AR-CPS Laboratory Analyst

at  CocaCola

Buenos Aires, Buenos Aires, Argentina -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate06 Nov, 2024Not Specified07 Aug, 2024N/AFood Safety,Analytical Skills,Leadership,Sanitation,Kaizen,Environmental Science,Continuous Improvement,Regulatory Compliance,Microbiology,Food Industry,Food Science,ChemistryNoNo
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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