Mega Vacancies in Medical – Pharmaceuticals and Food Companies
This is considered a comprehensive Mega Vacancies in Medical – Pharmaceuticals and Food Companies in different fields ( Quality Assurance – Quality Control – Production -Safety- Supply Chain and other medical jobs ) so keep reading and apply Now ..
1-Quality Control Inspector At Pharmaplast S.A.E.
Job description
We are currently searching for an experienced and highly-analytical Quality Inspector to join our production department. As the Quality Inspector, you will uphold the safety regulations of our company and supervise the production process to guarantee that all our products meet quality expectations.
The chosen candidate will perform regular product evaluations, record inspection results, and recommend improvements to the production process. To excel in this role, applicants should demonstrate great attention to detail with excellent technical and math abilities.
Responsibilities:
Company: Pharmaplast
Location: Alexandria/Al-Ajami area
Working hours from 3:30 pm to 12:00 night
Experience:0-2 years’ experience
Salary: negotiable
Email :
ahmed.abdelbaset@pharmaplast-online.com
Or
With mention in the title ” Quality Inspector ”
Details:
1) Monitor all supplied raw materials.
2) Monitoring the production process at different stages.
3) Selecting sample from production line at interval times for inspection and testing.
4) Carrying out tests on products by observing or measuring dimensions
5) Carrying out tests on products by observing or measuring weight
6) Carrying out tests on products by observing or measuring physical characteristics
7) Carrying out tests on products by observing or measuring chemical characteristics
8) Carrying out visual tests on products.
Requirements:
Academic Level/Bsc. Of science, or agriculture or any relevant Bachelor degree
· Experience: Fresh or 2+ experience accepted
· Excellent knowledge of MS Office.
· Good math and technical skills.
· Strong understanding of quality control standards and testing techniques.
– Skills:
– Goal setting.
– Effective planning.
– Effective management skills.
– Effective communication skills.
– Ability of keen observation.
– Analytical Skills, logical thought process and meticulous attention to details.
– Decision maker
– Ability to translate skills and knowledge to others.
2-Quality Assurance Specialist at Pharmaplast S.A.E.
Alexandria, Egypt
Job description
Pharmaplast company located in Free-zone, Alexandria, Egypt is hiring in QA Dept. Quality Assurance Specialist.
(Experience in Free-zones regulations is an addition)
Responsibilities:
The Medical Device Quality Assurance Specialist supports and reviews quality systems processes and serves to improve awareness, visibility, and communication on quality initiatives to support assigned quality goals and priorities.
Reports to QA Manager / Management to create new Quality System procedures/instructions.
Monitor and maintenance of existing processes.
Assist in internal and external audit.
Assist in creating and maintaining internal audit schedules and records including tracking CAPA activities as required.
Assist in and prepare for the execution of Notified Body audits and track progress of responses.
Assist in investigating quality issues and interact with products suppliers.
Review and investigate customer complaints, determine product failure root causes and evaluate risk of failures.
Ensure that the quality system is understood and applied throughout the organization on all levels by personnel concerned.
Authorizing product release to stock and completion of relevant records upon receipt.
Ensure that the change control process is done as per relevant SOPs and all related risks of the process is evaluated.
Doing and reviewing the data analysis of different QMS aspects and final validation reports.
To carry out any tasks given to him by the top management to achieve the objectives and any orientations in favor of the work.
Qualifications and Requirements:
Education Background: Bachelor’s Degree in Science, Pharmaceuticals.
Experience: 5+ years in QA activities
Alexandria resident is a must
Interested Candidates should send their C.Vs on HR@Pharmaplast-online.com with QA specialist in mail subject.
3-Microbiologist At Orchidia pharmaceutical
Orchidia pharmaceutical located in Oubor is hiring the below positions:
1- Microbiologist (Pharmacist, Science graduate- Minimum 1-3 year of experience).
Interested Candidates apply through this link
https://lnkd.in/eDbN_Fvz
4-Quality Engineer At Dreem Mashreq Foods
Excellent opportunity for ” Quality Engineer ” to join our factories in Borg Elarab
Engineering background is a MUST ,experience in quality is highly recommended
To Apply ,please send your CV on careers.dreem@mashreqgroup.com
, make sure to mention the job title in the Subject
5-QC Microbiologist Supervisor At Hikma Pharmaceutical
Job Summary:
Responsible for assisting a team of analysts, officers and/or technicians undertaking quality work. Job holders are involved in a full range of quality section responsibilities.
