Data Analyst, Data Integrity
at Labstat International Inc
Kitchener, ON N2C 1L3, Canada -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 24 Apr, 2025 | Not Specified | 25 Jan, 2025 | 3 year(s) or above | Statistics | No | No |
Required Visa Status:
Citizen | GC |
US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
Contract – W2 | C2H Independent |
C2H W2 | Contract – Corp 2 Corp |
Contract to Hire – Corp 2 Corp |
Description:
Certified Group is a leading North American provider of laboratory testing, regulatory consulting, and certification & audit services. Certified Group includes Food Safety Net Services (FSNS), Certified Laboratories, EAS Consulting Group, Labstat International Inc., Advanced Botanical Consulting & Testing (ABC Testing Inc.), Microconsult Inc., and Micro Quality Labs Inc. Certified Group provides laboratory testing and regulatory consulting services in the food & beverage, dietary supplements & NHP, cosmetics, OTC, tobacco, nicotine, cannabis, hemp, and other industries.
MINIMUM QUALIFICATIONS:
- BSc. or MSc. with a focus on a chemistry and/or biology related field.
- Experience with statistics is an asset
- Experience with computer programming and/or database application use is an asset. or as determined by Human Resources and Department Director/Manager
- At least 3 years’ experience working in an analytical laboratory is a necessity. Previous experience working in either a GLP or ISO17025 environment would be an asset. or as determined by Human Resources and Department Director/Manager
Responsibilities:
- Member of a team that is responsible for life cycle management of all nicotine, Configuration and maintenance of LIMS test code and related database settings.
- Validation of calculation blocks employed by LIMS
- Preparation of method validation reports either to finalize those prepared by other functions (i.e. Scientist) or from mined data.
- Maintenance of method validation statuses.
- Creation and maintenance of method summaries (standardization of method synopses and validation summary tables) which are used to support Client enquiries and the TPMF filed with FDA.
- Management of the list of limits of detection and quantification values used in reporting (i.e. through mLIMS test code configuration).
- Retrieval and use of data and information from previous studies and projects as necessary.
- The employee shall implement the Laboratory Quality Policy and perform their duties in accordance to existing project specific requirements, current Test Methods, study plans and Standard Operating Procedures (SOP).
- Comply with Health & Safety policies and procedures and wear required Personal Protective equipment at all times
- Other duties as assigned.
REQUIREMENT SUMMARY
Min:3.0Max:8.0 year(s)
Information Technology/IT
Pharma / Biotech / Healthcare / Medical / R&D
Software Engineering
Graduate
Proficient
1
Kitchener, ON N2C 1L3, Canada