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  1. 1. Provide a clear description of your needs and your expectations of an expert, consultant or job candidate and Zintro will match it with the most relevant professionals in our platform.
  2. 2. Within a day or two typically 6 - 12 Experts, who have opted-in, will contact you with a brief explanation of their qualifications and how they can help.
  3. 3. You can communicate back and forth, qualify each other, connect and pay fees to Experts through Zintro.
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Recent Qa Inquiries

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Quality Assurance

Job title: quality assurance manager - manufacturing location: west chester, pennsylvania reports to: president competitive salary and benefits. Relocation offered for the right candidate. The quality assurance manager is responsible for the development and implementation of the systems that ensure that our products and processes are meeting their goals for quality and improvement, in accordance with the quality policy and iso – certified quality management system, (qms). In order to achieve these strategic goals, the qa manager will lead a team of quality assurance roving inspectors and final inspectors as well as serve as the management representative for the iso 13485 qms. The qa manager will also communicate with customers on quality and other issues to ensure that effective steps are taken to measure and improve customer satisfaction, and serve as principal contact for quality audits, surveys, and corrective actions. Confidentiality this position requires strict confidentiality. Access to company information will not be discussed with anyone inside or outside the company. Responsibilities **manufacturing support** - work with management to develop specific and measurable goals, improvements and standards to continuously and consistently improve quality and reduce errors. - act on behalf of the customer to audit and maintain the accuracy and timely delivery of products. - ensure that first article inspections, (fai’s), are performed in a timely manner throughout the day. - make sure that roving inspections are done at all work stations on a routine daily basis and results are reported back to the machinist. - see to it that final inspections are done in a thorough manner and in accordance with shipping requirements and scheduling. - maintain iso 9001 and 13485 medical device quality management system certifications and compliance. Additional details of job description available upon request. Qualifications: **must haves** - bs engineering or related discipline, or asq certification, or equivalent experience. - 10+ quality experience in a precision machining environment. - experience with implementing and maintaining iso 9000 certification. - knowledge of statistical process control practices. - willing to work 40 or more hours weekly. - basic computer knowledge. Familiarity with ms word, excel and outlook. **desired** - cnc / swiss experience please note: we are seeking to hire a full-time employee and are not interested in responses from those only interested in consulting.

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    Sumit |Zintro Expert

    Dear Ma’m / Sir, Sub: In Reference to your requirement for a Quality Assurance Professional This i...

    2.1 Hours Later
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    Ravindran |General Manager(Operations)

    I have expertise in Quality Assurance and can take up this assignment.Thanks...

    2.3 Hours Later
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    maulin |Zintro Expert

    Dear Sir, I would like to express my interest in applying for Quality assurance Manager position, my...

    2.5 Hours Later
+75 Other Responses
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Automation Qa Testing

"we are an authorized zintro partner and our client requires a:  qa testing leadcolumbus, oh 6+ months looking qa testing lead with automation testing experience. Must have: ruby, xml.Xquery or gherkinselenium, or cucumber if possible, please attach your cv/resume in your response here. -kiran"

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    Denis |Head of Sales

    Kiran we have resources that can do this on a contract basis. Our *****emely competitive and w...

    1.4 Hours Later
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    Mohd |Apache Ofbiz Expert

    We have a resource that has over 10 years of total experience and 6 years of QA Testing Lead exper...

    1.4 Hours Later
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    Mounir |Senior Test Manager, SAP Test Manager, I

    Resume attached...

    2.8 Hours Later
+7 Other Responses
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Lab Qa/qc Management

Looking for experienced qa/qc managers in laboratory setting to help understand calibration of liquid equipment handling (handheld pipettes and automated systems)

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    Jonathan |Principal

    Good Afternoon. Our firm has resources with ***** and QC experience and experience with cali...

    3.4 Hours Later
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    David |Director of Quality Assurance

    Our company has the ability to perform many services: We is a professional services firm focused on...

    3.7 Hours Later
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    Charles |Director of Quality Laboratories; Qualit

    I'm not a company but an independent consultant with over 20 years of quality *****rience...

