Analyst, Quality Control
Hikma Pharmaceuticals
Remoto
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 1000 employees and 3 factories for the production of injectable medicines.
Hikma, intends to recruit an Analyst, Quality Control (m/f) to integrate Quality Control Department, on-site work.
Main Responsibilities:
- Initiate stability studies in all facilities: requesting the stability batches, preparing the samples, and placing them on the stability chambers.
- Sampling of stability batches for Quality Control, Analytical Research and Micro departments.
- Introduction of stabilty data on software LIMS and treat stability data from LIMS and Novatek.
- Receiving and login of stability samples.
- Reviewing and updating stability protocols in use.
- Ensure documentation practices according to the company quality requirements.
- Write/Review stability SOPs upon request.
- Elaboration of MEMOs, events, and deviation reports.
- Performs job tasks in strict adherence to Standar Operating Procedures (SOPs), company Good Manufacturing Practices (cGMPs) and Food and Drug Administration (FDA) requirements.
- Degree in Science/Technical, Engineering or related areas
- Excellent organization, communication, interpersonal, collaboration, and relationship skills
- Ability to work as part of a team
- Capability of working under pressure and meeting deadlines
- Good analytical and organizational skills and should have the ability to think critically
- Pharma experience is a plus
- Good knowledge of written and spoken English
- Availability to work rotating 8-hour shifts (morning and afternoon)
- Salary appropriate to the functions performed
- High career prospects