Team Leader

Job Title: Team Leader Division: QUALITY CONTROL Country: UNITED ARAB EMIRATES
Work Location: UAE (RAK head office) Job Type: Team Leader Employment Type:
Full Time Employment (Limited Contract) Job Description:* * Purpose:
Provide analysis and processing of bulk, finished products or Raw Material on
time by appropriate methods while respecting Good Manufacturing Practices.
Support resolution of technical issues in the laboratory. First contact in
case of analytical issue in the laboratory. Key responsibilities &
Accountability: • Management of a Lab Team (‎12-‎18 staff for laboratory
testing) • Release of commercial lots, testings for stability studies •
Follow-up of the quality system used in the laboratory, trend and reagents
follow-up … • Responsibility of the laboratory and the follow-up of the
equipments • Critical review of analytical data • Knowledge of deviation
process is an asset • Be a support to reach objectives targeted such as
planning adherence. • Manage Laboratories, Deviations, Investigation & CAPA
and the resolution of technical issues in the laboratory. • Act as Lead
Investigator, take in charge analytical projects • Train other technicians to
the QC analysis Escalates problems effectively to QC Managers • Equipment SME
• Perform double check of analytical tests to ensure the integrity of results
• Create SOPs and working documentation needed for QC laboratories • GMP
knowledge and experience to support the requirements expected by Swissmedic,
European union agencies and other regulatory bodies to assure that our
products meet all cGMP requirements together with our operations and
documentation system. • Respect all GMP standards. GMP knowledge and
experience to support the requirements expected by Swissmedic, European union
agencies and other regulatory bodies to assure that our products meet all cGMP
requirements together with our operations and documentation system. •
Maintains records and ensures proper documentation of the analysis and enter
data on SAP. • Ensure the quality of results provided by the department •
Quality documentation writing (deviations, CAPA, procedures, protocols,
reports …). • Transversal interactions with other teams in QC, with QA and
different MPU: Guarantee good communication for transversal interactions.
Qualifications: - Education Bachelor of Science in Chemistry or Chemical
Engineering or Pharmacy - Experience: • Minimum ‎6 to ‎8 years' experience in a
Pharmaceutical Environment (Finished product , preferable ) • Proven process
understanding (Pharma, GMP, investigation and method development) • Continuous
improvement experience (Lean, 5S, Problem Solving). - Training: Key
Competencies: • Safety, Quality, Result and Customer oriented • Basic speaker
(A2) English level • Strong Team spirit. Demonstrate exemplarity behaviours. •
Leadership skills • Open minded and flexible • Work under pressure • Excellent
interpersonal and intrapersonal skills Technical Competencies: