CV, Curriculum Vitae and Online Resumes Search

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Online Resumes with "cfr"

2 years oil field/ refinery operator experience. Few years in Landscaping/green industry.

Looking to utilize my experience in the landscape/green industry working and communicating with customers and seeking clientale. Open to use any of my on the job experience to obtain secured employment in the following fields: customer service, property management, sales, property maintenance, oil/gas industry. Open to all oppurtunities available. Education: Highschool graduate, with some college experience. Hazardou...

Tags for this Online Resume: oil/gas, property management, landcape/green industry

Sales Executive

Looking for sales or account management in the scientific vertical. I have over 15 years selling into Life Science, Pharmaceutical, Government, Educational and Chemical markets. Technical ability to sell complicated enterprise software to "C" level management. I take a consultative approach and would be considered a Hunter in the sales process.

Tags for this Online Resume: chromatography, Scientific Software, Scientific Distribution, HPLC, Life Sciences, 21 CFR Part 11, Validation, serevices, bio informatics, informatics, SDMS, technology, sales, hunter

QA/RA Manager / Senior Quality Engineer

I am seeking a like position with both challenge and room for unique contributions my background and experience can bring. I am willing to relocate for the right opportunity.

Ideal Companies: New Start-ups

Tags for this Online Resume: Company-Wide Quality Systems design, development & Certification to FDA/QSR, ISO13485 and all other associated regulatory requirements in both domestic and international markets for a broad range of Class I, II & III Medical Devices, Documentation/Data Control Management – CFR21 Part 11 Compliant, Develop/Manage Contractor-Supplier-Customer Partnerships (Internal & External) for Custom & Off-the-Shelf materials and components fabrication, assembly, sterilization, packaging, storage & distribution from Domestic & Global resources, Strategic Planning for Products / Budgets & P/L Responsibility, Lead Auditor for External QS Audits / Develop & Manage Internal Audit Programs, Post Market Surveillance Management, including Customer Service & Compliant Handling, for Continuous Improvement Program

Software Quality Specialist - 8 years experience

Results-oriented with reputation of critical quality analysis and enhancing customer satisfaction. Effective in streamlining processes to speed project deliverables.

Tags for this Online Resume: Software testing, Technical writing, Creative, Lean process, Quality, SDLC, Functional testing, Regression testing, 21 CFR Part 11, GMP, pharmaceutical, bug tracking

An innovator, a senior corporate executive with vast experience in aviation industry.

My career interest relates to landing an executive position (President, VP, or Director) in the aviation industry. Based on my skills in compliance with technical data, leadership and knowledge of US Title 14 CFR parts 91, 121, 135 and 145, I am confident that I would be a great addition to the company's management team to help the company with further success.

Tags for this Online Resume: Aviation Management, Airline Management, Aviation Repair Statton Management, Aviation Quality, Aviation Maintenance

sumary

In my almost 11 years of experience on safety and heath field, I develop skills including: leadership, self-taught individual, willing to learn and excellent in human relationships. My experience includes speaker in the AGC, auditing government project, pharmaceutical project inspection, complain file by CSHO agent, safety meeting, Attend the OSHA 29 CFR 1926 10 & 30 hour and developing OSHA outreach programs.

Tags for this Online Resume: ms word, ms excel, ms project, ms publicher, safety

Agricultural Technician

Tags for this Online Resume: capa, gmp, gdp, quality, cfr, fda

Senior Engineer - 20 years experience- Safety - Highway Applications

Seeking position in engineering where current engineering and practical knowledge will benefit employer, public and this individual.

Tags for this Online Resume: MSDS, JHA, HAZWOPER, OSHA HAZCOM, LOTO, 29 CFR

Laboratory operations manager 14 years experience cGMP 21CFR Quality Assurance Safety

I am looking for a pharmaceutical operations management position where I can utilize my advanced chemistry degree, expertise in quality assurance and background in safety compliance.

Tags for this Online Resume: Chemist, GMP, Quality, Safety, Compliance, Pharmaceuticals

Experienced Regional Manager/Sales Pro

Ideal Companies: Federal Government, Securitas, Sea Island Corporation, Southern Company

Tags for this Online Resume: Compliance, Sales, Security, Retail, Loss Prevention, Investigations, Implementation, CTPAT, MARSEC, 33CFR105

Senior Regulatory Writer (17 years experience)

I am seeking to end my present consulting status and return to an in-house position where continuity of projects is more realized. I have over 15 years experience writing regulatory medical documents that comprise CFR21 356h NDA/BLAs and eCTDs deliverables to the FDA/EU/Canadian regulatory authorities. I have written approximately 85 CSRs and can confidently say that ~40 of these were NCEs, early phase I/II and some pha...

Tags for this Online Resume: Regulatory Medical Writer Manager level

CTA

Seeking for a challenging career in a progressive organization offering the opportunity for contributing my skills services to the organization and personal growth and to work sincerely with maximum effort using best talents and with a challenge to achieve required goals and targets, abiding to the decisions of seniors and to earn a good reputation what ever required.

Tags for this Online Resume:  Develop, maintain and manage appropriate study documentation,  Developing, writing and presenting the clinical trial protocols,  Initiate, maintain and reconcile Trial Master File.,  Monitoring the trial throughout its duration which will involve visiting the Study centers on a regular basis to check the patient data in the case report forms (CRFs) and to sort out any problems which may arise.,  Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other Data collection tools by careful source document review Monitor data for missing of implausible data.,  Complete Serious Adverse Event (SAE) reporting, process production of Reports, narratives and follow up of SAEs and managing the clinical data intermilitently as per 21CFR USFDA guidelines,  Monitor study sites independently according to protocol monitoring guidelines, S.O.P.s, GCP and ICH Guidelines.,  Independently perform CRF review; query generation and resolution against established data review guidelines on client data management systems as assigned Perform other duties as assigned by management., , maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned