Cgmp Jobs in Berlin

Required Pharmaceutical Production Formulation SpecialistLocation: Ankleshwar Gujarat IndiaIndustry Pharma FormulationMust have 35 Years of Experience (Must be from Formulation Industry)Job Description:As a Pharmaceutical Production Formulation Specialist you will play a pivotal role 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...

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...

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...

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...

Quality Control Pharma FormulationRequired Quality Control AnalystLocation: Ankleshwar Gujarat IndiaIndustry Pharma FormulationMust have 35 Years of Experience (Must be from Formulation Industry)Job Description:As a Quality Control Analyst in pharmaceutical manufacturing you will pl 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...

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...

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...

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...

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 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...

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...