Cgmp Jobs in French Antilles
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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 More...
Job Title: CTM Associate (Clinical Trial Manufacturing) Length of Assignment: 12 months Shift/Schedule Details: Standard Business Hours MondayFriday 8am5pm Location: (Onsite) 100% Holly Springs NC 27540 Job Description: The CTM (Clinical Trial Manufacturing) Associate will be r More...
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 More...
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 More...
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 More...
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: More...
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 More...
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/ More...
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. More...
Quality Systems Specialist
Grifols Egypt For Plasma Derivatives Gepd New Cairo City, Egypt -
Cairo
-
Egypt
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. Establish a defined Deviation procedure and CAPA system, involving appropriate stakeholder More...
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 More...
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 More...
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 More...
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 More...
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 More...
Hplc Analyst
The Arab Company For Veterinary Medicines Industry -
Amman
-
Jordan
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 More...
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 More...
Job Description: Bio Process Associate 3rd shift roleso shift diff included on Rate Onsite in DevensLocal Candidates Only Operates control systems and processes in Biotechnology Pilot Plants as assigned. Prepares process buffers and reagents. Cleans equipment and maintain area in cle More...
Manufacturing Associate Biotechnologist Associate
Veerteq Solutions Inc. -
Portsmouth
-
UK
Job Title: Manufacturing Associate / Biotechnologist Associate Location: Portsmouth NH 03801 Duration: 12 Months Job Type: Contract Work Type: Onsite Position Description The Manufacturing Associate is responsible for the manufacture of therapeutic proteins (API) under c More...
Full Knowledge of cGMP/GSDP guidelines Knowledge of national/international guidelines and references (FDA, EU, PICs, ICH, etc) Experience in writing and reviewing SOP's, systems, protocols , reports , etc. Experience in the quality management system (QMS) Experience in condu More...
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