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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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Supervisor, Facilities Maintenance

CSL Behring - Kankakee, IL

Main Responsibilities and Accountabilities 1. Responsible for the Maintenance Department budget. Lead efforts in developing and maintaining of annual budgets and forecasts. 2. Coordinates the weekly and day-to-day operation schedule, setting facility priorities where needed. 3. Establishes adequate coverage to support scheduled manufacturing. Coordinates daily job assignments and identifies ov...more

From CSL Behring - 2/23/2018 5:45:29 AM

Cleaning Validation Program Lead

Catalent Pharma Solutions - Kansas City, MO

The Role •Strategic development of cleaning program and ongoing supporting rational development for regulatory and customer audits. •Coordination and oversight of cleaning procedure development and cross functional support for all commercial and potential commercial products. •Writes and/or facilitates Cleaning Engineering Studies and Cleaning Validations. •Defines, facilitates, collects da...more

From Catalent Pharma Solutions - 2/23/2018 5:44:34 AM

QA Associate

Catalent Pharma Solutions - Singapore, Singapore

Experience within a similar Quality Assurance role preferred Diploma qualification essential in engineering, quality engineering or Pharma based discipline   Degree qualification engineering, quality engineering or Pharma based discipline   What we offer you: • Competitive salary • Company benefits package About Catalent Catalyst + Talent. Our name combines these ideas. From drug and...more

From Catalent Pharma Solutions - 2/23/2018 5:44:34 AM

Associate QA Representative - Batch Record Review

Cook Pharmica - Bloomington, IN

Responsibilities - Issuance of drug product batch records and associated documentation - Review of drug product batch records and associated documentation - Disposition batch records, as required - Authoring and/or reviewing procedures, work instructions, etc. - Facilitate the resolution of job related questions and comments - Participate in generation of key team metrics ...more

From Cook Pharmica - 2/23/2018 5:44:17 AM

Senior Specialist, Quality Assurance IT

Merck & Co. - Rahway, NJ

Education: • Bachelor's degree in Science, Information Technology or equivalent. • IT experience related to Computerized Systems Development, Implementation and/or IT Operations. Required: •Hands-on experience or understanding of shop-floor systems supporting pharmaceutical manufacturing operations. •Minimum 5 years of experience in regulated pharmaceutical manufacturing with 2-3 year...more

From Merck & Co. - 2/23/2018 5:43:58 AM

Manager, Raw Materials

Novartis Pharmaceuticals - Morris Plains, NJ

Minimum requirements 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...more

From Novartis Pharmaceuticals - 2/23/2018 5:43:37 AM

QA Documentation Specialist II/III

AstraZeneca Pharmaceuticals - Philadelphia, PA

Requirements: Education Specialist II:  Associates Degree or relevant 3-5 years' experience Specialist III:  BS, BA with 5+ years' experience in biopharmaceutical/pharmaceutical industry Experience Specialist II:  3+ years' experience in biopharmaceutical/pharmaceutical industry. Specialist III:  5+ years' document management experience in biopharmaceutical/pharmaceutical industry. Special Skills/...more

From AstraZeneca Pharmaceuticals - 2/23/2018 5:43:24 AM

Pharmacokineticist I

Covance, Inc. a division of LabCorp® - Madison, WI

Education/Qualifications Minimum Required: - A Bioanalytical Chemistry or a Biological Life Sciences Degree Experience Minimum Required: - A minimum of 2 years of experience in clinical pharmacokinetic and/or pharmacodynamic analysis. - An understanding of, and the ability to apply, the principles of GLP and GCP as per the relevant UK Statutory Instruments.

From Covance, Inc. a division of LabCorp® - 2/23/2018 5:43:13 AM

Medical Technologist I - Chemistry

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

Education/Qualifications 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 chemical, physical or biological...more

From Covance, Inc. a division of LabCorp® - 2/23/2018 5:43:13 AM

Study Coordinator II Dose Analysis

Covance, Inc. a division of LabCorp® - Madison, WI

Education/Qualifications - Bachelor of Science (BS) degree in science or related field. - Experience may be substituted for education. - Ability to utilize word processing software, database, spreadsheet, and specialized software. - Skilled in concise writing. Writing should require little external review or edit. - Knowledge of grammar, punctuation, composition, and spelling. Ex...more

From Covance, Inc. a division of LabCorp® - 2/23/2018 5:43:13 AM

Lead Quality Engineer, Vision Care R&D

Novartis Pharmaceuticals - Johns Creek, GA

Minimum requirements Bachelor's degree in Engineering or Physical Sciences, Chemistry, Physics, etc. English 7 years of relevant experience and 5 years of demonstrated leadership.

