quality control analyst

Novo Nordisk, Inc.

<div><div><div><div><div>Senior Quality Control Equipment Analyst
</div></div></div></div><div><div><div><div>Facility: Quality
</div></div></div></div><div><div><div><div>Location:
Boulder, CO, US
</div></div></div></div><div><div><div><div><div>About the Department
</div><div>The Boulder Site is home to the specialized technical operations/CMC team for oligonucleotides and RNAi therapeutics. The CMC team works alongside Quality, Regulatory, Technical Operations and RNAi Early Development professionals at our Boulder, Colorado facility and works closely with our teams in Lexington, Massachusetts. Together, we are driving change. Are you ready to make a difference.</div> 
<div></div>
<div>
The Position</div>
<div>
Novo Nordisk, CMC Boulder, is building a Phase 1 and 2 API Pilot facility for oligonucleotide manufacturing in Boulder Colorado. As such, the Quality Control team is seeking a Senior Quality Control Equipment Analyst to support both the successful start-up and ongoing operation of the Quality Control laboratory supporting early phase manufacturing.</div> 
<div></div>
<div>
The Senior Quality Control Equipment Analyst will: Own all activities related to the establishment &amp; operation of the Quality Control Chemistry laboratory as it relates to equipment qualification and subsequent PM&rsquo;s and annual qualification. The position will also act as a back-up Global LIMS SME for the facility. This position is highly visible to Sr Management and is intended for a self-starter. This position is for a hands-on analyst familiar with Novo systems (TIMS, Global LIMS) and processes as they relate to GMP Quality Control.</div> 
<div></div>
<div>
Relationships</div>
<div>
Reports to Senior Manager, Quality Control.</div> 
<div></div>
<div>
Essential Functions</div>
<ul>
<li>Serve as QC lead (Equipment Responsible) for analytical equipment qualification to support the Boulder CMC API facility</li>
<li>Perform analytical equipment qualification and preventive maintenance, including hands-on execution and/or coordination with equipment vendors when activities are outsourced</li>
<li>Responsible for documenting the qualification and maintenance of analytical instrumentation, using Quality generated protocols and reports from the TIMS system when possible</li>
<li>Coordinate with internal subject‑matter experts and equipment vendors to troubleshoot and resolve equipment issues</li>
<li>Serve as the QC lead for the TIMS system a back-up for Global LIMS QC Super User</li>
<li>Assist with material qualification as needed</li>
<li>Develop processes, procedures and or protocols for QC lab equipment such as, but not limited to: HPLC, UHPLC, GC, Karl Fisher, UV, pH, Conductivity, TOC, endotoxin, ICP-MS and FTIR</li>
<li>Write/revise SOPs, technical protocols, change control and other quality related documentation</li>
<li>Lead &amp; coach team members, other specialists, providing leadership in problem solving for process &amp; quality issues</li>
<li>Evaluate and support corporate initiatives for new technology and process improvements</li>
<li>Represent Boulder QC on global and site level as needed for collaboration with other NN sites</li>
<li>Interact closely with QC analysts, analytical development, facilities, engineering, and quality assurance to ensure alignment with relevant stakeholders</li>
<li>Follow all safety &amp; environmental requirements in the performance of duties</li>
<li>Other accountabilities, as required</li></ul> 
<div></div>
<div>
Physical Requirements</div>
<div>
Ability to work in an open office environment with the possibility of frequent distraction. Ability to travel up to 10% of the time.</div> 
<div></div>
<div>
Qualifications</div>
<ul>
<li>High School Diploma or GED and 8+ years of experience, or Associate's degree with 6+ years of experience, or Bachelor's degree from an accredited university and 4+ years of experience, or Master's degree and 2+ years of experience is required</li>
<li>QC experience in a pharmaceutical or related (regulated) environment required</li>
<li>Experience with computerized laboratory systems (TIMS, Global LIMS, etc.) preferred</li>
<li>Demonstrated expert understanding of processes, procedures &amp; products associated with assigned areas required. Able to perform detailed analysis of events &amp; processes, develop appropriate responses to situational needs, &amp; convey information/results to various organizational levels as appropriate required</li>
<li>Excellent verbal &amp; written communication skills, investigative writing skills, &amp; computer skills required (MS Word, Outlook, Excel, PowerPoint, TIMS, and Global LIMS)</li>
<li>Demonstrated experience in practical problem solving &amp; process improvement methods required</li>
<li>Demonstrated ability to manage multiple tasks/deadlines &amp; prioritize properly based on process needs &amp; events. Demonstrated effectiveness in systematic follow-up required</li>
<li>Understand the processes and products at an advanced level required</li>
<li>Demonstrates understanding of project management and NN gate process flow preferred</li>
<li>Expert level of knowledge &amp; understanding regarding departmental SOP&rsquo;s &amp; their high-level inter-relationships required (i.e. how they work together to establish a system)</li></ul> 
<div></div>
<div>
The base compensation range for this position is $99,600 to 184,200. Base compensation is determined based on a number of factors. This position is also eligible for a company bonus based on individual and company performance.</div> 
<div></div>
<div>
Novo Nordisk offers long-term incentive compensation and or company vehicles depending on the position's level or other company factors.</div> 
<div></div>
<div>
Employees are also eligible to participate in Company employee benefit programs including medical, dental and vision coverage; life insurance; disability insurance; 401(k) savings plan; flexible spending accounts; employee assistance program; tuition reimbursement program; and voluntary benefits such as group legal, critical illness, identity theft protection, pet insurance and auto/home insurance. The Company also offers time off pursuant to its sick time policy, flex-able vacation policy, and parental leave policy.</div> 
<div></div>
<div>
The job posting is anticipated to close on April 7th, 2026. The Company may however extend this time-period, in which case the posting will remain available on our careers website at www.novonordisk-us/careers.com.</div><div></div><div> 
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.</div> 
<div></div>
<div>
At Novo Nordisk, we're not chasing quick fixes &ndash; we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and defeating diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger &ndash; a legacy of impact that reaches far beyond today.</div> 
<div></div>
<div>
Novo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, protected veteran status or any other characteristic protected by local, state or federal laws, rules or regulations.</div> 
<div></div>
<div>
If you are interested in applying to Novo Nordisk and need special assistance or an accommodation to apply, please call us at 1-855-411-5290. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.</div></div></div></div></div></div>

