Open Vacancies At Liptis Pharmaceuticals
1-Research and Development Methodology and Stability Specialist
Liptis Pharmaceuticals in Egypt is pleased to announce that there is a position opening for a "Research and Development Methodology and Stability Specialist”. We are looking for qualified and highly motivated professionals to apply to our state-of-the-art manufacturing complex which meets and exceeds all international standards.
JOB DESCRIPTION:
• Performing development for method of analysis of new product
• Performing comparative in-vitro dissolution studies of R&D trials against RLD products
• Execution of test method validation for new products
• Performing all chemical and physical tests for R&D trials
• Performing stability testing for R&D trials
• Operation, qualification, and calibration of Research and Development instruments
QUALIFICATIONS AND REQUIREMENTS:
• Bachelor’s Degree in Pharmacy, or Science
• Minimum 1 year of experience in the Methodology department
• PC User Skills
• cGMP
• GLP
COMPANY PACKAGE INCLUDES:
• Competitive Salary
• Health Insurance
• Life Insurance
• Transportation Provided
• Meals Provided
For those interested and who meet the criteria above please send your resume to recruitment.factory@liptis-pharma-eg.com
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2-Production Specialist
Liptis Pharmaceuticals in Egypt is pleased to announce that there is a position opening for a "Production Specialist”. We are looking for qualified and highly motivated professionals to apply to our state-of-the-art manufacturing complex which meets and exceeds all international standards.
JOB DESCRIPTION:
• Ensure production area is safe to work, is productive and has required inventory
• Maintain production machines and equipment
• Ensure equipment and work floor is clean, safe and well-maintenance
• Monitor and control processes using visual observation, process data and on-line testing
• Identify and debug problems in processes, products, equipment and work for solution
• Resolve practical problems and deal with variety of concrete situation variables where limited standardization exists
• Perform tasks assigned to operations
• Promote safe and healthy production environment and perform safe work practices always
• Establish and perform high performance standards characterized by integrity
• Support field personnel in production data management
• Lead and direct operators to ensure production integrity
• Support data management and technical evaluation efforts of team
• Recommend new approaches to streamline the team's data management
• Supervise strict implementation of cGMP regulations and SOPs in all aspects of production processes
• Avoiding errors, mix ups and contamination or cross contamination during processes
QUALIFICATIONS AND REQUIREMENTS:
• Bachelor Degree in Pharmacy
• A minimum of 1 year of experience in a reputable company is preferred
• Fresh graduates are welcome to apply
• Excellent Command of English Language (written and spoken)
• PC User Skills
• Office User Skills
COMPANY PACKAGE INCLUDES:
• Competitive Salary
• Health Insurance
• Life Insurance
• Transportation Provided
• Meals Provided
For those interested and who meet the criteria above please send your resume to recruitment.factory@liptis-pharma-eg.com.
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3-Research and Development Methodology and Stability Supervisor
Liptis Pharmaceuticals in Egypt is pleased to announce that there is a position opening for "Research and Development Methodology and Stability Supervisor”. We are looking for qualified and highly motivated professionals to apply to our state-of-the-art manufacturing complex which meets and exceeds all international standards.
JOB DESCRIPTION:
• Preparation and revision of all documents and SOPs
• Performing development for method of analysis of new products
• Performing comparative in-vitro dissolution studies of R&D trials against RLD products
• Preparation of cleaning validation protocols and reports
• Execution of test method validation for new products
• Performing all chemical and physical tests for R&D trials
• Performing stability testing for R&D trials
• Preparation of CTD file (methodology part)
• Preparation of CADC files
• Ability to deal with EDA and exportation comments
• Participate in cleaning validation
• Coordination with Quality control department in analytical method transfer
• Operation, qualification and calibration of Research and Development instruments
QUALIFICATIONS AND REQUIREMENTS:
• Bachelor’s Degree in Pharmacy or Science
• Minimum 5 years of experience in the Methodology department
• Good Command of English Language (written and spoken)
• PC User Skills
• cGMP
• GLP
COMPANY PACKAGE INCLUDES:
• Competitive Salary
• Health Insurance
• Life Insurance
• Transportation Provided
• Meals Provided
For those interested and who meet the criteria above please send your resume to recruitment.factory@liptis-pharma-eg.com.
