quality auditor

EmployHQ

<p><b>Key Responsibilities:</b></p><ul><li>Audit product coming out of all stages of production.</li><li>Check product for defects.</li><li>Measure product.</li><li>Enter all audit information into the computer.</li><li>Use a tablet/computer for reporting.</li><li>Any other duties as deemed necessary by the QA Manager.</li><li>Must be able to work in other buildings.</li><li>Overtime required as needed.</li></ul><p><b>Qualifications:</b></p><ul><li>Computer skills/data entry required.</li><li>May be asked to lift up to 40 lbs.</li></ul><p>Job Type: Full-time</p><p>Pay: $14.00 per hour</p><p>Work Location: In person</p>

Quality Auditor - 2nd shift

PCI Group

<div><div><p>__________________________________________________________________________________________________</p><p><b>
Job</b> <b>Position</b>: Quality Assurance Auditor</p><p><b>
Reports to: </b>Quality Assurance Manager</p><p><b>
Department</b>: Inserting</p><p><b>
Classification</b>: Overtime Eligible</p><p>
__________________________________________________________________________________________________</p><p></p><p><br>
PCI Group is the leading provider of mission critical communications for businesses where security of customer-centric data is paramount, precision and accuracy are crucial, and compliance is a must.</p><p></p><p><b><br>
Job Summary</b>:<br>
 The Quality Assurance (QA) Auditor Technician plays a pivotal role in maintaining PCI Group&rsquo;s commitment to excellence. This position is responsible for auditing, inspecting, and documenting the internal processes within the Inserting department. The primary objective is to ensure that all products meet our stringent quality standards, and that customers receive flawless output with no variations, defects, or missing components. This role requires a keen eye for detail, a deep understanding of quality assurance principles, and the ability to work collaboratively across teams to drive continuous improvement.</p><h2 class="jobSectionHeader"><b><br>
</b></h2><h2 class="jobSectionHeader"><b>
Some General Duties/Responsibilities:</b></h2><ul><li>
Perform audits and visual inspections to ensure printed and inserted materials meet quality and customer specifications.</li><li>
Review job tickets and verify materials, taglines, and sequence numbers for accuracy.</li><li>
Respond to machine quality lights for live divert checks and approve first pieces before full production.</li><li>
Stop production and document any quality defects such as blurry print, missing inserts, or damaged materials.</li><li>
Tag non-conforming products with red HOLD forms and notify appropriate personnel for segregation and review.</li><li>
Complete and follow up on Corrective Action Reports (CARS) and assist with internal and external audit readiness.</li><li>
Verify and record hand-stuff and damage values accurately on QA sheets.</li><li>
Ensure all diverted packages are tracked and reported on Reconciliation Reports.</li><li>
Report quality issues, discrepancies, or procedural gaps to the Quality Assurance Manager or other management.</li><li>
Perform additional duties and responsibilities as directed by the Quality Assurance Manager.</li></ul><p></p><p><b><br>
Education/Experience:</b></p><ul><li>
High School Diploma or G.E.D.; a vocational or technical school diploma or certificate in a related field is preferred.</li><li>
Proficiency in reading and writing English, with the ability to effectively communicate both verbally and in writing.</li><li>
Required background in quality control or quality assurance.</li><li>
Advanced proficiency in MS Office, particularly Word, Excel, and Outlook. Experience with report writing and preparing professional correspondence is required.</li><li>
The candidate should have a working knowledge of report writing, preparing professional verbal and written correspondences and email.</li><li>
Strong computer skills, including the ability to navigate production software, understand workflow processes, and accurately interpret job tickets.</li></ul><p></p><p><b><br>
Physical Demands:
</b></p><p><i>The physical demands described here are representatives of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Frequent hearing and talking required. </i><i>Must be able to stand and move for long hours May be required to lift up to 40 lbs</i>.</p><p></p><p><i><br>
Note: PCI Group retains the discretion to add to or change the duties of this position at any time.</i></p></div><br>
Thursday, Friday, Saturday, &amp; Every Other Sunday | Thur-Sat 7:00AM to 7:00PM | Sundays depending on volume 6 to 12 hour shift</div>

