISO 9001:2015 certified Swiss company with offices in Germany and Ireland. ITech Consult specialises in the placement of highly qualified candidates for recruitment in the fields of IT, Life Science & Engineering. We offer staff leasing & payroll services. For our candidates this is free of charge, also for Payroll we do not charge you any additional fees.
22/04/2024
Project-based
Quality System Specialist (m/f/d) - systems administration/support of laboratory systems/Windows Server/Active Directory/Client operating systems/Computerized System Validation/Network topology/English & German Project : For our customer a big pharmaceutical company in Basel we are looking for a highly qualified Quality System Specialist (m/f/d). Background : Are you passionate about Information (IT) and Automation Technology (OT) and aspiring to make a meaningful impact? You are a customer focused individual with aspiration to deliver high quality support in a GMP Lab environment. We Make Medicines! Behind every product sold by Roche is Pharma Global Technical Operations (PT). Starting with Phase I of the development process and continuing through to product maturity, PT makes lifesaving medicines at 11 locations, with the support of partners from around the world. Information (IT) and Automation Technology (OT) teams are key in producing and delivering medicine to patients. The organization is currently undergoing a transformation towards digitalization, advancing fundamental elements to meet future needs, such as leveraging new technologies. You as a System Process Specialist (SPS) will be acting in the 1-Stop-Shop and are part of the support and continuous improvement structure. The System Process Specialist has a profound process understanding and is collaborating with the Business Community to continuously improve business processes and underlying IT Assess & Release applications. By this, he/she acts as a trusted adviser of the end-user/key-user as well as a bridge between the end user and other roles in the Informatics support layers. The SPS can raise incidents on behalf of the user area or work with Process Owner & other local business roles to train (key-)users. In projects, the System Process Specialist can also represent the interests of the systems user group and has the responsibility of coordinating and bringing input from the area of responsibility to the project and communicating project goals, information and progress back to the business areas. The perfect candidate: The perfect candidate is familiar with ITSM processes and support tools for incident and change management. Also we are looking for someone who works independently within guidelines while receiving minimal guidance. Tasks & Responsibilities: * End-User-Support Laboratory Systems * End to End accountability for Assess & Release System support * Responsible for Assess & Release System support * Responsible for 24/7 on-call, nights and weekends on a rotational basis * Personal contact person for Key and End User out of the business department * Log incident/requests into a ticket system for further processing * Triages, prioritizes incidents/requests and performs root cause analysis in problem management (handling issue, data issue, authorization issue, IT issue). * Resolves or forwards incidents/requests based on individual knowledge or knowledge articles * Coordination of End User groups and escalation management as required * Distributes application issues and non-application issues that cannot be solved by him/her, or based on catalog to the 2nd level support * Supports issue clarification on request of 2nd level support * Validate the resolution proposals and performs the necessary test in case tests are required on request of the 2nd level support * Cooperate with 2nd level support team during analysis of reported incidents * Communicating and coordination of End User activities if there is a major incident. Interface Monitoring (Business Errors) * Support Execution of system actions * Support Implementation of new Systems and Equipment * Continuous Improvement of Laboratory Systems * Regular exchange with the Support network and or Business Process Experts (BPE) on support cases, best practices and process improvement proposals with network relevance * Helps the End User to submit new ideas for process improvements, allowing a comprehensive approach for assessing both the process interdependencies as well impact to all underlying * systems. * Describes the full life cycle of an integrated Change process to Business Process with System impact. This Framework combines the Assessment of the requirement, build and test work as well as deployment and possibly delivery of the added value to the End User. * Support Processes & Tools for Laboratory Systems * Local Labsystem and Lab Equipment Bundle, Application Support for eg Cedex Bio, Cedex HiRes, SoloVPE, Cary WinUV * Local Support of Informatics Products eg Central Label Management Software, Nextlab, Labx, Labware, Smartline Data Cockpit, Unicorn * Use of Service Now for incident, problem, request and change management Must Haves: * Relevant completed apprenticeship in IT area or equivalent and/or ideally an advanced degree in the IT or automation field * 3+ years professional experience in complex business environments * Knowledge and experience in systems administration and support of laboratory systems * Knowledge and experience in Windows Server, Active Directory and Client operating systems * Knowledge and experience in Computerized System Validation * Knowledge and experience in Network topology * Fluency German and English is a must (spoken and written) * Good communication skills * Service oriented attitude, being able to communicate with our customers, also in emergency situations * Teamplayer Nice to Have: * Knowledge and experience in systems administration in the manufacturing area (eg MES, PI, SCADA, PCS) * Trainer skills, methodology skills to perform trainings for end-users in specific area (refresh and new) Reference Nr. : 923283SDA Role : Quality System Specialist (m/f/d) Industrie : Pharma Workplace : Basel Pensum : 100% onsite Start: 01.05.2024 (latest Start Date: 1.6.2024) Duration : 12 Deadline : 25.04.2024 If you are interested in this position, please send us your complete dossier via the link in this advertisement. About us: ITech Consult is an ISO 9001:2015 certified Swiss company with offices in Germany and Ireland. ITech Consult specialises in the placement of highly qualified candidates for recruitment in the fields of IT, Life Science & Engineering. We offer staff leasing & payroll services. For our candidates this is free of charge, also for Payroll we do not charge you any additional fees.