Duties & Responsibilities:
Provides leadership to assigned staff by performing the following: leading organizational change; developing and empowering staff; cultivating relationships; putting staff in a position to succeed, meeting their personal career goals while also achieving organizational goals; building effective teams that apply their diverse skills and perspectives to achieve common goals; driving engagement, accountability, and creating a climate where staff are motivated to do their best.
Supervises employees in day-to-day operations by spending at least 50% of available time interfacing with employees to optimize the resources and to fulfill established dates or defined priorities.
Coordinate, reviews and approves laboratory analysis.
Update and/or review operational procedures and methods of analysis.
Participates in meetings of departmental inter groups to respond to the necessities of other departments suitable.
Participate and support during internal and external audits
Trains or coordinates the training of the personnel to its position in subjects, related to testing methods, operational procedures, good practices of laboratory and safety.
Assure that the activities of the laboratory are in fulfillment with the applicable Hikma policies.
Evaluates new methodology and technology.
Provides support to the management in the reduction and the minimum maintenance of deviations and discrepancies. In case of deviation, the Microbiology Supervisor will supports the areas in the generation of the investigations and the fulfillment of preventive actions within the considered time.
Ensures safety rules are carried out in the microbiological lab and takes action to resolve any problems identified
Job Qualifications:
5- 8 year of successful experience (Sterile Area).
B.Sc. degree in Pharmacy or Science.
Preferably (Cairo, Obour, New Cairo, Nasr City, Heliopolis, Badr, Zagazig, Sharqiyah, and 10th of Ramadan) residents
Location: EG
6-Procurement Officer At Hikma Pharmaceuticals
Job Summary:
To ensure purchasing of requested Materials on time by the best quality, cost and search for better alternatives.
Main Responsibilities:
Preparing the POs depending on current inventory levels in the warehouses and the delivery time from suppliers.
Analyzing and studying monthly and weekly purchasing plans in order to establish the POs of the raw and packaging materials accordingly
Preparing the POs depending on current inventory levels in the warehouses and the delivery time from suppliers
Following up on the delivery status of placed POs to ensure timely delivery, avoid shortages, and address any issues that may arise promptly
Preparing for the establishment of the administrative and spare parts purchasing orders by identifying the requirements of all Hikma functions
Processing offers and quotations obtained from suppliers and recommending on the most suitable
Building and maintaining a strong relationship with suppliers in order to facilitate the purchasing process and create additional value
Participating in evaluating suppliers as per the set criteria and updating the approved suppliers list accordingly
Updating the SAP system with the necessary transactions when ordering or receiving raw or packaging materials
Job Requirements
1-3 years’ experience in the same field
BSc Science (Chemistry , Biochemistry ), Business Administration (English Section), or Similar.
Excellent command of English.
Advanced user of Microsoft excel.
Negotiation, Analytical, Follow up Skills.
Attention to details.
Location: EG
7-Validation Supervisor At Hikma Pharmaceuticals
Job Summary:
Responsible for assisting a team of analysts, officers and/or technicians undertaking quality work. Job holders are involved in a full range of quality section responsibilities
Duties & Responsibilities:
Manages significant validation projects delivering agreed objectives and high level of resource utilization
Leads the validation area, monitor performance and ensure high standard of efficiency by managing employees’ workload and priorities to guarantee productivity and efficiency of out-puts
Participate in the decision making for issues concerning validation within the facility.
Communicate effectively with other departments to facilitate validation activities.
Reviewing validation master plan of the site.
Reviewing of products Process validation protocols & Cleaning validation and protocols.
Reviewing of Analytical method validation protocols and reports.
Reviewing of QC instruments qualification and calibration activities and plans.
Reviewing of Production machines, R&D machines qualification activities and protocols.
Reviewing of Facility utilities qualification activities and protocols.
Reviewing of Environmental Monitoring reports/trends..
Reviewing of media fill qualification activities and steps ((intervention, video revision, data sheet revision, report creation)
Reviewing of Computer system validation activities.
Conducts some aspects of validation training and carries out an ongoing review of the effectiveness of the training.
Job Qualifications:
5- 8 year of successful experience (Sterile Area).
B.Sc. degree in Pharmacy, Science or Engineering.
Preferably (Cairo, Obour, New Cairo, Nasr City, Heliopolis, Badr, Zagazig, Sharqiyah, and 10th of Ramadan) residents
Location: EG
8-Methodology & Stability Specialist At Apex Pharma
Job Description
Analysis R&D Trials and Comparative Dissolution of test product against reference.
Preform Comparative dissolution file for submission to MOH.
Analysis stability sample & prepare stability Report.
Perform method development & analytical method validation.
Preparation of NODCAR files.
