qc analyst

Coatinks (Private) Limited

<p>The Quality control Analyst is responsible for conducting tests and analyses to ensure the quality and performance of inks, coatings, and other printing materials. This role involves working closely with production teams to develop formulations and troubleshoot issues.</p><p><b>Key Responsibilities:</b></p><ul><li>Prepare samples of inks, chemicals, and substrates for testing.</li><li>Conduct tests to evaluate properties such as viscosity, pH, colour consistency, and drying time.</li><li>Assist in developing new ink and coating formulations to meet specific customer requirements.</li><li>Modify existing formulations based on performance feedback and testing results.</li><li>Utilize tools such as X-Rite for colour matching and ensure colour consistency across different batches and products.</li><li>Perform routine quality control tests to ensure materials meet established specifications and industry standards.</li><li>Document results and maintain accurate records of all tests performed.</li><li>Operate and maintain laboratory equipment and instruments.</li><li>Ensure all equipment is calibrated and functioning correctly.</li><li>Analyse test data and prepare reports summarizing findings and recommendations.</li><li>Collaborate with the QC team to communicate quality issues and develop solutions.</li><li>Adhere to safety protocols and proper handling procedures for hazardous materials.</li><li>Ensure compliance with environmental regulations and industry standards.</li><li>Work closely with production staff to troubleshoot issues and optimize printing processes.</li><li>Participate in cross-functional teams to improve product quality and performance.</li></ul><p><b>Qualifications:</b></p><ul><li>Associate's degree or higher in Chemistry, Printing Technology, or a related field.</li><li>2&ndash;3 years of previous experience in a laboratory setting, preferably in the printing, Paint or chemical manufacturing industry (ink and coatings experience is highly desirable). Strong analytical and problem-solving abilities.</li><li>Familiarity with laboratory equipment and testing procedures.</li><li>Excellent attention to detail and organizational skills.</li><li>Effective communication and teamwork skills.</li></ul><p>Job Type: Full-time</p>

QC Analyst

Hendrick Health

Responsible for preparing; scanning and quality control (QC) health records for correct chart order according to required standards set by hospital policies and procedures; Medical Staff Bylaws; Joint Commission Standards and Medicare and Medicaid requirements.
<br>JOB REQUIREMENTS
<br>Minimum Education
<br><br>
<ul>
<li>High School or equivalent</li>
</ul>
Minimum Work Experience
<br><br>
<ul>
<li>No experience required.</li>
</ul>
Required Licenses/Certifications
<br>Required Skills; Knowledge; and Abilities
<br><br>
<ul>
<li>Ability to follow the specifics of the chart order.</li>
<li>Input data into computer programs.</li>
<li>Ability to operate; perform user maintenance; and troubleshoot high speed scanners.</li>
<li>Effective interpersonal skills when working with others.</li>
<li>Ability to pay attention to detail to ensure documents for the correct patient go in the chart.</li>
<li>Ability to handle confidential information.</li>
</ul>
Designated Driver
<br><br>
<ul>
<li>No</li>
</ul>
OSHA Category
<br><br>
<ul>
<li>3 - Low Risk</li>
</ul>