Digital Microelectronic Verification Engineer (f/m/d) -Lab verification/Python/Oscilloscope/logic analyzer/SMU/C/C++/English Project : For our customer in Medical Device industry based in Zurich region we are looking for a highly Digital Microelectronic Verification Engineer (f/m/d) . Background : Research & Development delivers hearing solutions and services for hearing aid wearers, hearing care professionals, and further related people, in the form of hearing devices, accessories, web services, mobile applications, and PC software. Embedded in an international research and development team, you will work on ASIC verification at FPGA and silicon level. Our ASICs are emulated on FPGA systems to be able to verify the integrated IPs against the specification and to validate at system level against the requirements. On those systems an Embedded low level software is also running which needs to be tested for proper functionality. For the verification and validation activity we are looking for a 3+ years experienced and passionate digital microelectronic engineer with focus on verification. Tasks & Responsibilities: * ASIC design verification on FPGA and silicon : o Detail the verification plan according to IC requirements and IC specification o Execute IP block level verification and System level validation on FPGA prior ASIC tape out o Execute IP block level verification and System level validation on ASIC o Report findings and communicate with design house bugs and possible improvements * Test environment: o Develop and implement concepts for continuous testing o Collaborate with SW development team on test environment Must Haves: * University degree in microelectronic engineering or equivalent * 3+ years' experience in lab verification * Passionate about electronic design and technologies * Experience in Python Scripting * Experience in git * Experience with electronic test equipment like Oscilloscope, logic analyzer and SMU * Basic know how in C and C++ to understand and modify Embedded SW * Able to structure tasks, solution-oriented and quality aware * Willing to work in a distributed, diverse collaboration environment * Fluent in oral and written communication skills English Reference Nr.: 923384SDA Role : Digital Microelectronic Verification Engineer Industry : Pharma Workplace : Stäfa Pensum : 100% Start : 01.05.2024 Duration : 12 Deadline : 24.04.2024 If you are interested in this position, please send us your complete dossier via the link in this advertisement. About us: ITech Consult is an ISO 9001:2015 certified Swiss company with offices in Germany and Ireland. ITech Consult specialises in the placement of highly qualified candidates for recruitment in the fields of IT, Life Science & Engineering. We offer staff leasing & payroll services. For our candidates this is free of charge, also for Payroll we do not charge you any additional fees.
