, pub-2091334367487754, DIRECT, f08c47fec0942fa0 Collective Jobs in Quality - Production- Research - Safety

Collective Jobs in Quality - Production- Research - Safety

 Collective Jobs in Quality - Production- Research - Safety

Collective Jobs in Quality - Production- Research - Safety

Biologics R&D scientist At EVA pharma

Job Score Card
familiar with aseptic technique operations
perform passaging of viruses via egg-based platform
familiar with molecular biology & virology techniques, are you eager to learn new skills
Bachelor’s degree in Biotechnology/Veterinary/Science
0 - 3 years of experience in veterinary vaccine development
Proficient English language is a must.
Eager to learn new techniques, and ability to communicate and work in cooperation with other employees in the company environment.
Strong attention to detail and documentation skills are required, in addition to proficient knowledge in mathematics and computer skills are required.
Experience in egg-based vaccine production or development is an add-on.
Job Details
Job Location
Cairo, Egypt
Job Role
Research and Development
Employment Status
Full time
Employment Type
Number of Vacancies
Preferred Candidate
Career Level
Entry Level
Years of Experience
Min: 0 Max: 3

Apply Here

QC Serology & Virology Scientist At EVA Pharma

Job Score Card
Perform serological analyses such as ELISA & Immunoassays (HI, HA,)
Learn new techniques for virus vaccines characterization & release testing.
work in a controlled facility to produce high quality vaccines
adhere to QA/QC standards and assist with preparation and updating of SOPs and validating new assays
- Bachelor's Degree of Biotechnology/ Science / Veterinary

- 0-3 years’ experience in the same field

- Excellent command of Microsoft office Professional (word, Excel, Power Point, MS Outlook).

- Fluency in English is a must.

- Giza Or 6th Of October residents is preferred

Job Details
Job Location
Cairo, Egypt
Job Role
Quality Control
Employment Status
Full time
Employment Type
Number of Vacancies
Preferred Candidate
Career Level
Entry Level
Years of Experience
Min: 0 Max: 2
Bachelor's degree

Apply Here

Quality Specialist At Cleopatra Hospitals Group -Al Shorouk Hospital

Job Description
Ensure implementation of policies & procedures
Performing Inspections & Quality Test to ensure efficiency of quality system
Addressing and discussing issues and proposed solutions with superiors
Presents the quality evaluation of hospital services in the hospital quality meetings
Assist in internal surveys to measure the hospital performance on regular basis
Detect coaching needs and take actions in accordance with these needs in order to ensure compliance with quality standards
Actively participates on or facilitates committees such as: infection control, drug committee, blood bank, ..etc.
Performs other related duties as requested by the head of the quality department.
Job Requirements
Physician , Pharmacist , Dentist, Nurse
Male is Preferred
HealthCare Quality Management Certificate (TQM-CPHQ-MQM)
At least one-year experience in healthcare facility is a must
Advanced communication skills.
Organized and detailed orientated.

Apply Here

Pharmacists At EL Rezeiky Pharmacies

EL Rezeiky Pharmacies is  Hiring - Pharmacist

( Ain Shams – Abassia)


Education : Bachelor of pharmacy
Experience : 1 – 3 Years Solid Experience at Pharmacies
Software: Softech - Be connect - SAP
Interested Candidates can Send Their Resume to:
For Any Details Phone Us On: 01000404235

Quality Control Manager At first food industries

I’m #hiring for First for Food Industries. A Quality Control Manager  position with the following requirement:
** Bachelor’s Degree in Agriculture, Science, or any equivalent.
** Experience 2 - 5 years in the same position.
** Experience in Herbs, Pulses, or Spices is Must.
** Strong verbal and written communication skills.
** Ability to foster and promote a positive work environment.
** Working knowledge of AS ISO 9001, FSSC 22000, and BRC requirements.
** Must be able to multi-task and work in a fast-paced environment.
** Strong analytical skills.
** Proficient with Microsoft Office (Word, Excel, PowerPoint, Access).

