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Validation
Providing laboratory validation and quality control systems for life science companies is important. By verifying tests and checking on methods, you'll make sure that each test is working properly and that your company continues to succeed. HireLifeScience.com provides validation laboratory technician jobs for people who love the finer details and want to start a new career in life science.
Putting in applications for laboratory technician jobs is a breeze when you put in your application through HireLifeScience.com. Each of these listings features detailed information about the job, letting your know what it takes to work as part of the company's laboratory validation team. Furthermore, you can apply directly to each job from the listing, allowing you to apply to a number of jobs without having to click around. Learn more about lab validation and quality control systems by reading about each job featured here. We offer a wide array of jobs in the United States and other locations across the globe. 

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Senior Specialist, Clinical Systems Implementation

Merck & Co. - Upper Gwynedd, PA

Education Minimum Requirement: • B.S. Degree > +10 years experience; or M.S. / MBA / JD Degree >+8 years experience; or PhD +5 years experience. Required Experience and Skills: • System Validation, System Development Life Cycle Experience • Two to five years of clinical trials experience. • Recognized as "team player", possess good project management skills and committed to continuous ...more

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

Quality Assurance Validation Specialist

Glenmark Pharmaceuticals Inc., USA - Monroe, NC

Responsibilities include but not limited to: - Ability to read/interpret validation and engineering documents (protocols and reports). - Ability to interpret and relate Validation standards for implementation and review to functional areas. - Follow directions; performs well-defined tasks. - Investigate and troubleshoot problems which occur and determine solutions or recommendati...more

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

Scientist

Catalent Pharma Solutions - Morrisville, NC

The Role (daily responsibilities) •Usually works with some supervision, conferring with superior on unusual matters. May be assisted by laboratory technicians/assistants or associate level scientists. Assignments are broad in nature, requiring originality and ingenuity. Has appreciable latitude for un-reviewed action or decision. •Develop and execute analytical methods in a GMP environment •...more

From Catalent Pharma Solutions - 6/15/2018 5:54:52 AM

QC Chemist II API Job

Novo Nordisk Inc. - Clayton, NC

Chemist, Chemistry, Diabetes, Engineering, Healthcare, Laboratory, Science, Scientific, Scientist, Special Medicine

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

Sr. Specialist, Manufacturing Automation

Merck & Co. - West Point, PA

Education Minimum Requirement: • Bachelor's Degree in Engineering, Science, Information Technology or other relevant discipline Required Experience and Skills: •Minimum of 6 years experience in process automation or equivalent Preferred Experience and Skills: •Experience in Automation Platforms PLCs (Allen Bradley, Siemens), SCADA, DCSs (DeltaV), OSI PI •Experience with Computer System...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

Qualification & Validation Specialist Media Fill

Catalent Pharma Solutions - Brussels, Région de Bruxelles-Capitale

The Role: •Design the aseptic process simulation (Media fill, Sterile hold-time, Aseptic manipulation) •Supervise the annual program "Media fills" •Review annually the number and type of aseptic manipulations to be simulated •Ensure that all activities are performed according to the schedule •Ensure that all activities are properly documented •Write validation protocols and reports...more

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

Manufacturing Engineer, Varicella Bulk Facility Operations

Merck & Co. - Durham-RTP, NC

Education: • Bachelors Degree or higher in Chemical Engineering, Biochemical Engineering, or related field with a minimum of three (3) years of relevant GMP experience Required: • Experience in vaccine or biologics manufacturing within an aseptic, cGMP environment • Experience creating and revising standard operating procedures within a cGMP context • Experience working independently, ...more

From Merck & Co. - 6/13/2018 5:50:40 AM

Sr Specialist, Recovery Cleaning Validation Job

Novo Nordisk Inc. - Clayton, NC

Business Process, Developer, Diabetes, Document Management, Electrical, Engineer, Engineering, Facilities, Finance, Healthcare, Inspector, Management, Operations, Pharmaceutical, QA, Quality, Quality Assurance, Risk Management, Science, Six Sigma, Six Sigma Black Belt, Special Medicine, Technology

