Pharmaceutical Quality Control Jobs in Cambridge, MA

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QA Specialist - Equipment and Computer Systems  

Proclinical Staffing - Cambridge, MA, United States

. Ability to adapt, work under uncertainty and accommodate flexible work demands. Self-motivated; Sense of urgency. Knowledge and expertise of quality systems in a pharmaceutical environment

from: linkedin.com - 7 days ago

Quality Engineer  

BioTalent - Cambridge, MA, United States

/ Pharmaceutical industry Design Control and Change Controls experience Risk management and FMEA experience Strong experience working within a GMP compliant manufacturing facility

from: linkedin.com - 6 days ago

QC Operations Analyst  

Editas Medicine - Cambridge, Massachusetts

or pharmaceutical QC laboratory. Working experience in a cGMP Quality Control laboratory is required. Experience with biologics is preferred. Collaborative with partners to advance the Editas mission. Strong

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from: resume-library.com (+1 source) - 9 days ago

Director of Quality Assurance, Commercial GMP  

Life Sciences Recruitment - Lexington, MA, United States

procedures for GMP manufacturing of clinical materials. Implementing quality systems such as deviation management, CAPA, and change control. Preparing for and managing regulatory inspections and external

from: linkedin.com - 8 days ago

Senior Validation Specialist (Contract)  

a Medical Device Equipment located in near Lexington, MA - Lexington, MA, United States

validation input for quality systems such as CAPAs and change controls. Undertake other assigned duties and projects. Qualifications: Minimum 8-10 years of validation experience in pharmaceutical, medical

from: linkedin.com - 3 days ago

Quality Control Laboratory Support Technician  

Cambridge Isotope Laboratories, Inc. - Andover, Massachusetts

that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years. The Quality Control Laboratory Support

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from: resume-library.com (+1 source) - 2 days ago

Senior Validation Engineer  

a Medical Devices company in MA - Bedford, MA, United States

calibration or validation. Initiating and/or providing validation input on quality systems such as CAPAs and change controls. Responsible for other duties and projects as assigned. RESPONSIBILITIES Minimum 8

from: linkedin.com - 2 days ago

QC Chemist  

TalentBurst, an Inc 5000 company - Framingham, MA, United States

The Quality Control department supports the Seprafilm (medical device) and Sodium Hyaluronate (active pharmaceutical ingredient) GMP operations at the 74/76 NYA Manufacturing Facility. The department

from: linkedin.com - 5 days ago

Quality Assurance Change Specialist  

Cambridge Isotope Laboratories, Inc. - Tewksbury, Massachusetts

, biotech or pharmaceutical GMP regulated environment Advanced knowledge and experience using Microsoft office products including Word, Power Point and Excel Knowledge of cGMP and ISO documentation control

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from: resume-library.com (+1 source) - 6 days ago

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Senior Specialist, Clinical Supplies Project Manager  

Merck - Boston, MA

partner organizations such as Clinical Sciences and Study Management (CSSM), Regulatory, Chemistry, Manufacturing and Controls (CMC), Pharmaceutical Sciences, Formulation Development, and Global Development

from: Pharmadiversityjobboard.com - 17 days ago


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