Pharmaceutical Validation Specialist

**About the Role**Randstad Professionals is seeking a highly skilled Pharmaceutical Validation Expert to join our client, a leading pharmaceutical company in Lucerne. This exciting opportunity involves supporting the Qualification and Cleaning/Sterilization Validation projects within the Validation Unit team.The ideal candidate will be responsible for...

About the RoleWe are seeking a highly skilled Qualification and Validation Engineer to join our team in Lucerne, Switzerland.This position is part of the Validation Unit team and involves supporting Qualification and Cleaning/Sterilization Validation projects. The successful candidate will be responsible for implementing new systems and processes to ensure...

Job DescriptionThe role of Qualification and Validation Engineer is to implement new systems and processes to a state of permanent inspection readiness. This involves executing site projects related to Qualification, CSV, Cleaning/Sterilization Validation, and supporting coordination efforts with colleagues across the network to implement best practices and...

**Job Description**We are looking for a qualified Qualification and Compliance Specialist to support our client's Validation Unit team. The successful candidate will have a minimum of 5 years' experience in a pharmaceutical environment, with expertise in computer system validation, equipment qualification, and cleaning validation.The role involves executing...

Company OverviewRandstad, a leading staffing and recruitment agency, is proud to partner with a renowned pharmaceutical company based in Switzerland.

About the JobWe are seeking a skilled Pharmaceutical Laboratory Specialist to join our team at Gi Group SA. This role involves working in a QC Bioassay Lab, performing various tasks that require strong scientific knowledge and technical skills.Job DescriptionThe successful candidate will be responsible for:Culturing multiple human cell lines in vitro as CHO...

About the Role">We are seeking a highly skilled Quality Assurance Specialist to join our team at Randstad Professionals. As a key member of our quality operations team, you will be responsible for overseeing and supporting quality assurance activities in the space of Quality Operations and Compliance.

As a Regulated Industry Specialist, you will be responsible for ensuring compliance with Good Manufacturing Practice (GMP) regulations in the pharmaceutical industry.The role involves conducting quality reviews and approvals of GMP documentation, including calibration activity documentation, equipment periodic review, logbooks, training plans, and records....

Job DescriptionWe are seeking a highly skilled Process Engineer - II - P2 Specialist, Manufacturing Operations to join our team. This full-time, on-site position is focused on supporting GMP manufacturing activities and ensuring seamless integration within the existing team.About the RoleSet up, execute, and troubleshoot upstream, downstream, and support...

Pilatus Aircraft Ltd is a leading manufacturer of aircraft, and we are seeking a highly skilled System Control Specialist to join our dynamic team. This exciting opportunity will allow you to take your career to new heights by working on cutting-edge projects that drive innovation in the field of system control.About the Role:This role involves creating,...

Requirements and Qualifications">This role requires a Bachelor's or Master's degree in a relevant field. You should have at least 2 years of experience in a regulated industry, preferably in pharmaceuticals, biotechnology, or medical technology. Proficiency in IT is essential, and experience in conducting quality oversight activities is required. Strong...

Job DescriptionAs a skilled Process Engineer - II - P2 Specialist, Manufacturing Operations, you will play a critical role in supporting GMP manufacturing activities and ensuring seamless integration within the existing team.Responsibilities:Setting up, executing, and troubleshooting upstream, downstream, and support unit operations in continuous and...

About the JobWe are looking for a talented Process Engineer - II - P2 Specialist, Manufacturing Operations to join our team. As a key member of our Manufacturing Operations team, you will play a critical role in supporting GMP manufacturing activities.Key ResponsibilitiesDevelop and implement process improvements to ensure seamless integration within the...

For our client, a pharmaceutical company based in Lucerne, we are looking for a Quality Assurance Specialist. In this role you will be responsible for the oversight and support of certain quality assurance activities in the space of Quality Operations and Compliance. General Information: - Start Date: ASAP - Duration: 6 months contract - Extension:...

