Quality Control Specialist for Manufacturing

DelSiTech is a rapidly growing technology specialist in biodegradable silica-based drug delivery of small molecule drugs, biopharmaceuticals and viral vectors. The company provides drug development services for other pharma and biotech companies worldwide and develops its own in-house drug products. DelSiTech has its own clean room manufacture facility and it intends to start soon the manufacture of investigational medicinal products. To support our manufacture activities, we are seeking for an enthusiastic Quality Control (QC) Specialist, who has strong expertise in quality control under GMP.

Main tasks of the QC Specialist are:

  • Set-up, development and maintenance of DelSiTech’s microbiological QC laboratory
  • Coordination and supervision of outsourced QC activities
  • Sampling, analysis and documentation of environmental monitoring samples of our cleanroom
  • Preparation and development of quality system and quality documentation related to QC activities
  • Support of in-house manufacture team in QC related questions.

We expect the applicant to have a BSc or MSc education e.g. in microbiology, biotechnology, or biochemistry and at least several years practical work experience in microbiological QC. Good knowledge in GMP and cleanroom working practices are essential. Work experience and know-how in chemical analytical methods such as HPLC is appreciated.

We are looking for a team-player with good documentation skills, fluent in spoken and written English and capable to work under pressure.

DelSiTech offers a challenging position in a dynamic drug development company with competitive salary and benefits. Please apply for the position no later than 12 April, 2024, by sending your application by e-mail to: info@delsitech.com.

Want to know more? Please contact Mina Irenius, Quality Director tel. +358 40 1453097 on 4 or 5 April, 2024.