Cgmp Jobs in Stavanger

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...

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...

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...

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...

Job ID: AMAGJP Location: Thousand Oaks CA Duration: 3 months (Possible extension) This engineering position supports manufacturing activities associated with cGMP equipment and facilities at *** Thousand Oaks (ATO). The senior engineer works in partnership with the automation maint More...

Initiates the of EM related Standard Operating Procedures (SOPs). Performs environmental monitoring sampling according to established Standard Operating Procedures, as well as generating trend data from test results. Analyzing and reading Environmental Monitoring (EM) plates W 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...

Participate in the required investigations resulting from external audits and inspections, customer complaints, or any assigned projects, and follow up on the corrective and preventive actions as requested. Review and analyze the quality management systems and related work methods 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...

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...

Documentation Management like Issuance, Distribution, retrieval and destruction of documents i.e., SOPs, Formats, logbooks, Artwork, Lists, batch records, forms etc. and all other GMP documents. Preparation, review and revision of SOPs, Policies, Lists, SMF, Quality Manual etc 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...

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...

Ensures processes and products are compliant with cGMP and compatible with the regulatory environment required by our pharmaceutical client base. Understands how the European Medicines Agency (EMA) regulatory body impacts the design and development of single-use systems specific to More...

As the Technical Project Manager you will be responsible for overseeing the planning execution and closing of a complex automation project installation within a pharmaceutical environment. The project will involve installing new automated systems. ResponsibilitiesDevelop and maintain More...