Cgmp Jobs in Malmo
Cgmp Jobs in Malmo
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Overview: TekWissen Group is a workforce management provider throughout the USA and many other countries in the world. The below job opportunity is with one of our Biotech clients who researches develop and commercializes drugs. The company focuses primarily on antiviral drug More...
Job Title cGMP Cleaner Hours: 5 8 hours days 10:30pm 7:00am (mandatory 1 weekend day a week) Training hours: 1st three weeks Monday Friday 8am4:30pm Location: 100% Onsite Frederick MD Job Duration: 12 months Client is a cell therapy company that is focused on providing patients wit More...
Job Title: Cell Therapy Specialist Location: Frederick Maryland Duration 12 months contract Schedule: Initial 7 weeks: MonFri () for New Hire Orientation and Manufacturing Onboarding Technical Training. After 7 weeks: Fulltime 4/10 schedule with shifts directed by manager or depar 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...
Overview: TekWissen Group is a workforce management provider throughout the USA and many other countries in the world. Client is a leading provider of transfusion and transplantation diagnostic products worldwide. We strive to create a world where anyone anywhere in need of blood o More...
Overview: TekWissen Group is a workforce management provider throughout the USA and many other countries in the world. The below job opportunity is with one of our Biotech clients who researches develop and commercializes drugs. The company focuses primarily on antiviral drugs use 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...
JOB DESCRIPTION OF PROPOSED MANAGER QA Opthalmology Job Responsibilities Having 1520 years of experience in pharmaceutical industry and acting as site QA Head role since last 5 years (Oral solid dosage form/Injectable dosage form). To ensure overall compliance of cGMP/ More...
The Technical Services Materials Specialist has primary responsibility in supporting the cGMP manufacture of biological bulk drug substance (BDS) at our clients facility in Blanchardstown, Dublin. The Technical Services Materials Specialist will be responsible for providing support fo 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...
The Environmental Health and Safety Specialist (EHS) is responsible for various duties and responsibilities including:Acting as a subject matter expert in environmental health and safety and effectively communicating with internal and external stakeholders.Developing hazardous and che 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...
Key Responsibilities: Lead and motivate a team of associates and supervisors to achieve organizational goals in safety quality output and cost. Implement and manage lean manufacturing principles. Ensure compliance with SOPs Standard Work QMS policies and procedures. Optimize labor nee 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...
My Client a top company in the pharmaceutical sector is seeking a Quality Manager whose main responsibility will be to ensure products manufactured and imported are consistently of high quality efficacious and safe for patients in line with company s internal requirements whilst com More...
Job Title: Manufacturing Associate / Biotechnologist Associate Location: Portsmouth NH 03801 Duration: 12 Months Job Type: Contract Work Type: Onsite Position Description The Manufacturing Associate is responsible for the manufacture of therapeutic proteins (API) under c More...
About PSC Biotech Ltd 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 cloudbas More...
About PSC Biotech Ltd 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 cloudbas 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...
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