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Manager Development

Location:
Dombivli, Maharashtra, India
Salary:
100000. dollor
Posted:
September 25, 2019

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Resume:

RANJANA KADECHKAR

Mobile: +91-982******* // 965-***-****; E-Mail: adaf21@r.postjobfree.com

~ Research & Development(ANALYTICAL&FORMULATION)~

Formulation R&D Quality Control Commercial Operations Corporate Management Compliance of Data

Seeking a position in Research & Development (Formulation Analytical) to utilize my analytical experience to deliver a best science and best product development.

Linked with PRIVI LIFE SCIENCE – ASST.MANAGER

Career – At a Glance

Ambitious, self-directed, dedicated professional with 13+ years of experience in plant extract, flower extract formulation, Pesticide formulation, Mass Spectrometry, Chromatographic Sep’n like LC-MS, GC-MS & HPLC, Spectrophotometric technique UV Spectrophotometer and Brookfield viscometer.

Proficiency at Analytical Method Developments for unknown & new molecule.

Carrying out R&D activities to ensure highly innovative production techniques and methodologies that will increase production efficiency.

Creating a good database management system to maintain necessary documentations and records that can be utilized in future for reference purpose. Proficient in performing analysis using HPLC, GC,GC-MS,LC-MS/MS.

Keeping abreast with new developments and inventions about the field. Making full utilization of technological advancements to have in-depth understanding of the analytical issues.

Excellent time management skills with ability to work accurately and quickly prioritize, coordinate and consolidate tasks, whilst simultaneously managing the diverse range of function from multiple sources along with keen interest in Research & development.

An effective communicator with expertise in identifying & adopting emerging trends to achieve organizational objectives and profitability norms.

PERSONAL TRAITS

Strong analytical and interpersonal skills. Organized and detail oriented to handle complex and dynamic research projects. Possess good solving skills and ability to work independently. Ability to work independently and as part of a team.

OBJECTIVES

Seeking a position in Research & Development (Analytical) in Fragrances & Flavors, Pharmaceutical Industry that I can utilize my 13+ years of analytical experience to deliver a best science and best product development.

PROFILE VALUE

Mass Spectrometry(GC, GC-MS- Shimadzu 2010, Agilent [SingleQuadruple], GC- Head Space, LC-MS/MS- Waters, Electrospray Ionization.)

High Performance Liquid Chromatography :- HPLC- Waters, Agilent, UPLC

UV. Vis Spectrophotometry. –Shimadzu

FT-IR Spectroscopy

Potentiometric titration like: -Metlor, Karl Fischer.

Study of New molecule and their intermediates. (Identification, Characterization and Quantitation).

LC-MS(Thermo Scientific) and LC-MS/MS (Water’s,AB Sciex ),Brookfield viscometer DV2 .

Instrumentation Troubleshooting and Maintenance.

Clinical Plasma sample extraction analysis, Pesticide Residue Analysis. Method development for pharmaceutical, agrochemical Formulation mixtures.

Formulation development. Wet Chemistry, Plant scale up.

OCCUPATIONAL CONTOUR

Since Apr’19: PRIVI LIFE SCIENCE PVT LTD. FORMULATION DEVELOPMENT

Asst.Manager - R&D ( FORMULATION )

Responsibilities:

Develop and Commercialize Ecofriendly products which can be patented.

Developing and commercializing existing or third party products 2 Agricultural + 2 Ready to use products for gardening.

Reduction in Product Quality related Customer Complaints .

Managing the daily activity of Formulation Development Lab. Setting up the entire lab in terms of Formulation R&D. To lead the group of scientists whenever required.

A] Formulation Development

B] Stability studies

Interact with vendors /suppliers and contributing in seminars to ensure that up to date technologies and trends are used in new developments. Preparing and Implementing SOP for New Product Development.

Leading formulation R&D functions and monitoring of Physical, Inorganic test, Heavy metal analysis and testing activities for Raw Material (Chemical / Formulation), in process, Intermediates & A.I, finished products.

Developing and standardizing Formulation R&D methods as per CIB-RC, ECOCERT registration requirement for custom synthesis for different type and grade of the chemicals &Formulations.