Preparation of MOH stability files .
Job Requirements
Bachelor of Pharmaceutical science.
2-5 years of experience in similar position in reputable pharmaceutical companies.
Problem solving and analytical skills.
Attention to details.
Good Communication skills.
Good command of English.
Professional using Microsoft office.
9-R&D Formulation Specialist at Apex Pharma
Job Description
Working with product pipelines at various stages of development: developing formulae, specification and label declaration, and ensuring compliance with the finished production targeted specification.
Assist in scaling up of new and development products via plant trials, making changes to raw materials or components and process parameters to ensure that targeted product quality is maintained during large -scale production.
Reviewing published technical reviews, research pharmaceutical references to keep up to date with industry development and modern technology.
Apply GDP for appropriate handling and maintaining of department records,technical reports and specifications.
Job Requirements
Bachelor of Pharmaceutical science.
2-5 years of experience in similar position in reputable pharmaceutical companies.
Excellent knowledge acumen of pharmaceutical formulation techniques.
Problem solving and analytical skills.
Attention to details.
Good Communication skills for effective liaison and teamwork.
Good command of English.
Professional using Microsoft office.
10-QC Raw Materials Analyst at Apex Pharma
Job Description
Analyzing Raw materials samples and method validation.
Able to perform on different lab instruments (HPLC, GC, Atomic absorption) will be an advanced.
Prepare different volumetric solutions, chemical reagents used in routine analysis.
using different pharmacopeias
Job Requirements
Bachelor of Pharmaceutical science or Science.
3-5 years of experience in QC department in Pharmaceutical field.
Excellent knowledge of method validation.
Attention to details.
Problem solving skills.
Active learning.
Time Management skills.
Professional using Microsoft office.
11-Senior Regulatory Affairs Specialist At Apex Pharma
Job Description
Lead and plan the review of submission of the new/renewal of company products based on company plans, regulations and guidelines,
Obtain and ensure approvals are maintained as long as product in the market, working as interface between the regulatory authorities and the company, timely strict follow up for all regulatory tasks, perform duties as assigned.
Working with team and develop registration track record for company work.
Provide all the required reports.
Comply with company rules and regulatory department objectives, managing ,coordinating and documenting internal regulatory processes.
Follow up annual regulatory plan execution.
Job Requirements
Minimum 5 years of regulatory affairs experience
Bachelor of pharmaceutical science
High level of communication skills and priority setting
Awareness of all regulations and guidelines related to regulatory functions
Prompt respond to authorities requirements and promptness in deliverables
Good command of English language .
Professional using Microsoft office.
12-QA IPC Supervisor At EVA pharma
Giza, Al Jizah, Egypt
Job description
EVA Pharma is a company who fights for health and wellbeing as a human right, successfully operates in branded generics, OTC, food supplements, herbal medicines, and veterinary products. Being a Global Pharmaceutical company operates in more than 40 Countries, having a diverse top team of more than 100 professional associates across the globe, EVA Pharma is one of the leading branded generic pharmaceutical manufacturers in the MENA region.
EVA Pharma is looking to have a “QA IPC Supervisor“
Please Check the following questions?
-Are you responsible for tracking and trending results, in addition to participating in deviation and complaints’ investigations and change of control action plan?
-Are you able to ensure timely completion of QA procedures, manufacturing, and packaging and in- process sampling ?
To succeed in this role, you should have the following skills and experience:
– Bachelor’s degree of pharmacy.
– 5-6 years of experience in the same field.
– Fluency in spoken & written English.
– Giza Or 6th Of October Residents are preferred.
13-Production Shift Team Leader At Mars egypt
Do you wish to work on iconic brands like Galaxy, Twix and Jewels? Do you wish to work with a Company with a more than 100-year legacy of delighting people and pets? If you are an Engineer, we are looking for our next Production Shift Team Leader at our Egypt Factory located in 6th of October.
Lead teams and work in the house of widely loved brands. Start your tomorrow today with Mars! Apply on careers.middleeast@effem.com
14-Stability&Methodology pharmacist At pharo pharma
pharo pharma is hiring for it’s factory in borg Alarab-Alexandria
Job duties:
doing the necessary stability studies for the new Products (pilot)
Doing stability studies on the product containing the active ingredient from a new source.
doing stability studies in case of changing or modifying the composition statement for inactive substances.
