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techtippr
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EncryptedSite is Encrypted
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CountryHosted in United States
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Traffic rank#840,269 Site Rank
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Site age11 yrs old
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Site Owner informationWhois info
Website is Safe
Traffic rank
#840,269
#840,269
Site age
11 yrs
11 yrs
Location
United States
United States
Newest job postings for techtippr
via Salary.com
posted_at: 2 days agoschedule_type: Full-time
LGM Pharma is a leading contract development and manufacturing organization (CDMO) and provider of Active Pharmaceutical Ingredients (API). With excellent API sourcing and supply chain expertise together with our drug product contract development and manufacturing solutions, we are a premier end-to-end solutions provider to the global pharmaceutical industry.
We are a high-growth organization... looking to accelerate the development and commercialization
LGM Pharma is a leading contract development and manufacturing organization (CDMO) and provider of Active Pharmaceutical Ingredients (API). With excellent API sourcing and supply chain expertise together with our drug product contract development and manufacturing solutions, we are a premier end-to-end solutions provider to the global pharmaceutical industry.
We are a high-growth organization... looking to accelerate the development and commercialization of high-quality therapeutics worldwide. We have offices in California, Texas, Kentucky, Florida and Israel.
LGM Pharma is a leading contract development and manufacturing organization (CDMO) and provider of Active Pharmaceutical Ingredients (API). With excellent API sourcing and supply chain expertise together with our drug product contract development and manufacturing solutions, we are a premier end-to-end solutions provider to the global pharmaceutical industry.
We are a high-growth organization looking to accelerate the development and commercialization of high-quality therapeutics worldwide. We have offices in California, Texas, Kentucky, Florida and Israel.
We are looking for a Sr. R&D Technician to join our Quality Department, in Colorado Springs, CO.
RESPONSIBILITIES:
• Conduct hand, laboratory and pilot scale, new and reformulation product trials and write reports.
• Obtain raw materials and perform weighing; follow instructions to conduct product development trials and pilot batches.
• Perform product development equipment set-up, operation and clean-up.
• Perform visual inspection and physical testing on intermediates and finished trial products.
• Provide assistance to PI and formulators to prepare regulatory filing documents. Perform rework trials under the guidance of R&D supervisor.
• Perform new and secondary raw materials physical testing.
• Other related duties as required.
QUALIFICATIONS:
• High school diploma or equivalent, with some college preferred.
• Previous experience in a R&D and/or manufacturing environment preferred.
• Ability to read and interpret technical procedures, SOP’s, GMP’s and FDA regulations.
• Ability to work with MS Word and Excel and able to write reports and perform data entry.
• Strong communication skills, both written and verbal.
• Strong attention to detail.
• Ability to lift 25 plus pounds Show more details...
We are a high-growth organization... looking to accelerate the development and commercialization of high-quality therapeutics worldwide. We have offices in California, Texas, Kentucky, Florida and Israel.
LGM Pharma is a leading contract development and manufacturing organization (CDMO) and provider of Active Pharmaceutical Ingredients (API). With excellent API sourcing and supply chain expertise together with our drug product contract development and manufacturing solutions, we are a premier end-to-end solutions provider to the global pharmaceutical industry.
We are a high-growth organization looking to accelerate the development and commercialization of high-quality therapeutics worldwide. We have offices in California, Texas, Kentucky, Florida and Israel.
We are looking for a Sr. R&D Technician to join our Quality Department, in Colorado Springs, CO.
RESPONSIBILITIES:
• Conduct hand, laboratory and pilot scale, new and reformulation product trials and write reports.
• Obtain raw materials and perform weighing; follow instructions to conduct product development trials and pilot batches.
• Perform product development equipment set-up, operation and clean-up.
• Perform visual inspection and physical testing on intermediates and finished trial products.
• Provide assistance to PI and formulators to prepare regulatory filing documents. Perform rework trials under the guidance of R&D supervisor.
• Perform new and secondary raw materials physical testing.
• Other related duties as required.
QUALIFICATIONS:
• High school diploma or equivalent, with some college preferred.
• Previous experience in a R&D and/or manufacturing environment preferred.
• Ability to read and interpret technical procedures, SOP’s, GMP’s and FDA regulations.
• Ability to work with MS Word and Excel and able to write reports and perform data entry.
• Strong communication skills, both written and verbal.
• Strong attention to detail.
• Ability to lift 25 plus pounds Show more details...
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