Cgmp Jobs in Managua
Cgmp Jobs in Managua
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Role: Packing and Dispatch ManagerSalary: 35,000 - 40,000 per annum (DOE) Location: Tonbridge, Kent Hours: 7.30am to 4.30pm with 1 hour at lunch time.KHR has partnered with a rapidly expanding manufacturer with an excellent reputation for high-quality goods, who are recruiting More...
Packaging Manager 35,000 - 40,000pa Tonbridge, Kent Monday to Friday 7.30am to 4.30pmKHR has partnered with a rapidly expanding manufacturer with an excellent reputation for high-quality goods, who is recruiting for a Packing and Dispatch Manager to join their team on a permane More...
Position Title: Manufacturing OperatorLocation: Hauppauge or Central Islip New YorkShifts: 1st Shift (07:00 am 03:30 pm) 2nd Shift (03:00 pm 11:30 pm)Job Overview:As a Manufacturing Operator based in Hauppauge or Central Islip New York you will play a pivotal role in the pharmaceuti More...
Position: Material Handler Duration: 12 months (Possible to extend) Pay Rate: $20/hr on W2 Location: Germantown MD 20874 Shift: MF day Youll provide shipping receiving storage and order fulfillment services for clinical sites and laboratories. Pick pack sort arrange More...
Plan and Organize the Engineering department comprising of Mechanical Electrical HVAC Utilities and Project work. Exposure of cGMP of Pharmaceutical industries and exposure of Regulatory audits. Solid Understanding of Human machine interface and related software programming. Coordina More...
Job Title: Manufacturing Supervisor Synthesis and Production Microbiology Duration: 12 Month Shift: 7:00 am 3:00 pm PST Work Location: San Diego CA 92127 SUMMARY: The main responsibility for the Synthesis and Production Microbiology Supervisor is to lead and oversee all p More...
About PSC BiotechWho we arePSC Biotech is a leading Biotech Consultancy firm founded in 1996 headquartered in Pomona California USA with Global operations in Ireland India Singapore Australia and the US serving 350 clients in more than 23 countries worldwide. We provide cloudbased sof More...
618 years of experience in managing Industrial Pharmaceutical cGMP & FMCG Projects and Datacenter projects. Additional experience in interior design and landscape architecture would be preferred. Proficiency in AutoCAD and Revit. Knowledge of Photoshop 3D Max or Google Sketchup wou More...
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 More...
For further inquiries regarding the following opportunity please contact one of our Talent Specialists Rashi at Title: Quality Lab Associate I 3rd Shift Location: Round Lake IL Duration: 12 Months Description: Shift: 3rd Hours: 4 10hour shifts (Sunday to Thursday 10 pm to 8 More...
For further inquiries regarding the following opportunity please contact one of our Talent Specialists Meghna at Title: Quality Lab Associate I Location: Round Lake IL Duration: 12 Months Description: Shift: Weekend 2 other nights Hours :4 10hour shifts (Friday through Su More...
About PSC Biotech Who we are PSC Biotech is a leading Biotech Consultancy firm founded in 1996 headquartered in Pomona California USA with Global operations in Ireland India Singapore Australia and the US serving 350 clients in more than 23 countries worldwide. We provide cloudbased More...
Should be able to demonstrate strong understanding of USFDA/ MHRA/ EU or local guidelines. Responsible for setting strategy direction for the entire Quality Control & Microbiology Department and team. Conducts performance reviews for teams Development, review, revise and impl More...
Job Title: Material Handler (Packaging Operations) FLSA Classification: FullTime NonExempt/Hourly Professional Work Location: Fall RiverMA Work Hours: First Shift: 8:00 AM 5:00 PM (may vary based on business needs) Purpose: The purpose of this role is to serve as a Packaging Op More...
Job Title: Manufacturing Operator Job Type: FullTime NonExempt/Hourly Professional Work Location: Fall River MA and Central Islip NY Work Hours: First Shift: 8 AM 5 PM (may vary based on business needs) Reports To: Facilities Operations Manager Purpose: The purpose of this role i More...
Strong understanding of USFDA/ MHRA/ EU or local guidelines Responsible for setting strategy direction for the entire Production Department and team. To enforce the batch manufacturing as per cGMP requirements in order to obtain high quality products. To achieve targeted producti More...
Job Title: Manufacturing Operator FLSA Classification: FullTime NonExempt/Hourly Professional Work Location: Fall River MA and Central Islip NY Work Hours: First Shift: 8 AM 5 PM (may vary based on business needs) and 2nd Shift ( 3:00 PM 11:30 PM Purpose: The purpose of th More...
Sr. Engineer with working knowledge and experience with engineering practices and cGMP procedures on pharmaceutical/biotech production process facilities and equipment. Knowledge and experience in: Technical Writing Quality Risk Assessments such as FMEA and/or QRAESChange ControlNonCo More...
OverviewThe CMC Document Specialist is responsible for developing, reviewing, and managing technical documentation related to chemistry, manufacturing, and control (CMC) activities within the pharmaceutical industry. This includes preparation and submission of regulatory documents, de More...
Job Id OOJ 19838 Job Title Quality Assurance Document Supervisor Industry(ies) Biotechnology/ Life SciencesPharmaceutical Primary Skills Quality Assurance Professionals Location Lancaster SC Work Experience (Years) 315 Degree University Bachelors Degree/34 Year More...
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