QUALITY ASSURANCE AUDITOR | THUR-SAT

Newrest

<div><div><p>Newrest a leader in In-Flight Catering is looking for a Quality Control Auditor to oversee quality control processes. Duties include inspecting the product to ensure it meets the requirements of the specifications provided. This individual will be standing all day. Newrest values promoting people from within. If an individual shows capability and commitment, there is an opportunity for this individual to experience a career within Newrest.</p>
<p><b>Responsibilities:</b></p>
<ul><li>Strong attention to detail</li>
<li>Monitor and inspect to ensure quality and that specifications are met.</li>
<li>Complete all necessary records and reports in a timely and accurate fashion.</li>
<li>Conduct inbound processes of new merchandise in accordance with guidelines and following all prescribed procedures, ability to understand specificities for each airline.</li>
<li>Physical and administrative handling of merchandise</li>
<li>Inform the Team Lead, Supervisor, or Manager of daily activity and/or any issues/concerns.</li>
<li>Assist in maintaining Security and Health and Safety requirements.</li>
<li>Conduct inbound processes of new merchandise by guidelines and following all prescribed procedures.</li>
<li>Ability to understand the specificities of each airline.</li>
<li>Take appropriate action to label, store, sort, and dispose of merchandise as instructed.</li>
<li>Inform the Team Lead or Manager of daily activity and/or issues or concerns.</li>
<li>Assist in maintaining Security and Health and Safety requirements.</li>
<li>Perform other duties as required or assigned by the team lead or management.</li></ul></div><div><p><b><br>
Qualifications:</b></p>
<ul><li>Ability to lift items/packages (up to 50 lbs./15 kg)</li>
<li>Ability to stand for long periods.</li>
<li>Ability to handle pressure in a fast-paced environment.</li>
<li>Attendance, diligence, punctuality, reliability</li>
<li>Good work ethic</li>
</ul>
<p><b>Benefits</b></p>
<ul><li>Free company lunch daily</li>
<li>Medical, dental, and vision insurance</li>
<li>PTO</li>
<li>Paid company holidays</li>
<li>401(k)</li>
<li>Paid parental leave.</li>
</ul>
<p><b>PHYSICAL ENVIRONMENT</b></p>
<p>While performing the duties of this job, the employee is regularly required to sit, walk, talk, and/or hear. The employee is frequently required to use hands to handle or feel. The employee must also occasionally lift and/or move up to 50 pounds. The employee is also required to frequently inspect the manufacturing floor and will be exposed to noise levels that may range from moderate to loud.</p><br>
<div></div>
<p><b>ABOUT THE COMPANY</b></p>
<p>Newrest, established by Co-CEOs Olivier Sadran and Jonathan Stent-Torriani, has had a firm foundation in Group Catair since 1996. It is the only major catering company that operates across all segments of catering and hospitality, including airline catering, duty-free on-board, buy-on-board, contract catering, remote site and support services, airport and motorway retail, and rail catering. In 2017, Newrest achieved revenues of almost 1.8 billion Euros with a workforce of over 30,800 spreads across 49 countries, making it the foremost &quot;independent&quot; airline caterer globally. The company is steadfastly dedicated to continual progress and innovation for its clients, the prosperity and advancement of its employees and managers, sustainable and enduring development of the business, and unwavering respect for social and environmental values in all its operations.</p></div></div>