    7.3 Hours Later
+9 Other Responses
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Commercial Quality Assurance In California

This is a full time opportunity in california: sr. Director, quality assurance - commercial overview: this position will have oversight and leadership of the commercial quality and quality systems teams and be responsible to meet compliance and quality assurance requirements for commercial pharmaceutical manufacturing. Responsibilities: -effectively employ the principles of ich q9 (risk management) and ich q10 (pharmaceutical quality system) -develop and lead a risk based quality management system. -build and maintain robust quality program that will effectively support commercial manufacturing. -provide leadership and managerial oversight to the quality departments responsible for quality systems and commercial quality. -administer commercial quality systems including: -deviation -capa -change control -vendor management -training -internal/external audits -document control -quality management review -annual product review -product/customer complaints quality oversight of contract manufacturing organizations including: -auditing -deviation/change control -batch record review -batch release provide support as necessary to the vp global quality regarding gmp readiness, quality related projects and issues/concerns on a global basis. -conduct ongoing evaluations of quality programs, systems and initiatives to assure that product quality standards and regulatory compliance are achieved. -interpret regulatory authority regulations, guidelines and policies. Utilize internal audits and quality compliance assessments programs to evaluate dynavax processes and procedures. -conduct regular risk assessments to ensure processes and procedures are in compliance with cgmps. -supervise and develop quality personnel including the heads of applicable functional teams. Appropriately resource regulatory inspections. -direct the review and approval of the quality manual, quality policies, protocols, sops, batch records, test methods, raw material specifications, and annual product reviews. -provide quality expertise as needed for deviations reports and out-of-specification reports. -ensure that manufacturing processes, equipment, facilities and systems are validated and that a robust change control system and procedures are developed and maintained to meet state, federal, and international requirements. -ensure that suppliers and contract manufacturers are operating in compliance with state, federal, and international gxp regulations and guidelines through an external audit program. -hire and/or develop the team to establish and maintain efficient and effective quality systems and programs. -develop operational budgets, cost controls, cost estimates, capacity and resource plans as well as facility requirements to support corporate strategic business objectives.. qualifications: -ba/bs in a relevant scientific discipline and a minimum of 15 years industry experience with 7+ years of management experience providing both strategic and leadership guidance to an organization in quality assurance. For senior director level consideration, must have at least 2 years’ experience at the director level. -must have a quality background from the biotechnology/pharmaceutical industry with gmp experience and a successful track record in quality within fda and/or emea regulated environment. -experience in quality management and compliance systems. -in-depth knowledge of qa document control, gxp compliance, and qa auditing. -experience in development qa associated with pre-clinical development and commercial products. --a background in the development of analytical methods preferred. -must have a successful track record in managing fda/eu inspections. Contact us here on zintro for further details.

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    Stefan |Senior Researcher

    I am more than interested of your job offer and despite the fact of being of the age of more than 60...

    5.9 Hours Later
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    Arun Kumar |Associate

    I am keen to explore the said opportunity. Please provide your e-mail address so that I can provide ...

    6.9 Hours Later
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    EMMANUEL |Managing Partner - Independent Contracto

    Kunda Emmanuel Kalaba Address: 1 Tanamerah Kechil Road Singapore – Postal Code ***** Email: kunda....

    5.6 Days Later
+11 Other Responses
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Qa Functional Tester

Hi,   this is pranesh from orgspire inc. We have an immediate opening with one of our client. Kindly confirm your interest by replying to this email with your updated resume and convenient time/number to discuss further.  title: qa functional tester location: glendale, ca  duration: 9 months with possibility of extension  interview process: phone and then in person interview is required   responsibilities: performs complex testing functions and tasks performs analysis of requirements, test coverage and impact of proposed requirements changes ensure that testing activities allow applications to meet business requirements and identify existing or potential issues create and maintain testing deliverables based on user requirements and technical specifications tests software in accordance with established quality standards prior to implementation to ensure proper operation and freedom from critical defects analyze test results in order to report any defects, bugs, errors or configuration issues. Communicate testing progress, test results, and other relevant information to management. Cultivate and disseminate knowledge of quality assurance best practices. Requirements: minimum of 4 years into quality assurance – desktop and mobile application testing experienced in designing , writing and executing manual test cases strong knowledge of sql queries experience in  web services testing highly desired automation scripting using qtp or selenium preferred preferred experience in usability testing bachelor's degree in business, computer science or information systems or equivalent business experience  effective oral, written, and interpersonal communication skills   thanks & regards   pranesh

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    JeanAnn |Lead SQA Engineer

    Hello; I am highly experienced in designing testing projects, test strategy, test cases, executing, ...

    16.1 Hours Later
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    Shahid |Principal Software Quality Assurance and

    Hi Pranesh, The opportunity seems appealing and I am interested to avail it. I did MS in Software S...

    19.3 Hours Later
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    Rod |Deputy Quality Assurance Manager.

    With my experience in ***** quality assurance I feel I would be an asset....

    20.2 Hours Later
+5 Other Responses
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Qa Automation

Currently looking for a qa expert for a project in emeryville ca one qa automation expert who can provide guidance on the increasing automation (suggest tools, process changes, etc.), especially on the server side. The server side of qa has more potential for automation as it does not need devices for testing. The duration and the skill set will be same as #1 this is a 5 weeks to start than extend to 4 to 6 months. Someone that can give assessment and make recommendations.