Send your CV to

R&D Stability Pharmacist At Orchidia Pharmaceuticals 

Job Description
Participate in Translating business goals into plans that cover local market and export.

Participate in Preparation of new products stability files to be registered and launched onto the market in accordance with local regulatory requirements and requirements of export under the general supervision of the R&D manager.

Execute plan of stability studies covering first three batches, process validation, and change or add supplier, change composition & ongoing stability study covering for all products.

Monitor of stability temp. & humidity and ensure of archiving them

Prepare protocol for each stability studies containing summarized data and results.

send stability samples for micro analysis (sterility or preservative effectiveness test) for long, Acc. & in use

analysis of the new product under stability condition must meet the product specification especially impurities

update SOPs related to stability system & covering R&D activities

Report problems relating to products in stability chambers to R&D manager immediately.

Maintain & enhance capacity of stability chambers to cover different dosage form

Work according to R&D safety system.

Work according of GLP requirements

Bachelor's degree a must, in Pharmaceutical science.

One year of technical experience in stability, analytical method validation and training preferably in the pharmaceutical industry.

Scientific, technical background in pharmaceutical as well as cosmetics products is beneficial.

Using an advanced knowledge of stability and method validation techniques.

Excellent English, verbal / written communication.

Ability to communicate well and work through others.

Excellent computer skills.



Good problem solving skills.

Good communications skills.

Good self-management skills.

Capable of working in a team environment.

Interested Candidates send their CVs to Mentioning position name in subject

Quality Assurance Specialist (QA IPC) At Orchidia Pharmaceutical Company 

Job Description

Inspection on the dispensing process.

Inspection on the division of the ware house the release area, guarantee area and the reject area with the true identification labels.

Follow up the check list of the RH, Temp. At the different places at the ware house.

Inspection on the destruction process for the rejected finished products, raw materials and packaging materials.

Inspection on the raw and packaging materials and ensure its comply with the acceptance criteria.

Inspection on the gowning according to the SOP.

Inspection on the preparation process including check the weight of the raw materials, changing the filters, the CIP process and the SIP process.

Inspection on the autoclave activities with different sterilization programs.

Inspection on the filling process at the filling room and ensure that the area is clean from any previous product and that the machine is cleaned and sterilized for the new product.

Check the environmental monitoring for the sterile area.

Check the RH, the temp. And the Δp of all the sterile area according to its classification.

Check the weight, the shape and the sealing of the filled bottles.

Inspection on every process according to the batch record and ensure that the line clearance process are completed between every product.

Taking the samples to the Q.C department as the bulk sample: for ph. and assay, bio burden for microbiology.

Taking the samples to the Q.C department as S.F.P. sample: for finished analysis and sterility analysis.

Review the recording of all the production steps at the batch process and the batch packaging.

Release the batch to the guarantee area after the final reconciliation by the yellow label, then by the green label after the certificate of the chemical and microbiological analysis.

Include recording all the deviation which occurs at all the production process and writing the corrective and preventive action.

Recording any complain from any customer from any product and investigate about the reason of the problem and solving it.

Making internal audit on all the departments of the factory and recording the points which deviate from the right process and informing each department by its point to follow up this points and solving it then inform the QA by the corrective action which they did.


- BS in pharmacy, biology or chemistry.

- 1 - 3 year of experience in pharmaceutical operations.

- Understanding of methodologies and best QA practices

- Knowledge of documentation reviews and requirements analysis.

- Ability to troubleshooting and resolving complex issues effectively.

- Excellent English, verbal / written communication

- Ability to work well through others

- Excellent computer skills


Pharmacy or Science

Job Details

Job Location

Cairo, Egypt

Job Role


Employment Status

Full time

Employment Type


Manages Others


Number of Vacancies


Preferred Candidate

Career Level

Entry Level

Years of Experience 

Min: 1 Max: 3

Residence Location

Cairo, Egypt






Bachelor's degree

Interested Candidates send their CVs to Mentioning position name in subject

Medical Claims Assessment Coordinator At MEDMARK

MEDMARK is #hiringnow  Medical Claims Assessment Coordinator.

