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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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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

Manager, IT App Dev Commercial Application Systems

Amicus Therapeutics - Cranbury, NJ

Roles and Responsibilities The Manager, IT Applications Development will be responsible for: • Working closely with the Commercial Operations business managers and system administrators to deliver quality solutions for specified requirements • Managing multiple, high-complexity projects within the constraints of scope, quality, time, and cost to deliver specified requirements and meet customer sa...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 Systems Associate I

Catalent Pharma Solutions - Kansas City, MO

The Role •Client Service; Answering window, phone or email, completing client (internal) requests in a timely manner.  Includes but is not limited to checking out documents or laboratory notebooks, providing electronic scans of whole or partial documents upon request and checking in documents or laboratory notebooks when delivered to the Records Center. •Electronic Data Entry; Entry of doc...more

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

Food Project Microbiologist - Client Process Validation

Covance, Inc. a division of LabCorp® - Livermore, CA

Education/Qualifications B.S. or M.S. in Food Microbiology, Food Engineering or closely related area Experience 2-3 years of related experience in food industry or research and the ability to travel

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

Packaging Mechanical Technician - Trainee (2nd & 3rd Shift)

Merck & Co. - West Point, PA

Education: • Associate's Degree or higher in Applied Science - OR - High School Degree/GED in conjunction with equivalent Associate's Degree program or vocational certificate - OR -equivalent military course work NOTE: Equivalent programs will require training in courses such as: • Mechanical Pumps, Belts and Chain Drives • Lubrication and Installation of Bearings • Industrial Electr...more

From Merck & Co. - 4/19/2018 5:44:22 AM

Senior Specialist, Quality Assurance, Computer System Validation

Merck & Co. - West Point, PA

Education Minimum Requirement: • B.S. and/or M.S. degree in an appropriate Life Science, Computer Science, Information Technology or Engineering discipline. Required Experience and Skills: • Experience working in a Pharmaceutical/Biotechnology industry; experience working in a health authority regulated (e.g. GxP) environment. • A minimum of 5 years of industry experience including c...more

From Merck & Co. - 4/19/2018 5:44:22 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

Process Validation Specialist

Catalent Pharma Solutions - Brussels, Région de Bruxelles-Capitale

The Role •Ensure that all qualifications and validations are performed according to the regulatory and customer requirements •Validation of aseptic process  (formulation, filling, holding times)  •Ensure that all activities are performed according to the schedule •Ensure that all activities are properly documented •Write qualification and validation protocols and reports and other do...more

From Catalent Pharma Solutions - 4/18/2018 5:48:52 AM

Equipment Technician

Catalent Pharma Solutions - San Diego, CA

The Role (daily responsibilities ) •Equipment Cleaning •Support disassembly of manufacturing equipment prior to cleaning •Participate in manufacturing equipment cleaning •Sample manufacturing equipment for cleaning verification •Prep solutions for manufacturing equipment cleaning •Document cleaning verification results and submit results for approval •Data entry and analysis •Calibrati...more

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

Senior Quality Device Engineer

AstraZeneca Pharmaceuticals - West Chester, OH

Essential Job Functions: •Lead medical device and combination product Quality System initiatives at West Chester. Develop strategies, priorities, and plans as required. •Support activities related to the Combination Product and Medical Device Quality Management System, ensuring compliance to all applicable regulations. •Authoring, compilation and maintenance of Design History File content, C...more

From AstraZeneca Pharmaceuticals - 4/18/2018 5:47:39 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

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

Technical Steward, Packaging

Novartis Pharmaceuticals - Hicksville, NY

BSc. in Packaging Engineering or Mechanical Engineering. Desirable MSc. or equivalent experience. Fluent in English and proficient in site local language. Minimum 5 year experience in GMP manufacturing relevant to the specialist area of expertise. Proven process understanding (Pharma, GMP, Regulatory aspects).

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

QA Batch Manager

Novartis Pharmaceuticals - Morris Plains, NJ

BS/BA in Biological Sciences or equivalent relevant career experience Fluent in English written and oral. Minimum of 10 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 - 4/17/2018 8:00:17 AM

Process and Product Steward for Pharmaceutical Aseptic Manufacturing

Novartis Pharmaceuticals - Fort Worth, TX

Bachelor's degree or equivalent years of directly related experience Fluent in English 5 years directly related experience

From Novartis Pharmaceuticals - 4/17/2018 8:00:16 AM

Automation Engineer

Novartis Pharmaceuticals - Morris Plains, NJ

Bachelor's Degree required - Engineering or related field preferred. A minimum of 3+ years' experience with automation systems. Extended interdisciplinary technical knowledge. Knowledgeable in a GMP regulated environment (pharmaceutical preferable). Experience with automation systems (Continuum, Siemens, DeltaV, PLCs, etc). Knowledge of IT infrastructure/networks related to automation systems. S...more

From Novartis Pharmaceuticals - 4/17/2018 8:00:16 AM

Manager, Raw Materials

Novartis Pharmaceuticals - Morris Plains, NJ

Education: Bachelor's degree in Scientific discipline or equivalent work experience Experience: Min. 12-15 years' experience in an operational GxP area, in Manufacturing/Development or QA with knowledge in chemistry, pharmacy and/or biotechnology with Other Qualifications: •Strong interpersonal, written and communication skills along with problem solving and follow-up skills are required. •Deta...more

From Novartis Pharmaceuticals - 4/17/2018 8:00:16 AM

Sr Process Molding Engineer I

Novartis Pharmaceuticals - Houston, TX

Education Requirements • Minimum: Bachelor degree in Engineering or related technical discipline • Preferred: Bachelor degree in Plastics Engineering Experience Requirements • Minimum: 2 years experience in high volume molding and manufacturing environment • Preferred: 2 years experience in medical device manufacturing or other highly regulated industry • Working knowledge of Validation processes ...more

From Novartis Pharmaceuticals - 4/17/2018 8:00:16 AM
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