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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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Novo Nordisk Inc.
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Clayton, NC
CAD, Construction, Diabetes, Drafting, Electrical, Engineer, Engineering, Environmental Health & Safety, Facilities, Healthcare, Industrial Engineer, Maintenance, Manufacturing, Operations, Pharmaceutical, Science, Special Medicine, Technical Support, Technician, Technology
From
Novo Nordisk Inc. -
4/23/2018 5:44:38 AM
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2
793175
Scientist
Scientist
Catalent Pharma Solutions
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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.
•Execute analytical methods in a GMP environment
•Authors technical documents, such as protocols, test methods, text report...more
From
Catalent Pharma Solutions -
4/23/2018 5:44:20 AM
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Catalent Pharma Solutions
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Limoges, Région Île-de-France
The Role :
You will have two missions:
1) As part of the data integrity regulation, you are implementing data governance in the pharmaceutical quality system to meet regulatory expectations. You will assist the different departments of the site to optimize the manual GMP data processing systems. In addition, you apply ALCOA best practices in data management throughout the entire data lifecycle. ...more
From
Catalent Pharma Solutions -
4/23/2018 5:44:20 AM
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AstraZeneca Pharmaceuticals
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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
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Amicus Therapeutics
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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
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Amicus Therapeutics
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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
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Amicus Therapeutics
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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
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Catalent Pharma Solutions
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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
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Covance, Inc. a division of LabCorp®
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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
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Merck & Co.
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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
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Merck & Co.
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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
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Novartis Pharmaceuticals
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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
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Catalent Pharma Solutions
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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
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Catalent Pharma Solutions
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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
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AstraZeneca Pharmaceuticals
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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
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Covance, Inc. a division of LabCorp®
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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
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Novartis Pharmaceuticals
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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
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Novartis Pharmaceuticals
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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
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Novartis Pharmaceuticals
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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
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Novartis Pharmaceuticals
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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
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