Senior Quality Control Equipment Analyst

Georgia Department of Public Health

<div><div><div><h2 class="jobSectionHeader">Description</h2></div>
<div>Pay Grade: M<div> 
This is a FEDERAL GRANT FUNDED position and is subject to available grant funds. 
</div><div>
Click HERE for Video</div> 
Who We Are. We protect lives. The Georgia Department of Public Health (DPH) is the lead agency entrusted by the people of Georgia to protect lives and promote healthy lifestyles in communities throughout the state. We are committed to preventing disease, injury, and disability; promoting health and well-being; and preparing for and responding to disasters. 
 
What We Offer. As a member of the DPH team, you will join a group of passionate individuals dedicated to serving Georgians. Regardless of your role, you will contribute to protecting lives while enjoying a wide range of benefits.<ul><li>
Make a Professional Impact &ndash; Build your career where it matters and protect lives in the community where you live, work, and play.</li><li>
Enjoy Workplace Flexibility &ndash; Experience flexibility in how you work so you can be your best self for you and the people of Georgia.</li><li>
Work with a Dynamic and Diverse Team &ndash; Collaborate with employees who share ideas and leverage collective strengths.</li><li>
Achieve Career Longevity &ndash; Take advantage of opportunities for learning and development that support a long-term career.</li><li>
Take Part in a Hands-on Working Culture &ndash; Work in a unique culture of active engagement and problem-solving, no matter your role.</li><li>
Feel Pride in Where you Work &ndash; Be part of making an impact in public health alongside dedicated people just like yourself.</li></ul>
Within the Georgia Public Health Laboratory this position serves as a Quality Analyst on the Quality Assurance team. Under the supervision of the Quality Assurance Director, the Quality Analyst will work to assure compliance with the requirements of the Clinical Laboratory Improvement Amendments of 1988 (CLIA) for a high-complexity clinical laboratory, implement the facility&rsquo;s quality management system, and participate in continuous quality improvement activities.
The Quality Analyst will support implementation of our inventory management system (Odoo); assist with management of various applications within the Quality Management System (QMS) including the MediaLab document control system and Clinisys Laboratory Solutions (CLS); and play a key role in implementing CLS with the health districts.</div> 

