"Caring for People's Health as a Trusted Partner"

STADA is a leading manufacturer of high-quality pharmaceuticals. With a long-standing heritage rooted in pharmacies, we are perceived as a reliable and trustworthy partner since 1895. With our products we help people protect and regain a dignified and able life. With our proven Generics, we ensure that everyday health remains affordable.

At STADA, we follow our purpose of “Caring for People’s Health as a Trusted Partner”. In pursuit of this purpose, we are committed to further accelerating the successful trajectory of our company.

To our employees, we offer an attractive working environment in which they can develop personally. At the moment, we are looking for talents as:

QC MANAGER

RESPOSBILITY

• Plan and monitor QC activities, including raw material, in-process, finished product, stability testing.
• Review results of analytical method validation, process validation, cleaning validation and other validations, being followed in QC.
• Monitor collecting data, trend analysis, establish the alert limit, action limit for water systems, pure steam, compressed air, nitrogen systems.
• Responsible for monitoring and reporting of monthly and yearly KPI and report related to physiochemical laboratory.
• Collaborate with cross-functional teams, including Quality Assurance, R&D, Regulatory Affairs, and Manufacturing, to ensure seamless quality operations.
• Review and approve critical analytical data, OOS/OOT investigations, deviations, and CAPAs.
• Involve in procurement of analytical instruments in laboratory, installation/upgradation, and qualification of software’s.
• Spearhead continuous improvement initiatives, adopting advanced analytical technologies and risk-based approaches.
• Expertise in handling software’s related to analytical instruments and interpretation of chromatographic data.
• Participate internal and external inspections, assign appropriate actions against gaps and responsible for timely implementation of CAPA.

REQUIRMENT

Education:

University degree in chemical science, Pharmaceutical Sciences, or related field.

Languages:

Local Site language with capability to communicate in English as a second language.

Experience:

• 10+ years of experience in Quality Control within the pharmaceutical industry.
• Extensive experience in formulation (oral solids, injectables, other dosage forms) quality control, with strong expertise in analytical testing and regulatory compliance.
• In-depth knowledge of regulatory guidelines (EU GMP, WHO etc.)
• Proven track record of managing complex QC operations, audits, and regulatory inspections.
• Excellent communication in English and stakeholder management abilities.