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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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Chemist II - Coppell, Texas

AstraZeneca Pharmaceuticals - Coppell, TX

Responsibilities:  • Accurately complete all data entry requirements for methods or tasks performed, reviewing data for completeness and accuracy. • Prepare solutions and standards per Procedures, Analytical Procedures and/or SOPs, with appropriate documentation. • Clean and maintain the general laboratory facilities and notify appropriate maintenance  personnel as needed. • Develop and mai...more

From AstraZeneca Pharmaceuticals - 2/22/2018 5:46:04 AM

Chemist I - Coppell, TX

AstraZeneca Pharmaceuticals - Coppell, TX

Key Accountabilities: •         Ethical conduct and compliance •         Accurately complete all data entry requirements for methods or tasks performed, reviewing data for completeness and accuracy. •         Prepare solutions and standards per Procedures, Analytical Procedures and/or SOPs, with appropriate documentation •         Clean and maintain the general laboratory facilities •         D...more

From AstraZeneca Pharmaceuticals - 2/22/2018 5:46:04 AM

Information Center, Quality Assurance Specialist

AstraZeneca Pharmaceuticals - Wilmington, DE

Main Duties and Responsibilities You will be responsible for performing the tasks of the US product quality complaint (PQC) process to ensure consistent, clear, effective, and timely identification and communication of all PQCs to the appropriate investigation supply sites. Understand and support the PQC processes of external customers. Integrate across the organization by developing and maintain...more

From AstraZeneca Pharmaceuticals - 2/22/2018 5:46:04 AM

Associate Director, Quality Assurance Pharmacovigilance

Merck & Co. - Rahway, NJ

Education: • Bachelor's degree or equivalent in relevant area Required: • A minimum of 8 years of relevant experience in the pharmaceutical industry (i.e., drug development, clinical and/or non- clinical research, regulatory compliance, clinical study monitoring or Pharmacovigilance). • A substantial work history in pharmacovigilance and QA oversight activities. Preferred: • Previous ...more

From Merck & Co. - 2/22/2018 5:45:46 AM

Quality Control Inspection & Operations Job

Novo Nordisk Inc. - West Lebanon, NH

Diabetes, Electrical, Engineering, Healthcare, Housekeeping, Inspection, Inspector, Laboratory, Medical, Operations, Operations Manager, QA, QC, Quality, Quality Assurance, Quality Control Inspector, Science, Special Medicine, Technology

From Novo Nordisk Inc. - 2/21/2018 5:44:00 AM

Senior QC Associate

Catalent Pharma Solutions - Madison, WI

The Role • Accurately reviews analytical and/or microbiological testing following SOPs. • Reviews and verifies analytical and/or microbiological data and reports, ensuring accuracy and consistency. • Provides clear feedback for corrections needed. • Actively participates in team meetings. The Candidate • B.S./B.A. in Biotechnology, or related field, with minimum of 3 years experien...more

From Catalent Pharma Solutions - 2/21/2018 5:42:43 AM

Compliance Auditor

Catalent Pharma Solutions - Woodstock, IL

The Role •Manages, leads, and conducts audits (customer, external, and internal).  Includes risk assessments, scheduling, preparing documents prior to the audit, creating PRs in TrackWise and managing audit during execution, and closure. •Support preparations for planned Health Authority Inspections. •Support of site Supplier Review Board. •Support Central Supplier Quality Management ...more

From Catalent Pharma Solutions - 2/21/2018 5:42:42 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. •Review and approval of Validation of equipment documentation IQ, OQ, and PQs. •Support Equipment and Cleaning Validation. •Review cleaning veri...more

From Catalent Pharma Solutions - 2/21/2018 5:42:41 AM

Medical Technologist I - Genomics - Day Shift-Rotate Weekends!

Covance, Inc. a division of LabCorp® - Indianapolis, IN

Education/Qualifications Individual must qualify as testing personnel under the following CLIA 1988 and New York State Department of Health requirements: Bachelor's degree in Medical Technology or Clinical Laboratory Science or other life science with completion of at least a 12-month training program in Medical Technology. Or Bachelor's degree in a chemical, physical or biological ...more

From Covance, Inc. a division of LabCorp® - 2/21/2018 5:42:02 AM

Senior Specialist, Quality Assurance Pharmacovigilance

Merck & Co. - Rahway, NJ

Education: • Bachelor's degree or equivalent in relevant area Required: • A minimum of 5 years of relevant experience in the pharmaceutical industry (i.e., drug development, clinical and/or non- clinical research, regulatory compliance, clinical study monitoring or Pharmacovigilance). Preferred: • A substantial work history in pharmacovigilance and/or QA oversight activities, including c...more

