CURRICULUM VITAE

V.V.NIRANJAN RAO

CARREER OBJECTIVE:
Wants to be Professional in the stream of Production (API-Bulkdrugs) in a progressive
organization that gives me scope to utilize my knowledge and skills in accordance with the latest
technologies and to be apart of team that strives towards growth of organization and gain satisfaction
there off.

EDUCATIONAL QUALIFICATIONS:
B.Sc (Chemistry) from Acharya Nagarjuna University in the year – 1986(Andhra Pradesh)
Post Graduate Diploma in Computer Applications in the year 1986 form
Bharateeya vidya bhavan, Guntur (Andhra Pradesh)
SKILLS:
Participating in Production Planning and Inventory Control (PPIC)
Planning of Production as per market requirements and achieving production targets
Establishing production operations from pilot to plant scale
Looking after the training of subordinate employees and plant operations

PROFESSIONAL EXPERIENCE: + 35.0 years

Period Accountable:
Previous Organizations :
:Porus labs pvt limited unit-1 at kodad as Unit Head from May-2021to January 2023.
Reason for Resignination :Personal Problems.
: AGRISOL INDIA (PVT); LTD January As HEAD-Manufacturing 20 21 to January2023.
: ArchPharma Labs Ltd (Kazipally) (2009 to 2018) (WHO, GMP, ISO9001:2008 and ISO
14001:2004 certified) leading API Company .
: Aurobindo Pharma Limited, Unit-5 (2005 to 2009) USFDA and EDQM Approved Company
: Neuland Laboratories Limited Unit-1 and 2 (1992 to 2002) USFDA,TGA and EDQM Approved
: Sumithra Pharmaceuticals and Chemicals Limited (1990 to 1992)
: SIRIS Hyd,Limited L.B.Nagar (1987 to 1990

PROJECTS WORKED:
Establishing the process from pilot scale to plant scale of products at
NEULAND LABORATORIES LIMITED Unit-1 (Hyderabad, Telangana state)
Enhancing the plant capacity from 12.0 MT to 25.0 MT and upgrading the finished product area as
per USFDA and EDQM requirements. Established the process as per the required norms and
inspection and installation of the process equipment at NEULANDLABORATORIES
 LIMITED Unit- 2 (Hyderabad Telangana state)
Enhancing the plant capacity from 20.0 MT to75.0 MT and upgrading the finished product
area as per cGMP and WHO requirements. Established the process as per the required norms,
inspection and commissioning of the equipment at HIRAN ORGO CHEM LIMITED Unit-1&2
(Ankaleswar, Gujarat state)
Establishing of Penicillin products, to plant scale at AUROBINDO PHARMA LIMITED
Unit-5, (Hyderabad , Telangana state) including trail and validation
Enhancing the plant capacity from 10.0 MT to 25.0 MT and upgrading the product. Handling

Of Sodium cyanide in the process carefully without any incident at Arch Pharma Labs
Ltd (Hyderabad, Telangana state)

Establishing production operations at Agrisol India, (pvt); ltd with 6 different

Products (Dhone, Kurnool dist., Andhra Pradesh state)

1.1 Monthly production planning. and implementation

1.2 Responsible for regular plant inspection and to report’s status to the Plant Head.
1.3 Identifying scope for Planning, implementation and monitoring of technical changes to enhance
productivity.
1.4 Modifications in equipment, process flow, working practices, etc for controlling & reducing cost
per unit produced.
1.5 Conducting trial runs on production equipment with given appropriate operating parameters and
ensuring that the trail run is implemented smoothly to meet the required objective.
1.6 Spearhead value analysis of production cost and manpower utilization.
1.7 Conceptualize and implement strict measures in operating procedures to optimize resources and
capacity utilization.
1.8 Optimize man and machine utilization to achieve pre-set production targets.

2. Quality and Safety related activities:

2.1 Ensuring compliance of various quality measures & cGMP norms during manufacturing.
2.2 Co-ordinate in preparation, checking, maintaining and updating documents as per cGMP norms.
2.3 Involving in Preparation and facing of internal and external visits and audits.
2.4 Review of laid down procedures and standards for production department to avoid cross
contamination. Handling of Deviation and change controls.
2.5 Trail and validation batches reviewing, Preparation and review of BPCR’s
2.6 Preparation and review of Trail & Validation Protocols and reports.
2.7 Developing a frame work of quality standards, procedures & systems.
2.8 Maintaining the Safety awareness level and standards across the production department.
2.9 Revamping workflow of processes for integration of quality systems and effective implementation
of Quality Management systems.

Co-ordinating with inter-departments like warehouse, Quality control and Quality assurance.
2.10 Co-ordinate and ensure planned preventive maintenance of production equipment’s.
3. Training related activities:
3.1 Planning and scheduling training schedules for the associates.
3.2 Impart on-job training and conduct refresher course to improve the skill and efficiency of people
3.3 Reviewing and up-dating competency matrix for associates.
3.4 Carry out personal development of the people.
3.5 Coordinating with QAD in training evaluation programs and finding the training needs.
4. Auditing and Investigation Related Activities:
4.1 To Head -QA, in NC related activities.
 4.2 Assisting the MR in visits and Audits.

5. ISO Related Activities:

5.1 Implementation and recording of QMS procedures.
5.2 Value addition to the management review meetings.

Audits Faced:
US FDA, EDQM, TGA, ISO and CUSTOMER audits Like MERCK, PFIZER.
Language skills: Telugu Hindi and English.

Contact details:

Mobile: 9959888824
niranjanrao1965@ gmail.com

(V.V. NIRANJAN RAO)