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QA
Beginning your career as part of a lab quality assurance team starts at HireLifeScience.com. Our business provides you with listings for a number of laboratory quality assurance jobs, including compliance engineer, quality control reviewer, QA manager, or laboratory technician jobs. We have years of experience helping people find life science careers and are prepared to provide you with a wide array of great positions at locations throughout the country, in addition to other jobs across the planet. 

When you apply for lab quality assurance and laboratory technician jobs on our Website, you'll be able to get all of the information you need before you take the time needed to fill out an application. After you review the information provided, you can follow the link on listing to send your application to the company. Start working a new career today when you apply for laboratory quality assurance jobs online with HireLifeScience.com. 

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Manager Safety intelligence & Compliance Job

Novo Nordisk Inc. - Plainsboro, NJ

Compliance, Database, Defense, Diabetes, Government, Healthcare, Law, Legal, Management, Manager, Market Research, Marketing, Marketing Manager, Medical, Nursing, Pharmaceutical, QA, Quality, Quality Assurance, Registered Nurse, Research, Safety, Science, Service, Special Medicine, Technology

From Novo Nordisk Inc. - 6/18/2018 5:42:00 AM

Research Associate (NCI)

Leidos Biomedical Research, Inc. - FREDERICK, MD

Qualifications: BASIC QUALIFICATIONS To be considered for this position, you must minimally meet the knowledge, skills, and abilities listed below: - Possession of a B.S. degree or equivalent with emphasis in areas of Molecular Biology, Microbiology, Cell Biology, or Immunology from an accredited college or university according to the Council for Higher Education Accreditation. (Additional...more

From Leidos Biomedical Research, Inc. - 6/18/2018 5:41:46 AM

Research Associate (NCI)

Leidos Biomedical Research, Inc. - FREDERICK, MD

Qualifications: BASIC QUALIFICATIONS To be considered for this position, you must minimally meet the knowledge, skills, and abilities listed below: - Possession of a Bachelor's degree from an accredited college or university according to the Council for Higher Education Accreditation in a field related to biomedical research, such as molecular biology, oncology, or virology (Additional qua...more

From Leidos Biomedical Research, Inc. - 6/18/2018 5:41:46 AM

Quality Systems Administrator

Glenmark Pharmaceuticals Inc., USA - Monroe, NC

Education : - Minimum Associate's degree in scientific discipline (or closely related technical field of study) - Direct experience as a MasterControl Administrator may be used in lieu of degree requirements Experience: - MasterControl Implementation experience preferred. - Minimum of one (1) year of MasterControl Administrative experience required. - Prior pharmaceutic...more

From Glenmark Pharmaceuticals Inc., USA - 6/18/2018 5:41:23 AM

Principal QA Statistician

AstraZeneca Pharmaceuticals - West Chester, OH

Essential Requirements: •Masters of Science Degree in Statistics •5-10 years of statistical experience •Expert user of several statistical packages •A working knowledge in applying a wide range of statistical analyses to a pharmaceutical production/research environment •Knowledge and familiarity with cGMPs, compendia and regulatory standards and guidelines •Excellent written and oral comm...more

From AstraZeneca Pharmaceuticals - 6/18/2018 5:41:10 AM

Sr Specialist, QA GLP

Merck & Co. - West Point, PA

Education Minimum Requirement: • Bachelor's Degree or higher degree in an appropriate science or equivalent field (e.g., biology, chemistry, etc.). Required Experience and Skills: • Minimum of five (5) years' experience in the pharmaceutical industry, or Quality Assurance experience and familiarity with GLPs and international guidelines is required. Your role at Merck is integral to helpi...more

From Merck & Co. - 6/18/2018 5:38:06 AM

Compliance Auditor

Glenmark Pharmaceuticals Inc., USA - Monroe, NC

Responsibilities include but are not limited to: - Ensure financial prudence in resource planning, allocation and manage within approved budgets while building best in class quality processes and systems at site. - Maintain quality system controls to ensure state of compliance and no critical and major market complaints. - Ensure that all statutory and regulatory compliance are regul...more

From Glenmark Pharmaceuticals Inc., USA - 6/15/2018 5:58:38 AM

Quality Control Analyst (Temporary)

Glenmark Pharmaceuticals Inc., USA - Monroe, NC

Responsibilities include but are not limited to: - Be cost effective and vigilant of laboratory reagents, glassware, etcetera to ensure department is within the Revenue and Capex Budget as per spent analysis project. - Provide feedback to management with laboratory standard hours for financial prudence in resource planning, allocation and manpower to ensure within approved budgets while bu...more

From Glenmark Pharmaceuticals Inc., USA - 6/15/2018 5:58:38 AM

Technical Reviewer (Temporary)

Glenmark Pharmaceuticals Inc., USA - Monroe, NC

Education: - Minimum bachelor's degree in science or related discipline is required Experience: - Minimum of 2 years previous experience in related field - Intermediate-level professional contributor on a project or specialty work team - Occasionally a master's degree can substitute for some or all of the required previous experience in related field - Lab/analytical experience...more

From Glenmark Pharmaceuticals Inc., USA - 6/15/2018 5:58:38 AM

Quality Assurance Documentation Associate (Temporary)

