CURRICULLAM VITAE

BELLAMKONDA RAMAKRISHNA
ramasavi79@gmail.com
9640111166/6301359335

Dear Sir/Madam,
I am Writing to apply for good suitable position in your esteemed organization. Please find my
curriculum vitae attached next to the cover letter. I am an ambition, outgoing and
professional science graduate and have achieved outstanding results during my experience
in pharmaceutical industries. My Skills, attribute and experience make me an ideal applicant
for the position in your organization, which I see as an exciting opportunity and great
challenge. I enjoy the social nature of pharmaceutical industries and thrive on the pressure of
working and its targets.
Through organizing and conducting internal meetings with the team members and then
follow-up on those meetings. I have honed my technical information dissemination skills to a
fine art.
I am also self-motivated and work well automously, which is foreseen in my successful
territory planning and strategy.
Thank you for considering the application and I hope to have the prospect to further prove my
suitability for the role at the interview. I would highly appreciate the line reply.

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RAMAKRISHNA CAREER OBJECTIVE

BELLAMKONDA I have overall experience of about 16 years in the area of Quality
Contact Information: Control of APl division Stream. Having worthy exposure in Quality
Management system, compliance system and well versed in
Phone: +91 9640111166 pharmaceutical and professional stream with comprehensive skills
+91 6301359335
in Quality control activities seeking a good position in QC, where
these skills will add value for continual improvement of self and
E--mail id: organizational requirements.
ramasavi79@gmail.com PROFFISIONAL BACKGROUND
Name of the Period work Grade Key
Permanent Address: company,Location responsibility
S/o. B.srinuvasa Rao, Kekule life Science September- 30 team
Muchintala (Post), Ltd,Vijayawada 2023 to till Manager members with
Penuganchiprolu (USFDA) date QC team
(Mandalam), Rakshit
Krishna(Dist) pharmaceuticals July -2022 to Manager 45 team
Andhra Pradesh, ltd, August-2023 members with
PIN#521190 Visakhapatnam QC team
(EDQM certified)
Raks pharma pvt Handling a
Address for Lts June -2010
correspondence ( Amneal group) to Dy.Mange group
members
of 15-
team
B.Ramakrishna Visakhapatnam June -2022 r of different
D#: 4-473, (USFDA, EDQM, functions
STBL projects, KFDA)
Vutagedda Junction, Granules India pvt
Parawada mandalam, ltd
Bharnikam village, Visakhapatnam June 2007
Visakhapatnam, (USFDA, EDQM) to Sr.Chemist Worked as team
Andhra Pradesh, (Formaley Known May 2010 member
PIN#531021. as
Actus pharma Pvt
Ltd)
QUALIFICATION
 M.Sc in Analytical Chemistry With First Division
Andhra university, DR.LB College Visakhapatnam.
 B.Sc M.P.C with first Division
Acharya Nagarjuna University, K.V.R College Nandigama.
 Intermediate with First Division
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Personal Data: JOB RESPONSIBILITIES

Name `: B.Ramakrishna  About 16 years of experience in Quality control department in
Father Name: B.Srinuvasa Rao recognized API manufacturing companies.
 Currently the leading team has the strength of 30 members.
Date of Birth : 11th March- Currently leading by QC team (Wet lab, HPLC, GC and Stability
1984 
sections)
Sex: Male  Planning and monitoring of analysis.
Nationality: Indian  Experience in GLP section of Instrument Qualification, Calibration,
Marital Status:Married Standard Management and Analysts Qualification.
 Good exposure on calibration of various instrument of HPLC, GC,
Languages known: Auto titrator meter, conductivity meter, UV chamber, Polarimeter,
Telugu,English&Hindi IR, UV, LCMS, GCMS etc.
 Good communication with instrument vendor.
 Experience in Analytical method validation and method transfer
for API products.
 Investigation of incidents, OOS and OOT.
 Handling of change control, Deviation and CAPA.
 Handling of Raw material, Inprocess, Intermediate and API’s
products.
 Ensuring availability of required resources in laboratory.
 Ensuring timely completion of analysis and review activity by
following GLP and cGMP.
 Trouble shooting during the analysis activity.
 Review of analytical reports and raw data.
 Analytical Support for new products, market complaints and
regulatory queries.
 Co-ordination of with other departments like Quality assurance,
Manufacturing, Regulatory, AD and R&D.
 Qualification and calibration of instrument and review of
supporting documents.
 Ensuring data submission to RA in timely manner.
 Ensuring online documentation in laboratory.
 Identifying training needs and planning and implementing
training programs.
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 Participated in regulatory audits like USFDA, EDQM and
PERSONAL SKILLS: different customer audits.
 Good Motivator of the  Handled LIMS software.
team under all the Positive attitude and enthusiastic in team work.
circumstances. 

Very quick to adapt the situation and handled the issues.

 Maintain good 
relations.  Good organization and problem-solving skills.
the cross functional Good interpersonal skills, commitment, result oriented hand
teams. 
 Open to learn new working with a quest and zeal to learn new technologies and
things, undertake challenges.
Strong work ethics,
discipline and self
motivated. DECLARATION
 Committed to strive in
achieving team and I here by declare that the above stated information is true to the best
individual goals. of my
 Proficient in delivering Knowledge affirms the above provided information is true and
timely and productive reliable.
results in tight
deadlines.
Place: Visakhapatnam, India (Bellamkonda Ramakrishna)

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