17/04/2024
Project-based
Digital Microelectronic Verification Engineer (f/m/d) -Lab verification/Python/Oscilloscope/logic analyzer/SMU/C/C++/English Project : For our customer in Medical Device industry based in Zurich region we are looking for a highly Digital Microelectronic Verification Engineer (f/m/d) . Background : Research & Development delivers hearing solutions and services for hearing aid wearers, hearing care professionals, and further related people, in the form of hearing devices, accessories, web services, mobile applications, and PC software. Embedded in an international research and development team, you will work on ASIC verification at FPGA and silicon level. Our ASICs are emulated on FPGA systems to be able to verify the integrated IPs against the specification and to validate at system level against the requirements. On those systems an Embedded low level software is also running which needs to be tested for proper functionality. For the verification and validation activity we are looking for a 3+ years experienced and passionate digital microelectronic engineer with focus on verification. Tasks & Responsibilities: * ASIC design verification on FPGA and silicon : o Detail the verification plan according to IC requirements and IC specification o Execute IP block level verification and System level validation on FPGA prior ASIC tape out o Execute IP block level verification and System level validation on ASIC o Report findings and communicate with design house bugs and possible improvements * Test environment: o Develop and implement concepts for continuous testing o Collaborate with SW development team on test environment Must Haves: * University degree in microelectronic engineering or equivalent * 3+ years' experience in lab verification * Passionate about electronic design and technologies * Experience in Python Scripting * Experience in git * Experience with electronic test equipment like Oscilloscope, logic analyzer and SMU * Basic know how in C and C++ to understand and modify Embedded SW * Able to structure tasks, solution-oriented and quality aware * Willing to work in a distributed, diverse collaboration environment * Fluent in oral and written communication skills English Reference Nr.: 923384SDA Role : Digital Microelectronic Verification Engineer Industry : Pharma Workplace : Stäfa Pensum : 100% Start : 01.05.2024 Duration : 12 Deadline : 24.04.2024 If you are interested in this position, please send us your complete dossier via the link in this advertisement. About us: ITech Consult is an ISO 9001:2015 certified Swiss company with offices in Germany and Ireland. ITech Consult specialises in the placement of highly qualified candidates for recruitment in the fields of IT, Life Science & Engineering. We offer staff leasing & payroll services. For our candidates this is free of charge, also for Payroll we do not charge you any additional fees.
Bio Process Engineer vacancy for a globally operating Valais based company in the pharmaceutical sector . Your tasks: Executing production campaigns following cGMP guidelines, ensuring timely, quality, and cost-optimized product delivery Conducting risk analyses and implementing measures to ensure compliance with safety, quality, and regulatory standards Reviewing batch records and documentation for accuracy and compliance with internal procedures Collaborating with cross-functional teams to optimize processes, equipment, and procedures Documenting processes, prepare reports, and contribute to annual product reviews Identifying and pursuing opportunities for process improvement and efficiency enhancement Your experience/knowledge: 2+ years of experience in a similar role within the biotechnology or pharmaceutical industry Strong understanding of GMP, safety, and regulatory requirements Proficiency in MES/DeltaV or similar manufacturing execution systems Background in electronic batch record review and track handling Familiarity with CAPA handling, EMS Syncharge, and TrackWise Language skills: English - fluent in written and spoken, German is a strong plus Your soft skills: Ability to work in a fast-changing environment Excellent organizational and problem-solving skills Location: Valais, Switzerland Sector: Pharmaceutical Start: ASAP Duration: 09MM+ Ref .Nr.: BH21546 Take the next step and send us your resume along with a daytime phone number where we can reach you. Due to Swiss work permit restrictions, we can only consider applications from Swiss nationals, EU citizens as well as current work-permit holders for Switzerland. Ukrainian refugees are warmly welcomed, we will support you all the way. We welcome applications from individuals of all genders, age groups, sexual orientations, personal expressions, ethnic backgrounds, and religious beliefs. Therefore, there is no requirement to provide gender information or a photo in your application. As per client requirements, we need information about your marital status, nationality, date of birth, and a valid Swiss work permit. For applicants with disabilities, we are happy to explore potential solutions with our end client.
16/04/2024
Project-based
Bio Process Engineer vacancy for a globally operating Valais based company in the pharmaceutical sector . Your tasks: Executing production campaigns following cGMP guidelines, ensuring timely, quality, and cost-optimized product delivery Conducting risk analyses and implementing measures to ensure compliance with safety, quality, and regulatory standards Reviewing batch records and documentation for accuracy and compliance with internal procedures Collaborating with cross-functional teams to optimize processes, equipment, and procedures Documenting processes, prepare reports, and contribute to annual product reviews Identifying and pursuing opportunities for process improvement and efficiency enhancement Your experience/knowledge: 2+ years of experience in a similar role within the biotechnology or pharmaceutical industry Strong understanding of GMP, safety, and regulatory requirements Proficiency in MES/DeltaV or similar manufacturing execution systems Background in electronic batch record review and track handling Familiarity with CAPA handling, EMS Syncharge, and TrackWise Language skills: English - fluent in written and spoken, German is a strong plus Your soft skills: Ability to work in a fast-changing environment Excellent organizational and problem-solving skills Location: Valais, Switzerland Sector: Pharmaceutical Start: ASAP Duration: 09MM+ Ref .Nr.: BH21546 Take the next step and send us your resume along with a daytime phone number where we can reach you. Due to Swiss work permit restrictions, we can only consider applications from Swiss nationals, EU citizens as well as current work-permit holders for Switzerland. Ukrainian refugees are warmly welcomed, we will support you all the way. We welcome applications from individuals of all genders, age groups, sexual orientations, personal expressions, ethnic backgrounds, and religious beliefs. Therefore, there is no requirement to provide gender information or a photo in your application. As per client requirements, we need information about your marital status, nationality, date of birth, and a valid Swiss work permit. For applicants with disabilities, we are happy to explore potential solutions with our end client.
