QC Analytical Chemist

Essential Functions

• Carries out responsibilities in accordance with company policies, SOPs and state, federal and local laws
• Performs testing of raw materials, in-process (IP), finished products (FP) and/or stability sample (ST) samples including dissolution, assay, content/blend uniformity, particle size distribution and other tests according to the analytical methods, USP procedures in a regulated laboratory environment
• Analyzes and interprets test results
• Operates general analytical instruments during raw material, IP and FP testing such as High Pressure Liquid Chromatography (HPLC), Ultra Violet visible spectroscopy (UV/Vis), automatic titration, Infra-Red Spectroscopy (IR), Atomic Absorption (AA), Thin Layer Chromatography (TLC) and dissolution apparatus (Distek)
• Assists with the identification and troubleshooting of problems with instrumentation and analytical preparations
• Complies with all company policies and procedures, including safety rules and regulations
• Adheres to GMPs and current Good Documentation Practices (GDPs)

Qualifications

• Associate QC Analytical Chemist: Bachelors degree in Chemistry or related science field and 0-3 years lab experience in a cGMP related industry
• Hands-on experience with analytical instrumentation (i.e., UV, IR, HPLC, GC and/or dissolution instruments) in a pharmaceutical, biotechnology or academic setting
• QC Analytical Chemist I: Bachelor’s Degree in Chemistry or related science field and minimum 1-5 years lab experience in a cGMP related industry
• Hands-on experience with analytical instrumentation (i.e., UV, IR, HPLC, GC and/or dissolution instruments) in a pharmaceutical or biotechnology setting
• Strong hands-on experience performing and interpreting Related Compounds analysis (Impurity analysis)
• Demonstrated ability to apply good laboratory techniques while maintaining efficiencies required in a QC lab
• Chemist I: Bachelors degree in Chemistry or related science field and minimum 2-6 years lab experience in a cGMP related industry
• Chemist II: Bachelors degree in Chemistry or related science field and minimum 3-7 years lab experience in a cGMP related industry
• Chemist III: Bachelors degree in Chemistry or related science field and minimum 3-7 years lab experience in a cGMP related industry

Pay

• Associate QC Analytical Chemist: Anticipated salary range: $60-65k/yr.
• QC Analytical Chemist I: Anticipated salary range: $65-75k/yr.
• Chemist I: Anticipated salary range: $75-85k/yr.
• Chemist II: Anticipated salary range: $80-90k/yr.

Benefits

• Incentives, including, but not limited to: bonus eligible, medical, dental, vision, Rx insurance, 401K with match, life insurance, paid Company Holidays, PTO, Paid Volunteer Time and Employee Resource Groups
• Tris Pharma, Inc. offers a highly competitive compensation and benefits package

Company Information

• Tris Pharma, Inc. is a leading privately-owned U.S. biopharmaceutical company with a focus on development and commercialization of innovative medicines in ADHD, spectrum disorders, anxiety, pain and addiction addressing unmet patient needs
• We have >150 US and International patents and market several branded ADHD products in the U.S. We also license our products in the US and ex-US markets
• We have a robust pipeline of innovative products spanning neuroscience and other therapeutic categories employing our proprietary science and technology
• Our science and technology make us unique, but our team members set us apart; they are the engine fueling Tris’ passion and innovation
• We believe in each other and in respectful, open and honest communications to help support individual and team success