quality assurance tech

Chelten House Products LLC

<div><div><b>Quality Assurance Technician (Packaging)</b></div>
<div>(1st shift 5:00 am- 3:30 pm Monday-Thursday, overtime Friday requirements)</div>
<div></div><div><b>Who We Are:
</b></div><ul><li>Chelten House Products, Inc. is a fourth-generation, family-owned, food industry manufacturer with facilities in Swedesboro, New Jersey. We are an industry leader widely recognized for our commitment to crafting the finest-tasting pasta sauces, salad dressings, salsas, ketchups, and other sauces and blends.</li>
</ul>
<div></div><div><b>What We Have:</b></div>
<ul><li>Benefits such as medical, vision and dental</li>
<li>Company-wide perks, including (7) paid holidays and paid time off</li>
<li>Employee appreciation events</li>
<li>Supplemental benefits including life insurance and 401k contributions</li>
<li>Team training sessions and advancement opportunities</li>
<li>A diversified workforce committed to excellence and innovation</li>
<li>Transparent and accessible leadership team</li>
<li>Competitive hourly pay range $22-$24</li>
<li>Eligible annual performance bonus</li>
</ul>
<div></div><div><b>What We Need:</b></div>
<ul><li>We are looking for a Quality Assurance Technician to support efforts to maintain the highest quality standards for all of our products. The QA Technician will ensure all Quality standards are being met on the production floor with Packaging.</li>
</ul>
<div></div><div><b>What You Will Do:</b></div>
<div><ul><li>Inspect and document all quality assurance facility activities that take place on the production floor and report any discrepancies to the Quality Assurance Manager, involving cross-functional team members as needed.</li>
<li>Verify all personnel are wearing appropriate uniforms and required GMP and safety items.</li>
<li>Verify the correctness of: glass, case, cap, celon and labels per schedule and packing slip by material number and specification. Check each batch and every 20 minutes for cap security/vacuum and continued accuracy.</li>
<li>Verify with filler operator correct product, pack temperature and weight. Check each batch and every 20 minutes.</li>
<li>Verify lot codes into bottle and case coders are inputted correctly per schedule and packing slip. Verify on packaging spec data. Check UPC symbols. Check each batch and every 20 minutes.</li>
<li>Verify correct palletizing, tag information and label integrity at palletizer station.</li>
<li>Immediately take action for ANY product or packaging falling out of specification. Place on hold any items not meeting the required specification and report to Quality Assurance Manager.</li>
<li>Collect 1 bottle of each ID# for comparison sample, 2 from each batch for 24hour &amp; retains.</li>
<li>Collect customer required samples.</li>
<li>Document findings in formal report to departmental Leads, Supervisors and Manager.</li>
<li>Inspects and approves outgoing completed product aligned with proper inspection procedures, product specifications, transportation requirements, and food safety regulations.</li>
<li>Maintains measurement and testing equipment in operational condition on the shop floor, reporting any issues.</li>
<li>Maintains a safe and healthy work environment by following standards and procedures, including compliance with FDA, USDA, and company policies.</li>
<li>Follow Company SOPs and assure that appropriate department involvement takes place as needed, i.e. calling for maintenance to support machine issues that may affect quality or food safety and notifying Production Leadership assuring cross-functional involvement.</li>
<li>Any issues that are found where food safety or quality assurance is out of compliance must be addressed with corrective actions implemented in real time where possible, or a product hold, with involvement and escalation to the Quality Assurance Lead, Quality Assurance Manager and Production Team Leadership.</li>
<li>The employee constantly works in plant and production areas and is required to communicate with supervisors and operations employees, in a professional and effective manner.</li>
</ul></div><div><b>What You Need:</b></div>
<ul><li>High school diploma: associate degree or bachelor&rsquo;s degree in biology, chemistry, or microbiology preferred.</li>
<li>Experience with HACCP, USDA, and FDA standards.</li>
<li>Knowledge of quality assurance measuring, and testing equipment preferred.</li>
<li>Understanding of SSOP and sanitation verification preferred.</li>
<li>Working knowledge of quality systems preferred.</li></ul></div>

Quality Assurance Technician (1st shift)

3MD Inc.