Carrying out uninterrupted release of finished product by coordinating with production, ware-house and quality control. Identification of materials and equipments required for lab level, pilot and bulk level production of product

Using sophisticated instruments like GC-MS, GC & HPLC Agilent, AAS- Agilent Nitrogen Kjeldalh for carrying out analytical development activities @ ROHA chemicals.

Determining and setting controls for impurities in finished products by employing HPLC, GC, GC-MS LC-MS (Outsource) and carrying outstability Check study of stable formulations mixtures by performing Physical, Inorganic tests.Planned day to day activities analysis of samples and shared the results with synthetic R&D and prepared and executed validation protocols. .

Coordinating with plant & QC during technology transfer and between R&D synthesis lab and manufacturing unit, marketing unit, purchase department supply chain for technical related issues.

Molecules work :- Eucalyptol, Cedarwood oil, Cinnamom Oil, Eugenol, Citronellal, Citral, Menthol, Camphor, Azadirachtin, Gibbrellic acids, Quinoa-Saponins.

Since Oct’15: Mar’19 GODREJ AGROVET LTD 3 YEARS 5 MONTHS ANALYTICAL & FORMULATION METHOD DEVELOPMENT

ANALYTICAL R&D- EXECUTIVE

Responsibilities:

Heading the team and managing the daily activity of Analytical Development Lab.

Interact with vendors /suppliers and contributing in seminars to ensure that up to date technologies and trends are used in new developments.

Providing support on analytical R&D functions and monitoring of routine Analytical functions and testing activities for Raw Material( Chemical / Formulation), in process, Intermediates & A.I, finished products.

Developing and standardizing analytical methods as per ASTM or customer -specific requirement/ as per CIB registration requirement for custom synthesis for different type and grade of the chemicals & Fomulations.

Carrying out uninterrupted release of finished product by coordinating with production, ware-house and quality control.

Using sophisticated instruments like HPLC- Water’s E 2695- Empower -2 UV – Shimadzu and Karl-Fisher for carrying out analytical development activities related to specialty chemicals.

Determining and setting controls for impurities in finished products by employing HPLC or LC-MS (Outsource) and carrying outstability Check study of stable formulations mixtures by performing Physical, Inorganic tests.Planned day to day activities analysis of samples and shared the results with synthetic R&D and prepared and executed validation protocols.

Compiling and reviewing validation of analytical methods & analytical instruments, and Critical review of raw data during Analytical Method Validation.

Coordinating with plant & QC during technology transfer and between R&D synthesis lab and manufacturing unit, marketing unit, purchase department supply chain for technical related issues.

Highlights:

Developed method for non UV absorbent molecule i.e HOMOBRASSONOLIDE. Praise work by EX.R&D Head in front of Mr. NADIR GODREJ. Method development for different types of formulations.i.e 0.1 HBR, BPS+EPS, AZA ( Azadirachtin)

Authorized signatory for internal COA for molecules

Method development for specially for (NONUV ABDOSRBANT Molecules like HBR & Intermediates Tetrol, Pure-2 -ene), Cymoxanil, TPM, Glyphosate,Difenconazole, Propiconazole ( Formulation mixtures) more than 25 molecules MD done with in laboratory.

Individual responsible for HPLC Water’s maintainance, troubleshooting, decision maker for Mobile phase preparation, Column recovery, Linearity study of molecules, Development & Validation of molecules. UV –SPECTROPHOTOMTER calibration and maintenance& operation.

Molecules work : - BPS, QZP, Propaquizafop, Homobrassonides, AVG, Difenconazole, Propiconazole, EPS, Pure-2-ene, Lactone,

Aug’15 to Oct’15: HINDUSTHAN SPECIALITY CHEMICALS PVT LTD 3 MONTHS

SR.CHEMIST

Project: -- “Manufacturing of Epoxy Resin and allied products.

Responsibilities:

Assisted QC & QA Manager and prepared R&D Formulations under guidance of R&D Technical Manger (as per the requirement of market and customer) using different application like Brook field Viscometer DV2T, Differential Scanning Colorimeter (D.S.C.) and Metler-Toledo ( Potentiometric Titration).

