Gandhiji is seeking a position that utilizes his 12 years of experience in pharmaceutical production and quality assurance. He currently works as an Assistant Manager of Production at Medopharm in Chennai, where he oversees tablet and capsule manufacturing, implements lean manufacturing techniques, and ensures documentation compliance. Previously, he held production roles at multiple companies and has experience with equipment qualification and validation as well as developing training programs.

1. RESUME
E-mail: gandhiji_g@rediffmail.com
Mobile No: 7871708482,
8220517815.
G.GANDHIJI
I am in the pursuit of acquiring all the competencies for an escalating career and always
willing to face new challenges and critical task, which offer potential growth and development
through the spirit of teamwork.
PROFESSION SUMMARY:
A competent professional with 12.0 years of production experience as well as Production related
documentation in pharmaceutical formulations (solid dosage form).
COMPANY PROFILE:
MEDOPHARM, MHRA Chennai.
Designation : Asst. Manager-Production
Period of Working : From April 2015 to till date.
Capable of serving as the catalyst for achieving revenue objectives and organic growth through
effective contributions. I have done Master of Pharmacy coupled with expertise of around 10
years’ in Production operations, Maintenance, Quality Assurance & Man Management.
Furthermore I have expertise in Tablets & Capsules Manufacturing and also in OLD and SSD
formulations. Six sigma Green belt & Having experience in implementing Lean manufacturing
methodology & Six sigma tools to minimize the rejections and enhancing the Productivity with
the extreme quality & ensuring the documentation as per CGMP,WHO,MCC,MHRA,USFDA
guidelines.
Assessing customer requirements and ensuring that these are met. Recording, analyzing and
distributing statistical information. Effective training and development of working staff at regular
intervals. Co-ordination with cross functional team and validation activity. Manufacturing Solid
oral dosage forms viz. tablets, capsules.
Developing, managing and monitoring the performance of multi-skilled work force and
conceptualizing need-based training programs for maximizing operational efficiency.
Managing the functions of troubleshooting and predictive/preventive/shutdown maintenance for
reducing machinery downtime to minimum.

2. ARVIND REMEDIES LTD, IKKT
(Export Division for ROW market & constructed to comply with the
USFDA). (Company Profile: Well-constructed to cater solid oral, liquid orals, Ointment, Soft gel
and small volume parenteral dosage forms and can comply with USFDA).
Designation : Asst. Manager-Production
Period of Working : From April 2012 to 2015.
MADRAS PHARMACEUTICAL LTD
Designation : Sr.Executive Production
Period of Working : From March 2009 to March 2012.
MARAL LABS
Designation : Chemist
Period of Worked : From Sept 2003 to Aug 2006.
ARVIND REMEDIES LTD.
Designation : Executive-Production
Period of Worked : From May- 2002 to Aug 2003.
ROLES & RESPONSIBILIES IN ORAL SOLID DOSAGE FORM
ARVIND REMEDIES LTD.
 Lead the team and was qualified systems and all equipment’s of Design qualification (DQ),
Installation qualification (IQ), Operational qualification (OQ), Performance qualification
(PQ) in arvind remedies ltd.
 Lead the team to prepared Process validation protocol, master formula, BMR and BPR
Protocol - co-ordinate with QA, and Engineering Personnel.
 Determining, negotiating and agreeing in-house quality procedures, standards and/or
specifications
 Assessing customer requirements and ensuring that these are met.
 Recording, analyzing and distributing statistical information.

3.  Effective training and development of working staff at regular intervals.
 Co-ordination with cross functional team and validation activity.
 Manufacturing Solid oral dosage forms viz. tablets, capsules.
 Managing production operations involving preparation of production plans & schedules with
a view to ensure timely accomplishment of production targets within the time and cost
parameters.
 Coordinating to Q.A. was prepare Production related SOP’s.
MADRAS PHARMACEUTICAL LTD
 Online entry in SAP for production related activities.
 Documenting production activities like BMR, BPR and log sheets.
 Meet the safety norms during production.
 Planning of new product scale-up in coordination with Formulation Development team.
 Stabilization and improvement in the yields of new products.
 Safety Management by taking all safety measurements and bringing awareness of the safety
aspects in the working staff.
 Technical up gradation of the section by modification of processes and systems from time to
time.
MARAL LABS
 Granulation and Blending like RMG, FBD operating with PLC. Double cone blender, V-
Blender and octagonal Blender, Planetary Mixer, Vibratory Sifter, Tray Dryer.
 Compression machine like 45-station, 55-station & 35-station.
 Coating machines like Automatic Coating Machine of DNK make and Auto coater 60A of
Neocota make.
 Responsible for In-process checking and online entry.
 Generation and submission of reports to Asst-manager based on the daily production.
ARVIND REMEDIES LTD
 Responsible for In-process checking and online entry.
 Documenting production activities like BMR, BPR and log sheets.

4. COMPUTER SKILLS:
 Basic Knowledge about internet and computer which is related to my routine activities.
 Word processing, Basics of MS-Office.
PROFESSIONAL OUTLOOK:
 To make contribution to the organization to the best of my ability and to develop new skills
and share my knowledge while interacting with others and achieve new height
 Highly interpersonal relationships.
 Professional with complete commitment to the organization and responsibility.
ACHIVEMENTS IN MY CARRIER
 I have been Team leader to co-ordinate with Vendors, QA and Maintenance team to qualify
of all equipment had in oral solid dosage, semi-solid and liquid dosage dept. with DQ, IQ,
OQ and PQ.
 Co-ordinate with vendors to optimized and fine-tuned of all equipment’s in step by step.
 Prepared SOP's of all Equipment was present in oral solid dosage, semi-solid and liquid
dosage dept.
 Prepared process validation documentation and lead the team to workout innovated
formulation containing batches.
 Prepared under GMP Guideline containing BMR and BPR like OSD, OLD, and semi-solid
dosage.

5. EDUCATIONAL QUALIFICATION:
PERSONAL PROFILE:
NAME G.Gandhiji
SEX Male
MARITAL STATUS Married
LANGUAGES KNOWN English, Tamil and Hindi.
FOR FURTHER REFERENCES:
N. Satheesh,
Manager Quality assurances,
Strides Arco lab,
Bangalore.
Ph. 09972480366, Email ID, satheesh_natarajan@stridesarco.com
DECLARATION:
I hereby declare that the above furnished information’s are true and correct
to the best of my knowledge and belief.
Thank you,
Place : Chennai yours faithfully,
COURSE UNIVERSITY YEAR OF PASSING PERCENTAGE OF MARK
M.PHARM Annamalai university,
Chidambaram.
2006-2008 79%
B.PHARM The Tamil Nadu Dr. M.G.R.
Medical University,
Chennai.
1997- 2001 63%

6. G.Gandhiji

7. G.Gandhiji