<div><h2 class="jobSectionHeader">Job Responsibilities</h2></div>
<div><ul><li>Serve as subject matter expert in quality management systems, providing leadership and guidance to staff to ensure that quality policies, processes, and procedures are established, current, and followed by all laboratory staff.</li><li>
Oversee the facility&rsquo;s inventory management system (Odoo), assisting laboratory sections with entering and labeling items.</li><li>
Assist with managing the facility-wide document control system using MediaLab and newly implemented laboratory information management system (LIMS), Clinisys Laboratory Solutions (CLS).</li><li>
Coordinate the completion of documentation of non-conforming events and assure implementation of corrective action.</li><li>
Assist laboratory sections with completion of calibration/certification activities and assure participation in appropriate proficiency testing programs for all sections of the laboratory.</li><li>
Participate in internal audits and external assessments by various regulatory agencies.</li></ul></div> 

<div><h2 class="jobSectionHeader">Minimum Qualifications</h2></div>
<div>Bachelor's degree in a related field from an accredited college or university and two (2) years in a managerial or supervisory role in the area of assignment; or six (6) years of experience in the area of assignment, including three (3) years in a managerial role; or one (1) year of experience required at the lower level Mgr, Regulatory Compliance (RCM050) or position equivalent. 
Preferred Qualifications:<ul><li>
Experience with MediaLab products.</li><li>
Experience with using a laboratory information management system.</li><li>
Master&rsquo;s degree in a related field from an accredited college or university and 2 years of laboratory experience or 2 years of experience directing in a laboratory quality management system.</li></ul></div> 

<div><h2 class="jobSectionHeader">Additional Information</h2></div>
<div>The DPH Commissioner and agency leaders encourage all employees to engage in regular wellness activities and to make lifestyle choices that promote health and well-being.
The use of physical activity breaks during the workday is authorized to support this philosophy and help employees meet their wellness goals. A maximum of 30 minutes of physical activity may be allocated per workday, typically in the form of two 15-minute breaks or one 30-minute break.
Employment Information
State of Georgia employees are subject to the rules of the State Personnel Board regarding salary.
DPH accepts educational credentials recognized by the Council for Higher Education Accreditation (CHEA) and/or the US Department of Education (DOE) as valid. DPH will contact educational institutions to verify degrees, diplomas, licensures, and other relevant credentials.
The candidate selected for this position may be subject to pre-employment drug screening and a criminal background check.
Relocation assistance is not provided.
In the event of an identified emergency, you may be required, as a term and condition of DPH employment, to assist in meeting the emergency responsibilities of the department.
ADA Statement
DPH is committed to providing access and reasonable accommodation in its services, programs, activities, and employment for individuals with disabilities. To request a reasonable accommodation for the application or interview process, email DPH-ADA@dph.ga.gov. 
DPH is an Equal Opportunity Employer
_________________________________________________________________________________ 
Due to the volume of applications received, we are unable to provide information on application status by phone or e-mail. All qualified applicants will be considered, but may not receive an interview. DPH will contact selected applicants to proceed with the application process. Applicants who are not selected will not receive notification.
This position is subject to close at any time once a satisfactory applicant pool has been identified.
BENEFITS<div>
Standard Benefits for Full-Time Salaried Employees 
 In addition to a competitive salary, we offer a generous benefits package that includes a flexible schedule, training opportunities, health insurance, employee retirement plan (ERS GSEPS), deferred compensation, 13 paid holidays, vacation and sick leave, paid parental leave, dental, vision, long-term care, and life insurance.</div><div> 
Standard Benefits for Part-Time Employees</div>
Part-time employees are eligible to participate in the Georgia Defined Contribution Plan and receive paid parental leave.</div></div></div>

