Quality Control Technician

vor 5 Stunden

Berlin, Berlin, Deutschland Discover International Vollzeit

The Company:

This biotechnology organisation focuses on the research, development, and production of nucleic acid–based therapeutics. The site supports a broad range of activities - from early discovery and process development to large-scale manufacturing under GMP conditions. Its work focuses on innovative approaches to oligonucleotide and RNA-based medicines, serving partners across the pharmaceutical and biotech industries to bring cutting-edge therapies to market.

Role Overview:

As a QC Lab Technician, you will play a key role in ensuring the quality and compliance of nucleic acid–based therapeutics produced at our Berlin site. Working within a GMP-regulated environment, you'll perform analytical testing, support method qualification, and maintain accurate documentation to uphold the highest quality standards. This position offers the opportunity to contribute directly to the commercial manufacturing of innovative RNA and oligonucleotide medicines within a dynamic and growing biotechnology setting.

Responsibilities:

  • Perform routine and non-routine analytical testing of raw materials, intermediates, and finished products in accordance with GMP and internal quality standards.
  • Execute methods such as HPLC, UV/Vis spectroscopy, LC-MS, and other analytical techniques relevant to nucleic acid therapeutics.
  • Support method qualification, validation, and transfer activities in collaboration with analytical development teams.
  • Maintain accurate, compliant laboratory documentation and ensure data integrity in all QC activities.
  • Participate in equipment calibration, maintenance, and troubleshooting to ensure operational readiness.
  • Assist in deviation investigations, OOS/OOT analyses, and implementation of corrective and preventive actions (CAPAs).
  • Contribute to continuous improvement initiatives within the QC laboratory to enhance efficiency and quality performance.
  • Collaborate closely with manufacturing, QA, and development teams to support timely batch release and commercial production.

Qualifications:

  • 2–4 years of relevant experience in a GMP-regulated Quality Control environment, ideally within the biotechnology or pharmaceutical industry.
  • Practical experience with analytical techniques such as HPLC and related methods used for testing oligonucleotides or nucleic acid–based therapeutics.
  • Proven understanding of QC principles, documentation practices, and regulatory compliance in commercial production settings.
  • Strong technical and organizational skills with attention to detail and data integrity.
  • Fluent in German and proficient in English at a minimum C1 level (spoken and written).
  • Ability to work effectively in a collaborative, cross-functional environment and manage multiple tasks in a dynamic setting.

Benefits:

  • Competitive Remuneration.
  • Clear growth and development plan.
  • Make an impact on lives globally.

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