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Quality Assurance Control

Location:
Nunavut, Canada
Salary:
15lac/Year
Posted:
September 08, 2012

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Resume:

CURRICULAM VITAE

RAJKUMAR DHIMAN

Gali No. A-*, Near J.PS.S. Public School

Subhash Nagar Jwalapur Haridwar (U.K.),

PIN-249407

Mob : 093********

Mail ID ****************@**********.***

CAREER OBJECTIVE:

To achieve success with honesty and intentional efforts towards my profession and to sharpen my skills technically and professionally along with the growth of the organization.

ACADEMIC QUALIFICATION

M. Sc. (Organic Chemistry)

B.SC. (Zoology, Botany & Chemistry)

APPROVAL

Approved in Chemical Analysis, Instrumental Analysis and Microbiological Analysis.

TRAINING ATTENDED

• I have attended a training program in “National Institute of Pharmaceutical Education and Research” (NIPER) Sector 67, S.A.S. Nagar Punjab India Held on August 21-25 2006.

• I have successfully participated in a special Conference-Cum Workshop entitled “VALIDATION WEEK” Held on 10-14Jun 2008.

• PIGMP Consultant was haired by Akums Drugs & Pharmaceuticals Ltd. for regulatory approval. I was selected in the core team and worked in the guidance of consultant (PIGMP) ( Mr.Sushil Baukhandi and Dr. Sumant Baukhandi )

PROFESSIONAL EXPERIENCE

• Currently I am working in Akums Drugs & Pharmaceuticals Ltd. Haridwar WHO –GMP, ISO 9001: 2008, 14001:2004 Certified Company as An A.G.M Quality Assurance (QA Head) in Plant -1 form Ist Jun 2005 to till date.

• I have worked with Welcure Drugs & Pharmaceuticals Ltd. Bhiwadi (Rajasthan) WHO –GMP & ISO 9001: 2000 Approved Company as an “Asst. Analytical Chemist” since 13th Sep. 2004 to 30th May 2005.

• I have worked with Brawn Laboratories Limited Faridabad (Haryana) WHO –GMP & ISO 9001: 2000 Approved Company as a Quality control chemist since14th Jan 2004 to 31th Aug. 2004.

• I have worked with Medicamen Biotech Ltd. Bhiwadi (Rajasthan) WHO –GMP & ISO 9001: 2000 Approved Company as Quality Assurance Chemist as well as I was also engaged in testing of raw materials, packing materials, intermediate products and finished products since 16th Oct. 2002 to 14th Jan 2004.

• I have worked with Shamarat Pharmaceuticals (P) Ltd. Meerut Road Muzaffar Nagar (UP) as an “Analytical Chemist” since Nov. 2000 to Oct. 2002.

• I have started of my carrier with Shree Hari Chemicals Mill Muzaffar Nagar (UP) as an “Analytical Chemist” since Jan 1995 to Nov 2000.

CURRENT JOB PROFILE

Over all responsibility of Quality Assurance.

Audit face and compliance.

Daily Monitoring of Quality Assurance Activities.

Selection of Vendors for RM & PM.

Periodical Quality Audit.

Handling of Product Complaints.

Handling of Change Control, Deviation, OOS & OOT.

Product Recall.

Validation and Qualification.

Training on cGMP, GLP and Health Hygiene.

GMP Implementation in the Plant.

Co-ordination with various departments to implement GMP in Plant.

Market Authorization of Products.

Release of batches for Sale.

ACCOMPLISHMENTS

AT M/S WELCURE DRUGS & PHARMACEUTICALS LTD.

Preparation of new SOP/ Specifications and reviewing the existing ones.

To evaluate the adequacy of conditions for storage of Raw materials, Semi finished & finished products.

Evaluation of Quality control record and to ensure preservation of records & of control samples as specified period & ensuring the traceability of manufactured products.

Analysis of Finished products, Raw Materials and Packing Materials.

Analytical Method Validation.

AT M/S BRAWN LABORATORIES LIMITED FARIDABAD

Preparation of new SOP/ Specifications and reviewing the existing ones.

To evaluate the adequacy of conditions for storage of Raw materials, Semi finished & finished products.

Evaluation of Quality control record and to ensure preservation of records & of control samples as specified period & ensuring the traceability of manufactured products.

Analysis of Finished products, Raw Materials and Packing Materials.

Analytical Method Validation.

AT M/S MEDICAMEN BIOTECH LTD. BHIWADI

Preparation of SOPs, GTPs and STPs & tasting protocols specification & other Packaging related documents.

IPQA activities.

To evaluate the adequacy of conditions for storage of Raw materials, Semi finished & finished products.

Evaluation of Batch production Records & Quality control record and to ensure preservation of records & of control samples as specified period & ensuring the traceability of manufactured products.

To ensure satisfactory inspection before dispatch of finished products to the warehouse and to do terminal inspection (Final Inspection) of all finished goods & to release and not to release them for sale and distribution.

AT M/S SHAMARAT PHARMACEUTICALS (P) LTD.

Analysis of Finished products, Raw Materials and Packing Materials.

IPQC activities

AT M/S SHREE HARI CHEMICALS MILL MUZAFFAR NAGAR

Analysis of Finished products and Raw Materials.

Audit Faced

• WHO- GMP, ISO 9001-2008 & ISO 14001-2004 and

• I have audit faced so many companies eg. Aventis, Abbott, Mylon, UCB India, Anvida, Cipla, Lupin, Zydus Cadila, Lundbeck India etc.

Personal Status:

• Father’s Name : Late Shri Balwan Singh

• Date Of Birth : 15/02/1973

• Sex : Male

• Nationality : Indian

• Marital status : Married

• Languages Known : English, Hindi,

Current pkg. : 12 Lakh /Year

Expected pkg. :

I hereby declare that all the information given above is true to the best of my knowledge.

Dated :

Place : Haridwar (RAJKUMAR DHIMAN)



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