Cgmp Jobs in Casablanca

About PSC BiotechWho 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 clou More...

About PSC Biotech Ltd 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 More...

About PSC BiotechWho 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 clou More...

About PSC Biotech Ltd 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 More...

About PSC BiotechWho 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 clou More...

About PSC BiotechWho 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 clou More...

About PSC BiotechWho 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 clou More...

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 More...

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 More...

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 More...

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 More...

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 More...

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 More...

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 More...

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 More...

Education and/or ExperienceBachelor s degree in a scientific discipline.5+ years of quality assurance experience in a pharmaceutical or biotech environment.Extensive knowledge and understanding of cGMP regulations, Quality Systems and validation documentation.Technical writingProfic More...

Responsibilities: Direct reporting responsibility for some or all Reagent Manufacturing Associates. Facilitate team meetings as required. Recommends and/or initiates personnel activities such as selection, transfer, discharge, disciplinary actions and associates complaints in a fair, More...

Job Title: Senior Quality Control Technician Job Location: St. Louis, MO (Onsite) Job Duration: 12 Months Interview: Video Summary: Execute assigned laboratory tests and associated quality control procedures to ensure adherence to relevant SOPs and cGMPs. Give management and supervis More...

Job title: Senior Continous Improvement Engineer Job Location: St. Louis, MO Job Duration: 12 Months Contract Interview: Video Summary: The Senior Continuous Improvement Engineer carries out the plan for converting the strategy and objectives of client's NAs into effective, long-last More...

Description: 3rd shift role - 10pm - 8am Could be any of the following shift but will be set once they start working 3rd shift. MUST train on 1st for the first couple weeks. Sun-Wed, Mon-Thurs, Tues-Fri, or Wed - Sat - flexible to work OT on weekends 1. Can it extend - Yes 2. Is th More...