Qualifications required:

- #freshgraduates  graduates are welcome to apply.
- Pharmacy Graduates.
- 0-1 years of experience.
- Fluent English language.

Location: Cairo - Mohandesin.

If Interested please send your resume to

R&D Methodology Analyst At Alandalous Pharmaceuticals Industries

Alandalous Pharmaceuticals Industries is now hiring

R&D Methodology Analyst

Job Requirements 
-Bachelor degree of pharmacy or Science .
-Experience from 1:3 years in the same position .
-Pharmaceutical experience is a must .
-Preferably 6th October city residents or nearby.

If you are Interested, please send your updated CV to
E-mail subject should contain code 𝐑𝐃𝐌𝐞𝐭𝐡𝟎𝟎𝟏
,otherwise your CV will be ignored.

Health and Safety, Team leader At Noon

What you’ll do:

Ensure, in accordance with the Corporate guidelines, the implementation, updating, review and auditing of the Company HSE Systems

Enforce safety practices and procedures

Supervise and maintain the safety management process and procedures within the organization.

Ensure commitments to PPE to all staff and employees

Prepare safety toolbox talk topics.

Support the fulfillment department in their daily operations for any safety-related issues

Support implementing 5S projects

Provide monthly training to all employees

Support HSE Supervisor/Manager to conduct method statements, risk assessment..etc

Conducts Monthly checkup on the fire extinguishers

Conducts monthly inspection for First aid boxes

Carry out Weekly reports for the unsafe findings/acts

What you’ll need:

Bachelor's Degree in Engineering/sciences or relative fields

2-4 years of experience in E-commerce in a related field

Having NIOSH certificate is a Must

Excellent interpersonal and communication skills, with the ability to build relationships with internal and external stakeholders

English Language Level (reading/writing) = Good

Basic knowledge of HSE

Results-oriented and tenacious

Comfortable communicating at all levels of seniority within a large organization.

Experience managing change in multiple site environment and managing multiple direct reports

Risk assessment/management

Administrative policies and procedures

 Apply Here

Production Engineer At Scib Paints

Scib Paints looking for Production Engineer fresh graduate 1 up to 3 years in production filed, job location 6th October City, please send cv on

Quality & SAP Deputy Manager At Edita For Food Industries

Main Purpose:

Responsible for the business module of SAP within the industrial operation quality department with the main scope of (Designing, Creating, implementing and ensuring SAP processes in addition to participate in quality assurance responsibilities for warehouses and distribution centers


Lead the SAP business module and information security covering the IO department and manage the integration and implementation with stakeholders and supporting central functions
Manage the different module platforms according to business dynamics through developing SAP reports and queries to management.
Lead the quality assurance and system maintainability along with follow-up of corrective actions to ensure that the system is sealed.
Designing and initiating financial issues (Budget) required for the needs and feasibility of introducing new technologies that integrates with SAP for business efficiency and cycle’s improvement.
Partner with R&D department on current and new product development inspection setup creation and inspection plans, and build all Master Data & process concerning R&D and Keystone that regulates all internal processes of plants operation management.
Provide technical solutions to the ongoing challenges of R&D/NPD & Knowhow cycle.
Regularly audit suppliers to ensure compliance to Edita Standards & Specifications
Manage implementation of food safety standards cross Edita distribution centres.

Follow up the implementation of NFSA (National Food Safety Authorities) standards in Edita distribution centres and handling all related audits and raised findings.
Responsible for Edita raw material/packaging material Hub inspection for the abnormal incidents’ inspection
Generate monthly reports for the quality department KPI’s, quality system tools implementation and conformity rates, highlighting opportunities for improvement
Analyse trends related to food safety and quality system implementation using quality management tools and recommend corrective actions and improvement programs for defects reduction and coordinate these programs implementation.
Supervise the document controlling process and create new ideas for improving the documents approval cycle.
Manage the CCR (change control request) process

Job Requirements:

Education: B.Sc. Science

Experience: 5 to 7 years of experience in a similar field.

