تجميعه وظائف لكليات علوم-صيدله-زراعه-هندسه
QC Specialist At Unicharm Middle East & North Africa – Hygienic Industries – Babyjoy
Unicharm Middle East & North Africa – Hygienic Industries – Babyjoy Hiring: QC Specialist Job Location: 10th of Ramadan Job Requirements: -Preferred BS in Science -1 year of experience as QC Specialist (worked in packaging field is a MUST) -Excellent user of Microsoft Office (Word, Excel, & PowerPoint) -Familiar with ERP systems -Good Command of English -Very Good communication skills -Preferred Sharkya resident Suitable candidates shall send their CV to menna-ossama@unicharm.com , ahmed-tawfik@unicharm.com and mention job title in the email subject.
QA Vacancies At Gypto Pharma – Medicine City
1-Validation specialist at Gypto Pharma – Medicine City
Job Description
* Prepare validation, qualification and calibration plans procedures, protocols and reports related to process, cleaning, hold times and qualification.
* Follow up the execution and coordinate between departments in all validation and qualification activities.
* Participate in change control and risk assessments.
* Follow up and execution objectives and KPI’s for the validation section.
Job Requirements
* BSC of Pharmacy.
* Experience not less than 1 year to 3 years maximum in QA validation field in pharma is a must.
* Excellent command of English.
* Males are preferred.
If you are interested in the previously mentioned position please send your updated CV to:
karim.khaled@gyptopharma.com
-Please mention the job position you are applying for in the email subject, otherwise, your CV will be discarded.
2- IPC. specialist maximum 3 years Exp, sterile and non sterile
3-Documentation Specialist max 3 years EXP,
For positions IPC and Documentation
Kindly send CV, Ibrahim.youssef181119@gmail.com
Production Supervisor At Viatris Egypt
Key responsibilities for this role include:
Leading and guiding the direct reports for the execution & Ensuring adherence to production schedule/plan through coordination with other departments/cross functional team & solving moderately complex problems & technically support within his area of expertise.
Responsible for the performance of his respective area in the dimensions of Safety, Quality/compliance, Supply, Financials and People.
Ensure achieving team goals including as targeted OEE & All key performance indicators for through cascading objectives to direct reports & efficient resources utilization.
Responsible for SOPs and any other production related documents update/review.
Ensure him/team compliance with good documentation practice.
Participate in his area Quality/Safety investigations, changes & ensure implanting actions on time.
Ensure complete team/area adherence to SOPs, MBRs and any other instructions.
Ensure team/area compliance with cGMP, PQS (including data integrity/ALCOA principles), MOH & other regulatory requirements.
Conduct employee training in equipment operations or work procedures.
Manages the performance of direct reports through goal setting ,ongoing assessment & development, coaching with continuous feedback, appraising & recognition in addition to talent retention.
Participate in screening, interviewing and hiring new operators/workers.
Nourish continuous improvement culture within his team and lead by example.
Develop and maintain Viatris values within the team in day to day communications/activities.
Lead any assigned task/job from his manager.
The minimum qualifications for this role are:
Pharmacy bachelor degree or its equivalent.
Ability to effectively communicate within a diverse group resulting in desired outcomes.
Team player, with strong interpersonal and coaching skills.
Good verbal communication and ability to coach and provide guidance to others.
Demonstrates strong technical/functional knowledge needed to coach direct reports on day-to-day activities.
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Quality Control Senior Supervisor At Pepsico
New Cairo, Egypt
Job Description
Role:
Ensure that Pepsi products are consistently produced within PCI standards. Act as a liaison with local health officials and inspectors for the purpose of plant evaluation and auditing. Ensure plant operation, products and packages meet local beverage industry regulations and PCI requirements
Accountabilities:
Lead the implementation of the 3D quality system throughout the plant operations to assure sustaining B/G rating.
Manage the correct and efficient production of syrup and treated waters
Ensure that the laboratory is adequately equipped to perform the required tests at the appropriate degree of accuracy and frequency
Prepare and execute the departmental budget for staffing, consumables, testing equipment.
Manage line performance trials for the introduction of new packaging to ensure quality standards are maintained.
Lead product lifecycle management process to address and control the ongoing quality, performance, and cost.
Assure the Quality department staff and line personnel conducting quality tests are competent and proficient at performing their tasks. This includes line visual inspectors
Manage the execution and documentation of proper and timely calibration routines for all lab equipment, line gauges and other critical measuring equipment
Manage the implementation of quality assurance systems and procedures throughout plant operations. This includes the use of control charting and systematic monitoring and documentation of critical control point variability.
