Chemist A

Overview

Aurolife was founded in 2008 as part of a group of companies with a long history in generic pharmaceutical product development and manufacturing. Aurolife has a history of solid manufacturing practices in the solid oral dose arena. The Aurolife family consists of an experienced management team with expertise in manufacturing, R&D, Quality Assurance and Quality Control, and regulatory affairs. Aurolife aims to provide healthcare at economical prices to improve global health.

Chemist A will perform a variety of QC testing to assess the strength, identity and purity of test samples and/or materials. The Chemist will work as a member of a team to effectively plan and QC analytical testing using established (official and/or in-house) test procedures. The Chemist may execute 90% – 100% of their work at the bench level.

• Perform assigned sampling, physical, chemical tests and assay on raw materials, active pharmaceutical ingredients, in-process, finished and stability products, using various wet chemicals, physical and instrumental techniques (HPLC, GC, UV-Vis, IR, Particle Size Analyzer, KF Auto titrator, Bulk Density, and other routine QC instruments) as per USP monograph / in-house / any other compendial monographs.
• Independently plan and maintain adequate inventory of test reagents and solutions to perform work; ensure supplies are ordered as needed.
• Independently plan and execute testing to meet established timelines. Perform complicated testing with supervisory direction.
• Record data and results as specified in documentation procedures. Document work clearly and perform tests accurately.
• Prepare and/or review Test Procedures, SOPs, and Protocols as assigned.
• Perform maintenance and calibrations of laboratory instruments/equipment with supervisory direction/training.
• Perform troubleshooting and investigations under the direction of a supervisor.
• Comply with regulatory and in-house requirements (e.g., safety, housekeeping, laboratory chemical waste, cGMP, cGLP, documentation) when performing the assigned activity.
• Review of analytical documents as required.

• Minimum 2–3 years of experience in pharmaceuticals and 1–2 years in analytical testing (desirable).
• QC experience in generic pharmaceutical industries preferred.
• Knowledge of Good Documentation Practices; knowledge of USP/ICH/FDA guidelines.
• Ability to learn quickly and possess decision-making skills.

• Minimum BS in a scientific field; BS in Chemistry preferred.

• Various medical, dental, vision plans and life insurance options.
• Disability insurance, flexible spending accounts (FSA) and health savings account (HSA).
• 401(k) plan with employer match; fully vested after 3 years.
• Employee Assistance Program (EAP) – confidential and company-paid.
• Paid time off, vacation, holidays.
• Legal and identity theft protection options.

Min USD $50,000.00/Yr. Max USD $60,000.00/Yr.

• Work in a temperature-controlled office environment; travel may be required.
• Occasionally handle or feel objects; talk, hear, and walk during the course of employment.
• Some travel for business purposes; use of computer, phone, copier and other office equipment.
• Vision requirements include close, distance, color, peripheral vision, depth perception, and ability to adjust focus. Sedentary work with potential to lift up to 10 pounds occasionally.

Please note that we are not accepting unsolicited resumes or proposals from recruitment firms or agencies for this position. Thank you for your understanding.