Languages: Excellent Command of English Language

Computer Skills:

MS Word Skills Advanced

MS Excel Skills Advanced

MS PowerPoint Advanced

MS Outlook Skills Advanced

Apply Here

R&D Specialist At EVA Cosmetics

We are looking for an analytical and innovative "R&D Specialist (#Pharmacist)" to join our #Research_and_Development department at EVA Cosmetics
-         Responsible for launching new products as well as developing existing products.
-         Collaborating with all factory departments as well as Marketing department, to guarantee the best flow of product's life cycle in a quality and time framed pattern, and deliver successful products into the market.
-         Formulate cosmetics based on key and new ingredients that meet customer’s requirements.
-         Research and develop new technologies and trends to produce new products and to develop the existing ones to give our company the competitive edge in the cosmetics market place.
-         Complete stability study to guarantee a product that will remain stable throughout the claimed shelf life.
-         Analyze all active ingredients to ensure the efficacy of our products.
-         Work in parallel with the QC & the QA department to provide them with the specifications for the analysis of new products and the manufacturing procedures to monitor the production.
-         Prepare the registration files of new products and the re-registration files of old products every 10 years.
-         All the Scientific data should be claimed on the new products supplied by the R&D Department.
-         Ensure the implementation of HSE regulation.
-         Bachelor’s Degree in Pharmacy.
-         0-2  years of related experience in Cosmetics/Pharmaceuticals or FMCG Industry.
-         6th of October or Nearby Residents.
-         Excellent English Language Proficiency.
-         Computer Skills Proficiency.
-         Monthly Incentive.
-         Quarter Bonus.
-         Learning & Development Opportunities.
-         Career Progression.
-         Social and Medical Private Insurance.
-         Transportation.
If you are ready for your biggest career move, kindly submit your #CV to “

Warehouse Specialist At Rivapharma

A pharmaceutical company located in Nasr city is hiring warehouse specialist ( raw material)  with the below qualifications :

• Males only.
• B.SC. of science.
• 0-2 years experience in the same position
• Professional computer and MS-Office skills
• Good command of English
• Good communication skills.

Please send your updated CV with attached Picture at:

Production supervisor At rivapharma

A pharmaceutical company located in Nasr city is hiring Production supervisor with the below qualifications :

· Bachelor degree in pharmacy.

· 5-7 years in solid products production.

· Ability to work independently and as a part of a team.

· Actively seek to improve process, control and expand effectiveness and efficiency.

· Excellent communication and interpersonal skills.

· Excellent computer skills.

· Excellent command of English – both written and spoken.

Please send your updated CV with attached Picture at:

Formulation Specialist At Al-Esraa Pharmaceutical Optima

For the expansion plan of Al-Esraa Pharmaceutical Optima, we are looking to hire Formulation Specialist in R&D department, as follows: - 

Job Requirements: 

·       BSc. Of Pharmaceutical science or BSc. of Science 

·       Experience up to 3 years in same position

·       Analytical thinking skills 

·       Interpersonal skills

·       Communication skills 

·       Excellent in English (written and verbal communication)


If you are interested and fit to the job requirements, send your updated resume to :

QA Validation supervisor at Zeta Pharma

Zeta Pharma is hiring #Qa #Validation #supervisor

Location : Sadat City

~Job Description :

• Preparing and executing the master plan of the site.

• Preparing & executing process validation protocols, cleaning validation activities

• Collecting protocols’ data and reporting its status to departments for approval

• Reviewing of the Production machines, Lab equipment, R&D machines qualification activities and protocols.

• Managing and coordinating the Computer system validation with a third external party.

• Managing, following up and maintaining the calibration program for all measuring instruments.

• Prepare, collect, and report Facility utilities qualification activities.

• Reviewing and assessing the impact of any changes in process or equipment on the corresponding validation status.

• Coordinating & ensuring documentation submission completion

• Performing all business in accordance with SOPs and internal regulations

• Communicate effectively with other departments to facilitate validation activities.

• In addition to the above-mentioned tasks, other activities and responsibilities may be individually defined

~Requirements :

• Bachelor of Pharmacy or Science Degree in the pharmaceutical industry.

