لمشاهدة كل جديد تابعوا موقع وظائف داخل وخارج الااردن
job2jo.blogspot.com
مطلوب تخصص الصيدلة - الهندسة الكيميائية - الكيمياء للعمل لدى مجموعة محمدعمر بن حيدر القابضة في ابو ظبي
مطلوب تخصص الصيدلة - الهندسة الكيميائية - الكيمياء للعمل لدى مجموعة محمدعمر بن حيدر القابضة في ابو ظبي
تعلن في ابو ظبي - الامارات عن حاجتها الى :
١- R&D Manager - Pharmaceutical
- Ideal candidate will possess minimum 5 to 7 years experience as a R&D Manager in a Pharmaceutical manufacturing company.
- Overlooking production activities according to per-approved standard manufacturing procedures.
- Preparation and review of all production records.
- Maintain production facilities and equipment cleanliness and compliance.
- Ensure implementation of all approved SOP's
- Ensure production target achievement.
- Documentation related to batch history record e.g. Batch Manufacturing Order(BMO), Batch Packing Order (BPO), Standard Manufacturing Procedure (SMP) etc.
- Ensure safe operation, calibration and proper documentation of machines/equipment.
- Implement all manufacturing and packaging activities are as per cGMP guidelines and MOH, UAE, GCC & EU requirements.
المهارات
Must have UAE experience as a R&D Manager for Pharmaceuticals Manufacturing.Must have Bachelors Degree of Pharmacy.
-
-
Analytical Method Validation Manager - Pharmaceutical
- Analytical methods development
- Analytical methods validation according to ICH guidelines.
- Coordinate all equipment and facilities validation activities as related to plant operations.
- Review and approve all protocols, reports and studies as prepared and conducted for equipment and facilities validation.
- Perform validation assessments for all equipment and facilities related change controls.
- Review, revise and develop Standard Operating Procedures (SOPs)
applicable to equipment and facilities validation and assist in the review and development of plant-wide SOPs. - Oversee, review and approval of the site Validation Master Plan and Validation Project Plans.
- Support the generation of risk assessments for various equipment and facilities related validation activities.
- Represent validation during agency and client audits (as needed) on matters pertaining to equipment and facilities validation
responsibilities. - Coordinate and track the corrective/ preventive action follow-ups to audits for equipment and facilities related validation issues and activities.
- Manage resource loading and manpower requirements associated with equipment and facilities validation activities or in support of internal / external client projects.
- This includes managing external validation
resources. - Assist with the preparation of equipment and facilities validation budget for capital projects.
- Prepare request for proposals for external equipment and facilities validation resources.
- Review bids and prepare bid award recommendations for upper management approval.
- Determine and coordinate the training needs of employees directly involved in the functions associated with Equipment and Facilities Validation.
- Assist with the development and tracking of the department budget.
- Periodically update the management of relevant validation activities
- Support other site departments with periodic reviews and collaboration on computer system validation, aseptic media simulation programs, and environmental monitoring programs.
- Accomplishes staff results by communicating updated organizational information, job expectations & supporting their work Plans, monitors, and appraises direct reports including performance competencies, goals & job results Coaches, counsels, and conducts disciplinary actions
- Develops, coordinates, and follows organizational systems, policies, procedures, and follows labor and capacity standards
- Contributes to the overall operations and to the achievement of departmental goals
Perform job specific tasks in compliance with applicable Regulations, International Standards and Policies and Standard Operating Procedures. - Thorough understanding of Good Laboratory Practices and Good Manufacturing Practices
Other duties as assigned - May be required to assist in other departments
المهارات
A minimum of 5 years of experience as Validation Manager/Supervisor in the pharmaceutical industry in a validation or quality related position.BSc Degree in Pharmacy, Chemistry or Chemical Engineering