Quality Analyst

Barclays

<div><div>Date live: 04/02/2026
 Business Area: Wholesale Onboarding and Group FCO
 Area of Expertise: Banking Operations
 Contract: Permanent
 Reference Code: JR-0000092977
 Salary / Rate $70,000.00 - $100,000.00</div></div>
 <div>Champion Quality and Strengthen Our Financial Crime Controls &ndash; Bring your curiosity, attention to detail, and commitment to doing things right into a role that helps protect our customers and our business. Step into your important position as a Quality Assurance Analyst, where you will autonomously assess the effectiveness and consistency of AML investigative activity against established policies, procedures, and regulatory expectations. In your role, you&rsquo;ll identify, document, and escalate control, policy, and process gaps through structured QA reviews, ensuring every finding is accurate, evidence based, and applied with consistency. Your work will reinforce our risk and control framework by validating AML outcomes, spotting emerging trends, and contributing to governance, reporting, and remediation oversight. With a focus on &ldquo;right first time&rdquo; quality, you&rsquo;ll help ensure delivery within defined timelines and Enterprise Risk Management Framework (ERMF) requirements, providing reliable QA insights that support robust oversight and regulatory assurance across the organization.
To be successful in your role as a Quality Assurance Analyst, you should have:
<ul><li>An understanding of AML investigative processes, controls, and regulatory expectations
</li><li>Clear, professional written communication suitable for governance, audit, and regulatory audiences
</li><li>Great attention to detail and analytical capability to assess case work and supporting evidence
</li></ul>Other highly valued skills may include:
<ul><li>Experience performing AML Quality Assurance, Quality Control, or Transaction Monitoring
</li><li>Ability to engage with stakeholders constructively to discuss outcomes and reduce disputes or appeals
</li><li>Familiarity with continuous improvement, root cause analysis, and process enhancement
</li><li>Ability to work across multiple workstreams or within multi-layered AML environments
</li></ul>You may be assessed on the key critical skills relevant for success in this role, such as risk and controls, change and transformation, business acumen, strategic thinking, digital and technology, as well as job-specific technical skills.
This role is located in Whippany, NJ.
Minimum Salary: $70,000.00
Maximum Salary: $100,00.00
The minimum and maximum salary/rate information above include only base salary or base hourly rate. It does not include any other type of compensation or benefits that may be available.
Barclays employees are eligible for a suite of competitive and generous employee benefits, including medical, dental and vision coverage, 401(k), life insurance, and other paid leave for qualifying circumstances.
This position is eligible for an incentive award.
Purpose of the role
To determine, negotiate and agree internal quality procedures, service standards and specification to improve performance and quality directing objectives.
Accountabilities
<ul><li>Identification of industry trends and developments to implement best practice in quality assurance Services.</li>
<li>Collaboration with teams across the bank to align and integrate quality assurance processes.</li>
<li>Development and governance of internal quality assurance procedures, standards and specifications, and act as a catalyst for change, mitigate risks and maintain efficient operations.</li>
<li>Development of reports and presentations on quality assurance performance and communicate findings to internal senior stakeholders.</li>
<li>Identification of areas for improvement and providing recommendations for change in quality assurance processes and provide feedback and coaching for colleagues on these highlighted areas.</li>
<li>Execution of service quality assessments to monitor the quality objectives set by the bank, and ensure they comply with regulatory requirements.</li>
<li>Participation in projects and initiatives to improve quality assurance efficiency and effectiveness.</li>
<li>Determination of risk based on outcome of QA reviews, flagging risks that are outside of tolerance.</li>
</ul>Analyst Expectations
<ul><li>To perform prescribed activities in a timely manner and to a high standard consistently driving continuous improvement.</li>
<li>Requires in-depth technical knowledge and experience in their assigned area of expertise</li>
<li>Thorough understanding of the underlying principles and concepts within the area of expertise</li>
<li>They lead and supervise a team, guiding and supporting professional development, allocating work requirements and coordinating team resources.</li>
<li>If the position has leadership responsibilities, People Leaders are expected to demonstrate a clear set of leadership behaviours to create an environment for colleagues to thrive and deliver to a consistently excellent standard. The four LEAD behaviours are: L &ndash; Listen and be authentic, E &ndash; Energise and inspire, A &ndash; Align across the enterprise, D &ndash; Develop others.</li>
<li>OR for an individual contributor, they develop technical expertise in work area, acting as an advisor where appropriate.</li>
<li>Will have an impact on the work of related teams within the area.</li>
<li>Partner with other functions and business areas.</li>
<li>Takes responsibility for end results of a team&rsquo;s operational processing and activities.</li>
<li>Escalate breaches of policies / procedure appropriately.</li>
<li>Take responsibility for embedding new policies/ procedures adopted due to risk mitigation.</li>
<li>Advise and influence decision making within own area of expertise.</li>
<li>Take ownership for managing risk and strengthening controls in relation to the work you own or contribute to. Deliver your work and areas of responsibility in line with relevant rules, regulation and codes of conduct.</li>
<li>Maintain and continually build an understanding of how own sub-function integrates with function, alongside knowledge of the organisations products, services and processes within the function.</li>
<li>Demonstrate understanding of how areas coordinate and contribute to the achievement of the objectives of the organisation sub-function.</li>
<li>Make evaluative judgements based on the analysis of factual information, paying attention to detail.</li>
<li>Resolve problems by identifying and selecting solutions through the application of acquired technical experience and will be guided by precedents.</li>
<li>Guide and persuade team members and communicate complex / sensitive information.</li>
<li>Act as contact point for stakeholders outside of the immediate function, while building a network of contacts outside team and external to the organisation.</li>
</ul>All colleagues will be expected to demonstrate the Barclays Values of Respect, Integrity, Service, Excellence and Stewardship &ndash; our moral compass, helping us do what we believe is right. They will also be expected to demonstrate the Barclays Mindset &ndash; to Empower, Challenge and Drive &ndash; the operating manual for how we behave.</div>

