THE TIVOLI GROUP Delhi : Legal Liaison Manager

[Admin]

THE TIVOLI GROUP
www.tivoligarden.com

Keywords: laison , legal , hotel , tax , liaison

Designation: Liaison Manager
Experience: 8 - 13 Years
Location: Delhi
Compensation:
Best In the Industry
Education: UG - LLB - Law
PG - Any PG Course - Any Specialization
Industry Type: Hotels/ Restaurants/Airlines/Travel
Functional Area: Legal
Posted Date: 04 Dec 2008

Job Description
Should be able to handle Sales/Exise/Tax Matters.
* Should be able to liaise with Police authorities.
* Should be able to liaise with various Govt. Deaprtments.
* Should be able handle legal matters.
* Should be familiar with the working of a hotel.

Desired Candidate Profile
The individual should have worked in Hotel Industry.
LOCATION: North Delhi ( Near Rohini).

Company Profile
Tivoli gardens, the up market banqueting paradise in the heart of the South Delhi and very much part of the capital’s crème-de-la-crème. Whether it is a high profile theme party or an exclusive corporate do.

Executive Name: Mr. Tej Bahadur Singh

Address:
THE TIVOLI GROUP
Main Chattarpur Mandir Road
Near Chattarpur Mandir
Delhi,Delhi,INDIA 30

Email Address: hr@tivoligarden.com

Telephone: 91-011-26301111

Reference ID:
Liaison Manager

[Guest-IJT]

Name : manokaran
Email : manokar27 AT gmail.com
Designation / Skillset : Production Executive ( Hospirahealthcare india pvt ltd)

Resume :

