وظيفة في Glp في مسقط

اتبع لوائح توجيهات GMP وGLP وقواعد إجراءات التشغيل القياسية الداخلية. القيام بجميع أنشطة التحليل الكيميائي والفيزيائي. تحليل وتطوير والتحقق من صحة الأساليب التحليلية. الممارسة في استكشاف الأخطاء وإصلاحها التحليلية مع الأخذ في الاعتبار قسم إجراءات التشغيل الموحدة وقواعد GLP. خطط تحليل المزيد...

Responsibilities: Analytical testing of raw materials, in-process, samples, and finished products. Maintaining analytical instrumentation. Validating, verifying, and troubleshooting analytical methods. Method transfers. Author SOPs. Assist with audits. Requirements: BS المزيد...

Ensuring the quality and compliance of our pharmaceutical products including those in formulation through rigorous chemical analysis and testing. You will be responsible for overseeing and executing quality control activities related to the chemical aspects of product manufacturing en المزيد...

Executive / Sr. Executive Quality Control Officer For Reputed API Manufacturing Company Qualification: B.Sc. / M.Sc. Chemistry Experience: 01 to 07 years Location: Eklabara Salary: 3.00 to 5.00 Lacs P/A Job Description Urgent Job Opening for Executive / Sr. Executive المزيد...

Job Title: Laboratory Assistant 1 Location: Greensboro NC 27409 Duration: 6 Months Job Type: Contract Work Type: Onsite Overview: TekWissen the group is a workforce management provider throughout the USA and many other countries in the world.The below job المزيد...

London - 4 days on 4 days off - weekly pay A 2 month temp opportunity has arisen for a Laboratory Support – Track Assistant to maintain, support and develop the labs mechanical and analytical systems as and when required. This role is a night’s position working 8.30 pm to المزيد...

التعليم والمؤهلات: درجة البكالوريوس في الكيمياء، علم الأحياء، العلوم البيئية، الهندسة الكيميائية، أو مجال ذي صلة. شهادات مهنية متقدمة في مجال المختبرات (مثل GLP، ISO 17025) تعتبر ميزة إضافية. المهارات الفنية: معرفة قوية بأساليب وتقنيات التحليل المختبري. إتقان المزيد...

Title: Chemist I Duration: 6 months Location: 4701 International Blvd Wilson NC 27893 Interview Mode: 1st webcam/phone and 2nd In person Standard Hrs. Per Week: 40 hours Mon Thurs (10 hours/day excluding breaks) Shift time: 7:00 am 5:30pm Job Summary Performs a variety of ch المزيد...

التأكد من تنفيذ نظام ضمان الجودة، وإجراء عمليات تدقيق الجودة ومراقبة وتسجيل النتائج من العمليات والإجراءات داخل التصنيع وضمان الموثوقية المستمرة لعملية التصنيع. الإشراف وإجراء أنشطة ضمان الجودة (فحص RM/FG، وعمليات جودة الخط) التي تضمن تسليم نتائج دقيقة في الوقت المحدد وتنفيذ اختبار المزيد...

Hi Everyone Greetings from Randstad!! we are hiring for Quality Asurance executive for a pharma company in mumbai location . Responsibilities : Review of formulation & analytical documents preparation & review of SOPs review of specification/STP/TTM/AMV protocol المزيد...

About the jobExperience: 3 to 6 years in Analytical Development functionOperation calibration and trouble shooting knowledge of analytical instruments such as HPLC Dissolution tester Gas chromatograph UV visible spectrophotometer IR Viscometer etc.Experience of stability study of phar المزيد...

Ensuring compliance with regulatory standards (GMP GLP etc.).Managing quality systems and processes (SOPs audits CAPAs).Supporting quality control activities and validation processes.Overseeing supplier and vendor management.Providing training on quality systems and regulations.Monito المزيد...

Job Summary: This individual will be responsible for performing the technical aspects of assigned tests in compliance with GLP USDA and AAALAC guidelines. Essential Job Functions: Performs various tests that may include injections patching and wrapping implantation of test substance المزيد...

Job Summary Performs a variety of chemical analyses and GMP review in accordance with cGMP GLP DEA and company policies and procedures. Primary Responsibilities Perform routine testing (dissolution assay/degradant content uniformity and ID) of drug products in a cGMP laboratory المزيد...

Job Responsibilities To plan and manage all the activities of Quality Control Department. To assure the quality of all the products manufactured by the company. To coordinate with manufacturing department in controlling their process and products at every stage of manufact المزيد...

About the jobJob Description:We are seeking a talented and experienced Scientist specializing in In Vivo Pharmacology within the preclinical research domain. The successful candidate will be responsible for designing executing and analyzing preclinical in vivo studies to evaluate the المزيد...

Review Analytical documents Protocols and Reports of Stability Analytical Method Validation Analytical Method Verification and Analytical Method Transfer. Recording deviations and findings taking corrective and preventive actions defined and implemented in due time & trending of t المزيد...

Qualifications Education: B.S. in Bio/Chemical Engineering Biochemistry or related science 03 years work experience At least six months related laboratory experience preferably performing biologics purification steps General laboratory skills experience with pipettes O المزيد...

POSITION RESPONSIBILITIES o Working knowledge of basic laboratory techniques for application in all aspects of Reagent Bead production o Assist in the development and maintenance of procedures used in Reagent Bead manufacturing o Reagent Formulation Lab equipment maintenance o Maintai المزيد...

Qualifications Education: B.S. in Bio/Chemical Engineering Biochemistry or related science 03 years work experience At least six months related laboratory experience preferably performing biologics purification steps General laboratory skills experience with pipettes O المزيد...