Astrix
Analytical Chemist
Astrix, Aurora, Colorado, United States, 80010
Our client is a biopharmaceutical manufacturer that creates and develops high-purity chemicals to be distributed to client biotech companies. They are seeking an experienced
Analytical Chemist
to join their team in one of their state of the art manufacturing laboratories!
Located in Aurora, OH
Shift:
1st shiftPay:
$30-35/hour
Major Responsibilities:Method Development & Validation
Perform method development, verification, and validation using advanced analytical instrumentation such as UHPLC (RI, CAD, PDA) and GC (FID, TCD).
Regulatory Compliance
Adhere to current Good Manufacturing Practices (cGMP), current Good Laboratory Practices (cGLP), ISO 9001, and all safety regulations to ensure compliance in the Quality Control Lab.
Collaboration
Work closely with internal departments to achieve project and company goals, ensuring effective communication and support across teams.
Scientific Integrity
Ensure all projects are completed with the highest scientific and ethical standards, maintaining the integrity of data and results.
Lab Safety
Oversee the safe and secure operation of the laboratory to protect personnel, equipment, and the overall site. Ensure that all safety protocols are strictly followed.
Additional Duties
Perform other duties as assigned to support team goals and organizational success.
Qualifications:Education:Bachelor’s or Master’s degree in Chemistry, Biology, Biochemistry, or related field.Experience:Minimum of 4-5 years of experience in analytical chemistry, with a focus on HPLC, UPLC, and GC.3-4 years of experience in method development and validation, including hands-on experience with chromatographic techniques.Technical SkillsProficiency in chromatography techniques, including gas chromatography (GC) and high-performance liquid chromatography (HPLC).
Analytical Chemist
to join their team in one of their state of the art manufacturing laboratories!
Located in Aurora, OH
Shift:
1st shiftPay:
$30-35/hour
Major Responsibilities:Method Development & Validation
Perform method development, verification, and validation using advanced analytical instrumentation such as UHPLC (RI, CAD, PDA) and GC (FID, TCD).
Regulatory Compliance
Adhere to current Good Manufacturing Practices (cGMP), current Good Laboratory Practices (cGLP), ISO 9001, and all safety regulations to ensure compliance in the Quality Control Lab.
Collaboration
Work closely with internal departments to achieve project and company goals, ensuring effective communication and support across teams.
Scientific Integrity
Ensure all projects are completed with the highest scientific and ethical standards, maintaining the integrity of data and results.
Lab Safety
Oversee the safe and secure operation of the laboratory to protect personnel, equipment, and the overall site. Ensure that all safety protocols are strictly followed.
Additional Duties
Perform other duties as assigned to support team goals and organizational success.
Qualifications:Education:Bachelor’s or Master’s degree in Chemistry, Biology, Biochemistry, or related field.Experience:Minimum of 4-5 years of experience in analytical chemistry, with a focus on HPLC, UPLC, and GC.3-4 years of experience in method development and validation, including hands-on experience with chromatographic techniques.Technical SkillsProficiency in chromatography techniques, including gas chromatography (GC) and high-performance liquid chromatography (HPLC).