Are you a Quality Control Chemist who is looking to join one of the top companies in the Pharmaceutical industry?
Are you looking to further your career and grow?
Do you have experience with operating primary QC instruments like HPLC, GC, UV, IR, and Auto titrator?
If you answered yes to those three questions, then apply today!
Acara Solutions seeks highly qualified candidates to work Onsite with our client in Decatur, IL. Interested?
Here's what you'd do:
- Perform the sampling of raw materials, chemical and physical analysis of raw materials, bulk formulations, finished products, stability samples, and non-routine samples.
- Sampling and testing of raw materials per approved procedure.
- Physical and chemical testing of bulk and (pre-fill, finished product, and stability) products.
- Upkeep of laboratory notebook.
- Maintaining the work area in an orderly manner.
- Maintain lab inventory, such as a list of standards, chemicals, and reagents.
- Record daily activities such as PH verification, balance verification, and temperature and humidity monitoring of lab stability chambers, freezers, and refrigerators.
- Perform Finished product/in-process/cleaning validation and raw material analysis independently.
- Complete testing within specified timeframes and document results accurately
- Coordinate with vendor for instrument PM, calibration, and qualification activity.
- Provide necessary support.
- I maintained and monitored lab GLP activities, such as the instrument calibration/qualification schedule, preparation of instrument operating procedures, and coordination with the metrology team and vendor for scheduling period calibration/qualification activities.
- Performs calibration of lab instruments whenever possible.
- Cleaning of laboratory glassware.
- Responsible for writing SOP for instrument operation/ calibration.
- Provide necessary support for OOS/OOT investigation.
- Prepare the stability schedule and protocol and report per ICH requirements.
- Adhere to regulatory guidelines (FDA, ICH, GMP) and company quality standards during testing and documentation.
- Adhere to Good Laboratory Practices (GLP), Good Documentation Practices (GDP), and Good Manufacturing Practices (GMP) during testing procedures.
Here's what you'll get:
- Hours: 8/40 hours/week.
- Length: Direct Placement.
Sounds like a good fit?
APPLY TODAY
About Acara Solutions
Acara is a premier recruiting and workforce solutions provider-we help companies compete for talent. With a legacy of experience in various industries worldwide, we partner with clients, listen to their needs, and customize visionary talent solutions that drive desired business outcomes. We leverage decades of experience to deliver contingent staffing, direct placement, executive search, and workforce services worldwide.