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À propos de ce poste Quality Assurance Associate chez Biomapas

Biomapas · Sur site · Kaunas, Kaunas City Municipality, Lithuania

Join our Quality Assurance department as a Quality Assurance Associate.

Quality Assurance Associate supports in supervision of company’s quality management system and its improvements.

Position is in Lithuania, Kaunas office.

Role responsibilities:

  • Administrative support to QA department
  • Assisting in creation/review/revision/tracking of procedural and other quality documents
  • Administration of the electronic quality management system and oversight of the training compliance
  • Assisting in internal and external audits
  • Assisting is CAPAs coordination, liaising with CAPA owners with regards to corrective/preventive actions implementation, tracking and follow-up
  • Supporting eQMS administration
  • Technical supporting of collecting and reporting performance and quality metrics

Requirements

  • Fluent English and Lithuanian language
  • Knowledge of GCP, GPV and other GxP principles beneficial
  • Bachelor's degree or higher in Life Sciences or a related field; advanced degree preferred.
  • Advanced proficiency in MS Office
  • Strong attention to details and accuracy

Benefits

  • Professional growth and career opportunities
  • International team and environment
  • Bonus based on annual performance
  • Personal accident and business trip insurance
  • Additional health insurance
  • Influenza vaccines
  • Rewarding referral policy
  • Monthly lunch and fruit days
  • Team building, global meetings, B active events
  • Modern and new office in a city center with partly compensation for parking
  • Partly remote work possibility & flexible working hours, if agreed with manager

Salary range 1600 - 2000 Eur gross/month

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À propos de Biomapas

Biomapas is a functional and full outsourcing solution provider to the global life science industry.

As a trusted partner for biopharmaceutical, medical device, cosmetics, and food supplement companies, we have one-stop-shop clinical research capabilities in high recruiting countries, delivering regulatory and pharmacovigilance excellence across Europe, CIS, MENA, and LATAM regions through the entire product lifecycle.

Our in-house experience combined with a hands-on mindset allows for tailored solutions to complicated challenges that emerge on your path to commercialization. Our professionals execute your projects efficiently, cost-effectively and aspire to partner with you and become an integral part of your team from Early Development to Commercial success.

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