Quality Assurance Analyst

Cummins

<div>DESCRIPTION
We are looking for a talented Quality Analyst &ndash; Shipping to join our team specializing in Quality for our Cummins Inc. facility in Whiteland, IN.
In this role, you will make an impact in the following ways:
<ul><li>Ensure accurate, timely documentation and data entry that supports informed decision-making for the team, department, or organizational leaders.</li>
<li>Improve operational efficiency by researching information, preparing statistical reports, and responding effectively to routine and complex information requests.</li>
<li>Maintain data integrity by gathering, verifying, and compiling information across reports, presentations, forms, databases, and spreadsheets.</li>
<li>Enable smooth daily operations by coordinating meetings, conference calls, correspondence, and visitor interactions with minimal supervision.</li>
<li>Serve as a reliable point of contact by responding to or redirecting internal and external inquiries promptly, accurately, and professionally.</li>
<li>Support financial and vendor processes by preparing payment documentation, submitting requests in accounting systems, and resolving related inquiries.</li>
<li>Strengthen consistency and compliance by documenting, maintaining, and updating departmental policies and procedures.</li>
<li>Contribute to continuous improvement by participating in business improvement projects and acting as an informal resource for less-experienced colleagues.</li>
</ul>RESPONSIBILITIES
To be successful in this role you will need the following:
<ul><li>Demonstrate a proactive, customer-focused mindset by taking initiative on new challenges, communicating clearly across diverse audiences, and building strong relationships to deliver effective, customer-centric solutions.</li>
<li>Plan, prioritize, and execute work effectively while holding yourself and others accountable to meet commitments aligned with organizational goals.</li>
<li>Analyze qualitative and quantitative data to identify meaningful patterns and insights, applying sound business judgment, statistical principles, and problem-solving techniques.</li>
<li>Translate data into clear, actionable insights by validating data, drawing well-supported conclusions, and enabling data-driven decision-making.</li>
<li>Communicate complex findings effectively through clear data visualization, reports, and dashboards that tell the story of business problems, root causes, and solution options.</li>
</ul>Education/Experience
<ul><li>High school diploma or certificate of completion of secondary education or equivalent experience to the extent such experience meets applicable regulations.</li>
<li>This position may require licensing for compliance with export controls or sanctions regulations.</li>
<li>Requires significant relevant work experience or specialized skills obtained through education, training, or on-the-job experience.</li>
</ul>QUALIFICATIONS
Additional Information
<ul><li>College Degree Preferred</li>
</ul>Core Responsibilities:
<ul><li>Investigate shipment discrepancies, determine root causes, and implement preventive measures to ensure ongoing quality and compliance.</li>
<li>Support customer claims process and co-ordinate between shipping office and claims analyst team.</li>
<li>Actively support the Quality team with additional activities as needed to meet quality targets and drive continuous improvement.</li>
<li>Ability to occasionally lift up to 35 lb. as required to support operational activities.</li>
</ul>Skills Needed for the Role:
<ul><li>Strong ability to prioritize tasks, manage competing deadlines, and maintain attention to detail in a fast-paced environment.</li>
<li>Excellent verbal and written communication skills with a customer-focused mindset.</li>
<li>Strong computer skills and data analysis skills.</li>
<li>Demonstrated experience with data entry, report generation, and office productivity tools (e.g., Microsoft Excel, PowerPoint, databases).</li>
<li>Ability to handle sensitive information with professionalism and discretion.</li>
<li>Strong organizational and problem-solving skills.</li>
<li>Experience working cross-functionally with internal teams and external stakeholders with a collaborative mindset.</li>
<li>Ability to explain complex topics clearly to diverse audiences.</li>
</ul>Compensation (for United States)
Please note that the salary range provided is a good faith estimate on the applicable range. The
final salary offer will be determined after considering relevant factors, including a candidate&rsquo;s
qualifications and experience, where appropriate.
Job Quality
Organization Cummins Inc.
Role Category On-site with Flexibility
Job Type Office
ReqID 2426810
Relocation Package Yes
100% On-Site Yes
Due to the operational nature and specific job duties of this role, work is required to be completed 100% in person/On-site.
Cummins and E-Verify
At Cummins, we are an equal opportunity and affirmative action employer dedicated to diversity in the workplace. Our policy is to provide equal employment opportunities to all qualified persons without regard to race, gender, color, disability, national origin, age, religion, union affiliation, sexual orientation, veteran status, citizenship, gender identity and/or expression, or other status protected by law. Cummins validates the right to work using E-Verify and will provide the Social Security Administration (SSA) and, if necessary, the Department of Homeland Security (DHS), with information from each new employee&rsquo;s Form I-9 to confirm work authorization. Visit http://EEOC.gov to know your rights on workplace discrimination.</div>

