QC Analyst

TREATT USA INC•Lakeland, FL

About The Position

The objective of this role is to perform full analysis of flavor and fragrance raw materials that pass through the Quality Control laboratory. This encompasses the classical wet analysis, instrumental analysis to assess the acceptability of the profile, and organoleptic evaluation, to ensure that any material that enters or leaves the site is fit for purpose.

Requirements

A degree in a science-based discipline, preferably with chemistry-based modules, or industry experience relevant to the role.
Extensive chromatography experience (at least 2 yrs) and is comfortable operating, maintaining, troubleshooting, and calibrating GC and LC instrumentation, as well as confident analyzing the data for trends and anomalies.
Attention to detail, multitasker, effective communicator, and be able to lead when necessary.
A track record of taking the initiative to better themselves, the team, the business, systems/processes, etc.
Technical expertise: Classical wet analysis and instrumental analysis techniques in order to perform any testing required on the specification of material in accordance with the standard operating procedures.
Safe working practices to be adopted within the laboratory environment at all times ensuring appropriate use of PPE to prevent breaches of health and safety for yourself and colleagues.
Calibration and maintenance of equipment utilized to ensure it is correctly functioning at all times and troubleshooting those issues that arise, reporting these issues to the Quality Control manager.
Assessing and interpreting risks: Report any breaches in health and safety on the incident cards provided by the health and safety representative. Action should be made to prevent any such incidents where possible.
If material fails the assigned test specification, then testing should be<x_bin_455>repeated on the sample. If persistent failure is seen, where possible a re-sample should be requested for testing before reporting all findings from the analysis.
Understanding of where the Quality Control department fits within the company alongside building and maintaining relationships with key departments.
Operational knowledge of STARS for data entry on testing samples, and JDE for required applications for role.
Be competent at using Microsoft Office applications.
If required to correspond with Suppliers or Customers regarding the results of analysis, ensure that intellectual property on methodology is only shared when appropriate. Correspondence should be overseen by the Quality Control manager.
Ensure that testing of material is completed before the due date assigned in STARS 100% of the time, giving priority to those samples marked as urgent which should be completed on the day of receipt if before 12pm and the following morning if after 12pm.
Request re-samples in sufficient time taking into account service level agreements with Manufacturing and Goods In, and chase up samples if service level agreements are not met.
Notify the Quality Control manager if a sample is likely to go overdue with an explanation as to why so that this information can be cascaded to internal customers. All updates should be provided by 3pm.
If failures are observed with products, assess the possible route cause of this failure, and establish next best steps.
Utilise GCMS to identify any additional or absent compounds in a sample to ensure desired quality is met and advise why these observations may have been seen.
Look out for continuous improvement opportunities within the laboratory and share any possible proposals with the Quality Control manager.
Ensure open and consistent communication with all team members. Any issues which may result in late completion of sample analysis to be communicated to the Quality Control manager.
If assistance is required to maintain service levels, it is the responsibility of the analyst to communicate this need.
Alongside day to day analysis, when time allows, partake in method improvement or project work as applicable. To include but not exclusively, research into new techniques and knowledge development of specific project groups.
Essential within a Quality Control role to ensure accurate reporting of analysis.
Gain an understanding of those departments with which we have key relationships-Planning, Process Control, Procurement, Manufacturing, Goods In.
Ensure that all work carried out is both of the required quality, whilst also meeting the needs of internal customers where possible.

Nice To Haves

Leadership skills: Not required for this role. Open communication and teamwork is essential.

Responsibilities

Measure physical parameters of flavour and fragrance raw materials originating from various departments and external sources, which includes but is not exclusive to density, pH, refractive index, optical rotation, %Aldehyde, and Peroxide values.
Perform instrumental analysis on the above products which includes but is not exclusive to, UV spectroscopy, gas and liquid chromatography, and gas chromatography/mass spectroscopy.
Collect and analyze chromatographic data, being able to make conclusions on sample suitability and identify potential contamination, adulteration, or chromatography issues.
Perform general essential oil analysis but with further tests specific to the substance under analysis.
Participate in organoleptic evaluation of the products.
Prepare tasting solutions, arrange for a representative number of individuals to carry out analysis, and report data.
Prepare reagents for routine and non-routine analysis as well as analytical standards, to include accurately weighing and diluting stock standard materials for calibration purposes.
Identify problems, whether it be with a sample, process, or instrument, and propose solutions to address issues in a timely manner.
Carry out regular calibration and maintenance of the measuring instruments as prescribed by the working practices in the laboratory.
Perform internal microbiological testing.
Communicate with relevant departments for analytical samples to be sent for external analysis and collate the results.
Revise and review SOPs to ensure methods are up to date.
Assist in sample receipt to the Quality Control laboratory to maintain workflow of sample analysis to the required areas of the department.
Carry out day-to-day laboratory checks and housekeeping tasks, these includes washing up glassware and emptying the waste at the end of each day.
Capable of working independently and as a team player.
Contribute to the continuous improvement in the Quality Department (e.g. suggestions on improvements in efficiency, cost cutting, improvements in effectiveness of operations).
Follow any task and request as requested by Quality Control Supervisor or Quality Control manager
Assist Quality Control Supervisor in maintaining chemical inventory for the Quality Control laboratory and in the purchase of any items necessary for routine analysis.
Ensure that the working area in the laboratory is maintained in a clean and orderly condition and that any hazard or potential hazard is reported to the Quality Control Supervisor or Quality Control Manager.
Report any faults or deficiencies in equipment or analytical practices to the Quality Control Supervisor or the Quality Control Manager.
Always maintain your own and other staff’s healthy and safety ensuring a safe working environment.
Undergo training in areas specific to Treatt PLC business as required.
Undergo training in additional practices to those to aid the efficiency of the Quality Department as a whole.
Perform such other tasks that may be required from time to time.
Undertake a shift pattern where necessary to continue a high level of service to internal customers.
Act in the best interest of Treatt PLC always.