Highlights:

Potentiometer Metler Toledo ( Epoxy, Amine value), Binder Incubator, Durometer Standardization, calibration, maintenance, trouble shooting

Heading 2 people for QC/ QA activities.

Aug’11 to Jul’15: THE MINISTRY OF AGRICULTURE [ Contractual] 4 YEARS METHOD DEVELOPMENT

Growth Path:

Deputy Quality Manager :- Mar’14 to Jul’15

Deputy Technical Manager :- May’13 to Mar’14

Research Associate :- Aug’11 to Jul’15( ON CONTRACT )

Project: “Monitoring of Pesticide Residue on National Level (MPRNL) by”Dr.K.K.Sharma,Project Coordinator.

Responsibilities:

Analyzed pesticide residue in agriculture commodities like Vegetables, Fruits, Cereals, farm gate IPM & NON-IPM, JNPT import fruits like Apple,Grapes,Mandarin,Dragon fruit,Pear,Banana, and Mango.

Operation sophisticated equipments like GC-ECD & FPD Detector-Shimadzu, GC-MS (SHIMADZU)-QP-MS/MS and LC-MS/M.S Waters,ABScienx 2100. Procured and maintained the spare parts for the analytical equipment

Permissible limit for human consumption for food, industrial and modified pesticides products.

Developed and standardized analytical methods as per AOAC or customer or specific requirements.

Analytical method development/Validation for products. SOP,Protocols,ValidationReportwriting, Product related troubleshooting, Analytical Method related troubleshooting, Design of experiment (DoE),Trainingtoless skilled staff.

To lead the group of scientists whenever required. A] Formulation Development B] Stability studies

Processed trouble shooting and investigation of manufacturing.

Carried out 4 -ISO 17025 -NABL audits and prepared documents as per NABL standards for chemical testing laboratories.

Maintain the Laboratory’s Quality System. Perform analytical tests in the laboratory.Assist with laboratory administrative duties.Maintain smooth laboratory work flow.Obtain laboratory certifications and complete QA/QC assignments. Maintain the quality assurance of the laboratory by Schedule and successfully complete semi-annual proficiency testing for all analytes in NABL Scope of Accreditation.Promote good customer relations with all PRL -NABL clients.

Highlights:

Method Development & Method validation for SP, OC, OP,CARBAMATES,HERBICIDES almost 40 + molecules study on GC,GC-MS,LC-MS/MS

Gained exposure in 2- FAPAS-International PT Programme, while participating in the year 2013-2014 & 2014-2015 Cucumber Puree.

4 NABL Audits attended and successfully got certification for PRL, 5 Internal Audit conducted.

Certified with ISO/IEC 17025:2000 NABL Exposure in NABL AUDITS with Internal authorize signatory.

Heading team of 6 people.( 3 Ph.d fresher + 3 Contractual)

Given complete trainings for handling of GC & GC-MS& LC-MS Starts with sample preparation to till identification of molecules by using mass library.

Excellent exposure in maintaining Intermediate checks for C.R.M-Certified Reference Material and preparing of using Dr.Ehrenstofer Standards for working stocks in various level like 1000 Ppm,100Ppm,1Ppm as per requirements.

Feb’07 to Jan’11: BOMBAY BIORESEARCH CENTER- CRO – 4 YEARS

BIOANALYTICAL OFFICER- ANALYTICAL METHOD DEVELOPMENT

Responsibilities:

Analytical method development/Validation for CRO products, SOP, Protocols, Validation Report writing,

Product related troubleshooting, Analytical Method related troubleshooting, Design of experiment (DoE), Training to less skilled • staff.

Developed, validated and executed cleaning validation methods in support of manufacturing.

Performed analytical testing in support of stability studies. Developed analytical methods to solve challenging chemistry Troubleshoot technical problems. Designs experimental plans to address specific issues. Plan, write and executes validation protocols Interprets, analyze, and manage data .Write and disseminate technical data summaries and reports as needed. Ascertain the quality of final reported test results.

Direct and foster the professional development of scientific associates

Perform routine and non-routine analysis on raw materials, drug substances, reference materials and drug products using a variety of instrumental and wet chemistry techniques.

Search and scan relevant literature.

Document validation protocols, validation and progress reports as appropriate and assist in the preparation of study reports

Monitor and assess current analytical methods and assist in improvements and amendments according to cGMP practices.

