UNKNOWN

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OTHER

This position reports to the Director, Analytical Research and Development and will manage develop analytical methods and test various drug substances and drug products to support Medicinal Chemistry, Translational, Manufacturing, and CDMOs. The Chemist / Senior Chemist Analytical Method Development will serve as a key member of our development team, working on-site full-time, in our Redwood City laboratory, focusing on novel early and late-phase programs.

Programmable Medicine, a clinical stage biopharmaceutical company located in Redwood City, is seeking a motivated Chemist/Sr. Chemist Analytical Method Development. We are focused on developing novel nanomedicines, HD therapeutics (HDTs), to treat unmet medical needs in ophthalmology, neurology, inflammatory diseases, and neuro-oncology. Our HD platform builds therapeutics that are selectively taken up only by inflamed tissues, allowing us to treat diseases with unprecedented precision. This position reports to the Director, Analytical Research and Development and will manage develop analytical methods and test various drug substances and drug products to support Medicinal Chemistry, Translational, Manufacturing, and CDMOs. The successful candidate will be part of a dynamic, interdisciplinary team and require a high degree of creativity and initiative. This is an exciting opportunity to help drive the development of novel therapies for unmet medical needs in multiple indications. The Position The Chemist / Senior Chemist Analytical Method Development will serve as a key member of our development team, working on-site full-time, in our Redwood City laboratory, focusing on novel early and late-phase programs. Duties and Responsibilities - Essential Functions · Manage stability study and trend analysis such as design/review stability studies, prepare/review protocols, and monitor ongoing stability studies in-house and at various CDMOs. Develop various analytical methods.· Test various drug substance/drug product samples.· Manage, set up, and maintain all instruments in the analytical lab.· Keep and accurately maintain detailed electronic laboratory notebooks.· Perform tasks per protocols as required.· Additional responsibilities may be added as required. Job Requirements · BS degree in Chemistry, Analytical Chemistry, or closely related scientific area is required along with a minimum of 5 years of pharmaceutical industry experience.· In-depth expertise with stability study, analytical method development and validation with HPLC, UPLC. · Expertise in HPLC, HPLC/UPLC, LC-MS, SEC, and ICP-MS analytical techniques is preferred.· Prior experience with analytical method development and validation for small molecule drugs.· Experience with analytical method development and various tests for polymer-drug conjugates and/or biologics drug candidates are preferred.· Experience with injectable and oral dosage forms· Independent, problem-solving, and troubleshooting skills.· Knowledge of GLP & GMP requirements· Well organized and self-directed· Ability to communicate scientific findings and recommendations in one-on-one discussions, departmental meetings, and prepare reports.· Ability to work in a fast-paced, dynamic environment with multiple projects and priorities.· Must be able to work on site at our Redwood City facility, five days per week. About Programmable Medicine This is a unique opportunity to join a team focused on the development of a new class of precision medicines that selectively treat diseased cells in regions of inflammation. By making precision medicine even more precise, our nanomedicine technology has the potential to change the standard of care across ophthalmology, neurology, inflammatory diseases and neuro-oncology. You will have the opportunity to learn new skills and gain a better understanding of cutting-edge technology. We have a comprehensive compensation package including fully paid medical, dental and vision benefits for you and your family. We want our employees to become shareholders and offer new hire stock options. The company also offers participation in the annual bonus program. The salary range for MS candidates located in the Bay Area, with a minimum of 8 years of industry experience is $95,000 - $128,000, depending on years of experience and relevant skill sets.

Programmable Medicine Operatin

Chemist / Senior Chemist - Analytical Method Development

Analysis Skills

Analytical Chemistry

Analytical Development

Analytical Method Development

Analytical Method Validation

Biotech and Pharmaceutical

Chemistry

Clinical Medicine

Communication Skills

Disease

Dosage Forms

Drug Products

GLP (Good Laboratory Practices)

GMP (Good Manufacturing Practices)

High Performance Liquid Chromatography (HPLC)

Identify Issues

Inductively Coupled Plasma Mass Spectrometry (ICP-MS)

Inflammatory Diseases

Laboratory Notebook

Leading Edge Technology

Liquid Chromatography-Mass Spectrometry (LC-MS)

Manufacturing

Medical Products

Medical Treatment

Medicine

Multitasking

Neurology

Oncology

Ophthalmology

Organizational Skills

Polymers

Problem Solving Skills

Product Support

Reporting Skills

Research & Development (R&D)

Securities and Exchange Commission (SEC)

Small Molecule Drugs

Stability Analysis

Test Plan/Schedule

Trend Analysis

Trinet ATS Feed

Performing root cause investigations on failing or underperforming materials/components by scientifically examining the development, manufacturing or end-use environment of products specified for use in the construction, medical device, consumer electronics, and pharmaceutical industries. For over five decades, we've connected the lessons of past failures with tomorrow's solutions to advise clients as they innovate technologically complex products and processes, ensure the safety and health of their users, and address the challenges of sustainability.

