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Phaninder Ekkaladevi

Microbiology & Production Team Leader • Singapore • e************@gmail.com • +91*******048 • linkedin.com/••••• • drivetube.ai/•••••

Professional Summary

Microbiology & Production Team Leader with 15+ years of experience in food and pharmaceutical manufacturing microbiology, quality systems, validation and production support; skilled at leading teams, driving GMP/HACCP compliance, and implementing CAPA and continuous-improvement programs.

Technical Skills

Testing: GMP,HACCP,ISO 17025,BRCGS,Purified water analysis,WFI testing,DHS systems,CAPA,OOS investigations,Root cause analysis,Non-conformance management
Data and Analytics: Data trending,MS Excel,Report writing
Laboratory Information & ERP: LIMS,SAP,D365
Manufacturing & Control Systems: SCADA,HMI
Microbiology Techniques: Environmental monitoring,Sterility testing,Bacterial endotoxin testing,Microbial limit testing
Validation & Qualification: IQ,OQ,PQ,Equipment qualification,Cleaning validation,Hold-time studies
Continuous Improvement & Operations: Process optimization,Lean management,SOP development,Internal auditing
Laboratory Equipment & Utilities: Autoclaves,Incubators,Ovens

Work Experience

Oatly Singapore Operations & Supply Pte. Ltd.
Singapore
Microbiology & Production Team Leader
March 2022 – December 2024
Food manufacturing (plant producing oat-based dairy alternatives); provided microbiology and production support to ensure food safety and process reliability.
Tech Stack: LIMS, SCADA, SAP, MS Excel, CAPA systems
  • Led microbiological sampling program across critical process stages using settle/contact plates and swabs, ensuring timely analysis and adherence to internal sampling schedules recorded in LIMS.
  • Evaluated microbiology results and initiated CAPA and corrective actions with cross-functional teams, using root cause analysis to contain and resolve deviations while preserving production schedules.
  • Prepared and revised SOPs, CAPAs and non-conformance reports to align with BRCGS and internal standards; managed documentation and trending in LIMS to support audits and continuous improvement.
  • Validated and maintained sanitation and cleaning-in-place procedures for processing lines and utilities, coordinating verification activities and ensuring cleaning efficacy for product safety.
  • Coordinated investigations with QA and Engineering to troubleshoot quality issues detected via SCADA alarms and lab results, implementing process adjustments to stabilize microbial control.
  • Supported production optimization initiatives by integrating microbiological risk assessments into line-change and first-pass yield activities, enabling safe throughput improvements while maintaining compliance.
Wyeth Nutrition Pte Ltd, Singapore
Singapore
Process Technician
August 2019 – March 2022
Infant nutrition manufacturing (dairy-based nutrition products); supported GMP production, quality checks and manufacturing process control.
Tech Stack: SCADA, SAP, D365, MS Excel
  • Monitored dairy production processes under GMP and HACCP frameworks, using SCADA and process checklists to ensure control limits and prevent contamination risks.
  • Performed in-line and end-of-line quality checks and sampling, documenting results and releasing batches per QA criteria while maintaining production continuity.
  • Maintained production and quality documentation including batch records and deviation reports in SAP/D365 to support traceability and regulatory compliance.
  • Participated in lean-driven continuous improvement projects to reduce process variability and improve efficiency on the processing line.
  • Supported cross-functional teams during changeovers and validations, verifying cleaning and pre-run checks to ensure microbiological safety before production restarts.
  • Trained and coached operators on SOP adherence, sanitation practices and GMP behaviors to sustain a compliant production environment.
Wyeth Nutrition Pte Ltd, Singapore
Singapore
Assistant Microbiologist
June 2014 – August 2019
Quality laboratory support for infant nutrition manufacturing; executed environmental monitoring and equipment validation to maintain laboratory and plant compliance.
Tech Stack: LIMS, SAP, Autoclaves, Incubators
  • Executed environmental monitoring program using settle plates, contact plates, swabs and air sampling; analyzed trends and reported excursions to QA for timely action.
  • Performed microbiological testing of purified and deionized water systems and conducted hold-time studies to validate product stability and sampling integrity.
  • Managed CAPA and OOS investigation workflows, performing root cause analysis and implementing corrective actions to restore compliant operations.
  • Planned and executed qualification and validation of autoclaves, incubators, refrigerators and ovens following IQ/OQ/PQ protocols to maintain validated laboratory equipment.
  • Maintained laboratory compliance with GMP requirements, ensuring documentation accuracy, timely trend reporting and readiness for internal and external audits.
  • Prepared laboratory documentation and generated microbial trend analyses to support continuous improvement and regulatory reporting.
Symbiotic Pharma Lab Ltd., Indore
Indore, India
Microbiologist
January 2013 – May 2014
Contract pharmaceutical testing laboratory; provided microbiological testing and validation for raw materials and finished pharmaceutical products.
Tech Stack: SAP, LIMS, BET testing equipment
  • Performed microbial limit testing for raw materials and finished goods using standardized methods and documented results in SAP-based systems for client reporting.
  • Conducted bacterial endotoxin testing (BET) and supported method validation activities to ensure assays met acceptance criteria for client submissions.
  • Executed product validation studies and method validations, drafting validation reports and protocols to meet regulatory expectations.
  • Performed water analysis and environmental monitoring to verify facility hygiene and utility quality supporting pharmaceutical production.
  • Developed and executed IQ/OQ/PQ protocols for laboratory equipment, ensuring calibration and operational readiness for testing.
  • Generated microbiological trend reports and maintained SAP documentation to support client audits and quality review meetings.
Teena Bio Labs Pvt. Ltd., Hyderabad
Hyderabad, India
Microbiologist
August 2009 – December 2012
Pharmaceutical microbiology testing facility; responsible for sterility testing, endotoxin testing and routine lab operations under GMP.
Tech Stack: LIMS, Autoclaves, Incubators, MS Excel
  • Conducted sterility testing of pharmaceutical products and maintained chain-of-custody and test records to comply with GMP documentation standards.
  • Performed bacterial endotoxin testing of raw materials and finished products, interpreting results and reporting deviations to QA for investigation.
  • Managed microbial culture maintenance and preservation practices to ensure test organism integrity for routine assays.
  • Conducted water analysis for WFI and purified water systems, documenting results and supporting utility qualification activities.
  • Maintained laboratory records, GMP documentation and calibration logs to ensure regulatory readiness and traceability.
  • Supported validation activities and assisted in drafting SOPs and test procedures to standardize laboratory workflows.

Education

Jawaharlal Nehru Technological University (JNTU), Hyderabad
Bachelor of Technology (Biotechnology) • Hyderabad, India • 2009

Certifications

BRCGS Internal Auditor (Issue 8 & 9) — BRCGS
ISO 17025 Internal Auditor — ISO 17025
Food Safety & Hygiene Training
Incident Management Training
Leadership Development Program

Achievements

  • 15+ years of microbiology laboratory experience: Extensive hands-on experience across food and pharmaceutical microbiology, environmental monitoring, sterility testing and BET.
  • Regulatory and standards expertise: Certified internal auditor with working knowledge of GMP, HACCP, ISO 17025 and BRCGS corporate standards.
  • Validation and compliance delivery: Led equipment qualification and validation programs including IQ/OQ/PQ and cleaning validation across multiple facilities.
  • International manufacturing experience: Worked in regulated manufacturing environments in Singapore and India supporting product safety and production continuity.

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