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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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Director, Plasma Product Development Technical Operations

CSL Behring - Kankakee, IL

Provide effective leadership and management of Technical operations group and builds effective teams including: •Map, manage, motivate, and develop TO talent at all levels •Build strong talent pipeline and succession plan contributing to future hiring within TO, PPD, R&D and CSL •Preparation and assessment of performance objectives providing appropriate feedback across all levels of perfo...more

From CSL Behring - 4/19/2018 5:45:48 AM

Senior Auditor, Quality Assurance & Compliance

Covance, Inc. a division of LabCorp® - Princeton, NJ

Education/Qualifications - University/college degree BA/BS (life science preferred) - Knowledge, understanding, and experience applying ICH Guidelines, GCPs including applicable regulatory requirements for the conduct of clinical development programs - Knowledge of the drug development process from the perspective of a contract research organization - Spanish fluency perferred but not...more

From Covance, Inc. a division of LabCorp® - 4/19/2018 5:44:31 AM

Specialist, QA (International Release)

Merck & Co. - Wilson, NC

Education Minimum Requirement: BS degree in science or engineering related field Required Experience and Skills: A minimum of 4 years experience in a GMP pharmaceutical manufacturing facility either direct involvement in Quality functions supporting release and compliance activities or indirect involvement in Quality functions through execution of activities such as batch record/documentati...more

From Merck & Co. - 4/19/2018 5:44:23 AM

Specialist, Quality Assurance

Merck & Co. - Wilson, NC

Education Minimum Requirement: No minimum requirement. Required Experience and Skills**: A minimum of 3 years experience in a GMP pharmaceutical manufacturing facility either direct involvement in Quality functions supporting release and compliance activities or indirect involvement in Quality functions through execution of activities such as batch record/documentation reviews, investigations, co...more

From Merck & Co. - 4/19/2018 5:44:23 AM

Associate Director, Quality Assurance, GLP

Merck & Co. - West Point, PA

Education Minimum Requirement: •Bachelor's or higher degree in an appropriate science or equivalent field (e.g., biology, drug metabolism, etc.) with extensive experience in Good Laboratory Practices and computer validation. Required Experience and Skills: •Minimum of five (5) years experience in the pharmaceutical industry, auditing or quality experience and a thorough understanding of G...more

From Merck & Co. - 4/19/2018 5:44:21 AM

Director of Biometrics Automation and Tools

AstraZeneca Pharmaceuticals - Gaithersburg, MD

Main Duties and Responsibilities Reporting to the Head of B&I Technology Solutions you will be part of the Extended Programming Leadership Team and will have a number direct reports (2-10).  You will be responsible for continuous improvement and lifecycle management of B&I production technologies (software, environments, tools), in collaboration with internal/external groups. You will proactively...more

From AstraZeneca Pharmaceuticals - 4/19/2018 5:44:04 AM

(Senior) Pilot Production Supervisor

AstraZeneca Pharmaceuticals - Gaithersburg, MD

P ilot Production Supervisor Principal Duties: •First line authority figure for process area.   Responsible to initiate, monitor, and take appropriate actions related to process operations •Responsible for overseeing the accurate and timely completion of clinical manufacturing campaigns and the associated cGMP documentation •Direct/Assign junior staff (Tech 1 to Lead ) on daily/tactical...more

From AstraZeneca Pharmaceuticals - 4/19/2018 5:44:04 AM

Engineer II QA R&D

Novartis Pharmaceuticals - Lake Forest, CA

Minimum Qualifications: •Bachelor's Degree or equivalent years of directly related experience •The ability to fluently read, write, understand and communicate in English •2 Years of Relevant Experience Our generous benefits package includes the Novartis Investment Savings 401(k) Plan which provides a company contribution of up to 6%. In addition, after one year of service, employees are eligible ...more

From Novartis Pharmaceuticals - 4/19/2018 5:43:43 AM

Manager, External Supplier Quality

Novartis Pharmaceuticals - Fort Worth, TX

•Bachelor's degree or equivalent years of directly related experience. •The ability to fluently read, write, understand and communicate in English •7 Years of Relevant Experience •5 Years of Demonstrated Leadership

From Novartis Pharmaceuticals - 4/19/2018 5:43:43 AM

QA Specialist-Night shift

Catalent Pharma Solutions - St. Petersburg, FL

The Role (daily responsibilities) •Collaborates with management and supervisory personnel from Operations, Quality Control and Quality Assurance to resolve problems affecting product quality; collaboration includes reacting, investigating and following up with Operations for non-conformance issues and a working jointly towards resolution •Provide guidance and plan of action to the manufacturin...more

From Catalent Pharma Solutions - 4/18/2018 5:48:51 AM

QA Specialist - Compliance (NCI)