Prep/Scan/QC Analyst I

Avid Bioservices

<div><div>Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.<br>
</div><div><b>Your Role:</b>
</div><div>The <b>Analyst, Quality Control</b> will perform testing and sampling to support manufacturing, validation, process development and stability studies in a GMP environment.</div><ul><li>
Perform and review routine assays for HPLC, ELISA/cell-based immunoassays, and/or electrophoresis (SDS-PAGE/IEF) with strict adherence to written analytical test procedures.</li><li>
Perform aseptic sampling, visual inspection, pH, conductivity, osmolality, and spectrophotometry.</li><li>
Review, revise and write test methods, standard operating procedures. In addition to performing QC testing, the Analyst may support validation projects, investigations, and method development projects.</li><li>
Other functions include but are not limited to writing study protocols and reports; training other analysts; working with other departments in developing, revising, and implementing QC procedures and policies.</li><li>
Knowledgeable of company cGMPs as well as industry regulations that apply to all job functions.</li><li>
Participate in regulatory inspections.</li><li>
Support continuous improvement initiatives.</li><li>
Other duties as assigned.</li></ul><div><b>
Minimum Qualifications:</b></div><ul><li>
Bachelor&rsquo;s degree in biology, biochemistry, chemistry or equivalent scientific field or a minimum of 2 years of relevant, hands-on experience working in a QC or analytical lab or equivalent combination of education/experience.</li><li>
Experience with analytical testing and equipment, writing reports/procedures/specifications, GMPs and regulatory audits are essential.</li><li>
Must be proficient with ELISA, Analytical Biochemistry or chemistry.</li></ul><div><b>
Position Type/Expected Hours of Work:</b>
</div><div>This role is a full-time onsite position. Days and hours of work are Monday through Friday, 8:00a.m. to 5:00p.m. unless otherwise stated by Supervisor. The employee must also, if instructed, have the ability to work overtime and/or weekends when necessary.</div><div></div><div><b>
Compensation:</b>
</div><div>We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off.
</div><div></div><div>The compensation range for this role is $26.73-$30.00 hourly depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.
</div><div></div><div><b>Who you are:</b>
</div><ul><li>You have a &quot;bring it on!&quot; team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.</li></ul><ul><li>
Your written and verbal skills are out of this world, and you communicate with clarity and confidence.</li><li>
You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything.</li><li>
You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.</li></ul><div><b>
Physical Demands &amp; Work Environment:</b>
</div><div>In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 20 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.</div></div>

Analyst, Quality Control (Airway)

<div><div>Looking to join a passionate team dedicated to developing and manufacturing life-saving biopharmaceuticals? Avid Bioservices is a leading clinical and commercial biologics CDMO focused on creating innovative solutions to meet the needs of our clients and improve patient outcomes.
</div><div>
</div><div><b>Your Role:</b>
</div><div>The <b>Quality Control In-Process Analyst</b> will perform testing and sampling to support manufacturing, validation, process development and stability studies in a GMP environment for the Quality Control In-Process team.</div><ul><li>
Perform basic compendial test methods without supervision and with strict adherence to written protocols, analyze data and report results.</li><li>
Formulate buffers and reagents for the purpose of performing test methods.</li><li>
Write and revise test methods and procedures.</li><li>
Perform aseptic sampling, endotoxin, pH, conductivity, osmolality, A280 and endotoxin by LAL.</li><li>
Perform water testing and raw material sampling and testing.</li><li>
Perform QC testing for lot release, stability, development/validation projects, and investigations.</li><li>
Other functions include writing study protocols and reports.</li><li>
Work with other departments in developing, revising and implementing QC procedures and policies.
</li><li>Should be aware of company cGMPs as well as industry regulations that apply to all job functions.
</li><li>Perform sample pick up and sample locating without supervision and with strict adherence to written protocols.</li><li>
Other duties as assigned.</li></ul><div><b>
Minimum Qualifications:</b></div><ul><li>
Bachelor&rsquo;s degree or 2-4+ years of biotech industry experience working in a QC or analytical lab.
</li><li>Must have experience with analytical testing, writing reports, GMPs, and regulatory audits.
</li><li>Experience with most, if not all the methodologies listed above.
</li><li>Experience with basic maintenance and troubleshooting of analytical instrumentation is highly desirable.</li></ul><div><b>
Position Type/Expected Hours of Work:</b></div><ul><li>
This is a full-time position operating Sunday through Wednesday or Wednesday to Saturday on a 4x10(4 days x 10 hours) schedule.
</li><li>Will have an adaptable schedule to accommodate operational and scheduling demands.</li><li>
Availability needed for overtime and weekend shifts as necessary.</li></ul><div><b>
Compensation:</b>
</div><div>We offer competitive compensation packages for this role, including a base salary, performance-based bonuses, and comprehensive benefits such as health, dental, and vision insurance, 401(k) matching, and paid time off.
</div><div>
</div><div>The compensation range for this role is $26.73 to $35.63 hourly, depending on experience and qualifications. Additionally, we offer opportunities for career growth and development as well as a supportive and inclusive work environment.
</div><div>
</div><div><b>Who you are:</b>
</div><ul><li>You have a &quot;bring it on!&quot; team player approach and an unshakable positive attitude, always ready to tackle anything that comes your way.</li><li>
Your written and verbal skills are out of this world, and you communicate with clarity and confidence.</li><li>
You have exceptional multitasking skills and an unparalleled attention to detail that ensure the smooth running of everything.</li><li>
You are a master at building relationships, capable of establishing connections with anyone, be it team members, clients, vendors, or suppliers.</li></ul><div><b>
Physical Demands &amp; Work Environment:</b>
</div><div>In this dynamic role, expect a blend of regular activities like sitting, standing, and walking, with occasional physically engaging tasks such as lifting objects up to 20 pounds. The work environment might expose you to electrical shocks, toxic chemicals, vibrations, or loud noise levels occasionally. However, reasonable accommodations are available to enable individuals with different abilities to perform effectively, ensuring a supportive and adaptable work setting. Your visual acuity, including close, distance, and color vision, will be essential in navigating through the diverse day-to-day demands of this position.</div></div>

