Regulatory Affairs Specialist

il y a 3 semaines


Gent, Belgique DeLaval Temps plein

DeLaval is looking for a
**Regulatory Affairs Specialist** to strengthen the Regulatory Affairs team.

The position is based at DeLaval NV in Drongen, Belgium, but occasional international travelling might be required.

**Purpose of the role and key responsibilities**
- Play a key role in the regulatory information flow and follow-up on registration & compliance projects focussing on Europe
- Provide support to international dairy markets where DeLaval is active
- Collect needed scientific data, prepare regulatory & risk assessments, registration dossiers, MSDS, and support label instructions for new and existing products within the aftermarket portfolio
- Follow-up on legislation and guidelines related to BPR, veterinary medicines and hygiene aftermarket in Europe and other regions

In this role you will have regular contacts with:

- DeLaval Aftermarket Product Management, Regulatory Affairs & R&D colleagues (internal)
- Regulatory Authorities (external)
- External Suppliers (external)
- Contract labs and consultants (external)

**Qualifications and experience**

To be successful in this role we are looking for someone with:

- A university Degree in Sciences, Agricultural Sciences, Veterinary Sciences, or equivalent
- A minimum of 1-3 years’ experience in Regulatory Affairs (dossier preparation & submission, compliance, GMP, ISO, manufacturing and quality control of chemicals or pharmaceutical products)
- A minimum of 1-3 years’ experience in registration submission in Europe and/or other regions
- The ability to work independently but also interact in cross functional as well as cross cultural project teams
- Good knowledge of national and international chemical & pharmaceutical standards, R&D and field trials is an asset
- A fluent knowledge of English and Dutch. Basic understanding of other languages (e.g. German, French, Spanish) is an asset
- Very good communication skills (verbal/written) and computer literate

**Working at DeLaval**

**Our core values Passion, People, Professionals and Partnerships connect individuals across entities and geographies. Success is far more than knowledge - it is strongly related to behaviours. At DeLaval we are all guided by our three behaviours, Setting Direction, Make things happen and One DeLaval.**

We offer you a workplace like no other, where state-of-the-art technology goes hand in hand with animal welfare.

**Additional information**

We offer you:

- The opportunity to be part of a strong, international organisation
- A competitive salary with an attractive compensation package
- A flexible working schedule including home office
- The chance to work in a dynamic stimulating environment with a young and highly motivated team

**For further information, please contact**:
We look forward to hearing from you

**About DeLaval**

Our vision is to make sustainable food production possible. As a company built on innovation, we constantly work to find ways of helping our customers, dairy farmers, do more with less by providing world-leading milking equipment and solutions. Today, DeLaval has approximately 4,500 passionate professionals operating in more than 100 markets around the world. DeLaval is part of the Tetra Laval Group.


  • Regulatory Affairs Specialist

    il y a 2 semaines


    Gent, Belgique Jefferson Wells Temps plein

    Location: **Gent** **#23587** **Regulatory Affairs Specialist** Vast Contract - Regio Gent **#regulatory #affairs #specialist #food** Beschik je over een masterdiploma met een voorkeur voor een specialisatie in landbouw, voeding of chemie? Heb je min. 3 jaar ervaring in Regulatory Affairs? Ben je zelfstandig, zeer communicatief en computervaardig? Lees...


  • Gent, Flandre, Belgique Jefferson Wells Temps plein

    Location:**Gent****#23587****Regulatory Affairs Specialist**Vast Contract - Regio Gent**#regulatory #affairs #specialist #food**Beschik je over een masterdiploma met een voorkeur voor een specialisatie in landbouw, voeding of chemie? Heb je min. 3 jaar ervaring in Regulatory Affairs? Ben je zelfstandig, zeer communicatief en computervaardig? Lees dan vooral...


  • Gent, Belgique Elements Advisory Temps plein

    As a Junior Regulatory Affairs Specialist, you will be responsible for assisting in the management of regulatory affairs activities related to our biocide products. You will collaborate closely with the regulatory affairs team and other cross-functional departments to ensure compliance with relevant regulations and standards. **Responsibilities**: - Assist...


  • Gent, Belgique Nuwhï Temps plein

    We zijn op zoek naar een ervaren Senior Regulatory Affairs Specialist om ons team te versterken in regio Gent. In deze rol ben je verantwoordelijk voor het coördineren, implementeren en waarborgen van naleving van alle relevante wet - en regelgeving. Als Senior Regulatory Affairs Specialist ben je de expert in je vakgebied en zul je fungeren als interne en...


  • Gent, Belgique Elements Advisory Temps plein

    As a Senior Regulatory Affairs Specialist, you will be responsible for ensuring compliance with regulatory requirements for biocide products. You will work closely with cross-functional teams, regulatory authorities, and external partners to facilitate the registration and approval processes for biocide products in different markets. Your expertise in...


  • Gent, Flandre, Belgique DeLaval Temps plein

    DeLaval is looking for aRegulatory Affairs Specialist to strengthen the Regulatory Affairs team.The position is based at DeLaval NV in Drongen, Belgium, but occasional international travelling might be required.Purpose of the role and key responsibilities Play a key role in the regulatory information flow and followup on registration & compliance projects...


