Job Description :
Purpose : The main responsibility of the role holder is to adhere with the cGMP principles and to maintain them in an effective manner.
The role will also be responsible to ensure compliance of finished products in the physical lab. Key responsibilities & Accountability : Responsible for the inspection of finished products in JIII reference room.
Responsible to follow GMP and safety procedures and maintain hygienic conditions in lab. Responsible to collect samples and documents from all Julphar plants if needed.
Responsible to check temperature monitoring in reference rooms. Responsible to check and remove expiry products as per procedure.
Responsible to maintain batch archival in J-III and also main archival if needed as per procedure. Perform any other work assigned by the Team Leader / QA Manager.
Qualifications : - Education Any diploma course. - Experience : A minimum of 2-3 years of relevant experience in similar pharmaceutical facility.
Proven understanding and experience in sterile, non-sterile operations. Prior experience in handling similar role will ensure better fitment.
Must be able to manage tasks and priorities and easily adapt to changing situations. Good command in English (Communicating, writing and speaking).
Good prioritizing skills and being able to make a just decision also in case of (time) pressure. Flexible learning abilities, sufficient knowledge of product and GMP / Quality systems.
Must be highly organized, self-motivated to learn new things and implement them in building or updating quality system for Pharmaceuticals.
Technical Competencies : Excellent knowledge of reporting procedures and record keeping.