YEAR

About Exponent:
<a href="https://www.exponent.com/" rel="noopener nofollow noreferrer" target="_blank">Exponent</a> is the only premium engineering and scientific consulting firm with the depth and breadth of expertise to solve our clients’ most profoundly unique, unprecedented, and urgent challenges.   Our vision is to engage multidisciplinary teams of science, engineering, and regulatory experts to empower clients with solutions that create a safer, healthier, more sustainable world. For over five decades, we've connected the lessons of past failures with tomorrow's solutions to advise clients as they innovate technologically complex products and processes, ensure the safety and health of their users, and address the challenges of sustainability.   Join our team of experts with degrees from top programs at over 500 universities and extensive experience spanning a variety of industries. At Exponent, you’ll contribute to the diverse pool of ideas, talents, backgrounds, and experiences that drives our collaborative teamwork and breakthrough insights. Plus, we help you grow your career through mentoring, sponsorship, and a culture of learning. Thanks for your interest in joining our team!    Key statistics: <ul><li>950+ Consultants </li><li>640+ Ph.D.s </li><li>90+ Disciplines </li><li>30+ Offices globally </li></ul>

Our Opportunity:
We are currently seeking a Chemist/Polymer Scientist for our <a href="https://www.exponent.com/expertise/polymers-chemistry" rel="noopener nofollow noreferrer" target="_blank">Polymers & Chemistry</a> Practice in Menlo Park, CA. In this role you will work as part of an interdisciplinary team contributing to a diverse set of projects from industries such as pharmaceutical, medical device, consumer products, construction, infrastructure and automotive. This position requires some travel and will involve collaborating with scientists and engineers from other Exponent offices and practices. A long-term goal for a successful candidate will be to develop business by obtaining new projects and bringing new clients to the firm.  

You will be responsible for:
<ul style="margin-top:0in"><li style="color:black;margin-bottom:0in;font-family:'arial' , 'helvetica' , sans-serif;font-size:12pt">Inspecting, testing and analyzing various polymeric materials to assess their specifications and/or reliability in a variety of applications from a wide range of industries</li><li style="color:black;margin-bottom:0in;font-family:'arial' , 'helvetica' , sans-serif;font-size:12pt">Performing root cause investigations on failing or underperforming materials/components by scientifically examining the development, manufacturing or end-use environment of products specified for use in the construction, medical device, consumer electronics, and pharmaceutical industries</li><li style="color:black;margin-bottom:0in;font-family:'arial' , 'helvetica' , sans-serif;font-size:12pt">Analyzing information and conveying technical conclusions to individuals in engineering, business, law, and industry, as well as communicating testing rationale in the context of product development, product defect claims, and intellectual property disputes</li></ul>