Quality Control Auditor Grave Shift

Markel Corporation

<div><div>What part will you play? If you&rsquo;re looking for a place where you can make a meaningful difference, you&rsquo;ve found it.</div>
The work we do at Markel gives people the confidence to move forward and seize opportunities, and you&rsquo;ll find your fit amongst our global community of optimists and problem-solvers. We&rsquo;re always pushing each other to go further because we believe that when we realize our potential, we can help others reach theirs.
Join us and play your part in something special!
The Quality Assurance Auditor performs multiple internal audits of quality, customer service, productivity and timeliness and reports accurate results within the required time frame. In addition, this position is responsible for assisting the Lead and Manager with training and performing new internal audits for various departments.<div></div><div>
Essential Functions:</div><ul><li>
Independently conduct performance studies according to guidelines by gathering, tracking, organizing and analyzing data for multiple quality and timeliness audits.</li><li>
Verify accuracy of results/reports prior to issuing and prior to lead review within the defined timeframes, meeting with management to review results (as appropriate).</li><li>
Measure compliance with internal procedures in conducting audit-the-auditor studies of inbound and outbound calls by following established audit procedures.</li><li>
Provide clear and immediate communication to appropriate members of management regarding non-compliance with performance standards and internal procedures. Proactively identify recurring problems and make recommendations for solutions.</li><li>
Enhance/refine studies and schedules in conjunction with Supervisors/Managers from other departments.</li><li>
Stay abreast of changes in processes, accounts, or procedures that affect audit areas by attending specified meetings, training, or reading communication materials.</li><li>
Provide training when required on approved processes, call standards, and etiquette.</li><li>
Facilitate monthly calibration sessions with appropriate members of management. Recommend changes for improving the quality assurance process.</li></ul><div></div><div>
Additional Responsibilities:</div><ul><li>
Identify additional areas of potential improvement revealed during administration of studies that were not obvious during the development of study guidelines</li><li>
Provide feedback on audit trends to Training Department</li><li>
Assume project/special duties as assigned by Lead or Manager</li></ul><div></div><div>
Knowledge/Skills/Abilities:</div><ul><li>
Intermediate or higher level of knowledge of Microsoft Office products or equivalent programs, particularly Excel spreadsheets and charts.</li><li>
Maintain high standards and measures despite pressing deadlines, doing work right the first time, and inspecting material for errors.</li><li>
Able to follow detailed procedures and ensure accuracy in documentation and data, concentrate on routine work details, and organize a system of records.</li><li>
Able to prepare for emerging customer needs, manage multiple projects, determine project urgency in a meaningful and practical way, use goals to guide actions and create detailed action plans, and organize and schedule people and tasks.</li><li>
Able to act in accordance with established guidelines, policies and procedures.</li><li>
Able to display enthusiasm, promote a friendly group working environment, and work closely with other departments as necessary.</li></ul><div></div><div>
Education/Experience:</div><ul><li>
High School Diploma or equivalent required</li><li>
Some college education preferred</li><li>
2-3 years of prior experience in audit/relevant department knowledge</li><li>
2 years of QA experience preferred</li></ul><div></div><div>
#LI-Hybrid</div><div>
#Markel-IND</div><div></div><div>
US Work Authorization</div><div></div><div>
US Work Authorization required. Markel does not provide visa sponsorship for this position, now or in the future.</div><div></div><div><div><div>