Manage the implementation of quality assurance, HACCP, ISO FSSC 22000 and QAS systems throughout Plant operations.
Lead the implementation and ensure compliance and continuous improvement of the AIBI, , NFSA and food safety requirements.
Ensure all packaging materials & raw materials tests are conducted to ensure materials meet PI Specs and keep good communication channels with suppliers to resolve quality issues and maintain quality packaging supply.
Manage the provision of analytical services and technical leadership to all plant operation through, informal and formal training of personnel, the prevention and resolution of quality issues and the reduction of process variability.
Manage the execution and documentation of proper and timely calibration routines for all lab equipment, line gauges and other critical measuring equipment.
Ensure proper handling of consumer/customer complaints by the plant in accordance with company guidelines
Implement the standard company procedures for the management of raw materials and products release or hold
Follow-up on the implementation of all corrective action as a result of a GMP, Local or IQA audit
Ensure safe operating conditions exist throughout the processing and laboratory. Promptly correct unsafe conditions.
Coaches and provides constant feedback for the development and improved performance of quality personnel
Prepare and execute the departmental budget for staffing, consumables, testing equipment.
Ensure that an annual performance review is being conducted with all quality personnel
Communicate quality performance and activities regularly to Plant Managers, Senior Quality Manager, and other department heads
Assist in the coaching and implementation of the EHS programs in the field.
Qualifications/Requirements
7+ years of experience in an FMCG company preferably beverages.
Degree in biochemical / chemical or food technology field
Firm foundation in the application of problem-solving tools, statistical methods and HACCP systems
Good communication skills in English & Arabic
Proficient with computer usage, including Word processing, Spreadsheets and Database
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Agriculture Officer At Egyptian Food Bank
Cairo, Egypt
Job description
o Main Purpose
Advise farmers on improved methods of agriculture and agricultural work such as farm management, crop rotation, soil conservation, use of new machinery, marketing, coordinate and contribute to economic quantitative and qualitative analysis on a broad range of issues in relation to the project decision support tool and the analytical studies.
o Main Responsibilities
Collects and analyzes data related to land productivity, crop yield and financial reports to measure performance.
Researches and keeps up to date with any relevant developments in agriculture particularly smart agriculture methods and techniques.
Advises on how to improve the soil, use of fertilizers, weedkillers or other materials used on farms and advising on the best types of seeds to use.
Support in developing program design related to agriculture empowerment and rural development.
Develops and maintains close relations with government officials and key stakeholders in the agriculture sector.
Develops and strengthens technical networks relevant to sustainable cropping systems, and participates in outreach events such as webinars, workshops and conferences with strategic partners (academic/research institutions and centers of excellence, national, regional and sub-regional institutions, organizations and bilateral assistance agencies).
Provides technical advice and guidance to key external partners to advance our understanding of agriculture led economic growth capacities and measurement in order to improve development outcomes.
Plans, organizes and participates in technical meetings, conferences, seminars, intergovernmental discussions to promote practices and policies for sustainable crop production.
o Job Dimensions
o Internal Stakeholders: Supply chain – Field operations – Finance
o External Stakeholders: Farmers – Ministry of agriculture – Research Centers- NGOs
o Qualifications and Education Requirements
5-7 years of relevant experience in the agriculture centers (NGOs, government, private sector, research institutions).
Communicate effectively, both in writing and orally, with clients, colleagues and members of the public.
Bachelor’s degree in agriculture.
Strong knowledge of crop and plant science, environmental science, horticulture, and soil science.
Expertise in monitoring and evaluation of agriculture activities to improve data collection and analysis along with reporting preferred.
Demonstrated ability to provide capacity building within teams and/or with government partners such as ministries and NGOs so that the team is better able to achieve agriculture results.
Strong interpersonal, communication, analytical and negotiating skills.
Excellent command of English & Arabic and writing skill in both languages
o Competencies
Innovating and seeking creative solutions
Driving for results
Collaborating & influencing
Acting with integrity
Proficiency in research & analysis
Familiarity with economics
Project Management
Additional Notes
Personality traits:
Integrity, morally driven and team player
Seniority level
Entry level
Industry
Nonprofit Organization Management
Employment type
Full-time
Job functions
ManagementManufacturing
Apply From Here
Plant Quality Leader At Electrolux
Your role
To Ensure Compliance of all Inward Materials (Component – processed material – raw material assembled parts), prevent the usage of defected parts to be assembled on production lines
A typical day
Manage & lead quality staff engaged in Process and final inspection activities.
