Quality Assurance Engineer - Senior Associate

Pwc Tampa , FL 33602

Posted 2 months ago

A career in our Innovation Development practice, within Innovation services, will provide you with the opportunity to help our clients' redesign, redefine, and redeploy their assurance and/or tax departments to be a strategic asset across the enterprise. You'll focus on assisting clients as they incorporate increased automation, machine learning, data & analytics, Open Source technologies into their processes to deliver better quality output and contribute more strategically to organisational decision making. Our team helps our clients create a guided path to innovation by developing the right methods that generate insight based ideas, and to select, produce and commercialise the most valuable and viable results. You'll focus on software driven innovation strategy, software technology diligence, operating model design, software product planning and management, and software architecture and cloud strategy.

Responsibilities

As a Senior Associate, you'll work as part of a team of problem solvers with extensive consulting and industry experience, helping our clients solve their complex business issues from strategy to execution. Specific responsibilities include but are not limited to:

  • Proactively assist in the management of several clients, while reporting to Managers and above

  • Train and lead staff

  • Establish effective working relationships directly with clients

  • Contribute to the development of your own and team's technical acumen

  • Keep up to date with local and national business and economic issues

  • Be actively involved in business development activities to help identify and research opportunities on new/existing clients

  • Continue to develop internal relationships and your PwC brand

Job Requirements and Preferences:

Basic Qualifications:

Minimum Degree Required:

Bachelor Degree

Required Fields of Study:

Computer and Information Science, Computer Engineering, Computer Programming, Engineering, Management Information Systems, Systems Engineering

Minimum Years of Experience:
3 year(s)


Required Knowledge and

Skills:

Demonstrates thorough abilities and/or a proven record of success as a team leader including:

  • Developing and leading the automation strategy/effort and generate scripts to perform automated testing cycles using Selenium & similar tools;

  • Demonstrating in depth experience in building custom test automation frameworks and automation scripts for BVT, FVT and regression testing solutions for Continuous Integration/Continuous Delivery process;

  • Demonstrating experience in leading/mentoring other engineers in building and deploying test automation frameworks; and,

  • Demonstrating ability to work closely with development teams designing requirements, test plans and strategy in an Agile environment.

Preferred Qualifications:

Preferred Knowledge/Skills:

Demonstrates a thorough level of abilities with, and/or a proven record of success as both an individual contributor and team member, identifying and addressing client needs by:

  • Demonstrating ability to work cross-functionally with multiple teams and stakeholders and to juggle multiple time-sensitive projects efficiently;

  • Demonstrating account management, follow-through, resourcefulness, attention to detail, and verbal and written communication skills;

  • Demonstrating ability to collaborate with multiple diverse groups across teams;

  • Demonstrating ability to work on multiple projects at one time;

  • Demonstrating interpersonal and collaboration skills in both oral, written communication, and presentations skills as evidenced by publications or cover letter; and,

  • Demonstrating analytical and problem-solving skills.

All qualified applicants will receive consideration for employment at PwC without regard to race; creed; color; religion; national origin; sex; age; disability; sexual orientation; gender identity or expression; genetic predisposition or carrier status; veteran, marital, or citizenship status; or any other status protected by law. PwC is proud to be an affirmative action and equal opportunity employer.


icon no score

See how you match
to the job

Find your dream job anywhere
with the LiveCareer app.
Mobile App Icon
Download the
LiveCareer app and find
your dream job anywhere
App Store Icon Google Play Icon
lc_ad

Boost your job search productivity with our
free Chrome Extension!

lc_apply_tool GET EXTENSION

Similar Jobs

Want to see jobs matched to your resume? Upload One Now! Remove
Quality Assurance Associate

Osmotica Pharmaceuticals Plc

Posted 1 week ago

VIEW JOBS 4/12/2019 12:00:00 AM 2019-07-11T00:00 Position Overview The QA Associate is responsible for supporting Trigen and contract manufacturing and packaging organizations (CMO, CPO) activities in order to meet cGMPs (21 CFR 111 and 211), quality specifications and company goals. Perform day to day technical activities supporting CMO/CPO for dietary supplements and drug product manufacturing, i.e. review and approval of documentation (batch manufacturing record and/or packaging, deviation, investigation, etc.), process changes, trouble shooting and improvements. The QA Associate position will need a robust understanding of applicable regulations, standards, and applicable company policies and procedures to ensure compliance. The QA Associate performs quality related activities of diverse scope, makes decisions and implements those actions in partnership with other departments at the site. This position will escalate compliance issues to QA Management. Duties and Responsibilities * Perform documentation review (i.e. batch manufacturing and/or packaging records, Certificate of Compliance, Certificate of Analysis, etc.) with high attention to detail using working knowledge of quality concepts and internal procedures. Based on review, perform product release and disposition within company ERP system. * Initiate, write, drive/lead deviations and investigations to ensure that all critical and major quality issues are thoroughly addressed and documented with appropriate associated CAPA. * Participate in Change Control activities affecting procedures, processes and systems. * Receive product quality complaints and perform activities to lead to closure and customer satisfaction. * Write, review, and approve standard operating procedure (SOPs) and other applicable operation related GMP documents. * Support and participate in trending of quality measures, CAPA plans, and annual reports. * Escalate potential issues and concerns immediately to QA Management. * Participate and assist in the GMP auditing program for internal and external audits including FDA, DEA, and FL-DBPR. * Support the development, improvement and maintenance of Quality Systems including procedure development, process mapping in collaboration with other technical and business areas. * Guide, develop and train others in areas of subject matter expertise. * Follow and complete training according to the assigned training curricula. Execute and perform those activities that have been trained * Accomplish quality and organization goals by completing related activities as assigned, thoroughly and in a timely manner. * Maintain a safe and healthy work environment by following written standards and procedures; complying with applicable regulatory requirements. * Prompt and regular attendance. Other duties as assigned by senior management. Requirements * Bachelor's Degree in Science or Engineering or relevant scientific discipline from an accredited college or university. * Minimum of three (3) years' experience in pharmaceutical quality assurance or quality. * Strong knowledge of cGMPs (21 CFR 111, 211) and related FDA and International Conference on Harmonization (ICH) guidance documents. * Good written and verbal communication and problem solving skills. * Proficiency in MS Word, Excel, PowerPoint, and Outlook. * Proficiency in English usage, spelling, grammar and punctuation. * Effective planning and organizational skills. * Requires flexibility and ability to multi-task. About Us Osmotica Pharmaceutical is a global specialty pharmaceutical company with a proven history of developing commercially successful pharmaceutical products using a proprietary osmotic technology platform. In February 2016, Osmotica Pharmaceutical combined with Vertical Pharmaceuticals, LLC and Trigen Laboratories, LLC to create a world-class, fully-integrated specialty pharmaceutical and generics company. Vertical Pharmaceuticals, LLC was founded in 2003 with a mission to develop, market, and acquire products offering therapeutic benefits for patients and healthcare providers. Vertical Pharmaceuticals supplies branded prescription products, specializing in Neuroscience and Women's Health with brands such as Lorzone®, Divigel®, and OB Complete®. Trigen Laboratories, LLC is a generic pharmaceutical company offering unique products across an increasing array of categories. Trigen seeks to bring value-driven generic products to its customers, working vigorously with its partners to identify and develop products which face an assortment of challenges. Additionally, Trigen identifies unique marketing opportunities and is steadfast in its pursuit to deliver products to best serve these markets. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, national origin, age, disability or veteran status. Osmotica Pharmaceuticals Plc Tampa FL

Quality Assurance Engineer - Senior Associate

Pwc