Who we are:</div></div><div><div>
Markel Group (NYSE &ndash; MKL) a fortune 500 company with over 60 offices in 20+ countries, is a holding company for insurance, reinsurance, specialist advisory and investment operations around the world.</div></div><div></div><div><div><br>
We&rsquo;re all about people | We win together | We strive for better</div></div><div></div><div><div><br>
We enjoy the everyday | We think further</div></div><div></div><div><div><br>
What&rsquo;s in it for you:</div></div><div></div><div><div>
In keeping with the values of the Markel Style, we strive to support our employees in living their lives to the fullest at home and at work.</div></div><div><ul><li><div>
We offer competitive benefit programs that help meet our diverse and changing environment as well as support our employees&rsquo; needs at all stages of life.</div></li></ul></div><div><ul><li><div>
All full-time employees have the option to select from multiple health, dental and vision insurance plan options and optional life, disability, and AD&amp;D insurance.</div></li></ul></div><div><ul><li><div>
We also offer a 401(k) with employer match contributions, an Employee Stock Purchase Plan, PTO, corporate holidays and floating holidays, parental leave.</div></li></ul></div><div></div><div><div><br>
Are you ready to play your part?</div></div><div></div><div><div>
Choose &lsquo;Apply Now&rsquo; to fill out our short application, so that we can find out more about you.</div></div></div><div></div><div><div><div><br>
Caution: Employment scams</div></div><div></div><div><div>
Markel is aware of employment-related scams where scammers will impersonate recruiters by sending fake job offers to those actively seeking employment in order to steal personal information. Frequently, the scammer will reach out to individuals who have posted their resume online. These &quot;job offers&quot; include convincing offer letters and frequently ask for confidential personal information. Therefore, for your safety, please note that:</div></div><div><ul><li><div>
All legitimate job postings with Markel will be posted on <div>Markel Careers</div>. No other URL should be trusted for job postings.</div></li></ul></div><div><ul><li><div>
All legitimate communications with Markel recruiters will come from Markel.com email addresses.</div></li></ul></div><div></div><div><div><br>
We would also ask that you please report any job employment scams related to Markel to <div>rarecruiting@markel.com</div>.</div></div><div></div><div><div><br>
Markel is an equal opportunity employer. We do not discriminate or allow discrimination on the basis of any protected characteristic. This includes race; color; sex; religion; creed; national origin or place of birth; ancestry; age; disability; affectional or sexual orientation; gender expression or identity; genetic information, sickle cell trait, or atypical hereditary cellular or blood trait; refusal to submit to genetic tests or make genetic test results available; medical condition; citizenship status; pregnancy, childbirth, or related medical conditions; marital status, civil union status, domestic partnership status, familial status, or family responsibilities; military or veteran status, including unfavorable discharge from military service; personal appearance, height, or weight; matriculation or political affiliation; expunged juvenile records; arrest and court records where prohibited by applicable law; status as a victim of domestic or sexual violence; public assistance status; order of protection status; status as a smoker or nonsmoker; membership or activity in local commissions; the use or nonuse of lawful products off employer premises during non-work hours; declining to attend meetings or participate in communications about religious or political matters; or any other classification protected by applicable law.</div><div></div><div><br>
Should you require any accommodation through the application process, please send an e-mail to the <div>rarecruiting@markel.com</div>.</div><div></div><div>
No agencies please.</div></div></div></div>

