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QC
Laboratory quality assurance jobs are some of the most important jobs in the laboratory. By working as part of the laboratory QC process, you make sure that ever little bit of data that leaves your lab is of the utmost quality. HireLifeScience.com, an online source for life science and laboratory technician jobs, features many great QA jobs for scientists and medical specialists who are looking for new careers in the life science field. Available jobs include analytical chemist, research associate, and QA manager, just to name a few.
Click on the current laboratory QC jobs we have featured here and see if there is a job available for you. We always have plenty of listings for laboratory technician jobs as part of the QC team. Each listing features important information you need to know about the job, as well as a link that you can click on to apply for the position. See if you can find a new career as part of a laboratory quality assurance specialist when you apply through HireLifeScience.com.
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Covance, Inc. a division of LabCorp®
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Greenfield, IN
Education/Qualifications Recommended:
High school diploma or equivalent Experience
Computer literacy, willingness to learn and desire to work in a team oriented environment
From
Covance, Inc. a division of LabCorp® -
4/20/2018 5:50:53 AM
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Novartis Pharmaceuticals
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Morris Plains, NJ
BA or MS or advanced degree in biology, chemistry, biochemistry, microbiology or other related science or equivalent work experience.
Experience:
0 - 5 years of relevant experience in the pharmaceutical, biologics, microbiology, sterile manufacture, or medical device industry. • Knowledge of cGMP and an understanding of the concepts of GLP, good clinical practices and FDA guidelines, applicable s...more
From
Novartis Pharmaceuticals -
4/20/2018 5:49:51 AM
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Novartis Pharmaceuticals
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Morris Plains, NJ
BA or MS or advanced degree in biology, chemistry, biochemistry, microbiology or other related science Fluent in English Greater than 5 years of relevant experience in the pharmaceutical, biologics, microbiology, sterile manufacture, or medical device industry. • Knowledge of cGMP and an understanding of the concepts of GLP, good clinical practices and FDA guidelines, applicable state and foreign ...more
From
Novartis Pharmaceuticals -
4/20/2018 5:49:50 AM
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Amicus Therapeutics
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Cranbury, NJ
Roles and Responsibilities
- Prepare, author, review, coordinate or maintain simple and complex regulatory submissions, including original IND/IMPD, IND/IMPD amendments, annual reports and agency meeting briefing documents in accordance with applicable regulations
- Manage all the regulatory submission documents and the associated supporting documents
- Coordinate the authoring, review and c...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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Amicus Therapeutics
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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
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Catalent Pharma Solutions
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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
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Catalent Pharma Solutions
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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
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Catalent Pharma Solutions
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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
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Leidos Biomedical Research, Inc.
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BETHESDA, MD
PREFERRED QUALIFICATIONS
Candidates with these desired skills will be given preferential consideration:
- Analytical assay experience
- Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/210/211)
Leidos Overview:
Leidos is a global science and technology solutions leader working to solve the world's toughest challenges in the defense, intelligence, home...more
From
Leidos Biomedical Research, Inc. -
4/19/2018 5:44:48 AM
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Covance, Inc. a division of LabCorp®
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Indianapolis, IN
Education/Qualifications
B.S. degree in Chemistry or Biology from accredited college or university Experience
1 year minimum experience performing extractions and working with LC-MSMS systems in production environment (not research)
From
Covance, Inc. a division of LabCorp® -
4/19/2018 5:44:31 AM
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Covance, Inc. a division of LabCorp®
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Princeton, NJ
Education/Qualifications
- 5 years of postgraduate of relevant experience in the application of PK and PD to clinical trials for employees with a BSc in the field of Bioanalytical Chemistry or a Biological Life Sciences Degree (minimum). Experience
- Strong knowledge of Clinical Development.
- Proficient in compartmental/non-compartmental data analysis.
- Specialist in WinNonLin. ...more
From
Covance, Inc. a division of LabCorp® -
4/19/2018 5:44:31 AM
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Merck & Co.
