Ph. D. in Business candidates should provide authentic personal statements to each of the five following questions/prompts reflecting on their own personal interests. In the event that any outside resources are used, resources should be cited in APA format. Submissions should be a maximum of 500 words to 200 words per question. It is best to respond to each prompt/question individually for clarity of the reviewer. Documents should be submitted in Microsoft Word format.
1. Provide a brief introduction focusing on your education, career, and decision to apply to University of the Cumberlands.

2. In relation to your doctoral program application, what area of recent research in the field would you want to study, and why?

3. How does your current vocation relate to your application to the doctoral program?

4. How will your experiences and personal skills help you to be successful in your program?

5. What long-term goals do you have for applying your learning from your doctoral program?
Brief description about the candidate-
worked in  medical devices manufacturing companies as project lead. Presently studying MS in Project Management. Kindly refer the attached resume and the SOP to  know more about the candidate and answer the questions accordingly. Try to answer each question >200 words.Result-driven professional, targeting managerial assignments in Quality Assurance and Supervision | Sales
Engineering domain
Location Preference:

Production, Planning & Control
Quality Assurance

Sales Engineering

Supervision & Surveillance
Process Enhancement
Inspection Management

Process Validation

Supplier Quality
Design Verification

Equipment Qualifications
A professional with over 5 years of experience in Quality Assurance & Sales
Engineering; dynamic experience in Lean Six Sigma, Cost Estimation, Quality
Control, Continuous Improvement Techniques, Logistics & Client
Relationship Management across Medical Device industry
Currently associated with Abbott, California as Quality Engineer – providing
functional support to TPM, ISO, QMS and SHEMS policy, compliance to legal
Increased market share for underground drills in eastern region; experience
of working closely with B2B clients across domains such as Pharma,
Manufacturing to understand their technical requirements and delivered key
solutions to meet their needs
Performed dedicated sales and marketing activities across various business
segment throughout
Expertise in Process Validation, Test Method Validation, Protocol/Report
Writing, Statistical Analysis, NCRs, CAPAs, Supplier Quality, Design Verification
and Equipment Qualifications across product design and manufacturing
environment; experienced in statistical data analysis using Minitab
Implemented Change Management/Control; reviewed Corrective and
Preventive Actions (CAPA) and highlighted their mediation plans to mitigate
the non-compliance
Superior knowledge in risk assessment, 21 CFR Part 11 assessment, and
reviewing validation plans
Gained expertise in meeting business units objectives and goals, ensuring safe
and efficient operation of the plants, formulating and implementing the
operational SOPs with emphasis on safe, reliable and system performance
and efficient operation of the plants
Jun’18- Present: Abbott, Texas
As Manufacturing Engineer
• Spearheading Quality Assurance activities for manufacturing and engineering, validations of processes and equipment
in accordance with FDA and ISO guidelines
• Writing, reviewing and approving Engineering Change Orders and Engineering Change Records, Design History File
documents, IQ, OQ, PQ, TMV reports for accuracy and correctness
• Performing GAP Analysis of existing Risk Management Plans, Process Documents and suggesting Remediation activities;
conducting Hazard Analysis, PFMEA, DFMEA
• Preparing detailed inspection documentation such as written descriptions of inspection results including deviations
from engineering specifications
• Participating in weekly CAPA Review meetings, managing and issuing weekly CAPA status reports and ensuring CAPAs
are closed on time
• Assessing existing Quality Control Processes and identifying and implementing improvements

Authored and executed IQ, OQ and PQ protocols, and wrote reports summarizing the validation activities and deviations
resulted during execution and their closure with necessary root cause investigation per GMP regulations
• Ensured Risk Management Plan and Report follows QSR 820 and ISO 14971
• Authored test methods for some existing work instructions and developed strategies to validate them
• Resolved product complaints and initiated CAPAs
Jul’17- Jun’18: Zimmer Biomet, Warsaw, Indiana
As Quality Engineer
• Created Process Validation Plans, Process Maps, Process Requirements, PFMEA, protocols and reports for IQ, OQ, PQ,
and MVP’s for remediation of process and equipment
• Authored and managed Validation Matrices, Technical Reviews, PFMEA and Risk Files

Updated Device Master Records (DMR) as required to ensure that they were fully aligned with the procedures in force
as well as the DHF (s)
Jan’12 – Apr’14: Sandvik Asia Pvt. Ltd., Kolkata
As Engineer-MIS
• Ensured machinery and mechanical equipment operations including preventive maintenance equipment on engines,
motors, pneumatic tools, conveyor systems, and production machines; following diagrams, sketches, operations
manuals, manufacturer’s instructions, and engineering specifications; troubleshooting malfunctions.
• Conducted root-cause-analysis of problems observed in mechanical devices
• Identified and defective parts by dismantling devices; using hoists, cranes, and hand and power tools; examining form
and texture of parts
• Performed Fleet Planning, Financial Management, Information Verification
• Conducted Defect analysis and ensuring maintenance envelope is constantly being reviewed for improvement
Apr’10 – Jan’12: Sandvik Asia Pvt. Ltd., Kolkata
Sales Engineer
• Spearheaded the complete Mining Equipment sales activities for the Eastern part of the Country;
• Generated inquiry from customer ends and followed up for forthcoming project; coordinated design, modifications,
enhancements of products and sold Mining Equipment sales as per client specifications
• Managed Notice Inviting Tender’s pertaining to Various Govt. / Semi Govt. & Special enquires Pertaining to private sectors
• Administered Machine Application, Business operations, Order booking reports
• Generated Monthly Marketing Report & various business analysis reports
• Ensured service and maintenance Coordination with the branches
• Performed techno-commercial negotiation prior to order finalization
• Maintained healthy Customer Relationship (Discussion and finalization of contracts, invoicing and payment settlements
and availability of equipment)
• Created reports for tracking lead conversion at every step of the sales funnel and worked with the sales team for
plugging leaky funnels
• Led a team of engineers to meet the agreed targets; troubleshot business problems and implemented creative, highly
effective solutions
• Prepared instrument index, tender bidding and technical documents for project study
Jun’16 – Jun’17: CSS Tech Solutions, Chicago
As Intern Quality Engineer
Validation Protocols (IQ, OQ, PQ)
CAPA Audit, NCR, Root Cause Analysis (RCA)
Nonconformance Material Reports (NCMR)
Risk Management & Remediation Activities
QSR 21 CFR Part 820, ISO 13485, ISO 14971
Test Method Validation (TMV)
Gage (R&R) Statistical Process Controls (SPC)
Fish Bone, Fault Tree Analysis, 5-WHY Analysis
Supplier Scorecards, SCAR & Supplier Metrics
Minitab, (GD&T), Six-Sigma, Lean & Kaizen
Design Control, Design Changes
Statistical Process Controls (SPC)
AutoCAD, Lean certification, CSSGB, CQE
2015: Master’s in mechanical engineering from Texas A&M University-Kingsville
2009: Bachelor’s in mechanical engineering from Priyadarshini Institute of Engineering and Architecture,
Under Nagpur University, AICTE affiliated
Date of Birth
: 17th February 1985
| Languages Known
: 13248 Mossvine Dr,Frisco, TX 75035
: English, Bengali & Hindi

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