01\/19\/2016 <\/p>\n
R&D Chemist needed for small custom manufacturing chemical company located in Spartanburg SC. Chemical synthesis and plant scale up experience required. Analytical experience utilizing GC and HPLC equipment required. Education- minimum BS in Chemistry or Chemical Engineering. Experience - 3+ years preferred. _cn_ Santolubes Manufacturing _rfc_ JRC-7398... <\/p>\n
01\/19\/2016 <\/p>\n
Premier client looking for MSW in Lansdale area. Responsibilities: Works in collaboration with the Care Coordination Manager. The Senior Social Worker helps patients\/families as part of Discharge Planning including regulatory requirements, obtaining appropriate insurance authorizations, identify discharge planning preferences of patients and families, facilitation of discharge transportation an... <\/p>\n
01\/19\/2016 <\/p>\n
We are currently recruiting for a Research and Development Lab Tech. If you have the experience and skills listed below, fill out an application at http:\/\/www.manpowerjobs.com<\/a> and then call us at 812.474.7485 to get set up with next steps. Job Duties\/Requirements: * Effectively use and maintain basic food lab instrumentation (i.e. pH meters, viscometer , balances, water activity meter, powder tester, ... <\/p>\n 01\/19\/2016 <\/p>\n Required Skills: Microbiology Experience, R & D Project Experience, Lab Experience Please note that this is a 1 year contract. Perform raw material, intermediate, final product testing; and routine and non-routine microbiological testing. Document results clearly and accurately. Interpret results by comparing against appropriate specifications or requirements. Perform Data reviews and release ... <\/p>\n 01\/19\/2016 <\/p>\n Job Number: 435257 Senior SAS Programmer OVERVIEW Coordinate programming activities across several trials with a given compound including publication and regulatory submission activities. Program according to specifications, analysis datasets, pooled datasets, listings, and figures across several trials with a given compound Develop and comply with project\/study programming standards and spec... <\/p>\n 01\/19\/2016 <\/p>\n Position Title: Environmental Health Specialist Reports To: Director of Environmental Health Status: Non- Exempt (Fulltime 35hrs base workweek with benefits) Hours: 8:00am to 4:00pm Monday- Friday (some nights and weekends) Position Summary: The purpose of this classification is to perform specialized work functions to prevent the transmission of disease through the environment. This is accom... <\/p>\n 01\/19\/2016 <\/p>\n Job Description: The Manager, Program Coordination provides coordination support to the Clinical functional teams as assigned to ensure completion of deliverables that are balanced for quality, timeliness and resources Assists Program Manager in providing planning and resource management support to the Compound Development Teams (CDTs) Facilitates team communications by maintaining and tracking... <\/p>\n 01\/19\/2016 <\/p>\n SUMMARY: Prepare FDA and international submissions for new products and product changes, including labeling, to ensure timely approval for market release in accordance with applicable regulations, standards, and guidance. Maintain regulatory affairs application files to support compliance with requirements and standards. Interact and respond to regulatory agencies. Supervise regulatory affairs sp... <\/p>\n 01\/19\/2016 <\/p>\n SUMMARY To formulate and develop products - with an emphasis on oral, nasal, and topical\/ skin care formulations for contract customers. The products would include semi-solid and liquid dosage forms such as creams, lotions, ointments, gels, suspensions, solutions and aerosols. This person is expected to work under moderate supervision - both in the case of work progress and results. ESSENTIAL DU... <\/p>\n 01\/19\/2016 <\/p>\n Job Summary: Seeking a highly motivated biologist with at least 5 years of industry experience to join the in vitro biology team working for a client located in Cranbury, New Jersey. This vital position will independently design and execute studies to advance new small-molecule drug candidates in the Oncology portfolio. Responsibilities will include developing, characterizing, and running biochem... <\/p>\n 01\/19\/2016 <\/p>\n Amec Foster Wheeler (www.amecfw.com) designs, delivers and maintains strategic and complex assets for its customers across the global energy and related sectors. With pro-forma 2014 annualized scope revenues of 5.5 billion and over 40,000 people in more than 55 countries, the company operates across the whole of the oil and gas industry from production through to refining, processing and distr... <\/p>\n 01\/19\/2016 <\/p>\n BIOLYPH (pronounced Bio-Life) is a dynamic and rapidly growing, 22 year old privately-owned Biotechnology service provider for the In Vitro Diagnostic and Research Use Only markets. Due to our tremendous growth, BIOLYPH is in the process relocating to a larger facility located in Chaska, MN. BIOLYPH is looking for a GMP experienced Production Scientist who is team oriented, enthusiastic and frie... <\/p>\n 01\/19\/2016 <\/p>\n Sequence, Inc. is excited to announce our arrival in Kansas City, MO, with an outstanding employment opportunity. Founded in 2002 as a Validation Consulting firm, Sequence, Inc. has grown our service offerings to include Software Management, Remote Monitoring, Quality Programs, and Engineering Services. We are currently looking for an experienced Validation Engineer who has the skill and knowledg... <\/p>\n 01\/19\/2016 <\/p>\n Seeking an Clinical SAS Programmer for a contract position working in Cambridge, MA 02139. Coordinate programming activities across several trials with a given compound including publication and regulatory submission activities. Program according to specifications, analysis datasets, pooled datasets, listings, and figures across several trials with a given compound Develop and comply with pr... <\/p>\n 01\/19\/2016 <\/p>\n Title: Chemistry State Regulatory Affairs Specialist Type: Contract Time Period: February 2016 through August 2016 Description We are seeking a highly motivated individual for a period of 6 months to assist with regulatory submission of products. The successful candidate will be responsible for assisting the Regulatory Affairs Manager in filing necessary applications for state product registra... <\/p>\n 01\/19\/2016 <\/p>\n Clinical Research Associate Conduct and manage of post marketing commitment studies, focusing in the areas of protocol development, study planning and implementation, site monitoring and management, enrollment and data quality Demonstrated ability to monitor all visit types independently Knowledge of ICH & GCPs Strong organizational, written and oral communication skills Experience as a CRA i... <\/p>\n 01\/19\/2016 <\/p>\n Theradex is an international contract research organization providing complete professional services for the clinical research and development of pharmaceutical compounds, medical devices and diagnostic test in the areas of oncology and life-threatening diseases for over 30 years. Theradex conducts studies which lead to marketing approval of significant advances; and has built a reputation on as... <\/p>\n 01\/19\/2016 <\/p>\n Patheon is one of the worlds largest contract manufacturing and development organizations (CDMOs) offering end-to-end, fully integrated services for both drug substances and drug products. We facilitate both large and small biopharma companies ability to deliver life changing therapies to their customers. Our biologics division is on a strong growth trajectory continuously investing in our glob... <\/p>\n 01\/19\/2016 <\/p>\n Patheon is one of the worlds largest contract manufacturing and development organizations (CDMOs) offering end-to-end, fully integrated services for both drug substances and drug products. We facilitate both large and small pharma companies ability to deliver life changing therapies to their customers. Our biologics division is on a strong growth trajectory continuously investing in our global ... <\/p>\n 01\/19\/2016 <\/p>\n Patheon is one of the worlds largest contract manufacturing and development organizations (CDMOs) offering end-to-end, fully integrated services for both drug substances and drug products. We facilitate both large and small pharma companies ability to deliver life changing therapies to their customers. Our biologics division is on a strong growth trajectory continuously investing in our global ... <\/p>\n <\/p>\n Read the original post: 01\/19\/2016 R&D Chemist needed for small custom manufacturing chemical company located in Spartanburg SC. Chemical synthesis and plant scale up experience required. Continue reading
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