1. QUALITY MANAGER
Description of the position
As a Quality Manager you are responsible for developing and maintaining the Company’s quality system in accordance with GMP, especially in the sterile product manufacturing.
At first, you will be responsible for setting up QA/QC quality practices together with the Head of manufacturing and other department Heads. You also play an important role in reviewing and approving cleanroom validation documentation. In addition, the work includes quality assurance of raw materials, packaging materials and the final product.
Requirements
To be successful in this position, we expect you to have a previous working experience in a pharma industry, especially the experience in IMPs and sterile manufacturing would be an advantage. The deep knowledge of relevant EudraLex and FDA regulations is appreciated.
Fluent oral and written communication and presentation skills in English are mandatory. You are ready to travel for business if needed. As a person, you are team-player and work effectively even under pressure.
We offer
We offer a unique opportunity to join a rapidly growing drug development/drug delivery technology company with a highly interesting global business. We also offer you a career development opportunity to become Head of Quality as we move on to the GMP phase. As a small dynamic company, we have a great working climate and co-workers with common values and mutual trust. We offer a competitive salary and benefits.
2. SENIOR VALIDATION ENGINEER
Description of the position
As a Validation Engineer, your primary responsibility is to validate and maintain the Company’s sterile manufacturing facilities and equipment in accordance with GMP. Your work includes monitoring and maintenance of B- and C-classified cleanrooms, as well as validations and calibrations of production equipment. In addition, you will participate as a technical expert in GMP-compliant documentation and risk assessment.
Requirements
To be successful in this position, we expect you to have a several years’ work experience as a validation engineer and practical experience in cleanroom environment. The previous experience in the pharma industry would be an advantage. Fluent oral and written communication and presentation skills in English are mandatory. You are ready to travel for business if needed. As a person, you are team-player and work effectively even under pressure.
We offer
We offer a unique opportunity to join a rapidly growing drug development/drug delivery technology company with a highly interesting global business. In this position you will be able to influence and develop our manufacturing operations. As a small dynamic company, we have a great working climate and co-workers with common values and mutual trust. We offer a competitive salary and benefits.
Interested?
For both opportunities, please send your application and CV to info@delsitech.com by 30 May, 2022. For additional information please call CEO Lasse Leino, tel. +358 408494694 for position 1, and Head of Manufacturing Outi Heikkilä, tel. + 358 503228388 for position 2. Please leave a voice message, if not answered immediately.