Glenmark Pharmaceuticals Inc., USA - Monroe, NC

Responsibilities include but not limited to: - Maintain quality system controls to ensure state of compliance and no critical and major market complaints. - Take appropriate steps to reduce wastages and losses in the analysis process and build improved efficiency. - Executes the initiation, processing, routing, distribution and archiving of all GxP documentation. - Manages recor...more

From Glenmark Pharmaceuticals Inc., USA - 6/15/2018 5:58:38 AM

Manager, Quality Assurance

Glenmark Pharmaceuticals Inc., USA - Paramus, NJ

Key Responsibilities : - Independently conducts internal systems audits of various departments and procedures, including Pharmacovigilance, as assigned. Prepares audit reports independently, with review by CQA management as necessary. - Reviews the audit reports of contracted auditors, and forwards to QA management for final review. - Suggests internal and external audit targets to CQA m...more

From Glenmark Pharmaceuticals Inc., USA - 6/15/2018 5:58:38 AM

QMS Manager

Glenmark Pharmaceuticals Inc., USA - Paramus, NJ

Key Responsibilities : - Ensure the management of Quality Documents in the CR&D Quality System with coordination of their review, approval and release, respectively deviation management. - Review, approve (where necessary), and track the procedural document request and revision forms. - Conduct the QA review of all procedural documents, discuss and agree release and effective date...more

From Glenmark Pharmaceuticals Inc., USA - 6/15/2018 5:58:38 AM

QA Document Control Specialist (NCI)

Leidos Biomedical Research, Inc. - FREDERICK, MD

Qualifications: BASIC QUALIFICATIONS To be considered for this position, you must minimally meet the knowledge, skills, and abilities listed below: - Possession of a Bachelor's degree from an accredited college or university according to the Council for Higher Education Accreditation. (Additional qualifying experience may be substituted for the required education). Foreign degrees must be ...more

From Leidos Biomedical Research, Inc. - 6/15/2018 5:51:46 AM

Compliance and Inspection Readiness Principal

AstraZeneca Pharmaceuticals - Gaithersburg, MD

Responsibilities: •Identify opportunities for and drives the enhancement of existing processes and partnerships through knowledge of internal and external environment. •Working with the P&P  leads, and  Patient Safety and Regulatory experts, develop, establish, monitor, report and assess global  KPIs related to safety and regulatory data reporting. •Utilise safety and regulatory knowledge to...more

From AstraZeneca Pharmaceuticals - 6/15/2018 5:48:33 AM

Senior Specialist Quality Assurance Training Management Job

Novo Nordisk Inc. - Plainsboro, NJ

Administrative, Curriculum, Document Control, Education, Healthcare, Laboratory, Management, Manager, Operations, Pharmacovigilance, QA, Quality, Quality Assurance, Quality Manager, Science, Technology, Training

From Novo Nordisk Inc. - 6/14/2018 5:49:29 AM

Specialist, Quality Assurance

Merck & Co. - West Point, PA

Education Minimum Requirement: • Bachelor's Degree in a science or engineering discipline or related field • A minimum 5 years' experience in the QA IT industry with understanding of the use and validation of laboratory systems from the end-users perspective • Hands-on experience and understanding of major Lab Systems (like NuGenesis, LIMS, Empower, LabWare, Nucleus etc.) supporting pharmace...more

From Merck & Co. - 6/14/2018 5:48:01 AM

Sr Specialist MRL QA Technology

Merck & Co. - Rahway, NJ

Position Qualifications : Education Minimum Requirement: • B.A./B.S. in Computer Science, Information Systems or Science Required Experience and Skills: • Minimum of 3 years pharmaceutical or related industry experience, including work in IT/IS systems validation and/or GxP business quality Preferred Experience and Skills: • Knowledge of Good Clinical Practice and 21 CFR Part 11...more

From Merck & Co. - 6/14/2018 5:48:01 AM

Quality Assurance Associate II

Catalent Pharma Solutions - San Diego, CA

The Role (daily responsibilities) •Performance of general QA activities such as line clearances, internal audits, issuing documents, change control and investigation numbers, etc. •Review and approve equipment calibration or qualification reports. •Support Equipment and Cleaning Validation including review and approval of Validation of equipment documentation IQ, OQ, and PQs and also review ...more

From Catalent Pharma Solutions - 6/13/2018 5:51:34 AM

Quality Assurance Specialist

AstraZeneca Pharmaceuticals - Coppell, TX

Key Accountabilities: • Develop, implement and maintain Quality Assurance processes and systems. • Business Process Owner for External Audit process • BPO for complaint process (PQCs, direct material suppliers), including Super User role for GCM. •Lead / participate in internal Quality System / cGMP audits. • Escalates to QA Line Manager po tential issues of non-compliance. • Writ...more

From AstraZeneca Pharmaceuticals - 6/13/2018 5:51:08 AM

Senior Scientist, Statistical Programming

Merck & Co. - North Wales, PA

• MS in Statistics, Applied Mathematics, Clinical Research Administration, or related field. • 3 years of SAS programming experience in a clinical trial environment, including the following: generating reports and necessary analysis required for NDA and FDA submissions; developing analysis and reporting deliverables (data, analyses, tables, graphs, listings); SAS/MACRO, SAS/GRAPH; performing v...more

From Merck & Co. - 6/13/2018 5:50:41 AM
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