Cgmp Jobs in Bucharest

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...

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...

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...

Key Responsibilities: Vendor Development and finalising them Responsible for overall Purchase of R & D & Manufacturing sites. Responsible for procurement of Capex Purchase and Opex Purchase for Engineering. Managing a wide number of functions like Engineering 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...

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...

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...

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...

POSITION RESPONSIBILITIES o Working knowledge of basic laboratory techniques for application in all aspects of Reagent Bead production o Assist in the development and maintenance of procedures used in Reagent Bead manufacturing o Reagent Formulation Lab equipment maintenance o Maintai More...

For further inquiries regarding the following opportunity please contact one of our Talent Specialists Rashi at Title: Quality Lab Associate I 3rd Shift Location: Round Lake IL Duration: 12 Months Description: Shift: 3rd Hours: 4 10hour shifts (Sunday to Thursday 10 pm to 8 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: Material Handler (Packaging Operations) FLSA Classification: FullTime NonExempt/Hourly Professional Work Location: Fall RiverMA Work Hours: First Shift: 8:00 AM 5:00 PM (may vary based on business needs) Purpose: The purpose of this role is to serve as a Packaging Op 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...

Job Title: Manufacturing Operator Job Type: FullTime NonExempt/Hourly Professional Work Location: Fall River MA and Central Islip NY Work Hours: First Shift: 8 AM 5 PM (may vary based on business needs) Reports To: Facilities Operations Manager Purpose: The purpose of this role i More...

Review Analytical documents Protocols and Reports of Stability Analytical Method Validation Analytical Method Verification and Analytical Method Transfer. Recording deviations and findings taking corrective and preventive actions defined and implemented in due time & trending of t More...

Please share your resumes at Job Role: Validation Engineer Contract: W2 Location: Newark CA Position Overview/Responsibilities: Ensure quality and compliance with established procedures and standards. Generate review and approve baselevel documents such as the Valid More...

Qualifications B.S./M.S. degree in appropriate engineering/scientific field Minimum of 03 years postBachelors degree experience in a cGMP environment (e.g. Production Development Process Engineering Technical Services or related field) in pharmaceutical/ biotech industry P More...