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CURRICULUM VITAE

Bikash Chandra Mahanta AT – RAMCO COURT FLAT NO:- B/35, MOMBASA ROAD NAIROBI, KENYA CONTACT NO:- +254- 753171779 MAIL ID: bikash_1431@rediffmail.com Skype ID: bikash.mahanta3

OBJECTIVE:

Seeking for challenging assignment in the field of pharmaceutical organization. I would like to be a part of organization team that has the potential of recognition as well as enhancement of my skills. QUALIFICATION: Bachelor in Pharmacy from North Orissa University in the year 2002.

EXPOSURE TO QUALITY ASSURANCE:

Oral Liquids, Tablets, Hard Gelatin Capsules, Soft gelatin Capsules, Parenteral (Ampoule /Small volume / large volume /Powder filling).

EXPOSURE TO REGULATORY AUDIT: USFDA: United states of food and drug administrations (USA)
MHRA: Medicines and Health care products Regulatory Agency (UK) TGA: Therapeutic goods and administrations (Australia) WHO: World Health Organization (Geneva) ANVISA: Brazil

EXPOSURE TO LOCAL AUDIT: Local FDA Audit.
Customers Audit like Ranbaxy, Cipla, Cadila health care, Johnson & Johnson, Aventis, Dr.Redy. Galpharm (UK), Millpharm (UK), Gold shields (UK).

EXPERIENCE:
In Mercury Labs LTD.Baroda, (Gujarat) as a chemist QA from May 2002 to June 2004.

RESPONSIBILITY: Sampling of Raw materials to QC department for analysis and release.
Monitoring and in process checks in shop floor activities in accordance with cGMP. Sampling of semi finished or finished product to QC department. Issuance and retrieval of batch documents from production department. Handling non conformances in shop-floor and maintaining its record. Promoted to: Officer QA. Reporting to: Manager QA. In Glenmark Labs LTD. Verna, (GOA) as officer QA from June 2004 to September 2006.

RESPONSIBILITY: Monitoring and in process checks in shop floor activities in accordance with cGMP.
Sampling of semi finished or finished product to QC department. Issuance and retrieval of batch documents from production department. Handling non conformances in shop-floor and maintaining its record. Handling deviations and change control as per SOP and maintains its record. Calibrating all in process instruments and weighing balances as per schedule and maintains its record. Reporting to: GM QA

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Active member in GMP committee. Making of monthly report . Handling non conformances in shop-floor and maintaining its record. Handling non conformances in shop-floor and maintaining its record Handling deviations and change control as per SOP and maintains its record. Allocating daily jobs to QA officers/ IPQA personnel Reporting to: Head QA In Laboratory & Allied Ltd. Handling deviations and change control as per SOP and maintains its record.(Formerly known as Dabur pharma Ltd. Making statistical data to control waste management. Doing sample management in LIMS (Reserve samples. Reviewing final batch documents before batch release. Giving training to colleagues/sub-ordinates about GXP. Reviewing final batch documents before batch release. Sampling of semi finished or finished product to QC department. ACHIEVEMENTS: Getting Scholarship in class-7th & in class-10th. Baddi (Himachal Pradesh) as Sr.In Glenmark Pharma LTD. RESPONSIBILITY: Making of Batch Documents and SOP's Making and Execution of Process Validation Protocols and Reports. (Nairobi. in. Reporting to: DGM QA In Fresenius Kabi Oncology Ltd. Active participation on USFDA/MHRA audits in Fresenius kabi oncology.process & Finish product samples). RESPONSIBILITY: Monitoring and in process checks in shop floor activities in accordance with cGMP. Calibrating all in process instruments and weighing balances as per schedule and maintains its record.officer QA from September 2006 to February 2007. Reporting to: Manager QA/Company Pharmacist/ Managing Director. RESPONSIBILITY: Making of Batch Documents and SOP's Making and Execution of Process Validation Protocols and Reports. Making and Execution of DQ/IQ/OQ/PQ of Facilities/Instruments/Machineries. Release final batch. Page 2 of 3 .)Baddi (Himachal Pradesh) as Executive QA from March 2007 to January 2010. Release final batch through SAP. Kenya) as Asst. Handling non conformances in shop-floor and maintaining its record Handling deviations and change control as per SOP and maintains its record. Making of APQR of products which are manufactured throughout the Year. Making of APQR of products which are manufactured throughout the Year.) Allocating daily jobs to QA officers/ GMP training officer/ IPQA personnel. Monitoring sample management (Reserve samples. Active participants in new plant project (Lab & allied ltd. Issuance and retrieval of batch documents from production department. Assisting regulatory persons for making of dossier for new product registrations. Monitoring daily/monthly calibration schedule of all balances and service contract for the same. In process & Finish product (samples). Making of year planner for preventive maintenance & training. Manager QA from February 2010 to till date.

Passion of Willing. Oriya & Bengali.2018 COMPUTER SKILLS: INTEREST & HOBBIES: PASSPORT DETAILS: Passport No Issue from Date of Issue Validity PRESENT SALARY: SALARY EXPECTED: D 1500 USD per month Negotiable E C L A R A T I O N I do hereby declare that all the information furnished above is true to the best of my knowledge and belief. Place: Nairobi Date: Signature (Bikash Chandra Mahanta) Page 3 of 3 . . Excel & Power Point) Listening Old Hindi movie songs Internet Surfing : : : : H0258518 Bhubneshwar (Orissa) 25th Sept. Sector-15 Rourkela. EXTRACURRICULAR ACTIVITIES: STRENGTH: Active participation in sports and extra curricular activities at both school and college level.2008 24th Sept. Ability to think innovative. MS Office (Word.PERSONAL: Father's Name: Permanent Address: Date of Birth: Marital Status: Languages Known: Mr. Sundergarh Orissa-769 003 30/06/1978 Married English. No. Hindi. Effective communication skills. Mahendra Nath Mahanta Qrs.A/229.