Quality Assurance Specialist for Pharmaceutical Industry

We are seeking a Quality Assurance Specialist for Analytical Data to join our team at Randstad (Schweiz) AG.About the JobThis is a 12-month contract opportunity to work with a leading pharmaceutical company in Aubonne, Switzerland.Your role will be to ensure the quality oversight and compliance of QC activities and the data integrity of QC analytical data in...

Job DescriptionRandstad is seeking a highly skilled QA Specialist for Quality Assurance to join our team in Aubonne. As a QA Specialist, you will play a crucial role in ensuring the quality oversight and compliance of QC activities and the data integrity of QC analytical data.Your Role:To ensure the timely delivery of high-quality results and maintain the...

Job OverviewAs a Quality Assurance – Documentation and Training Specialist, you will be responsible for ensuring the accuracy and integrity of documentation and training processes within our client Merck's organization in Aubonne. This is a 12-month position that requires a detail-oriented individual with excellent organizational skills.

We are seeking a highly skilled Quality Assurance Specialist to join our team at SOPHiA GENETICS. In this role, you will be responsible for managing and improving our quality control processes to ensure compliance with regulatory requirements.Key Responsibilities:Ongoing review and compliance of previous NCs to ensure readiness for auditsCollaboration with...

Quality Assurance SpecialistWe are seeking a Quality Assurance Specialist to support our team during periods of absence and increased workload. The ideal candidate will have experience in quality assurance with NCs and CAPA, and be available for a contract opportunity.Key Responsibilities:Ongoing review of previous NCs to ensure compliance ahead of our next...

About the RoleWe are seeking a Senior Quality Assurance Specialist to join our team at Randstad. This is an exciting opportunity for a qualified professional to take on a key role in ensuring the quality of our services.Job DescriptionThe successful candidate will be responsible for supporting laboratory new equipment implementation, working closely with the...

Quality Assurance SpecialistWe are seeking a Quality Assurance Specialist to join our team at SOPHiA GENETICS. As a Quality Assurance Specialist, you will be responsible for ensuring all software used in design, manufacturing, and quality management processes comply with ISO 13485 standards.Your Key Responsibilities:Assist in gathering software validation...

We are seeking a Quality Specialist to support our quality team during periods of absence and increased workload. This role will be responsible for NC and CAPA management, ensuring compliance ahead of our next audit.Key ResponsibilitiesNC and CAPA ManagementThe successful candidate will be responsible for ongoing review of previous NCs to ensure compliance,...

At Randstad, we are looking for a skilled Lead Computerized System Validator to join our team. As a Regulatory Compliance Specialist or CSV Operations Manager, you will play a crucial role in ensuring the validation of computerized systems and software development adheres to industry standards and best practices.Job DescriptionJob Title: Lead Computerized...

About the RoleWe are seeking a highly skilled Quality Engineer to join our team at SOPHiA GENETICS. As a Quality Engineer, you will play a critical role in ensuring the quality and compliance of our software used in design, manufacturing, and quality management processes.Key ResponsibilitiesAssist in gathering software validation documentation and supporting...

Job OverviewA highly skilled Regulatory Compliance Specialist is required to join our client Randstad in a Medium priority role. This position involves overseeing the creation, management, and implementation of GxP documentation processes as well as providing training for various areas within the company.About the RoleThis exciting opportunity allows you to...

Job DescriptionOur client Merck in Aubonne is seeking a 'Cleaning Validation Expert' until the end of 2025.The Cleaning validation within the Fill & Finish Department leads and manages all the cleaning validation activities within our site to ensure new production equipment and product implementation, business continuity, and Product-Lifecycle activities on...

We are seeking a highly experienced Regulatory Affairs Specialist to join our team at Intuitive Surgical. As a Senior Regulatory Affairs Specialist, you will play a critical role in ensuring the compliance of our medical devices with EU and global regulations.The ideal candidate will have a minimum of 8+ years of experience in regulatory affairs within the...

Job DescriptionOverviewAt Intuitive Surgical, we seek a highly skilled Senior Regulatory Affairs Specialist to join our Regulatory Affairs Department. This key role will focus on providing advanced regulatory support for New Product Development (NPD) and sustaining operations across designated Business Units.Key ResponsibilitiesRegulatory Submission...

Randstad is seeking a skilled Process Validation Expert to join our team on a Medium priority basis.Estimated Salary: $80,000 - $110,000 per annumJob Description:Company OverviewWe are a leading provider of workforce solutions and consulting services, with a strong presence in the biotechnology industry. Our client is a renowned pharmaceutical company that...

Overview"> In a world where minimally invasive care is revolutionizing healthcare, we seek an exceptional Senior Regulatory Affairs Specialist to drive innovation and excellence. As a pioneer in robotic-assisted surgery, Intuitive is committed to fostering an inclusive and diverse team, dedicated to making a meaningful impact. Salary & BenefitsWe offer a...

Job DescriptionThe MSAT DP within the Fill & Finish Department is responsible for leading and managing all drug product site technical activities to ensure the supply of New Biologic Entities and business continuity for legacy products. This role requires compliance with specifications, registration, and GMP requirements.To succeed in this environment, we...

We are looking for an experienced Accountant Specialist to join our team at {company}.The Accountant Specialist will be responsible for providing high-quality financial services, including financial planning, budgeting, and reporting. They will work closely with the management team to ensure accurate and timely financial information.Key responsibilities...

About the JobWe are seeking a skilled Validation and Compliance Specialist for our client Merck in Aubonne.Job DescriptionThe successful candidate will lead and manage all cleaning validation activities within our site to ensure business continuity and compliance with specifications, registration, and GMP requirements.

Job SummaryWe are seeking a highly experienced Transformational Leader to drive education and consulting initiatives for our medical device solutions in Europe and the UKI region. This role requires a strategic thinker with strong leadership skills, ability to influence cross-functional teams, and expertise in adult learning principles.**Key...