Pharma Production supervisor : Resume CV

[aarun]

RESUME :
A.ARUN
Email ID : aarun126 AT rediffmail.com

OBJECTIVE :
Seeking a responsible position in a growth oriented organization with simulated work environment that allows me to utilize my technical knowledge and practical experience to obtain the goals of the organization.

ACADEMIC PROFILE :
- Diploma in Chemical Technology in PMC Tech., Hosur.
- HSC Science Group in Nalanda H.S.School in Krishnnagiri.
- SSLC G.B.H.S.School in Krishnnagiri.

PROFESSIONAL EXPERIENCE :
- Presently working as a Production Assistant I in Apotex Pharmachem India Pvt. Ltd., (Canada based MNC) in Bommasandra Industrial Area, Bangalore from FEB-2007 to till date.
- Worked as a Production supervisor in INTERMED LABS PVT LTD (MNC)
in Bangalore fromMay-2004 to JAN -2007.

INDUSTRIAL EXPOSURE :
- Handling Reactors like Glass lined Reactors, Stainless Steel Reactors & Hastalloy Reactors.
- Filtration Equipments like Nutch filter, Centrifuge, Leaf filter, Sparkler filter, Robo filter.
- Driers like Tray drier, Fluid bed drier, rotary cone vacuum drier & Multi mill, Blender.
- Operation and maintenance of De-mineralized water plant and also maintaining all the records related to DM water plant.
- To coordinate with engineering to minimize production losses due to maintenance Breakdown and compliance to all safety requirements.
- To coordinate with R&D in follow up of user trials scale up batches in pilot plant for the better suggestions of new process and existing process.
- To ensure all log sheets and records are updated online with the operations are carried out.

RESPONSIBILITIES :
- Maintaining all the Records as per cGMP Standard.
- Good at inter personal relationship and communication.
- Responsible to handle equipments as per standard operating procedures.
- Responsible for documentation of batch production control records and general
Cleaning records as per procedures.
- Responsible for daily usage log, equipment usage log calibration log.
- Controlling and maintaining process parameters as per BPCR.
- Production Planning, Supervising unit operations.
- To evaluate potential ability of man power handling.
- Trouble shooting the problems coming across.
- To achieve production targets.
- Handling Pilot Plant instruments.
- Maintaining the records as per ISO norms.
- To follow 5S.

ADDITIONAL QUALIFICATION :
- Diploma in Industrial Safety in Annamalai University, Chidambaram
Tamilnadu.

OTHER SKILLS :
- Under gone Training programs about cGMP, Basic Safety, First-Aid, Fire fighting.
- Handling of all types of Extinguishers & Fire hydrant.
- Undergone training in on-site emergency plan.

PERSONAL PROFILE :
Sex : Male.
Date of Birth : 01-02-1984.
Nationality : Indian.
Language Known : Tamil, English & Kannada.

DECLARATION :
I hereby declare that the information provided above is true, complete and correct to the best of my knowledge.

Yours truly,
(A. ARUN)

[Guest]

RESUME :
VISHAL KUMAR MISHRA
E-mail :vishalkmishra AT rediffmail.com

CAREER OBJECTIVE : -
To implement and ensure the all cGMP norms to keep organization in state of best compliance level of national and international regulatory requirements.To follow the management policies along with required updation in existing practices through awareness for quality at all levels by continuous improvement of technical skills.

PRESENTLY ENGAGED IN : - “M/s Cipla Ltd." Sikkim, as a Management
Staff since 2nd June 2011 to till date.

WORKING EXPERIENCE (+ 5.8 years) :-
- 2.9 years with J.B.CHEMICALS & PHARMACEUTICALS PVT. LTD. Daman, in both Production & Packing Department as a Production-Packing officer from August 2008 to May 2011.
- 2.4 years with Gujarat Liqui Pharmacaps Pvt. Ltd., as a
Production Pharmacist in Production Department from April 2006 to
August 2008.

AUDITS FACED :-
- Nigeria Audit at GLPL, Vadodara.
- FDA inspection at JBCPL, Daman.
- Internal audits at JBCPL, Daman.
- TGA at JBCPL, Daman.
- MCC at JBCPL, Daman.
- WHO at Cipla, Sikkim.

Technical efficiency :-
- To increase the productivity of good quality products, through time-management, planning and less changeover time.
- Minimization of the probabilities of line clearance failures by providing training to the concerned about the critical points to be checked during line clearance, so as to avoid product mix-up at any stage.
- In process checks including the challenging of interlocks and controls of the machines and the provided systems, so as to ensure their proper working.
- Rejection control & analysis, to minimize the loss of packing materials.
- Supervision of manufacturing and packing processes in the machineries like, Vibratory-Sifter, Multimill, Octagonal- Blender, Planetary mixer, Encapsulation machine, Sachet/pouch packing machines : PAKONA 92 TWIN, PAKONA AG90, Blister pack machines: EPI-2500, EPI-3000FB, EPI-3010PDA, BQS, Strip pack machines: Satellite Engineerings, Precision Gears & Marchesini.
- Machine wise spare list preparation and ensuring availability in change-parts storage area.
- Review of quality related issues in packing materials with suppliers.
- Control of process deviations, on line rejection of packing materials.
- Line clearance activity with supervision of area and equipment cleaning.
- Stereo management i.e, order, procurement, storage & destruction of stereos.
- Review & compliance of BMR, BPR, SOPs, log books and all other documents related to production and packing.
- Batch packing reconciliation.
- Product & equipment history record maintenance.
- Machine log, temperature, RH and pressure differntial monitoring.
- Electronic weigh balance & checkweigher daily verification & calibration.
- First pack verification, raising of PRRF, packed stock inspection, reweighing of the packed shippers and their contents before their transfer to the BSR along with Daily Production Report.
- Unit operation of machine and packing line.
- Annual product review along with data collection of the batches being manufactured.
- Training of machine operators & casual workers for awareness of product & process.
- Calculations for active pharmaceutical ingredients and excipients i.e raw materials for the batches to be dispensed for the manufacturing processes of tablets, soft gelatin capsules and oral powders on the basis of data provided by quality control and work-order.
- General cleaning & status labeling of manufacturing areas, primary packing cubicles, packing lines, staging area, charging area & packed stock inspection zone.
- In process checks for soft gelatin capsule encapsulation, pouch/sachet filling, tablet granulation, compression and packing.
- Break down rectification and co- ordination with maintenance department.
- Fumigation arrangement and recording.
- Calculation, dispensing, yeild reconcillation, EMRM & EMCM of primary and secondary packing materials.
- Offline packing & printing planning, supervision and segregation of pre-printed packing materials for further packing activities.
- Manpower handling and their work allocation as per the requirement.

EDUCATIONAL QUALIFICATION :
- BACHELOR OF PHARMACEUTICAL SCIENCES from (Gayatri College of Pharmacy, Sambalpur, Orissa, securing 65.3% as aggregate marks in the year 2005-06. under BPUT.
- 10+2 from Government Higher Secondary School, Haldibadi Chirimiri, Dist. KOREA (Chattisgarh), securing 50.2% of Marks under M.P.Board in the year 2001.
- Xth from Kendriya Vidyalaya Chirimiri (CBSE BOARD) securing 50.2% of Marks in the year 1999.