Key Responsibilities:

• Be familiar with standard analytical lab equipment usage in the pharmaceutical industry.
• Compile and record data for documentation needed for testing and report preparation.
• Review and update SOPs related to quality control.
• Ensure regulatory compliance by working with GLP and GMP environments.
• Interact with Operations and Quality Assurance.
• Operate and implement analytical lab instrumentation.
• Maintain and manage accurate, precise documentation.
• Support testing to comply with schedules by team-oriented processing.
• Conduct laboratory evaluation of samples.
• Record data in LIMS following standard operating methods.
• Comply with standard procedures and quality control to improve products.
• Performs chemical analysis of raw materials, in-process materials, and finished drug products in accordance with OSHA, FDA, cGMP, and other appropriate regulatory requirements.
• Collection, handling, and documentation of raw materials, chemical reagents, laboratory standards, and sample vessels (handle and move compressed gas cylinders) by OSHA, FDA, cGMP, and other appropriate regulatory requirements.
• Calibration and preventative maintenance of analytical instruments by OSHA, FDA, cGMP, and other appropriate regulatory requirements.
• Review other analysts’ work.
• Maintain standard and supply inventory levels. Organize laboratory supplies and equipment
• Perform routine housekeeping activities; create and submit HOLD alerts, deviation reports, work orders, etc.

U.S. PERSON REQUIREMENTS

Due to compliance with U.S. export control laws and regulations, the candidate must be a U.S. Person, which is defined as a U.S. citizen, a U.S. permanent resident, or have protected status in the U.S. under asylum or refugee status.

YOU MUST HAVE:

• Minimum: High School Diploma with two years in compressed gas industry.
• 1+ year of experience in a working laboratory
• 15 hours of College Chemistry

We Value:

• Bachelor’s degree from an accredited institution in a technical discipline such as the sciences, technology, engineering or mathematics
• Understand, internalize and apply cGMPs and cGLPs; knowledge of laboratory processes
• Effective interpersonal skills, written and oral communication skills; organization skills and detailed-oriented, effective computer skills (Microsoft Word and Excel).
• Basic knowledge of laboratory analyzers, such as GC, Karl Fisher, and FTIR, used to perform chemical analyses as well as basic wet chemistry techniques, such as titration.
• Preference for applicants who understand and can operate OpenLab GC software.
• Able to work as part of a team.

Physical Demands:

• Ability to work in an upright and/or stationary position for up to eight (8) hours per day
• Frequent mobility needed
• Light to moderate lifting and carrying (or otherwise moves) objects including laboratory equipment, laboratory supplies, and laptop computer with a maximum lift of 30 pounds
• Ability to access and use a variety of computer software
• Ability to communicate information and ideas so others will understand, with the ability to listen to and understand information and ideas presented through spoken words and sentences
• Frequently interacts with others to obtain or relate information to diverse groups
• Requires multiple periods of intense concentration
• Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence
• Ability to perform under stress and multi-task
• Regular and consistent attendance

Additional Information

• JOB ID: HRD227263
• Category: Integrated Supply Chain
• Location: Ontario & Lupine Streets,Baton Rouge,Louisiana,70821-2830,United States
• Nonexempt

Honeywell is an equal opportunity employer. Qualified applicants will be considered without regard to age, race, creed, color, national origin, ancestry, marital status, affectional or sexual orientation, gender identity or expression, disability, nationality, sex, religion, or veteran status.