وظيفة في Cgmp في San Diego

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 المزيد...

Fremont CA Contract Duration: 636 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a MES Technical Writer in the Fremont CA area. Responsible for understanding all the complexities of the MES system revise and create SOPs test protocols technical docum المزيد...

Fremont CA Contract Duration: 1136 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a MES MBR Designer in the Fremont CA area. Responsible for understanding all the complexities of the BioMES system revise and design new electronic batch records tro المزيد...

Fremont CA Contract Duration: 3036 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a QC Associate III in the Fremont CA area. Performs tasks and activities related to supplier/material qualifications and supplier change notifications (e.g. review of v المزيد...

Athens GA Contract Duration: 636 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a Packaging Technician in the Athens GA area. 1st shift: Monday to Friday 6:30AM 3:00PM To perform the duties associated with labeling inspecting and packaging of المزيد...

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 المزيد...

Title : Specialist Quality Assurance Type: W2 Visa: USC/GC/EADS Preferred OPT/CPT (If they dont have any employer already) H1B (If open for H1B transfer) Provide quality onthefloor support of manufacturing reviewing documentation and providing realtime support of manufacturing iss المزيد...

Roles & Responsibilities: CQV Lead Engineer for all CIP Equipment in the DSM Buildings initially responsible for review of all Design deliverables from Jacobs including Drawings Datasheets specifications and Engineering Lists. Lead generation of all CQV CIP Documentation FAT wrap المزيد...

QC Lab Supervisor (OOJ 19650) Lancaster South Carolina USA Industry(ies) Pharmaceutical Primary Skills Pharmaceutical Companies Qc Chemmist Secondary Skills Qc Lab Occupational Categories Science/ Life Science/ Biotechnology Work Experience (Years) 37 Degree University Bachelors Deg المزيد...

Coppell TX Contract Duration: 936 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a Production Operator in the Coppell TX area. (onsite) Team D: As a member of the Manufacturing team the operator will contribute through performing varying tasks related المزيد...

Our direct client is looking for a QA Analyst in Massachusetts(Onsite). Job Title: QA Analyst Location: Tyngsborough MA Type: Full Time W2 SUMMARY: The Quality Assurance Manager will be responsible for managing the quality management system and ensuring regulatory compliance for the المزيد...

No Sponsorship is available now or in the Future. The Quality Assurance Manager will be responsible for managing the quality management system and ensuring regulatory compliance for the companys products processes and services. RESPONSIBILITIES: Oversee the companys adherence to dome المزيد...

Title: Project Manager Location: Remote Duration: 1 year Responsible for planning executing and delivering projects within scope budget and timeline. Responsible for managing the project team stakeholders and resources ensuring that the project goals and objectives are met. Re المزيد...

Associate Technical Engineer: Lets do this. Lets change the world. In this role you will provide technical engineering support on all system/equipment optimization strategies upgrades replacements repairs and modifications. You will evaluate and determine if process equipment maintena المزيد...

The purpose of this position is to lead review and contribute to validation planning risk assessment system requirements formulation design specifications qualification protocol and remediation efforts. The person will act as a crossfunctional interbusiness unit resource. As such t المزيد...

*Job Summary:* Direct management of an FDA cGMP Polymer Bulk Manufacturing and Unit Packaging facility. This includes overseeing production maintenance warehouse quality assurance operational excellence processes quality control and safety processes. Responsibilities also encompass e المزيد...

Summary of the Position: The Automation and Controls Engineer reports to the Manager of Manufacturing Engineering and is responsible for developing new automation concepts as well as maintaining existing automated manufacturing systems. The Automation and Controls Engineer will identi المزيد...

Principal Specialist Validation Athens GA Full time Description As an employee of Boehringer Ingelheim you will actively contribute to the discovery development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees المزيد...

Quality Assurance Manager MA Tyngsborough MAMust be a US Citizen or Green Card holderThe Quality Assurance Manager will be responsible for managing the quality management system and ensuring regulatory compliance fo المزيد...

SUMMARY: The Quality Assurance Manager will be responsible for managing the quality management system and ensuring regulatory compliance for the companys products processes and services.RESPONSIBILITIES:Oversee the companys adherence to domestic and international regulatory standards المزيد...