Quality Assurance Auditor - State National

Organon Pharmaceuticals

<p></p><div><p><b>The position</b></p><p>
The Associate Director, Pharmacovigilance (PV) Quality Assurance Auditor, is responsible for ensuring quality and compliance with local and international regulatory requirements by conducting audits of Organon Processes, Affiliates, Vendors, Business Partners, and Investigator sites. The Associate Director is responsible for accepting audit assignments, performing audit pre-work, conducting audits and ensuring post audit activities are completed within defined timeframes. This role provides guidance to internal stakeholders, assisting in the establishment of the company's compliance strategy and the resolution and prevention of compliance risks.</p><p></p><p><b>
Responsibilities:</b></p><ul><li><p>
Schedule and conduct assigned PV audits in accordance with the global audit plan ensuring compliance with local and international guidelines and regulations.</p></li><li><p>
Prepare audit reports and manage follow-up activities within established timelines.</p></li><li><p>
Maintain broad-based expertise in Organon Policies, Procedures and Guidelines, local and global regulatory requirements, etc., pertinent to GVP. Maintain awareness of evolving industry and regulatory trends/regulations.</p></li><li><p>
Obtain and maintain cutting-edge knowledge, and application, for various Quality auditing topics.</p></li><li><p>
Generate and present comprehensive presentations/summary of audit issues for effective communication to all levels, as needed.</p></li><li><p>
Leads initiatives / drive results in various projects, as assigned, to maintain the effectiveness and efficiency of the audit program, and to ensure the audit program continues to meet company and regulatory expectations.</p></li><li><p>
Supports the implementation and maintenance of the PV risk-based strategy, including assistance in the development of the annual audit plan and maintenance of the audit tool.</p></li><li><p>
Reviews and provides input into the quality sections of the Pharmacovigilance System Master File (PSMF).</p></li><li><p>
Supports regulatory inspections and external audits, when required.</p></li><li><p>
Train and mentor junior team members.</p></li></ul><p><br>
</p><p><b>Required Education, Experience, and Skills</b></p><ul><li><p>
A minimum of a Bachelor&rsquo;s degree in a relevant scientific field (Pharmacy, Life Sciences, etc.).</p></li><li><p>
Fluency in written and spoken English; additional language skills a plus.</p></li><li><p>
Minimum of ten (10) years of experience in the pharmaceutical industry or regulatory agency related to Quality Systems and Quality Assurance (e.g., clinical trial quality, pharmacovigilance, regulatory).</p></li><li><p>
Minimum of one (1) year of experience in PV auditing with EU/FDA /global regulatory requirements.</p></li><li><p>
Strong knowledge of EMA, FDA and ICH guidelines in GVP and proficiency in interpreting and applying regulatory requirements and guidelines.</p></li><li><p>
Attention to detail and ability to work independently in a virtual environment.</p></li><li><p>
Proficiency in Microsoft applications (Word, Excel, PowerPoint, Outlook).</p></li><li><p>
Excellent/accomplished communication, negotiation, facilitation, influencing, and strategic thinking skills at all levels of organization Availability to travel up to 20% of time.</p></li><li><p>
Collaboration and Partnering: Demonstrates ability to work in partnership with others within the Company and external partners to accomplish quality goals; possesses advanced leadership skills.</p></li><li><p>
Communication Skills: Strong verbal skills and experienced effective writing skills.</p></li><li><p>
Project Management: Demonstrates ability to organize work efforts, prioritization of tasks and utilize appropriate resources to deliver or support work products in accordance with timelines and appropriate regulations.</p></li><li><p>
Decision Making: Demonstrates skills to utilize knowledge, networks, and data to make rapid and appropriate decisions and to determine when escalation of issues is necessary.</p></li><li><p>
Business Operations/Knowledge of Field: Demonstrates knowledge of regulations. Regulatory and business trends and applies this knowledge to optimize daily activities and ensure the functional areas within Research and Development are compliant with regulations and appropriate procedures.</p></li></ul><p></p><p><b>
Secondary Job Description</b></p><p></p><p><b>
Who We Are:
</b></p><p>Organon delivers ingenious health solutions that enable people to live their best lives. We are a $6.5 billion global healthcare company focused on making a world of difference for women, their families and the communities they care for. We have an important portfolio and are growing it by investing in the unmet needs of Women&rsquo;s Health, expanding access to leading biosimilars and touching lives with a diverse and trusted portfolio of health solutions. Our Vision is clear: A better and healthier every day for every woman.</p><p></p><p>
As an equal opportunity employer, we welcome applications from candidates with a diverse background. We are committed to creating an inclusive environment for all our applicants.</p><p></p><p><b>
Search Firm Representatives Please Read Carefully</b><br>
Organon LLC, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.</p><p></p><p><b>
Annualized Salary Range</b></p><p></p><p><b>
Annualized Salary Range (Global)</b></p><p><b>
Annualized Salary Range (Canada)</b></p><p><b>
Please Note: Pay ranges are specific to local market and therefore vary from country to country.</b></p><p></p><p><b>
Employee Status:
</b></p>Regular<p></p><p><b>
Relocation:</b></p>
No relocation<p></p><p><b>
VISA Sponsorship:</b></p>
No<p></p><p><b>
Travel Requirements: Organon employees must be able to satisfy all applicable travel and credentialing requirements, including associated vaccination prerequisites</b></p><p></p><p><b>
Flexible Work Arrangements:</b></p><p></p><p><b>
Shift:</b></p><p></p><p><b>
Valid Driving License:</b></p><p></p><p><b>
Hazardous Material(s):</b></p><p></p><p><b>
Number of Openings:
</b></p>1<p><b><br>
Requisition ID:</b>R539374</p></div>

