مطلوب رئيس قسم امن صناعي لمصنع جلود بقويسنا:
خريج هندسة أو علوم او ما يعادلها
السن من 28 الي 42 سنة
خبرة من 5 سنوات
يفضل من ساكني قويسنا أو المنوفية أو ما يجاورها
مرتب من 12000 إلى 13000 + وجبة أو بدل وجبة + إنتقالات في خطوط محددة في المنوفية
على ان يرسل السيرة الذاتيه على الايميل التالي
hr@italystandard.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
-----------------------
We Are Hiring
For a New Project In New Capital the following jobs:-
- Site Manager – Finishing.
- Site Engineer – Finishing.
- Technical Office Manager - (Site Based).
- Technical Office Engineer - (Site Based).
- Quality Control Engineer (Finishing).
- Documents Controller - (Site Based).
- مشرفين تشطيبات
If you interested kindly send your CV to hr@heavyrock-eg.com, and mention job code and position in the subject.
مطلوب للتعيين
لمشاريع الشركة بالعاصمة الإدارية الجديدة الوظائف التالية:-
- مدير موقع (تشطيبات).
- مهندسين تنفيذ (تشطيبات).
- مدير مكتب فني (بموقع المشروع).
- مهندس مكتب فني (بموقع المشروع).
- مهندس جودة (تشطيبات).
مراقب مستندات (بموقع المشروع).
- مشرفين تشطيبات
إذا كنت مهتمًا ، فيرجى إرسال سيرتك الذاتية إلى hr@heavyrock-eg.com ، واذكر كود و أسم الوظيفة في خانة الموضوع بالبريد الإلكتروني.
------------------------
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
--------------------------
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
-------------------------
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
----------------------
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
----------------------
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
-----------------------------------
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
--------------------------------------
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
----------------
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 .
-----------------------
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