Provide technical expertise & instruction to his subordinate.
Evaluate his team performance against their job requirement and define training needs on regular bases to upgrade their skills.
Ensure that all products under processing are produced according to their related specs.
Ensure the availability of all measuring equipment & inspection instruments needed for in process inspection.
Use and apply statistical tools to analyze and expire the product related data of the being inspection and/or tested.
Discus on daily bases with production manager & senior the product defects to prevent & reduce cause of defect occurrence.
Issue the inspection of in process products related documents (work instruction, inspection instruction,…etc.)
Follow up & supervise all inspection activities & relating or affecting activities
Report on regular bases to Quality Manager on in process & final products quality, cause of defects, repeated defects, suggestions and prevent recurrence.
Monitor the final products returned from Customers & After sales service sector reports
Establishing the required action plans to improve final product & customer returns KPIs
Aware and implement the requirement of quality management system ISO 9001-2008.
Aware and implement the requirement of environmental management system ISO 14001-2004
Aware and implement the requirement of OHS management system OHSAS 18001-2007
Ensure that all used testing equipment and/or tools under his supervision are subjected for calibration program follow the program implement for each.
Generate & create ideas and techniques for continuous improvement related to this area of interest to minimize the cost of processing or inspection
Responsible for Plans, coordinates, and directs maintenance procedures in hisher section.
Introduces efficient Maintenance methods.
Initiates and directs procedures to increase the section output. Controlling and maintaining the scrap
Initiate and lead continuous improvements projects (CIP) in her/his area (like SMDC) with coordination with the cross functional teams of the relevant departments and her/his team to realize Electrolux 5 pillars.
Plans, coordinates, and directs maintenance procedures in his section. Regulates and coordinates functions of office and shop.
Minimum Qualification
Who you are
Minimum 3 years of experience in manufacturing environment
Experience in managing diversified teams
Excellent English
Communicative. You can communicate plans and articulate your ideas with colleagues at all levels.
Team player. You nurture and develop the relationships that implement innovation.
Analytical. With an eye for detail and the ability to interpret complex data, you can also translate this into meaningful, useful information that informs decision-making.
A leader. You have a vision and a purpose, and you can inspire and influence others to not only share it but apply their abilities to achieving it.
Problem-solver & resilient. You see challenges as opportunities and chances to make things even better than before. Strong knowledge of Lean Tools / Six Sigma is preferred
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Production Engineer At Abu Auf
Production Engineer is urgently needed for Abu Auf for Nuts, Coffee and healthy food. Responsibilities: Responsible for general supervision of production. Responsible for the production schedules for all manufacturing department. Work closely with the production team to increase productivity and profitability within the manufacturing operation. Responsible to implement all the continuous improvement activities to enhance the production process. Responsible for validation and commissioning for the process and packaging areas. Lead the troubleshooting process during the process activities. · Coaching, Motivating, and Mentoring the production team. Qualifications: Bachelor’s Degree in agriculture engineering . 3 to 5 years experience in F&B Manufacturing Company. Strong computer skills. Strong leadership, team building and advanced coaching skills. Interested Candidates please send your updated CV to: jobs@abu-auf.com
Packaging and Development Officer At
Dabur International Ltd
10th of Ramadan, Sharkia, Egypt
Dabur Egypt Ltd. World largest ayurvedic company is hiring:
PACKAGING & DEVELOPMENT OFFICER
Who will be reporting directly to the Pack & Dev J. Manager and will be responsible for:
Product Development and Upgradation
Assists in New Product Development and upgrade existing designs.
Undertake long-term and short-term projects for developing innovations in primary and secondary packaging.
Benchmarks against same or similar products in domestic and international markets.
Runs & Apply Cost Reduction Programs.
Ensures that there is no degeneration in quality as a result of cost reduction.
Selects vendor providing goods at best quality along with cost benefits.
Creates network of reliable and efficient vendors who use the best possible technologies.
Prepares and maintains different documents such as BOM, Specifications, Artwork copy, Shade card and Packaging software such as (Mold/Artwork management systems) as well as packaging instructions.
Under take new/existing mold commissioning process till finalization & documentation.
Attend online proofing at the supplier end for NPDs and existing Products (MKTG), technical.
Art works, and (existing new designee) files to be circulated between Purchase and marketing.
Skills:
1-3 years of experience in experience in the same role.
Very good of both speaking and writing English.
FMCG experience is a preferable.