Analyst (In-Process), Quality Control

Vertex Pharmaceuticals

<div>Job Description:
<div>
The Vertex Cell and Gene Therapy (VCGT) Type 1 Diabetes (T1D) Quality Control (QC) team is responsible for the testing of samples and associated workflows within our stem-cell based T1D program. VCGT T1D QC carries out all activities under Good Manufacturing Practices (GMP) guidelines.</div><div></div><div><br>
The Quality Control Specialist is responsible for supporting a variety of analytical functions that occur in the Quality Control (QC) department supporting validation, testing and reporting of in-process, release and stability samples. This role also helps ensure activities occur in an efficient and cGMP compliant manner while fostering the Vertex vision and values.</div><div></div><div><b><br>
Shift: Sunday - Wednesday 12:30pm-11:00pm</b></div><div></div><div><b><br>
Key Responsibilities:</b></div><ul><li>
Typical test methods performed include flow cytometry, qPCR (MycoTOOL), ELISA, cell counts, sterility (BACT), Gram stain and endotoxin (LAL) testing.</li><li>
Performs technical reviews of raw data.</li><li>
Records test results and maintains raw data and accurate laboratory records.</li><li>
Performs general lab and equipment maintenance duties.</li><li>
Performs other duties as assigned.</li><li>
Weekend shift work: Typical workweek is a 4 day week, 10 hours a day, Sunday to Wednesday 12:30 PM &ndash; 11:00 PM.</li></ul><div></div><div><b><br>
Knowledge and Skills:</b></div><ul><li>
Performs tasks with strict adherence to cGMP and cGDP principles.</li><li>
Has an understanding of basic laboratory equipment and practices.</li><li>
Is proficient in the use of spreadsheets and word processing software.</li><li>
Is dependable and able to work well within a team.</li><li>
Is interested in learning new things. Open to change.</li><li>
Is optimistic and displays a positive attitude even during periods of adversity.</li><li>
Shows initiative; acts independently with management approval.</li><li>
Possesses a high attention to detail.</li></ul><div><br>
</div><div><b>Requirements:</b></div><ul><li>
A minimum of a Bachelor's degree in Sciences is required.</li><li>
4 + years of experience in the GMP pharmaceutical/biopharmaceutical industry</li></ul><br>
<div></div>
Pay Range:
<div><b>
$40-$50/hr</b></div>
Requisition Disclaimer:
<p>
This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals (&ldquo;Vertex&rdquo;). The individual selected for this role will be offered the role as an employee of a third- party agency partner; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements</p><div></div><div><br>
By applying for this position, you agree to the Atrium Terms and Conditions and you direct Atrium to share your application materials, which may include your CV/Resume, email address or phone number, with Vertex. For more information on how Vertex handles your personal data related to your job application, please see Vertex&rsquo;s Careers Privacy Notice. Agreeing to the Atrium Terms and Conditions, includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings, profiles, articles, news, and other employment-related information, as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners</div><div>
(collectively, &ldquo;Atrium Alerts&rdquo;). Atrium Alerts may be sent by email, phone, or text message. Your personal information will be safely stored within the Atrium &amp; Vertex databases. Atrium does not sell your personal information to third parties. Text message and data rates may apply. To OPT OUT of text messaging or to modify your communication preferences for Atrium Alerts at any time, please contact Atrium at privacyadministrator@atriumstaff.com.</div><div></div><p><br>
If you do not agree with the Atrium Terms and Conditions, you can still complete your application for this position by emailing your resume to our team at tempstaffing@vrtx.com. Please include the job title in the subject of your email.</p><div></div><div><b><br>
No C2C or Third-Party Vendors</b></div></div><div></div>

