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Control Room Technician API Job

Novo Nordisk Inc. - Clayton, NC

Business Process, CAD, Diabetes, Drafting, Electrical, Engineer, Engineering, Environmental Health & Safety, Facilities, HVAC, Healthcare, Inspector, Maintenance, Management, Manufacturing, Medical, Operations, Procurement, Quality, Special Medicine, Technical Support, Technician, Technology, Wastewater, Water Treatment

From Novo Nordisk Inc.- 2/20/2018 7:02:58 AM

Environmental, Health & Safety Prof Job

Novo Nordisk Inc. - Clayton, NC

Diabetes, Emergency Management, Engineering, Environmental Engineering, Environmental Health & Safety, Facilities, Government, Healthcare, Medical, Operations, Pharmaceutical, Safety, Science, Service, Special Medicine

From Novo Nordisk Inc.- 2/20/2018 7:02:58 AM

GMP Partner - Automation API Job

Novo Nordisk Inc. - Clayton, NC

CAPA, Compliance, Diabetes, Engineer, Engineering, Facilities, Healthcare, Legal, Management, Medical, Medical Device, Operations, Pharmaceutical, Project Manager, QA, Quality, Quality Assurance, Science, Special Medicine, Technology

From Novo Nordisk Inc.- 2/20/2018 7:02:58 AM

Educator Diabetes Ohio North Job

Novo Nordisk Inc. - Sandusky, OH

Bilingual, Compliance, Curriculum, Diabetes, Diabetes Educator, Education, Endocrinology, Healthcare, Law, Legal, Medical, Nursing, Registered Nurse, Special Medicine, Training, Travel Nurse

From Novo Nordisk Inc.- 2/20/2018 7:02:58 AM

Manager Sales Reporting & Forecasting Job

Novo Nordisk Inc. - Plainsboro, NJ

Consulting, Diabetes, Healthcare, MBA, Management, Manager, Marketing, Marketing Manager, Medical, Outside Sales, Pharmaceutical, Pharmaceutical Sales, Project Manager, Sales, Sales Management, Sales Rep, Science, Special Medicine, Technology

From Novo Nordisk Inc.- 2/20/2018 7:02:58 AM

Global Medical Director - Transplant

CSL Behring - King of Prussia, PA

Qualifications: •M.D. with relevant Transplant experience required •Proven medical and scientific expertise in Transplant Medicine required.  •Minimum of 6 years relevant medical- or bio-pharmaceutical Med Affairs industry experience preferred. Worker Type: Employee Worker Sub Type: Regular

From CSL Behring- 2/20/2018 7:02:43 AM

Inside Sales Specialist I

Teva Pharmaceuticals USA - Weston, FL

Qualifications Required Knowledge and Skills: • Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements. • Business English usage, spelling, grammar and punctuation. • Business and personal computer hardware and software applications. • Pharmaceutical industry, pharmacy and other retail distribution channels. • ...more

From Teva Pharmaceuticals USA- 2/20/2018 7:02:29 AM

Customer Service Specialist II

Teva Pharmaceuticals USA - Weston, FL

Qualifications Minimum Qualifications: High School diploma or equivalent GED Certificate, and three (3) years customer service experience, preferably in a drug, food or cosmetic manufacturing environment; or, an equivalent combination of education and/or experience. Knowledge of: • Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulat ...more

From Teva Pharmaceuticals USA- 2/20/2018 7:02:29 AM

Manufacturing Operator - Drug Product Primary - Prep & Fill 3rd Shift

Cook Pharmica - Bloomington, IN

Responsibilities - Safely operate basic equipment - Support cleaning and organizational efforts, including maintaining visual factory - Read, understand, and follow GMP documents - Demonstrate a basic understanding on Operational Excellence concepts - Participate in area continuous improvement activities - Report safety and quality concerns and recommend improvements - ...more

From Cook Pharmica- 2/20/2018 7:02:00 AM

Manager, QA (Audit)

Cook Pharmica - Bloomington, IN

Responsibilities - Managing and monitoring quality assurance site audit functions working with Catalent Corporate Quality (i.e., internal and customer audits) - Provide support and participate in regulatory agency inspections (US FDA, ROW) - Providing oversight for processes to ensure regulatory compliance to FDA regulations, global regulations and Catalent internal directives in the m ...more

From Cook Pharmica- 2/20/2018 7:02:00 AM

QC Laboratory Assistant

Catalent Pharma Solutions - Dartford, London

Job Description Catalents +1,500 strong, international quality team is focused on delivering nearly 7,000 products to patients in over 80 countries with the highest level of quality standards across multiple superior drug delivery and manufacturing technologies at more than 30 facilities. Catalent require a Lab Assistant at our Dartford facility. The successful candidate will be responsible for ...more