You will have the following skills and qualifications:
<ul style="margin-top:0in"><li style="color:black;margin-bottom:0in;font-family:'arial' , 'helvetica' , sans-serif;font-size:12pt">Ph.D. in Chemistry, Polymer Science, Materials Science, or a related field  </li><li style="color:black;margin-bottom:0in;font-family:'arial' , 'helvetica' , sans-serif;font-size:12pt">Well-developed understanding of small molecule, polymer and materials characterization</li><li style="color:black;margin-bottom:0in;font-family:'arial' , 'helvetica' , sans-serif;font-size:12pt">Knowledge of polymer bulk physical properties, and/or polymer processing preferred</li><li style="color:black;margin-bottom:0in;font-family:'arial' , 'helvetica' , sans-serif;font-size:12pt">Strong background and hands-on experience in polymer/chemical characterization techniques, such as FTIR, GC-MS, LC-MS, GPC, NMR, ICP-MS, ICP-OES, DSC, TGA, and DMA.</li><li style="color:black;margin-bottom:0in;font-family:'arial' , 'helvetica' , sans-serif;font-size:12pt">Knowledge of medical device testing and manufacturing standards, such as ISO 10993, ISO 13485, ISO 14971</li><li style="color:black;margin-bottom:0in;font-family:'arial' , 'helvetica' , sans-serif;font-size:12pt">Experience with the design, assembly, and execution of novel or non-standard testing  </li><li style="color:black;margin-bottom:0in;font-family:'arial' , 'helvetica' , sans-serif;font-size:12pt">Excellent verbal and written communications skills </li><li style="color:black;margin-bottom:0in;font-family:'arial' , 'helvetica' , sans-serif;font-size:12pt">Must be able to convey complex technical information to individuals in engineering, business, legal and related industries</li><li style="color:black;margin-bottom:0in;font-family:'arial' , 'helvetica' , sans-serif;font-size:12pt">Ability to work within project teams with strong desire to contribute; have potential for technical and project managerial leadership</li><li style="color:black;margin-bottom:0in;font-family:'arial' , 'helvetica' , sans-serif;font-size:12pt">Strong educational and publication credentials</li><li style="color:black;margin-bottom:0in;font-family:'arial' , 'helvetica' , sans-serif;font-size:12pt">This is a Menlo Park, CA -based position. The successful applicant must live in (or be willing to relocate to) the Menlo Park, CA area AND be enthusiastic about regularly working in the office</li><li style="color:black;margin-bottom:0in;font-family:'arial' , 'helvetica' , sans-serif;font-size:12pt">Presently legally authorized to work in the United States.  No immigration sponsorship or processing required</li></ul> Applicants are encouraged to submit a CV (Curriculum Vitae) with publications (feel free to include publications that are in review or pending) [not restricted to 1 page].

Life @ Exponent:
To learn more about life at Exponent and our impact, please visit the following links: <a href="https://www.exponent.com/careers/life-exponent" rel="noopener nofollow noreferrer" target="_blank">https://www.exponent.com/careers/life-exponent</a> <a href="https://www.exponent.com/company/our-impact" rel="noopener nofollow noreferrer" target="_blank">https://www.exponent.com/company/our-impact</a> Attracting, inspiring, developing, and rewarding exceptional people with diverse backgrounds and expertise are central to our corporate culture. Our diverse team allows us to provide better value to our clients and enjoy an enriched work environment.   Our firm is committed to offering a variety of programs and resources to support health and well-being. We believe that providing competitive benefits as well as compensation and recognition programs empowers our staff to do work that makes a difference. 

Work Environment:
At Exponent, we have found that in-person interactions deepen employee engagement and are crucial for development, for realizing the full potential of our talented and diverse teams, and for​ building a more inclusive workplace where all have a sense of belonging. In our offices, you can expect a supportive culture and a collaborative, dynamic, multi-disciplinary work environment.Our consultants engage in-person in the office unless they are traveling for client work or other business activities.  We value the rich lives our colleagues enjoy outside of work and understand that work/life balance is critical to our employees and their well-being. Consultants have the autonomy to balance their work and personal schedules so you can meet with clients, visit inspection sites, attend conferences, and make time for priorities outside of work, too. It is this flexible, agile work style and working hours that allow our teams to drive innovation and results in their own ways, while meeting the needs of clients. #LI-Onsite

Compensation:
Our consultants are rewarded for their technical and business contributions and have an opportunity to plan for future success and career growth. Exponent's total compensation plan is consistent with its expectations of the quality and quantity of work performed and with the professional standards set by Exponent. At the Associate and Senior Associate level, total compensation includes base salary, bi-weekly bonuses for high-intensity efforts, annual bonus and 401(k) employer contribution of 7% of base salary. The base salary range for this position is dependent on experience and capabilities which will be assessed during the interview process.

Salary Range:
USD $140,000.00 - USD $162,000.00 /Yr.

Benefits you will enjoy:
<div>Access benefits information on our Life@Exponent page: </div><div><a href="https://www.exponent.com/careers/life-exponent" rel="noopener nofollow noreferrer" target="_blank">https://www.exponent.com/careers/life-exponent</a>  </div><div>Exponent is a proud equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, veteran status, disability, sexual orientation, gender identity, or any other protected status.  </div><div>If you need assistance or accommodation due to a disability, you may email us at HR-Accommodations@exponent.com.  </div>

Job Locations:
US-CA-Menlo Park

Exponent Inc.

Chemist/Polymer Scientist (Ph.D.)