From Merck & Co. - 2/21/2018 5:41:48 AM

Senior Mechanical Design Engineer

Novartis Pharmaceuticals - Lake Forest, CA

Minimum requirements •BS Mechanical Engineering or related discipline and two years relevant work experience OR equivalent mix of education and experience. •Excellent written and verbal English communication skills. Preferred Requirements •Ability to take responsibility for multiple concurrent design activities •Must possess fundamental, theoretical and applied knowledge related to general m...more

From Novartis Pharmaceuticals - 2/21/2018 5:41:32 AM

Quality Engineer I

Novartis Pharmaceuticals - Sinking Spring, PA

Minimum requirements Bachelor's degree or equivalent experience. English. 2 years in QA cGMP manufacturing role that included investigations / CAPA preferred

From Novartis Pharmaceuticals - 2/21/2018 5:41:32 AM

GMP Partner - Automation API Job

Novo Nordisk Inc. - Clayton, NC

CAPA, Compliance, Diabetes, Engineer, Engineering, Facilities, Healthcare, Legal, Management, Medical, Medical Device, Operations, Pharmaceutical, Project Manager, QA, Quality, Quality Assurance, Science, Special Medicine, Technology

From Novo Nordisk Inc. - 2/20/2018 7:02:58 AM

Manager, QA (Audit)

Cook Pharmica - Bloomington, IN

Responsibilities - Managing and monitoring quality assurance site audit functions working with Catalent Corporate Quality (i.e., internal and customer audits) - Provide support and participate in regulatory agency inspections (US FDA, ROW) - Providing oversight for processes to ensure regulatory compliance to FDA regulations, global regulations and Catalent internal directives in the m...more

From Cook Pharmica - 2/20/2018 7:02:00 AM

Associate, QA Systems

Catalent Pharma Solutions - Madison, WI

Education / Experience: •Bachelor's Degree in technical discipline (e.g. biology, biotechnology, engineering) or related life science; or •Associates Degree in technical discipline (e.g. biology, biotechnology, engineering) or related life science with minimum two years related experience.

From Catalent Pharma Solutions - 2/20/2018 7:01:39 AM

Associate Quality Assurance Inspector 1st shift

Catalent Pharma Solutions - Somerset, NJ

The Role •Provide QA support to manufacturing for clinical and commercial batches. •Performs Line Clearances, equipment releases and AQL inspections.  •Audit of raw materials and facility logs.  •Interdepartmental communication for obtaining information.      •Comply with and ensure compliance of the department with Health, Safety, and Environmental responsibilities.     •Assist with batc...more

From Catalent Pharma Solutions - 2/20/2018 7:01:39 AM

CSS Director, Continuous Improvement, Technology and Engineering

Catalent Pharma Solutions - Kansas City, MO

•Experience in maintaining regulatory compliance thru audits, validation, change management, risk assessments, qualified drawings, corrective action plans, FMEA, and deviation support. •Utilize and promote Operational Excellence, Six Sigma & Lean methodologies to all work flows with ability to run Kaizen Events •Provide oversight and technical expertise during the development of new strategic ...more

From Catalent Pharma Solutions - 2/20/2018 7:01:39 AM

Raw Material Chemist

Catalent Pharma Solutions - Woodstock, IL

The Role • Perform analytical testing and calculations on raw materials including excipients, resins, foils, and active pharmaceutical ingredients • Operate analytical instrumentation such as FTIR and UV-Vis •Coordinate testing with peers and prioritize testing depending upon supply chain and production needs • Prepare test reports and perform cGMP documentation in all areas of the laborat...more

From Catalent Pharma Solutions - 2/20/2018 7:01:39 AM

QA Associate, Operations

Novartis Pharmaceuticals - Morris Plains, NJ

Minimum requirements BS/BA in Biological Sciences or equivalent relevant career experience English Minimum of 2 years GMP manufacturing and/or QA related experience, at least 1 year of which are in the area of quality assurance and/or compliance or equivalent experience.

From Novartis Pharmaceuticals - 2/20/2018 6:59:44 AM

QA Specialist, Operations

Novartis Pharmaceuticals - Morris Plains, NJ

Minimum requirements BS/BA in Biological Sciences or equivalent relevant career experience English Minimum of 7 years GMP manufacturing and/or QA related experience, at least 5 years of which are in the area of quality assurance and/or compliance or equivalent experience.

From Novartis Pharmaceuticals - 2/20/2018 6:59:44 AM
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