AR-CPS Laboratory Analyst
at CocaCola
Buenos Aires, Buenos Aires, Argentina -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 06 Nov, 2024 | Not Specified | 07 Aug, 2024 | N/A | Food Safety,Analytical Skills,Leadership,Sanitation,Kaizen,Environmental Science,Continuous Improvement,Regulatory Compliance,Microbiology,Food Industry,Food Science,Chemistry | 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:
At The Coca-Cola Company, we are constantly transforming our ways of working and our workforce to meet the demands of our diverse consumer base and global operations.
We are looking for a dedicated and skilled Laboratory analyst to join our team in Buenos Aires. If you have a passion for excellence and a drive to make a difference, we want to hear from you.
WHAT ARE THE QUALIFICATIONS NEEDED
- Degree in Food Science, Chemistry, Microbiology, or a related field.
- It´s desirable to have experience in a quality control or quality assurance role, preferably within the beverage or food industry.
- Strong analytical skills with a solid understanding of physical-chemical, microbiological, and sensory analysis.
SKILLS:
Leadership; Product Development; Chemistry; Kaizen (Continuous Improvement); Continual Improvement Process; Environmental Science; Researching; Problem Resolution; Communication; Food Safety and Sanitation; Data Entry; Laboratory Testing; Data Compilation; Quality Control (QC); Green Solutions; Environmental Regulatory Compliance; Recordkeepin
Responsibilities:
As a Lab analyst, you will be responsible for the effective implementation of quality control and quality assurance systems to maintain a high level of performance and ensure compliance with the policies, procedures, practices, and standards of the Company and local regulatory agencies.
Your key duties and responsibilities will include:
- Conducting physical-chemical, microbiological, and sensory analysis of raw materials, intermediate and finished products, environment, and packaging, ensuring proper use of quality documentation and procedures, and accurately interpreting and recording results.
- Ensuring all analyses are performed according to and meet Company specifications with integrity and objectivity.
- Making usage decisions (approval or rejection) over analyzed materials.
- Supporting the measurements follow-up to assure effective control of operational processes.
- Defining necessary actions to demonstrate continuous improvement of operational processes and ensuring a positive impact on Plant key indicators.
- Actively participating in preparing and implementing laboratory workstreams TIPs.
- Executing analytical activities in the Quality Control laboratory with a focus on waste reduction and process optimization according to the analytical planning.
- Observing behaviors compatible with Operational Excellence (OE) culture and complying with standards and guidance established by the Plant Management System.
- Promoting a culture of continuous improvement in GMP (Good Manufacturing Practices), GLP (Good Laboratory Practices), and the Management System of the laboratory.
- Actively participating in and complying with the Laboratory Management System program (ISO 17025).
- Performing calibration and troubleshooting of laboratory equipment and maintaining results and dispositions registered in information systems on time.
- Monitoring analytical results through Statistical Process Control (SPC) to identify trends and using statistical problem-solving tools effectively.
- Implementing new methods of analysis validated and approved by Corporate.
- Conducting Shelf life extension processes according to Company requirements.
- Performing trainings according to the Skill Matrix and writing, reviewing, and performing work instructions of the Integrated Management System of the Laboratory.
- Supporting compliance with the Quality Assurance program of the Integrated Management System.
- Participating in sensory evaluation panels and maintaining the Sensory Panel of the Plant according to Company requirements.
- Participating in department meetings, internal work teams, and necessary meetings to comply with Plant and global metrics.
- Performing internal audits of the Management System and prioritizing product safety by maintaining personal hygiene, avoiding cross-contamination risks, and complying with FSSC 22000 risk analysis.
- Communicating identified situations that may impact safety and assuming the OE Change Agent role during workstream and tool implementation.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Chemistry
Proficient
1
Buenos Aires, Buenos Aires, Argentina