Job Description :
Purpose : Jr. Specialist the role holder is responsible to adhere cGMP principles and maintain them ineffective manner and perform In- Process Quality checks.
Responsible for the implementation of allJulphar’s procedures, and policies. Overall support & organize smooth functioning of QA In-Processquality activities.
The role holder responsibilities include preforming in-process quality checks in production and / orpackaging area (Tablets / Capsules / liquids / Semi solids / Injectable) and captures test results in batchrecords, and monitor process.
Perform a quality review of log books, participate in Internal andExternal Audit program’s. Assist in preparation of Annual Product Quality Review reports.
As well asensure the in-process check equipment’s are adequately calibrated and functions properly. Key responsibilities & Accountability : In this role you will be responsible to adhere and ensure compliance cGMP principles andmaintain them in effective manner.
Perform in-process quality check activities according to SOP in production / packagingdepartments (Tablets / Capsules / liquids / Semi solids / Injectable) in complying with cGMPprinciples 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 unacceptablematerials.
Revise all documents for in process control and perform a quality review of log books. Responsible to revise and document for inspection results and complete all requireddocuments for in process control by completing reports and logs, summarizes re-work andwaste, and inputs data into quality database on SAP system.
Participate in Internal and External Audit program’s. Assist in preparation of Annual Product Quality Review reports. Ensure the in-process check equipment’s are adequately calibrated and functions properly.
Perform and check the line before start (production / packaging) and give the clearance forthe work. Check all material required for manufacturing steps (production / packaging).
Maintain accurate records and perform tests on all activities conducted in the plant. Plan and assign daily job duties to fulfill the plan.
Accomplish quality and organization goals by completing related results as needed. Maintain safe and healthy work environment by following standards and procedures, andcomplying with regulations.
Updates job knowledge by participating in educational opportunities and reading technicalpublications. Preform any other work assigned by manager and support colleagues whenever necessary.
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 learners mind to understand and grasp new learnings. Motivated, organized, focused & overall compliance.
Must be able to manage tasks, plan workload effectively, priorities and easily adapt tochanging situations. Ability to understand new learnings and implant in workplace.
Qualifications : - Education 4 years Bachelor’s Degree in Science / Diploma in similar field. - Experience : At least 3-5 years’ experience in Pharmaceutical Company is desirable, proven experience inquality assurance or a similar field.
Good Command in English (communicating, writing and speaking). Technical Competencies : Functional knowledge of with GMP and all SOPs, MFM, and SAP.