<div><b>*Full Time on-site requirement in Denver, CO*</b><p><b><br>
Benefits</b></p><p>
 U.S.-based employees have access to medical, dental, and vision insurance, a 401(k) plan and company contribution, short-term and long-term disability coverage, basic life insurance, and wellbeing benefits, among others. U.S.-based employees also receive, per calendar year, up to 6 scheduled paid holidays. Additionally, eligible hourly/non-exempt and exempt employees accrue up to 112 hours of PTO based on years of service and may annually take up to 8 hours of paid volunteer time. Additional paid sick leave is also provided if required by state or local law.</p><div></div><div><p><b><br>
Summary of Position:</b></p><p>
The IT Quality Assurance plans, executes, and completes the analysis of IT-quality-related issues along the Software Development Life Cycle (SDLC) and deliverables. Assists in identifying, evaluating, and monitoring processes, systems, and procedures to meet IT-quality requirements and Internal Audit findings. Ensures that the quality of the delivered products is aligned with the Quality Assurance methodology.</p><p><b>
Essential Functions:</b></p><ul><li>
Design, Develop, and Execute test cases and test suites focusing on efficiency and maintainability while ensuring the highest in quality standards</li><li>
Collaborate closely with Software Development Engineers in Test to maximize re-usable automation scripts.</li><li>
Perform exploratory testing beyond defined test methods with a focus on efficiency and risk mitigation</li><li>
Consult and advise management regarding software readiness and critical issues</li><li>
Create strategic core test plans encompassing functional, regression, and smoke tests with meaningful test steps and expected results based on functional requirements and User Stories</li><li>
Review and reconcile project deliverables aligned with strategic IT-quality standards</li><li>
Conceptualize, document, and communicate solutions concerning IT-Quality</li><li>
Requires competency in customer focus, change &amp; innovation, strategic thinking, relationship building &amp; influencing talent management, results focus, and inspirational leadership</li><li>
Demonstrates working knowledge of Software Development Life Cycle (SDLC) methodology (processes, and deliverables) and can work with the process and application teams to identify and close the gaps concerning IT-quality issues as well as provide metrics for monitoring purposes and measures of success</li><li>
Demonstrates knowledge to conceptualize, document, and communicate solutions concerning IT-Quality issues</li><li>
Ensures review of Quality Assurance documentation for accuracy, feasibility, consistency, and completeness.</li><li>
Executes initiatives to improve processes, procedures, and tools for IT-quality purposes utilized by the cross-functional teams</li><li>
Creates and delivers articulate and effective oral presentations to a variety of audiences, large or small, internal, or external</li></ul><p><b>
Competencies:</b></p><ul><li>
Ensures Accountability</li><li>
Tech Savvy</li><li>
Communicates Effectively</li><li>
Values Differences</li><li>
Customer Focus</li><li>
Resourcefulness</li><li>
Drives Results</li><li>
Plans and Prioritizes</li><li>
Decision Quality</li><li>
Self-Development</li></ul><p><b>
Work Environment:</b></p><p>
This job operates in a professional office environment. This role routinely uses standard office equipment such as computers, phones, photocopiers, filing cabinets, and fax machines.</p><p><b>
Physical Demands:</b></p><p>
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.</p><p>
While performing the duties of this job, the employee in this position frequently communicates with other co-workers/clients who have inquiries about the various projects and other needs. Must be able to exchange accurate information in these situations. The employee must be able to remain in a stationary position 75% of the time. The employee in this position needs to occasionally move about inside the office to access file cabinets, office machinery, etc. Constantly operate a computer and office machinery such as a calculator, keyboard, copy machine, and printer. Frequently moves boxes with equipment weighing up to 25 lbs across the building and/or to other offsite buildings for various project needs.</p><p><b>
Required Education and Experience:</b></p><ul><li>
High School Diploma or general equivalent</li><li>
3+ Years of Experience</li></ul><p><b>
Qualifications:</b></p><ul><li>
3 years minimum experience with a formal SDLC</li><li>
3 years minimum experience creating SDLC deliverables (Requirements, Functional, Design, and Test Requirements Specification Documents Management and communication of project status, budgets, and risk registers</li><li>
Ability to analyze and solve complex problems quickly and creatively</li><li>
Experience with client-server systems and understanding the types of issues that may arise</li><li>
Ability to learn quickly in a dynamic environment</li><li>
Excellent oral, written, and interpersonal communication skills</li><li>
Self-motivated and team player</li><li>
Ability to handle multiple tasks and priorities</li></ul><p><b>
AAP/EEO Statement:</b></p><p>
3MD Inc. is an equal opportunity employer and does not discriminate based on gender, sex, age, race, color, religion, marital status, national origin, disability, sexual orientation, gender identity or expression, veteran status, or any other category that is protected by applicable law.</p><p><b>
Other Duties:</b></p><p>
Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties,</p></div></div>