2nd shift Quality Control Specialist (contract) 28670

dsm-firmenich

<div><p><b>QA/QC Specialist</b></p><p><b>
Gebze (Kocaeli), Turkey</b></p><p><b>
Onsite, Temporary for 16 months</b></p><p></p><p><br>
Join our Quality team as a QC/QA Specialist, where you will play a critical role in safeguarding product quality across our value chain. In this role, you will combine hands‑on analytical laboratory work with Quality Assurance activities, supporting production, supply chain, and customers while ensuring compliance with international quality standards. This is a challenging and rewarding position offering exposure to advanced analytical techniques and quality systems in a global manufacturing environment.</p><p></p><p><b><br>
Your key responsibilities</b></p><ul><li>
Perform or implement complex analytical testing methods using advanced techniques (e.g. GC/MS, HPLC/MS, NMR, IR) and routine quality control analyses</li><li>
Ensure accurate documentation, review of test results, and reporting against specifications</li><li>
Support qualification, calibration, and validation of laboratory equipment and analytical methods</li><li>
Participate in deviation investigations, root cause analysis, and continuous improvement activities</li><li>
Support Quality Assurance processes including audits, SOP preparation, training (GMP, SOPs), and product release activities</li><li>
Contribute to maintaining and improving ISO, HACCP, GMP, GLP, and FAMI‑QS compliant quality systems</li><li>
Follow up of yearly analysis plan, check of supplier documents as a part of raw material QC monitoring plan</li></ul><p></p><p><b><br>
We offer</b></p><ul><li>
A rich history and a promising future of bold scientific innovation and passionate creation with our customers</li><li>
A space to grow by encouraging and supporting curiosity and an open mindset</li><li>
A culture that prioritizes safety and well-being, both physically and mentally</li><li>
The opportunity to work for a company where sustainability is much more than a claim and is core to our strategy and purpose;</li><li>
A firm belief that working together with our customers is the key to achieving great things</li><li>
An eagerness to be one team and learn from each other to bring progress to life and create a better future;</li></ul><p></p><p><b><br>
You bring</b></p><ul><li>
Bachelor&rsquo;s degree in chemistry, analytical chemistry, or a related engineering/science field</li><li>
3&ndash;5 years of experience in Quality Control and/or Quality Assurance within a manufacturing or laboratory environment</li><li>
Strong knowledge of analytical techniques and best laboratory practices (GLP)</li><li>
Good understanding of quality management systems and standards (ISO, GMP, HACCP, Feed/Food/Pharma)</li><li>
Strong problem‑solving skills, attention to detail, and ability to work with complex data</li></ul><p></p><p><b><br>
Our application process</b></p><p>
Interested in this role? Then please apply online only via our career portal.</p><p>
Recruiter: Aylin Toy</p><p></p><p><b><br>
About ANH</b></p><p>
ANH, in the process of separating from dsm-firmenich, is a global leader in animal nutrition and health, as well as vitamins, carotenoids, and aroma ingredients - driven by its strong purpose: feeding the planet without costing the earth. Together, we make it possible. www.dsm-firmenich.com/ANH</p><p></p><p><b><br>
About dsm-firmenich</b></p><p>
At dsm-firmenich, we don&rsquo;t just meet expectations &ndash; we go beyond them.</p><p>
Join our global team powered by science, creativity, and a shared purpose: to bring progress to life.</p><p>
From elevating health to making fortified food and sustainable skincare, the impact of your work here will be felt by millions &ndash; every single day. Whether it&rsquo;s fragrance that helps you focus, alternative meat that&rsquo;s better for the planet, or reducing sugar without losing flavor, this is where you help shape the future of nutrition, health, and beauty for everyone, everywhere.</p><p>
And while you&rsquo;re making a difference, we&rsquo;ll make sure you&rsquo;re growing too. With learning that never stops, a culture that lifts you up and the freedom to move across businesses, teams, and borders. Your voice matters here. And your ideas? They&rsquo;re essential to our future.</p><p>
Because real progress only happens when we<b> go beyond, together.</b></p><p></p><p><b><br>
Inclusion, belonging and equal opportunity statement</b></p><p>
At dsm-firmenich, we believe being a force for good starts with the way we treat each other. When people feel supported, included, and free to be themselves, they do their best work &ndash; and that&rsquo;s exactly the kind of culture we&rsquo;re building. A place where opportunity is truly equal, authenticity is celebrated, and everyone has the chance to grow, contribute, and feel they belong.</p><p>
We&rsquo;re proud to be an equal opportunity employer, and we&rsquo;re serious about making our hiring process as fair and inclusive as possible. From inclusive language and diverse interview panels to thoughtful sourcing, we&rsquo;re committed to reflecting the world we serve.</p><p>
We welcome candidates from all backgrounds &mdash; no matter your gender, ethnicity, sexual orientation, or anything else that makes you, you.</p><p>
And if you have a disability or need any support through the application process, we&rsquo;re here to help &ndash; just let us know what you need, and we&rsquo;ll do everything we can to make it work.</p><p></p><p><b><br>
Agency statement
</b></p><p>We&rsquo;re managing this search directly at dsm-firmenich. If you&rsquo;re applying as an individual, we&rsquo;d love to hear from you. We&rsquo;re not accepting agency submissions or proposals involving fees or commissions for this role.</p></div><p></p>

