Cgmp Jobs in UAE

Description:Perform one or more of the following duties and responsibilities in support of site Quality Assurance program under minimal supervision. Review and approve product MPs. Approve process validation protocols and reports for manufacturing processes. Request Quality on inciden More...

Allen Spolden is actively recruiting for a Director of Quality. This is a perm (Direct Hire) opportunity. Relocation assistance will be provided.Location: Gulfport, MS (100% onsite is required.)Work Schedule: M-F, flexible startSalary: Dependent on experience. Job Summary:The Directo More...

Ability to work overtime/weekends, as required Demonstrated understanding of cGMP regulations related to QA Warehouse and Inspection applications. Strong attention to detail. Proficient in computer system applications. Ability to organize and prioritize multiple tasks, highly fle More...

Qualifications CRITERIA Kennis en complexiteit Kennisniveau Hoger Middelbaar Onderwijs of gelijkwaardig door ervaring Technische scholing is een pluspunt. Minimaal 1 jaar ervaring in een commerciële , distributie of industriële omgeving is een pluspunt. API-SM erva More...

Qualifications Master scientific degree or equivalent experience. 4 - 6 years' experience in pharmaceutical or chemical industry. Knowledge of cGMP/Qualification compliance (21 CFR Parts 211; EU Directive 2003/94/EC and annex 15; ICH Q7,...) Experience with Equipment Quali More...

Description: Conduct routine compendial purity and impurity testing of pharmaceutical release stability and in-process samples by internally developed qualified and validated test methods. Utilize UV/VIS, CGE, capillary gel electrophoresis, imaged capillary isoelectric focusing for More...

Develop and perform assays that support development, release and stability testing of pharmaceutical drug substance and drug products. Documents laboratory work in accordance with GxP expectations, company policy, and legal requirements. Review of experiments, stability protoc More...

Overview:The QC department is responsible for microbiological and analytical cGMP testing of sterile and non-sterile products, raw materials, components and utilities. This includes routine microbiological and analytical testing of products for release and stability, development and More...

Operate processing equipment in accordance with SOPs, in all classified areas (Grade A/B/C) Complete all necessary paperwork associated with investigations, deviations and remarks. Use proper aseptic technique while performing tasks in the Grade A/B areas to include filling line, More...

Description: With direction from the Lead and Supervisor, produces various food ingredients, learning good manufacturing practices, and how to follow standardized formulas for weighing, measuring and mixing raw materials. Sets up, and controls processes, i.e. blending, drying, b More...

The Director of Operations is accountable for meeting production demand that supports corporate top-line revenue while improving efficiency to bottom-line This position is responsible for all day-to-day manufacturing operations, including purchasing, production planning, manufactur More...

Operate processing equipment in accordance with SOPs, in all classified areas (Grade A/B/C) Complete all necessary paperwork associated with investigations, deviations and remarks. Use proper aseptic technique while performing tasks in the Grade A/B areas to include filling li More...

Uses regulatory guidance and industry best practice, and scientific and technical experience, to develop innovative approaches to process or viral clearance or process validation. Plans, executes and reports process or viral clearance validation studies through process sciences More...

Product life cycle: Support the technical aspects of a product during product transfer product troubleshooting and change assessment in accordance with regulatory requirements implement stage 2 (product qualification) based on stage 1 (product development) Improvements/recommendations More...

Product life cycle: Support the technical aspects of a product during product transfer product troubleshooting and change assessment in accordance with regulatory requirements implement stage 2 (product qualification) based on stage 1 (product development) Improvements/recommendations More...

EURHASI recruits for its client a CSV Engineer Our client is a Swiss company composed of a passionate team of experienced Life Sciences Since 2014 we deliver outstanding industry s expertise and support to our clients in the complete product life cycle such as: R&D, Engineering More...

About PSC Biotech Who we are?PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with Global operations in Ireland, India, Singapore, Australia and the US, serving 350 clients in more than 23 countries worldwide. We provide clou More...

Design and implement all material plans and ensure compliance to all purchasing policies and manage all communication for all engineering activities and assist to buy all supplies and equipments and maintain quality for same. Evaluate all quotes and coordinate with vendors to provide More...