Indian Immunologicals Ltd Hyderabad : Executive Techinical Training

[mskavi]

Indian Immunologicals Ltd.
http://www.indimmune.com


Keywords: Training

Company Profile
Indian Immunologicals Limited
A Wholly owned subsidy of NDDB


Executive - Techinical Training


Experience:
6 - 10 Years
Location:
Hyderabad / Secunderabad
Education:
UG - B.Sc - Biology, Botany, Chemistry, Microbiology

PG - M.Pharma - Pharmacy;M.Sc - Any Specialization;M.Tech - Any Specialization
Industry Type:
Pharma/ Biotech/Clinical Research
Functional Area:
Healthcare, Medical, R&D
Posted Date:
04 Sep


Job Description
Will be responsible for all the training activities across the organisation with respect to QA/QC , TQM and other techinical trainings
Should be able to plan and implement the entire gamut of training activities
Should be able to generate results with respect to trainings
Must act as good communicator for the implementation of trainings

Desired Candidate Profile
Candidate must be Post graduate in any branches science and having 6 to 8 years of Experience in QC/QA in a biologicals manufacturing industries.The candidate must have exposure to handle technical training department/organizing training classes.

Contact Details
Executive Name:
C.V Kumar

Address:
Indian Immunologicals Ltd
Rakshapuram
Gachibowli Post
Hyderabad,A.P,INDIA 500032

Email Address:
cvkumar@indimmune.com

Telephone:
91-040-23000211

Reference ID:
TT01/08

[Natrajkumar]

CURRICULUM VITAE
NATARAJ KUMAR. ADIPUDI
Plot No: C-97, Phase-II,
Near Bus stop, Allwyn Colony,
Kukatpally,HYDERABAD
e-mail : natraj9949982017 AT yahoo.co.in & natrajadipudi AT yahoo.co.in
Mobile : 9949982017, 9700211363
--------------------------------------------------------------------------------------------------------
WORK EXPERIENCE:
Total Experience: 7 Years 11 Months (Quality Control)
Present Experience : 11 Months
Place of work : Aurobindo Pharma Ltd (USFDA)
Formulation Unit-III Bachupally (Village) Medak (Dist)
Designation : Sr.Executive –IV (Group Leader)
Interested Areas : Quality control & Quality Assurance
Location Preference : Hyderabad & Sec’bad
Position applied for : Suitable Position
Present Job role in APL:- (Group Leader)
- In QC Department Daily any non compliance activity observed and Reporting
- Everyday twice in a day GLP rounds and all Instrument Logbooks checking
- Daily Balances calibration and KF Factor and pH meter documents checking and Room temperatures’ and Relative humidity monitoring in the Lab.
- Asper schedule Working standards preparation planning and volumetric solutions preparation and standardizations’ planning and updating the LIMS (2.0 & 3.1 )
- All Instruments Calibrations of all Lab Instruments (HPLC,GLC,UV,IR,Dissolutions etc…..) and maintenance of all Calibration records as per Master Schedule planning and follow up the Master instruments calibrations.
- New instrument received IQ,OQ,PQ completed after Operation and Calibration SOP’s preparation.
- New SOP’s Preparations and SOP’s review (Up version and Routine revision) and Updated SOP’s (Calibration and Operation)filing and Operational SOP’s displayed at the Instrument.
- All Instrument Calibration documents and working standards preparation documents checking and reviewed the HPLC systems and related work also checking like Ref.std consumption and column performance and Instrument log entry etc…
- Procurement of the Reference standards and Impurities (USP& BP& EP& IHS) as per requirement after receiving updating the LIMS systems and filing the Certificates.
- Every month Issue to QC related formats (Daily and Monthly) and Issue to Instrument Log book when ever requirement.
- Any Audit Related products working standards and Calibration documents review
- Joined Freshers to be completing the Analyst Qualifications, and SOP’s trainings allotted section.
- To be arrange in the QC Lab Safety items and First Aid box items.
- Handling of change controls and deviation whenever required to be raised.
- Audits :- Completely and actively involved in various regulatory audits such as USFDA,WHO (Australia) ANVISA (Brazil), MHRA, TGA, Sanofia, North star ,Astrazenica and Internal Audits by QA.
Previous Experience : 3 ½ Years
Place of work : Dr.Reddys Laboratory’s (Formulations)
FM-1 Bollaram (Village) Medak (Dist)
Designation : Sr.Executive
Pervious Job role in DRL:- (GLP Team)
- Calibrations of all Lab Instruments (HPLC,GLC,UV,IR,Dissolutions etc...) and maintenance of all Calibration records, calibration standards and Calibration certificates and Preparation of SOP’s for operation and calibration of new received instruments.
- Preparation of Master Calibration Plan- Monthly and Half Yearly and Yearly.
- Maintenance of all analytical laboratory standards and updation of relevant formats as per SOP for regulatory compliances.
- Characterization and standardization of Working standards by comparison with Official Pharmacopoeia Reference standards or with In-House reference standards.
- Procurement of Primary standards, Official Pharmacopoeia Reference standards and Calibration standards
- Reference Standards , Impurity Standards , Stock solution stock cards , Working standards Preparations and maintains of stock cards