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4-Export Regulatory Affairs Specialist
Liptis Pharmaceuticals in Egypt is pleased to announce that there is a position opening for an "Export Regulatory Affairs Specialist”. We are looking for qualified and highly motivated professionals to apply to our state-of-the-art manufacturing complex which meets and exceeds all international standards.
JOB DESCRIPTION:
• Provides direct assistance with the registration of new and existing products supplied by the plant to foreign markets
• Gathering, evaluating, organizing, managing and collating all export regulatory related information on registration instructions and regulations in a variety of formats
• Manage and facilitate all export registration related activities
• Studying export scientific and legal documents
• Complete forms and requests originating from foreign government agencies
• Obtains and/or generates information to be submitted to foreign regulatory authorities and prepares required regulatory documentation and dossiers
• Ensuring compliance with the MOH regulations in export countries
• Liaising and negotiating with foreign regulatory authorities
• Keeping up-to-date with changes in export regulatory legislation and guidelines
QUALIFICATIONS AND REQUIREMENTS:
• Bachelor’s Degree in Pharmacy, Science or Vet
• Minimum of 3 years of experience in a similar position in local and export RA
• Background knowledge of regulatory applications and procedures
• Good Command of English Language (written and spoken)
• PC User Skills
• High interpersonal and communication skills
• Careful planning to achieve accurate and timely results
• Ability to work precisely according to procedures, rules and regulations
• Recognize recurring issues and analyze their causes in order to reach a solution
COMPANY PACKAGE INCLUDES:
• Competitive Salary
• Health Insurance
• Life Insurance
• Transportation Provided
• Meals Provided
For those interested and who meet the criteria above please send your resume to recruitment@liptis-pharma.com.
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5-Microbiology Analyst
Liptis Pharmaceuticals in Egypt is pleased to announce that there is a position opening for a "Microbiology Analyst”. We are looking for qualified and highly motivated professionals to apply to our state-of-the-art manufacturing complex which meets and exceeds all international standards.JOB DESCRIPTION:
• Analyze the received samples including raw materials, finish samples, and stability samples
• Analyze all different kinds of water samples
• Perform the environmental monitoring for the production area, warehouse, and microbiology laboratory
• Perform the microbiological suitability studies for the finished products
• Perform disinfectant efficacy studies
QUALIFICATIONS AND REQUIREMENTS:
• Bachelor's degree of Pharmacy, Veterinary, or Science
• A minimum of 1 year of experience in a similar position in a reputable company
• Excellent Command of English Language (written and spoken)
• PC User Skills
• Office User Skills
COMPANY PACKAGE INCLUDES:
• Competitive Salary
• Health Insurance
• Life Insurance
• Transportation Provided
• Meals Provided
For those interested and who meet the criteria above please send your resume to recruitment.factory@liptis-pharma-eg.com
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6-QC Raw Material Supervisor
Liptis Pharmaceuticals in Egypt is pleased to announce that there is a position opening for a "QC Raw Material Supervisor”. We are looking for qualified and highly motivated professionals to apply to our state-of-the-art manufacturing complex which meets and exceeds all international standards.
JOB DESCRIPTION:
• Creating raw and packaging materials specifications
• Creating raw and packaging materials test methods
• Preparing validation/verification protocols for raw materials test methods
• Creating analytical worksheets for raw and packaging materials
• Checking chemical analysis of water
• Reviewing and checking prepared volumetric solutions
• Reviewing and checking internally prepared working standards
• Training of newly hired QC Raw Specialists
QUALIFICATIONS AND REQUIREMENTS:
• Bachelor's degree of Pharmacy, Veterinary, or Science
• A minimum of 5 years of experience in a similar position in a reputable company
• Excellent Command of English Language (written and spoken)
• PC User Skills
• Office User Skills
COMPANY PACKAGE INCLUDES:
• Competitive Salary
• Health Insurance
• Life Insurance
• Transportation Provided
• Meals Provided
For those interested and who meet the criteria above please send your resume to recruitment.factory@liptis-pharma-eg.com