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cGMP
cGMP stands for Current Good Manufacturing Practices (cGMP) and the regulations are set by the Food and Drug Administration (FDA). As you begin your job search is good to familiarize yourself with different industry terms and abbreviations. There seem to be a fair amount to know. 
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Quality Control Analyst II

Teva Pharmaceuticals USA - Cincinnati, OH

Qualifications EDUCATION & EXPERIENCE BS or higher in science related discipline Minimum 2 years of experience in a pharmaceutical environment Connect With Us! Not ready to apply? Connect with us for general consideration. Do YOU have great ideas? Want to work in an environment that will nurture your professional development? Come and join Teva on its journey of growth. Teva...more

From Teva Pharmaceuticals USA - 2/16/2018 5:51:10 AM

Critical Systems Operator

Teva Pharmaceuticals USA - Irvine, CA

Qualifications Education Required: High School diploma or equivalent. Education Preferred Completion of vocational courses in areas such as welding, mechanics, control systems, electrical, refrigeration, HVAC, or Freeze drying is desirable. Refrigeration license or technical school certificate is highly desirable. Experience Required: Experienced in repair, installation or maintenance to H...more

From Teva Pharmaceuticals USA - 2/16/2018 5:51:10 AM

Group Leader Quality Control

Teva Pharmaceuticals USA - Cincinnati, OH

Qualifications Education: •Bachelor's of Science Degree in Chemistry or related quantitative scientific discipline required Experience: •Minimum 5 years of progressive pharmaceutical QC laboratory experience required Technical Skills: •Excellent knowledge of cGMPs and their application to a pharmaceutical QC laboratory; thorough knowledge of compendia USP, EP and ICH guidel...more

From Teva Pharmaceuticals USA - 2/16/2018 5:51:10 AM

Specialist, cGMP Biomanufacturing - 2nd Shift Wednesday through Saturday

Catalent Pharma Solutions - Madison, WI

Responsibilities: • Performs daily review of executed cGMP documentation (BPRs, forms). Executes and properly documents cGMP Biomanufacturing activities. • Operates and troubleshoots cGMP Biomanufacturing equipment such as pH/conductivity meters, mixing tanks (SUMs), tubing fusers/sealers, filter integrity testers, peristaltic pumps, balances and      Biosafety Cabinets (BSC) or Laminar Flow H...more

From Catalent Pharma Solutions - 2/16/2018 5:50:47 AM

cGMP Biomanufacturing Manager

Catalent Pharma Solutions - Madison, WI

The Role •The cGMP Biomanufacturing group is responsible for current Good Manufacturing Practices (cGMP) production activities, including Master/Working Cell Bank production, Upstream cell culture, Downstream protein/mRNA purification, and/or Fill/Finish. This position requires a variety of skills necessary for a cGMP Biomanufacturing environment. Independently perform Biomanufacturing operati...more

From Catalent Pharma Solutions - 2/16/2018 5:50:47 AM

Product Development Manager

Catalent Pharma Solutions - Swindon, Wiltshire

Job Description Catalent offers rewarding opportunities to further your career " join the global drug development and delivery leader! You will help develop some of the nearly 200 products we launch each year or help supply some of the over 7,000 products for patients around the world. Our highly skilled, dedicated global team of over 9,500 is passionate about improving the health of patients by...more

From Catalent Pharma Solutions - 2/16/2018 5:50:46 AM

Associate, BioManufacturing (Wed-Sat. 4/10 Shift)

Catalent Pharma Solutions - Madison, WI

Responsibilities • Perform aseptic techniques within in a clean room environment • Execute and document cGMP Biomanufacturing activities • Operate cGMP Biomanufacturing equipment such as pH/conductivity meters, mixing tanks (SUMs), tubing fusers/sealers, filter integrity testers, peristaltic pumps, balances and BioSafety Cabinets (BSC) or Laminar Flow Hoods (LFH) • Maintain effectiveness...more

From Catalent Pharma Solutions - 2/16/2018 5:50:46 AM

Project Manager

Catalent Pharma Solutions - San Diego, CA

The Role (daily responsibilities) •Work directly with Client-side Project Managers to develop, write and process work orders as part of the RFP process. •Liaise between clients, science and manufacturing teams to drive project and process solutions. •Prepare and present monthly/quarterly (or as required) project updates to client management via telephone and at client sites. •Manage all cli...more

From Catalent Pharma Solutions - 2/16/2018 5:50:46 AM

Associate Principal Scientist - GMP Laboratories

Merck & Co. - West Point, PA

Education: • PhD in Molecular Biology, Biochemistry, or related discipline with 4 years relevant experience in biotech industry, OR MS in Molecular Biology, Biochemistry, or related discipline with 8 years relevant experience in biotech industry, OR BS in Molecular Biology, Biochemistry, or related discipline with 12 years relevant experience in biotech industry. Required: • Knowledge, under...more