Receive Deviation from production to conduct the necessary stability study for it and determine the results
Conducting accelerated stability studies to test a new formulation of the product
follow up Registration process in different log books of Department.
development Analysis Methods for some products to be (stability indicating)
Follow up the department’s stock of chemicals
Job requirements:
Bachelor of pharmaceutical Science
1-2 years of experience in pharmaceutical analysis
Good computer skills&English language
Problem solving
Creativity&innovation
Teamwork player
Alex Residents only
انهاء/الغاء التكليف الحكومى
if you are interested, kindly send your CV at careers@pharopharma.com mention job title in subject “Stability&Methodology pharmacist”
15-Filling & Packaging Supervisor at EVA Cosmetics
Job Objective:
Assist Production Manager in achieving production output in the most efficient way through applying lean concepts.
Job duties & Responsibilities:
Responsible for ensuring that production activities in the plant are performed in accordance to codes of Good Manufacturing Practice (GMP)
Responsible for all aspects of mixing development activities that include upgrading of products quality, process validation and trouble-shooting.
To liaise with other departments in day-to-day operation.
Controls production process and production facilities and ensure that manufacturing activities comply with all standard yields along production lines are maintained.
Ensures the general cleanliness and hygienic conditions of the manufacturing areas and production personnel.
Prepares, review and analyze daily/weekly/monthly production reports indicating relevant KPI’s.
Responsible for the electronic production monitoring system for tube filling machines, review data posted.
Ensuring that the safety, environmental and health regulations are being adopted and properly applied
Coordinating with the Quality function to ensure compliance of processes to quality guidelines and SOP’s
Conducting regular maintenance investigations to check and ensure efficiency of production machines at the shop floor and recommending corrective and preventive maintenance actions when the need arises
Assist in manage risk assessment for product operation and equipment used.
Manage with production staff the periodic shut down for maintenance schedule and report malfunction in machines that have severe impact on the production plan implementation to the production manager.
Assist in monitor & enhance the performance of different manufacturing machines and Filling & Packaging lines and direct the team to carry necessary improvements to run smooth manufacturing sequence and to achieve required production plan on time.
Ensure the process validation and clean validation plans to production staff, handle deviations in these plans.
Deliver on job training for new hires in order to guarantee compliance of production operations to proper procedures according to recently updated SOPs
Responsible for change control issuance and follow up with the action plan
Responsible for deviation handling system in production area, follow up for the CAPA
Responsible for production projects’ management.
Job Requirements
Bachelor’s Degree in Agriculture or Science majors.
5-7 years of experience in the Cosmetics or Pharmaceutical Industry.
Management skills
Experience in process design and validation.
Interested candidates can apply through mail hr@eva-cosmetics.com mentioning job title
16-مشرف أنتاج في شركه كوكي أمريكانا
شركة كوكي- أمريكانا تبحث عن استقطاب المواهب بوظيفة
#مشرف #أنتاج (بمجزر النوبارية).
المسئوليات الوظيفية:
– مسئول عن أجراء الفحص الظاهري لقطعان الدواجن الحية والتأكد من عدم وجود أي علامات مرضية وخلو الدواجن من أي فيروسات وكذلك التأكد من سلامة الشهادات الواردة من المزارع.
– تنفيذ الخطة الإنتاجية والأشراف عليها من عمليه الذبيح
– التأكد من سلامة عملية الذبيح حسب الشريعة الإسلامية ومتطلبات الجودة وذلك بحضور مسئول قسم الجودة.
– الأشراف على عمليه الاستبعاد الطبي للدواجن النافقة والغير صالحة.
– تجهيز العينات بطريقة صحيحة تضمن عدم التداخل أو التلوث وعدم التأثير في دقة الفحص أو سلامة النتائج
– توزيع المرؤوسين طبقا للأعمال الإشرافي في نطاق عمله واحتياجات العمل.
– تطبيق انظمة ومعاير الجودة العالمية بشكل فعال على سلامة المنتجات التي تحقق سياسات الجودة بالشركة.
معايير الوظيفة:
– بكالوريوس طب بيطري.
– خبرة سنة أو سنتين في مجازر الدواجن.
– إجادة مهارات التعامل مع برامج مايكروسوفت اوفيس.
– اجادة المهارات القيادية والقدرة على تقديم الحلول المناسبة للمشكلات.
مميزات العمل:
– تأمين اجتماعي وتأمين طبي خاص.
– صندوق زمالة.
– منح مالية مجزية بالأعياد والمدارس.
– أرباح سنوية مجزية.
– وسيلة مواصلات.
