quality control analyst

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

Vendify TM

<p><b>Vendify</b> is seeking a detail-oriented <b>Quality Assurance (QA) Analyst</b> to oversee the call quality and compliance of our international POS sales campaigns. The ideal candidate will have deep expertise in the POS industry and a proven track record of improving sales conversion through rigorous call monitoring and feedback.</p><p><b>Role Overview</b></p><ul><li><b>Location:</b> On-site &ndash; Gulshan-e-Iqbal, Karachi.</li><li><b>Shift:</b> Night Shift (08:00 PM &ndash; 05:00 AM).</li><li><b>Tenure:</b> Full-time / Permanent.</li></ul><p><b>Key Responsibilities</b></p><ul><li><b>Call Monitoring:</b> Audit live and recorded outbound sales calls to ensure adherence to POS campaign scripts and USA/Canada compliance standards.</li><li><b>Performance Analysis:</b> Evaluate &quot;POS Closers&quot; and &quot;Lead Gen&quot; agents based on communication, tone, objection handling, and closing techniques.</li><li><b>Feedback &amp; Coaching:</b> Conduct one-on-one feedback sessions and group workshops to address performance gaps and improve campaign KPIs.</li><li><b>Reporting:</b> Prepare daily and weekly QA reports for the Recruitment and Operations Managers to track the quality of the &quot;New Room&quot; and existing teams.</li><li><b>Compliance:</b> Ensure all agents follow SOPs regarding merchant data security and ethical sales practices.</li></ul><p><b>Requirements</b></p><ul><li><b>Experience:</b> Minimum <b>2 years of experience</b> specifically in a QA role for <b>POS campaigns</b> (Point of Sale/Merchant Services).</li><li><b>Education:</b> Minimum Bachelors or equivalent.</li><li><b>Industry Knowledge:</b> Deep understanding of the North American POS market, merchant processing, and common sales objections.</li><li><b>Communication:</b> Exceptional verbal and written English skills with a sharp ear for nuances in international sales calls.</li><li><b>Analytical Skills:</b> Ability to identify trends in agent performance and suggest data-driven training solutions.</li></ul><p><b>What We Offer</b></p><ul><li><b>Market-Leading Salary:</b> Based on experience and POS domain expertise.</li><li><b>Incentives:</b> Performance-based bonuses and recognition.</li><li><b>Transport:</b> Dedicated <b>Pick &amp; Drop facility</b> for female staff covering 11+ major Karachi areas.</li><li><b>Growth:</b> A professional environment with opportunities to lead the QA department.</li></ul><p><b>How to Apply</b></p><p>Interested professionals meeting the 2-year POS experience criteria are encouraged to apply.<br/><b>Email:</b> contact@vendify.info<br/><b>WhatsApp:</b> 0332-0757648</p><p>Pay: Rs50,000.00 - Rs70,000.00 per month</p><p>Location:</p><ul><li>Karachi Gulshan-E-Iqbal (Required)</li></ul><p>Work Location: In person</p>

Quality Assurance Officer

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

StandardAero

<div><p><b>Build an Aviation Career You&rsquo;re Proud Of
</b></p><p>At StandardAero, we use our ingenuity and know-how to find solutions for the simple to the most complex challenges in aviation. Together, we get the job done and done well. Our stability, resources, and respectful culture supports you in building a solid career with a great team you can count on day in and day out for the long term.
</p><p>As a <b>Quality Analyst, Sr </b>you will participate in quality activities of the business unit in order to improve the processes, procedures, methods and materials used in the repair and overhaul of aero-engines, components and other related processes to ensure product quality is maintained while striving for continuous improvements. This includes creation and facilitation of CAR, performing and participating in Internal and External Audits, leading and participating in incident investigations, reviewing and creating process improvements, reviewing and updating work instructions and developing tools to help ensure compliance to required technical and regulatory processes and procedures.
</p><p><b>What you&rsquo;ll do:
</b></p><ul><li>Continuously monitor quality data (warranty, product rectification, customer satisfaction, etc.) for improvement opportunities across the business unit. Work with the business unit strategic group to select, manage, and facilitate continuous improvement initiatives.
</li><li>Assist in the maintenance of methods and systems for measuring the degree by which the business unit&rsquo;s quality goals, objectives and standards are being met.
</li><li>Participate in the business unit quality audits and corrective action process by providing training, facilitation, recommendations and leadership, as required, to achieve optimal results.
</li><li>Monitor, review and conduct sub-contractor audits in liaison with supplier development.
</li><li>Interface with marketing, operations and engineering to establish quality requirements on individual products and services on the basis of customer needs, the fit, form and function of the product, and to ensure that quality considerations are properly addressed as early as possible in the product or process design stage.
</li><li>Monitor warranty procedures including investigation, root-cause, corrective action and follow-up to ensure that continuous improvement is occurring.
</li>Analyze, evaluate, and present information concerning factors such as business situations, production capabilities, remanufacturing problems, statistical trends, and proposed process changes.<br>
<li>
</li></ul><p></p><p><b>Minimum Qualifications
</b></p><ul><li>Must be certified in AS9100, or AS9110 or ISO 9001
</li><li>5 years work experience in Quality Assurance or equivalent
</li><li>5 years work experience in quality methodologies for implementation in support of business unit strategic initiatives.
</li><li>3 years work experience in PowerBI and Microsoft suites
</li>Bachelor's degree in Mechanical, Industrial or Aerospace Engineering or similar technical field of Study or equivalent experience.<br>
<li>
</li></ul><p></p><p><b>Desired Characteristics
</b></p><ul><li>5-year work experience in Aviation or MRO
</li><li>3 years&rsquo; experience in identifying and reporting flight/product safety concerns
</li>Participate in proactive risk analysis of flight/product safety for critical parts and processes<br>
<li>
</li></ul><p></p><p><b>Benefits that make life better:
</b></p><ul><li>Comprehensive Healthcare
</li><li>401(k) with 100% company match; up to 5% vested
</li><li>Paid Time Off starting on day one
</li><li>Bonus opportunities
</li><li>Health- &amp; Dependent Care Flexible Spending Accounts
</li><li>Short- &amp; Long-Term Disability
</li><li>Life &amp; AD&amp;D Insurance
</li>Learning &amp; Training opportunities<br>
<li>
</li></ul><p></p><p><b>Raising the Standard of Excellence since 1911
</b></p><p>With over a century of proven excellence, StandardAero has become an industry leader in MRO services and customized solutions in the aerospace field. Our shared values and learning-based culture inspire our team to exceed their potential and power our customers&rsquo; missions worldwide. With on-the-job training, advancement opportunities, and excellent benefits, StandardAero invites you to experience a fulfilling and meaningful career with us.
</p><p><b>Inclusivity Is Our Standard
</b></p><p>StandardAero offers equal employment opportunities for all. Our supportive environment celebrates diversity with no room for harassment or discrimination of any kind. We invite you to bring your authentic self to our team and experience our welcoming culture.</p></div><p></p>

