Expert Associate in Starting Materials Compliance

vor 2 Wochen

Bad Vilbel, Deutschland STADA Arzneimittel AG Vollzeit

**Hemofarm** is a member of STADA Group, one of the largest global generic pharmaceutical companies, which successfully operates in both the markets of Serbia and Western Balkans. Hemofarm produces high quality pharmaceutical products within the leading pharmacotherapeutic groups, observing the key corporate values: Agility, Integrity, Entrepreneurship and ONE STADA.- STADA Global Quality Starting Materials Compliance Team is looking for:
**Expert Associate in Starting Materials Compliance team**

**Place of work: Belgrade**

**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

**Role & Responsibilities**:

- Active participation in Quality system processes, such as GMP documentation management, change control, qualification and requalification activities 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

**We ffer**:

- Dynamic and responsible position;
- Continuous learning environment;
- Chance for a professional and personal development;
- Good working conditions and positive working atmosphere

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