التقديم على الرابط أدناه:
https://lnkd.in/d7tkUFrv
17-HSE Supervisor At Unicharm Middle East & North Africa – Hygienic Industries
Unicharm Middle East & North Africa – Hygienic Industries –Babyjoy Hiring: HSE Supervisor Job Location: 10th of Ramadan Job Requirements: · Bachelor’s degree in (Science / Engineering). · Experience 5-8 Years included 2 years for senior position. · Work for FMCG Industry (Manufacturing, FMCG) is a must. · Has the certificates (شهادة اخصائى سلامة معتمدة سارية / شهادة أعضاء لجان ). · Hold NEBOSH/ or IOSH is a must. · Very good experience in ISO audits (9001,14001,45001) . · Excellent communication, leadership skills. · Ability to work without direct supervision. Suitable candidates shall send their CV to
ahmed-tawfik@unicharm.com and mention job title in the email subject.
18-Food Safety Supervisor (Bani Suef factory)) At Olam
Responsibilities
He will be accountable to ensure that all Food Safety Management Systems (FSMS) and processes are in place.
To ensure the development of systems, training, implementation, audit and progress review and effectiveness of implementation and ensuring sustainability.
Support activities to achieve compliance with Olam Quality Management System requirements and other applicable instructions and standards.
Develop Pathogen Monitoring Plans for the Factory.
Integrated Pest Management (IPM) Specialist & Contact Point for the Factory.
Regular traceability audit & report to management
Analyze trend of the results & follow-up for the deviating results
Qualifications
Preferably Bani Suef residents (Work location – Bani Suef)
3-5 years of experience in the Food industry.
BSc. of Agriculture or science.
Analytical thinking, Decision maker, and problem solver.
People-oriented and Detailed oriented.
Very Good MS Office skills particularly in Excel, Word, and Powerpoint.
Quality Standards
19-Quality Manager At Cilantro
Qesm El Maadi, Cairo, Egypt
Job description
Cilantro is one of the fastest-growing tech-enabled F&B chains in Egypt with a network of 85+ stores that operate all across the country. The company is on a mission to become the #1 F&B operator in the region, and to do this we’re looking to build a team of superstar “A” players.
Cilantro, a Cairo-born brand established in 2001, has always been a first-mover and a pioneer in the local F&B market. Our aim at Cilantro is to Create Magic Moments every day through Outstanding Hospitality, Delicious products, Best Value, and Great Convenience.
We have a culture that rewards results and impact. We are data-informed, we work in teams and we respond fast to market and consumer needs. Our team is agile, results-driven, and passionate about delivering amazing customer experiences.
Key Responsibilities & Duties
Embed a Quality mindset into all business partners to focus on the consumer.
Lead quality escalations to mitigate the impact, define root cause, and implement robust corrective action.
Lead quality KPIs discussion, focusing on improvement actions to meet the target.
Establishes work procedures and processes that support standards, procedures, and strategic directives.
Assists with development, compliance, documentation, and maintenance of standard operating procedures (SOPs) across the entire company.
Measure performance and identify any areas of weakness, recommending and implementing improvements through aligning with departments’ heads.
Liaise with other managers and staff and provide training plans, tools, and techniques to enable others to achieve quality standards.
Lead a team of internal auditors, conducting quality and safety audits of production sites, warehouses, and retail points for compliance with national laws and internal
Restructuring Quality Dep.
Recruiting, staffing, and coaching A players in the Quality team
Developing 1 Q manager successor and creating a second line of potential Q managers
Developing, implementing, and improving all Q Processes and Key Processes.
promote fact decision base in the company
visualize and Digitalize Quality attributes (complaints, CAPA, Audits, ) to facilities decisions
The ideal applicant should have:
Bachelor’s degree in Food Science, Chemistry, or related science field.
Minimum 3 years of experience in a similar role leading Quality Management systems
At least 5 years of people management experience with the ability to connect, motivate and change behavior.
A strong F & B industry is a must.
Internal Audit, PCQI, HACCP, and SFQ Practitioner certification preferred
Quality control certification is advantageous.
Excellent verbal and written communication.
Data analysis and statistical aptitude.
Good interpersonal skills.
Highly conscientious and diligent.
A keen eye for detail and a results-driven approach.
20-Senior R&D Specialist – Pharmaceutical at CIRA Pharma
Cairo, Egypt
Job Purpose:
Design the formula – Formulate – Test – Develop Prototypes whenever necessary – Validate and test stability – create pilot scale and liaise with production for large scale
Main duties & Tasks
Including but not limited to: –
– Formulate, research, test, stabilize, troubleshoot, validate specifications, and perform other research activities related to the Cosmetic industry.
– Successfully prepare creams, shampoos, solutions, gels, emulsions, ointments, and lotions formulations.
– Prepare presentations for new products range.
– Develop batches from scratch; and improve upon and scale up existing batches.
