Cgmp Jobs in Porto-Novo
Cgmp Jobs in Porto-Novo
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Responsibilities:Maintaining work place good House Keeping as per cGMP.Operation and cleaning of Equipment as per SOP.Receipt and Storage of raw material in day stock area for the batch as per Request slip.Carry out the process as per LMR and operation verification.All safety rules/pr More...
0-1 yrs experience with High School Diploma Ability to work independently or in collaboration with others on assigned tasks Ability to comply with cGMP standards Must possess computer skills Ability to follow instruction and directions Desirable Skills/Experience: More...
Overview TekWissen Group is a workforce management provider throughout the USA and many other countries worldwide. The job opportunity below is for one of our clients specializing in biotechnology product development services. Our client is dedicated to supplying laboratory eq More...
CAPA Specialist (College station TX) Environment: The CAPA specialist will be responsible for supporting a backlog of the clients CAPAs. They must have experience in several aspects of tracking coordination and closure of CAPAs change controls and deviations and ists in supporting th More...
Title: QC Microbiology Analyst Location: Miami FL Onsite experience need : 6years TOP QUALITIES INCLUDE: Thorough knowledge and understanding of current Good Manufacturing Practices (cGMP) FDA Guidance and ICH Guidelines Strong microbiology skills with a focus on drug product c More...
Regulatory Data Integrity/Data Migration Specialist Houston TX (onsite) We have a new position on site just outside Houston TX. They are looking to add one maybe two consultants to help with Data migration. Scope: Support client with the data migration (data entrydata verifica More...
Title: QC Microbiology yst Location: Miami FL Onsite experience need : 6years JD: Thorough knowledge and understanding of current Good Manufacturing Practices (cGMP) FDA Guidance and ICH Guidelines Strong microbiology ss with a focus on drug product contamination control and e More...
Accountabilities: As a QC Microbiology Analyst, you will be responsible for implementing methods and techniques for analysis of cell therapy products, such as: bioburden, endotoxin, gram staining, and sterility. You will handle routine QC lab tasks such as technical transfer test More...
Accountabilities: As a Senior Process Facilitator, you will provide direction to PET personnel, promote safe work practices, ensure cGMP’s are used and followed during production, and promote a positive work environment. You will also be responsible for training of PET pe More...
About the Job Oleson specialises in delivering highquality talent and solutions that enhance the capabilities and operational excellence of our global customers. We are focused on matching the dynamic needs of Data Centre and Life Science clients with skilled professionals thereby d More...
About PSC Biotech 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 cloudbased More...
Job Title: QA Associate Work Location: Basel Country: Switzerland Duration: 6 months Rate: CHF 35.13 CHF 44.87 (8 hours per day) depending on experience Your main duties as a QA Associate will include:Supporting the timely release of GMP relevant documents and batches and More...
Field QA Specialist Pharma (Onsite Devens MA) We are looking for a Field QA specialist for a Global pharmaceutical Company. You will be responsible for quality activities for the Single Use Facility in accordance with the clients policies standards procedures and Global cGMP. Funct More...
CK Group are recruiting for a number of Shift QC Analysts, to work within a Quality Control Laboratory for a leading pharmaceutical organisation that develop and manufacture veterinary products. The QC Analyst will be working on site in Dundee on a permanent basis.This client is offer 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...
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...
Would you like to join a leading Digital Solution Company and contribute to innovative solutions that are built on a daily basisOur client is a leading global provider of IT solutions and services known for their customercentric approach to digital transformation. With a rich history More...
Would you like to join a leading Digital Solution Company and contribute to innovative solutions that are built on a daily basisOur client is a leading global provider of IT solutions and services known for their customercentric approach to digital transformation. With a rich history More...
Stewardess Charter Italyfrance 30m My
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...
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