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Resume
Anupam Das
E-mail: anupamdas78@gmail.com
anupamdas78@yahoo.co.in
Mobile: +919903122639
Objective
Looking forward to work in a challenging environment to enhance my skills and grow
in an esteemed organization.
Education and Technical Background
B. Pharmacy with first class from ‘Maharashtra College of Pharmacy', Nilanga, Latur
under ‘Swami Ramanand Teerth Marathwada University', Nanded, Maharashtra.
Summary
A Quality Assurance professional with a record of increased responsibility. Proficient
in prioritizing and completing tasks in a timely manner, yet flexible to multitask when
necessary. Quality focused with diverse industry experience over 10 years including
Manufacturing, QA and DQA. Highly proficient in Microsoft Word, Excel. Enjoys
learning new programs and processes. A team player who is attentive to detail and
able to work in a fast paced environment.
Area of Expertise:
• Documentation for Regulated Market specially BMRs, BPRs, MFRs, MPRs.
• Complete Documentation for Domestic Market with compliance with GMP.
• State excise calculation and rules.
• Market complains investigation and handling.
• In-house Calibration of instrument and devices.
• Compiling new drug endorsement papers.
Professional Experience
1. Working with ‘Mendine Pharmaceuticals Pvt. Ltd., Kolkata' in ‘Quality
Assurance Department' from 7th
December 2009 to till date as Manager
Quality Assurance.
2. Worked with ‘Micro Advanced Research Center, Micro Labs Limited,
Bangalore' in ‘Development Quality Assurance Department' from 25th
July
2008 to 28th
November 2009 as ‘DQA Officer'.
3. Worked with ‘Aristo Pharmaceuticals Private limited, Mandideep, Bhopal'
in ‘Quality Assurance Department' from 10th
July 2005 to 20th
July 2008 as
‘QA Officer'.
4. Worked with ‘Cheryl Laboratories Pvt. Ltd.' Mahape, New Mumbai ‘Quality
Assurance Department' from 2nd
April 2005 to 7th
July 2005 as ‘Quality
Assurance Chemist'.
5. Worked with ‘Dew Pharmaceuticals', Durgapur in Capsule, Tablet & Liquid
Department from 21st
December 2003 to 15th
Mar 2005 as ‘Junior Production
Chemist'.
Current Job profile
1. Preparation and implementation of quality system.
2. Preparation and review of MFRs and BMRs new & existing products.
3. Preparation and review of Process Validation Protocols and Stability Protocols.
4. Preparation, review and Updating of RM specifications, PM specifications, In-
process and Finished product specifications of new & existing products.
5. Preparation, implementation and training of SOPs.
6. Define Responsibilities & Train Personnel.
7. Calibrating instruments & Devices (in house and third party).
8. Investigating Product Quality Complaints.
9. Coordinating State Regulatory Audits (State Drug Control, State Excise).
10. Compiling Site Master Files.
11. Ensuring compliance with GMP.
12. Reviewing Batch Manufacturing Records & authorizing disposition of batches.
13. Compiling & ensuring compliance with SOPs.
14. Preparation of Price list and Calculation of Excise Duty of finished products by
coordinating with Excise Officer and Other Department.
15. Review of Art-work for new & existing products.
16. Conducting Stability Studies and Process Validation.
17. Preparation of Document required for Endorsement of New Drug to State
Drug Control Department.
Previous Job profile
1. Preparation and review of MFRs, MPRs, BMRs and BPRs of new products.
2. Review of Process Optimization Protocols, Process Validation Protocols,
Stability Protocols.
3. Preparation and review of RM specifications, PM specifications, In-process and
Finished product specifications of new and existing products.
4. Preparation, implementation and training of SOPs in R & D department.
5. Review of Analytical and formulation work records.
6. In-process quality checks of Manufacturing, Packing of Tablet, Capsule, Liquid
and Parental (Powder & SVP)
7. Internal auditing of BMR.
Additional Strength
1. Committed to the task, sincere
2. Focused objective oriented approach
3. Active and consistence in achieving set targets.
Computer Proficiency:
1. MARG: Pharmaceutical Manufacturing Software
MARG customization course from software manufacturer.
2. MS office (2003, 2007 and 2010).
Inplant Training:
In ‘Bengal Chemicals & Pharmaceuticals Ltd. Kolkata' for 9 weeks.
Personal Information:
Name
Anupam Das
Father's Name
Mr. Amiya kumar Das
Sex
Male
Date of Birth
12th
February, 1978
Marital Status
Married
Permanent Address
112, Sarada Moni Lane,
Power House Para,
Burdwan, West Bengal
Pin Code- 713101
Phone: 0342-2567077
Languages known
Bengali, Hindi, English.
References:
1. Mr. Sachin Mundade
General Manager
MARC, Micro Labs Limited,
Banglore - 560068.
