No Relocation Assistance Offered 86733 : Guatemala, Guatemala, Guatemala
Objective of the Position
To guarantee and ensure the quality of analytical and microbiology laboratory analyzes according to the Colgate Palmolive Guiding Standards (QS and G) and coordinate the implementation of new methods for raw material, product in process and / or finished product complying with Colgate Palmolive quality standards, EOHS, FP and R.
Functions and Responsibilities
Perform physicochemical and microbiological analysis of raw material, product in process, water, environment and finished product according to KRS (Key Release Specification), KPC (Key Process Control) and microbiological specifications to give approval or rejection of according to the current procedures approved using validated methods.
Report and interpret results and identification of product or materials out of specification communicating immediately to the plant and documented planning all in a Laboratory Research Report.
Operate and verify the correct operation (system suitability) of the equipment during the analyzes.
Maintain accurate and up:to:date laboratory records and books, guaranteeing the permanence of unchanged and traceable registered documents that verify the validity of the results.
Provide support in the validation of manufacturing processes and supplier evaluation coordinated by the technology transfer engineers or requested by the plant.
Prepare Standard Operating Procedures and other procedures when required.
Support investigations related to Non:Conformities so that they are documented in SAP.
Actively participate in continuous improvement activities related to your position.
Conduct qualification and training in good laboratory practices and documentation to minilab Analysts.
Implement new methodologies according to established standards and following all the guidelines of the global technology centers for the analytics area.
Carry out the annual analysis of raw materials for all categories.
Support microbiologists in the support provided to the plant for the development of microbiological control, cleaning and sanitation programs, control points, environmental program, validation of the water system, implementation of good manufacturing practices to maintain MVA and awareness microbiological (Micro Awareness).
Transfer the results of the quarantine release of the finished product of Liquids, Fabric Care and Oral Care, to Quality Assurance, so that it is released into the SAP system once the microbiological specifications have been met.
Feed the Global QAMPI database with the results of finished product, water and raw material on a daily or monthly basis, as appropriate.
Maintain the quality assurance program of the Microbiology laboratory, complying with the requirements indicated in the QS: 023 Microbiological Control.
Report the micro incidents that occurred to the Division in the global QAMPI base and to the Managers of the area involved.
Participate in risk analysis and root cause meetings when a microbiological incident occurs in micro sensitive products.
Maintain the updated list of microsensitive raw materials.
:University Degree in Biological Chemistry, Biochemistry and Microbiology or related degree.
:Experience: From 1 to 2 years in a similar position.
:Knowledge of the English language by 75
:Knowledge in the handling of advanced analytical laboratory equipment.
:Basic microbiology knowledge
:Related quality control programs, for example GMPs
:Management of MS Office
Its nice to have:
:Requires Knowledge of Good Laboratory Practices.
:Experience in microbiology laboratories
Equal Opportunity Employer
Colgate is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity, sexual
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