From Merck & Co. - 2/16/2018 5:49:54 AM

BioProcess Technical Support Technician

Merck & Co. - DeSoto, KS

Education: Associates Degree in Biology, Microbiology, or related science, OR High School diploma with 2 years relevant work experience Required : • Must have good writing and communication skills • Must have good mathematical abilities • Must be familiar with common laboratory procedures • Must be able to follow written or verbal instructions without extensive supervision Preferred...more

From Merck & Co. - 2/16/2018 5:49:54 AM

Manager, Maintenance (Millsboro, DE)

Merck & Co. - Millsboro, DE

Education: Associate’s degree in Engineering or other Scientific/Technical Area OR Master’s License in Trade (Electrical, HVAC, HVAC/R, Plumbing, etc.) Required: • A minimum of 8 years’ industry experience as an engineer, supervisor, or technical lead in a maintenance department that supports a manufacturing setting. • 3 year’s management and or lead role experience (people/budget/or...more

From Merck & Co. - 2/16/2018 5:49:54 AM

QSIP Site Lead

Merck & Co. - Elkton, VA

Minimum Requirements: • B.S., B.A. degree in Science, Engineering, or Business •A minimum of 7 years in a GMP environment with 4 years leadership experience •Experience with Quality Systems enhancement and improvement •Project management experience •Experience leading teams in a matrix environment •Change management experience •Strong working knowledge of CFR, Eudralex and other regulat...more

From Merck & Co. - 2/16/2018 5:49:54 AM

Senior Scientist - GMP Laboratories

Merck & Co. - West Point, PA

Education: • MS in Molecular Biology, Biochemistry, or related discipline with four ( 4 ) years relevant experience in biotech industry; OR BS with a minimum of seven ( 7 ) years relevant experience Required: • Knowledge, understanding, and experience performing biochemical and cell-culture assays • Formal training and experience with analytical instrumentation (e.g. HPLC, plate reader) ...more

From Merck & Co. - 2/16/2018 5:49:54 AM

Specialist

Merck & Co. - West Point, PA

Education: • Bachelor’s Degree or higher in Science or Engineering discipline Required: • Minimum of 1 year of experience working in/or supporting manufacturing in cGMP Operations • Willing and able to work alternate shifts and weekends during start-up and demonstration to meet critical business needs • Good verbal and written communication skills • Ability to effectively respond...more

From Merck & Co. - 2/16/2018 5:49:54 AM

Quality Control_ Associate Microbiologist

Novartis Pharmaceuticals - Broomfield, CO

Minimum requirements HS or GED required. Associate Degree in related discipline is preferred. Fluent in written and spoken English. At least 2 months of Novartis/Sandoz experience successfully demonstrating company behaviors and values.

From Novartis Pharmaceuticals - 2/16/2018 5:49:38 AM

Operator

AstraZeneca Pharmaceuticals - Coppell, TX

Key Accountabilities: •         Ethical conduct and compliance •         Performs process manufacturing tasks including operation of large scale equipment, weighing, measuring, monitoring of raw materials to assure batches contain proper ingredients, quantities and process outputs •         Performs in-process testing as specified within manufacturing documentation. •         Identifies and ...more

From AstraZeneca Pharmaceuticals - 2/16/2018 5:49:06 AM

Associate Director

AstraZeneca Pharmaceuticals - Gaithersburg, MD

Essential Requirements: •Advanced degree in the life sciences, chemistry or appropriate engineering discipline is required. •Minimum 8-10 years of increasing documented success in biopharmaceutical field, with at least 5 of those years in regulatory affairs biotechnology CMC.  •Strong background in cGMP, facilities and post-marketing submissions.  •Experience with monoclonal antibody manufa...more

From AstraZeneca Pharmaceuticals - 2/16/2018 5:49:06 AM

Lean Six Sigma Lead

AstraZeneca Pharmaceuticals - Newark, DE

Main Duties and Responsibilities The Lean/Six Sigma Process Owner is responsible to assist line management in implementation of the AZ Supply System.  The individual will be a site Lean/ Six Sigma Subject Matter Expert, driving standardized ways of working and building capability across the site in Manufacturing Excellence.  Responsibilities include the proper application of Lean/Six Sigma Tools,...more

From AstraZeneca Pharmaceuticals - 2/16/2018 5:49:04 AM

Senior Manager, Production

Teva Pharmaceuticals USA - Cincinnati, OH

Qualifications POSITION REQUIREMENTS Education/Certification/Experience: • Requires bachelor's degree • Requires a minimum of 7 years of relevant experience in a regulated industry • Requires a minimum of 5 years in a leadership role Skills/Knowledge/Abilities: • Inspire, motivate, and lead • Self-directed with ability to organize and prioritize work • ...more

From Teva Pharmaceuticals USA - 2/15/2018 5:48:10 AM

Operator I

Teva Pharmaceuticals USA - Cincinnati, OH

Qualifications Position Requirements Any equivalent combination of education, training and/or experience that fulfills the requirements of the position will be considered. Preferably extruding experience Education/Certification/Experience: • Requires High School Diploma or equivalent. • Prefer previous experience in a manufacturing environment within pharmaceutical, nutraceut...more

From Teva Pharmaceuticals USA - 2/15/2018 5:48:10 AM
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