Job Title: Chemistry, Manager
Location: St. Louis, MO
Duration: permanent (Full Time)
Job Role:
• This position will supervise a group of chromatography analysts for compendial, material and drug product testing in a cGMP environment and will be required to develop resource plans that meet revenue goals with regards to safety, quality, output and cost.
• The supervisor will conduct investigations for OOS results, errors and deviations.
• The position requires regular communication with clients in a timely and professional manner.
• The supervisor is responsible for ensuring proper staff training and that deliverables are met or expectations are proactively managed towards alternative solutions.
Key Job Responsibilities:
• Optimizes efficiency of the working environment of the group.
• Ensures training of the group is complete.
• Ensures adherence to personnel and equipment SOPs and other regulatory requirements.
• Pays specific attention to equipment operating practices and conditions to minimize equipment down time, lower maintenance costs, reduce time to run project and repeat of work.
• Makes project/work assignments with communication of the expected timeline.
• Monitors the progress against the timeline.
• Provides troubleshooting support as needed.
• Monitors the quality of the group.
• Effectively communicates with clients and internal groups.
• Evaluates personnel in a timely manner.
• Conducts investigations individually and in conjunction with clients.
• Must be proficient in technical writing.
Qualifications:
• An MS/BS in Chemistry or related field with 5+ years of experience in chromatography (HPLC and GC) techniques.
• Must have a minimum of 3 years in pharmaceutical cGMP laboratory.
• This position requires strong verbal and written communication skills, a thorough understanding of client management, and ability to train staff.
• Previous supervisory experience strongly preferred.
Experience:
• Compendial Testing and wet chemistry techniques
• Experience with OOS investigations to include deviations, LIRs, Kappas
• Method development/validation (Chromatography method development and validation, method verification and method transfer is desired)
• Protocol and report writing, and technical trouble-shooting skills in a GMP environment.
• Routine and non-routine testing using LC/MS and/or GC/MS
• Experience in structural characterization of small molecules by LC-MS/MS and mass spectrometric analysis of biologics including analysis of intact proteins, peptide mapping, and characterization of glycans
Job details are sourced from the employer's original posting.
Open job postingAbout the company
Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.