Cgmp Jobs in Vieste

Direct Hire. 4555/hrFull time. El Segundo CA Responsibilities: The Senior Maintenance Technician will be responsible for the maintenance and repair of manufacturing and production equipment including calibration troubleshooting and preventative maintenance. This involves working wit More...

Temp Packaging Operator needs 2 years experienceTemp Packaging Operator requires:InventoryPackagingWarehouseProductionQualitycGMPTemp Packaging Operator duties: Setup operate and clear packaging line equipment and/or ancillary support equipment to meet efficiency expectations. Repleni More...

ProQR Therapeutics is a biotechnology company listed on NASDAQ with offices in Leiden the Netherlands and Cambridge Massachusetts USA. ProQR is focused on the development of life changing RNA therapies to meet the unmet need of individuals and families with common and rare diseases. A More...

Perform project electrical and pneumatics hardware and PLC/HMI software design including test and validation activities on equipment and systems in accordance with applicable regulatory standards and to cGMP and GAMP 5 guidelines for the pharmaceutical industry. Liaise with associa More...

Our client is seeking a Direct Hire for an Senior Automation Engineer for its Wilmington MA office. The position requires proven technical proficiency in implementing automation solutions using PLC DCS HMI and SCADA platforms with a strong focus on leadership and project management.K More...

Description: Performance of MFG formulation protocols Performance of QC testing protocols (Instrument proficiency MFG and QC protocols) Data Review batch record review Knowledge of Microsoft Office Foster Team Environment Calibration and Maintenance of Lab Equipment Lab Duties More...

Laboratory Support Technician II We are looking for a Lab Support Technician II to join our team. The Lab Support Technician II will ensure that all Buildings are cleaned and all equipment (tanks buckets and bottles) used in the manufacturing of SLI products are cleaned and stored pro More...

Project Manager Onsite preferred but flexible for hybrid Santa Monica CA Job Responsibilities This role is responsible for supporting and managing a diverse range of projects within Global Supply Chain Organization. The responsibilities include: Overseeing multiple assigne More...

Should be able to demonstrate strong understanding of USFDA/ MHRA/ EU or local guidelines. Responsible for setting strategy direction for the entire Quality Control & Microbiology Department and team. Conducts performance reviews for teams Development, review, revise and impl More...

Dear Partner Good Morning GreetingsfromNukasanigroupInc!Wehavebelowurgentlongtermcontractprojectimmediatelyavailable for****Research Associate Quality Control Somerville NJ**** need submissions you please review the below role if you are available could you please send me updated wor More...

We are hiring for QC AnalystDesignation Sr ExecutiveLocation NetherlandsQualifications Bachelors/Master of Science in Chemistry with Experience and working knowledge of CGMP regulations is required. Key Skills English language is required. To ensure the compliance with More...

About PSC Biotech Who are wePSC 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...

Strong understanding of USFDA/ MHRA/ EU or local guidelines Responsible for setting strategy direction for the entire Production Department and team. To enforce the batch manufacturing as per cGMP requirements in order to obtain high quality products. To achieve targeted producti More...

Overview: We are seeking a Senior Automation Engineer with strong expertise in PLC DCS HMI and SCADA platforms. This role involves leading a team of engineers working directly with clients to identify requirements and delivering innovative automation solutions.Key Responsibilities:Dev More...

Experience Required: 7 years of experience in procurement preferably in the Pharma/Nutra industry. Proven track record in vendor management contract negotiation and procurement operations. Strong knowledge of cGMP guidelines and quality compliance in materials management. Pers More...

QC Analyst/Sr. ExecutiveFor FTE Min 1 to 3 yrs experienceFor Contarct BSc FresherQualifications BSc/Master of Science in Chemistry with Experience and working knowledge of CGMP regulations is required.Should be Experienced in :Maintenance of the Laboratory Reporting of abnormal obs More...

We are seeking a proactive Quality Assurance Coordinator to join our team. In this role you will support all Quality Systems to ensure quality manufacturing of products as defined by current Good Manufacturing Practices (GMP). You will assist other departments with quality and GMP iss More...

Job Description RESPONSIBILITIES Reports to the Facilities Manager interface with internal management and external auditors. Ensures activities on the Master Cleaning Schedule (MCS) are performed and documented Ensures that cGMP and Quality requirements are followed throu More...

JOB PURPOSE: To perform pharmaceutical microbiological procedures in compliance with FDA regulations and other regulatory/audit groups in order to ensure the accuracy of test results and raw data generated. KEY ACCOUNTABILITIES: Policies, Processes & Procedures: Follows a More...

OverviewThe CMC Document Specialist is responsible for developing, reviewing, and managing technical documentation related to chemistry, manufacturing, and control (CMC) activities within the pharmaceutical industry. This includes preparation and submission of regulatory documents, de More...