- Daily Calibration Updating.(Balences,pH meters,K.F Inst etc…)
- Supporting regulatory departments by providing Finished Product COA’s
(Export COA’s) and Working standards for registering the products in various countries.
- New HPLC & GC columns Performance records maintained.& old HPLC Columns Regeneration with records
- To ensure that no errors in the completed, checked and approved documents of
finished products, In-process and raw materials by reviewing the complete
documents daily.
- Strictly observed the GLP in the laboratory and All Instruments log books updates
- Joined as Senior Executive-QC and responsible for analysis of In-process, Finished products and Process validation samples in the form of Tablets, Capsules, Pelletes injections and analysis of Packaging Materials.
- Complete analysis & Reporting of Finished Products, and In-process and Raw materials.& Packing material analysis
- Injectables samples (C.C.D& Non-CCD) in bulk stage & Finished stage analysis
- In-process Validation Samples analysis and Hold Time analysis.
- Raw Materials analysis (API’& Excepients) and Volumetric So1lutions Preparation & Standardization and maintenance of Records
- I had done in primary Packaging Materials analysis in 6months.
- Analytical experience on sophisticated instruments like
- HPLC (Agilent 1100 & 1200 with Chemstation software and Waters Auto Sampler Model 2996 ,Empower and waters Softwares)
(To Developed in Instrument Methods and processing Methods)
- Gas Chromatography with Head space (Agilent Model 6890 with 7694 and Shimdju 14A & 17B Empower software )


- FTIR (Perkin Elmer-1000 & Agilent 4800s),
- U.V. Agilent 4893 & Shimdju-2201)
- Dissolutions ( Elecrolab Auto & manuals and Disteck 2200 Models) .
Known Instruments handled
Karl fisher apparatus, Loss on Drying
Auto titrator’s Disintegration ,
T.L.C , Hardness of the tablets machine,
Melting range, Oven & Vacuum Oven,
Optical Rotation by Polari meter, Bursting strength,
pH meter , Muffle furnace,
Conductivity, Bulk Density,
Audits :- Completely and actively involved in various regulatory audits such as ANVISA
(Brazil), NDA (Uganda),NAFDAC (Nigeria),USFDA(local),Kenya pharmacy ,
NAFDC(Indonesia)& GRAC (Internal Audits).
Previous Experience : 2 YEARS
Place of work : NATCO PHARMA LIMITED (Formulations)
Kottur.Mahaboob Nager (Dist)
Designation : Executive
- Finished products (Tab’s , Caps , Dry powders and suspensions)
- Raw Materials API’s & Excepients and also Oncology Products
- Volumetric Solutions Preparation & Standardization
- Working standards Preparations
- Preparation of Reagents, Indicators & standard solutions
Previous Experience : 1½ YEARS
Place of work : DIVIS LABORATORIES LIMITED .Hyd &Vizag.
Designation : Chemist
- Pharma ( Final & Finished Products )
- Raw Materials (Solids & Liquids)
- Volumetric Solutions Preparation Standardization(Daily , Weekly & Monthly)


- Preparation of Reagents, Indicators & standard solutions
- Analysis of water in plant (Hard, Soft ,Boiler & D.M water)
- Packaging Materials (HDPE Drums & LDPE Polythene Bags)

EDUCATIONAL QUALIFICATIONS:
M.Sc., (Org. Chem.) S.R.M.T.University, Nanded (M.H)
Marks: 62% First class (2000 – 2002)
B.Sc., Nagarjuna University, Guntur.(A.P)
Marks: 72% Distinction (1997 - 2000.)
COMPUTER SKILLS:
Windows ‘95/’98 & MS-Office.
S.A.P.(System Applicable Procedure) in Industrial Purpose.
Raw materials, Finished COA Results entered in SAP System .
PERSONAL PROFILE

Name : NATARAJ KUMAR. ADIPUDI
Father’s Name : Satyanarayana .A (Late)
Date of Birth : 15th July, 1975
Nationality & Religion : Indian & Hindu
Sex / Martial Status : Male – Married
Language known : Telugu, English & Hindi
Permanent Address : S/o. Saraswathamma. A
Pusapadu (Post), Inkollu (MD),
Prakasam (Dist). PIN : 523190.

Yours faithfully,
Place: Hyderabad
Date : (A.NATARAJKUMAR)

[Guest]

CURRICULUM VITAE
K.PitchiReddy,
Email : kandibio10 AT gmail.com

___________________________________________________________________________
OBJECTIVE :
To be a part of an organization, wherein I can contribute to the growth of company and enhance my current capabilities. To obtain a challenging position in the industry that unfolds my Potency, contribute my Best to ever-escalating field and wish to move with a high growth company where more knowledge and great¬er job satisfaction can be achieved.
PERSONAL STRENGTHS :
- Good interpersonal and Communication skills.
- Ability to learn faster and a good listener.
- Flexible and adaptable to any environment.
- Work effectively and efficiently as per situation.
- Ability to reach organization goals under intense pressure.
EDUCATIONAL QUALIFICATIONS :
- M.Sc. from Bharatidasan University, Tamilnadu (73%).
- B.Sc from Acharya Nagarjuna University, Guntur, A.P (65%).
EXPERIENCE :
Current Working Experience
Company : Working in MSN laboratories Hyderabad- Unit-II since February 2010 till 0.date.
Current Role : Jr Executive - Quality Control

Current Job Responsibilities : Analysis of Finished samples.
JOB RESPONSIBILITIES :
- Maintenance of Control samples for Finished Products
- Responsible for Analysis of Finished Products.
- Responsible for Maintenance and Calibration of Instruments like KFR, SOR &FTIR Spectrophotometer.
- Preparation of the Method Validation Protocols.
INSTRUMENTS HANDLED :
- Gas Chromatography
- FTIR Spectrophotometer
- UV Spectrophotometer
- Karl Fishcher Titrator
- Specific Optical Rotation(SOR)
- Particle Size Analyser (PSD)
REGULATORY AUDITS FACED :
- USFDA
- Other Customer Audit
SUMMARY :
1+ Years of Total Experience in Pharma Industry.