Quality Analyst - Shipping

DCD Vehicle Corp

Location: Orlando, FL 32809 Department: Quality Control Reports to: Quality Control Manager Employment Type: Full-timeJob DescriptionWe are seeking a diligent and detail-oriented Quality Control Inspector to join our golf car manufacturing operation. This role is essential in ensuring that each vehicle meets quality standards before reaching our customers. Inspectors are responsible for conducting full inspections, coordinating with other departments for repairs or touch-ups, and verifying final readiness for shipment.Key Responsibilities<ul><li>Fully inspect each incoming golf car using standardized QC forms to ensure all components meet quality requirements.</li><li>Maintain workflow in the QC area, ensuring the space is clean, organized, and operating efficiently.</li><li>After initial inspection, direct the vehicle to the appropriate department&mdash;mechanics, paint, or detail&mdash;based on identified issues.</li><li>Conduct re-inspections of vehicles after repair or detailing to confirm all issues have been resolved.</li><li>Relocate fully approved vehicles to the designated shipping area.</li><li>Ensure each golf car is updated to the latest settings/configurations and apply a sticker on the windshield to confirm the update.</li><li>Torque battery terminals (positive and negative) to the proper specification on each unit.</li><li>While overtime is not mandatory, it is expected during peak production periods and will impact bonus eligibility and performance reviews.</li></ul>Qualifications<ul><li>High school diploma required; bachelor&rsquo;s degree preferred.</li><li>1&ndash;2 years of experience in quality inspection, preferably in automotive or manufacturing environments.</li><li>Familiarity with quality control methods such as Six Sigma is a plus.</li><li>Experience with measuring tools, including meters, gauges, computers, and calipers.</li><li>Ability to read blueprints or technical diagrams is preferred.</li><li>Strong written and verbal communication skills.</li><li>Competence in basic math, computer use, and data entry.</li><li>High attention to detail, strong analytical and documentation skills.</li><li>Mandarin language proficiency preferred for team communication.</li></ul>Additional Information<ul><li>Health insurance is provided.</li><li>Other benefits will be discussed during the interview.</li><li>This is a key position with long-term development opportunities for individuals who demonstrate strong performance and reliability.</li></ul>Job Type: Full-timePay: $4,000.00 - $6,000.00 per monthBenefits:<ul><li>Health insurance</li></ul>Work Location: In person

