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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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Trainee GLP QA Auditor

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

Education/Qualifications - A Bachelor's degree in science or a related field or a combination of education, training, and experience Experience - Strong drive for process optimization and data integrity - Excellent communication and interpersonal skills with great attention to detail - Familiarity with clinical research - Experience working in a regulated environment is a plus

From Covance, Inc. a division of LabCorp® - 4/20/2018 5:50:54 AM

Senior Specialist Quality Assurance -IT Systems

Merck & Co. - Madison, NJ

Education: •Bachelor of Science degree (minimum) in science, engineering, or other relevant field (advanced degree preferred). Required: •A minimum of 3 years of relevant experience in a pharmaceutical IT QA role (21 CFR Part 11, GLP OECD 17, GMP Annex 15, GAMP) •A high level of professionalism, demonstrated oral and written communication skills, demonstrated understanding of related ...more

From Merck & Co. - 4/20/2018 5:50:42 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 management, biosta...more

From AstraZeneca Pharmaceuticals - 4/20/2018 5:50:18 AM

Fill-Finish Process Engineer (Associate Scientist II/Scientist I)

AstraZeneca Pharmaceuticals - Gaithersburg, MD

The candidate should have capability, skill and/or knowledge in most of the following areas: •biopharmaceutical drug product development •fill-finish unit operations including formulation, mixing, filtration, fill and lyophilization •biopharmaceutical degradation pathways and mechanisms •QbD, experimental design, statistics, modeling •technical writing and documentation •cGMP, asept...more

From AstraZeneca Pharmaceuticals - 4/20/2018 5:50:18 AM

QA Technical Specialist - (Louisville, KY)

AstraZeneca Pharmaceuticals - Shepherdsville, KY

Essential Job Functions: •Serving as local business process owner (BPO) for several AZ quality system elements (e.g. change control, investigations, complaints, self-inspection, supplier quality management, etc.) to ensure their compliant and timely execution and continuous improvement. •Ensuring site operations, equipment, processes and product comply with local, regional, and corporate proc...more

From AstraZeneca Pharmaceuticals - 4/20/2018 5:50:18 AM

QA Analyst I

Novartis Pharmaceuticals - Huntington, WV

Bachelor's degree in a Science Discipline or 8 years of directly related experience English No prior experience required. Prior Laboratory testing and analysis experience preferred.

From Novartis Pharmaceuticals - 4/20/2018 5:49:51 AM

Operations Planner

Novartis Pharmaceuticals - Fort Worth, TX

Education : •Minimum: Technician with continuing education (EU) or BS/MS or equivalent •Desirable: MS or equivalent Experience: •Successfully demonstrated several years (mini-mum of 3 years) of directly related experience as scientist or 3-5 years (for BS) or 1-3 years (for MS). •Knowledge of cGMP and Annex 13 requirements •Strong scientific and technical knowledge skills: in product manufacturin...more

From Novartis Pharmaceuticals - 4/20/2018 5:49:50 AM

Operations Planner

Novartis Pharmaceuticals - Fort Worth, TX

Education : •Minimum: Technician with continuing education (EU) or BS/MS or equivalent •Desirable: MS or equivalent Experience: •Successfully demonstrated several years (mini-mum of 3 years) of directly related experience as scientist or 3-5 years (for BS) or 1-3 years (for MS). •Knowledge of cGMP and Annex 13 requirements •Strong scientific and technical knowledge skills: in product manufactur...more

From Novartis Pharmaceuticals - 4/20/2018 5:49:50 AM

Executive Director, Global Head of Safety and Pharmacovigilance

Amicus Therapeutics - Cranbury, NJ

Roles and Responsibilities - Lead the Global Drug Safety and Pharmacovigilance function - Have direct managerial responsibilities pertaining to the function as appropriate - Be responsible for oversight of global drug safety processes and drug safety deliverables - Build on the existing Drug Safety and Pharmacovigilance function at Amicus. - Provide detailed, accurate and timely medical...more

From Amicus Therapeutics - 4/19/2018 12:59:21 PM

Manager, Quality Systems Administration and CSV Compliance

Amicus Therapeutics - Cranbury, NJ

Roles and Responsibilities - Experience in QA / Validation performing protocol review and approval associated with the implementation and maintenance of computerized systems in pharma/biotech environments. - Provide QA assessment and approval for GXP computer system changes. - Demonstrates in-depth knowledge of QA systems principles, concepts, industry practices, and standards. - Support a...more

From Amicus Therapeutics - 4/19/2018 12:59:21 PM

Microbiology Manager

Amicus Therapeutics - Cranbury, NJ

Roles and Responsibilities - This role is responsible for overseeing the Quality Control (QC) microbiology testing function in support of testing services of Phase I-III and commercial appropriate Microbiological testing and Environmental Monitoring functions performed at CMO and CLOs. - Provides Microbiological technical QC expertise at site, within and outside of department, in area of speci...more

From Amicus Therapeutics - 4/19/2018 12:59:21 PM

Quality Control Associate (Contract)

Amicus Therapeutics - Cranbury, NJ

Roles and Responsibilities - Understanding statistical data-listings, tables and figures to ensure they are incorporated and interpreted appropriately into the written document. - Verifying source data to written document in clinical study reports and regulatory submission documents. - Assisting in the resolution of comments from Quality Assurance. - Cross functional interactions include m...more

From Amicus Therapeutics - 4/19/2018 12:59:21 PM

Associate Director, Quality Operations and Management

Amicus Therapeutics - Cranbury, NJ

Roles and Responsibilities - Develop and implement quality management strategy and plans, including resources, systems, timescales, and financials to support the organization's annual business plan and long term strategy. - Based upon strategic Program Plans, develop long range plans and high level timelines. - Ensure detailed plans and timing meet strategic intent and achieve critical miles...more

From Amicus Therapeutics - 4/19/2018 12:59:20 PM

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

Associate Scientist

Catalent Pharma Solutions - Morrisville, NC

The Role Under general supervision, performs work that is varied and that may be somewhat difficult in character, but usually involves limited responsibility. Some evaluation, originality or ingenuity is required. Follows established protocols and work plans. May be assisted by laboratory technicians /assistants. •Execute laboratory work plan / schedule developed with input from supervisor •...more

From Catalent Pharma Solutions - 4/19/2018 5:45:03 AM

Laboratory Associate

Catalent Pharma Solutions - Morrisville, NC

The Role •Under close supervision and guidance, performs tasks from detailed instructions and established procedures.  After conducting basic analysis, interpretation and evaluation of results, work is reviewed for soundness of judgment and adherence to procedure. •Execute laboratory work plan / schedule developed by supervisor or senior team member. •Edits technical documents, such as t...more

From Catalent Pharma Solutions - 4/19/2018 5:45:03 AM

Laboratory Associate

Catalent Pharma Solutions - Morrisville, NC

The Role •Under close supervision and guidance, performs tasks from detailed instructions and established procedures.  After conducting basic analysis, interpretation and evaluation of results, work is reviewed for soundness of judgment and adherence to procedure. •Execute laboratory work plan / schedule developed by supervisor or senior team member. •Edits technical documents, such as t...more

From Catalent Pharma Solutions - 4/19/2018 5:45:03 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
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