Required Quality Assurance At Gurgaon

Job Description

The Requirement Details are As Follows,Position :-Quality Officer (Quality Assurance /Quality Control)Location: Bangalore -GurgaonJob Code :-QC GurgaonResumes to be send :- hidden_email / hidden_emailType of Industy :- An Sterlisation Provided based CompanyOur Client had been pioneers in providing sterilisation and bio-burden reduction services, since 1983. The Company provides Ethylene oxide (EtO) Sterilisation, Gamma Radiation Sterilisation (GRS) and Natural Pasteurisation Services (NPS) from19 facilities across India and South Asia.Thanks to our diverse portfolio of services, we have become the only service provider offering Total Sterilisation Solutions to the Healthcare, Foods and Cosmetics industries not only in the country but in Asia.They provides sterilisation and bio-burden reduction services to the following industries; manufacturers and processors ofDisposable Medical Devices Packaging Components Spices & Herbs Food Ingredients Herbal Extracts & Formulations Pharmaceutical Raw Material & Formulations Cosmetic Raw Material, Finished Products & AccessoriesThe sterilisation process is one, by which all micro-organisms are inactivated (e.g. disposable medical devices, pharma formulations etc.) rendering the product sterile. In the case of bio-burden reduction, total bacterial load in the products(agro-produce like herbs, spices, pharma & cosmetic raw material) is substantially lowered and pathogens destroyed rendering respective products usable.The services offered help manufacturers, processors, consumers and exporters meet quality norms both, domestic and in importing countries, resulting in earning higher value for their produce, meeting all Regulatory (including international phytosanitary) requirements, extension of shelf-life (thereby helping reduce wastage), addressing food safety issues thus rendering the respective product usable.To address the growing needs of customers, we expanded our services to include GRS & NPS to our EtO process.Actual users, including exporters, demand hygienic and quality products void of all contamination, hence, the importance of an appropriate method that would not affect the properties of the product and yet, be acceptable to customers.The Healthcare, Food & Pharma industries prefer outsourcing their sterilisation / bio-burden reduction needs to specialists instead of doing it themselves due to the high level of expertise required for optimal results, capital investment involved and lack of economy-of-scale.In sum, the process that best meets customers requirements becomes the method of choice. Further, all our processes have been developed bearing in mind Food safety laws (PFA) and respective statutory regulations.They have revolutionised the concept of Quality enhancement by creating domestic awareness to match international standards resulting in ready-to-use-products, since 1983; over the years, Established facilities atBaddi, Gurgaon, Manesar, Bawal, Unjha, Vasai, Mahape, Bengaluru, Edayar, Kolenchery, Rajapalayam, Tuticorin and Guntur. In 2006,MICROTROLs first overseas EtO facility became operational on the outskirts of Ho Chi Minh City, Vietnam.Job Profile :-
1. Liaise with the in Process and QC Personnel for product/process conformity and documentation/reports
1. Release the treated product while ensuring compliance with the respective protocol / technical agreement; observe and record deviation, if any.
1. Ensure the awareness of regulatory and customer requirements throughout the organisation through training/meetings/notices/personal briefings etc.
1. Analyse all quality performance of the Company by reviewing Quality records, Internal Quality Reports, etc.
1. Be responsible, as applicable, for the GMP and Pharmaceutical Quality Systems requirements with respect to processing.
1. Attending/facing Quality Audits and preparing related documentation
1. Co-ordinate all Corrective and Preventive Actions.
1. Irrespective of his responsibilities, when appointed as Management Representative (MR), will be responsible for ensuring that process of Quality Management Systems are established and maintained at the plant. He shall be responsible for the preparation of the Agenda and Minutes of Management Review Meetings.
1. MR will report to the Top Management on the performance of QMS, including need for improvement in management review meeting or/any other meeting. He / She shall also liaise with the Corporate QA / MR on all issues related to quality systems.
if Shortlisted, will update u with Interview DetailsFrom,Ravi Dawra & HR Department

Keyskills :
quality assuranceqms