Analyst, Quality Sr

Advocate Program, Inc

<p>The SSVF Compliance &amp; Quality Assurance Specialist is responsible for ensuring the quality and compliance of all program activities under the Supportive Services for Veteran Families (SSVF) grant. This includes regular file reviews, case planning oversight, TFA and shallow subsidy approvals, HMIS data integrity checks, and providing corrective guidance to program staff. The role helps safeguard program compliance with VA regulations and organizational policies, while supporting continuous improvement in service delivery. Serving veterans across South Florida, consistent monitoring is essential to maintain compliance with VA guidelines, Council on Accreditation (COA) standards, and organizational quality benchmarks.</p><p><b>Qualifications</b></p><ul><li><i><b>Master&rsquo;s degree in social work, public administration, or a related field; or</b></i></li><li><i><b>Bachelor&rsquo;s degree in a related field with 2&ndash;3 years of direct experience in program compliance or quality assurance within human services.</b></i></li><li><i><b>At least 2&ndash;3 years of experience in program compliance and quality assurance, within human services.</b></i></li><li>Familiarity with SSVF guidelines, HMIS systems, and federal grant compliance strongly preferred.</li><li>Excellent attention to detail, organizational, and analytical skills.</li><li>Strong communication and training facilitation skills</li></ul><p><b>Key Responsibilities:</b></p><ul><li>Conduct quality assurance reviews of client files, including case planning, temporary financial assistance, and documentation.</li><li>Perform regular HMIS data checks to ensure accuracy and compliance.</li><li>Lead and coordinate internal audits to prepare for VA and external monitoring visits.</li><li>Ensure program practices align with Council on Accreditation (COA) standards.</li><li>Participate in and support Performance &amp; Quality Improvement (PQI) activities, including data tracking, outcomes measurement, and reporting.</li><li>Identify trends, provide feedback for staff, and support continuous improvement initiatives.</li><li>Deliver or support staff training on compliance, documentation, and quality standards.</li><li>Update department policies and procedures accordingly to ensure continued compliance.</li><li>Collaboration &amp; Stakeholder Reporting: Partner with internal teams and external stakeholders (funders, auditors, VA representatives) to provide compliance data, respond to inquiries, and support monitoring visits or site reviews.</li><li>Attend VA/SSVF trainings, webinars, and conferences to stay current with program regulations, HMIS updates, and compliance best practices; share knowledge and provide training to staff.</li></ul><p><b>TRAVEL: </b></p><ul><li>This position requires travel to attend trainings, workshops, or professional development opportunities as assigned.</li><li>Employees must be available to travel locally within Florida or to other locations as required by the organization.</li><li>Travel may include day trips and/or overnight stays, depending on training location and schedule.</li><li>All travel expenses will be covered in accordance with company policy.</li></ul><p>This is a <b>full-time position</b> offering benefits such as health insurance, PTO and 401K enrollment.</p><p>Pay: $55,000.00 - $65,000.00 per year</p><p>Benefits:</p><ul><li>401(k)</li><li>Dental insurance</li><li>Employee assistance program</li><li>Health insurance</li><li>Life insurance</li><li>Paid time off</li><li>Vision insurance</li></ul><p>Education:</p><ul><li>Bachelor's (Required)</li></ul><p>Experience:</p><ul><li>program compliance and quality assurance: 2 years (Preferred)</li></ul><p>Willingness to travel:</p><ul><li>25% (Preferred)</li></ul><p>Work Location: In person</p>