From Novo Nordisk Inc. - 6/12/2018 5:45:41 AM

QA Calibration 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. - 6/12/2018 5:45:24 AM

NPI Project Coordinator

Catalent Pharma Solutions - Brussels, Région de Bruxelles-Capitale

The role of the NPI Project Coordinator is to collaborate with both the client and the internal departments to ensure completion of the project. What we offer is a diversified and transversal role within a very dynamic and fast-paced company. This position will not only allow you to work with all departments (Supply Chain, Procurement, Quality, Maintenance and Engineering, etc.) but also enjoy clo...more

From Catalent Pharma Solutions - 6/12/2018 5:44:53 AM

Qualification Specialist QC

Catalent Pharma Solutions - Brussels, Région de Bruxelles-Capitale

The role •Plan, follow-up and perform routine calibration & qualification activities according to the site validation master Plan •Perform initial & periodical Computerized System validation for QC equipment at site 21 CFR Part 11 •Ensure that all activities are performed according to the schedule. •Ensure that all activities are properly documented, according to SOP, customer and regu...more

From Catalent Pharma Solutions - 6/12/2018 5:44:53 AM

Quality Assurance Specialist II

AstraZeneca Pharmaceuticals - Philadelphia, PA

Qualifications: Education: • Bachelors degree in a Science / technical field such as Pharmacy, Biology, Chemistry or Engineering or any Bachelors degree.   Required: •Minimum of three (3) years' experience in the pharmaceutical industry in roles covered by GMP oversight. • Strong ability and motivation to learn. more

From AstraZeneca Pharmaceuticals - 6/12/2018 5:44:00 AM

Senior GLP Quality Assurance Auditor

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® - 6/11/2018 5:49:28 AM

Analyst, Contract Admin

Merck & Co. - West Point, PA

Education Minimum Requirement: BS/BA degree required Required Experience and Skills ** : • Prior work or internship experience in sales, customer service, training, teaching, finance, accounting, or technology fields Preferred Experience and Skills: • A personable team player with strong communication skills • A self-starter with the ability to solve complex problems • Strong anal...more

From Merck & Co. - 6/11/2018 5:49:00 AM

QA Technical Specialist/Quality Engineer - (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 - 6/8/2018 5:49:21 AM

Laboratory Technician I

Organovo - San Diego, CA

Laboratory Technician I Skills and Experience: Previous lab experience preferred but not required Experience in one of the following preferred: mammalian tissue culture, ELISA, qPCR, histology, flow cytometry AA or BS in Biology, Bioengineering or a related field. Experience with mammalian cell culture and asceptic techniques preferred but not required. Strong math skills Highly organized ...more

From Organovo - 6/7/2018 7:52:34 AM

Technical Transfer Lead

Novartis Pharmaceuticals - Huntington, WV

Bachelor degree in Engineering/ Physics or related discipline Masters degree in. Engineering/ Physics or related discipline Excellent knowledge of English and proficient in Site local language. Minimum: 7 years experience in high volume manufacturing environment with experience of process engineering, automation implementation and project management Preferred: 5-10 years experience in medical devi...more

From Novartis Pharmaceuticals - 6/7/2018 5:45:09 AM

QC Sr Mgr

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

Education/Qualifications - 6+ years experience leading/managing teams, developing strategies, execution of projects, 4+ years partnering/guiding clients at management levels, 2+ years leading large IT validation projects. - Familiar with various validation methodologies (SDLC), and their implementation in an IT organization - Knowledgeable of regulatory compliance requirements in the pha...more

From Covance, Inc. a division of LabCorp® - 6/7/2018 5:44:42 AM

Medical Technologist III - Chemistry - First Shift

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

Education/Qualifications - S. Requirements 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 chemi...more

From Covance, Inc. a division of LabCorp® - 6/7/2018 5:44:42 AM
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