Business Development

Business Law

Compensation and Benefits

Conferences

Construction

Consulting

Consumer Electronics

Cross-Functional

Diversity

Fourier-Transform Infrared Spectroscopy (FTIR)

Gas Chromatography-Mass Spectrometry (GC-MS)

ISO (International Organization for Standardization)

Infrastructure Construction

Intellectual Property (IP)

Leadership

Legal

Material Science

Materials Analysis

Medical Equipment

Medical Tests

Mentoring

Nuclear Magnetic Resonance

Presentation/Verbal Skills

Product Development

Regulations

Root Cause Analysis

Safety/Work Safety

Small Molecules

Sustainability

Team Player

Testing

Willing to Travel

Writing Skills

[AW]-iCims

About Us:
Rivian is on a mission to keep the world adventurous forever. This goes for the emissions-free Electric Adventure Vehicles we build, and the curious, courageous souls we seek to attract.  As a company, we constantly challenge what’s possible, never simply accepting what has always been done. We reframe old problems, seek new solutions and operate comfortably in areas that are unknown. Our backgrounds are diverse, but our team shares a love of the outdoors and a desire to protect it for future generations. 

Responsibilities:
<ul><li>Lead the development for adhesives, seals, potting, and thermal interface materials (TIMs) for high-performance battery packs. </li><li>Leverage your deep chemistry expertise to develop novel formulations while benchmarking market-leading solutions. </li><li>Identify materials opportunity by establishing key metrics, such as, cost, performance, reliability, and safety </li><li>Conduct hands-on characterization (DSC, TGA, DMA) to identify failure modes and optimize adhesion, sealing, dielectric, and thermal performance. </li><li>Collaborate closely with cross-functional teams specializing in module and pack design, simulation, manufacturing, and Supply Chain to balance performance, cost, reliability, and safety. </li><li>Document data and analysis clearly and make presentations to communicate findings to stakeholders and leadership</li></ul>

Qualifications:
<ul><li>BS with 5+ years, MS with 3+ years, or a fresh PhD in Chemistry, Materials Science, or Chemical Engineering with a focus on polymer chemistry. </li><li>Experienced in polymer formulation/chemistry of acrylics, polyurethanes, silicones, and epoxies with strong knowledge of the interplay between polymer backbones, chain length, and mechanical/thermal/environmental functionality. </li><li>Proven ability to quantify adhesive joint integrity, CTE matching, flame retardancy, and environmental performance </li><li>Proficient in a wide array of characterization techniques such as DSC, TGA, DMA, rheometry, FTIR, and Instron. </li><li>Strong project planning and execution skills, with the ability to define clear objectives, break down complex tasks, and establish realistic timelines for successful project delivery.</li><li>Effective communication skills, with the ability to summarize and present insights from large datasets clearly and concisely. </li><li>Availability to travel up to 25% to collaborate with material suppliers and internal manufacturing sites, ensuring seamless technology transfer from the R&D lab to high-volume production.</li></ul>

Pay Disclosure:
The salary range for this role is USD 117,200 - 146,500 for California based applicants. This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to, specific competencies, relevant education, qualifications, certifications, experience, skills, geographic location, shift, and organizational needs. The successful candidate may be eligible for annual performance bonus and equity awards. We offer a comprehensive package of benefits for full-time and part-time employees, their spouse or domestic partner, and children up to age 26, including but not limited to paid vacation, paid sick leave, and a competitive portfolio of insurance benefits including life, medical, dental, vision, short-term disability insurance, and long-term disability insurance to eligible employees. You may also have the opportunity to participate in Rivian’s 401(k) Plan and Employee Stock Purchase Program if you meet certain eligibility requirements. Full-time employee coverage is effective on their first day of employment. Part-time employee coverage is effective the first of the month following 90 days of employment. More information about benefits is available at <a href="http://rivianbenefits.com" target="_blank" rel="noopener">rivianbenefits.com</a>. You can apply for this role through <a href="http://careers.rivian.com" target="_blank" rel="noopener">careers.rivian.com</a> (or through <a href="http://internal-careers-rivian.icims.com" target="_blank" rel="noopener">internal-careers-rivian.icims.com</a> if you are a current employee). This job is not expected to be closed any sooner than March 20, 2026.

