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Supervisor, quality control

Sintra
Hikma Pharmaceuticals
Coordenador
Anunciada dia 30 setembro
Descrição

Founded by Samih Darwazah over 40 years ago in Jordan, Hikma's purpose is to provide affordable, quality medicines to the people who are competent. Based on very solid foundations, we continue to innovate daily and find practical solutions to transform the lives of the millions of people we serve.

At the end of the 1980s, we extended ours beyond the Middle East and acquired land in Portugal for the construction of a sterile factory for injectable pharmaceutical products. This was an important turning point for the company, and our first step into a new region. Today, in Portugal, we have more than 900 employees and 3 factories for the production of injectable medicines.

Hikma, intends to recruit an Supervisor, Quality Control (m/f) to integrate Quality Control Department, on-site work.

Main Responsibilities:

1. Stays updated with regulatory and quality standards, evolutions in GXPs compliance and follow GMPs rules.
2. Setting the analysis plan and review laboratory notebooks and raw data, to ensure the completion and accuracy of information and generated data archieving the target due date for the assigned tasks and objectives
3. Supervision of the daily activities of the laboratory staff, ensuring the personnel, premises and the equipment in the laboratories is appropriate to the tasks
4. Fills out relevant documention, including generating reports and filling Certificate of Analysis
5. Supports the Sr. Quality Control Supervisor and/or Quality Control Manager of critical documents and CAPA
6. Acts as primary contact for the other Quality Unit or Operation groups to support achieving the department and site objectives
7. Performs qualifications protocols and reports according to lab tasks

Profile:

8. Degree in chemical engineering, chemistry or a related field
9. At least 4 years of previsous QC work-related experience in a regulated analytical lab environment is essential
10. Demonstrated knowledge of working in an analytical lab environment, of the cGMPs, and ability to generate, review, and follow SOPs and policies
11. Demonstated ability and skill to perform and evaluate feasibillity for required analytical techniques and to operate and troubleshoot the associated equipment and software
12. Capabillity of working with others and as part of a team is essential
13. Good problem-solving techniques is needed to make necessary adjustments and to prioritize tasks
14. Exhibited ability to work in a highly structured regulated environment, including the capacity to follow directions, have attention to detail, meet deadlines and multi-task
15. Good command of Windows operating system, namely in the software Office (Word, Excel and PowerPoint)
16. English Intermedium/Advanced Level
17. Project management skills, is preferred

We offer:

18. Direct contract with Hikma
19. Salary appropriate to the functions performed
20. Life insurance
21. Health insurance
22. Annual Performance Bonus
23. High career prospects

If you think this is a good opportunity for your professional career, join us and contribute to Better Health, within everyone's reach, every day

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