IT Quality Assurance - DTS

Desi Fresh Foods

<p><strong> About Us </strong></p><p> <strong>Desi Fresh Foods</strong> is a leading "cultured" dairy manufacturer with over 23 years of experience. We produce high-quality and consistent products, which include yogurt (Dahi or Indian, Greek and traditional), smoothies / yogurt drinks, sour cream, and dips from single serve options to the food service side. We are currently seeking a skilled Quality Assurance Technician to join our team and contribute to the ongoing success of our facility in Winchester, Virginia! </p> <p><strong> About the Role </strong></p><p>The <strong>Quality Assurance Technician</strong> plays a critical role in ensuring the production of high-quality finished goods within our food production facility. This position is responsible for implementing and monitoring comprehensive food safety and quality control programs. The technician's diligence ensures compliance with regulatory standards, customer specifications, and company policies.</p><p><strong>Hours:</strong> 3rd Shift: 11 pm - 7 am</p><p>This is a Monday to Friday role, with some weekends or overtime as needed.</p><p><strong> Commitment to Excellence </strong></p><p>The Quality Assurance Technician is dedicated to upholding the highest standards of product quality and food safety. Through meticulous attention to detail and a proactive approach, this role ensures that our consumers receive products that are safe, consistent, and of the highest quality.</p> <p><strong> Responsibilities </strong> </p><ul><li><p>Adhere to the company's Code of Conduct, GMP policies, and all internal procedures, while performing additional duties as assigned by management.</p></li><li><p>Monitor production processes for compliance with company programs and policies, including but not limiting to GMPs, HACCP, as FDA regulations.</p></li><li><p>Conduct quality checks on raw materials, in-process products, finished goods, CCP verification, packaging, and labeling.</p></li><li><p>Perform pre-operational inspections and daily sanitation verifications to ensure plant cleanliness and readiness.</p></li><li><p>Collect samples for microbiological and chemical testing with accurate record-keeping.</p></li><li><p>Identify and escalate food safety or quality issues, implementing corrective actions as needed.</p></li><li><p>Inspect packaging materials and labels for accuracy and compliance with specifications.</p></li><li><p>Maintain detailed records for inspections, tests, and corrective actions per HACCP, SQF, and other programs.</p></li><li><p>Support customer, regulatory, and third-party audits with preparation and participation.</p></li><li><p>Provide food safety and quality training to production staff while supporting compliance efforts.</p></li><li><p>Collaborate with other teams, including production to troubleshoot and recommend process improvements.</p></li><li><p>Support the QA Manager in maintaining quality and food safety programs, including HACCP, GMP, and SQF.</p></li><li><p>Conduct physical, analytical, and sensory testing of finished products, as needed, ensuring adherence to standards.</p></li><li><p>Propose process improvements, participate in risk assessments for new or improved products or systems, and develop action plans to address recurring quality or food safety challenges.</p></li></ul> <p> <strong> Qualifications </strong> </p><ul><li><p>Bachelor's degree in Food Science, Chemistry, Biology, or a related field preferred.</p></li><li><p>2 years of experience in food manufacturing quality assurance or a related field.</p></li><li><p>HACCP certification and knowledge of SQF, AIB, and FDA standards.</p></li><li><p>Strong organizational and analytical skills with attention to detail.</p></li><li><p>Proficiency in Microsoft Office (Excel, Word, Outlook) and other data entry systems.</p></li><li><p>Ability to multitask and prioritize in a fast-paced environment.</p></li><li><p>Excellent communication and teamwork skills.</p></li><li><p>Bilingual (English/Spanish) is a plus.</p></li></ul><p><strong> Physical Demands and Work Environment </strong></p><ul><li><p>Ability to lift up to 30 pounds; perform repetitive tasks such as bending, squatting, and reaching.</p></li><li><p>Ability to stand for extended periods and work in noisy, cold, or hot environments with appropriate safety gear.</p></li><li><p>Occasional travel to off-site locations, such as farms or co-packers, may be required.</p></li></ul> <p><strong> We offer a competitive hourly rate of $22-24/hour plus benefits. </strong></p><p>Desi Fresh Foods is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.</p> PandoLogic. Category:Quality Control,<img src="https://www.jobg8.com/Tracking.aspx?idZ%2bdN1PYqUCitioqKdWheY6GD47tgGIn" width="0" height="0" />

