We are looking for Expert Associate in our Staring materials Quality management team to assure execution of all activities and processes in order to align with department and corporate goals and compliance with all regulatory requirements.
Expert Associate
Requirements:
- Faculty of Technology, Pharmacy or Chemistry;
- Active knowledge of the English language – B2 mandatory, C1 level advantage;
- Advanced level of knowledge of MS Office package;
- Excellent communication and negotiation skills;
- Ability to work in a fast-paced, dynamic, environment;
- Team-oriented, precise, analytical, responsible, independent;
- Fast learner and easily adaptable to changes;
Your duties and tasks:
- Active participation in Quality system processes, such as GMP documentation management, change control, qualification and requalification activities, audits and others;
- Maintaining and compiling GMP documentation – such as specifications, analytical procedures, risk assessments, different reports, questionnaires and other;
- Evaluating GMP documentation in line with the applicable GMP guidelines and files approved by regulatory authorities;
- Ensure ongoing abidance by industry regulatory and quality requirements;
- Drive improvements in Quality Documentation and processes;
- Inspect data to detect areas for improvement;
- Performing other tasks at the order of direct superior;
Job offer:
- Dynamic and responsible position;
- Continuous learning environment;
- Chance for a professional and personal development
Place of work: Vršac, Serbia
If this position is of interest for you please send your application (CV and cover letter).
For further information on Hemofarm, please visit the website hemofarm.com
Hemofarm AD
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