For our client, a leading pharmaceutical company based in Lucerne, we are looking for a Quality Assurance Specialist.In this role, you will be responsible for the oversight and support of certain quality assurance activities in the space of Quality Operations and Compliance.General Information:Start Date: ASAPDuration: 6 months contractExtension: unlikely...

Job ResponsibilitiesExecutes site projects related to Qualification, CSV, Cleaning/Sterilization Validation.Supports coordination efforts with colleagues across the network to implement best practices and ensure site systems meet all quality and regulatory expectations.Assists in the development, review, and improvement of Qualification and CSV,...

1 year temporary project with possibility of extensionFlexible hybrid working arrangementsAbout Our ClientOur client, a global leader in pharmaceutical life sciences, seeks a Digital Marketing Specialist to drive integrated, omnichannel strategies for healthcare products in Switzerland. The ideal candidate brings strong technical marketing skills, industry...

Direct message the job poster from Aristo GroupMSP Lead | MSP Partnering at Aristo Group | Empowering Life Science with the Perfect MatchThe Qualification, CSV and Cleaning/Sterilization Validation Engineer is a role within the Validation Unit team. This function supports Qualification and Cleaning/Sterilization Validation projects. It is the responsibility...

Get AI-powered advice on this job and more exclusive features.Direct message the job poster from Aristo GroupMSP Lead | MSP Partnering at Aristo Group | Empowering Life Science with the Perfect MatchAs a Quality Assurance Specialist, you will be responsible for the oversight and support of certain quality assurance activities in the space of Quality...

Responsibilities:Coordination, organization, and controlling of temperature-controlled Air and Ground transportation of national and international shipments.Coordination and planning of shipping activities in close collaboration with internal and external requestors.Act as the contact person for export/import questions.Check and control compliance aspects...

We are looking for a scientist with a strong technical background and hands-on experience in biochemical analytical methods to join our Biologics Analytical Department located in Lucerne/Schachen, Switzerland. You will be part of a multidisciplinary team and support the development of novel biopharmaceuticals.The Biologics Analytical Department provides...

Providing Flexible Resourcing SolutionsFounded in 1997 and headquartered in Basel, Switzerland, CTC is a specialist life-sciences recruitment organisation. We place specialist talent into contract and permanent positions in the pharmaceutical, biotech, medical devices and CRO industries.An in-depth experience in life-sciences recruitment combined with an...

Providing Flexible Resourcing SolutionsFounded in 1997 and headquartered in Basel, Switzerland, CTC is a specialist life-sciences recruitment organisation. We place specialist talent into contract and permanent positions in the pharmaceutical, biotech, medical devices and CRO industries.An in-depth experience in life-sciences recruitment combined with an...

**My duties** - Create supply plan for Finish Goods, Bulk and API (up to 36-months-horizon) - Manage Purchase Order/Stock transfer orders - Adhere to Escalation Management, Information flow and escalation in Tier process. - Participate and representing Product portfolio in Site Supply Reviews, - Global Supply Review and Demand Review - Allocation Management...

**My duties** - Provide administrative support to a department or individual - Record keeping, project management, - Budget tracking - Handling/controlling PO (Purchase Order) and invoice processes - Support compliance procedures and following guidelines while storing all documentation accordingly - Support the team with an holistic approach, thinking along...

We are looking for a Process Engineer - I (P1) Associate Specialist to join the Manufacturing Operations team for one of our clients. This full-time, on-site position is focused on supporting GMP manufacturing activities and ensuring seamless integration within the existing team. Contract: temporary contract via Randstad Start Date: 03/02/2025 End Date:...

job details We are looking for a Process Engineer - I (P1) Associate Specialist to join the Manufacturing Operations team for one of our clients. This full-time, on-site position is focused on supporting GMP manufacturing activities and ensuring seamless integration within the existing team. Contract: temporary contract via Randstad Start Date:...

At MSD our teams are passionate about bringing our vaccines to customers. For our Swiss subsidiary in Global Human Health based in Lucerne, we are currently looking for a Sales and Stakeholder Manager Vaccines who will be responsible for building a world class vaccine sales force to support the MSD Vaccine portfolio. As the Sales and Stakeholder Manager you...