Covering Letter
Dear Sir/Madam,
I Ramesh Singh Yadav wish to offer my candidature for suitable in your
esteemed organization.
Over 17 years of dynamic career in Pharma OSD Production
Operations (Oral Solid dosage forms i.e Tablets, capsules, Pellets, ER
tablets etc.), in Pharmaceutical sector in USFDA, MHRA, TGA and
others approved reputed organizations.
Expertise in Production operations coordinating, planning and implementing
changes to technology.
Dynamic change agent skilled in repositioning organization to achieve
operational and manufacturing excellence like thats....
Astt. Manager , Dy Manager, Manager OSD production, Troubleshooting,
Downtime Reduction, Cost Reduction, Yield Improvement, Capacity Planning,
Resource Management, CGMP Compliance, In Process Inspection, QMS, CAPA,
SAP, OEE.
Presently working in Production (OSD) department as Manager, Hetero
Drugs Ltd, Hyderabad from January 2016 to till Date.
Experience: 17 years
Thanking you sir,
Yours sincerely
Ramesh Singh Yadav
Contact No.9727992548 & 9100091725
Curriculum Vitae
RAMESH SINGH YADAV
Job Code: Production Department
Experience: 17 years
Email id: rameshsingh7519@[Link]
Cont. no: +919727992548
Objective:
Seeking a challenging career to excel my performance. Looking forward for
an opportunity to work in a well projected environment where my knowledge
can be shared and enriched.
Professional Qualification:
B. Pharmacy from SRMSCET (UPTU), Lucknow during the year of 2003 -
2007
Value Profile:
● Responsible for manufacturing operation as per cGMP /regulatory norms.
● Responsible for ensuring fulfilment of monthly production commitment
against plan.
● Responsible for making strategy and improvement plan to improve
productivity and compliance of department.
● Responsible for keeping area all time ready for audit and comply and
audit observation.
● Responsible for investigation of market complaints deviations OOS/OOT
and other non conformances from production end.
● Responsible for QMS documentation and manufacturing records,
preparation and review of Batch manufacturing Records (BMR), SOP and
change controls, deviations, CAPA etc.
● Tasking of daily output report with weekly, monthly production and
managing the assembly line workforce for achieving periodic production
target.
● Identifying the area of improvement and recommending process
modification.
● Responsible for ensuring manufacturing equipments are running as per
21CFR Part 11 compliance in topical facility.
● Schedule equipment maintenance and inspection of regular basis.
● Organize job trainings to team member to achieve production goals.
● Ability to grasp new technologies and apply them in a specific context.
● Recommended to cost reduction initiatives while maintaining quality
standard.
● Ensure to team Follows Company polices safety standard.
Career Timeline: (Latest 4 Associations)
Oct-2008 – Nov-2009 Dec-2009 – Apr-2015 May-2015 – Dec-2015 Since Jan-2016
Previous Companies Experience
● Worked with Zydus cadila Ltd, in Production (Wruster) dept. as sr.
executivefrom (May 2015 to Dec 2015) handling of molecules like
Tamsulosin /Venlafaxine HCL/Omeprazole / Esomeprazole /
Lansoprazole/Divalproex sodium capsules and etc.
● Worked with Dr. Reddy’s Labs Ltd, in Production (Wruster) dept. as
team leader from December 2009 to April 2015. (In Dr. Reddy’s Labs
handling of molecules like Omeprazole mg
DR/Omeprazole/Esomeprazole / Lansoprazole/Divalproex sodium
capsules and also top spray granules like Zafirlukast/ metobeta /
Diclofenace sodium and Esomeprazole etc.
● In Dr. Reddy’s Labs, production (Compression) dept. also handling of
molecules like Omeprazole, Divalproex sodium tablets, Zafirlukast/
metobeta tablets etc.
● Worked with Sun Pharmaceutical Pvt. Ltd. Jammu & Sikkim as officer,
in Granulation & Compression dept. from Nov 2008 to Nov 2009.
● Worked with M/S Acme Formulation Pvt. Ltd. Nalagarah Sloan (H.P.)
India, as officer in Granulation dept. (WHO & cGMP Certified company),
from Jul. 2007 to 10thNov.2008.
Current Company Profile:
Presently working with Manager in Hetero Drugs Ltd Jadcherla,
Hyderabad from January 2016 to till Date. It is a reputed formulation
manufacturing company of both Injectable and oral solid Dosages form that
plant is approved by in USFDA, MHRA, TGA and others regulatory bodies.
Work Profile in Previous Companies:
INPROCESS ACTIVITIES:
● Execution of Process Validation, and Hold time study as per the
protocol.
● Execution of Process characterization as per approved protocols and
the respective SOPs.
● Responsible for co-ordinate to all in process Production.
● Preparation of Batch manufacturing record.
● Supervise production team to manage and execute production
process activity.
● Work with team to plan schedule and assign to daily workload to
team member.
● Handling of deviations and incidents during process.
● Responsible for attending trainings and maintaining Shop floor GMP
compliance
● Involved in the regulatory Audits.
Strengths:
● Flexibility to work hard for long hours and patient enough until the goal
I accomplish.
● Excellent Communication Skills.
● Coordination with the people in a professional manner.
Reference: Mr Sudhir Kumar, contact no. 8898890490
Salary: Present salary: 16.20 L/A
Declaration:
I herebly declare that all the information mentioned above is true to the best
of my knowledge.
Yours Sincerely,
Ramesh Singh Yadav
Ghazipur, Uttar Pradesh