Quality Control Inspector (Mandarin Required)

Custom Filters Direct

<div>
 
 
 
 
 
 
 
 Job Title: Quality Control Specialist (Full-Time)
 
 
 
 
 
 
 
 
 
 
 
 
 
 Company: Custom Filters Direct
 
 
 
 
 
 
 
 
 
 
 
 
 
 Location: Bloomsburg, PA
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 Have experience in quality control and take pride in ensuring products meet the highest standards?
 
 
 
 
 
 
 
 
 
 
 
 
 
 Custom Filters Direct is seeking a detail-oriented Quality Control Specialist to support inspections, audits, and continuous improvement across our manufacturing operations.
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 Schedule:
 
 
 
 
 
 
 
 
 
 
 
 
 
 Monday through Friday
 
 
 
 
 
 
 
 
 
 
 
 
 
 7:00 AM &ndash; 3:30 PM (Overtime may be required based on business needs)
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 Compensation &amp; Benefits:
 
 
 
 
 
 
 
 
 
 
 
 
 
 &bull; Salary based on experience
 
 
 
 
 
 
 
 
 
 
 
 
 
 &bull; Medical, Dental, and Vision insurance available after 90 days
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 About Us:
 
 
 
 
 
 
 
 
 
 
 
 
 
 Custom Filters Direct is a growing manufacturer specializing in custom air filters for eCommerce companies and direct fulfillment. We are committed to delivering high-quality products and continuously improving our processes to meet customer expectations.
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 Position Overview:
 
 
 
 
 
 
 
 
 
 
 
 
 
 The Quality Control Specialist is responsible for inspecting and evaluating incoming materials, in-process production, and finished goods to ensure compliance with company and industry standards. This role supports quality assurance processes, documentation, audits, and continuous improvement initiatives.
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 Key Responsibilities:
 
 
 
 
 
 
 
 
 
 
 
 
 
 &bull; Conduct inspections of incoming materials, in-process production, and finished products
 
 
 
 
 
 
 
 
 
 
 
 
 
 &bull; Ensure compliance with quality standards, specifications, and work instructions
 
 
 
 
 
 
 
 
 
 
 
 
 
 &bull; Perform quality checks including product specifications and weight verification
 
 
 
 
 
 
 
 
 
 
 
 
 
 &bull; Identify defects, non-conformances, and areas for improvement
 
 
 
 
 
 
 
 
 
 
 
 
 
 &bull; Support root cause analysis and corrective/preventive actions (CAPA)
 
 
 
 
 
 
 
 
 
 
 
 
 
 &bull; Maintain accurate quality documentation, reports, and inspection records
 
 
 
 
 
 
 
 
 
 
 
 
 
 &bull; Create and analyze quality trends and reports
 
 
 
 
 
 
 
 
 
 
 
 
 
 &bull; Support internal quality audits and process evaluations
 
 
 
 
 
 
 
 
 
 
 
 
 
 &bull; Work cross-functionally with production to resolve quality issues
 
 
 
 
 
 
 
 
 
 
 
 
 
 &bull; Ensure adherence to quality control procedures and standards
 
 
 
 
 
 
 
 
 
 
 
 
 
 &bull; Assist with continuous improvement initiatives
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 Qualifications:
 
 
 
 
 
 
 
 
 
 
 
 
 
 &bull;
 
 
 
 
 
 
 
 
 
 
 
 
 Previous quality control experience in a manufacturing environment required*
 
 
 
 
 
 
 
 
 
 
 
 
 
 &bull; Familiarity with quality systems, inspections, and documentation
 
 
 
 
 
 
 
 
 
 
 
 
 
 &bull; Experience with audits, root cause analysis, or CAPA preferred
 
 
 
