Cgmp Jobs in Hong Kong

Should be able to demonstrate strong understanding of USFDA/ MHRA/ EU or local guidelines. Responsible for setting strategy direction for the entire Quality Control & Microbiology Department and team. Conducts performance reviews for teams Development, review, revise and impl 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...

Athens GA Contract Duration: 936 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a Validation Engineer I/ II in the Athens GA area. (onsite) Perform Smoke studies and assist in semiannual Media fill qualifications as a SME Perform requalification/period More...

Strong understanding of USFDA/ MHRA/ EU or local guidelines Responsible for setting strategy direction for the entire Production Department and team. To enforce the batch manufacturing as per cGMP requirements in order to obtain high quality products. To achieve targeted producti 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...

Job Title: SYSTEMS ENGINEER Job Location: Boston MA(HybridThree days onsite with two days Remote) Job Duration: LongTerm Job Description: REQUIREMENTS: MUST HAVE SOP Documentations GENERATION experience! 8 or more years of Systems Engineering experience with a degree in bio tec More...

Coppell TX Contract Duration: 936 months Rate: Negotiable Responsibilities: Excellent employment opportunity for a Production Operator in the Coppell TX area. (onsite) Team D: As a member of the Manufacturing team the operator will contribute through performing varying tasks related More...

OverviewThe CMC Document Specialist is responsible for developing, reviewing, and managing technical documentation related to chemistry, manufacturing, and control (CMC) activities within the pharmaceutical industry. This includes preparation and submission of regulatory documents, de More...

Qualifications 3rd Shift Role Education: BS in life science (e.g. Chemistry biology microbiology immunology virology etc.) or engineering (e.g. biomedical chemical). Years of experience: At least 2 years. Required Experience/Skills: Must have excellent communication docume More...

For further inquiries regarding the following opportunity please contact one of our Talent Specialists Rakeshwar at Title: Quality Lab Associate I (3rd shift) Location: Round Lake IL Duration: 12 Months Description: 3rd shift role 10 pm 8 am Could be any of the following shi More...

Job Title: Manufacturing Operator FLSA Classification: 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) and 2nd Shift ( 3:00 PM 11:30 PM Purpose: The purpose of th More...

To execute works as per procedure and compliance with ISO 9001 standards Quality Management System Compliance cGMP standards ISO 14001 & Halal HACCP standards. Sound knowledge in electrical maintenance in API PlantsCandidate should read and understand SLD and electrical diagra More...

Our direct client is looking for a QA Analyst in Massachusetts(Onsite). Job Title: QA Analyst Location: Tyngsborough MA Type: Full Time W2 SUMMARY: The Quality Assurance Manager will be responsible for managing the quality management system and ensuring regulatory compliance for the 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 Prev More...

Job Title: Technical Services Senior Associate Job Duration: 09 months Contract on W2 Job Location: Thousand Oaks CA 91320 Note: US Citizen or Perm Residents/GC required for this position Job Description: Complete daily tasks assigned by the artwork planner. Ensures high More...

Job description Job Title: Junior Quality Control Chemist Job Summary: The Quality Control Chemist plays a crucial role in ensuring the quality and safety of products in various industries including pharmaceuticals cosmetics food and beverages and manufacturing. The primary resp More...

Job Id OOJ 19838 Job Title Quality Assurance Document Supervisor Industry(ies) Biotechnology/ Life SciencesPharmaceutical Primary Skills Quality Assurance Professionals Location Lancaster SC Work Experience (Years) 315 Degree University Bachelors Degree/34 Year 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...

Job Title: Reagent Fill Technician III Duration: 6 Month with the possibility of extension Work Location: San Diego CA 92127 Summary: Responsible for performing manufacturing and assembly of clinical and commercial products. Weighs measures and checks raw materials and/or manu More...

Job Title: Reagent Fill Technician IV Duration: 6 Month with the possibility of extension Work Location: San Diego CA 92127 Job Description Summary: Responsible for performing manufacturing and assembly of clinical and commercial products. Weighs measures and checks raw materia More...