- Operate as QA Specialist focused on the follow-up of stability studies.
- Support in the issue of stability studies documentation (i.e. Protocols/Reposts), in
line with current Regulations, internal procedures and business needs.
- Ensure compliance with GMP, corporate standards/Company’s procedures (SOP), Regulatory
requirements and industry standards
- Statisticalevaluation of Stability Data
Skills required:
· At least a Bachelors Degree (Pharmacy, Pharmaceutical Chemistry, Microbiology, Chemistry, Engineering)
· At least 3 years of relevant work experience;
· Good knowledge of cGMP guidelines and Data integrity principles
· English Fluent (mandatory)
· Full availability to travel domestically and abroad
Our collaborators are engaged, developed, challenged and well-rewarded for performance. We recognize the importance of leadership at all levels of our organization in order to succeed in a challenging business environment, and we are committed to providing practical processes and programs to identify, develop and inspire all our current and future leaders.
Working at PQE Group
As a member of the PQE team, you will be part of a challenging, multicultural company that values collaboration and innovation. PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world.
If you are looking for a rewarding and exciting career, PQE Group is the perfect place for you.
Apply now and take the first step towards an amazing future with us.
Summary of role requirements:
- Looking for candidates available to work:
- Monday: Morning, Afternoon
- Tuesday: Morning, Afternoon
- Wednesday: Morning, Afternoon
- Thursday: Morning, Afternoon
- Friday: Morning, Afternoon
- 2-3 years of relevant work experience required for this role
- Working rights required for this role
- Expected salary: $70,000 - $80,000 per year