Automation Engineer vacancy for a globally operating Neuchatel company in the pharmaceutical sector . Your tasks: Being responsible for technical support, investigating, maintaining, and improving the automation of the production equipment in use Collaborating with cross-functional teams to driving site improvements and changes Providing support for automation validation activities Administering automated systems linked to production equipment Supporting the demands of different partners Your experience/knowledge: 2+ years of experience in the biotechnology or pharmaceuticals industry Proficient in writing functional and design specifications Excellent grasp of GMP requirements and industry regulations pertaining to qualification and validation Familiarity with standard computer tools, experience with OsiSoft PI and Inmation Emerson would be advantageous Bachelor's degree in Sciences or relevant field Language skills: French - fluent in written and spoken, English would be an advantage Your soft skills: Ability to effectively partner and collaborate across teams Highly self-motivated, self-directed, organized, and detail oriented Location: Neuchatel, Switzerland Sector: Pharmaceutical Start: ASAP Duration: 06MM+ Ref .Nr.: BH21547 Take the next step and send us your resume along with a daytime phone number where we can reach you. Due to Swiss work permit restrictions, we can only consider applications from Swiss nationals, EU citizens as well as current work-permit holders for Switzerland. Ukrainian refugees are warmly welcomed, we will support you all the way. We welcome applications from individuals of all genders, age groups, sexual orientations, personal expressions, ethnic backgrounds, and religious beliefs. Therefore, there is no requirement to provide gender information or a photo in your application. As per client requirements, we need information about your marital status, nationality, date of birth, and a valid Swiss work permit. For applicants with disabilities, we are happy to explore potential solutions with our end client.
16/04/2024
Project-based
Automation Engineer vacancy for a globally operating Neuchatel company in the pharmaceutical sector . Your tasks: Being responsible for technical support, investigating, maintaining, and improving the automation of the production equipment in use Collaborating with cross-functional teams to driving site improvements and changes Providing support for automation validation activities Administering automated systems linked to production equipment Supporting the demands of different partners Your experience/knowledge: 2+ years of experience in the biotechnology or pharmaceuticals industry Proficient in writing functional and design specifications Excellent grasp of GMP requirements and industry regulations pertaining to qualification and validation Familiarity with standard computer tools, experience with OsiSoft PI and Inmation Emerson would be advantageous Bachelor's degree in Sciences or relevant field Language skills: French - fluent in written and spoken, English would be an advantage Your soft skills: Ability to effectively partner and collaborate across teams Highly self-motivated, self-directed, organized, and detail oriented Location: Neuchatel, Switzerland Sector: Pharmaceutical Start: ASAP Duration: 06MM+ Ref .Nr.: BH21547 Take the next step and send us your resume along with a daytime phone number where we can reach you. Due to Swiss work permit restrictions, we can only consider applications from Swiss nationals, EU citizens as well as current work-permit holders for Switzerland. Ukrainian refugees are warmly welcomed, we will support you all the way. We welcome applications from individuals of all genders, age groups, sexual orientations, personal expressions, ethnic backgrounds, and religious beliefs. Therefore, there is no requirement to provide gender information or a photo in your application. As per client requirements, we need information about your marital status, nationality, date of birth, and a valid Swiss work permit. For applicants with disabilities, we are happy to explore potential solutions with our end client.
