Cmc Technical Writer

CMC Technical Writer – DP Drug Product Lyophilization (M/F)Location: Basel, SwitzerlandWho is Aixial Group?Aixial Group is a renowned CRO (Clinical Research Organization) specializing in Life Science. We collaborate with various laboratories to offer technical assistance for clinical projects spanning phases I to IV and post-market phases. Since 2014, we...

The RoleAs Head of CMC, you will ensure that late development and lifecycle plan are translated in sustainable reality. For this, you can rely on a team of CMC project lead and CMC dossier managers. They manage end to end complex technical CMC projects, including budget and reporting, CMC regulatory strategy and scientific writing. You will work closely with...

The Role:In addition, the Global Stability Technical Writer will be responsible for supporting Global processes for harmonizing and integration of stability-related activities. Global Stability Technical Writer will also assist during HA Audits and will lead the governance of stability related processes and systems at Global level.Here's What You'll...

Sobi offers the opportunity to work at an international pharmaceutical company focused on specialty pharmaceuticals meeting the high medical needs of rare disease patients and providing treatment and services to them. Our employees come from a variety of backgrounds within research, healthcare, industry and the academic sphere.Head of CMC Program...

Sobi offers the opportunity to work at an international pharmaceutical company focused on specialty pharmaceuticals meeting the high medical needs of rare disease patients and providing treatment and services to them. Our employees come from a variety of backgrounds within research, healthcare, industry and the academic sphere.CMC Dossier Manager:Role &...

Regulatory Affairs Manager CMCFor our client in Basel, we are looking for RA CMC Manager who will be responsible for global CMC submission activities for assigned projects.Responsibilities: Identify the required documentation and any content, quality and/or timeliness issues for global submissions and negotiate the delivery of approved technical source...

The Life Science Career NetworkOur client is a leading global player in the Pharmaceutical industry with global headquarters in Basel, Switzerland. They are undergoing a transformation with respect to culture and outside perception. The organisation focusses on novel therapies in Oncology and Ophthalmology and is also currently developing a world-leading...

CMC Dossier ManagerThe CMC Dossier Manager works in the Sobi Technical Operations Department within in the CMC Program Management unit. The role is responsible for technical oversight and the coordination of generation of CMC documentation. Within the scope is the source documentation for process development, process validation, GMP and non-GMP manufacture...

For our customer located in Basel/Switzerland we are currently looking for a: Regulatory Affairs CMC Manager (M/F/x)Tasks & Responsibilities / Must Haves Responsible for regulatory activities specifically related to chemistry, manufacturing, and control (CMC). Activities such as the preparation & publication of REG CMC documentation for submissions to Health...

The Life Science Career NetworkOur client, an innovative and dynamic bio-pharmaceutical company headquartered in Switzerland, covering multiple therapeutic areas, is looking for an Regulatory Affairs CMC Manager for 18 month contract role based in Basel, Switzerland.As Associate Manager within our Global Regulatory Affairs CMC team, you support timely...

CMC ChemistResponsibilities: You will be part of a team of process research, scaleup & supply chemists, purification and analytical sciences experts Support a diverse portfolio of small molecule, peptides and nucleic acid discovery projects. Develop synthetic routes for small molecules suitable for early toxicological and clinical phase I campaigns. Be...

A Regulatory Affairs CMC Manager is required to join a global pharmaceutical company based in Basel on an 18-month contract.What you will be doing: Support all global CMC submission activities (planning, authoring, reviewing, coordination, submission) for assigned projects/products. Identify the required documentation and any content, quality and/or...

Posted: Today Location: Basel, Switzerland Job Ref: BH Job Type: Contract Salary:CHF40 CHF44 per hourExpiry date: 1/18/2023 Contact:Audwin CheungXplore Life Sciences are recruiting for an Associate Regulatory Affairs CMC Manager to work for a Global Leader in Pharmaceuticals based in Basel.This is an 18 Month freelance contract and you must have valid right...

For our customer located in Basel/Switzerland we are currently looking for a:Regulatory Affairs CMC Associate Manager (M/F/x)**- pay rate range - given by our client: 51 chf/h*Hiring Manager Job Description: As Associate Manager within our Global Regulatory Affairs CMC team, you support timely preparation of high quality CMC regulatory documentation for our...

For our client, a leading pharma company in Basel, we are looking for a Regulatory Affairs CMC Associate Manager to start asap.Contract duration: 18 months with extension possibleWorkload:100%Location: Basel cityDescription:As Associate Manager within our Global Regulatory Affairs CMC team, you support timely preparation of high-quality CMC (Chemistry,...

Technical Author (with work experience in the aerospace industry) Establish the aircraft maintenance manual (AMM) supplements Establish the Illustrated Parts Catalog (IPC) supplements Produce isometric illustrations Tracks the design revisions Prepare the customer documentation packages Mother tongue English German a huge advantageJob Types: 100%,...

Salary:CHF CHF165000 per annumJob type:PermanentLocation:Basel, SwitzerlandFunction:Technical Operations, Quality Control, ChemistPosted:05/05/2023Ref:BBBH2220- Hi I'mChristopher, I manage this roleHobson Prior are seeking for a CMC Lead Drug Substances to join a fantastic biotech establishment on a permanent basis located in Basel. Our client is focused on...

Senior Manager – CMC Dossier Manager (M/F) Location : Basel, Switzerland Who is Aixial Group ? Aixial Group, we are a CRO (Clinical Research Organization), specialized in Life Science. We work with laboratories to provide technical support on clinical projects from phases I to IV and post market. Since 2014, we have been part of the Alten...

766 million lives were touched by Novartis medicines in 2021, and while we're proud of this, there is more we can do to help improve and extend people's lives In Global Regulatory Affairs CMC, our work starts when a compound goes into clinical trials. Novartis has a unique and promising portfolio. All of these innovative projects are aimed at making a...

Technical Project & Product Lead - Drug Product (Oral Dosage ADAOur 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 for a Technical Project & Product Lead - Drug Product (Oral Dosage Form) for a...