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Manufacturing operations concern the operation of a facility, as opposed to maintenance, supply and distribution, health, and safety, emergency response, human resources, security, information technology and other infrastructural support organizations.
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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

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

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

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

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

Quality Complaints Specialist

Catalent Pharma Solutions - Winchester, KY

The Role •Primary internal quality contact for all Customer Complaints received.  The qualified individual is expected to become the Subject Matter Expert for the process. •Responsible for supporting parts of internal, client and regulatory audits that are related to Customer Complaints System. •Responsible for trending procedures that monitor the health of the Customer Complaint System....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

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

Director Clinical Development

AstraZeneca Pharmaceuticals - Gaithersburg, MD

Main Duties and Responsibilities The Director of Clinical Development (DCD) is a key leadership role within the Clinical Program Team (CPT), responsible for program management of the clinical elements of drug development.  The role involves driving the clinical development program and also integrating strategy, design, feasibility and operational planning to produce business-focused clinical drug...more

From AstraZeneca Pharmaceuticals - 2/20/2018 7:01:05 AM

Metrology Technician/Maintenance

AstraZeneca Pharmaceuticals - Mount Vernon, IN

Main Duties and Responsibilities: •Performs, as needed, a variety of installation, calibration, maintenance, troubleshooting, and repair duties on complex laboratory, process and utility instrumentation, working closely with the Maintenance, Operations and Automation groups, in a paper based and paperless work environment, following SOPs in a cGMP facility. •Assists in qualification activitie...more

From AstraZeneca Pharmaceuticals - 2/20/2018 7:01:05 AM

Project Controls Director

AstraZeneca Pharmaceuticals - Gaithersburg, MD

Required Skills & Knowledge •Degree in Construction Management or Engineering •Considerable bio-pharmaceutical experience & knowledge •Extensive experience in project controls including planning & scheduling, cost management, and estimating •Expert level knowledge in cost estimation, cost management and planning/scheduling. •Experience in major scheduling software including Microsoft...more

From AstraZeneca Pharmaceuticals - 2/20/2018 7:01:05 AM

QA Associate, Operations

Novartis Pharmaceuticals - Morris Plains, NJ

Minimum requirements BS/BA in Biological Sciences or equivalent relevant career experience English Minimum of 2 years GMP manufacturing and/or QA related experience, at least 1 year of which are in the area of quality assurance and/or compliance or equivalent experience.

From Novartis Pharmaceuticals - 2/20/2018 6:59:44 AM

QA Specialist, Operations

Novartis Pharmaceuticals - Morris Plains, NJ

Minimum requirements BS/BA in Biological Sciences or equivalent relevant career experience English Minimum of 7 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 - 2/20/2018 6:59:44 AM

Innovation Director, Trial Management

Novartis Pharmaceuticals - East Hanover, NJ

Minimum requirements Bachelor's Degree required, preferred in Life Sciences ; Advanced Degree in science or business preferred 1. At least 10 years of experience in pharmaceutical development, preferably in global strategy, innovations or clinical operations role 2. Thorough understanding of process control techniques such as Statistical Process Control (SPC), Six Sigma, Lean Sigma. Six Sigma ...more

From Novartis Pharmaceuticals - 2/20/2018 6:59:43 AM

Engineer I - QA

Novartis Pharmaceuticals - Houston, TX

Minimum requirements Minimum requirements •B.S. Engineering or Physical Sciences (e.g. Chemistry, Physics) •English Experience Requirements •No previous experience require •Preferred: 2 years of relevant experience

From Novartis Pharmaceuticals - 2/20/2018 6:59:43 AM

Principal Engineer - PMO Obsolescence, Continuity

Novartis Pharmaceuticals - Irvine, CA

Minimum requirements -Bachelor's or greater, preferably a Master of Science in engineering or physics discipline or educational equivalent is required. -7 years of directly related experience in a systems engineering, technical supply chain, technical project mgt., or process development role. -In depth understanding of electro-mechanical, optical, software controlled medical ophthalmic equipmen...more

From Novartis Pharmaceuticals - 2/20/2018 6:59:42 AM

Finance - Clinical Operations Manager (COM)

Merck & Co. - Montreal (Kirkland), CA

•Bachelor's Degree (or comparable) in Business Finance/ Administration/ Life Science or equivalent Health Care related experience •Five to seven years clinical research experience •Extensive experience in clinical project management and coordination •Expertise in core clinical, regulatory and financial systems, tools and metrics •Extensive knowledge of local regulatory environment and subm...more

From Merck & Co. - 2/20/2018 6:59:23 AM

Oncology Specialty Representative - (Charlotte, NC)

Merck & Co. - Winston-Salem, NC

Education: • Required: BA/BS • Preferred: MBA/MS Required Experience: • Minimum of (3) years successful Pharmaceutical Sales experience • Minimum of (5) years Sales/Marketing experience in a Pharmaceutical and/or Health Science industry • Documented history of strong performance in Sales • Demonstration of strategic and execution oriented competencies • A...more

From Merck & Co. - 2/20/2018 6:59:23 AM

Associate Director, Cyber Security Engineering

Merck & Co. - Czech Republic, Prague

Education Minimum Requirement: • Bachelor's Degree with preference in computer science, electrical engineering, or other technical discipline. Required Experience and Skills: . • Must have 2 years of staff management or team leadership experience • Must have experience or a good level of exposure to project finances. • Solid proven experience with engineering...more

From Merck & Co. - 2/20/2018 6:59:22 AM

Associate Director, HRIS Talent Management Solutions

Merck & Co. - Kenilworth, NJ

Education: • Bachelor's degree Required: •Minimum of 5 years of progressive experience in an HRIS, IT, HR Operations function •Implementation or operational management experience in one of the following HCM Cloud software providers: SuccessFactors, Oracle, or Workday •Project leadership expertise, managing in a deadline driven environment and proven ability to deliver as a team leader o...more

From Merck & Co. - 2/20/2018 6:59:22 AM
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