FIELD SERVICE ENGINEER Covering UK&IRE £40,000 - £50,000 + Excellent benefits Monday - Friday - door to door (44 hours) One of the UK's leading suppliers of highly complex process sterilisation and quality process equipment is now recruiting for a Field Service Engineer to join their busy and expanding field service engineering team to cover UK&IRE. As the field service engineer, you will be required to travel to customer sites in the pharmaceutical and life-sciences field, carrying out repair and maintenance on a diverse range of technologies including autoclaves/sterilisers, RO systems, steam generators etc. Key responsibilities as the Field Service Engineer: You will be required to travel across the UK and Ireland and will include nights away from home. Provide preventative maintenance, calibration and technical support, to a standard consistent with the high quality of the equipment and services the organisation supply and with the reasonable expectations of the customers. Undertake fault finding/rectification assignments as delegated by the management team Creating, preparing and managing servicing and calibration documentation as delegated by the management team Managing specific service spares Role specific administration such as reporting, expenses, and time sheets Proper management of the organisations equipment, including test equipment, computer equipment etc. Support the training of other Field Service Engineers Provide FAT support as required. Additional administrative duties as required, including but not limited to, protocol review, document creation as per QMS. Adhering to policies and procedures at all times Experience required - Field Service Engineer: ONC/HNC or equivalent in engineering (mechanical, electrical, electronic etc.) Multi-skilled engineer who has carried out service, repair and maintenance on industrial sized electro-mechanical machinery Industry background could be; FMCG, Ex-Military (Navy, REME, RAF etc.), Automation, Robotics, Pharmaceutical, Biotechnology, Semi-Conductor, Oil & Gas etc. Flexible to travel and stay away as and when required as a field service engineer Valid, UK driving licence Package/benefits: £40,000 - £50,000 depending on experience Company performance bonus Paid overtime x1.5 - Monday Friday any hours over 44 hrs (door to door travel) Overnight stay allowance - £20 for first night away raising an extra £10 per night for consecutive nights (Capped at £110/night). Once fully out on your own - Night 1-4 -£62 p/n, nights 5-7 - £80 p/n, nights 8 onwards is £100p/n. Lunch allowance Company vehicle included for personal use or the option for business use only Company Pension scheme 25 dyas holiday + bank Company phone & laptop Tools and uniform supplied Annual salary reviews (linked to inflation) plus continuously review salary in relation to performance. If you are and experienced multi-skilled field service engineer interested in making an application, please click APPLY NOW and a CBSbutler representative will be in touch to discuss this exciting opportunity.
16/04/2024
Full time
FIELD SERVICE ENGINEER Covering UK&IRE £40,000 - £50,000 + Excellent benefits Monday - Friday - door to door (44 hours) One of the UK's leading suppliers of highly complex process sterilisation and quality process equipment is now recruiting for a Field Service Engineer to join their busy and expanding field service engineering team to cover UK&IRE. As the field service engineer, you will be required to travel to customer sites in the pharmaceutical and life-sciences field, carrying out repair and maintenance on a diverse range of technologies including autoclaves/sterilisers, RO systems, steam generators etc. Key responsibilities as the Field Service Engineer: You will be required to travel across the UK and Ireland and will include nights away from home. Provide preventative maintenance, calibration and technical support, to a standard consistent with the high quality of the equipment and services the organisation supply and with the reasonable expectations of the customers. Undertake fault finding/rectification assignments as delegated by the management team Creating, preparing and managing servicing and calibration documentation as delegated by the management team Managing specific service spares Role specific administration such as reporting, expenses, and time sheets Proper management of the organisations equipment, including test equipment, computer equipment etc. Support the training of other Field Service Engineers Provide FAT support as required. Additional administrative duties as required, including but not limited to, protocol review, document creation as per QMS. Adhering to policies and procedures at all times Experience required - Field Service Engineer: ONC/HNC or equivalent in engineering (mechanical, electrical, electronic etc.) Multi-skilled engineer who has carried out service, repair and maintenance on industrial sized electro-mechanical machinery Industry background could be; FMCG, Ex-Military (Navy, REME, RAF etc.), Automation, Robotics, Pharmaceutical, Biotechnology, Semi-Conductor, Oil & Gas etc. Flexible to travel and stay away as and when required as a field service engineer Valid, UK driving licence Package/benefits: £40,000 - £50,000 depending on experience Company performance bonus Paid overtime x1.5 - Monday Friday any hours over 44 hrs (door to door travel) Overnight stay allowance - £20 for first night away raising an extra £10 per night for consecutive nights (Capped at £110/night). Once fully out on your own - Night 1-4 -£62 p/n, nights 5-7 - £80 p/n, nights 8 onwards is £100p/n. Lunch allowance Company vehicle included for personal use or the option for business use only Company Pension scheme 25 dyas holiday + bank Company phone & laptop Tools and uniform supplied Annual salary reviews (linked to inflation) plus continuously review salary in relation to performance. If you are and experienced multi-skilled field service engineer interested in making an application, please click APPLY NOW and a CBSbutler representative will be in touch to discuss this exciting opportunity.