Quality Assurance (QA) Technician, 3rd Shift

Astellas

<div><p>Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are driven to develop and deliver innovative and effective new medicines to patients and physicians. If you want to be part of this exciting work, you belong here!
</p><p>We are a leading pharmaceutical company conducting business in more than 70 countries around the world. We are committed to turning innovative science into medical solutions that bring value and hope to patients and their families. Keeping our focus on addressing unmet medical needs and conducting our business with ethics and integrity enables us to improve the health of people throughout the world.
</p><p>This position is based in Bengaluru, India. We recognize the importance of work/life balance, and we are proud to offer a hybrid working solution allowing time to connect with colleagues at the office with the flexibility to also work from home. We believe this will optimize the most productive work environment for all employees to succeed and deliver. Hybrid work from certain locations may be permitted in accordance with the Responsible Flexibility Guidelines.
</p><div><b>Purpose and Scope:<br>
</b></div><div></div><div>Responsible for managing and executing the Technology and Data Quality Assurance (TDQA) audit and validation oversight programs related to regional Digital X processes for computer systems, technology solutions, clinical and commercial systems, data integrity processes, and related process improvement initiatives within QA.
</div><div>Provides operational management to drive consistent cGxP compliance and validation approaches to ensure compliance with standards, policies, and procedures.
</div><div>Ensures compliance with global Electronic Records / Electronic signatures regulations and related cGxP regulatory requirements.
</div><div>Responsible for managing the TDQA audit program related to audits of vendors, service providers, and internal processes in support of computerized system validations for new system implementations, system upgrades, change controls, and periodic reviews for computer systems.
</div><div>Develops, facilitates, and implements process improvements and supports new technology initiatives as continually invests in new technology solutions and computerized systems.
</div><div>Contributes to the development, implementation, and successful execution of the QA mission, objectives and 3-5 year strategic plan.<br>
</div><div></div><div><div><div><div><p><b>Responsibilities and Accountabilities:
</b></p></div></div><br>
</div></div><ul><li>Responsible for directing and executing the TDQA program to oversee the computerized systems validation program, clinical, commercial, and R&amp;D electronic systems.
</li><li>Performs and ensures issue resolution, audits, and regulatory authority inspection preparation.
</li><li>Facilitates and leads the development and implementation of related continuous process improvement programs within Information Technology and business departments.
</li><li>Develops and drives the implementation of quality strategies and tactics related to Electronic Systems, technology solutions, and overall Quality discipline that ensure long term success for the quality assurance function. Translates strategies into prioritized short- and long-term objectives for the TDQA and QA department.
</li><li>Leads initiatives and programs across multiple departments, regions, business functions, and internal/external partners. Establishes and prioritizes quality initiatives to ensure execution of multiple projects concurrently.
</li><li>Responsible for the overall management of QA oversight of IT processes, electronic systems, technology solutions, and validation projects to assure quality of output as well as compliance with standards, policies, procedures, and regulations. Presents and defends validation strategy during Regulatory Authority and 3rd Party Inspections. Utilizes risk-based approaches to process oversight.
</li><li>Directs the establishment and execution of internal and vendor audit program related to computer software providers and computer related service providers utilized.
