3rd Shift QC Chemist - Vandalia, United States - Adare Pharma Solutions

Description

Job Description

Are you ready to join a growing, global drug development and manufacturing organization that puts people first? Come to Adare We work closely with our pharmaceutical industry partners during all phases of drug development with a mission of improving the lives of patients and medicines essential to people all over the world. Each role and every department within Adare offer you a unique, customized experience with a chance to make a real impact, and is critical to our success. With the help of people like you dedicated to our mission, Adare is transforming lives by transforming drug delivery

Join our mission at Adare

What can Adare offer you?

• Medical/dental/vision/life – low employee premiums
• 401k with a highly competitive match
• Generous PTO, including floating holidays
• Career growth and internal opportunities
• Tuition reimbursement
• Relocation assistance
• Performance-based bonus
• Employee Recognition Programs

We are seeking to hire a QC Chemist I - 3rd Shift to join our Quality Control Team...

If any of the below describes you, we would love to meet you

JOB SUMMARY

The QC Chemist I is an essential part of the lab Quality team and will be expected to perform physical and chemical testing of intermediate and finished products according to written procedures.

RESPONSIBILITIES AND LEARNING OPPORTUNITIES

• Demonstrate knowledge of various test methods and instrument analysis techniques including sample preparation, titration, analytical balances, extractions, dilutions, chromatography, pH, and dissolution.
• Prepare various standards, mobile phases and buffers as needed for various test methods.
• Perform physical and chemical testing of raw materials, intermediate, and finished products as described in the documented procedures to support product release and process validation protocols. Suggest method modifications as required. Understanding of USP methods.
• Perform testing requiring rotating bottle, titrations, dissolution baths, and other basic laboratory equipment.
• Perform test methods that utilize instruments such as UV, FTIR, GC, and HPLC. Demonstrate the ability to operate the instrument software application, set up basic sequences and report data.
• As required, perform swabbing and analysis of equipment cleaned by manufacturing with minimal supervision.
• Perform assigned calibrations for equipment in the laboratory as required and maintain the required documentation for compliance.
• Recognize and report Out of Specification results, Out of Trend results and deviations to Supervisor. Assist with investigation steps as required for LIR/OOS Investigations.
• Accurately maintain notebooks and files compliant with current GMPs and internal Standard Operating Procedures. Peer review and/or audit others work as required for verification of GMP compliance.
• Demonstrate consistent ability to perform testing with minimal need for investigation and repeat
• analyses. Ability to accurately report test data in various formats.
• Maintain laboratory equipment and working areas in good working condition.
• Observes all safety procedures and regulations.
• Assist with training of temporary personnel.

Requirements

• Bachelors Degree in Chemistry or related field
• 1+ years of experience working in a Quality Control or Research and Development Laboratory, preferably in the pharmaceutical industry
• Excellent interpersonal written and oral communication skills
• Working knowledge of current Good Manufacturing Practices (GMPs).
• Proficient in Microsoft Excel, Word. Microsoft Access experience a plus.
• Basic knowledge of technical writing coupled with good oral communication skills.

Physical Requirements:

• Stand, walk, push, pull, twist, reach overhead, and bend to the floor
• Occasionally move items or equipment weighing up to 50 pounds
• Occasionally required to climb ladders and/or steps to reach equipment.
• Requires reading precision measuring equipment, machine dials, gages, and thermometers; must be able to observe fine details utilizing a microscope.
• Must have sense of smell to detect odors of unacceptable compounds and/or mixtures.
• Must have steady hands and good physical coordination in order to handle delicate laboratory instrumentation and equipment.
• The employee may be required to wear personal protective equipment (PPE) during certain phases of the operation; such as high noise areas from machinery, exposure to a variety of chemicals, or exposure to dust, mists, and fumes.
• Any employee whose position requires exposure to these conditions receives training in Hazardous Communication Standards and use of mandatory personnel protective equipment. Employee is required to wear such approved personal protective equipment whenever thus exposed.
• Engineering controls are in place to minimize or eliminate exposure to these conditions wherever practical. Adare Pharmaceuticals, Inc. complies with all applicable OSHA, and EPA, standa

Benefits

• Medical/dental/vision/life – low employee premiums
• 401k with a highly competitive match
• Generous PTO, including floating holidays
• Career growth and internal opportunities
• Tuition reimbursement
• Relocation assistance
• Performance-based bonus
• Employee Recognition Programs

Adare Pharma is an equal opportunity employer & prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital & veteran status.

PRINCIPALS ONLY
NO AGENCIES OR THIRD PARTIES