PRODUCTION EXECUTIVE – PHARMACEUTICAL INDUSTRY
Offering an experience of 4 years in pharmaceutical production; seeking a challenging assignment with Pharmaceutical manufacturing organization of repute which provides me avenues for professional learning and makes good use of my technical skills and encourages individual growth
________________________________________
PROFILE
- Adroit & diligent Production Executive, professionally & technically competent in all aspects of the pharmacy production, with an experience of around 4 years in the pharmaceutical industry. Currently spearheading as Executive – Production with Hospira Healthcare India Pvt. Ltd.
- Hands on experience in production planning & control, budgeting, resource management and manpower supervision in the manufacturing environment; expertise in worker handling, maintaining house keeping records, checking & packaging, maintenance & use of Production Equipments/ Facilities, Clinical/ Pharmaceutical Aspects,, Pharmacy Acts & Regulations, Occupational Health & Safety Acts/ Principles
- Demonstrated ability to manage human, financial and material resources towards the achievement of stated objectives, to plan and manage work programs and to lead, motivate and provide effective guidance to a team of professional and support staff
- Effective resource planning/ optimization, focusing on waste reduction, enhancing productivity & profitability with ability to use sound judgment, decision-making skills and thrive in a deadline intensive environment, multi-task, performs under pressure and meet deadlines
- Proficient in managing operation & maintenance of machines & equipments in reducing downtime and enhancing operational effectiveness of equipment with expertise in handling diverse range of machinery
CORE COMPETENCIES
Production Operations - Planning & Control - Process Improvement - Project Management - Quality Control & Quality Assurance - Liaison & Coordination - Human Resource Management
________________________________________
PROFESSIONAL EXPERIENCE
HOSPIRA HEALTHCARE INDIA PVT. LTD., _______ `March 2010 – till date
(Hospira Healthcare is approved from UK MHRA, USFDA, ANVISA-Brazil, HEALTH CANADA, WHO and MCC South Africa etc. Hospira healthcare Ltd is a leading pharmaceutical organization having formulation & bulk facilities. Formulation plants are capable of manufacturing Sterile Products, Tablets, Capsules & Dry Syrups to cater world wide with latest cGMP practices)
Executive – Production
- Prepare & review SOP’s of equipment, engaged in performance monitoring of all key elements of materials management including taking corrective action wherever appropriate
- Develop, verify & maintain the computerized product formulation database to ensure accuracy and completeness of all derived formulae. Supervise and participate in the formulation, preparation, and provision of Dry Powder Injectables; responsible for overall activity carried out in Injectable section and Injectable packing section including packing of batches, documentation of Batch Records and supervision and monitoring the area activity and drug product inspection and to maintain completion of Batch Manufacturing and Batch Packing Records in online .
- Ensure cGMP in the production and packing area are carried out in compliance with National & International regulatory norms; comply with the policies & procedures, guidelines relating to hospital pharmacy manufacturing practice, the therapeutic goods administration's code of good manufacturing practice, occupational health, welfare & safety requirements & professional standards
- Preparing complete qualifications of equipments and area, performing operational qualification of equipment and installation of the new equipment and to ensure the qualification& requalification of visual inspectors & carried out as per schedule.
- Plan manpower required for daily & monthly production batches in coordination with Production Head and Administration department; training and evaluation of subordinates, technical staff, operators & casuals to achieve efficient utilization of manpower
- Responsible for Planning & supervision of Vial Washing activities, Sterilizations, Manufacturing, Filling, Sealing,
and optical testing, X-ray inspection and Packing activities of Dry Powder Injectables.
- Carrying out the execution of the Aseptic Media Fill Validations for the following vials
- 10 ml conventional vial , 20 ml conventional vials , 30 ml conventional vial , 50 ml conventional vial
& 100 ml conventional vial
- Monitoring of Sanitation and Cleanliness of the Area, equipments & their documentation
- Maintaining Quality, Output /Yeild and Losses at all critical stages as per respective BMR of Products.
- Maintaining the sterile manufacturing area in validated and qualified state by performing the periodic performance verifications of the following
- Performance verification of Autoclave
- Performance verification of Dry heat tunnel sterilizer
- Performance verification of Vial washer
- Performance verification of Sterile dosage area w.r.t AHU’s
- Performance verification of LAF’s/UDF stations
- Accountable to generate daily & monthly production reports and check the monthly stock statements in coordination with PPIC department; maintaining and updating cGMP records
- As a team member of Internal Audit Committee, participating in self Audits in other department and ensure that the Rules & Regulations of the Organization are followed
- Continuously reviewing and revising the procedures and systems according to current GMP and regulatory requirements
- Handling of incidents & deviations report & preventive and corrective action.
- Having experience in facing the external audits. Faced more than 15 audits of USFDA, MCA (MHRA), MCC, TGA and Brazil regulatory audit etc…. Continuously reviewing and revising the procedures and systems according to current GMP and regulatory requirements
- Operate & maintain equipment used in the delivery of these services in accordance with standing operating procedures. Advise & direct the Pharmacy Assistants & Purchasing Officer to ensure adequate supplies of pharmaceuticals, raw materials, consumables and supplies are stocked to meet the needs of the Service
- Control the materials & resources to meet production schedules & internal company requirements; formulate & maintain manufacturing objectives & coordination with quality control to maximize product reliability
- Ensure that calibration & maintenance cycles are adhered to and documented throughout the QC/ Production Department. Carry out audit tasks as required by the Quality System Audit Schedule
- Carrying out the Performance verification for critical equipments like Autoclave, Sterilization tunnel , vial washing and LAF’s
- To carryout preventive maintenance programme to reduce break down of the equipments and Carrying out
any modifications to improve the productivity and quality in coordination with Maintenance department.
- Involved in Validation of :
- Personnel Qualification
- Sterile area Qualification
- Miscellaneous validations with respect to microbial loads
- Process Qualifications (Cleaning validation, Process validation etc…)
- Handled equipment validations (Installation qualifications, Operational qualifications and performance qualifications etc...)
- Vial Labeling Machine
- CVC vial labeling machine
- X ray Vial Inspection Machine
- Tray Packer with SYSTECH vision system fully automated ROBOT operated multi-carton packaging system.
- Carton semiautomatic over coding machine
- Carton online over printing and over coding machine
ORCHID CHEMICALS&PHARMACEUTICALS LTD. Oct. 2007 – March 2010
Junior Executive ( Production Dry powder & injectables)
________________________________________
AUDITS FACED
- WHO : World Health Organization - Facility Audit
- USFDA : United States Food And Drug Administration
- MHRA : Medicines and Healthcare products Regulatory Agency – UK
- ANVISA : Agentia Nationale Vigilance Sanitaria - Brazil Consultant Authority for Marketing
- HEALTH CANADA : Facility Audit
- VAN ZYL AUDIT : Consultant Audit for WHO
- GSK : Glaxo Smithkline
- PLIVA : UK Based Consultant –For Facility Audit
- SCHEDULE M : Drug Control Authority - INDIA
- UNICEF : United Nations International Children’s Emergency Fund.
- PFSB (JAPAN) : Pharmaceuticals and Food Safety Bureau
- CDSCO (INDIA) : Central drug standard control organization.
________________________________________
ACADEMIA
MS (PHARMA. TECH.), 2011 - Vinayaka mission University, Salem India; 66%
B. Pharmacy, 2007 - Vel’s college of Pharmacy, Chennai; 70%
HSC (XII), 2003 - K.C.S.M. Marticulation Higher Secondary School; 83%
SSLC (X), 2000 - K.C.S.M. Matriculation Higher Secondary School; 66%
COMPUTER PROFICIENCY :
DCA (Diploma in Computer Application) - SAP (Production and Packing) - Windows, MS Word, MS Excel, MS PowerPoint and Internet Applications
________________________________________
Languages : English & Tamil; Hobbies: Watching TV and listening to music;
-------------------------------------------------------
More Information about this submission and submitter :-
___________________________________________________
Submission ID : 4354264
Date & Time : 10th Jul 2011 2:49 PM (UTC)
IP Address : 12.144.110.131
Browser Info : Mozilla/4.0 (compatible; MSIE 7.0; Windows NT 5.1; .NET CLR 1.1.4322; .NET CLR 2.0.50727; .NET CLR 3.0.4506.2152; .NET CLR 3.5.30729)
Predicted Country : United States

[Guest]

Bio-data
Name - Arshvinder Singh.
E-mail -singh.arshvinder AT yahoo.com

Educational Qualifications-Matriculation,Bachelor of Arts,Master of Arts[History],L.L.B[Bachelor of Law].
Work Experience-
Started practicing as a lawyer in the High Court of Punjab and Haryana at Chandigarh in the year 2000 in Criminal law,represented the state of Punjab in the high court as Assistant Advocate General from September 2005 till march 2007,as Deputy Advocate General from may 2009 till april 2011 ;and then as Additional Advocate General from April 2011 till October 2011;and now practicing independently in Criminal law in the High court of Punjab And Haryana at Chandigarh.