Are you ready to take your career to the next level in a role that truly makes a difference? As a Quality Compliance Specialist at Zentiva, you’ll be at the forefront of ensuring pharmaceutical quality and regulatory compliance.
You will have the opportunity to:- Lead investigations for deviations and complaints, ensuring timely root cause analysis and effective CAPA implementation.
- Coordinate and monitor change control processes, ensuring compliance and timely execution of change plans.
- Review and approve manufacturing batch records and local documentation in alignment with GxP and quality system requirements.
- Participate in internal audits, external inspections, and compliance gap assessments, escalating risks as needed.
- Monitor quality system performance indicators, support training oversight, and follow up on validation, maintenance, and calibration activities.
- You have a degree in Pharmacy or Chemistry and 3–5 years of experience in the pharmaceutical industry.
- You possess strong knowledge of GMP and regulatory requirements.
- You are a great communicator with excellent interpersonal and conflict management skills.
- You have strong investigational and analytical thinking and can simplify complex technical issues.
- You are proficient in MS Office and have upper-intermediate English language skills.
We will empower you with the freedom and autonomy to shape your work, make key decisions, and take ownership of your success. We will trust you to lead, innovate, and make an impact from day one.
And we will also bring you:A collaborative and inclusive work environment where your voice matters.
Opportunities to grow within a leading pharmaceutical company committed to innovation and excellence.
Exposure to cross-functional projects and international teams.
A culture that values continuous learning, development, and recognition.
Our Recruitment Process:To be considered for this role, please apply in our Applicant Tracking System and refrain from sending your CV via email. Upon the completion of the sourcing period, all received applications will be reviewed by our Recruitment experts and evaluated against the needs of the open role. Successful candidates will be contacted by our Recruiting experts for an initial screening interview during which further details about the selection process will be shared. Successful candidates will progress to interviews with line managers, while not selected candidates will be informed in a written form as soon as possible.
Top Skills
What We Do
Zentiva is a Pan-European Platform developing, manufacturing and providing high-quality and affordable medicines to more than 100 million people in Europe. Zentiva has 4 wholly owned manufacturing sites and a broad network of external manufacturing partners to ensure supply security. We offer solutions in key therapeutical areas like Cardiology & Circulation, Diabetes, Oncology, Respiratory, CNS and focus on expanding our portfolio in self-care. The company is Private Equity owned, delivering sustainable double-digit growth, with an ambitious 5-year plan for further strong (organic and inorganic) growth across Europe.
We are a team of almost 5,000 unique talents bonded together by our mission to deliver high-quality and affordable medicines to people who depend on them every day. We want Zentiva to be a great place to work, where everyone feels welcomed and appreciated and can be their true selves contributing to the best of their ability.
