Cgmp Jobs in Stuttgart

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...

Prepare and review SOP’s related to Quality Systems following the guidelines established according to Egyptian regulations and the guidelines established according to cGMP requirements. Establish a defined Deviation procedure and CAPA system, involving appropriate stakeholder More...

Our Client is a leading multinational company operating in the Pharmaceutical industry. They are dedicated to innovation wellness and sustainability with a rich legacy of trust and excellence in the healthcare industry. The client is setting up a stateoftheart pharmaceutical manufactu More...

Title: Chemist I Duration: 6 months Location: 4701 International Blvd Wilson NC 27893 Interview Mode: 1st webcam/phone and 2nd In person Standard Hrs. Per Week: 40 hours Mon Thurs (10 hours/day excluding breaks) Shift time: 7:00 am 5:30pm Job Summary Performs a variety of ch 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...

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...

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...

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...

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...

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 (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...

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...

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...

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...

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 Title: Manufacturing Operator FLSA Classification: FullTime NonExempt/Hourly Professional Work Location: Fall River MA Work Hours: First Shift: 8 AM 5 PM (may vary based on business needs) and 2nd Shift: 3:00 PM 11:30 PM Reports To: Facilities Operations Manager Purp More...