SAP knowledge is a preferable.
Education:
Bachelor degree (chemistry, mechanical engineering) or any relevant degree from reputable university
Work context:
Normal working from 8.30 AM to 5.00 PM based at Dabur factory at 10th of Ramadan city
Days off: Friday’s & Alternative Saturday’s
Apply NOW & send your updated resume to:
HR.Egypt@Dabur.com
And Mention the job title in the subject
Senior Health and safety Specialist At Elif Global
Senior Health and safety Specialist is required for a packaging company with the below requirements :
1-At least 3 Years of experience in industrial Safety is a must 2-Engineering / Science Background .
3-Very Good in English.
4-Certificates in occupational health and safety – OSHA , HSE Specialist ,Civil Defense & First Aid are mandatory .
5-Excellent knowledge of legislations and procedures .
6-Excellent knowledge of potentially hazardous materials or practices .
7-Experience in Preparing reports .
8-Experience with writing policies and procedures for health and safety .
9-Familiarity with conducting data analysis and reporting statistics . Proficient in MS Office .
10-Working knowledge of safety management information system . Outstanding organizational skills.
11-Critical thinker and problem-solving skills .
12-Preferred NEBOSH or Equivalent Certificate .
13- Maximum age is 30 .
If you you’re interested and matching these requirements kindly send your updated Cv to sandyashraf@elif.com mention in the subject Senior Health and Safety Specialist , and kindly read the requirements very carefully you should have all these requirements to apply .
Vacancies At VITABIOTICS – Egypt for pharmaceutical industries
VITABIOTICS – Egypt for pharmaceutical industries is looking to hire the following positions: –
1. Raw Material Control Specialist (In QC Department ) with the following specifications:- • Alexandria Resident is a must • Males is preferred due to working condition • Bachelor of Science (preferred microbiology major) • Experience 0 – 3 years in pharmaceutical industry • Strong English (oral and writing skills) • Excellent computer skills
2. IPQA specialist to follow IPC and GMP rules. With the following specifications:- • Alexandria Resident is a must • Males is preferred due to working condition • Bachelor of Science. • Experience 1 – 3 years in pharmaceutical industry • Strong English (oral and writing skills) • Excellent computer skills We are offering: • Very attractive salary • Family medical insurance • Transportation • Daily meal Working condition: • Location; Borg Al-Arab • 5 working days / 8 hours • Two days off (Friday / Saturday) If you are interested, please send your updated resume to careers@vitabiotics-egypt.com mention the job title in email subject
Solid Production Specialist At Marcyrl Pharmaceutical industries
Marcyrl Pharmaceutical industries are looking to hire
Solid Production Specialist
Marcyol
Bachelor’s degree in Pharmaceutical Science.
From 1 to 2 years of experience.
Strong Solid manufacturing background
– Excellent communication and interpersonal skills.
– Flexible to operate in shifts (preferred males)
Kindly sent your updated C.V to:-
hr@marcyrl.com
QC stability officer At Copad Pharma
a pharmaceutical factory based in Obour industrial zone is seeking to hire a qualified candidate to wotk as (QC stability officer) in QC dept., with the following requirements:
– Qualification Bsc. in Pharmacy, or Science
– Experience 2-4 years in QC
– Residency Obour city,Cairo,or nearby
– Gender males or females
interested candidates may send their CV with a recent photo – and to mention job title (QC stability officer) in the subject – to the following email
Copadpharmajobs@gmail.com
Warehouse Manager At REDA Chemicals
Job description
Are you looking for a new challenge?
At REDA Chemicals, we passionately market and distribute a unique and innovative portfolio of specialty raw materials and industrial chemicals. We are the largest distribution network with local services in 30 countries in the Middle East, Africa, India, Pakistan, Central Asia, Southeast Asia, and China.
You and REDA, it’s more than just chemistry. And we are currently searching for a proactive and competent Warehouse Manager to join our team in Egypt.
