Ankamma Rao Resume

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Ankammarao Bollimuntha

Assistant Manager
Email: [email protected] | Phone: 9603468379

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Professional Summary
I am a strategic quality professional with extensive leadership experience in pharmaceutical
Quality of OSD, API, and injectable. I am proficient in developing strategies, budgets, and
organizations. In my leadership roles, I have built, managed, and transformed quality
organizations (team sizes varied from 10 to 70 people) to implement strategies for
obtaining product/facility approval. My specialties include Laboratory, Analytical Quality
Assurance, Audit & Compliance, Remediation plans, Quality Management System (QMS),
and Analytical Method Validation.

Skills
• Regulatory Exposure: USFDA, TGA, EDQM, WHO
• Laboratory Investigations
• Audit & Compliance
• Remediation Plans
• Cleaning Validation
• Quality Risk Management
• Vendor Qualification
• Resource Management
• Standard Operating Procedure (SOP)
• Internal Audit Management
• Team Management
• Quality Management System (QMS)
• Green Field Projects
• Batch Release

Work Experience

Itaan Pharma (May 2023 - Present)


Assistant Manager - Quality Control Department

• Reviewed raw material analysis documents


• Reviewed and monitored water analysis documents and trends
• Ensured GLP and GDP compliance
• Managed LIMS for document preparation and review (finished, raw materials, packing
materials, in-process, and other analytical documents)
• Prepared and reviewed stability protocols using LIMS
• Developed worksheets and general test procedures
• Actively participated in various customer audits, including USFDA
• Ensured proper documentation compliance with GLP in LIMS online
• Followed SOP and STP
• Maintained reference and working standards
• Raised OOS (Out of Specification), OOT (Out of Trend), and obvious errors as required
during analysis
• Conducted active investigations on QMS elements
• Maintained analytical columns
• Reviewed team documents and performed sequence checking and online monitoring

Aspiro Pharma (Nov 2021 - May 2023)


Senior Executive - Quality Control Department

• Managed shift handling analysis planning


• Handled QMS-related activities including LIR incidents, OOS, OOT, CCF, and risk
assessments in consultation with cross-functional teams
• Conducted training sessions

Graviti Pharma (Oct 2018 - Nov 2021)


Associate - Quality Control Department

• Reviewed all analytical documents


• Handled HPLC, GC, and WET analysis systems
• Maintained GLP documents

Dr. Reddy’s (Oct 2013 - Oct 2018)


Analyst - Quality Control Department

• Conducted raw material and tanker sampling


• Calibrated analytical instruments
• Sampled and analyzed packing materials
• Performed analyses of packing materials, raw materials, in-process, intermediates, and
finished products
• Attended LDM meetings

Instruments
• FTIR (Perkin Elmer & Spectrum Two)
• HPLC (Waters Agilent with Empower 3)
• UV (Shimadzu with UV Probe Software)
• pH Meter, KF Titrator, Conductivity Meter, SOR, Analytical Balance, FT-NIR, Halogen
Moisture, TLC, Oven LODs, Residue of Ignition (ROI)
• GC (Agilent Instruments) with Empower 3
Education
• MSC (Organic Chemistry) - ANU University
• BVOC (Pharmaceutical Chemistry) - A+ Grade
• Intermediate - K.V.S.R.T. Junior College, Chilumuru, A.P.
• S.S.C - C.V.R. High School, A.P.

Personal Details
• Name: B. Ankamma Rao
• Father's Name: Venkata Krishna Rao
• Gender: Male
• Marital Status: Unmarried
• Nationality: Indian
• Religion: Hindu
• Languages Known: Telugu, English
• Address: Kakarlamudi (V), Chadalawada (PO), Vemuru (M), Guntur (D), Andhra Pradesh
- 522301

Declaration
I hereby declare that the information furnished above is correct to the best of my
knowledge and I bear the responsibility for the correctness of the above-mentioned
particulars.

Place: Hyderabad

Date:

(Ankamma Rao)

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