Quality Assurance Specialist

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:...

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.

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...

Randstad Professionals seeks a seasoned Quality Assurance Professional to join our team. In this role, you will be responsible for ensuring compliance with Good Manufacturing Practice (GMP) regulations in the pharmaceutical industry.Your primary responsibilities will include conducting quality reviews and approvals of GMP documentation, supporting quality...

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....

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...

Your Responsibilities">Conduct quality reviews and approvals of Good Manufacturing Practice (GMP) documentation, including calibration activity documentation, equipment periodic review, logbooks, training plans and records, SOPs. Provide support for quality oversight activities under the responsibility of the Quality Operations and Compliance area, such as...

About Our ClientOur client, a leading global player in the pharmaceutical industry located in the Lucerne area, is looking for a service and customer-oriented Quality Auditor (m/f/d) who will support the Quality Operations and Compliance organization on clinical quality activities, ensuring accountability for Good Manufacturing Practice (GMP) compliance....

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...

We are seeking a highly motivated and skilled Airframe Support Specialist to join our team at Pilatus Aircraft Ltd. As a key member of our Field Support maintenance activities, you will play a vital role in ensuring the success of our customers.About UsPilatus Aircraft Ltd is a leading manufacturer of innovative aircraft. We take pride in our commitment to...

About the JobWe are looking for a highly skilled Aircraft Software Specialist to join our team at Pilatus Aircraft Ltd. As a software development engineer, you will be responsible for designing and developing high-quality software for certified avionic systems on trainer and business aircraft.Key ResponsibilitiesYou will develop software that meets the...

Type of Employment: temporary through nemensis ag, 100%ID: 22406Duration: 01.02.2025 - 31.07.2025 (maternity cover)Salary: CHF 7375 monthly - CHF 8962 monthlyResponsibilitiesReview and approval of GMP documentation, including calibration records, equipment periodic reviews, logbooks, training plans and records, and SOPsSupport quality oversight activities in...

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...

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...

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...

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...

About Us\helpers{Pilatus Aircraft Ltd is a leading manufacturer of innovative aircraft.}\helpers{We are a committed team dedicated to pushing the boundaries of aviation technology.}\Helpers{Our commitment to innovation drives us to develop cutting-edge avionic systems that set new standards in the industry.}\helpers{With our expertise in engineering and...

Key ResponsibilitiesSetting up, executing, and troubleshooting upstream, downstream, and support unit operations in continuous and fed-batch manufacturing processes under GMP guidelines.Managing documentation for process execution, deviations, changes, and CAPAs while collaborating with Quality Assurance and other internal stakeholders.Contributing to...

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:...