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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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Critical Systems Operator

Teva Pharmaceuticals USA - Irvine, CA

Qualifications Education Required: High School diploma or equivalent. Education Preferred Completion of vocational courses in areas such as welding, mechanics, control systems, electrical, refrigeration, HVAC, or Freeze drying is desirable. Refrigeration license or technical school certificate is highly desirable. Experience Required: Experienced in repair, installation or maintenance to H...more

From Teva Pharmaceuticals USA - 2/16/2018 5:51:10 AM

Project Manager

Catalent Pharma Solutions - San Diego, CA

The Role (daily responsibilities) •Work directly with Client-side Project Managers to develop, write and process work orders as part of the RFP process. •Liaise between clients, science and manufacturing teams to drive project and process solutions. •Prepare and present monthly/quarterly (or as required) project updates to client management via telephone and at client sites. •Manage all cli...more

From Catalent Pharma Solutions - 2/16/2018 5:50:46 AM

BioA Study Coordinator II

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

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. - Skilled in concise writing. Writing should require little external review or edit. - Knowledge of grammar, punctuation, composition, and spelling. Ex...more

From Covance, Inc. a division of LabCorp® - 2/16/2018 5:50:15 AM

Principal Engineer (Design Control)

Novartis Pharmaceuticals - Fort Worth, TX

Minimum requirements Minimum Qualifications-- •Bachelor's degree in Engineering •6 years directly related experience •Proficiency in the English Language Preferred Qualifications- • Advanced degree in engineering • Demonstrated experience with ISO 14971 • DFSS (Design for Six Sigma) experience • Demonstrated experience in new product development (focus on Design Control and/o...more

From Novartis Pharmaceuticals - 2/16/2018 5:49:38 AM

QA Area Specialist - Complaints Job

Novo Nordisk Inc. - Clayton, NC

Compliance, Customer Service, Diabetes, Healthcare, Human Resources, Legal, Medical, Medical Device, Performance Management, Pharmaceutical, QA, Quality, Quality Assurance, Science, Special Medicine, Technology

From Novo Nordisk Inc. - 2/16/2018 5:49:20 AM

Associate Director

AstraZeneca Pharmaceuticals - Gaithersburg, MD

Essential Requirements: •Advanced degree in the life sciences, chemistry or appropriate engineering discipline is required. •Minimum 8-10 years of increasing documented success in biopharmaceutical field, with at least 5 of those years in regulatory affairs biotechnology CMC.  •Strong background in cGMP, facilities and post-marketing submissions.  •Experience with monoclonal antibody manufa...more

From AstraZeneca Pharmaceuticals - 2/16/2018 5:49:06 AM

Quality Inspector

Catalent Pharma Solutions - Philadelphia, PA

The Role •Responsible for ensuring that Standard Operating Procedures are consistently followed and that cGMPs are observed, in the course of incoming inspection, distribution, label control, destruction and returns. This may require the simultaneous auditing and/or monitoring of one or more processes. •Verifies and inspects incoming materials and works accordingly with Quality and Projec...more

From Catalent Pharma Solutions - 2/15/2018 5:47:32 AM

Validation Specialist / Validation Specialist II

Novartis Pharmaceuticals - Morris Plains, NJ

Minimum requirements Education: BS degree in Scientific discipline or other related field with significant prior experience or equivalent. Skills/Experience: • 5+ years of Pharmaceutical industry experience and 5 + years of Facilities, Utilities, Equipment and Analytical Instruments experience required for Validation Specialist. • 8+ years of Pharmaceutical industry experience and 8 + years ...more

From Novartis Pharmaceuticals - 2/15/2018 5:46:30 AM

Principal Engineer - PMO Obsolescence, Continuity

Novartis Pharmaceuticals - Irvine, CA

Minimum requirements -Bachelor's or greater, preferably a Master of Science in engineering or physics discipline or educational equivalent is required. -7 years of directly related experience in a systems engineering, technical supply chain, technical project mgt., or process development role. -In depth understanding of electro-mechanical, optical, software controlled medical ophthalmic equipmen...more

From Novartis Pharmaceuticals - 2/15/2018 5:46:30 AM

Study Technician Dose Form

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

Education/Qualifications Required: - Bachelor of Science/Arts (BS/BA) degree in chemistry or related scientific field - Experience may be substituted for education. - Ability to perform basic computer skills (e.g., Word, Excel). Experience Required: - No experience required.

