Cgmp Jobs in Shanghai

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...

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...

Job Description: Overall incharge of Process Development Lab Activity. Solving/Guiding the entire QC related queries/problems inline with Quality Management System and the entire QC related problems to work consistently without any interruption. Responsible for More...

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...

Regulatory Affairs OfficerLocation: Delhi (Office Only)Experience: 25 YearsMustHave: USFDA Regulation 510(K) Compliance as per 21CFR 821. Coordinate with QC QA R&D MSAT Regulatory affairs teams on daytoday activities.Job Responsibility Responsible for product submis More...

Analytical Engineer Manufacturing Support Location: Thousand Oaks CA Duration: 12 months (Possible extension) Key Responsibilities: Verification Leadership: Take individual accountability for verification deliverables on key capital projects. Assist in identifying critical qual 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...

Overview: TekWissen group is a workforce management provider throughout the USA and many other countries in the world. Our client is a leading biotechnology company that combines technological insight with worldclass manufacturing scientific expertise and process excellence and helps More...

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...

Job Description: Primary Purpose SummaryThe Quality Control Technician performs dimensional and functional testing on Aptar Congers product to ensure compliance with established quality standards and customer specifications. The Quality Control Technician is responsible for documentin More...

Lead Mechanic Westbury NY Full time/ Permanet/ 2nd shift: 3:00pm11:30pmWhat you will be doing:Responsible for machine related aspects such as packaging projects equipment maintenance parts and serviceReview daily mechanical activities to assure compliance with company cGMP s and SOP 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...

Job Responsibilities: Interfaces with Quality Assurance Production and Engineering departments on process requirements for new and current products. Equipment qualification including automation and computerized systems. Writes and executes evaluation protocols for all processing steps 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...

Job ProfilePlanning & Execution1. Planning for respective shifts and Execution of Warehouse activity2. Coordinate with different departments such as production QA QCDocumentation1. CGMP regulation in the warehouse department.2. Monitoring and Documentation of warehouse activities. More...

Description:Perform one or more of the following duties and responsibilities in support of site Quality Assurance program under minimal supervision. Review and approve product MPs. Approve process validation protocols and reports for manufacturing processes. Request Quality on inciden 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 so 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...

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...