Ensure cGMP compliance is maintained. Looked after Pharmacodynamics & Pharmacokinetics and made documents as per regulatory & sponsor auditors

Contribute to the development and/or implementation of new technology.

Review work from various sources, may assign work to others, and train less experienced employees.Formulation Development (Liquids). Stability studies Extracted plasma sample analysis, bioavailability & bioequivalence of drug.

Maintained record for all HPLC, LCMS, chemical storage, deep freezer, balance calibration, testing and conductivity of water.

Looked after maintenance & archival of documents, maintenance of Library of analytical books; distribution and archiving of LNB & Log books, prepared purchase indents of stationary, chemicals & other laboratory items, and correspondence.

Handled HPLC-Agilent Technologies and planned & organized for timely installation of analytical equipments in ANALYTICAL R&D

Highlights:

Documented as per requirements for audits like US-FDA, AN-VISA, WHO & Sponsors Archival of study & validation files and proficiency in liaising with the authorities.

Jun’05 to Dec’06: ASTEC CHEMICALS PVT LTD. 1 YEAR 6 MONTHS

Research & Development Chemist

Responsibilities:

Provided research &development support to department activities while managing the wide spectrum of tasks including development of Procedures about New compound synthesization.

Estimated the demand for the product, analyzed, reported, gave recommendations and developed strategies to improve quality and quantity by using different method. responsible for in-process reaction monitoring, solvent recovery, in-process testing and raw material analysis.

Creating & Maintaining the formulas, process to manufacture, Raw material and finish product specification and other R&D related documents

Performed assessment and reporting on daily basis for individual synthesis batch by maintaining reports and coordinating with concern manager.

Highlights:

Efficiently improved purity & percentage level of compounds using different methods and lining up batches as per instructions given by R&D manager.

Exposure on instrument GAS CHROMATOGRAPHY Head space.( Learn in addition along with R&D activity).

Aug’04 to Oct’04: CIPLA PHARMACEUTICAL LTD 3 MONTHS

Industrial Training Programme

Responsibilities:

Trainee chemist in Quality Control, responsible for in-process reaction monitoring, solvent recovery, in-process testing and raw material analysis.

Worked on Stability study of bulk drugs and formulations (antibiotics) Highlights.

Physical Characterization of API and drug products using Particle sizer (Light scattering), Zeta sizer (Zeta potential), DSC, Microscopy imaging technique (Clemex), Rheometry, HPLC, UPLC etc.SOP writing for Cleaning validation program

Analytical Method Development for Nano suspension Analysis

Dissolution method development for drug devices

Academic Credentials

2004 Master of Science (M.sc)in Analytical Chemistry from S.N.D.T University -Second Class 58.00 %

2002 Bachelor of Science (B.sc)in Chemistry from Mumbai University -Second Class 59.25 %

Trainings Undergone

Underwent Certified Training of Handling GC & GC-MS from Regional Plant Quarantine Station-Chennai.

Underwent Training General Requirement for the Competence of Testing & Calibration Laboratories and Internal Audit as per ISO/IEC 17025:2005. From I.D.E.M.I- MUMBAI

APWSS International Conference at Hyderabad.

Seminar Launch Program on ‘New! Thermo Scientific Vanquish UHPLC’ by “THERMOFISCHER SCIENTIFIC”

QaD Application & advantage of detector. – WATERS INDIA ( SEMINAR)

LC-MS/MS Practical Hands on experience on instrument by WATER’S INDIA PVT LTD

LC Trouble shooting by WATERS INDIA PVT LTD.

SOFTWARE SKILLS

Empower-2

Chemstation

GC-MS Solution.

LC-MS Solution

Personal Snippets

Date of Birth : 9thApril 1982

Permanent Address : 3rd Floor / Flat no 32, Shree raviraj C.H.S,Jaihind Colony, Vishnunagar, Gupte Road, Dombivli-West.

Current Address : 1stFloor / 103 SitaApartment,PanchayatBawadi, Chedda Road, Near Sai baba temple,Dombivli-East

Language Known : English, Hindi, Marathi; German (Beginner),

Passport no : Z-5153890



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