Global Quality Regulatory Api Specialist

Who we are?Today, we are a pharmaceutical group with a track record spanning over 45 years and a footprint in more than 50 countries, led by Leandro and Lucas Sigman.Our overarching goal is to improve people's health all over the world, providing accessible, effective, safe, quality medicines through our various business units, underpinned by continuous...

At Sandoz, quality is a key factor embedded in our purpose of pioneering access for patients. As Manager Regulatory Affairs API in our Palafolls site, you'll provide timely preparation of high-quality CMC regulatory documentation for active ingredients/intermediates under your responsibility; formulate and lead global regulatory strategy for drug substances...

DescriptionThis position needs to ensure Galderma products meet the Company quality standards and comply with the relevant government regulations according to the product applicable classification: cGMP, GDP, ISO, ICH, or any relevant regulations and guidance.As ESO Quality Specialist, this person will rely on regulatory, industry, and technical expertise to...

Description This position needs to ensure Galderma products meet the Company quality standards and comply with the relevant government regulations according to the product applicable classification: cGMP, GDP, ISO, ICH, or any relevant regulations and guidance.As ESO Quality Specialist, this person will rely on regulatory, industry, and technical expertise...

Description This position needs to ensure Galderma products meet the Company quality standards and comply with the relevant government regulations according to the product applicable classification: cGMP, GDP, ISO, ICH, or any relevant regulations and guidance. As ESO Quality Specialist, this person will rely on regulatory, industry, and technical expertise...

At Galderma, we are advancing dermatology for every skin story. As a specialist in regulatory affairs strategy, you will play a crucial role in delivering innovative global regulatory strategies for clinical trial registration with health authorities.About the RoleThis is an exciting opportunity to join our team and contribute to our mission of empowering...

Description This position needs to ensure Galderma products meet the Company quality standards and comply with the relevant government regulations according to the product applicable classification: cGMP, GDP, ISO, ICH or any relevant regulations and guidance. As ESO Quality Specialist, this person will rely on regulatory, industry and technical...

We are seeking a seasoned Senior Quality and Regulatory Specialist to join our team in Barcelona.This role will focus on leading the entire quality and regulation area, ensuring that products meet the highest standards and regulatory requirements.The ideal candidate will have extensive experience in manufacturing, with a strong background in ISO 9001 and...

Job Description: As a Regulatory Affairs Senior Director of Quality, you will lead and manage a team of regulatory professionals within the Regulatory API (RAPI) department, driving the delivery of high-quality documentation to support successful submissions to regulatory authorities. Your key responsibilities include:

The Regulatory Affairs department at Werfen is seeking a highly skilled Quality and Regulatory Affairs specialist to join our team in Barcelona, Spain.As a Quality and Regulatory Affairs specialist, you will be responsible for supporting the execution of pre and post-market regulatory affairs departmental functions. This includes assisting in the preparation...

.Job Details: Regulatory Affairs Specialist- EBD Full details of the job.Vacancy NameVacancy Name Regulatory Affairs Specialist- EBDVacancy NoVacancy No VN309Employment TypeEmployment Type Full-TimeLocationAbout the JobSinclair is looking for a Regulatory Affairs Specialist to manage the global product registration and regulatory approvals for our...

.Job Details: Regulatory Affairs Specialist- EBD Full details of the job. Vacancy Name Vacancy Name Regulatory Affairs Specialist- EBD Vacancy No Vacancy No VN309 Employment Type Employment Type Full-Time Location About the Job Sinclair is looking for a Regulatory Affairs Specialist to manage the global product registration and regulatory approvals for our...

.Job Details: Regulatory Affairs Specialist- EBDFull details of the job. Vacancy Name Vacancy Name Regulatory Affairs Specialist- EBD Vacancy No Vacancy No VN309 Employment Type Employment Type Full-Time Location About the JobSinclair is looking for a Regulatory Affairs Specialist to manage the global product registration and regulatory approvals for our...

At Centrient Pharmaceuticals Netherlands, we are a leading manufacturer of beta-lactam antibiotics and provider of next-generation statins and anti-fungals.We produce and sell intermediates, active pharmaceutical ingredients, and finished dosage forms.We strive to be at the centre of modern healthcare as a maker of essential and life-saving medicines.Our...

About The Zonal Group: As a global medical aesthetics organisation, we deliver an extensive product range with an in-house commercial infrastructure, including manufacturing and a network of distributors in leading global markets. Our products are sold in 55 countries worldwide.Job Description: We are seeking a Regulatory Affairs Specialist to manage the...

.Ecolab, Purolite Resins, the world leader in resin-based separation, purification and extraction technology, is seeking a Senior Regulatory Affairs Specialist.We manufacture products which help our customers around the globe, mainly in pharmaceutical and life science sectors, with technology which are critical to safe manufacture of their products. It's an...

About UsBoehringer Ingelheim España, S.A. is a leading pharmaceutical company dedicated to delivering innovative solutions for human and animal health.Job Title: Senior Labeling Specialist - Global Regulatory ComplianceEstimated Salary: €85,000 - €110,000 per annum, depending on experience.Job Description:We are seeking an experienced Senior Labeling...

About the RoleWe are seeking a skilled individual to join our team as a Global Pharmacovigilance Specialist.The Key ResponsibilitiesThis role will involve providing operational support for global pharmacovigilance activities, ensuring that pharmacovigilance deliverables meet global regulatory reporting timelines and maintaining the highest quality.The Ideal...

Ecolab, Purolite Resins, the world leader in resin-based separation, purification and extraction technology, is seeking a Senior Regulatory Affairs Specialist.We manufacture products which help our customers around the globe, mainly in pharmaceutical and life science sectors, with technology which are critical to safe manufacture of their products. It's an...

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...