Regulatory Affairs Manager

Manager, Regulatory Affairs page is loadedManager, Regulatory AffairsLocation: CH - Visp, CH - BaselTime Type: Full timePosted On: Posted YesterdayJob Requisition ID: R61013Title: Manager, Regulatory Affairs (CMC)Hybrid Working Pattern: 2 WFHRelocation support is provided – subject to criteria.Today, Lonza is a global leader in life sciences operating...

Title: Manager, Regulatory Affairs (CMC)Hybrid working pattern: 2 WFHLocation: Basel or VispRelocation support is provided – subject to criteria.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...

Job DescriptionThe Regulatory Affairs Manager, as part of the Lonza CMO/CDMO Regulatory Affairs Biologics department, will provide regulatory support and advice for internal and external customers in line with defined regulatory plans.This exciting role involves coordinating regulatory activities for clinical development, product license applications, and...

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, big and small,...

Job Description:The Regulatory Affairs Manager will be responsible for coordinating regulatory activities across various stages of biologics projects. This includes authoring and reviewing Module 3.2 dossier sections, representing the Regulatory Affairs department in project teams, and leading submission-related activities to ensure timely delivery of...

About the RoleWe are seeking a highly skilled Regulatory Affairs Manager to join our CMO/CDMO Regulatory Affairs Biologics team. As a key member of the team, you will provide regulatory support and advice for internal and external customers.This role offers an excellent opportunity to work on challenging projects, develop your skills, and contribute to the...

ResponsibilitiesThe Regulatory Affairs Manager will be responsible for the following key areas:Regulatory Support:Provide regulatory support and advice for internal and external customers.Develop and implement regulatory strategies to meet business needs.Regulatory Coordination:Coordinate regulatory activities for clinical development, product license...

Social network you want to login/join with:Associate Director Regulatory Affairs Small Molecules (f/m/d), VispClient:Location:Job Category:OtherJob Reference:3a4171bf38cfJob Views:10Posted:21.01.2025Expiry Date:07.03.2025Job Description:Today, Lonza is a global leader in life sciences operating across three continents. Our greatest scientific solution is...

Key Responsibilities:As a Regulatory Affairs Manager at Lonza, your responsibilities will include authoring and reviewing Module 3.2 dossier sections, tracking and negotiating source document availability, and preparing responses to health authority submission review questions.You will represent the Regulatory Affairs department in project teams, lead...

About UsPanda International is a leading Contract Manufacturing Organization (CMO) dedicated to delivering high-quality products and services to the biotechnology industry. We are committed to excellence and innovation, and we seek like-minded individuals to join our team.Role Overview:This role offers the opportunity to work in a fast-paced environment with...

Job OverviewWe are seeking a highly skilled Quality Assurance Professional to join our team at Real Staffing. In this role, you will be responsible for ensuring compliance and regulatory requirements are met across various projects and initiatives.You will work closely with cross-functional teams to establish and maintain quality agreements, address...

Must-Have QualificationsTo be successful in this role, you will need:Demonstrated experience in QA commercial drug substance/drug product environments or equivalent aseptic processing and cell therapy manufacturing experience.Knowledge of GMP compliance and Part 11 compliance principles.Experience overseeing aseptic processing and associated international...

Regulatory Compliance ExpertWe are seeking a highly skilled Regulatory Compliance Expert to join our team at Real Staffing. In this role, you will be responsible for ensuring compliance with regulatory requirements across various projects and initiatives.You will work closely with cross-functional teams to establish and maintain quality agreements, address...

Job description: On behalf of our client, a leading global life sciences company, we are seeking an experienced Quality Assurance Manager to oversee compliance and customer quality agreement (QAA) activities for Drug Product Visp. This role requires strong collaboration with cross-functional teams and external stakeholders to ensure regulatory compliance...

About the RoleThis senior level position is responsible for supervising compliance and customer quality agreement activities for drug production. The successful candidate will work closely with drug product services teams to establish and negotiate quality agreements.Main Responsibilities:Manage quality agreements (QAAs) in collaboration with DPS and DS...

We are looking for a highly skilled Quality Agreement Manager 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:Quality Agreement Manager...

Succeed as a Process Engineer in our dynamic team by overseeing the design and execution of biotechnological and pharmaceutical plant projects. Your expertise will drive innovative projects in the biotech and pharmaceutical sector.Your Role:Evaluate and compare supplier proposals based on technical and regulatory criteria.Define technical specifications for...

About the RoleWe are seeking a highly skilled Senior Quality Systems Manager to ensure seamless compliance with ISO/cGMP quality system requirements.The ideal candidate will possess in-depth knowledge of PICS Guide to Good Manufacturing Practices (Parts 1 and 2) or the EU Guidelines to Good Manufacturing Practice for Medicinal Products for Human and...

Hobson Prior are looking for an EHS Manager Project to join a fantastic pharmaceutical establishment on a contract basis. Our client is focused on facilitating a healthier society. Please note that to be considered for this role you must have the right to work in this location. **Key Responsibilities**: - For this potion, you will supervise EHS stats of...

**Product Safety Specialist (f/m/d)**: 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...