– Review current formulations and optimize for better performance and optimal ingredients.
– Optimize manufacturing processes of current and new products lines.
– Analyze all changes to existing formulas to determine proper testing and stability effects.
– Assist manufacturing with adjustments/troubleshooting relative to formulation batching/mixing.
Qualification:
– Bachelor’s Degree in Pharmacy only
– 2-3 years of experience in the same job title preferably in the cosmetic industry
– QC-QA courses /Masters in Pharmaceutical Sciences in any of these fields: Pharmaceutics / Pharmacology / Clinical is an additional privilege
– Excellent command of English.
– Very good user of the MS office package.
– Analytical thinker and critical problem solver.
– Time manager and independent worker.
What we are offering
– Very attractive package
– A healthy work environment for learning, development, and growth within the company.
– A knowledgeable, high-achieving experienced team.
– The chance to be a part of a rapidly growing startup and the next success story.
Seniority level
Entry level
Industry
Pharmaceuticals
21-Supply Chain Quality Officer At Pfizer egypt
Organization overview
The key role of Pfizer SCQ is to establish and maintain an appropriate and sustainable Product Quality System and Quality Culture within Pizer and any contractor related to GMP/GDP activities, so that compliance with Pfizer and Regulatory authority expectations and protection of Pfizer patients/customers from any product quality risk are ensured. SCQ is the main point of contact for the investigation and resolution of all product quality issues discovered or originating in the PCO and for interacting with the relevant stakeholders and local regulatory authorities on such issues. Coordinates and monitors the product quality and compliance activities at the PCO to ensure that current regulatory expectations are met and facilitates internal and regulatory GDP inspections.
Role description and Main responsibilities
1- Maintenance of the compliance to the local BOH regulations
Coordinate the product quality and compliance activities at the PCOs, to ensure current BOH expectations are met.
Act as the Qualified / Responsible Person to local authorities or support Qualified Person activities for all Pfizer Product Quality Compliance issues in the market.
2. Governance & internal organization
Supports timely implementation of all applicable Product Quality SOPs (issued by SCQ) within the PCO.
Ensures that all relevant PCO colleagues are appropriately trained in the Product Quality SOPs.
Assess new quality system and local regulatory requirements to enhances and align local systems and processes when required.
Conducts and documents periodic assessments to determine if a revision, retirement, administrative change or no change is required for the Product Quality SOPs (issued by SCQ) within the PCO.
Quality Metrics Management
Commitment Tracking Management
Change Controls
Handles any planned, permanent and temporary changes of GMP/ GDP related activities and systems in the PCO.
Participates in the changes committee as appropriate and ensures the required approvals.
Ensures change actions completion as per the agreed timelines.
Inspection and Internal Audit
3 Product quality assurance & operations
Notification to Management
Informs SCQ manager of any significant deviations and complaints, that could lead into a NTM.
Ensure notification is done within the appropriate timeline and process.
Deviation Management
Perform, if needed, investigation of product quality incidents that occur within the responsibility of Pfizer country office in cooperation with the relevant internal/external functions.
Track the preventive and corrective actions until completion within the set due dates.
Product Complaint Handling
Manage the intake and triage of complaints from the markets under PCO responsibility, classify the product complaint, and forwards them to the appropriate investigating PGS/Contractor manufacturing site via the global complaints management system (QTS-CITI).
Develops and issues responses to complainants in a timely manner
Tracks complaint responses.
Notifies the Management when needed.
Local Product Disposition & Temperature excursion
Review all documents and records relevant to the imported products and perform the necessary activities to provide a disposition decision to the products to the market sale in compliance with local regulatory requirements and Pfizer procedures.
Communicate the disposition decision with internal and external stakeholders.
Document any temperature excursion and coordinate with manufacturing site for assessment and via the global Quality Tracking System (QTS).
Years of experience: 2-5 years in the Pharmaceutical or related regulated industry
Technical skills
Has an appropriate education in science or quality topics; Bachelor’s degree, pharmacist, Engineer.
Has basic knowledge of the Quality principles, concepts of Quality and basic technical skills
Has basic knowledge about Quality Systems (Change Control, deviations, complaint management, documentation management, audits, inspections, etc.)
Able to Participate effectively in cross-functional team
Analytical skills
Basic level in English
22-Production Section Head at ARMA Group
Arma Group is hiring Production Section Head as follows:-
-Job Requirements:-
1-Bachelor Degree in Engineering (Chemical-Industrial-Production) Major
2-Experience from 5 to 8 Years in Production
3-FMCG Experience is Preferred
4-Cairo or Sharqia Resident is preferred
-Work location :-
10Th of Ramadan-Sharkia(Transportation provided)
-Duties :-
1- Review day-to-day productivity and compile production report to ensure that Production plan is achieved .