Company Statements:
<h4>Equal Opportunity</h4>Rivian is an equal opportunity employer and complies with all applicable federal, state, and local fair employment practices laws. All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, ancestry, sex, sexual orientation, gender, gender expression, gender identity, genetic information or characteristics, physical or mental disability, marital/domestic partner status, age, military/veteran status, medical condition, or any other characteristic protected by law. Rivian is committed to ensuring that our hiring process is accessible for persons with disabilities. If you have a disability or limitation, such as those covered by the Americans with Disabilities Act, that requires accommodations to assist you in the search and application process, please email us at <a href="mailto:candidateaccommodations@rivian.com?subject=Application%20to%20Rivian%20-%20Assistance%20Request" target="_blank" rel="noopener">candidateaccommodations@rivian.com</a>.<h4>Candidate Data Privacy</h4>Rivian may collect, use and disclose your personal information or personal data (within the meaning of the applicable data protection laws) when you apply for employment and/or participate in our recruitment processes (“Candidate Personal Data”). This data includes contact, demographic, communications, educational, professional, employment, social media/website, network/device, recruiting system usage/interaction, security and preference information. Rivian may use your Candidate Personal Data for the purposes of (i) tracking interactions with our recruiting system; (ii) carrying out, analyzing and improving our application and recruitment process, including assessing you and your application and conducting employment, background and reference checks; (iii) establishing an employment relationship or entering into an employment contract with you; (iv) complying with our legal, regulatory and corporate governance obligations; (v) recordkeeping; (vi) ensuring network and information security and preventing fraud; and (vii) as otherwise required or permitted by applicable law.  Rivian may share your Candidate Personal Data with (i) internal personnel who have a need to know such information in order to perform their duties, including individuals on our People Team, Finance, Legal, and the team(s) with the position(s) for which you are applying; (ii) Rivian affiliates; and (iii) Rivian’s service providers, including providers of background checks, staffing services, and cloud services.  Rivian may transfer or store internationally your Candidate Personal Data, including to or in the United States, Canada, the United Kingdom, and the European Union and in the cloud, and this data may be subject to the laws and accessible to the courts, law enforcement and national security authorities of such jurisdictions.   Please note that we are currently not accepting applications from third party application services.

Rivian

Sr. Polymer Chemist

Adhesives

Background Investigation

Benchmarking

Chemical Engineering

Data Analysis

Data Sets

Demographics

Disability Insurance

Information/Data Security (InfoSec)

Metrics

Production Volume

Project Execution

Project Planning

Reference Verification

Simulation

Social Media

Supply Chain

PERMANENT

Never stop experimenting and learning with Qualitest Tech academy: 3000+ training courses, mentorship programs, technical tribes, sponsored certifications, leadership programs and much more. •Hands on experience with instrument hardware, software, assay chemistry related to high pressure liquid chromatography and or immunoassays, ELISA or similar technologies.