Email: sachinmundade@gmail.com
Mobile: +919008778888
2. Mr. Subrata Kundu
Sr. Scientist
Vergo Pharma Research Goa,
Email: kundusubrato@gmail.com
Mobile: +917350522868

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Resume ANUPAM

  • 1. Resume Anupam Das E-mail: anupamdas78@gmail.com anupamdas78@yahoo.co.in Mobile: +919903122639 Objective Looking forward to work in a challenging environment to enhance my skills and grow in an esteemed organization. Education and Technical Background B. Pharmacy with first class from ‘Maharashtra College of Pharmacy', Nilanga, Latur under ‘Swami Ramanand Teerth Marathwada University', Nanded, Maharashtra. Summary A Quality Assurance professional with a record of increased responsibility. Proficient in prioritizing and completing tasks in a timely manner, yet flexible to multitask when necessary. Quality focused with diverse industry experience over 10 years including Manufacturing, QA and DQA. Highly proficient in Microsoft Word, Excel. Enjoys learning new programs and processes. A team player who is attentive to detail and able to work in a fast paced environment. Area of Expertise: • Documentation for Regulated Market specially BMRs, BPRs, MFRs, MPRs. • Complete Documentation for Domestic Market with compliance with GMP. • State excise calculation and rules. • Market complains investigation and handling. • In-house Calibration of instrument and devices. • Compiling new drug endorsement papers. Professional Experience 1. Working with ‘Mendine Pharmaceuticals Pvt. Ltd., Kolkata' in ‘Quality Assurance Department' from 7th December 2009 to till date as Manager Quality Assurance. 2. Worked with ‘Micro Advanced Research Center, Micro Labs Limited, Bangalore' in ‘Development Quality Assurance Department' from 25th July 2008 to 28th November 2009 as ‘DQA Officer'. 3. Worked with ‘Aristo Pharmaceuticals Private limited, Mandideep, Bhopal' in ‘Quality Assurance Department' from 10th July 2005 to 20th July 2008 as ‘QA Officer'. 4. Worked with ‘Cheryl Laboratories Pvt. Ltd.' Mahape, New Mumbai ‘Quality Assurance Department' from 2nd April 2005 to 7th July 2005 as ‘Quality Assurance Chemist'. 5. Worked with ‘Dew Pharmaceuticals', Durgapur in Capsule, Tablet & Liquid Department from 21st December 2003 to 15th Mar 2005 as ‘Junior Production Chemist'.
  • 2. Current Job profile 1. Preparation and implementation of quality system. 2. Preparation and review of MFRs and BMRs new & existing products. 3. Preparation and review of Process Validation Protocols and Stability Protocols. 4. Preparation, review and Updating of RM specifications, PM specifications, In- process and Finished product specifications of new & existing products. 5. Preparation, implementation and training of SOPs. 6. Define Responsibilities & Train Personnel. 7. Calibrating instruments & Devices (in house and third party). 8. Investigating Product Quality Complaints. 9. Coordinating State Regulatory Audits (State Drug Control, State Excise). 10. Compiling Site Master Files. 11. Ensuring compliance with GMP. 12. Reviewing Batch Manufacturing Records & authorizing disposition of batches. 13. Compiling & ensuring compliance with SOPs. 14. Preparation of Price list and Calculation of Excise Duty of finished products by coordinating with Excise Officer and Other Department. 15. Review of Art-work for new & existing products. 16. Conducting Stability Studies and Process Validation. 17. Preparation of Document required for Endorsement of New Drug to State Drug Control Department. Previous Job profile 1. Preparation and review of MFRs, MPRs, BMRs and BPRs of new products. 2. Review of Process Optimization Protocols, Process Validation Protocols, Stability Protocols. 3. Preparation and review of RM specifications, PM specifications, In-process and Finished product specifications of new and existing products. 4. Preparation, implementation and training of SOPs in R & D department. 5. Review of Analytical and formulation work records. 6. In-process quality checks of Manufacturing, Packing of Tablet, Capsule, Liquid and Parental (Powder & SVP) 7. Internal auditing of BMR. Additional Strength 1. Committed to the task, sincere 2. Focused objective oriented approach 3. Active and consistence in achieving set targets. Computer Proficiency: 1. MARG: Pharmaceutical Manufacturing Software MARG customization course from software manufacturer. 2. MS office (2003, 2007 and 2010).
  • 3. Inplant Training: In ‘Bengal Chemicals & Pharmaceuticals Ltd. Kolkata' for 9 weeks. Personal Information: Name Anupam Das Father's Name Mr. Amiya kumar Das Sex Male Date of Birth 12th February, 1978 Marital Status Married Permanent Address 112, Sarada Moni Lane, Power House Para, Burdwan, West Bengal Pin Code- 713101 Phone: 0342-2567077 Languages known Bengali, Hindi, English. References: 1. Mr. Sachin Mundade General Manager MARC, Micro Labs Limited, Banglore - 560068. Email: sachinmundade@gmail.com Mobile: +919008778888 2. Mr. Subrata Kundu Sr. Scientist Vergo Pharma Research Goa, Email: kundusubrato@gmail.com Mobile: +917350522868