• knowledge of shipping regulations and policies

• Analytical mind, Problem-solving

• 5 to 7 years of experience in the same role

~If interested kindly send your cv to

mention your job title in the subject

Production section head At Zeta Pharma

Zeta Pharma is hiring #Production #section #head  

Location : Sadat City 

Job Requirements :

- Bachelor degree of pharmacy 

- 6 to 9 years experience 

- Have experience in solid dosage forms 

Job Description :

- Manage and control the production to meet agreed plan 

- Monitor the performance of production department according to GMP and zeta standards 

- Manage MOH logs 

- Control process deviation 

- Coordination with other department to achieve the plan 

~If interested kindly send your cv to 

mention your job title in the subject

Compliance Section Head At Zeta Pharma

Zeta Pharma is hiring #compliance_Section_Head
Location : Sadat City

~Job Description :
•    Responsible for reviewing departmental procedures and SOP 
    from the quality side prior to approval
•    Provide employee training on compliance related topics, 
     policies, or procedures.
•    Maintain quality system and Investigate quality deviations.
•    Prepare quality plans for any changes in pre-assessed 
•    Responsible for implementation of auditing program and all 
     relevant activities.
•    Deals with external audits and follow up on implementation of  
    corrective/preventive actions’ plans.
•    Reporting Annual products quality review
•    Deals with customer complaints investigations
•    Generate quality improvement projects. 
•    Responsible for Supplier Qualification
~Requirements :
• Bachelor of Pharmacy or Science Degree in the pharmaceutical industry.
• 5 to 7 years of experience in the same role
~If interested kindly send your cv to
mention your job title in the subject

Lab Specialist At As-salam International Hospital

As-salam International Hospital Maadi Branch is now hiring Lab Specialist for the below; 

- Differential blood film, Retics counting.

- Immunofluorescence technique.

- Reporting of panic values.

- QC follows up.

- Check & correlate& verify the lab results.

- Bone marrow aspiration and biopsy.


- Education: Master degree of clinical pathology for lab specialist and master degree of histopathology for histopathology specialist.

- Experience: At least 3year experience in the same field

- Training: LIS , Infection control and quality control

- Skills: Communication skills, leadership skills

If you're Interested and your qualifications are matching the above criteria, please send your updated resume to; mentioning the job tittle in the subject.

Senior Mixing Specialist At EVA Cosmetics - Egypt

Job description

 Receiving the "Batch Record" from the Control Department.

 Follow up on the exchange of raw materials to be manufactured and recorded in the batch record from the weighing department before starting manufacturing.

 Receipt of a certificate of conformity with the analysis of distilled water from the control department before starting the production process via e-mail.

 Ensure that the manufacturing premises are cleared of any belongings related to previous operations in accordance with the instructions of "GMP-Line clearance".

 Follow up the cleanliness of the manufacturing halls to reach the highest quality by directing the cleaner to the places to be cleaned (machines - floors - walls - ceilings - tables - production requirements).

 Receiving and reviewing the batch (raw materials) in terms of compliance with weight, physical shape and expiry date - and QC No. And sign each material by reviewing and matching it on time. In the event of a complaint about any physical change in the material, the immediate notification to the control department is taken to take the necessary action and follow up the diffraction report and nominate the root causes while providing the necessary corrective and preventive measures

 Follow up on machines during work and washing by following the S.O.P of manufacturing each product by following up on workers’ addition of raw materials and methods of filtering them before they enter the machine, with daily assurance that all filters (stainless filters) are present at all entrances and exits of the machine and recording all data and timings On Time.

 Follow up on the application of good GDP codification practices in operating records and documents

 Handing over the half-factory to the official of the half-factory store and handing it over to the stores after obtaining the permission to deliver the half-factory and entering the data into the (Oracle) program.

 Delivery of BMR paper to the control department after manufacturing within 2 working days.

 Follow up and implement all requirements required by ISO certificates, environmental protection policy, occupational safety and health, and record all requirements in records (recording temperature and humidity - cleaning production areas - calibrating scales - recording washing time - recording machine malfunctions).

