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Experience
5 - 8 Years
Job Location
Dubai(Dubai Investment Park) - United Arab Emirates (UAE)
Education
Bachelor of Pharmacy(Pharmacy)
Nationality
Any Nationality
Gender
Male
Vacancy
1 Vacancy
Job Description
Roles & Responsibilities
Responsible for Change control, Deviation, CAPA and Complaint Caliber modules.
Periodic review of Re-Qualification of Equipment and Utilities.
Periodic review of Process validation Program.
Monitoring of other VMP deliverables.
Conducting & Coordinating for Internal audits and Third party audits.
Conducting & Coordinating for Training.
Periodic review and management of Quality Third party.
Preparation and review of SOP’s.
To check and approve of BMR’s/BPR’s.
Review and control of all the technical documents.
Provide validation support to plants for new projects assigned.
Assisting QA Management for the preparation of Regulatory audit response.
Reporting the non-compliance instances to GMPs and regulatory requirements to Head of Quality.
To assist Head of Quality for the proper implementation of cGMP and problem solving in quality related matters.
Desired Candidate Profile
Bachelors of Pharmacy or Science degree with relevant experience in the Pharmaceutical industry.
Experience and Knowledge:
Min 5 years in the pharmaceutical industry field.
Languages:
Excellent Communication skills in English.
Skills:
Well versed with MS-Office, QMS, SAP & other computer software, must have good presentation skills.
Employment Type
- Full Time
Company Industry
Keywords
- CAPA
- Equipment Qualification
- Process Validation
- Audits
- SOP Review
- SOP Preparation
- BMR
- BPR Review
- Regulatory Audits
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Globalpharma Co LLC
Nimmy Biju - HR Recruiter
Globalpharma, street 35, Dubai Investment Park 1 PO Box 72168 Dubai UAE, Dubai, United Arab Emirates (UAE)
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