  • Gent, Flandre, Belgique Elements Advisory Temps plein

    As a Senior Regulatory Affairs Specialist, you will be responsible for ensuring compliance with regulatory requirements for biocide products. You will work closely with cross-functional teams, regulatory authorities, and external partners to facilitate the registration and approval processes for biocide products in different markets. Your expertise in...


  • Gent, Flandre, Belgique Nuwhï Temps plein

    We zijn op zoek naar een ervaren Senior Regulatory Affairs Specialist om ons team te versterken in regio Gent. In deze rol ben je verantwoordelijk voor het coördineren, implementeren en waarborgen van naleving van alle relevante wet- en regelgeving. Als Senior Regulatory Affairs Specialist ben je de expert in je vakgebied en zul je fungeren als interne en...


  • Gent, Belgique Eastman Temps plein

    **The job**: We are looking for a Regulatory Affairs Specialist to support the global product stewardship and regulatory affairs Crop Protection team. In close collaboration with business, technology and product management, you give support in protecting the existing portfolio of products and actively engage in projects to extend our growth worldwide. This...


  • Gent, Flandre, Belgique Eastman Temps plein

    The job:We are looking for a Regulatory Affairs Specialist to support the global product stewardship and regulatory affairs Crop Protection team. In close collaboration with business, technology and product management, you give support in protecting the existing portfolio of products and actively engage in projects to extend our growth worldwide. This is a...


  • Gent, Belgique Nuwhï Temps plein

    Do you want to be an expert in **medical affairs** - **market access** and **regulatory affairs**? We have a great opportunity to be able to learn and to get an expert in these fields. The great thing about it, is that this mix of RA and Medical affairs or Market access is not that common in the field. This could be the reason why you as an RA professional...

  • Regulatory Affairs Officer

    il y a 14 heures


    Gent, Belgique Nuwhï Temps plein

    Do you want to be an expert in **medical affairs** - **market access** and **regulatory affairs**? We have a great opportunity to be able to learn and to get an expert in these fields. The great thing about it, is that this mix of RA and Medical affairs or Market access is not that common in the field. This could be the reason why you as an RA professional...


  • Gent, Flandre, Belgique Nuwhï Temps plein

    Do you want to be an expert in medical affairs - market access and regulatory affairs?We have a great opportunity to be able to learn and to get an expert in these fields.The great thing about it, is that this mix of RA and Medical affairs or Market access is not that common in the field. This could be the reason why you as an RA professional can step out of...


  • Gent, Flandre, Belgique Eastman Temps plein

    Founded in 1920, Eastman is a global specialty materials company that produces a broad range of products found in items people use every day. With the purpose of enhancing the quality of life in a material way, Eastman works with customers to deliver innovative products and solutions while maintaining a commitment to safety and sustainability. The company's...


  • Gent, Flandre, Belgique Eastman Temps plein

    Founded in 1920, Eastman is a global specialty materials company that produces a broad range of products found in items people use every day. With the purpose of enhancing the quality of life in a material way, Eastman works with customers to deliver innovative products and solutions while maintaining a commitment to safety and sustainability. The company's...


  • Gent, Belgique Nuwhï Temps plein

    **About the role** The Regulatory Affairs Manager is responsible for managing the lifecycle of the medicines from the preparation of the registration dossier, including the follow-up and finalization of new registrations, the preparation to market access, compilation, submission, and follow-up of variation dossiers in the Benelux. Basically the RA manager...


  • Gent, Flandre, Belgique Nuwhï Temps plein

    About the roleThe Regulatory Affairs Manager is responsible for managing the lifecycle of the medicines from the preparation of the registration dossier, including the follow-up and finalization of new registrations, the preparation to market access, compilation, submission, and follow-up of variation dossiers in the Benelux.Basically the RA manager ensures...


  • Gent, Belgique FrieslandCampina Temps plein

    Ben jij op zoek naar een uitdagende functie waarin je een belangrijke rol speelt bij het waarborgen van de kwaliteit en veiligheid van lekkere zuivelproducten? Ben jij een expert op het gebied van wet - en regelgeving en wil je jouw kennis graag toepassen in een dynamische en internationale omgeving? Dan zijn wij op zoek naar jou! Wat we vragen - Je bent...


  • Gent, Flandre, Belgique FrieslandCampina Temps plein

    Ben jij op zoek naar een uitdagende functie waarin je een belangrijke rol speelt bij het waarborgen van de kwaliteit en veiligheid van lekkere zuivelproducten? Ben jij een expert op het gebied van wet- en regelgeving en wil je jouw kennis graag toepassen in een dynamische en internationale omgeving? Dan zijn wij op zoek naar jouWat we vragen- Je bent...


  • Gent, Belgique Cooper Consumer Health Temps plein

    Requisition ID - 39 - Job Family 1- Regulatory & PSRM - Country 1- Belgium - Location 1- Hybrid - About us - **Cooper Consumer Health** is a leading European consumer healthcare player that develops, produces, and distributes a diverse range of OTC (over-the-counter) products with strong brands such as Valdispert, Oenobiol, Excilor, Vitascorbol, Lashyle and...