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Open nowPosted 15 days ago

Galenic Development Specialist (m/f/d)

almirall53 open roles

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REINBEK
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Your applicationOpen nowGalenic Development Specialist (m/f/d)almirall · REINBEK
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The clock on this job

Early applications get read.

12.7% of postings close within 7 days. Measured by our own scanner across the market. almirall postings stay open a median of 14 days.

Share of postings closed within
  1. 2.2%1 day
  2. 4.5%3 days
  3. 12.7%7 days
  4. 20.4%14 days
  5. 35.6%30 days
  6. 58.7%60 days
This job: posted 15 days ago

almirall median: 14 days open

The posting

We’re building the future of medical dermatology by focusing on unmet patient needs and giving people the space to think independently, take ownership and make an impact that matters.

Our purpose is simple: to transform patients’ lives by addressing real needs. We work with care, act with courage, keep things simple and focus our innovation where it makes a difference.

Recognised as a Top Employer in Spain since 2008 and in Germany since 2025, we continue to invest in an environment where people can grow and move forward.

If you care differently, you belong here.

Uncommon by Nature. Patient-focused by Purpose.

At Almirall, we consciously choose to take a different path. As a specialized biopharmaceutical company with a clear focus on medical dermatology, we combine scientific excellence with an entrepreneurial mindset and a culture that empowers people to do things differently. Uncommon by Nature means approaching challenges with curiosity, courage, and a strong sense of ownership.

Your Contribution

As a Galenic Development Specialist (m/f/d), you will be part of our Industrial Development Team, supporting pharmaceutical and cosmetic products throughout their entire lifecycle. You will serve as a key interface between Development, Manufacturing, Quality, and Regulatory Affairs, helping to successfully transfer new products into commercial production.

Your Responsibilities

  • Plan, execute, and document development, optimization, and technology transfer projects for pharmaceutical and cosmetic products
  • Support scale-up activities and the transfer of new products into manufacturing
  • Prepare and maintain technical, GMP-relevant, and regulatory documentation
  • Support validation, qualification, and stability studies
  • Analyze and resolve technical issues within the manufacturing environment (troubleshooting)
  • Collaborate closely with Manufacturing, Quality, Regulatory Affairs, Supply Chain, and external partners
  • Contribute to the continuous improvement of formulations and manufacturing processes

Your Profile

  • Degree in Pharmacy, Chemistry, Physics, or a related scientific discipline; a PhD in Pharmacy or Pharmaceutical Technology is an advantage
  • Initial professional experience in galenic development, formulation development, technology transfer, or pharmaceutical manufacturing is beneficial
  • Basic knowledge of GMP requirements and pharmaceutical development processes
  • Strong analytical and structured approach to work, combined with excellent problem-solving skills
  • Team-oriented mindset and enthusiasm for collaborating across different functions
  • Excellent written and spoken English; German language skills are an advantage

Our Benefits

  • 37.5-hour work week
  • Up to 35 days of paid annual leave
  • Company pension scheme and capital-forming benefits
  • Supplementary company health insurance
  • Employee cafeteria
  • Performance-based bonus and incentive programs
  • Health and wellbeing initiatives (Urban Sports Club membership, bike leasing)
  • Training and professional development opportunities
  • Employee events
  • Employee discounts through our staff sales program

The Galenic Development Specialist is responsible for the development, optimization, scale-up, and technology transfer of pharmaceutical and cosmetic formulations throughout the product lifecycle. The role supports formulation development, commercial manufacturing, regulatory submissions, and lifecycle management by planning and evaluating development studies, preparing and reviewing technical and regulatory documentation, supporting validation and stability activities, and providing technical expertise to manufacturing and project teams. Working closely with QC, A, Regulatory Affairs, Operations, R&D, and external partners, the position contributes to resolving technical challenges, supporting product registrations and variations, improving manufacturing processes, and driving innovative solutions while ensuring compliance with GMP and applicable regulatory requirements.

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