Compliance & Quality Assurance Specialist for Veterans

NRG Energy

<div><p>As an NRG employee, we encourage you to take charge of your career and development journey. We invite you to explore exciting opportunities across our businesses. You&rsquo;ll find that our dynamic work environment provides variety and challenge. Your growth is key to our ongoing success&mdash;take the lead in shaping your career development, goals and future!</p><br>
<p></p>
<div><b>
Job Summary:</b></div><div><br>
</div><div>NRG Business is seeking a detail-oriented and innovative Operations Analyst to join our dynamic team in the energy sector. This role is pivotal in maintaining and optimizing product and billing configuration across our existing product suite, while also contributing to the development of new and forward-thinking commodity and non-commodity offerings. The analyst will serve as a subject matter expert in billing configuration and product implementation, ensuring accuracy and efficiency through quality control processes and system troubleshooting. The position is responsible for developing and maintaining complex billing configurations, ensuring accurate revenue recognition for over 480,000 service locations and $675M in monthly billed revenue. Acting as a subject matter expert, the analyst collaborates cross-functionally with Sales, Billing, Pricing, Customer Care, Forecasting, Finance and other teams to implement innovative product structures and resolve escalated customer issues.</div><div><br>
</div><div>Ideal candidates will possess strong problem-solving abilities, excellent communication and interpersonal skills, and a strong grasp of process optimization and control methodologies. Success in this role requires strong analytical skills, attention to detail, and the ability to navigate dynamic market conditions with precision and agility. The role operates with limited supervision and has a direct impact on enhancing the customer experience through accurate product and billing configuration to support timely billing execution.</div><div></div><div><b><br>
Essential Duties/Responsibilities:</b></div><ul><li>
Support the development, launch, and optimization of commercial commodity and non-commodity products, including billing configuration and product setup across ISO markets.
</li><li>Create and maintain accurate billing configurations for over 480,000 service locations, ensuring timely and complete billing of $675M+ monthly revenue. Monitor quality control and resolve system issues impacting billing.</li><li>
Partner with Sales, Billing, Finance, Pricing, and other teams to ensure consistent product treatment, costing structures, and revenue recognition.</li><li>
Analyze regulatory/legal changes and support operational implementation. Calculate net metering accounts based on tariffs and usage</li><li>
Address complex customer or system issues and provide expert guidance on product configuration and billing across ISO markets</li><li>
Contribute to continuous improvement initiatives and identify system efficiencies in collaboration with management and SMEs.</li><li>
Perform related tasks and duties as assigned with limited supervision, maintain a proactive and solution-oriented mindset</li></ul><h1 class="jobSectionHeader"><b><br>
</b></h1><h1 class="jobSectionHeader"><b>
Working Conditions:</b></h1><ul><li>
Open office environment or fully remote work options available.</li><li>
Travel: Less than 5%.</li></ul><div></div><div><b><br>
Minimum Requirements:
</b></div><ul><li>Minimum of 2 years energy industry experience, especially an understanding of wholesale energy markets, the market drivers, settlement processes and intricacies of regional markets</li></ul><div><b><br>
</b></div><div><b>Preferred Qualifications:
</b></div><ul><li>Bachelor&rsquo;s degree preferred; concentration in Economics, Finance, Business, or related area</li><li>
Self-starter with strong mathematical, analytical, and problem-solving skills; detail-oriented; under limited supervision, ability to communicate findings and make recommendations; comfortable working with individuals in different organizational levels; with support, effective at managing multiple activities and meeting deadlines</li></ul><div></div><div><b><br>
Additional Knowledge, Skills and Abilities:</b></div><ul><li>
Demonstrates expertise in utilizing Microsoft Excel, Power BI, Visio, PowerPoint, and Access</li><li>
An effective communicator with excellent written, verbal, and presentation skills</li><li>
An understanding of process control techniques, policies, and procedures is a plus especially experience that leverages technology as part of the solution is preferred</li><li>
Self-motivated and very detail-oriented; ability to work with limited supervision in a fast-paced environment with multiple deadlines</li></ul><div></div><div><b><br>
Physical Requirements:</b></div><ul><li>
Most of the time is spent sitting in a comfortable position and there is frequent opportunity to move about.</li></ul>
<p>
NRG Energy is committed to a drug and alcohol-free workplace. To the extent permitted by law and any applicable collective bargaining agreement, employees are subject to periodic random drug testing, and post-accident and reasonable suspicion drug and alcohol testing. EOE AA M/F/Vet/Disability. Level, Title and/or Salary may be adjusted based on the applicant's experience or skills.</p><p>
Official description on file with Talent.</p></div>

Operations Analyst

Search 10000+ Quality control analyst jobs near you this June. New roles added regularly across leading industries. Apply today.