GMP Compliance Manager

About the PositionWe are seeking an experienced expert to lead our cleaning operations and ensure compliance with GMP standards in a mammalian manufacturing facility.This role requires a strong understanding of manufacturing operations, quality compliance, and cleaning validation. The ideal candidate will have experience in Manufacturing Specialist or...

EPM Scientific - Phaidon International is seeking an experienced QA Manager to join our team in Switzerland. As a key member of our drug product services team, you will be responsible for overseeing GMP compliance and customer quality activities.About the Role:You will supervise quality agreements and compliance activities, ensuring that our products meet...

Key ResponsibilitiesThe GMP Compliance Trainer will be responsible for ensuring that our production operations comply with Good Manufacturing Practice (GMP) regulations. You will achieve this by assessing training needs, designing and implementing comprehensive training concepts, and ensuring regulatory compliance.In addition, you will evaluate the...

About the JobWe are looking for a highly skilled GMP Compliance Trainer to join our team. As a key member of our organization, you will be responsible for developing and delivering training programs to support our business goals.Key ResponsibilitiesDesign and deliver comprehensive training programs to ensure compliance with GMP regulations.Collaborate with...

Job Description:We are seeking a highly motivated LIMS/SAP Systems Support Specialist to join our Quality Unit Support team. In this role, you will be responsible for providing technical support, coordinating system changes, and ensuring GMP compliance.Key Responsibilities:Provide technical support and troubleshooting for users of the LIMS software...

Are you a motivated individual looking for a challenging role in a state-of-the-art Biologics Drug Substance facility? We are seeking a highly skilled GMP Compliance Floor Support specialist to join our team at BioAtrium.BioAtrium is a dynamic organization with a focus on delivering high-quality products. As a key member of our team, you will be responsible...

Job Description:About the Role:The successful candidate will develop and implement a training strategy and roadmap for the site, aligning with BioAtrium QA GMP Training Manager, local and global strategy and roadmap.Develop effective training programsTrain and qualify other trainersSupport technical and GMP trainingLiaise with operations teamSupport...

TN Switzerland is a global leader in life sciences with a strong commitment to innovation and collaboration. We are seeking a dedicated Senior Quality Assurance Specialist for Analytics to join our team.In this role, you will work closely with our Quality Control and Analytical Development departments to ensure the quality of GMP-relevant activities. This...

About the RoleThis is an exciting opportunity to join our EPM Scientific - Phaidon International team as a Thermal Validation Subject Matter Expert.You will be working in a GMP-compliant bio-technology environment, ensuring the qualification and validation of process and support equipment.Responsibilities:Validation of process and support equipment,...

Job DescriptionOur client is seeking an experienced quality assurance professional to join their team. The ideal candidate will have a strong background in quality management and a proven track record of success in a similar role.Key Responsibilities:Negotiate and maintain quality agreements (QAAs) in collaboration with DPS and DS sites.Manage...

We are seeking a GMP Specialist Lead to oversee the implementation of quality systems and ensure compliance with regulatory requirements. This includes adhering to ISO/cGMP standards, PIC/S GMP (part 1-2) or EU Guidelines (Annex 1).The successful candidate will have 5-10 years of QA experience in commercial drug substance/product or aseptic processing,...

Lonza is a global leader in life sciences, operating across three continents. Our success is built on the dedication and expertise of our people. We work together to devise solutions that help businesses improve the world.The Supplier & Material Qualification Specialist III is a key member of our team, responsible for ensuring that our suppliers and...

Senior QA Specialist Role SummaryTN Switzerland is seeking a Senior Quality Assurance Specialist to join its team in Visp. In this role, you will oversee quality assurance activities related to raw materials and collaborate with interdisciplinary teams to ensure product quality throughout the manufacturing process.ResponsibilitiesMaintain quality standards...

Key ResponsibilitiesAs a Senior Quality Systems Manager at Actalent, you will be responsible for:Ensuring adherence to ISO/cGMP quality system requirements.Providing expert guidance to operations and quality control staff on compliance matters.Making informed quality-related decisions leveraging regulatory and compliance expertise.Evaluating and improving...

We are looking for a highly skilled GMP Quality Assurance Expert to supervise compliance and customer Quality Agreement activities for drug production.This role requires close collaboration with Drug Product Services (DPS) teams in Basel/Stein sites (e.g., Slough/Visp) to establish and negotiate Quality Agreements.Responsibilities:GMP Quality Assurance...

About the RoleThis is an exciting opportunity for a Senior GMP Production Coordinator to join our team at SRG. The successful candidate will be responsible for coordinating and overseeing the production of high-quality drug products.The ideal candidate will have a minimum of 2 years' experience in a GMP environment, preferably in sterile manufacturing. They...

Regulatory ComplianceThis is an exciting opportunity for a Regulatory Compliance Associate to join our team at SRG. The successful candidate will be responsible for ensuring compliance with GMP guidelines and regulations, as well as supporting process-related investigations and decision-making on production issues.The ideal candidate will have a strong...

We are looking for a Biotechnology Research Scientist with expertise in GMP to join our team at Capgemini Engineering. As a key member of our pharmaceutical manufacturing operations, you will be responsible for ensuring compliance with Good Manufacturing Practices (GMP) guidelines and identifying areas for process improvement.About the RoleThe ideal...

BioTalent Ltd is hiring a Quality Systems Compliance Officer to guarantee adherence to regulatory requirements. This includes ensuring compliance with ISO/cGMP standards, PIC/S GMP (part 1-2) or EU Guidelines (Annex 1).The role involves providing oversight, making independent quality decisions, and overseeing audits, validation, change controls, CAPAs, and...

Job RequirementsTo be considered for this role, you must have:In-depth knowledge of Good Manufacturing Practices (GMP) and regulatory requirements for cleaning processes.Strong background in process improvements using methodologies like Lean Six Sigma and Kaizen.Ability to work effectively across teams and manage internal projects.What We OfferWe offer a...