Job description Responsibilities: - Perform laboratory tests and procedures to assist in diagnosing, monitoring, and treating diseases or conditions - Prepare samples for analysis and conduct laboratory tests according to established procedures and protocols - Analyze and interpre المزيد...

JOB DESCRIPTION: We have a Sr. Automation Engineer position available in our Wilmington, MA office. This position requires demonstrated technical proficiency in implementing automation solutions with PLC, DCS, HMI, and SCADA platforms. This position requires demonstrated technical pr المزيد...

Regulatory and Quality Systems Manager, IVDDirect Hire (Hybrid OK) San Diego, CATalentry is looking for a professional Compliance Manager who can manage the quality management systems and ensure continued compliance. The right person will develop and implement the quality systems, lea المزيد...

Frederick MD Contract Duration: 6-18 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a Distribution Specialist in the Frederick MD area. 100% On site Role - No option for remote or hybrid Night Shift: Monday thru Friday (early Sat morning) 6PM 3A المزيد...

Sr. Business Analyst Location: Foster City, CA Contract: 1 year Work Type: Remote / onsite (2-3 day per week) Job Responsibilities Work closely with data science leaders, data scientists, software developers and business SMEs to deliver end-to-end data science solutions Respon المزيد...

Description: CAPA/NCR writers Description: Essential Duties and Responsibilities: 1. Perform non-conformance (NCR) investigations within the Track Wise 8 Management System. 2. Execute implementation of CAPAs associated with NCR investigations. 3. Maintains a high level of expertise المزيد...

Responsibilities: Excellent employment opportunity for a Manufacturing Associate in the Fremont, CA area. Independently executes all routine unit operations in Purification including change-over procedures, scheduling within the shift team, equipment cleaning and set up. Able المزيد...

Description: Position Overview: As a member of the Component Testing Group, this individual will be expected to perform routine and non-routine testing on a variety of materials used in the manufacture of In Vitro Diagnostics (IVD) assays. Additional responsibilities of this positio المزيد...

Description: Position Overview: As a member of the Component Testing Group, this individual will be expected to perform routine and non-routine testing on a variety of materials used in the manufacture of In Vitro Diagnostics (IVD) assays. Additional responsibilities of this position المزيد...

Description: Performs quantitative and qualitative analysis, such as sampling, testing, and measuring using specialized equipment. Completes the compiling, analyzing, and interpreting of results. Performs periodic equipment inspections and preventative maintenance work. Performs basic المزيد...

Frederick, MD Contract Duration: 6-18 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a Cell Therapy Specialist in the Frederick, MD area. 100% onsite roles - No flex or Work from Home available Successful candidate must meet the Company Covid Vaccina المزيد...

Fremont, CA Contract Duration: 5-36 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a Manufacturing Technician in the Fremont, CA area. Independently executes all routine unit operations in Purification including change-over procedures, scheduling with المزيد...

Responsibilities : Take ownership of the management of SLT GEMBA process execution and subsequent action items, create communication and training materials for site operations personnel, Identify opportunities or implement changes to improve products or reduce costs. Drive site imple المزيد...

Responsibilities : The Quality Product Compliance (QPC) Project Coordinator will support the execution of Quality Assurance activities that fall within the Global Quality Key Brands organization. This includes support of marketing and post-marketing changes, global change management المزيد...

Fremont, CA Contract Duration: 5-36 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a QC Associate I in the Fremont, CA area. Day to day duties will include but not limited to: Collect routine Environmental Monitoring and Utility samples from Manufactur المزيد...

Responsibilities: Work with Round Lake, CL project engineering, and Quality engineering to develop new medical device molds in the CL plant. This will include developing and conducting training, writing JIBs, writing SOPs and writing preventive maintenance procedures. Start up and de المزيد...

Responsibilities: The following duties and responsibilities are intended to be representative of the work performed by the incumbent(s) in this position and is not all-inclusive. The omission of a specific duty or responsibility will not preclude it from the position. Determines comp المزيد...

Responsibilities: Performs instrument optimization functions after final assembly: laser alignment, pressure adjustments, electrical adjustments, etc. Performs final production testing and inspection to ensure products meet performance specifications and standards. Analyzes test resu المزيد...