From Novartis Pharmaceuticals - 2/22/2018 5:46:30 AM

Chemist II - Coppell, Texas

AstraZeneca Pharmaceuticals - Coppell, TX

Responsibilities:  • Accurately complete all data entry requirements for methods or tasks performed, reviewing data for completeness and accuracy. • Prepare solutions and standards per Procedures, Analytical Procedures and/or SOPs, with appropriate documentation. • Clean and maintain the general laboratory facilities and notify appropriate maintenance  personnel as needed. • Develop and mai...more

From AstraZeneca Pharmaceuticals - 2/22/2018 5:46:04 AM

Chemist I - Coppell, TX

AstraZeneca Pharmaceuticals - Coppell, TX

Key Accountabilities: •         Ethical conduct and compliance •         Accurately complete all data entry requirements for methods or tasks performed, reviewing data for completeness and accuracy. •         Prepare solutions and standards per Procedures, Analytical Procedures and/or SOPs, with appropriate documentation •         Clean and maintain the general laboratory facilities •         D...more

From AstraZeneca Pharmaceuticals - 2/22/2018 5:46:04 AM

Information Center, Quality Assurance Specialist

AstraZeneca Pharmaceuticals - Wilmington, DE

Main Duties and Responsibilities You will be responsible for performing the tasks of the US product quality complaint (PQC) process to ensure consistent, clear, effective, and timely identification and communication of all PQCs to the appropriate investigation supply sites. Understand and support the PQC processes of external customers. Integrate across the organization by developing and maint...more

From AstraZeneca Pharmaceuticals - 2/22/2018 5:46:04 AM

Associate Director - Quality Assurance

Merck & Co. - West Point, PA

Minimum requirement: • B.S or M.S. in Scientific or Engineering field or equivalent experience in the pharmaceutical industry • Minimum 8 years in Pharmaceutical Quality, Regulatory, or related experience with progressive and demonstrated Quality decision making responsibility • Demonstrated interpersonal skills including flexibility, collaboration and inclusion skills, and ability to ...more

From Merck & Co. - 2/22/2018 5:45:46 AM

Associate Director, Quality Assurance Pharmacovigilance

Merck & Co. - Rahway, NJ

Education: • Bachelor's degree or equivalent in relevant area Required: • A minimum of 8 years of relevant experience in the pharmaceutical industry (i.e., drug development, clinical and/or non- clinical research, regulatory compliance, clinical study monitoring or Pharmacovigilance). • A substantial work history in pharmacovigilance and QA oversight activities. Preferred: • Previous ...more

From Merck & Co. - 2/22/2018 5:45:46 AM

Quality Control Inspection & Operations Job

Novo Nordisk Inc. - West Lebanon, NH

Diabetes, Electrical, Engineering, Healthcare, Housekeeping, Inspection, Inspector, Laboratory, Medical, Operations, Operations Manager, QA, QC, Quality, Quality Assurance, Quality Control Inspector, Science, Special Medicine, Technology

From Novo Nordisk Inc. - 2/21/2018 5:44:00 AM

Senior QC Associate

Catalent Pharma Solutions - Madison, WI

The Role • Accurately reviews analytical and/or microbiological testing following SOPs. • Reviews and verifies analytical and/or microbiological data and reports, ensuring accuracy and consistency. • Provides clear feedback for corrections needed. • Actively participates in team meetings. The Candidate • B.S./B.A. in Biotechnology, or related field, with minimum of 3 years experien...more

From Catalent Pharma Solutions - 2/21/2018 5:42:43 AM

Compliance Auditor

Catalent Pharma Solutions - Woodstock, IL

The Role •Manages, leads, and conducts audits (customer, external, and internal).  Includes risk assessments, scheduling, preparing documents prior to the audit, creating PRs in TrackWise and managing audit during execution, and closure. •Support preparations for planned Health Authority Inspections. •Support of site Supplier Review Board. •Support Central Supplier Quality Management ...more

From Catalent Pharma Solutions - 2/21/2018 5:42:42 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. •Review and approval of Validation of equipment documentation IQ, OQ, and PQs. •Support Equipment and Cleaning Validation. •Review cleaning veri...more

From Catalent Pharma Solutions - 2/21/2018 5:42:41 AM
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