Cgmp Jobs in Rio de Janeiro

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...

The Packaging Operator is pivotal in the MDI product packaging process at the manufacturing site ensuring compliance with cGMP customer specifications and SOPs. They are tasked with executing packaging operations safely and efficiently to uphold product quality standards. This role ho More...

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

Look for someone whos having good experience in Radiochemistry. Job Role: GMP Manufacturing Technician Location: Watertown MA 02472 Fulltime Role Reporting: Associate Director Clinical Manufacturing Description: We are seeking an experienced GMP Manufacturing Technician advancing 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 cloudbas 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 cloudbas More...

Job Title: CQV Engineer Location: Greater Los Angeles area CA USA Job Description: Join our team as a CQV Engineer for a 2year project to support the expansion of a pharmaceutical facility in the Greater Los Angeles area. Starting in the 2nd week of July youll bring your 5 years o More...

Job Title: Process Engineer Manufacturing Investigations Location Frederick MD Onsite Kite is seeking a highly motivated individual with biotechnology experience to work on innovative TCell therapies for cancer treatment. As a member of the Operations and Compliance Support 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...

My Client a top company in the pharmaceutical sector is seeking a Quality Manager whose main responsibility will be to ensure products manufactured and imported are consistently of high quality efficacious and safe for patients in line with company s internal requirements whilst com 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...

Qualifications Bachelor's degree in chemistry or engineering with a chemistry component. 3 years' experience working in a pharmaceutical environment. Experience with ETQ, SAP, Veeva, QMS document management. Experience with Root Cause Analysis, CAPA (Corrective and pre 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...

Job Summary Performs a variety of chemical analyses and GMP review in accordance with cGMP GLP DEA and company policies and procedures. Primary Responsibilities Perform routine testing (dissolution assay/degradant content uniformity and ID) of drug products in a cGMP laboratory More...

Education BSc(Life Sciences)/MSc(Life Sciences)/B.Pharm/M.Pharm/B.Tech(biotechnology)/M.Tech(biotechnology) or equivalent. Experience of 10 15 years in bioprocess activities (upstream and downstream) and formulations with special reference to monolayers in T flasks Rollers Cell st More...

What you'll do: Oversee construction project management including vendor selection Determine scope of work, evaluate job bids, complete RFQ/RFI Establish and maintain the budget, troubleshoot issues and determine options Supervise subcontractors/consultants for various proje More...

Job Description:The Manufacturing Operator position is pivotal within the metered dose inhalation (MDI) products project site in Fall River MA. The role entails overseeing manufacturing operations related to MDI products ensuring adherence to Current Good Manufacturing Practices (cGMP More...

Job Title: Process Engineer Manufacturing Investigations (Biotech/TCell Therapy) Location Frederick Maryland Onsite 12 months duration Manager is seeking a highly motivated individual with biotechnology experience to work on innovative TCell therapies for cancer treatment. As More...

Ensuring the quality and compliance of our pharmaceutical products including those in formulation through rigorous chemical analysis and testing. You will be responsible for overseeing and executing quality control activities related to the chemical aspects of product manufacturing en More...

Veterinary, Human Pharma, Aseptic manufacturing operations in clean rooms and hoods/biological safety cabinets etc… Pesticides Production plants ( Insecticides, Fungicides, herbicides,…). QMS application and compliance experiences to include : Full cGMP complia More...