From Covance, Inc. a division of LabCorp® - 2/15/2018 5:46:17 AM

Medical Information Specialist

CSL Behring - King of Prussia, PA

Main Responsibilities and Accountabilities: 1. Leads efforts in researching, writing, and reviewing database of accurate, evidence-based, balanced medical information SRLs and FAQs for US and Global Medical Affairs that results in effective communication with our internal and external stakeholders. Establishes and conducts periodic review of current literature for evaluation and inclusion in resp...more

From CSL Behring - 2/14/2018 5:44:13 AM

Senior QA Technician

Cook Pharmica - Bloomington, IN

Responsibilities - Provide clerical support to the Quality Assurance department (e.g., issuing records and other documents, posting documents for client review) - Providing administrative support for Quality initiatives designed to enhance the Quality Management System and to ensure successful completion of key Quality projects. Qualifications High School/GED - Technical Certif...more

From Cook Pharmica - 2/14/2018 5:43:18 AM

QA Technician

Cook Pharmica - Bloomington, IN

Responsibilities - Provide clerical support to the Quality Assurance department (e.g., issuing records and other documents, posting documents for client review) - Providing administrative support for Quality initiatives designed to enhance the Quality Management System and to ensure successful completion of key Quality projects. Qualifications - High School/GED - Technical Certi...more

From Cook Pharmica - 2/14/2018 5:43:18 AM

Sample Coordinator - Part Time

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

Education/Qualifications - Associates Degree (Experience may be substituted for Education) - Working Knowledge of computers Experience - Minimum Required: - Customer service skills including attention to detail, accuracy, confidentiality and communication skills (is preferred). - Ability to identify and communicate client's service needs.

From Covance, Inc. a division of LabCorp® - 2/14/2018 5:42:22 AM

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

Novartis Pharmaceuticals - Fort Worth, TX

Minimum requirements 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). ...more

From Novartis Pharmaceuticals - 2/14/2018 5:42:12 AM

Associate Specialist, Quality Assurance - Sample Examination

Merck & Co. - Wilson, NC

Education Minimum Requirement: • Bachelors or Masters degree Required Experience and Skills: • Minimum of 4 years experience within a GMP pharmaceutical manufacturing facility. • Experience investigating and resolving production issues. • Knowledge of regulatory requirements/cGMPs. • Excellent written and oral communication skills. • Excellent leadership and teamwork skills, including c...more

From Merck & Co. - 2/14/2018 5:41:54 AM

Director of Biometrics Safety Reporting

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 (4-20).  You will ensure the Biometrics Safety Reporting group develops, implements, and champions relevant standards for data integration and analysis and reporting. You will ensure consistent approaches to safety da...more

From AstraZeneca Pharmaceuticals - 2/14/2018 5:41:32 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 - 2/14/2018 5:41:32 AM

Clinical Project Manager/Senior Clinical Project Manager

AstraZeneca Pharmaceuticals - Gaithersburg, MD

Requirements/Qualifications: Education : •University degree, preferably in a biologic/scientific discipline Experience : o   5 + years of biotech and/or pharmaceutical industry experience Special Skills/Abilities : •Thorough understanding of country level regulations, ICH and GCP guidelines •Thorough understanding of cross-functional clinical processes including data managemen...more

From AstraZeneca Pharmaceuticals - 2/14/2018 5:41:32 AM

Product Quality Specialist

Catalent Pharma Solutions - Winchester, KY

The Role •Primary quality liaison for clients and internal customers. Is expected to become the Subject Matter Expert for the client products, processes and requirements.   •Serves as NPI support member for products/processes which may not have a specified QA representative. •Responsible for supporting internal, client, and regulatory audits through coordination and/or leadership of the audi...more

From Catalent Pharma Solutions - 2/13/2018 5:49:05 AM
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