 Submitting a daily report for the department that includes (what was produced - percentage of plan achievement - percentage of losses - Deviation report-Down time)

 Follow-up on the performance of workers in terms of: Providing personal protective equipment for workers - Following up on the implementation of the instructions for entering individuals with the clothes assigned to the manufacturing departments - Completing the general appearance of workers - Daily attendance and departure.

 Coordinating the nights and shifts process to achieve the plan and notifying the concerned departments (movement, security and engineering) in the nights and shifts, sending the names of workers and pick-up stations and registering them on the watch program.

 Notify the Operations Department and the concerned departments (director of departments - planning - stores - engineering - control) via e-mail about any obstacles that hinder the implementation of the plan, whether today's plan (malfunctions - water outages ... etc.) if something happens that impedes the implementation of the plan today or the next day before Implementation within a maximum of 24 hours and during the day to take the necessary.

 Reviewing the manufacturing plan with the Planning Department to ensure that the plan can be achieved.

 Entering the new recipe (Recipe) for the new products on the Orcal program.

 Reviewing and updating the S.O.P every half year and taking the necessary corrective action.

 Commitment to implementing the instructions of occupational safety and health and environmental protection and holding a daily awareness meeting with the workers to set the work system.

 Follow up the work of the annual calibration of (devices - machines - scales - temperature and humidity meters) and implement their PR-PO on the Orical program

Participate in continuous improvement and provide the necessary CCR to develop and improve the production process while reducing industrial waste.

Qualifications: Bachelor of Science or Bachelor of Agricultural Science

Experience: Not less than 2 years.

Computer: Microsoft Office, Proficiency in using software

Apply From Here


Vacancies At kirovest pharmaceutical company

A leading pharmaceutical company

located  in Al-obour city  looking for

new colleagues for the flowing positions ;

1. :Raw material specialist 

2. QC senior 

3. Laboratory technicianفنى معمل


* Bachelor’s degree of Pharmaceutical Science  for position 1.2.

* (1-4 ) years experience in QC field 

* good knowledge in QC work

*very good in computer skills.

* Strong attention to details.

* 0-4 years experience for position 3 فنى معمل حاصل على دبلوم معهد فنى كيماوى يفضل خبرة   

If you are interested, kindly send your updated C.V with a recent

photo to

mentioning( QC analyst) in the subject

Vacancies At Mash Premiere Pharmaceutical and Cosmetic Industries

Mash Premiere Pharmaceutical and Cosmetic Industries
Located in badr city is hiring the following 
1-QA IPC Senior 
2-R&D formulation Senior
  Minimum 2 years experience in asimilar role.
Requirements: Bachelor's degree in pharmaceutical sciences
Or sciences
Males only 
If you are interested send your updated cv to:
mentioning the vacancy in the e-mail subject.

QC Specialist At Global Napi Pharmaceuticals

Job Description

Performs qualitative and/or quantitative analysis of raw & packaging material and bulk or finished products.

Performs stability analysis of pharmaceutical products.

Performs analysis of drug concentrations using HPLC, GC , FTIR , UV……..etc.

Calibrates instruments according to work instructions to ensure compliance to standards.

Troubleshoots and resolves operations issues.

Job Requirements

Bachelor Degree of Sciences (Chemistry) or Pharmaceutical Sciences

Good English Language.

Good Computer skills proficiency.

Not less than  1-3 year of professional experience in the QC department

Apply Here

Pharmacists At Misr pharmacies 

صيدليات مصر تعلن عن حاجاتها لتعيين صيادله للفروع الأتيه : 

( شبرا -وسط البلد - المقطم -التجمع الثالث-مدينه الفردوس )

للتقديم برجاء تسجيل البيانات على اللينك التالى :

أو التوجه لمقر الاداره (29ش القدس الشريف من ش شهاب , ميدان لبنان.المهندسين) من الأحد الى الخميس من الساعه 10 صباحا حتى 3 عصرا

اللوكيشن الخاص بالإداره

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