2- Increase production, assets capacity and flexibility while minimizing unnecessary costs and maintaining current quality standards to Maximize the production and minimize cost.
3- Discuss, analysis and solve section achievements and obstacles to stand on section pros and cons to continuous success and overcome difficulties.
4- Appraise labors performance quarterly, coach and mentor daily progress to improve People performance.
5- conduct weekly maintenance plan in cooperation with engineering dept.
6- Ensure the implementation of the requirements of industrial security to Maintain safety at work.
If you are interested, please send your CV on :- ramy.mokhtar@arma.com.eg writing the Job title in the email subject
23-Senior HSE Specialist At EVA Cosmetics
Job requirements
BSc in Science, Agriculture or Engineering with an overall grade good or above
with post graduate studies in HSE, First Aid & Firefighting
Good Computer skills proficiency
Very Good English Language Proficiency
Must have minimum of 2 years’ experience in the area of Cosmetics /Pharmaceutical HSE department
To apply: submit your CV to
hr@eva-cosmetics.com
mentioning HSE Senior Specialist in the e-mail subject
24-QA Manager At Viatris Egypt
Key responsibilities for this role include:
Ensure that GMP standards, as they apply to the individual products and the site, are in compliance with Viatris and regulatory standards
Design, implement and improve QA systems and auditing procedures.
Insure implementation of data integrity program within QA and on-site operations level.
Review and approve SOP’s, validation protocols and reports, annual product review as required.
Responsible for QA resource planning including preparation of budgets and monitoring budget adherence with QO manager.
Coaching and developing QA colleagues towards achieving high performance.
In-process control activities: insures that a system is in place that a predetermined control stages that insure building of quality inside the product.
Approve Deviations / Complaint handling system: Assure that all deviations are properly investigated prior to the release of the batches, Managing all quality issues regarding investigations & complaints
Change Control system: Be a key member of the Site Change Control Board and assure adherence of change control procedure
Assure follow-up of the changes with Regulatory Impact.
Periodic product review: Approval of risk assessments for annual review plan insures its implementation and approve of annual product reviews.
Product complaint: Review and Approval of Quality related product complaints investigation.
Manage the overall assurance and disposition of products produced at the manufacturing site.
Ensure a system is in place for validation/qualification/
Approve validation master plans and SOPs.
Review/Approval of validation protocols and reports.
Approval of calibration program, calibration plan.
Member of routine and Ad hoc SQRT meetings.
Prepare monthly quality metrics to follow-up the performance of quality functions.
Coordinate Technology Transfer activities of Manufacturing Procedures to other sites.
Plan the preparation for and management of quality-related audits conducted by Corporate and regulatory agencies.
Support and identify site Right First-Time initiatives; this includes coaching of M1 and M2 Projects and Light Lean (Kaizen) projects
Ensure that appropriate systems are in place to meet or exceed the requirements of the company and the regulatory authorities for the quality of the products manufactured on site or by approved vendors.
Implement appropriate QO self-appraisal processes to ensure compliance of VIATRIS-Cairo operations with Viatris and regulatory requirements.
Interface with regulatory agencies to discuss lot records, manufacturing procedures, test results, and labeling.
Responsible for implementation of Data integrity program in the relevant work area and Insure following up ALCOA principles all over operations.
Active implementation of Notification to Management procedures.
Responsible for compliance with Viatris Quality Standards.
The minimum qualifications for this role are:
Personal and Technical Skills
Robust Knowledge of GMP Guidelines in Pharmaceutical Industry
Strong Advocate for Quality and GMP Compliance
Lead Auditor
Good command of English both written and spoken
Leads by example and follows through on commitments
Strong Project Management Skills
Good Communication and Problem-Solving Skills
High Precision and Accuracy
Decision making skills
Education and Experience:
Bachelor’s degree in Pharmaceutical Sciences
Minimum 8 years’ experience in pharmaceutical operations with minimum of 2 years in managerial role
Quality management certification is a plus
At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others.
25-Yeast Cell Culture Fermentation Specialist At Minapharm Pharmaceuticals
Summary
Perform fermentation processes in yeast cell culture area of RM-BG, and all related tasks ensuring successful fermentation runs to achieve the company’s goals.
Tasks
Strongly obey all GMP rules related to the field of employment.