QA/QC Specialist

Openkyber

<div><p>OpenKyber, Inc., (OpenKyber), is searching for a Business Analyst for a CONTRACT assignment with one of our premier Regulatory clients in Rockville, MD, Tysons, VA or Washington D.C. The Business Analyst conducts moderate-to-high complexity analysis of automated surveillance systems that detect potential violations of regulatory rules. This role is responsible for understanding, validating, enhancing, and supporting surveillance patterns across multiple asset classes and regulatory domains. The analyst serves as the bridge between regulatory requirements and the technical implementation of surveillance logic, ensuring patterns produce accurate, complete, and defensible results. The analyst is expected to actively leverage generative AI tools to accelerate analysis, documentation, and automation - serving as the domain expert who directs AI capabilities while ensuring regulatory accuracy and completeness of all outputs.</p>
<b>Responsibilities :</b>
<ul><li>Surveillance Pattern Analysis &amp; Knowledge Management Reverse-engineers surveillance pattern source code to build comprehensive knowledge documentation covering data pipelines, business rules, exception logic, and output schemas</li>
<li>Maintains a knowledge base of surveillance patterns across multiple regulatory domains</li>
<li>Performs requirements-vs-code gap analysis to identify discrepancies between documented business requirements and implemented logic, flagging risks to surveillance coverage</li>
<li>UAT &amp; Release Validation Validates new surveillance pattern releases by comparing production vs. UAT outputs, analyzing exception counts, volumes, and firm-level impacts</li>
<li>Builds local testing environments to execute query scripts against sample data, enabling independent verification of pattern logic before production deployment</li>
<li>Designs multi-scenario test cases covering edge cases to ensure comprehensive test coverage</li>
<li>Packages release artifacts (scripts, QC results, requirements documentation) following standardized release structures</li>
<li>Ad-Hoc Data Analysis &amp; Investigation Support Writes complex queries to support analyst investigations into surveillance exceptions</li>
<li>Performs firm-level statistical analysis and produces reports for management review</li>
<li>Maintains reference data sets used by downstream surveillance patterns</li>
<li>Assesses data incident impacts by cross-referencing affected data sources against the surveillance pattern dependency map</li>
<li>Process Automation &amp; Tooling Develops automation tools for ticket management, release documentation, and workflow optimization</li>
<li>Builds local testing frameworks that replicate production environments for rapid pattern testing and iteration</li>
<li>Creates data visualization and comparison reports with interactive views, summary statistics, and color-coded differentials</li>
<li>Generative AI Integration &amp; Prompt Engineering Leverages AI coding assistants as a force multiplier - directing AI agents to reverse-engineer source code, build knowledge documentation, generate test frameworks, and produce data comparison reports</li>
<li>Designs structured AI workflows including pattern study pipelines, workflow assistants, and automated documentation generation</li>
<li>Maintains a curated AI project workspace with standing instructions, conventions, and context files that enable consistent, high-quality AI-assisted output</li>
<li>Coordinates multi-step analytical tasks through AI - from reading source code and drafting requirements, to generating test harnesses and producing comparison reports - reducing turnaround from days to hours</li>
