1. V.V.NIRANJAN RAO
Email:
niranjanrao1965@yahoo.in
Mobile:
9959888824
Address for Communication:
Easha Sadan,
Flat No: A-1,
Vivekananda Nagar Colony,
Rama Krishna Street,
Kukatpally,
Hyderabad -500072.
Telangana state.
Personal Details:
Father’s Name: Narayana Rao
Date of Birth: 15th,August 1965
Marital Status: Married
Languages Known: Telugu, English,
and Hindi
Technical Qualifications:
1. B.Sc(chemistry)
2. PG. Diploma in Computer
Applications
Key Skills:
1. Achieving the production targets
2. Controlling, maintenance of
production documents
3. Participating in Production planning
and inventory control (PPIC).
4. Assisting MR in external visits and
audits.
Audits Faced: US FDA, WHO GMP,
EDQM, GSK, MERCK, PFIZER, ISO
and other customer audits.
Drugs Handled: Antibiotics,
Antiretrovirals, Antihypertensives,
Antiasthmatics
Objective
Want to be Professional in the stream of Production (API) in a
progressive organization that gives me scope to utilise my
knowledge and skills accordance with latest technologies and to be
a part of team that dynamically makes towards growth of
organization and gain satisfaction there off…
ENLIGHTENMENT:
 Currently working for Arch Pharma Labs Ltd a WHO GMP, ISO
9001:2008 and ISO 14001:2004 certified leading API Company.
 Previously worked for Aurobindo Pharma Limited and Neuland
laboratories limited and facilities are in compliance with WHO
cGMP Standards, USFDA approved, EDQM approved company.
PROFFESSIONAL EXPERIENCE:
Organization Name : Arch Pharma Labs Ltd (Hyderabad)
Period : Since February 2009
Accountable : Manager (Production)
Organization Name : Aurobindo Pharma Limite (Hyderabad)
Period : 2004 to 2009
Accountable : Dy.Manager (Production)
Organization Name : Hiran Orgochem Limited(Ankaleswar,Gujarat)
Period : 2002 to 2004
Accountable : Manager (Production)
Organization Name : Neuland Laboratories Limited (Hyderabad)
Period : 1992 to 2002
Accountable : Dy.Manager (Production)
Organization Name : SumitraPharmaceuticalsand Chemicals
limited(Hyd)
Period : 1990 to 1992
Accountable : Shift in-charge (Production)
Organization Name : SIRIS(HYD) Ltd (Hyderabad)
Period : 1987 to 1990
Accountable : Shift in-charge (Production)
28 YEARS OF EXPERIENCE IN PHARMACUITICAL INDUSTRY(BULKDRUGS –PRODUCTION)

2. DUTIES AND RESPONSIBILITIES:
Presently working as a Manager (Production) and also playing active role in the
implementation of cGMP system and Production Planning in the organization.
1. Production Planning and control related activities:
 Monthly production planning. Process Enhancement & Cost Control.
 Responsible for regular plant inspections and reporting to the Unit Head.
 Identifying scope for Planning, implementation and monitoring of technical
changes to enhance productivity.
 Responsible for controlling & reducing conversion cost per unit produced.
Like modifications in equipment, process flow, working practices etc.
 Conducting trail runs on production equipment by providing appropriate
operating parameters and ensuring that the trail run is implemented smoothly to
meet the required parameters.
 Spearhead value analysis of production cost and manpower utilization.
 Conceptualize and implement strict measures in operating procedures to
optimize resources and capacity utilization.
 Optimize man and machine utilization to achieve pre-set production targets.
2. Quality and Safety related activities:
 Ensure compliance of various quality measures & GMP norms during
manufacturing.
 Co-ordination in preparation, checking, maintaining and updating documents as
per GMP norms.
 Involved in preparation and facing of internal and external audits.
 Review of laid down procedures and standards for production department to
avoid cross contamination. Handling of Deviation and change controls.
 Online Trails and validation batches reviewing, Preparation and review of
BPCR’s.
 Preparation and review of Trail & Validation Protocols and reports.
 Developing a framework of quality standards, procedures & systems.
 Maintaining the safety awareness level and standards across the production

3. department.
 Revamping workflow processes for integration of quality systems and effective
implementation of Quality Management systems.
 Co-ordinate with inter-departments like warehouse, Quality control and Quality
assurance.
 Co-ordinate and ensure planned preventive maintenance of production equipment.
3. Training related activities:
 Planning and scheduling training schedules for the associates.
 Impart on-job training and conduct refresher course to improve the skill and
efficiency of people.
 Reviewing and up-dating competency matrix for associates.
 Carry out personal development of the people.
 Co-ordinating with QAD in training evaluation programs and finding the training
needs.
4. Auditing and Investigation Related Activities:
 To QA department, Production HEAD and in NC related activities.
 Assisting the MR in Audits.
 Playing the role of Auditor for production and other departments.
5. ISO Related Activities:
 Implementation and recording of QMS and EMS procedures.
 Value addition to the management review meetings.
 Preparing the management review agenda for Production.
ACADEMIC QUALIFICATION:
B.Sc (Chemistry) from Acharya Nagarjuna University – Batch of 1986
PG.diploma in computer applications from Bharateeya Vidya Bhavan in 1987
The above furnished information is true to the best of my knowledge. I request for
placement in your firm suitably.
Place:
Date:

4. (V.V.NIRANJAN RAO)