Operate production equipment necessary for production process in YCC fermentation area, perform yeast fermentation processes according to production plan, supervise the technicians during the production process, and support continuously analyzing the production process aiming at process understanding and improvement.
Follow up maintenance of production equipment as per defined plan.
Receive and keep documents (SOPs, validation protocol, change control, etc.), issue new SOPs and revise approved SOPs according to revision plan according to instructions.
Notify timely supervisor and QA about all incidents, participate in investigation and assessment of incidents, deviations and changes, perform root cause analysis and contribute to SMART corrective and preventive actions for audit findings, implement CAPA, additional controls, change control actions, annual report actions and management review actions according to instructions.
Participate in process and cleaning validation as defined in relevant protocol, participate in equipment internal calibration according to instructions.
Issue materials and tools dispensing order needed for the production process and follow up relevant stocks.
Support supplier qualification for raw materials and consumables used in production process.
Contribute to quality risk management projects, support continuous process improvements, report and support assessing environmental hazard aspects and impacts, report and support assessing health and safety risk assessment.
Strongly cooperate with other departments (for instance DSP, QA, QC, warehouse) aiming at smooth and efficient production and process flow.
Experience:
From 2 to 3 years in bioprocess manufacturing.
Education:
Bachelor’s degree in Sciences, Pharmaceutical Science, or related fields.
Knowledge:
Basic GMP.
Knowledge of Biotechnology processes.
Basic analytical methods.
Abilities:
Ability to apply the biotechnology production process.
Ability to understand and follow written instructions.
Ability to express him/herself in clear language.
Quick learner.
Computer Literate.
Fluent in the English Language.
Behavioral Competencies:
Self-organizing skills.
Communication skills to all levels of staff.
Analytical skills with attention to detail.
Flexibility according to the needs of the processes.
If you are interested, please send your resume to aisaac@minapharm.com quoting the job title in the subject field
26-Process Specialist At Novartis Egypt
Job Description
Shift Lead II -Represent production management to the team members and promote Novartis values within the team -Line responsibility and shift walkthrough -Engage and motivate the team and delivers strong results with an empowered team -Process Expert -Provide front line expert support for all process-specific issues to production -Act as Subject Matter Expert (SME) for the product and process -Coordinate and ensure the completion of all production operations on time, in accordance with the documentation and in compliance with GMP, SSE and 5S rules Operation Scheduler -Is responsible to provide a feasible plan to the shop floor in terms of materials and capacity availability -Establish optimized sequence of orders within the Planning Time Fence and keep it up to date, based on rules agreed by manufacturing, Quality and other support functions and in accordance with Customer requirements -Provide the planning status in the daily production meeting -Manufacturing Systems Expert -Define User requirement specifications (Voice of customer) -Design and create electronic batch files (EBR) with respect for quality, costs and deadlines -MBR / BOM/ Recipe creation in production IT systems -Participate in the qualification and risk assessment processes -Technical Trainer -Delivers engaging technical training programs, using multiple delivery methodologies (OJT, Classroom, virtual classroom etc.) to support qualification of associates to perform technical tasks and develop technical capabilities -Design and develop technical training programs, aligned with the site strategy and local training plans -Present site training strategy and respond to auditor questions -HSE and Quality -Promote and improve the HSE culture, by implementing the necessary systems and actions in line with the evolution of the site -Promote and improve the Quality culture in collaboration with Quality Assurance. -Ensure overall inspection readiness for area of responsibility
Minimum requirements
Operations Management and Execution Project Management Collaborating across boundaries Functional Breadth People Challenges Major Change English Transportation Manufacturing Process Execution General HSE Knowledge Managing business continuity Knowledge of relevant tools and systems
27-Medical audit and rejection coordinator at Dar Al Fouad Hospital
Dar Al Fouad Hospital Nasr city is hiring Medical audit and rejection coordinator with following requirements:
– Bachelor degree in Medicine and surgery
– At least 2 years experience in insurance industry
– At least 1 year experience in reconciliation and rejection management is preferred
– Excellent command of English
– Excellent communication skills
– Data analysis skills is preferred
Interested candidates can send their updated resume to
Careers.nc@daralfouad.net with title of ” Medical Audit and rejection
28-Infection Control At City Hospital
Job description
We are hiring for City Hospital .. (part time)
-Infection control specialist
Excellent organizational skills.
Excellent communication skills.
Good presentation skills.
Experience : 4 years in hospitals (minimum)
Education: ( medicine- pharmacy-vet- nursing)
Gender : Both
Location : Alexandria
Type of work : Part Time Job
Our Mail to send your resume :
jobs.healthcare.ch@gmail.com OR WHATS APP01550992089