</li><li>Develops and drives the implementation of policies, procedures, standards, and tools in support of validation processes, data integrity processes, and quality systems and interfaces across multiple departments and levels of management. Responsible for facilitating and collaborating with cross functional areas to resolve complex and diverse problems with decision making responsibility for issues with major impact to stakeholder relationships, dossier approvals, compliance status, and the company&rsquo;s credibility and/or revenue. Authors, reviews, and approves departmental Quality System Documents as necessary. Participates in the biennial review of Quality System documentation.
</li><li>Ensures inspection readiness for regulatory inspections, 3rd Party inspections and internal audits.
</li><li>Provides leadership to functional areas with minimal management oversight. Provides guidance to functional areas across for validation, and quality systems related consultations. Represents QA management on process improvement project teams to provide regulatory compliance and technical expertise in all areas of continuous improvement, innovation, and validation.
</li><li>Manages the development and utilization of tools to track, trend and report quality metrics to management to assure that systems and procedures comply with external regulatory authority requirements for compliance. Collects and shares metrics to facilitate the Management Review process.
</li><li>Ensures close and effective collaboration with functional colleagues across the company for validation oversight, process improvements, and execution of audit scheduling, audit conduct, validation process, and validation oversight.</li></ul></div>
<br><div><p><b>Required Qualifications:
</b></p><ul><li>University degree required (Science or IT preferred)
</li><li>Minimum of 7 years in the pharmaceutical industry, with a minimum of 3 years in a Quality Assurance role.
</li><li>Demonstrated leadership skills, including the ability to lead and manage projects and staff in a matrixed, global setting.
</li><li>Demonstrated knowledge of global industry standards and regulatory requirements for, software development, computer system validation, Electronic Records / Electronic Signatures regulations, Good Clinical Practices (GCP), Good Manufacturing Practices (GMP), and Good Laboratory Practices (GLP), and related GxP regulations in the global regulatory environment including GAMP5, 21 CFR Part 11, EU Annex 11, and Japan Notice 0401022.
</li><li>Comprehensive knowledge of quality assurance of computer system validation process management in a pharmaceutical manufacturing and clinical development environment.
</li><li>Demonstrated knowledge of development, management, and execution of internal and vendor auditing processes, audit reporting systems, and audit/CAPA management.
</li><li>Demonstrated experience in facilitating and supporting regulatory agency inspections and third party audits pertaining to Data Integrity and Electronic Records/Electronic Signatures compliance with successful outcomes.
</li><li>Demonstrated experience facilitating and leading global process improvement and harmonization activities, especially in the areas of Data Integrity, computing environment development, validation, control, and maintenance.
</li><li>Demonstrated competence to resolve complex and diverse problems with decision making responsibility that has a major impact within Quality and/or with functional groups globally.
</li><li>Effective written and oral communication and interpersonal skills, facilitation and influencing skills with an ability to interface globally across multiple departments and across various levels of management and with external stakeholders.
</li><li>Domestic and international travel of 5-10% is required.
</li></ul><p>&quot;Beware of recruitment scams impersonating Astellas recruiters or representatives. Authentic communication will only originate from an official Astellas LinkedIn profile or a verified company email address. If you encounter a fake profile or anything suspicious, report it promptly to LinkedIn's support team through LinkedIn Help&quot;</p></div><p></p>

