Cgmp Jobs in Frankfurt
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Overview: TekWissen group is a workforce management provider throughout the USA and many other countries in the world. Our client is a leading biotechnology company that combines technological insight with worldclass manufacturing scientific expertise and process excellence a More...
Responsibilities:IPQA Officer for General Injectables:Perform inprocess quality checks during manufacturing and packaging of general injectable products.Conduct line clearance and equipment checks to ensure compliance with Standard Operating Procedures (SOPs).Monitor critical process More...
Supervising operators in liquid during the production process, assuring the process flow according to cGMP rules. Coaching of the Supervisors and Operators Responsible for new projects and Validation processes Aligning with Quality team and engineering all the calibration and pr More...
Roles & Responsibilities: Knowledge required in International codes such as ASME API TEMA etc Preparation of standard operating procedures specification and standard testing procedures Documentation of analytical data and preparation of STP. Responsible for compliance t More...
Role: Packing and Dispatch ManagerSalary: 35,000 - 40,000 per annum (DOE) Location: Tonbridge, Kent Hours: 7.30am to 4.30pm with 1 hour at lunch time.KHR has partnered with a rapidly expanding manufacturer with an excellent reputation for high-quality goods, who are recruiting More...
Packaging Manager 35,000 - 40,000pa Tonbridge, Kent Monday to Friday 7.30am to 4.30pmKHR has partnered with a rapidly expanding manufacturer with an excellent reputation for high-quality goods, who is recruiting for a Packing and Dispatch Manager to join their team on a permane More...
Position Title: Manufacturing OperatorLocation: Hauppauge or Central Islip New YorkShifts: 1st Shift (07:00 am 03:30 pm) 2nd Shift (03:00 pm 11:30 pm)Job Overview:As a Manufacturing Operator based in Hauppauge or Central Islip New York you will play a pivotal role in the pharmaceuti More...
Job Profile: To Perform shop floor compliance to cGMP and GDP and facility/equipment up keeping. As a Section QA Role in Track wise to Perform Activates like Preliminary Investigation Interrogation with Persons related to deviation approval of change controls Initiation of change More...
Athens GA Contract Duration: 636 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a Packaging Technician in the Athens GA area. 1st shift: Monday to Friday 6:30AM 3:00PM To perform the duties associated with labeling inspecting and packaging of More...
Position: Material Handler Duration: 12 months (Possible to extend) Pay Rate: $20/hr on W2 Location: Germantown MD 20874 Shift: MF day Youll provide shipping receiving storage and order fulfillment services for clinical sites and laboratories. Pick pack sort arrange More...
Job Title: Manufacturing Supervisor Synthesis and Production Microbiology Duration: 12 Month Shift: 7:00 am 3:00 pm PST Work Location: San Diego CA 92127 SUMMARY: The main responsibility for the Synthesis and Production Microbiology Supervisor is to lead and oversee all p More...
QUALIFICATIONS NEEDED: Degree or diploma in Chemistry / Analytical Chemistry / Biochemistry /Biotechnology or equivalent. NECESSARY EXPERIENCE AND INDUSTRY KNOWLEDGE: At least 8 years of experience in the vaccine/pharmaceutical/biotech manufacturing industry. At least 5 years o More...
Quality Control Lead Chemistry Material Handling Pharma
Abc Worldwide -
Cape Town
-
South Africa
QUALIFICATIONS NEEDED: Degree or diploma in Chemistry / Analytical Chemistry / Biochemistry /Biotechnology or equivalent. NECESSARY EXPERIENCE AND INDUSTRY KNOWLEDGE: At least 8 years of experience in the vaccine/pharmaceutical/biotech manufacturing industry. At least 5 years More...
Plan and Organize the Engineering department comprising of Mechanical Electrical HVAC Utilities and Project work. Exposure of cGMP of Pharmaceutical industries and exposure of Regulatory audits. Solid Understanding of Human machine interface and related software programming. Coordina More...
Title : Specialist Quality Assurance Type: W2 Visa: USC/GC/EADS Preferred OPT/CPT (If they dont have any employer already) H1B (If open for H1B transfer) Provide quality onthefloor support of manufacturing reviewing documentation and providing realtime support of manufacturing iss More...
Roles & Responsibilities: CQV Lead Engineer for all CIP Equipment in the DSM Buildings initially responsible for review of all Design deliverables from Jacobs including Drawings Datasheets specifications and Engineering Lists. Lead generation of all CQV CIP Documentation FAT wrap More...
QC Lab Supervisor (OOJ 19650) Lancaster South Carolina USA Industry(ies) Pharmaceutical Primary Skills Pharmaceutical Companies Qc Chemmist Secondary Skills Qc Lab Occupational Categories Science/ Life Science/ Biotechnology Work Experience (Years) 37 Degree University Bachelors Deg 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...
618 years of experience in managing Industrial Pharmaceutical cGMP & FMCG Projects and Datacenter projects. Additional experience in interior design and landscape architecture would be preferred. Proficiency in AutoCAD and Revit. Knowledge of Photoshop 3D Max or Google Sketchup wou More...
For further inquiries regarding the following opportunity please contact one of our Talent Specialists Meghna at Title: Quality Lab Associate I Location: Round Lake IL Duration: 12 Months Description: Shift: Weekend 2 other nights Hours :4 10hour shifts (Friday through Su More...
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