Pharmaceutical Regulatory Expert

Kymos Group is a leading European contract research organization that provides innovative services to the pharmaceutical industry.Job OverviewWe are seeking an experienced Legal Counsel to develop this role for all Group companies. The ideal candidate will have 3-4 years of experience in the pharmaceutical or biotech industries and a deep understanding of...

Panda International is a leading global player in the pharmaceutical industry, and we are committed to innovation and excellence. We are seeking a Pharmaceutical Process Optimization Expert to join our team in Barcelona, Spain. This permanent position offers a competitive salary of €90,000 - €110,000 per annum, depending on experience.About the RoleThis...

About AizonAizon is a software-as-a-service provider that transforms manufacturing operations in life science industries using advanced analytics and artificial intelligence. Our mission is to improve global health by optimizing how medicines are manufactured.Industry Specialist Consultant RoleThe Industry Specialist Consultant will play a crucial role in...

Job OverviewWe are seeking a highly skilled Pharmaceutical Regulatory Expert to join our team at FARMAPROJECTS SAU. This is an exciting opportunity for a professional with a strong background in regulatory affairs to contribute to the success of our organization.

We are seeking an expert in Regulatory Affairs to join our team at Galderma. This role will focus on preparing and updating the CMC (Chemistry, Manufacturing and Control) dossier sections of assigned products.The ideal candidate will have experience in CMC Regulatory Affairs and a background in the pharmaceutical industry. They will be responsible for...

At Alira Health Group, we value innovation and initiative. Our global team is dedicated to collaboration, where physical boundaries don't limit, but encourage, mutual growth. We explore all contributions and new ideas with an open mind and drive our work by shared values: be courageous, be accountable, be honest, be inclusive, and elevate others.About the...

Farmaprojects SAU is a B2B Pharmaceutical Laboratory company offering a broad portfolio of generic pharmaceutical products and value-added medicines. We are looking for a Regulatory Affairs Senior Specialist to join our Regulatory Affairs Department.Key responsibilities include:Developing assessments and strategic regulatory plans for strategic product...

About the RoleWe are seeking a highly skilled IT Senior Consultant with expertise in the Pharmaceutical and/or Med Tech industry to join our System Operations team as Veeva Configuration Specialist.The successful candidate will be responsible for providing post-implementation consultancy, designing, implementing and supporting technology solutions, L2...

Job Title: Senior Legal Counsel - Pharmaceutical IndustryAbout the Role:We are seeking a highly skilled Senior Legal Counsel to join our team at Kymos Group. As a key member of our legal department, you will be responsible for providing expert legal advice and support to our business units.Key Responsibilities:Develop and implement legal strategies to ensure...

Company OverviewGalderma is a leading dermatology category leader, operating in approximately 90 countries worldwide. Our innovative, science-based portfolio of premium flagship brands and services spans the full spectrum of the fast-growing dermatology market, including Injectable Aesthetics, Dermo-cosmetics, and Therapeutic Dermatology.We have dedicated...

Welcome to the Kymos Group, where we are committed to delivering high-quality services to our clients. We are currently looking for a skilled Pharmaceutical Quality Control Manager to join our team.This role involves managing and executing ICP-MS and AAS studies for pharmaceutical, veterinary, health, and cosmetic products. Key responsibilities...

Job Title:Regulatory Affairs SpecialistGalderma Pharma S.A is seeking a highly skilled Regulatory Affairs Specialist to join our team. As a Regulatory Affairs Specialist, you will be responsible for delivering innovative, breakthrough global regulatory strategies for clinical trial registration with health authorities.The ideal candidate will have a strong...

We are seeking an expert in Regulatory Affairs to join our team at Galderma. As a Regulatory Affairs CMC Specialist, you will be responsible for preparing and updating the CMC dossier sections of assigned products. This includes assessing regulatory impact, reviewing data, and writing/ assembling CMC sections of regulatory submissions.Key responsibilities...

Job DescriptionWe are seeking a highly skilled Regulatory Affairs Expert to join our team. The ideal candidate will have a strong background in CMC Regulatory Affairs and experience with topical and/or systemic drugs.Key Responsibilities:Contribute to global regulatory CMC strategies.Assess regulatory impact of proposed CMC changes and contribute to the CMC...

Job Title: Senior IT Project Manager - Pharmaceutical Industry ExpertWe are seeking a highly skilled and experienced Senior IT Project Manager to lead and manage complex IT projects within our organization. The ideal candidate will have extensive experience with Kinaxis RapidResponse and a strong background in the pharmaceutical industry.Main...

Job Title: Senior Pharmaceutical LawyerKymos Group is a leading European contract research organization dedicated to providing innovative services to the pharmaceutical industry. Our team is growing, and we are seeking a skilled Senior Pharmaceutical Lawyer to develop this role for all Group companies.Job Summary: We are looking for a highly motivated and...

About the RoleWe are seeking a highly skilled IT Senior Consultant with expertise in the Pharmaceutical and/or Med Tech industry to join our System Operations team as Veeva Configuration Specialist. The successful candidate will be responsible for providing post-implementation consultancy, designing, implementing and supporting technology solutions, L2...

We are seeking a highly skilled Regulatory Affairs Specialist to join our team at Galderma. As a key member of our Regulatory Affairs department, you will be responsible for preparing and updating the CMC (Chemistry, Manufacturing and Control) dossier sections of assigned products. This will involve contributing to global regulatory CMC strategies, assessing...

Job Title: Regulatory Affairs CMC SpecialistWe are seeking an experienced Regulatory Affairs CMC Specialist to join our team at Galderma. As a key member of our Regulatory Affairs department, you will be responsible for preparing and updating CMC dossier sections for assigned products.Key Responsibilities:Contribute to global regulatory CMC strategies and...

About FARMAPROJECTS SAUFARMAPROJECTS SAU is a B2B Pharmaceutical Laboratory company offering a broad Portfolio of Generic Pharmaceutical Products and Value Added Medicines.We are looking for a new Regulatory Affairs Senior Specialist to join our Regulatory Affairs Department and contribute to the business.About the RoleAs a Regulatory Affairs Senior...