 
 
 
 
 
 
 
 
 
 
 &bull; Strong attention to detail and problem-solving skills
 
 
 
 
 
 
 
 
 
 
 
 
 
 &bull; Ability to analyze data and identify trends
 
 
 
 
 
 
 
 
 
 
 
 
 
 &bull; Strong communication and leadership skills
 
 
 
 
 
 
 
 
 
 
 
 
 
 &bull; Ability to work independently and as part of a team
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 Physical Requirements:
 
 
 
 
 
 
 
 
 
 
 
 
 
 &bull; Ability to stand for extended periods
 
 
 
 
 
 
 
 
 
 
 
 
 
 &bull; Frequent walking, bending, reaching, and working on the production floor
 
 
 
 
 
 
 
 
 
 
 
 
 
 &bull; Comfortable working in a manufacturing environment
 
 
 
 
 
 
 
</div>

Quality Control Specialist

United Biosource Corporation

<div>As a pharmaceutical support industry leader, UBC is devoted to empowering health solutions for a better tomorrow. We take pride in improving patient outcomes and advancing healthcare. At UBC we provide services to enhance the entire drug development process and commercialization lifecycle - From clinical trial support to real-world evidence generation.
Embark on a rewarding career journey with UBC! Grow your career while making a meaningful impact on the world around you. UBC fosters a culture built on our Core Values being: Collaborative, Conscientious, Curious, Consultative, and Compassionate. We believe in an inclusive workplace that fosters creativity.
If you are seeking a career that will challenge, inspire, and reward you, join us at UBC! 
Quality Control Specialist 
 
Brief Description:
Responsible for completing quality control checks on assigned programs and assisting in the implementation, maintenance and documentation of quality control practices, procedures and programs. 
Specific job duties:<ul><li>
Perform quality control checks on assigned programs, identify corrective and preventive actions, and perform follow-up activities.</li><li>
Review associates&rsquo; documentation for accuracy.</li><li>
Print and review daily reports for assigned programs.</li><li>
Assist operational staff in developing and implementing operational quality control processes utilizing appropriate tools (checklists, double-data entry, etc).</li><li>
Monitor the effectiveness of the implemented quality control procedures and report summarized results of all quality control processes to the Director, Program Management &amp; Quality Control and Senior Manager, Quality Assurance.</li><li>
Promote quality awareness.</li><li>
Other duties as assigned by the Director, Program Management &amp; Quality Control and as determined by UBC SOPs.</li></ul> 
Desired Skills and Qualifications:<ul><li>
High School Graduate; college degree preferred.</li><li>
Knowledge of Post Marketing Drug Surveillance programs</li><li>
Quality Control related experience in call centers, health care or pharmaceutical care</li><li>
Working knowledge of Microsoft Word, Excel, PowerPoint and other Office tools as required</li><li>
Well-organized</li><li>
Strong attention to detail</li><li>
Good written/verbal skills</li><li>
Good interpersonal skills</li><li>
Good time management skills</li></ul> 
Benefits:
At UBC, employee growth and well-being are always at the forefront. We offer an extensive range of benefits to ensure that you have everything you need to thrive personally and professionally.
Here are some of the exciting perks UBC offers:<div><ul><li>
Remote opportunities</li><li>
Competitive salaries</li><li>
Growth opportunities for promotion</li><li>
401K with company match*</li><li>
Tuition reimbursement (after 90 days of employment)</li><li>
Flexible work environment</li><li>
20 days PTO</li><li>
Paid Holidays</li><li>
Employee assistance programs</li><li>
Medical, Dental, and vision coverage</li><li>
HSA/FSA</li><li>
Telemedicine (Virtual doctor appointments)</li><li>
Wellness program</li><li>
Adoption assistance</li><li>
Short term disability (after 90 days of employment)</li><li>
Long term disability</li><li>
Life insurance</li><li>
Discount programs</li></ul></div> 
UBC is proud to be an equal opportunity employer and does not discriminate because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, and basis of disability or any other federal, state, or local protected class. We are committed to a diverse, equitable and inclusive culture that fosters respect for each other, our clients, and our patients.</div>

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