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Durham-RTP, NC
Position Qualifications
Education Minimum Requirement
BS degree in Engineering or Science
Required Experience and Skills
• Minimum 5 years of experience within in the Pharmaceutical industry in Quality, Technical, Manufacturing Operations, or related Business Operations working with Deviation Management, CAPAs, Product Quality Complaints, and Adverse Event investigations
• Experience performing ...more
From
Merck & Co. -
4/19/2018 5:44:23 AM
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Merck & Co.
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Millsboro, DE
Position Qualifications:
Education Minimum Requirement:
• BS in Microbiology or Biology with focus in Microbiology
Required Experience and Skills**:
• 3 + years of experience in GMP environment, Pharmaceutical/Biological Quality or Technical function supporting manufacturing or testing operations, or related industry experience in a laboratory, manufacturing, science related or regulated se...more
From
Merck & Co. -
4/19/2018 5:44:22 AM
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Merck & Co.
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Whitehouse Station West, NJ
Education Minimum Requirement:
• Degree in Life Sciences, Engineering or related relevant discipline.
Required Experience and Skills**:
• Minimum of 6-8 years' experience in the FDA and/or EU regulated pharmaceutical environment; preferably in a manufacturing site/GMP environment in site/global quality, operational excellence and/or project management roles.
• Demonstrated senior-level ...more
From
Merck & Co. -
4/19/2018 5:44:22 AM
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AstraZeneca Pharmaceuticals
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Gaithersburg, MD
Main Duties and Responsibilities
•Assists in the writing/editing of clinical regulatory and other supporting documents for assigned studies/indications, and assists in the management of the overall development and approval process. Assists in the analysis, synthesis, and presentation of complex information. Provides QC review support as needed.
•Assists in the writing of clinical abstracts, p...more
From
AstraZeneca Pharmaceuticals -
4/19/2018 5:44:04 AM
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AstraZeneca Pharmaceuticals
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Gaithersburg, MD
P ilot Production Supervisor Principal Duties:
•First line authority figure for process area. Responsible to initiate, monitor, and take appropriate actions related to process operations
•Responsible for overseeing the accurate and timely completion of clinical manufacturing campaigns and the associated cGMP documentation
•Direct/Assign junior staff (Tech 1 to Lead ) on daily/tactical...more
From
AstraZeneca Pharmaceuticals -
4/19/2018 5:44:04 AM
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Leidos Biomedical Research, Inc.
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FREDERICK, MD
PREFERRED QUALIFICATIONS
Candidates with these desired skills will be given preferential consideration:
- Combination of QA and QC or manufacturing experience
- Working knowledge of quality systems and TrackWise
- Experience with the GMP manufacture of Phase I/II clinical material
Expected Competencies:
- Advanced level professional providing professional input to complex assi...more
From
Leidos Biomedical Research, Inc. -
4/18/2018 5:48:33 AM
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Merck & Co.
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West Point, PA
Education Minimum Requirement:
• B.A./B.S. in life sciences, chemistry, engineering, or related relevant discipline.
Required Experience and Skills**:
• Minimum of 10 years' experience in the FDA and/or EU regulated pharmaceutical environment; preferably in a manufacturing site in leading manufacturing and/or quality roles and/or in Global Quality; experience in vaccines, biologics, devic...more
From
Merck & Co. -
4/18/2018 5:48:08 AM
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Covance, Inc. a division of LabCorp®
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Montreal, Quebec
Education/Qualifications
- In lieu of the above requirement, candidates with a High School Diploma or equivalent AND a minimum of 5 years work experience in clinical research, including a strong working knowledge of the ICH guidelines and FDA, IRB/IEC regulations will be considered
- Ability to drive and possess a valid driver's license
- Ability and willingness to present at internal...more
From
Covance, Inc. a division of LabCorp® -
4/18/2018 5:47:57 AM
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