P. Murthy Raju is a Production Officer with over 8 years of experience in the pharmaceutical industry. He is looking for a challenging position in manufacturing that allows him to grow professionally. He has a MSc in Chemistry and has worked at Mylan Laboratories and Divis Laboratories. Some of his responsibilities include production planning, supervision, achieving targets, ensuring quality, technology transfer, process improvements, audits, and safety training. He has knowledge of SAP, process validation, cGMP guidelines, troubleshooting, and change control. He aims to contribute to organizational goals through his technical and communication skills.

1. CURRICULUM VITE
P.MURTHY RAJU,
S/o P.PEDDIRAJU
D.NO:1-43,
SABBE VARI PETA
PALAKOL
West Godavari (district)
Andhra Pradesh(state)
Cell: 9177610621,
9010695709.
E-mail: murthy.600.mr@gmail.com
CAREER OBJECTIVE :
Looking for a challenging position in Manufacturing
Department in a Pharmaceutical industry that demands technical skill and innovative
qualities for development of the company and for my growth, both professionally and
personally that leads to a successful career. Ready to work with commitment and zeal
both as a team and individual.
Academic Qualification: MSc. (Chemistry)
Experience: Totally, 08+ years’ Experience
 Presently working in MYLAN Laboratories limited, unit-8
as a PRODUCTION OFFICER from june 2009 Onwards.
 Previously I worked in DIVIS Laboratories limited, Unit-2
with 1 year 1 month Experience (From 2008 April to 2009
june) as a Chemist.
Present Designation: PRODUCTION OFFICER in Production
WORK AREA: PILOT BLOCK
Handling of Instruments:
 Reactors (SSR,GLR,MSR)
 Dryers( RD,VD,TD and Spray Dryer)
 Filters(CF,NF,CD,MF,ANF,PNF,LF,SF)

2. Professional Competencies :
 Target focused professional with over 08 years’ experience in manufacturing of APIs.
 Confident in managing Process Validations, cleaning validation, Equipment
Qualifications, Handling of Change Control , Training , Deviations, Batch Failure
Investigation and its CAPA
 Deftness in handling regulatory documentation and audit compliance, follow and
implementing ICH Q7 & 21 CFR GMP Guidelines
 Experience in facing regulatory audits like i.e. USFDA, ISO ,WHO, TGA, MCC,
MHRA, EU, GMP and customers of MNCs and Indian to without non compliances
Personal Attributes:
 Strong work ethics and self-motivated
 Team work and Leadership quality
 Ability to adopt and learn new technologies
 Positive thinking to contribute my functional role towards
organizational requirement.
 Excellent interpersonal communication skills
 Quick learner and result oriented
Key Skills:
 Knowledge in SAP
 Knowledge in Process validation.
 Working under c GMP, ICH Guideline.
 Self Confidence, Time management analysis of the
problems, Communication.

3. Responsibilities include:
 Responsible for production planning & timely execution, supervision of
manufacturing activities
 Achieve the production targets and dispatch targets by maintaining budgeted
consumption Norms with Targeted yield, Quality and Safety.
 Responsible for Effective Utilization of Manpower and & machines runs for
enhancing the Productivity.
 Responsible to generate Monthly reports, including monthly reconciliation of
raw material and finish product
 Responsible for scale up of new API’S & its intermediates from Pilot scale to
large commercial scale, Optimizations of process parameters, timings, raw
materials & Process Stabilization in commercial Scale.
 Ensure smooth scale up of new products and DMF validation batches in
coordination with QA & R&D
 Technology Transfer from bench scale to Production scale through Pilot Plant
Studies and successful Validation of new products for DMF filing.
.
 Responsible and ensure for the quality monitoring, time cycles & process
improvements, trouble Shooting of plant problems, manpower management,
with major emphasis on safety and cost effectiveness Reporting, evaluation and
investigation of critical Deviations like Un planned deviations
 Evaluating proposed changes in product, process or equipment through Change
Control
 carry out root cause analysis for the Non conformity (OOS investigations) and
take CAPA
 Ensure All-time preparedness for all Regulatory and Safety audits and
adherence to compliances.
 Identifying safety needs during operations of the process and training of the
personnel on awareness of safety precautions and MSDS of raw materials etc.
 Organizing HAZOP and Risk Assessment Studies etc and
Implementation of safety Recommendations
 SAP online document improvement in production

4. Personal profile:
Name : PADAVALA MURTHY RAJU
Date of Birth : 09-03-1986
Father’s Name : PEDDI RAJU
Sex : Male
Nationality : Indian
Marital Status : Married
Languages Known : English, Telugu and Hindi
Permanent Address : S/o P.PEDDIRAJU
D.NO:1-43,
SABBE VARI PETA
PALAKOL
West Godavari (district)
Andhra Pradesh(state)
Cell: 9177610621.
POSITIVE TRAITS:
Positive thinking, ability to work in intergraded teams and
willingness to take on responsibilities.
PLACE:
DATE: (P.MURTHY RAJU)