Associate Director, Quality Assurance and Compliance

Job Description: Associate Director Quality Assurance and Compliance The Associate Director, Quality Assurance and Compliance (QAC) - Europe serves as the operational manager to direct, oversee, and manage all European clinical quality assurance (QA) activities, and provides hands on administration and management of Quality Systems and ensures compliance...

**Ridgeline Discov**ery is looking for an (Associate) Director, Quality Assurance**. Ridgeline Discovery, a Versant Ventures Discovery Engine, creates and operates Versant-financed innovative biotech companies in partnership with entrepreneurs, industry, and leading academics across Europe. In recent years, Ridgeline has assembled an international team of \...

**Organizational Overview**: Immunovant, Inc. is a clinical-stage biopharmaceutical company dedicated to enabling normal lives for people with autoimmune diseases. As a leader in FcRn inhibitor technology, we are boldly developing innovative therapies for a range of debilitating autoimmune diseases with significant unmet patient needs. Our investigational...

**The Role**: Reporting to the Sr. Director of Global Quality Control, the Associate Director, Sterility Assurance, will be collaborating closely with Moderna’s network of Microbiological Laboratories, internal and external (affiliated Contract Testing Organizations (CTOs)/Contract Manufacturing Organization (CMOs)), providing guidance and direction about...

Gi Group SA is seeking a highly experienced Senior Quality Assurance Director to join our team in Basel, Switzerland.About the RoleThis is a unique opportunity for a seasoned quality professional to lead our Quality Assurance team and drive excellence in quality management. As Senior Quality Assurance Director, you will be responsible for ensuring the...

The Quality Difference at Thermo Fisher Scientific: What makes our quality teams unique is a shared passion for getting it done right the first time and working for the right reasons with our customers always in mind. Our team of Quality professionals understand our customers rely on the accuracy, safety, and effectiveness of our products and services that...

The Role Joining Moderna offers the unique opportunity to be part of a pioneering team that's revolutionizing medicine through mRNA technology with a diverse pipeline of development programs across various diseases. As an employee, you'll be part of a continually growing organization working alongside exceptional colleagues and strategic partners worldwide,...

**The Role**: Reporting to the Director of Quality Management Systems, the Quality Standards and Policies Associate Director is responsible for enabling quality and compliance excellence by interpreting regulatory intelligence to support translation into the necessary Quality Standards. Working in collaboration with key stakeholders in Quality and across...

**The Role**: Reporting to the Head Quality, International Organization, the Director of Quality Assurance Disposition will be responsible for providing QA oversight and support of Moderna’s international organization’s product disposition for clinical and commercial product manufactured at contract manufacturing organizations (CMO) and tested at...

General Description: Under the direction of the General Manager Sub Region Europe, this individual is responsible for the local representation of regulatory affairs and quality assurance in SRE. The incumbent provides dynamic leadership, strategic direction and close oversight of all regulatory affairs and compliance activities in SRE across BeiGene's...

Are you looking for a patient-focused, innovation-driven company that will inspire you and empower you to shine?Join us as an **Associate Director, GRA Regional Compliance - EU/Extended EU**, based in Zurich. **Here, you will be a vital contributor to our inspiring, bold mission.** **OBJECTIVES**: - Provide direction and leadership in the identification,...

Apsida Life Science is looking for a QA Compliance Manager.Key Responsibilities:Ensure compliance with GMP standards at both third-party service providers and internal facilities.Develop and assist with the annual plan for external QA audits and internal self-inspections.Conduct GMP/GDP audits and self-inspections, coordinating with internal teams and...

Job SummaryWe are seeking a highly skilled Quality Assurance Engineer to join our team at agap2 - HIQ Consulting. As a QA Engineer, you will play a crucial role in ensuring the compliance of our clients' projects with regulatory requirements and industry standards.The ideal candidate will have a strong background in quality assurance, excellent analytical...

Associate Director, R&D Quality Systems, Strategy, and Excellence (International & Affiliate) BeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share...

Our client is a Medical Device Company Your next Responsibilities: - To be the Quality Management representative for the site as well as the Person Responsible for Regulatory Compliance - Establishes and maintains quality assurance programs, procedures and controls including quality control, quality engineering, product release, CAPA and non-conformances,...

**The Role**: Reporting to the Director, Product Quality Lead the Associate Director, Product Quality Lead will be responsible for developing, approving, monitoring and maintaining critical quality standards, identifying quality risks, ensuring quality management of product and processes lifecycle, leading improvement and alignment with current regulatory...

Switzerland, Basel Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas,...

Proclinical are proud to announce our exclusive partnership with Ultragenyx Pharmaceuticals in support of their ongoing European expansion. Ultragenyx are a US based biotech committed to the development of innovative therapies for patients with serious rare and ultra-rare genetic diseases. Their unique approach has led to the successful development of...

**The Role**: Reporting to the Director Quality Systems & Compliance the AD Regulatory Compliance will be responsible to be the liaison function between Quality and the Regulatory CMC functions of Moderna. The role will implement and continuously improve required processes to ensure the compliance of Moderna’s product with the registered...

**The Life Science Career Network** Our client, an innovative and dynamic bio-pharmaceutical company headquartered in Switzerland, covering multiple therapeutic areas, committed into delivering products on the market over the next 5 years, is looking a: **PVQA (Pharmacovigilance and Quality Assurance) Manager** for a 12 months-contract based in the area of...