Assessor Resource

FDFTEC5001A
Manage and evaluate new product trials

Assessment tool

Version 1.0
Issue Date: May 2024


This unit applies to the management of the trial in a production environment. New product trials typically involve working with a team of area specialists including product development and engineering experts.

This unit of competency covers the skills and knowledge required to plan, monitor and evaluate the trialing of new products in production.

You may want to include more information here about the target group and the purpose of the assessments (eg formative, summative, recognition)

Employability Skills

This unit contains employability skills.



Evidence Required

List the assessment methods to be used and the context and resources required for assessment. Copy and paste the relevant sections from the evidence guide below and then re-write these in plain English.

The Evidence Guide provides advice on assessment and must be read in conjunction with the performance criteria, required skills and knowledge, range statement and the Assessment Guidelines for the Training Package.

Overview of assessment

Assessment must be carried out in a manner that recognises the cultural and literacy requirements of the assessee and is appropriate to the work performed. Competence in this unit must be achieved in accordance with food safety standards and regulations.

Critical aspects for assessment and evidence required to demonstrate competency in this unit

Evidence of ability to:

establish parameters and conditions and requirements for product trial

establish, document and communicate the procedure for the trial

monitor and evaluate trial outcomes against objectives and set conditions

document all aspects of trial to ensure repeatability and collection of evidence.

Context of and specific resources for assessment

Assessment must occur in a real or simulated workplace where the assessee has access to:

trial objectives and parameters

new product specifications

raw materials/ingredients, packaging components and consumables

related production equipment

relevant Standard Operating Procedures (SOPs)

communication systems

workplace information recording systems, requirements and procedures.

Method of assessment

This unit should be assessed together with core units and other units of competency relevant to the function or work role. An example could be:

FDFPPL4005A Establish process capability.

Guidance information for assessment

To ensure consistency in one's performance, competency should be demonstrated on more than one occasion over a period of time in order to cover a variety of circumstances, cases and responsibilities, and where possible, over a number of assessment activities.

Submission Requirements

List each assessment task's title, type (eg project, observation/demonstration, essay, assingnment, checklist) and due date here

Assessment task 1: [title]      Due date:

(add new lines for each of the assessment tasks)

Assessment Tasks

Copy and paste from the following data to produce each assessment task. Write these in plain English and spell out how, when and where the task is to be carried out, under what conditions, and what resources are needed. Include guidelines about how well the candidate has to perform a task for it to be judged satisfactory.

Required skills

Ability to:

identify trial objectives and information requirements, including clarifying reporting requirements and formats

identify trial participants, including clarifying roles, responsibilities and levels of authority (participants may include technical experts, related functions such as planning, quality assurance and engineering and trial process operators)

establish and maintain effective communication processes to meet the information requirements of all stakeholders

assess final product specifications against recipe/formulation and processing method to confirm capability

identify production targets and timeframes against equipment and process capability

confirm availability of resources to meet trial schedule, such as stock levels, equipment availability and capacity, personnel and storage capacity

identify competencies required by trial operators and confirm availability, such as arranging training prior to trial

confirm that all hazards have been identified and appropriate methods of control are in place to control environmental, food safety and OHS hazards (control methods should be selected consistent with the control hierarchy)

establish a detailed trial schedule to manage the process

ensure that relevant documentation is available in appropriate formats, including product specifications/recipe formulations, process parameters and operating procedures

monitor trial progress against detailed plan to identify variances and identify factors that may need to be adjusted to achieve schedule, which may require consultation with operators and other experts

investigate and report on causes of variation and identify opportunities for improvement, such as participating in/facilitating problem solving processes

use project planning, scheduling and monitoring skills, such as use of relevant software applications

collect and evaluate trial information, such as participating in/facilitating an evaluation team

report on trial outcomes and related improvement opportunities to meet reporting requirements of the trial process

use communication skills to interpret and complete work information to support operations of work team or area

demonstrate and support cooperative work practices within a culturally diverse workforce