Role Functions
Ensure the warehouse operates at peak efficiency, with customer satisfaction being the primary goal, by supervising, organizing, directing, and training warehouse employees and establishing, monitoring, and managing operation goals
Manage the warehouse operations system and storage requirements, equipment utilization, inventory management, and deliveries to customers
Train and manage the warehouse team to solve day-to-day operational issues and reach short and long-term performance goals
Oversee daily operations while controlling and managing inventory
Review and prepare workflow, managing and space requirements, and customer service standards are met
Maintain a safe and healthy work environment by establishing, following, and enforcing standards and procedures while complying with legal regulations
Knowledgeable of the nature of chemicals, especially with DG materials, and storing them perfectly in safe conditions
Oversee and manage the transport of products to customers and internal facilities, communicating with drivers and ensure the on-time delivery to customers
Skills and Qualifications
University degree, preferably in chemistry, science
3+ years experience in a warehouse lead role, preferably in chemical warehouses
Proficient knowledge of warehouse procedure and policy
Excellent problem-solving skills and leadership qualities
Ability to work with all levels of company staff
Bilingual (Arabic and English)
ERP system skills required
Proficiency in MS Office and Outlook are essentially required
Interested candidates are encouraged to respond with an updated CV.
Alternatively, you can also submit your application to careers@redachem.com
Compliance & Validation Section Head At Rivapharma
Qualification:
– Experience: 6 to 8 years.
– Bachelor degree in Science or Pharmaceutical.
– duties :
1- Follow up calibration ,qualification & validation plan
2- Review Protocols & Reports
3- Qualify the calibration & Qualification service provider.
4- Internal & External audit follow up
5- Follow up change control system ,deviation ,investigation & CAPA
-Work location: Nasr city – Free Zone.
Please send your updated CV to:
randa_magdy@rivapharma.com
Regional Regulatory affairs strategist manager At Pfizer
JOB SUMMARY
Summarize the primary purpose & key accountabilities of the job.
Manage projects and Handle related regulatory strategies for allocated Products, and ensure communication/clarity of regulatory timelines and strategy.
Single point of contact for global/product strategists, and In-Country Regulatory Team on regional issues to facilitate the best in class support for product registration and product life cycle management activities.
Responsible for ensuring that regulatory documentation meets relevant regulatory requirements.
To apply knowledge and best interpretation of regulatory requirements in the assigned countries to the drug development process, including promulgation of health authority marketing authorization dossiers to enable efficient and effective registration of medicinal products consistent with the supported regions commercial objectives.
To ensure business continuity between global/product Strategists and In-Country Regulatory Team.
JOB RESPONSIBILITIES
Indicate the primary responsibilities critical to the job.
Maintain knowledge base of country requirements and regulatory environment, Maintain effective regional relationship with stakeholders to ensure communication /clarity of regulatory strategy and timelines.
Apply regulatory expertise for assigned Products/countries to enable preparation of high quality documentation and assure compliance with departmental procedures.
Provide regional input to global regulatory strategy for the development of products in-line with business objectives, Assist and liaise with GCMC, global/product strategists, PGS, Submissions Management, In-Country Regulatory , ILG, ALIM, Cluster/Market, and any other key stakeholders to ensure the filing strategies are defined and executed and BoH requirements are met, ensuring a submission ready dossier. Ensure that the appropriate regulatory requirements systems and database are updated in a timely manner when changes occur in market regulations. Ensure a submission planning and forecasting tool is utilized to update timelines.
Assist and support all product lifecycle regulatory work, and liaise with GCMC, Submissions Management, Cluster/Market, and any other key stakeholders.
Assist and oversee the preparation of regulatory strategies and plans for assigned countries, including review of existing regulatory guidelines and relevant literature.
Dispatch dossiers to In-Country Regulatory .
Develop detailed understanding of regulatory guidelines and technical requirements in assigned countries and ensure that global/product strategists are aware of regulatory requirements (e.g., department presentations and Regulatory Requirements Database) Regularly follow up with In-Country Regulatory Team on progress of registration submission and approval activities, and ensure line management are advised of progress in regulatory filings.
Maintain Pfizer systems and databases, and applicable Pfizer policies and procedures.
Responsible for ensuring product strategies, submission and approval time lines, and country registration requirements/guidelines are accurately captured and current in applicable systems/regulatory databases.
Responsible for ensuring notifications of proposed regulatory changes are communicated to relevant stakeholders in a timely manner.
Participate in-functional project teams in line with business needs, Responsible for ensuring that comprehensive records of country requirements (communication of requirements for RRM updates) and regulatory status, are maintained.
To regularly follow up progress on regulatory submissions with In-Country Regulatory.
Contributes to the development of filing and approval goals for the region.
Ensure systems are in place and adhered to, to optimize process efficiency with out-sourced and in-house contractors, where applicable.
QUALIFICATIONS / SKILLS
Indicate qualifications and skills that are necessary for performance of responsibilities including: education, relevant experience, licenses, certifications and other job-related technical and managerial skills.
Scientific Degree. A higher degree (Pharmacy, BSc) may be an advantage but is not essential.
Appropriate Regulatory Experience : 4-6 years’ experience
Proven ability to manage complex regulatory or drug development issues.
Proven ability to consistently deliver to time, cost and quality standards.
Attitude: Right mindset, Outward looking, Strategically minded, Project management skills preferred
Country/regional knowledge (For AfME only – specifically, MER, NEAR, South Africa, Maghreb)
Knowledge of the Regional and Global regulatory environment and how this impacts regulatory strategy and implementation.
Knowledge of drug development practice, rules, regulations and guidelines.
Technical skills with respect to understanding of CMC submissions, BoH Requirements to identify potential risks
good communication, negotiation and interpersonal skills
Strategic thinking
Ability to manage complexity and negotiate skillfully under these circumstances
Change agile
Analytical thinking
Detail- and compliance orientation
Big picture thinking
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Operations Specialist At Majestic BioPharma Ltd
Job Description Summary:
1. Quality Checks for all company’s Finished Products and Packaging Materials.
2. Create Standard Documents for all Products.
3. Coordinate between our toll manufacturers about any quality issues.
4. Create all necessary documents to maintain a high-quality level for all our products.
Requirements Summary:
– 1 to 3 Years of experience in Quality Control
-Six Sigma Holder is a plus
– Very Good E-mail skills
– Very Good English writing skills
– CAIRO RESIDENTS ONLY Close to our Warehouse Location: Tagmo Industrial Zone ( الف مصنع )
– Pharmaceutical or Cosmetics industry experience is a plus
– Good Excel and Word Skills
– Owning a car is a plus.
Ø If interested, send your resume at: hoda.khalil@majestic.bio
Ø And mention “Operations Specialist “in the mail subject
Quality Vacancies At Grifols a multinational healthcare company
1-Quality System Specialist At Grifols
Grifols a multinational healthcare company is hiring:
Quality System Specialist
Requirements:
– science / pharmacy background
– 2 years experience
– TQM / CPHQ preferred
JD :
– Establish a defined Deviation procedure and CAPA system, involving appropriate stakeholders for investigation and closure.
– Prepare and review SOP’s related to Quality Systems following the guidelines established according to Egyptian regulations and the guidelines established according to cGMP requirements
-Compile all the information related to the different processes referred to Key Process indicators established for the Quality system
working conditions: Full Time – 5 days – 8 Hours
if you are interested kindly send your cv at
Doniaashraf776@gmail.com
2-Quality Compliance Specialist At Grifols
Grifols a multinational healthcare company is hiring:
Quality Compliance Specialist
Requirements:
– science / pharmacy background
– 2 years experience
– TQM / CPHQ preferred
JD :
– Prepare all the documentation related to Technical Information referred to Blood Establishments (Plasma Centers, Plasma Logistic Centers (PLC) and Plasma testing laboratory).
-Prepare Site Master file of all Blood establishments
– Compile all the information related to the different processes referred to Key Process indicators established
working conditions: Full Time – 5 days – 8 Hours
if you are interested kindly send your cv at
Doniaashraf776@gmail.com
3-Plasma Document Control Specialist At Grifols
Requirements:
– science / pharmacy background
– 2 years experience
– TQM / CPHQ preferred
JD :
– Prepare and review SOP’s related to Documentation Lifecycle Systems
-Compile all the information related to Documentation Lifecycle
-To ensure that documentation should be designed, prepared, reviewed and distributed with care
– To ensure that Documents containing instructions should be approved, signed and dated by appropriate and authorized persons
working conditions: Full Time – 5 days – 8 Hours
if you are interested kindly send your cv at
Doniaashraf776@gmail.com
4-Audit & Supplies Specialist At Grifols
Grifols a multinational healthcare company is hiring: Audit & Supplies Specialist Requirements: – Bachelor ‘s Degree in Health-related Sciences – Knowledge of Quality Audits preferred. – Knowledge of cGMP requirements preferred – 2 years experience – TQM / CPHQ preferred Job Description : – To perform Audits to all critical suppliers according to the established program. – To oversight for GMP audit activities, including training and continuous development of GMP auditors, and reporting on the GMP risks, trends and effectiveness of the quality systems to Quality Systems – Manager for further evaluation. – To carry out GMP audits of critical suppliers, subcontracted activities as well as corporate audits of Blood establishments and GMP systems. – To receive 3rd party audits as well as Health Competent authorities’ inspection. working conditions: Full Time – 5 days – 8 Hours if you are interested kindly send your cv at Marinageorgy96@gmail.com