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Laboratory Operations Expert 2

In Wisconsin / United States

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Laboratory Operations Expert 2   

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JOB TITLE:

Laboratory Operations Expert 2

JOB TYPE:

JOB SKILLS:

JOB LOCATION:

Madison Wisconsin / United States

JOB DESCRIPTION:

Description
client is a contract development and manufacturing organization (CDMO) of active pharmaceutical ingredients (API’s). The Analytical Development group is responsible for developing and transferring methods (especially HPLC methods) along with supporting the Process Development group’s testing needs using HPLC, GC, LCMS, NMR, FT-IR and Karl Fischer (KF) among other common analysis methods for organic molecules.


PURPOSE OF THE POSITION

The Associate Scientist is responsible for the analysis of samples from Process and Analytical Development (PAD), related paperwork, troubleshooting analysis issues, and general laboratory tasks. Analysis involves the use of HPLC, GC, LCMS, DSC, TGA, FTIR, NMR and XRPD, among other instrumentation, along with wet chemical assays. The Associate Scientist is responsible for transferring and evaluation of analysis techniques used to release starting materials, intermediates, and final products as well as in process controls. The Associate Scientist may be responsible for developing or assisting in the development of analytical methods to support Development for eventual validation.

Working with colleagues in PAD, the Associate Scientist is part of a team of professionals advancing pharmaceutical candidates to cGMP manufacturing. The Associate Scientist has a good foundation in general practice and concepts of their scientific/technical discipline. Demonstrates an ability to execute experiments and displays a developing judgment in scientific and technical situations. The Associate Scientist is recognized as an individual contributor in the scientific and technical areas within PAD.

ESSENTIAL JOB FUNCTIONS

• Analytically test non-GMP final products, intermediates, and raw materials. Testing will involve the use of HPLC, GC, LCMS, DSC, TGA, FTIR, NMR and XRPD among other tests and instruments
• Properly document lab work
• Transfer and evaluate analytical test methods from the customer
• Work in a safe manner and maintain the cleanliness of the work environment
• Interpretation of analytical data (including HPLC, GC, FT-IR, 1H NMR, MS)
• Assist with maintenance and calibrate/verify analytical and related equipment
• May develop test methods for products, intermediates and raw materials
• Work on and solve problems of moderate scope
• Perform job responsibilities with some guidance
• Write reports, protocols, SOP’s and other documentation
• Work with clients (internal and external) to achieve project goals
• Work in accordance with FDA, OSHA, EPA, DNR, DOT, and other regulatory agency guidelines

BASIC QUALIFICATIONS

Education: B.S./M.S. in Chemistry or related sciences.

Experience: Suggested entry experience of 0-3 years in an analytical laboratory environment operating under GLP or cGMP conditions.

Essential and Critical Skills: Excellent communication skills. Ability to work in a team environment. Ability to work in an Analytical testing lab with hazardous and toxic chemicals. Adequate technical writing skills to generate development reports.


ADDITIONAL LOCAL NEEDS:

Environmental conditions: Works near moving mechanical parts. Is frequently required to wear appropriate protective gear, (hard hats, glasses / goggles, chemical resistant suites, gloves, safety shoes) and other personal protection equipment “PPE” to protect themselves from toxic or corrosive chemicals in the forms of liquids, solids, vapors or airborne particles. Must be willing to work with highly potent / hazardous materials requiring the utilization of proper personal protective equipment which could include half/full face respirators, Saranex and / or Tyvek suits with powered respiration.

Position Details

POSTED:

Apr 20, 2022

EMPLOYMENT:

INDUSTRY:

Health Care

SNAPRECRUIT ID:

S164442240906978

LOCATION:

Wisconsin / United States

CITY:

Madison

Job Origin:

Jobsrus_organic_feed

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Laboratory Operations Expert 2    Apply

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Description
client is a contract development and manufacturing organization (CDMO) of active pharmaceutical ingredients (API’s). The Analytical Development group is responsible for developing and transferring methods (especially HPLC methods) along with supporting the Process Development group’s testing needs using HPLC, GC, LCMS, NMR, FT-IR and Karl Fischer (KF) among other common analysis methods for organic molecules.


PURPOSE OF THE POSITION

The Associate Scientist is responsible for the analysis of samples from Process and Analytical Development (PAD), related paperwork, troubleshooting analysis issues, and general laboratory tasks. Analysis involves the use of HPLC, GC, LCMS, DSC, TGA, FTIR, NMR and XRPD, among other instrumentation, along with wet chemical assays. The Associate Scientist is responsible for transferring and evaluation of analysis techniques used to release starting materials, intermediates, and final products as well as in process controls. The Associate Scientist may be responsible for developing or assisting in the development of analytical methods to support Development for eventual validation.

Working with colleagues in PAD, the Associate Scientist is part of a team of professionals advancing pharmaceutical candidates to cGMP manufacturing. The Associate Scientist has a good foundation in general practice and concepts of their scientific/technical discipline. Demonstrates an ability to execute experiments and displays a developing judgment in scientific and technical situations. The Associate Scientist is recognized as an individual contributor in the scientific and technical areas within PAD.

ESSENTIAL JOB FUNCTIONS

• Analytically test non-GMP final products, intermediates, and raw materials. Testing will involve the use of HPLC, GC, LCMS, DSC, TGA, FTIR, NMR and XRPD among other tests and instruments
• Properly document lab work
• Transfer and evaluate analytical test methods from the customer
• Work in a safe manner and maintain the cleanliness of the work environment
• Interpretation of analytical data (including HPLC, GC, FT-IR, 1H NMR, MS)
• Assist with maintenance and calibrate/verify analytical and related equipment
• May develop test methods for products, intermediates and raw materials
• Work on and solve problems of moderate scope
• Perform job responsibilities with some guidance
• Write reports, protocols, SOP’s and other documentation
• Work with clients (internal and external) to achieve project goals
• Work in accordance with FDA, OSHA, EPA, DNR, DOT, and other regulatory agency guidelines

BASIC QUALIFICATIONS

Education: B.S./M.S. in Chemistry or related sciences.

Experience: Suggested entry experience of 0-3 years in an analytical laboratory environment operating under GLP or cGMP conditions.

Essential and Critical Skills: Excellent communication skills. Ability to work in a team environment. Ability to work in an Analytical testing lab with hazardous and toxic chemicals. Adequate technical writing skills to generate development reports.


ADDITIONAL LOCAL NEEDS:

Environmental conditions: Works near moving mechanical parts. Is frequently required to wear appropriate protective gear, (hard hats, glasses / goggles, chemical resistant suites, gloves, safety shoes) and other personal protection equipment “PPE” to protect themselves from toxic or corrosive chemicals in the forms of liquids, solids, vapors or airborne particles. Must be willing to work with highly potent / hazardous materials requiring the utilization of proper personal protective equipment which could include half/full face respirators, Saranex and / or Tyvek suits with powered respiration.


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