<div>Are you interested in working with the World’s leading AI-powered Quality Engineering Company? Ready to advance your career, team up with global thought leaders across industries and make a difference every day? Join us at Qualitest!We are looking for a Junior Chemist to join our growing team in Hercules, CA!Role - Junior ChemistLocation - Hercules, CA (on-site) Job Description <ul><li>Assist in the creation of serum/plasma autoimmune and infectious diseases samples for Clinical Diagnostic verification and validation.</li><li>Execute experimental protocols with guidance from senior team members.</li><li>Assist in data analysis and documentation of the experimental results.</li><li>With guidance from senior team members identify and resolve technical challenges that may arise during sample development.</li><li>Assist and collaborate with a team of research scientists and associates to achieve shared goals.</li></ul> What the Candidate Brings: •Education: Bachelor’s degree in life science or related discipline (Biochemistry, Biotechnology, Chemistry, Biological Sciences, etc.)•Work Experience: 0-2 years of relevant laboratory experience. Experience performing verification and validation studies is a plus.•Coordinate, prioritize and plan lab tasks to meet deadlines.•Ability to work in a team and make decision of limited scope, subject to review.•Hands on experience with instrument hardware, software, assay chemistry related to high pressure liquid chromatography and or immunoassays, ELISA or similar technologies.•Working knowledge of Microsoft Office tools – Excel and Word.•Committed to customer satisfaction; quality focused; resourceful; able to work independently and in a team environment. Why QualiTest?<ul><li>Be a part of a company who strives to support for diversity and inclusion in the workplace – we are one, we are many at Qualitest. Celebrate culture, share knowledge with engineers from around the globe, and inspire each other through our differences.</li><li>Local and global opportunities – we offer you internal rotation and international mobility opportunities to grow your career.</li><li>Clear view of your career and progression with the company – Qualitest is growing massively and giving you the opportunity to grow with us.</li><li>Work hard and play harder with our flexible and casual culture. Take a break from work and join an employee event, or enjoy the amenities and games provided from one of our Employees Centers.</li><li>Save your earnings and prepare for your future by enrolling in our 401k plan where Qualitest will match your contributions accelerating your savings plan.</li><li>Take care of health with enrollment into one of our competitive healthcare benefits. Qualitest will match towards your HSA if you choose to participate.</li><li>Never stop experimenting and learning with Qualitest Tech academy: 3000+ training courses, mentorship programs, technical tribes, sponsored certifications, leadership programs and much more</li><li>Stay active and get rewarded with our Corporate Wellness Program. We pay your Gym membership and giving you opportunities to Earn additional vacation times for attendance the gym!</li><li>Salary of $80,000 annually. </li><li>Earn bonuses via our Client Referral and Employee Referral Program’s. Refer and earn – tap your network for net-worth.</li><li>Planning a vacation? Looking for car insurance? Get access to Qualitest Employee Perks for discounts on anything from travel to electronics. With so many offerings the savings are endless!</li></ul>Intrigued to find more about us?<ul><li>Visit our website at <a href="https://www.qualitestgroup.com/careers/" rel="nofollow">Careers - Qualitest Group</a></li></ul>If you like what you have read, send us your resume and let’s start talking!</div><div>Are you interested in working with the World’s leading AI-powered Quality Engineering Company? Ready to advance your career, team up with global thought leaders across industries and make a difference every day? Join us at Qualitest!We are looking for a Junior Chemist to join our growing team in Hercules, CA!Role - Junior ChemistLocation - Hercules, CA (on-site) Job Description <ul><li>Assist in the creation of serum/plasma autoimmune and infectious diseases samples for Clinical Diagnostic verification and validation.</li><li>Execute experimental protocols with guidance from senior team members.</li><li>Assist in data analysis and documentation of the experimental results.</li><li>With guidance from senior team members identify and resolve technical challenges that may arise during sample development.</li><li>Assist and collaborate with a team of research scientists and associates to achieve shared goals.</li></ul> What the Candidate Brings: •Education: Bachelor’s degree in life science or related discipline (Biochemistry, Biotechnology, Chemistry, Biological Sciences, etc.)•Work Experience: 0-2 years of relevant laboratory experience. Experience performing verification and validation studies is a plus.•Coordinate, prioritize and plan lab tasks to meet deadlines.•Ability to work in a team and make decision of limited scope, subject to review.•Hands on experience with instrument hardware, software, assay chemistry related to high pressure liquid chromatography and or immunoassays, ELISA or similar technologies.•Working knowledge of Microsoft Office tools – Excel and Word.•Committed to customer satisfaction; quality focused; resourceful; able to work independently and in a team environment. Why QualiTest?<ul><li>Be a part of a company who strives to support for diversity and inclusion in the workplace – we are one, we are many at Qualitest. Celebrate culture, share knowledge with engineers from around the globe, and inspire each other through our differences.</li><li>Local and global opportunities – we offer you internal rotation and international mobility opportunities to grow your career.</li><li>Clear view of your career and progression with the company – Qualitest is growing massively and giving you the opportunity to grow with us.</li><li>Work hard and play harder with our flexible and casual culture. Take a break from work and join an employee event, or enjoy the amenities and games provided from one of our Employees Centers.</li><li>Save your earnings and prepare for your future by enrolling in our 401k plan where Qualitest will match your contributions accelerating your savings plan.</li><li>Take care of health with enrollment into one of our competitive healthcare benefits. Qualitest will match towards your HSA if you choose to participate.</li><li>Never stop experimenting and learning with Qualitest Tech academy: 3000+ training courses, mentorship programs, technical tribes, sponsored certifications, leadership programs and much more</li><li>Stay active and get rewarded with our Corporate Wellness Program. We pay your Gym membership and giving you opportunities to Earn additional vacation times for attendance the gym!</li><li>Salary of $80,000 annually. </li><li>Earn bonuses via our Client Referral and Employee Referral Program’s. Refer and earn – tap your network for net-worth.</li><li>Planning a vacation? Looking for car insurance? Get access to Qualitest Employee Perks for discounts on anything from travel to electronics. With so many offerings the savings are endless!</li></ul>Intrigued to find more about us?<ul><li>Visit our website at <a href="https://www.qualitestgroup.com/careers/" rel="nofollow">Careers - Qualitest Group</a></li></ul>If you like what you have read, send us your resume and let’s start talking!</div>

QualiTest is the world’s second largest pure play software testing and QA company. Testing and QA is all that we do! 
 We design and deliver contextualized solutions that leverage deep industry-specific understanding with technology-specific competencies and unique testing-focused assets. 
 QualiTest delivers results by combining customer-centric business models, critical thinking and the ability to gain a profound comprehension of customers’ goals and challenges.

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