Specialist / Quality Assurance Specialist
KARIERA
Specialist / Quality Assurance Specialist
Place of work: Poznan
Responsibilities:
Management of Pharmaceutical Quality System documentation including review and registration of new system documents and monitoring and updating of lists
Planning, conducting and documenting internal and external audits
Co-create annual training and product quality review schedules
Managing the change control process, CAPA and APR
Archiving of system documentation
Participate in inspections and audits and supervise the implementation of post-audit recommendations
Prepare annual reports including: documentation review, audit results, training, corrective and preventive actions, and risk analysis
Expectations:
University degree — preferable in quality assurance / quality control or related field
At least 3 years of experience in the quality assurance area
Knowledge of pharmaceutical law requirements, good manufacturing practice and HACCP
Knowledge of English at the level of min. B1
Very good operation of MS Office software
Time management, communication skills, ability to work in a team, willingness to learn and develop, ability to work under time pressure
Very good work organization and planning
Accuracy, meticulousness and attention to procedures
Ability to work in a team, communication skills and willingness to learn and develop
We offer:
Employment under an employment contract in a pharmaceutical company with more than 155 years of tradition
Working with an ambitious and supportive team that is willing to share knowledge and experience
Opportunity for growth through additional training
Tools necessary for the job — including a laptop and phone and the possibility of hybrid work
Social package ZFŚS, medical package, group insurance on preferential terms, subsidized Multisport card or holidays under the rubble
2 paid days off per month under the Work-Life Balance concept
Kariera
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