Regulatory Affairs Manager at Neumüller Personalberatung Regina Neumüller eK
berlin, Berlin, Germany -
Full Time


Start Date

Immediate

Expiry Date

14 Jan, 27

Salary

45000.0

Posted On

16 Oct, 26

Experience

1 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Industry

Healthcare & Life Sciences

Description

Company: Neumüller Personalberatung Regina Neumüller eK

Working time models: Part-time - morning, Part-time - afternoon, Part-time - evening, Full-time

Work location: Nuremberg, Middle Franconia (DE)

Job description:

For over 20 years, Neumüller, an owner-managed company with more than 300 employees, has been providing recruitment and application support, as well as personnel and engineering services.

Appreciation, honesty, and self-realization characterize our work.


Neumüller has received numerous awards for its sustainable practices, including recognition for gender equality, health management, and as a "Great Place to Work."


As a Regulatory Affairs (RA) Manager (m/f/d), you will be responsible for the following tasks:


- Managing drug approval processes.

- Providing regulatory support for development substances at the national level.

- Contributing to market launches.

- Conducting regulatory approval processes for clinical trials with the BfArM and PEI.

- Maintaining databases to ensure regulatory compliance.


Your qualifications:


- Completed degree in a natural science (or equivalent)

- Experience in Regulatory Affairs or an MDRA degree is desirable

- Strong communication and teamwork skills

- Excellent written and spoken German and English skills


Our offer to you:


- Attractive compensation - Various compensation models to suit your needs

- Flexible working hours - Working hours that fit your lifestyle

- Individual professional development - Tailored training programs for your career advancement

- Long-standing network - Collaboration with medium-sized companies to international corporations in future-oriented industries

- Work in future-oriented industries - Exciting activities in future-oriented research and development fields

- Mobility at work - Company car, job ticket, company bike, etc., also for private use

- Individual career coaching - After consultation, your application will be presented directly to decision-makers at several top companies

- Supported onboarding - Organized and supported mentoring to help you settle into your new job

Content: © Federal Employment Agency – Reference number: 10001-1003830787-S

Apply now

How To Apply:

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Responsibilities

Company: Hays Professional Solutions GmbH

Working time model: Full-time

Work location: Berlin (DE)

Job description:

Your benefits:


- Support throughout the entire application process

- Ongoing project support from our team


Your responsibilities:


- Development and implementation of regulatory strategies for new and existing drugs

- Preparation, coordination, and submission of regulatory documents to authorities

- Management of the entire product lifecycle (variations, renewals, change notifications, lifecycle management)

- Monitoring of national and international regulatory requirements and evaluation of legislative changes

- Collaboration with internal departments such as Medical Affairs, Market Access, Clinical Operations, Quality, and Commercial

- Establishing and maintaining contacts with regulatory authorities

- Ensuring compliance with regulatory requirements and internal SOPs


Your qualifications:


- A degree in pharmacy, natural sciences, biotechnology, or a comparable field

- Experience in regulatory affairs

- Sound knowledge of national and international drug approvals

- Excellent English skills

- Strong communication and project management skills


About Hays:


With over 15 years of experience in the traditional pharmaceutical, biotechnology, chemical, and medical technology industries, we know the key contacts who advertise challenging positions with potential. The high demand for personnel opens up exciting opportunities for dedicated professionals and managers to develop their careers and advance their professional development. As a specialized recruitment consultancy with an international network, we offer you decisive advantages – completely free of charge. Register now and benefit from interesting and suitable positions and projects.

Content: © Federal Employment Agency – Reference number: 13319-893545/1_622588LS-SCompany: Neumüller Personalberatung Regina Neumüller eK

Working time models: Part-time - morning, Part-time - afternoon, Part-time - evening, Full-time

Work location: Nuremberg, Middle Franconia (DE)

Job description:

For over 20 years, Neumüller, an owner-managed company with more than 300 employees, has been providing recruitment and application support, as well as personnel and engineering services.

Appreciation, honesty, and self-realization characterize our work.


Neumüller has received numerous awards for its sustainable practices, including recognition for gender equality, health management, and as a "Great Place to Work."


As a Regulatory Affairs (RA) Manager (m/f/d), you will be responsible for the following tasks:


- Managing drug approval processes.

- Providing regulatory support for development substances at the national level.

- Contributing to market launches.

- Conducting regulatory approval processes for clinical trials with the BfArM and PEI.

- Maintaining databases to ensure regulatory compliance.


Your qualifications:


- Completed degree in a natural science (or equivalent)

- Experience in Regulatory Affairs or an MDRA degree is desirable

- Strong communication and teamwork skills

- Excellent written and spoken German and English skills


Our offer to you:


- Attractive compensation - Various compensation models to suit your needs

- Flexible working hours - Working hours that fit your lifestyle

- Individual professional development - Tailored training programs for your career advancement

- Long-standing network - Collaboration with medium-sized companies to international corporations in future-oriented industries

- Work in future-oriented industries - Exciting activities in future-oriented research and development fields

- Mobility at work - Company car, job ticket, company bike, etc., also for private use

- Individual career coaching - After consultation, your application will be presented directly to decision-makers at several top companies

- Supported onboarding - Organized and supported mentoring to help you settle into your new job

Content: © Federal Employment Agency – Reference number: 10001-1003830787-S

Apply now

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