Required knowledge

Knowledge of:

trial project parameters, constraints and criteria for evaluating outcomes

sources of expertise available to support the trial process

process documentation procedures and requirements to ensure that the process meets trial outcomes and is consistent with legislative and company policy objectives, including relevant legislation

factors to be taken into account in planning and monitoring the trial process

proposed formulations and preferred processing method to assess constraints and opportunities for improvement, including equipment capability, typical materials usage rates to achieve a given production outcome, and area experts in related roles, such as product development and engineering, where required, to provide additional expertise

systems and procedures for managing OHS, environmental management and food safety through the trial process consistent with the hierarchy of control

investigation and process improvement techniques and processes, including techniques to collect and evaluate trial data

recording systems and requirements

The range statement relates to the unit of competency as a whole. It allows for different work environments and situations that may affect performance. Bold italicised wording, if used in the performance criteria, is detailed below. Essential operating conditions that may be present with training and assessment (depending on the work situation, needs of the candidate, accessibility of the item, and local industry and regional contexts) may also be included.

Trial conditions

Trial conditions are consistent with company policies and procedures, regulatory and licensing requirements, legislative requirements, and industrial awards and agreements and takes account of OHS and environmental impact of scheduling arrangements

Achieving schedule

Achieving schedule involves meeting product specifications within given resource allocations and timelines

Trial processes

Trial processes typically involve a multi-disciplinary team

Factors to be taken into account in planning and monitoring the trial process

Factors to be taken into account in planning and monitoring the trial process may include but are not limited to:

product specifications

raw materials/ingredients, packaging components and consumables

storage capacities

production capacity, configuration and availability

processing parameters

labour requirements and availability

trial production targets/timelines

related OHS, food safety and environmental hazards and controls

Copy and paste from the following performance criteria to create an observation checklist for each task. When you have finished writing your assessment tool every one of these must have been addressed, preferably several times in a variety of contexts. To ensure this occurs download the assessment matrix for the unit; enter each assessment task as a column header and place check marks against each performance criteria that task addresses.

Observation Checklist

Tasks to be observed according to workplace/college/TAFE policy and procedures, relevant legislation and Codes of Practice Yes No Comments/feedback
New product specifications are defined 
Production resource requirements are identified 
Project budget and timeline are established 
Trial size is appropriate to provide reliable process and production information 
New product recipe/formula is scaled to suit trial production 
Raw materials/ingredients, packaging components and consumables are identified and confirmed to meet trial requirements 
Production equipment is identified, available and suitable for use 
Production personnel are available and have the required competencies to operate the trial process 
Environmental, food safety and health and safety hazards of the trial process are identified and appropriate control methods determined 
Trial documentation format and procedures are agreed 
The trial schedule timeline is established and barriers/constraints to achieving schedule are identified, monitored and addressed 
Personnel in related work areas and functions are kept informed of trial status and progress 
Operators directly participating in the trial are advised of trial parameters, roles and responsibilities 
Advice on product specifications and operating procedures is communicated to the project team 
The trial process is monitored to identify actual and potential barriers to achieving the schedule 
Trial product is produced within specification 
Out-of-specification or unacceptable outcomes are identified and investigated 
Unusual or atypical conditions that could affect the achievement of the schedule are identified 
Modifications are made and reported as required according to trial arrangements 
Trial objectives are identified 
Resource allocations are assessed against plan 
Trial product is assessed against specifications 
Production parameters/operating conditions are compared with scheduled performance 
Significant variances are identified and investigated 
Improvement opportunities are identified and reported 

Forms

Assessment Cover Sheet

FDFTEC5001A - Manage and evaluate new product trials
Assessment task 1: [title]

Student name:

Student ID:

I declare that the assessment tasks submitted for this unit are my own work.

Student signature:

Result: Competent Not yet competent

Feedback to student

 

 

 

 

 

 

 

 

Assessor name:

Signature:

Date:

Assessment Record Sheet

FDFTEC5001A - Manage and evaluate new product trials

Student name:

Student ID:

Assessment task 1: [title] Result: Competent Not yet competent

(add lines for each task)

Feedback to student:

 

 

 

 

 

 

 

 

Overall assessment result: Competent Not yet competent

Assessor name:

Signature:

Date:

Student signature:

Date: