وظيفة Cgmp في عمان

Overview: TekWissen Group is a workforce management provider throughout the USA and many other countries in the world. The below job opportunity is with one of our Biotech clients who researches develop and commercializes drugs. The company focuses primarily on antiviral drug المزيد...

Job Title: Cell Therapy Specialist Location: Frederick Maryland Duration 12 months contract Schedule: Initial 7 weeks: MonFri () for New Hire Orientation and Manufacturing Onboarding Technical Training. After 7 weeks: Fulltime 4/10 schedule with shifts directed by manager or depar المزيد...

Job Title cGMP Cleaner Hours: 5 8 hours days 10:30pm 7:00am (mandatory 1 weekend day a week) Training hours: 1st three weeks Monday Friday 8am4:30pm Location: 100% Onsite Frederick MD Job Duration: 12 months Client is a cell therapy company that is focused on providing patients wit المزيد...

Role and Responsibilities:As an Officer Production your primary responsibility will be to maintain workplacegood housekeeping as per cGMP standards and ensure the operation and cleaning of equipment as per SOP. You will be responsible for the receipt and storage of raw materials in t المزيد...

0-1 yrs experience with High School Diploma Ability to work independently or in collaboration with others on assigned tasks Ability to comply with cGMP standards Must possess computer skills Ability to follow instruction and directions Desirable Skills/Experience: المزيد...

Overview: TekWissen Group is a workforce management provider throughout the USA and many other countries in the world. Client is a leading provider of transfusion and transplantation diagnostic products worldwide. We strive to create a world where anyone anywhere in need of blood o المزيد...

Overview: TekWissen Group is a workforce management provider throughout the USA and many other countries in the world. The below job opportunity is with one of our Biotech clients who researches develop and commercializes drugs. The company focuses primarily on antiviral drugs use المزيد...

JOB DESCRIPTION OF PROPOSED MANAGER QA Opthalmology Job Responsibilities Having 1520 years of experience in pharmaceutical industry and acting as site QA Head role since last 5 years (Oral solid dosage form/Injectable dosage form). To ensure overall compliance of cGMP/ المزيد...

Oversee the planning scheduling and execution of production activities to meet production targets while maintaining optimal efficiency and costeffectiveness. Ensure compliance with cGMP (current Good Manufacturing Practices) regulatory requirements and company policies and procedures. المزيد...

Primary Purpose / Regulatory Responsibilities: Establishment of robust fit for purpose biological drug product manufacturing processes for the different development phases (FIM Ph2 Ph3). Defining and selecting drug product manufacturing processes and parameters for clinical m المزيد...

Production Management: Oversee all aspects of production operations includingmanufacturing processes capacity planning scheduling and inventory management toensure timely and costeffective production of highquality pharmaceutical products incompliance with regulatory requireme المزيد...

The Technical Services Materials Specialist has primary responsibility in supporting the cGMP manufacture of biological bulk drug substance (BDS) at our clients facility in Blanchardstown, Dublin. The Technical Services Materials Specialist will be responsible for providing support fo 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...

Our Client is a leading multinational company operating in the Pharmaceutical industry. They are dedicated to innovation wellness and sustainability with a rich legacy of trust and excellence in the healthcare industry. The client is setting up a stateoftheart pharmaceutical manufactu المزيد...

The Environmental Health and Safety Specialist (EHS) is responsible for various duties and responsibilities including:Acting as a subject matter expert in environmental health and safety and effectively communicating with internal and external stakeholders.Developing hazardous and che المزيد...

Our Client is a leading multinational company operating in the Pharmaceutical industry. They are dedicated to innovation wellness and sustainability with a rich legacy of trust and excellence in the healthcare industry. The client is setting up a stateoftheart pharmaceutical manufactu المزيد...

Independently plans and executes that support research, development and validation activities Support cGMP testing activities by performing analytical methods including UPLC/HPLC, Dissolution, GC, Thermogravimetric DSC/TGA, and KF titration. Perform data analysis and troubleshoot المزيد...

The successful candidate will be responsible for providing technical and/or engineering support for Finished Product (FP) manufacturing providing packaging engineering support through all phases of the commercial finished product lifecycle including technology transfer validation and المزيد...

Key Responsibilities: Lead and motivate a team of associates and supervisors to achieve organizational goals in safety quality output and cost. Implement and manage lean manufacturing principles. Ensure compliance with SOPs Standard Work QMS policies and procedures. Optimize labor nee المزيد...

Responsibilities:Analytical QA Officer:Execute analytical quality assurance activities as per standard operating procedures (SOPs) and regulatory requirements.Perform review and approval of analytical test methods validation protocols and reports.Conduct audits and inspections of anal المزيد...