<li>Evaluates and validates AI-generated outputs for regulatory accuracy before use in production workflows</li>
<li>Project Management Support Manages work across project tracking boards, tracking enhancement tickets, bug fixes, and new pattern development</li>
<li>Drafts and updates Business Requirements Documents (BRDs) for surveillance pattern enhancements</li>
<li>Coordinates release activities including documentation, QC, and UAT sign-off tracking</li>
</ul><p>OTHER RESPONSIBILITIES Participates on special projects as assigned. Serves as a mentor for less experienced analysts. Keeps management updated on notable trends in industry practices, regulatory changes, and emerging technology capabilities (including AI tooling). Champions adoption of AI-assisted workflows within the team.</p>
<b>Required Skills :</b>
<ul><li>Bachelor's degree and 5+ years of experience in financial regulatory technology, surveillance systems, or capital markets data analysis</li>
<li>Proficiency in SQL for large-scale data analysis on distributed platforms</li>
<li>Proficiency in at least one scripting/programming language for data analysis, automation, and tool development</li>
<li>Experience reading and interpreting complex data processing pipelines and business logic in source code</li>
<li>Strong analytical skills with the ability to independently investigate data discrepancies and validate system outputs</li>
<li>Excellent documentation skills - ability to translate complex technical implementations into clear business-facing knowledge documents</li>
<li>Advanced proficiency in spreadsheet tools for business and operational analysis</li>
</ul><b>Preferred Skills :</b>
<ul><li>Major in Business Administration, Finance, Computer Science, or related field; advanced degree preferred</li>
<li>Knowledge of SEC/FINRA regulatory rules and reporting requirements</li>
<li>Experience with distributed query engines and big data platforms</li>
<li>Experience with project management and documentation tools and their APIs</li>
<li>Familiarity with surveillance pattern architectures (exception generation, scoring, aggregation, reconciliation)</li>
<li>Experience with source code management and release branch workflows</li>
<li>Experience leveraging generative AI tools (LLMs, AI coding assistants) to accelerate data analysis, code comprehension, documentation, and automation workflows</li>
<li>Ability to design effective AI prompts and structured project contexts that produce reliable, domain-accurate outputs in a regulated environment</li>
</ul><p>OpenKyber is a technology and resource solutions provider driven to stand out. We are a women-owned business. Our mission: to solve big IT problems with a more personal, boutique approach. Each year, we match consultants like you to more than 1,000 engagements. When we say let's work better together, we mean it. You'll join a diverse team built on these core values: customer service, employee development, and quality and integrity in everything we do. Be yourself, love what you do and find your passion at work.</p>
<p>SGA is an Equal Opportunity Employer and does not discriminate on the basis of Race, Color, Sex, Sexual Orientation, Gender Identity, Religion, National Origin, Disability, Veteran Status, Age, Marital Status, Pregnancy, Genetic Information, or Other Legally Protected Status. We are committed to providing access, equal opportunity, and reasonable accommodation for individuals with disabilities in employment, and our services, programs, and activities.</p>
<p>Please visit our company to request an accommodation or assistance regarding our policy.</p>
<p><b>For applications and inquiries, contact:</b> hirings@openkyber.com</p></div>

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