Leidos Biomedical Research, Inc. - FREDERICK, MD

PREFERRED QUALIFICATIONS Candidates with these desired skills will be given preferential consideration: - Combination of QA and QC or manufacturing experience - Working knowledge of quality systems and TrackWise - Experience with the GMP manufacture of Phase I/II clinical material Expected Competencies: - Advanced level professional providing professional input to complex assi...more

From Leidos Biomedical Research, Inc. - 4/18/2018 5:48:33 AM

Associate Director, External Quality

Merck & Co. - Whitehouse Station West, NJ

Education Minimum Requirement: • Bachelor's degree or higher in a scientific or technical discipline Required Experience and Skills**: •Minimum 7 years applied professional work in the pharmaceutical industry. Minimum 5 years experience with master's degree or higher. •Strong working knowledge of change control processes •Working knowledge of GCM Trackwise Preferred Experience and S...more

From Merck & Co. - 4/18/2018 5:48:08 AM

Director, GMP Compliance

Merck & Co. - West Point, PA

Education Minimum Requirement: • B.A./B.S. in life sciences, chemistry, engineering, or related relevant discipline. Required Experience and Skills**: • Minimum of 10 years' experience in the FDA and/or EU regulated pharmaceutical environment; preferably in a manufacturing site in leading manufacturing and/or quality roles and/or in Global Quality; experience in vaccines, biologics, devic...more

From Merck & Co. - 4/18/2018 5:48:08 AM

Tissue Operations Expert (Associate Director Regional HCT Processing)

Novartis Pharmaceuticals - Dallas, TX

University degree with an advanced degree in science preferred (e.g., MS, PhD., Pharm. D., MD, RN) English 10+ years of GxP pharmaceutical experience or at least 5 years pharmaceutical experience and experience in GTP • Working with US or international blood/tissue requirements. • Understanding of drug development and submission requirements. • Understanding of commercial material/product expectat...more

From Novartis Pharmaceuticals - 4/18/2018 5:47:26 AM

Vice President- R&D External Innovation and Partnerships North America Job

Novo Nordisk Inc. - Boston, MA

Biology, Biotech, Business Development, CAPA, Executive, Management, R&D, Research, Sales, Science, VP

From Novo Nordisk Inc. - 4/18/2018 1:27:23 AM

Senior GLP Quality Assurance Consultant

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

Education/Qualifications - A Bachelor's degree, preferably in science or a related field Experience - At least 5 years of experience in a GCP/GLP-regulated environment with at least one year of auditing experience - Working knowledge of current regulatory guidelines including GCP/GLP and 21 CFR Part 58 and a general knowledge of ICH GCP compliance - Strong working knowledge of FDA ...more

From Covance, Inc. a division of LabCorp® - 4/17/2018 8:02:48 AM

Study Coordinator BioA

Covance, Inc. a division of LabCorp® - Madison, WI

Education/Qualifications - Bachelor of Science (BS) degree in science or related field. - Experience may be substituted for education. - Ability to utilize word processing software, database, spreadsheet, and specialized software. Experience - Minimum of 1.5 years of related experience. - Excellent communication, presentation, and interpersonal skills. - Excellent attention t...more

From Covance, Inc. a division of LabCorp® - 4/17/2018 8:02:48 AM

QA Specialist - Lot Release (NCI)

Leidos Biomedical Research, Inc. - FREDERICK, MD

PREFERRED QUALIFICATIONS Candidates with these desired skills will be given preferential consideration: - Combination of QA and QC or manufacturing experience - Working knowledge of quality systems and TrackWise - Experience with the GMP manufacture of Phase I/II clinical material Expected Competencies: - Intermediate professional role, responsible for delivery of professional activ...more

From Leidos Biomedical Research, Inc. - 4/17/2018 8:00:55 AM

Aseptic Processing/Product Lifecycle Steward - Pharma, Med. Device

Novartis Pharmaceuticals - Fort Worth, TX

BSc in Pharmacy, Pharmaceutical Technology, Chemistry or equivalent scientific degree. Preferred: MSc, or equivalent experience. Fluent in English 5 years directly related experience in process support role on the shop floor of pharmaceutical manufacturing and/or QA/QC. Preferred: 15 years experience Proven process understanding (Pharma, GMP, Regulatory aspects). Sound experience of data handlin...more

From Novartis Pharmaceuticals - 4/17/2018 8:00:17 AM

Senior Lead Quality Auditor

Novartis Pharmaceuticals - Houston, TX

Minimum: Bachelor's degree in sciences or engineering from an accredited college or university English Minimum: • 5 years of quality assurance experience in a regulated industry (FDA, ISO) • 2 years' experience in auditing in a regulated industry • 1 year managing direct reports Preferred: • 2-3 years' experience managing direct reports • 2-3 years' experience in developing, implementing, e...more

From Novartis Pharmaceuticals - 4/17/2018 8:00:17 AM
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