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    Imran |IT Program Manager

    I will be able to provide a UI based(Black-box ) testing framework for the product....

    33 Minutes Later
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    Gail |Software Quality Assurance /Test Analyst

    I would be happy to assist you with your QA *****ect. I have extensive experience in HP...

    5.9 Days Later
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    Jeff |President/CEO

    Hi, Do you expect this to be a full-time engagement (40 hours/week) both during the initial 5 week ...

    6.9 Days Later
+3 Other Responses
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Quality Assurance Service

Hello ,   this is mafas we have an immediate opening with one of our client. Kindly confirm your interest by replying to this email with your updated resume and convenient time/number to discuss further. In case if you are not currently available or not interested in the below position, i apologize for the inconvenience and request you to forward my mail to your friends or colleagues whom you feel would excel this opportunity   job details:    job title: qa- quality assurance location: pleasanton, ca terms: contract to hire   summary of experience :   ·         good experience in a linux and db2 (or similar sql) environment. ·         automation tool soap ui, java not required but a plus. ·         any deployment with anthil or jenkins a plus. ·         experience with transaction processing, particularly financial – also a plus     thanks & regards   mafas

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    Iulian |GM, Senior business Consultant, Program

    Hi, I am interested and available within 2 weeks. Note, I am a Romanian citizen, living in Romania. ...

    2.6 Hours Later
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    prem |Production manager

    I am very much interested to take up this project ...

    4.5 Hours Later
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    Murali |Chief Consultant

    Hi I am interested in this assignment. It is convenient for me if you can call before 12 noon EDT ...

    9.8 Hours Later
+5 Other Responses
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Quality Assurance Development In California

This is a sr. Director of quality assurance,development full time position opportunity in california. Overview: this position will have oversight and leadership of developmental quality assurance programs to meet phase appropriate compliance, validation, and gxp quality assurance requirements. Responsibilities: -establish and maintain a robust quality program that will effectively support the various phases of drug development – preclinical through phase 3, plus product/process improvements. -employ the principles of ich q8 (pharmaceutical development) and q9 (risk management) to the development of manufacturing processes. -ensure a systematic approach to development is employed that begins with pre-defined objectives and emphasizes product and process understanding and process control based on sound science and quality risk management. -provide leadership and managerial oversight to the quality department responsible for development qa. -establish and maintain a phase appropriate approach to product/process development qa. -as project team member, represent qa on product development teams including pre-clinical, phase 1, 2, and 3 development studies, and manufacturing improvement teams. -responsible for document review and qa release of ds/dp to be used in phase 1, 2, and 3 clinical studies. -responsible for phase appropriate quality systems implementation for ds/dp manufactured for use in phase 1, 2, and 3 clinical studies. -acts as technical advisor to vp global quality on topics related to development and commercial quality. -develop and implement effective development qa programs aligned with corporate strategic initiatives and business goals. -interpret regulatory authority regulations, guidelines and policies. Utilize internal audits and quality compliance assessments programs to evaluate processes and procedures as they pertain to product development activities. -must be able to maintain a “big picture” perspective without losing site of the details necessary to meet deliverables and deadlines. -supervise and develop quality personnel. -direct the review and approval of the applicable sops, batch records, test methods, raw material specifications. -provide quality expertise as needed for deviations reports and out-of-specification reports. -ensure that manufacturing processes, equipment, facilities meet phase appropriate gmp requirements. -ensure that suppliers and contract manufacturers associated with product/process development are operating in compliance with state, federal, and international gxp regulations and guidelines as necessary through an external audit program. -hire and/or develop the team to establish and maintain efficient and effective quality systems and programs as they relate to product/process development. -develop operational budgets, cost controls, cost estimates, capacity and resource plans to support corporate strategic business objectives. Qualifications: -ba/bs in a relevant scientific discipline and a minimum of 15 years industry experience with 7+ years of management experience providing both strategic and leadership guidance to an organization in quality assurance. For senior director level consideration, the ideal candidate must have at least 2 years’ experience at the director level. -must have a development quality background from the biotechnology/pharmaceutical industry. -experience in quality management and compliance systems. -in-depth knowledge development qa and experience implementing phase appropriate quality systems to achieve gxp compliance. Contact us here on zintro for further details.

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    Frederick |President

    Thank you for the opportunity- but this is way outside my area of expertise. Best wishes and good l...

    13.4 Hours Later
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    Monica |QA Specialist

    I`m interested in the proposal, please let me know where I can send you my resume. I have to say tha...

    21.9 Hours Later
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    Michael |CMSO , Chief Medical Strategies Officer

    Thanks...but i live in NY.....great opportunity!...

