Jr. Specialist

Ras al-Khaimah, United Arab Emirates

Job Description

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Position Summary :
  • In this role you will be responsible for adhering to and ensuring compliance with cGMP principles and maintaining them in an effective manner.
  • Perform in-process quality check activities according to SOP in production / packaging departments (Tablets/Capsules/liquids/Semi solids/Injectable) in complying with cGMP principles and captures test results in batch records.
  • Check the required tests for all products during production / packaging process.
  • Inspect and check incoming materials by confirming specifications and return unacceptable materials.
  • Revise all documents for in process control and perform a quality review of logbooks.
  • Responsible to revise and document for inspection results and complete all required documents for in process control by completing reports and logs, summarizes re-work and waste, and inputs data into quality database on SAP system.
  • Ensure the in-process check equipments are adequately calibrated and functions properly.
  • Perform and check the line before start (production/packaging) and give the clearance for the work.
  • Perform Initial investigations for reported incidents and deviation in the respected site
  • Participate in the preparations of APQRs of the respected site.
  • Maintain safe and healthy work environment by following standards and procedures and complying with regulations.
Core Competency :
  • In terms of competency, you are highly result oriented with strong sense of accountability & ownership.
  • High on compliance adherence, having strong attention to detail, proactive and flexible
  • Good communication, interpersonal, and collaboration skills.
  • Should be having good learning agility to understand and grasp new learnings.
  • Motivated, organized, focused & overall compliance.
  • Must be able to manage tasks, plan workload effectively, priorities and easily adapt to changing situations.
  • Ability to understand new learnings and implant in workplace.
Qualifications, Key Experiences / Functional Knowledge Requirements:
  • Bachelor of degree in pharmacy/Science
  • Minimum 0 to 3 years in quality operation in Sterile manufacturing
  • Knowledge of QMS system Agile, Track wise, Ampelogic
  • Proficient in English.
  • Quality and Business decisions taker
  • Good Knowledge and command on cGMP
  • Risk Assessment knowledge

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Job Detail

  • Job Id
    JD1682219
  • Industry
    Not mentioned
  • Total Positions
    1
  • Job Type:
    Full Time
  • Salary:
    Not mentioned
  • Employment Status
    Permanent
  • Job Location
    Ras al-Khaimah, United Arab Emirates
  • Education
    Not mentioned