Regulatory Affairs Specialist

Regulatory Affairs Consultant in Biocidal ProductsAre you ready to make a significant impact in the field of regulatory affairs? Join our team as a Regulatory Affairs Consultant, where you will play a crucial role in the redaction of regulatory dossiers for biocidal products. We are seeking a talented individual who can bring their expertise and enthusiasm...

Redebel Regulatory Affairs (RRA) is looking for a Master in sciences or Bio-Engineer for the preparation of Bio stimulant dossiersRRA is a growing company dealing with regulatory affairs from more than 30 years with successful registrations of plant protection products and approval of new active substances.We started the RRA adventure 30 years ago, with two...

Redebel Regulatory Affairs (RRA) is looking for an experienced Regulatory Manager in REACH Dossiers.RRA is a growing company dealing with regulatory affairs from more than 30 years with successful registrations of plant protection products and approval of new active substances. We take pride in our dedication to innovation, sustainability, and compliance...

Write, review, and assemble high-quality regulatory submissions, including but not limited to Preparation of IND and IMPD modules EMA/FDA Interactions and CorrespondanceRegulatory Sciences: Participate in the definition and implementation of regulatory strategies for the development of ATMPs Provide support for the preparation of Agency meetings (EU and US)....

Redebel Regulatory Affairs (RRA) is looking for a Business Support Officer/management assistant (M,W,X)RRA is a growing company dealing with regulatory affairs from more than 30 years with successful registrations of plant protection products and approval of new active substances.We started the RRA adventure 30 years ago, with two people. During the journey...

Description:ROLE Support the compilation and verification of documentation provided relating to the requirements of MHRA guidance for the importing of IMPs into Great Britain from approved countries. Verification will involve the review of documentation provided by the clinical trial study sponsor and /or external contract giver, as applicable, to verify a...

Our client is a pioneer in the development and commercialization of Intravascular Lithotripsy (IVL) to treat complex calcified cardiovascular disease. It aims to establish a new standard of care for medical device treatment of atherosclerotic cardiovascular disease through its differentiated and proprietary local delivery of sonic pressure waves for the...

**Regulatory Affairs Consultant in Biocidal Products** Are you ready to make a significant impact in the field of regulatory affairs? Join our team as a Regulatory Affairs Consultant, where you will play a crucial role in the redaction of regulatory dossiers for biocidal products. We are seeking a talented individual who can bring their expertise and...

**Redebel Regulatory Affairs (RRA) is looking for an experienced Regulatory Manager in REACH Dossiers.** RRA is a growing company dealing with regulatory affairs from more than 30 years with successful registrations of plant protection products and approval of new active substances. We take pride in our dedication to innovation, sustainability, and...

Redebel Regulatory Affairs (RRA) is looking for a Master in sciences or Bio-Engineer for the preparation of Bio stimulant dossiers RRA is a growing company dealing with regulatory affairs from more than 30 years with successful registrations of plant protection products and approval of new active substances. We started the RRA adventure 30 years ago, with...

Redebel Regulatory Affairs (RRA) is looking for a Master in sciences or Bio-Engineer for the preparation of Plant Protection Product dossiers. RRA is a growing company dealing with regulatory affairs from more than 30 years with successful registrations of plant protection products and approval of new active substances. We started the RRA adventure 30...

Write, review, and assemble high-quality regulatory submissions, including but not limited to - Preparation of IND and IMPD modules - EMA/FDA Interactions and Correspondance **Regulatory Sciences**: - Participate in the definition and implementation of regulatory strategies for the development of ATMPs - Provide support for the preparation of Agency...

_Our mission is supported by an ambitious vertically integrated approach: design & manufacture of small satellites combined with development of earth observation services._ - Since its creation in 2018, the company has already grown substantially. Our team gathers more than 25 engineering expertise, from hardware design to software development & data...

**_Mont-Saint-Guibert_**_, _**_Belgium_**_ _** **Our mission is supported by an ambitious vertically integrated approach: design & manufacture of small satellites combined with development of earth observation services. Since its creation in 2018, the company has already grown substantially. Our team gathers more than 25 engineering expertise, from hardware...

**_Mont-Saint-Guibert_**_, _**_Belgium_**_ _** **Our mission is supported by an ambitious vertically integrated approach: design & manufacture of small satellites combined with development of earth observation services. Since its creation in 2018, the company has already grown substantially. Our team gathers more than 25 engineering expertise, from hardware...

**We are growing, grow with us!** Are you looking for a dynamic company with daily new challenges and opportunities? Then, Pharmalex is your career opportunity! Pharmalex is one of the leading service companies for the Pharmaceutical Industry globally and is specialized in all aspects of drugs and medical devices approval, of the market development and any...

SEC Newgate EU is a Brussels-based advocacy and communications consultancy with global reach as part of the SEC Newgate Group.We are looking for an experienced consultant to join our trade and external relations team.The successful applicant will support public and private clients on foreign policy and trade issues.This is an exciting opportunity for a...

SEC Newgate EU is a Brussels-based advocacy and communications consultancy with global reach as part of the SEC Newgate Group. We are looking for an experienced consultant to join our trade and external relations team. The successful applicant will support public and private clients on foreign policy and trade issues. This is an exciting opportunity for a...

The company is an international consulting company Job description As an HR Administration and Payroll Specialist you are in charge of: Managing the monthly payroll process for all employees and ensure the highest standards of payroll administration, in partnership with Finance colleaguesOrganizing monthly payroll process in coordination with social...

This role is accountable for performance and compliance for assigned protocols in a country in compliance with ICH/GCP and country regulations, Labcorp Drug Development client's policies and procedures, quality standards and adverse event reporting requirements internally and externally. Under the oversight of the SCOM or CRD, the person is responsible for...

Labcorp Drug Development has supported the pharmaceutical industry in developing more medicines worldwide than any other company, including the top 50 best-selling drugs on the market today. Join us and see why more than 90% of the top 20 global pharmaceutical companies are repeat customersIf you are looking to take on responsibility and leverage your...

As a Project Engineer (M/F/X) in the Nuclear Pressure Equipment team, you will work within the Energy & Process Industries (EPI) Business Unit. EPI supports its customers in the energy and process industries, offering advanced solutions and advice from experienced specialists. EPI assists a wide range of customers such as players in the nuclear sector,...

A family-owned company, bioMérieux has grown to become **a world leader in the field of in vitro diagnostics**. For almost 60 years and across the world, we have imagined and developed **innovative diagnostics solutions** to **improve public health**. Today, our teams are spread across 45 countries and serve 160 countries with the support of a large...

Within our MSAT team in Mont-saint-Guibert (Belgium) there is one position immediately available for a Process Engineer. ***: **The position**: The Process technology transfer Lead reports to the MSAT Director. He/She acts as a reference expert at the level of the Company in all aspects surrounding the technology, processes and knowledge transfer...

Within our MSAT team in Mont-saint-Guibert (Belgium) there is one position immediately available for a Process Engineer. ***: **The position**: The Process technology transfer Lead reports to the MSAT Director. He/She acts as a reference expert at the level of the Company in all aspects surrounding the technology, processes and knowledge transfer...

The mission of Cellistic/ Ncardia Belgium is to understand human iPSC and developmental biology, and harness this knowledge to develop and manufacture iPSC therapeutics that significantly improve patient outcomes. We are convinced that pluripotent stem cell technology is the key to get better, more efficient treatments to patients faster. To achieve this...

**Description**: **ROLE** - Support the compilation and verification of documentation provided relating to the requirements of MHRA guidance for the importing of IMPs into Great Britain from approved countries. Verification will involve the review of documentation provided by the clinical trial study sponsor and /or external contract giver, as applicable, to...