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SANJAY KUMAR
CAREER OBJECTIVE
Contact No. To work in an organization where I can acquire new knowledge and sharpen
+91 8750838281 my skills & pay my best efforts in achieving the organizational as well as
+91 8010069886 individual goal.
WORK PORTFOLIO
Work Planning.
Shift handling.
Date of Birth: Manpower training and handling.
07th February 1988. ACHIEVEMENT
Other Personal Data: - Worked with Hindustan Syringes Pvt. Ltd. as a Quality Control Supervisor
which is situated in Sector 58, Faridabad from Aug- 2008 to Dec- 2010.
WORK POFILE
Linguistic Ability: Check out product at In-Process activities at moulding stage.
English & Hindi To ensure quality of product (BCT) at different stages of manufacturing.
In-process report preparation at different stages of manufacturing.
Moulded & mould component evaluation of BCT.
All testing related to product in In-process.
Strength: Finished product testing of BCT (Blood Collection Tube).
Punctual. Preparation of test certificate of product.
Male. Worked with La-med Healthcare Pvt. Ltd. As a Quality Control Supervisor
from April 2013 to March 2015.
WORK POFILE
Moulded & mould component evaluation of new mould samples
(Visual/Dimensional/Operational).
To ensure quality of products (I. V. Cannula, I.V. Set, B.T. Set, Burette Set
Nationality: and other common/tubing disposable products at different stages of
manufacturing.
Indian.
All testing related to product in In-process.
In-process inspection report preparation at different stages of
Manufacturing, Assembly & Packaging of products.
Approval of packing label as per approved art work.
Finished product physical testing.
Preparation of finished product report of all products.
Marital Status: Preparation of COC & COA of all products according to product
standards.
Married
Media Preparation and handling Bio-burden & sterility testing.
Pre dispatch inspection (PDI) of Sterilized product.
EXPERIENCE
Presently working with Degania Medical Devices Pvt. Ltd. as Sr. Officer-
Quality Assurance from March 2015 to till date.
WORK POFILE
Responsible for developing and implementing QMP, SOPs, Work
Instructions and Formats.
Handling of ECO/ECR.
Periodically document review and change control.
Training to the concern personnel related to change.
Periodically internal Audit of production Hall’s and other than Production
Salary Expected: Hall’s according to ISO 13485.
Negotiable
Involvement to improve the process and Procedure.
Identifying relevant process-related training needs and delivering training
for the development of the employees.
Ensure safety and identify risk during work.
Analyzing of customer complaints and corrective actions to solve the same
and adopting different methods to avoid complaints.
Participate in internal as well as external audits like Customer audit,
USFDA, ANVISA, Certification as well as Regulatory audits.
ATTRIBUTES
Hard working and believe in teamwork.
Result oriented and diligent person.
Love to learn new things.
A good helper towards those who need it.
Can adjust myself to adverse situations.
Passion for Challengeable job.
Eager to learn new innovative techniques and way of working.
DECLARATION
I hereby declare that the above-mentioned statements are true and correct
up to my knowledge and belief. I pledge that the work assigned to me will
Date:………………..
be completed up to the expectation of the organization.
Place:………………
(Sanjay Kumar)