    1.7 Days Later
+13 Other Responses
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Us Banking Software Qa

We are an authorized zintro partner looking to better understand quality assurance in software testing development in the north american banking industry. Ideally i am looking to speak with an individual formerly in a qa role for a large us based bank. Specifically looking to understand software development/testing processes best practices including defining test scopes, resources, schedule, etc. And testing process in a pure agile environment/in an agile-like environment (some variation) including waterfall.

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    George |Consultant

    Hi... I worked for a large US/Canadian bank for 3 years as a Test Management Consultant. I am confi...

    47 Minutes Later
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    Erick |Associate Director

    Global models for systems ***** the key fact projects success. Support by the business ...

    2.5 Hours Later
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    John E. |Principal; Member-Manager

    My specialty is software testing / verification, ***** ***** meeting U.S. FDA C...

    4.8 Hours Later
+12 Other Responses
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Software Qa Process Improvement California

We need a software qa process improvement consultant to work with our team at a client site. This consultant should be able to : a) analyze and recommend a road-map to re-implement hp alm projects including defining the asset workflows,/lifecycle, field creation and behavior customization,, and designing targeted metric/reporting output. B) analyze and recommend the best defect escape analysis approach given the customer's unique environment and future process changes c) analyze and recommend the best approach to calculating cost of quality including process and tool changes. Additional concerns: > this person should be willing to travel short term to spend time with client resources during the discovery and implementation phases. > this person should demonstrate strong interpersonal skills and the ability to work as an individual contributor. We are not implementing based on client direction; we are setting direction. > this person should have advanced qa experience and have contributed to the community via conference participation, white page publications, or some similar demonstration of thought leadership. If this sounds interesting to you, kindly respond with a brief description of your background and relevant experience. Thank you.

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    Balu |Independent Consultant / Freelancer

    Hi, I will help you but i am ***** India. Let me know client place . Thanks balu...

    18.8 Hours Later
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    Purvi |Senior Software Testing Specialist

    Hi, I am highly interested to work Software QA Process Improvment. Please let me know. I have worke...

    22.8 Hours Later
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    SUNIL |Vice President

    I want understand what is period of engagement ,do you offer sponsorship or take consultant on contr...

    1 Day Later
+24 Other Responses
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Laboratory Quality Assurance In Uae

Job title: qa director this job post has been authorized by zintro. **job overview**: - this is a responsible, professional, supervisory, and technical position in the administration of a specific department of the medical laboratory. - the quality assurance director plans and directs the quality management system programs and practices of the lab to ensure patient safety, compliance with all local and international accreditation standards, and scientific best practices. - the director works closely with all members and levels of the our team to ensure compliance with the aforementioned. Responsibilities are performed with considerable independence with accountability to the medical director and the chief executive officer. **key job summary**: - ensure the overall quality of services rendered to laboratory clients relative to reliability, accuracy, and precision. - provide proactive leadership in the identification and rapid resolution of problem issues which adversely affect quality - direct quality programs including the implementation of policies and systems which lead to continuous quality improvement. - promote a culture of quality throughout the laboratory system through communication and increased quality awareness. - direct the daily operations of the qa/qc department. - maintain standard performance of laboratory staff and technical operations to ensure accurate and consistent testing procedures. - train, mentor, and evaluate laboratory staff to ensure quality control, safety, and record maintenance, in coordination with technical leadership. - ensure every laboratory is inspection-ready. ** preferred experience**: - communicate qa programs to technical and administrative staff. - establish standard operating procedures and safety standards - knowledge of cap / jci / iso 15189 accreditation requirements - international certification on quality management (preferred) - american society of clinical pathologists (ascp) certified iso 15189 experience. - work autonomously **minimum qualifications and experience**: - bsc in medical technology with appropriate clinical internship/ laboratory technology or biomedical science - minimum of seven (7) years as a quality assurance manager/director in a college of american pathologists accredited laboratory.

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    Michael |Senior Principal Consultant

    I would love to be considered for this role...

    2.4 Hours Later
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    Babatunde |Senior HSE Engineer

    I have interest and available in the UAE for this job-opening of "*****ity Assurance". Ple...

    1 Day Later
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    Zerela |Owner & CEO

    I'm interested in this opportunity. Please contact me....

    2.8 Days Later
+3 Other Responses
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Strawberry Qa

I am conducting a search for a very good company in the monterey bay area. They have an opening for a qa manager for berries. They would prefer strawberries if possible and bilingual. The company is a billion plus respected organization. The office is in watsonville, ca, but the responsibilities are for the west coast. Compensation - 60 to 100k. If you know of anyone looking, please pass this along. Thanks

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    Nisar |Manager

    If u need Agricultural training expert , I can help. amr _ nisar @ hot mail com...

    17.8 Days Later
+1 Other Responses
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