Trainee at Hikma Pharmaceuticals PLC

Sahab, Amman, Jordan -

Full Time

Start Date

Immediate

Expiry Date

18 Apr, 26

Salary

0.0

Posted On

18 Jan, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Validation, Temperature Mapping, Humidity Mapping, Calibration, Process Validation, Environmental Monitoring, Air Particle Count, HEPA Filters Integrity, Air Velocity, Recovery Time Study, Air Change, Requalification, Training Files, Validation Documents, cGMP, English

Industry

Description

Location: Amman, Jordan Job Type: Full-time Hashtag: #LI-OS1 About Us: For over 45 years, Hikma Pharmaceuticals has been putting better health within reach, every day, by creating high-quality medicines and making them accessible to those who need them. We are helping to shape a healthier world that enriches all our communities, and our global team of 9,500+ empowered employees are central to this mission. As a trusted and reliable partner of over 800 high-quality generics, specialty and branded pharmaceutical products, we are driven to improve access to medicine. Through our 29 manufacturing plants, 9 R&D centers across the MENA, North America and Europe, our footprint allows us to play a critical role in serving patients. Description: We are looking for a talented Trainee, Quality Validation to join us. At Hikma you’ll be supported by a culture of progress and belonging where people are encouraged to develop, wellbeing is prioritised and our inclusive approach values contributions from all. We’re seeking candidates who embody our values: Innovative, driven to keep learning; Caring, genuinely compassionate in their work; and Collaborative, eager to solve problems together. If you want to be part of a team that cares about impact, this is the place for you. Role Summary: Trainee to learn and support the validation/qualification initiatives to internal project teams and external validation firms in order to ensure schedules are met and that systems, both computer and equipment are in compliance with regulatory requirements. KEY ACCOUNTABILITIES:· Perform temperature and Humidity Mapping studies for warehouses, stability chambers & refrigerators and prepare related protocols with mapping reports. Arrange with external calibration agencies to keep tools ,weights & balances within calibration due dates. · Preparing process validation protocols and arrange of process validation activities· Prepare process validation reports Conduct periodic environmental monitoring activities to maintain quality and pharmaceutical regulatory standards1. Air particle count test2. Air smoke test3. HEPA filters integrity test4. Air velocity5. Recovery time study6. Air change· Perform requalification for sampling booth & QC lab cabinets.· Arrange training files.· Arrange validation documents approval between departments. Minimum Qualifications:Bachelor’s degree in Chemical Engineering. Familiar with computer & office app Familiar with cGMP. Very good in English writing & speak Minimum Experience: 0-1 year of experience working in Engineering or related Quality fields.Training period: One year/ Paid

Responsibilities

The Trainee will learn and support validation and qualification initiatives for internal project teams and external validation firms. Responsibilities include performing temperature and humidity mapping studies, preparing validation protocols, and conducting environmental monitoring activities.