Participation in validation and transfer of analytical methods including preparation/review of documentation and performing experimental activities in the laboratory.
Participation in testing of stability samples and performing other stability related studies including preparation/review of documentation and performing experimental activities in the laboratory.
Preparation of documentation required for registration of finished pharmaceutical products, including responding to inquiries from regulatory authorities and customers.
Participation in adopting new technologies in GMP Laboratory.
Managing change control process, laboratory investigations/deviations and CAPAs.
Participation in laboratory process improvement initiatives.
Participation in internal and corporate global quality inspections, and regulatory inspections.

Master’s degree in the relevant field (Chemistry, Pharmacy, Biotechnology, Chemical engineering or related studies)
Preferable experience with injectable products
Knowledge of GMP requirements for product development, manufacturing and analysis
Team player, proactive and approachable; able to formulate and implement design strategies within cross functional teams
Proven ability to handle multiple tasks in a global competitive-paced pharmaceutical industry environment
Fluency in English language (spoken and written)

Collaboration across teams and functions, building relationships with colleagues from different departments and regions
A dynamic international work environment that values curiosity, growth, and innovation
Permanent full-time position
Competitive compensation package
Annual health check-up and incident insurance policy
Monthly food and travel allowances
Free drinks, fruit and parking slot

Hikma Pharmaceuticals

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