From Catalent Pharma Solutions- 2/20/2018 7:01:40 AM

Assistant General Counsel, Regulatory and Commercial, Europe

Catalent Pharma Solutions - Cham, Canton Zug

Responsibilities for this position will require you to: •Provide legal counsel in Europe and elsewhere as needed for the development and administration of regulatory processes and systems to maintain compliance with regulations of the European Medicines Agency (EMA), the U.S. Food and Drug Administration (FDA), and similar counterpart agencies around the world, including the development of a ...more

From Catalent Pharma Solutions- 2/20/2018 7:01:39 AM

Cleaning Validation Scientist

Catalent Pharma Solutions - Swindon, Wiltshire

Educational Requirements:  Science graduate or higher with proven experience of laboratory operations in a cGXP environment or extensive industry experience. Cleaning validation experience preferable. Why Work for Us: Our Vision is to be the worlds most trusted, reliable and innovative drug development and delivery partner by upholding the highest industry standards and exceeding customer exp ...more

From Catalent Pharma Solutions- 2/20/2018 7:01:39 AM

Raw Material Chemist

Catalent Pharma Solutions - Woodstock, IL

The Role • Perform analytical testing and calculations on raw materials including excipients, resins, foils, and active pharmaceutical ingredients • Operate analytical instrumentation such as FTIR and UV-Vis •Coordinate testing with peers and prioritize testing depending upon supply chain and production needs • Prepare test reports and perform cGMP documentation in all areas of the laborat ...more

From Catalent Pharma Solutions- 2/20/2018 7:01:39 AM

Senior Regulator Affairs Specialist

Catalent Pharma Solutions - St. Petersburg, FL

The Role (daily responsibilities) •Preparation and submission of ANDA submissions (initial, amendments, supplements, annual reports, 15-day Alert Reports); drug master files (initial, amendments, annual reports); plant/site master files; licenses, permits, and registrations to meet FDA and State requirements (especially Florida); other submissions as required •Prepare and submit all federal, s ...more

From Catalent Pharma Solutions- 2/20/2018 7:01:39 AM

CSS Director, Continuous Improvement, Technology and Engineering

Catalent Pharma Solutions - Kansas City, MO

•Experience in maintaining regulatory compliance thru audits, validation, change management, risk assessments, qualified drawings, corrective action plans, FMEA, and deviation support. •Utilize and promote Operational Excellence, Six Sigma & Lean methodologies to all work flows with ability to run Kaizen Events •Provide oversight and technical expertise during the development of new strategic ...more

From Catalent Pharma Solutions- 2/20/2018 7:01:39 AM

Director, Bioassay

Catalent Pharma Solutions - Kansas City, MO

The Role The methodologies and techniques used in this group are Cell based Potency assays (bioassays or ELISA assays), impurity assays (DNA by qPCR, HCP, Protein A, Insulin, beta glucan, rLongR3), kinetic binding assays or quantitation assays (Octet (BLI) or Biacore (SPR)) and any new assays or new technologies identified and implemented to support industry needs. The Director will oversee the B ...more

From Catalent Pharma Solutions- 2/20/2018 7:01:39 AM

Production Quality Testing Associate - D shift

Catalent Pharma Solutions - Woodstock, IL

The Role •Standardization and use of simple analytical instrumentation (pH meter, osmometer, torque meter, balance) and measurement devices (ruler, micrometer, go/no go gauges) •Material/Product sampling per a pre-defined schedule •Evaluation of materials/products for conformance to visual and functional specifications •Complete, accurate, detailed and legible documentation of sampling ...more

From Catalent Pharma Solutions- 2/20/2018 7:01:39 AM

Associate Quality Assurance Inspector 1st shift

Catalent Pharma Solutions - Somerset, NJ

The Role •Provide QA support to manufacturing for clinical and commercial batches. •Performs Line Clearances, equipment releases and AQL inspections.  •Audit of raw materials and facility logs.  •Interdepartmental communication for obtaining information.      •Comply with and ensure compliance of the department with Health, Safety, and Environmental responsibilities.     •Assist with batc ...more

From Catalent Pharma Solutions- 2/20/2018 7:01:39 AM

Associate, QA Systems

Catalent Pharma Solutions - Madison, WI

Education / Experience: •Bachelor's Degree in technical discipline (e.g. biology, biotechnology, engineering) or related life science; or •Associates Degree in technical discipline (e.g. biology, biotechnology, engineering) or related life science with minimum two years related experience.

From Catalent Pharma Solutions- 2/20/2018 7:01:39 AM
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