CMC Manager / Pharmacist / Chemist (m/f/d)

TN Germany; Eggenstein-Leopoldshafen; Vor Ort; EUR 50.000 - 70.000; Vollzeit

Zusammenfassung

A leading company in the pharmaceutical industry is seeking professionals to join their innovative team. Candidates should have a university degree in pharmaceutical sciences or chemistry, along with industry experience in production or quality assurance. The role involves supporting radiopharmaceutical development, ensuring compliance with GMP requirements, and collaborating with various teams. If you are a creative problem solver and a team player, this opportunity is for you!

Qualifikationen

• At least 2 years of industry experience in production, quality control, or quality assurance.
• Knowledge of GMP requirements.

Aufgaben

• Support current and new radiopharmaceutical development projects.
• Assist in implementing and maintaining production processes.
• Participate in regular internal project meetings.

Kenntnisse

Problem Solving

Creativity

Team Player

Fluency in English

Ausbildung

University degree in pharmaceutical sciences

University degree in chemistry

Jobbeschreibung

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Job Reference:

be04539dca4d

Job Views:

1

Posted:

16.05.2025

Expiry Date:

30.06.2025

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Job Description:

About us

We are a team of hands-on professionals and creative minds who appreciate the challenges in our small, innovative environment with a family atmosphere. Driven by our international environment, we reliably deliver state-of-the-art drugs from 9 locations in 3 countries to patients who benefit from our sustained and growing service.

Join our expanding team and continue to develop with us!

Your profile

• University degree in pharmaceutical sciences, chemistry, or related scientific discipline.
• Knowledge of GMP requirements.
• At least 2 years of industry experience in production, quality control, or quality assurance of radiopharmaceuticals.
• Experience in technology transfer.
• Ability to identify and solve critical problems.
• Ability to think creatively and challenge current CMC development strategies.
• Being a team player.
• Willing to travel.
• Willing to work in a remote team.
• Fluency in English.
• Support current and new radiopharmaceutical development projects.
• Assist in implementing and maintaining production processes and quality control testing.
• Write and update GMP documents.
• Track the progress of projects.
• Participate in regular internal project meetings to discuss and plan projects.
• Participate in meetings with contract organizations to update progress via teleconference or site visits as appropriate.
• Maintain records documenting all relevant communications related to projects.
• Monitor timelines and contracts for accuracy and follow up on discrepancies with contractors and internal personnel.
• Work closely with Site Manager, Head of Quality, Head of Production, Head of Quality Assurance, Head of Operations, and contract givers.