Lead, Quality Assurance, Technology & Data

Almarai - المراعي

<div>
 <p>
  QA Technician, Abu Dhabi, United Arab Emirates
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   The Company:
  </strong>
 </p>
 <p>
  Almarai is the world&rsquo;s largest vertically integrated dairy and the region&rsquo;s largest food and beverage manufacturing and distribution company. Headquartered in the Kingdom of Saudi Arabia, Almarai Company is ranked as the #1 FMCG Brand in the MENA region and is a market leader in all its categories across the GCC. &ldquo;Almarai currently employs over 46,000 employees servicing some 110,000 retail outlets and has reported net income of SAR 2.31 billion on sales of SAR 20.97 billion in 2024.&rdquo;
 </p>
 <p>
  <br/>
 </p>
 <p>
  An aggressive expansion program together with acquisitions in new vertical markets have created an exciting opportunity to join a dynamic multinational team dedicated to furthering growth plans for the group.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   About the Role:
  </strong>
 </p>
 <p>
  Carry out the predetermined range of chemical, organoleptic and bacteriological tests required to monitor quality parameters from raw materials through to finished product and associated services to assist in identifying causes of non-conformance.
 </p>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Requirements
  </strong>
  :
 </p>
 <p>
  Potential candidates must meet the requirements mentioned below:
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Bachelor&rsquo;s degree in microbiology.
  </li>
  <li>
   Fresh Graduate is preferred / 2 years of hands-on experience in a microbiology laboratory, preferably in a food/pharmaceutical.
  </li>
  <li>
   Proficient in media preparation, sample handling, serial dilution, plating techniques (pour plate, spread plate, membrane filtration), experience in incubation, colony counting, and identification of microorganisms, familiarity with aseptic techniques and laboratory hygiene protocols.
  </li>
  <li>
   Knowledge of ISO 17025, GMP, or GLP standards.
  </li>
  <li>
   Willingness to work in shifts
  </li>
  <li>
   Basic computer skills (MS Excel, Word, etc.).
  </li>
  <li>
   Good Communication Skills (English).
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  Almarai offers a competitive package, generous leave, medical coverage, discretionary bonus, training, and development etc.
 </p>
 <p>
  <br/>
 </p>
 <p>
  This is a great opportunity to join a successful and expanding global business, offering an excellent remuneration and benefits package
 </p>
</div>


Quality Assurance Technician

شركة المراعي

<p>QA Technician, Abu Dhabi, United Arab Emirates</p><p><strong>The Company:</strong></p><p>Almarai is the world's largest vertically integrated dairy and the region's largest food and beverage manufacturing and distribution company. Headquartered in the Kingdom of Saudi Arabia, Almarai Company is ranked as the FMCG Brand in the MENA region and is a market leader in all its categories across the GCC. "Almarai currently employs over 46,000 employees servicing some 110,000 retail outlets and has reported net income of SAR 2.31 billion on sales of SAR 20.97 billion in 2024."</p><p>An aggressive expansion program together with acquisitions in new vertical markets have created an exciting opportunity to join a dynamic multinational team dedicated to furthering growth plans for the group.</p><p><strong>About the Role:</strong></p><p>Carry out the predetermined range of chemical, organoleptic and bacteriological tests required to monitor quality parameters from raw materials through to finished product and associated services to assist in identifying causes of non-conformance.</p><p><strong>Requirements</strong>:</p><p>Potential candidates must meet the requirements mentioned below:</p><ul><li>Graduate in food/ or Bakery science or other related discipline.</li><li>3 years' experience in the food / pharmaceutical industry or a similar environment</li><li>Having Chemical handling skills.</li><li>Should be a good team player.</li></ul><p>Almarai offers a competitive package, generous leave, medical coverage, discretionary bonus, training, and development etc.</p><p>This is a great opportunity to join a successful and expanding global business, offering an excellent remuneration and benefits package</p><img src="https://www.jobg8.com/Tracking.aspx?D9MLp94I7TMOb3ncw9In9LmgdeHnF0g8d" width="0" height="0" />

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