5 Lowongan kerja di Reckitt Benckiser Indonesia PT
DESKRIPSI PEKERJAAN Requirements : Candidate must possess at least a Diploma, Bachelor's Degree, Engineering (Industrial) or equivalent. At least 1 year of working experience as admin planning / PPIC. Preferably Staff (non-management & non-supervisor)s specializing in Planning / PPIC. Familiar with Microsoft Excel & ERP System (SAP, JDE, Oracle). Good communication in Bahasa and English (passive & active). Contract position available. Willing to work at Cileungsi, Bogor. Job Description : Coordinate and call off raw materials from suppliers of Personal Care according to existing contract. Coordinate and call off packaging materials from suppliers of Personal Care according to existing contract. Manage inventory record of Personal Care raw and packaging materials. Prepare and print Purchase Order (PO) according to plan. Arrange delivery date of RMPM with suppliers. Refresh stock on hand Personal Care RMPM daily.
DESKRIPSI PEKERJAAN Candidate must possess at least a Bachelor's Degree, Engineering (Chemical), Engineering (Electrical/Electronic), Engineering (Industrial), Engineering (Mechanical) or equivalent. Required language(s): English, Bahasa Indonesia At least 1 year(s) of working experience in the related field is required for this position. Applicants must be willing to work in Cileungsi,Bogor. Preferably Supervisor / Coordinators specializing in Manufacturing/Production Operations or equivalent. 3 Full-Time position(s) available. Fresh graduates are welcome to apply Job Description: Manage and supervise a series of production activities, which includes ensuring quality of produced outputs. Manage and supervise the usage of raw material. Manage and set up work rotation schedule for related team members, and ensure their attendance during on-going production shift. Provide guidance, SOP refreshment, direction, and disciplinary to subordinates, to ensure a productive working environment amongst team members to support manufacturing process. Supervise and ensure implementation of a safe working behavior amongst team members. Ensure all the equipment and facilities in best shapes and in good condition:- Work actively with related parties to ensure preventive and corrective maintenance performed as scheduled.- Rise, record, plan action, monitor and ensure execution for maintenance work in Personal Care proactively. Support production manager to provide report production weekly and monthly especially for OEE & wastage report.- Make initiation and program for continuous improvement:- Identify critical and potential issue in Personal Care which impact quality, safety and delivery Make action plan, proactively coordinate with related party, taking help from production team and support from production manager
DESKRIPSI PEKERJAAN Candidate must possess at least a Bachelor's Degree, Biology, Chemistry or equivalent. Required language(s): English, Bahasa Indonesia At least 2 year(s) of working experience in the related field is required for this position. Applicants must be willing to work in Cileungsi,Bogor. Preferably Supervisor / Coordinators specializing in Quality Control/Assurance or equivalent. Full-Time position(s) available. Scope : Responsible for handling validation process, qualification of equipment with coordination with other support group (QC, Project, Engineering, Process Development, Operation, M&E, HSE) Job Description : Responsible to prepare, maintain, or review validation and compliance documentation, such as change controls, deviation, protocols, report etc. Assist in training equipment operators or other staff on validation protocols and standard operating procedures. Conduct validation or qualification tests of new or existing processes, equipment, in accordance with internal protocols or external standards. Create, populate, or maintain databases for tracking validation activities, test results, or validated systems. Design validation study features, such as sampling, testing, or analytical methodologies. Prepare detailed reports or design statements based on results of validation and qualification tests or reviews of procedures and protocols. Conduct validation of cleaning process or performance qualification of equipment to ensure compliance with internal or regulatory requirements. Direct validation activities, such as protocol creation or testing. Prepare validation or performance qualification protocols for systems, or equipment for production. Maintain validation test equipment Analyze validation test data to determine whether systems have met validation criteria or to identify root causes of production problems. Identify deviations from established process standards and provide recommendations for resolving deviations. Responsible to support Cleaning Validation or disinfectant efficacy studies. Execution of protocols of cleaning validation with coordination with other support groups, Process validation, Operations and QC department. Execution of sampling, visual inspection and testing associated with cleaning validation. Responsible for generation of validation protocols and reports to support Validation of Microbiological Test method validation such as ensuring that all test method meet the USP and regulatory requirements. Methods include but not limited to Bioburden, Growth Promotion, Microbial Identification, disinfectant efficacy and Preservative studies. Development and Validation of Microbiological Analytical Methods to support new Validation Activities associated with manufacturing changes, new product introduction and changes to the site bioburden and flora. Act as subject matter expert for investigations, CAPA, change control and external inspections.
