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Manager*in GMP Compliance – Oligonukleotide (m/w/d)

Berlin, BE, de💼 Full-time🗓 2026-09-17 → 2026-09-26

Core

Ensure GMP compliance and develop standards for oligonucleotide production.

Role type

Manager in GMP Compliance (Oligonucleotides)

Builds

Scalable compliance management systems and quality assurance processes for RNA therapeutics.

Domain

Life Sciences / Pharma / Oligonucleotide Manufacturing

Deliverable

production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work

Required skills

GMP regulatory experience, risk analysis, SOP creation, change control management, audit support, analytical thinking, organizational skills

Preferred skills

Degree in Chemistry, Pharmacy, or related natural science, experience in GMP-regulated environments, proficiency with quality management systems

Technologies

MS Office, Quality Management Systems

Responsibilities

Secure highest GMP compliance and continuously develop standards, design efficient and scalable compliance management to minimize risks, analyze deviations and implement corrective measures, identify risks early through targeted risk analyses, create and review SOPs, change controls, and qualification documents, strengthen compliance culture through training and active audit support

Seniority

Manager, hands-on leadership

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