DESKRIPSI PEKERJAAN Candidate must possess at least a Bachelor's Degree, Master's Degree / Post Graduate Degree, Chemistry or equivalent. Required language(s): English, Bahasa Indonesia. Good understanding of regulatory and GMP requirements relevant to a regulated product e.g. EU GMP, WHO, PIC/S, CFR 21 Part 210/211. 5 - 7 years experience working in a Quality Control / Laboratory Testing function in FMCG, Food, Pharmaceutical, and other related industry at middle management level with at least 2 – 3 years in similar capacity. Appropriate qualifications in auditing is an advantage. Applicants must be willing to work in Cileungsi,Bogor. Preferably Manager / Assistant Managers specializing in Quality Control/Assurance or equivalent. Full-Time position(s) available. Scope of Role The role holder continuously interacts internally with the QA and QMS team, the Procurement team for Laboratory, Production team, and Warehouse. She externally interacts with the vendor on Raw Material and Packing Components suppliers, Laboratory Equipment suppliers, and External laboratory for carrying various tests. Responsibilities Ensure that all quality control of RB manufacturing are well maintained and implemented as per global quality standards Ensure that good manufacturing practice and good laboratory practices, safety & environmental requirement are updated implemented and maintained on all RB manufacturing. Ensure testing and inspection of all raw materials, packaging materials, finished goods and bulk are carried out as per TDS specifications. Responsible for the releasing process of all raw materials, packaging materials, bulk as per approved SOP and global requirements before they are used for the production process; also responsible for the release process of all finished goods as per approved SOP and global requirements before they are released for distribution with consideration from head of Quality Guarantee all raw materials and packaging materials used in the manufacturing process are from approved vendors; also to ensure that the COA specifications from the suppliers for all incoming materials comply with the TDS specifications. Confirm all In Process Quality Control (IPQC) systems on RB manufacturing lines are implemented and maintained as per approved standards and global requirements. Lead an investigation an appropriate investigation in case of any on site quality related issues and corrective action implementation so as to mitigate root causes. Perform validation, qualification and calibration activities on RB manufacturing sites as per approved guidelines. Make sure the change control management process for all activities which have the potential to impact quality on all RB manufacturing sites; document and review the same. Issue the "good for sale" certificate for the first delivery for all NPD/EPD/Squeeze projects. Prepare and provide for quality agreements with countries from which we export products. Establish self and/or team member follow GMP and other regulation related to safety and environment.
DESKRIPSI PEKERJAAN This role plays an important part in supporting the implementation of category management strategies, consisting of all aspects of 4P strategy with the specific customer. This position is focused on driving in-marketing activity that leads to improved sales/share. He or she will heavily interact with filed sales, key account managers, finance, and marketing.
Reckitt Benckiser Indonesia PT
- Sudah Tidak Bekerja
- Accounting / Finance
- 19 Juni 2016
- Gaji & Benefit
- Work/Life Balance
- Senior Manajemen
- Nilai & Budaya
- Jenjang Karir
- Rekan kerja yang selalu support sehingga persaingan kerja yang ada di sini sportif tidak ada tindakan yang macam-macam dari karyawan lainnya.
- Job yang diberikan oleh perusahaan menyita waktu karyawan, sehingga waktu istirahat menjadi kurang dan waktu untuk keluarga pun menjadi berkurang.