Associate Director, Pharmacovigilance Quality Assurance Auditor

Hormel Foods

<div><div><b>Pay Rates</b> start at $22.50 per hour with a differential pay of $1.00 per hour worked.</div><div><b>
Benefits</b>: This position has a strong benefits package including medical, dental, vision, prescription drug coverage, 401(k) and match, Wellness Program, life insurance, tuition reimbursement, paid time off, and more.</div><div><b>
RESPONSIBILITIES:</b></div><ul><li>Conducts Quality Evaluations of products and practices according to procedures and specifications.</li><li>Conducts Food Safety activities CCP, monitoring GMP/Process auditing and product sampling.</li><li>Conducts Regulatory activities for Microbiological swabbing and Label verifications.</li><li>Communicates with the appropriate operations personnel to resolve day-to-day problems.</li><li>Assures the proper handling of products and services when not meeting Hormel and regulatory requirements.</li><li>Assists in the monitoring of departmental and plant-wide goals to improve quality, maximize efficiencies and minimize costs.</li></ul><div><b>
QUALIFICATIONS:</b></div><div><b>
Required</b></div><ul><li>Previous manufacturing experience</li><li>Ability to read and write in English</li><li>Ability to understand safety rules, operating and maintenance instructions, and procedure manuals. Ability to complete required documentation, including the use of tables, PCs, and scanners.</li><li>Ability to tolerate temperatures of 25 degrees or &gt;90F or below for the entire shift and lift 35lbs.</li></ul><div><b>
Preferred:</b></div><ul><li>High School Diploma</li><li>QA experience</li><li>Ability to manage time well, deal with multiple tasks and handle stressful situations.</li><li>Good communication and reasoning skills to retrieve information from co-workers and to relay information to and from all employee levels.</li></ul><div></div><p><b><br>
Hormel Foods provides equal employment opportunities to applicants and employees without regard to race; color; sex; gender identity; sexual orientation; religious practices and observances; national origin; pregnancy, childbirth, or related medical conditions; status as a protected veteran or spouse/family member of a protected veteran; or disability.</b></p></div>

Fontanini Food Quality Control Auditor- 2nd Shift

Keel

<div>Description:
<p><b>
First shift Monday through Friday 6:00 am to 4:30 pm</b></p><p><b>
PTO upon hire, Medical, Dental, and Vision Benefits are offered after 90 days of employment, 401K after 6 months</b></p><p><b>
Overview: </b>As a Quality Inspector / Auditor I for Keel Midwest, you will be responsible for the dimensional and physical inspection and testing to verify that the product and/or processes conform to the customer requirements. On the job training is provided as necessary.</p><p><b>
Job Functions</b>:</p><ul><li>
Performs product or process inspection utilizing standardized inspection methods.</li><li>
Visually and physically check parts against blueprint or work order specifications using precision measuring instruments.</li><li>
Completes quality packages that conform to customer standards.</li><li>
This position is consider to be in training towards a Level II Inspector / Auditor</li></ul><p><b>
Physical Demands</b>: Frequent standing, sitting, bending, stooping, and twisting. Must be able to lift up to 50 lbs. without mechanical assistance. This position requires regular computer and inspection tool usage as well as physical handling of parts.</p><p><b>
Work Environment:</b> Inspection room and shop floor environment, so exposure to moving parts, dust, debris, and loud noise is common. PPE is required at all times on the manufacturing floor.</p>
Requirements:
<ul><li>High School Diploma or GED required.</li><li>
One (1) year of experience in a quality-related position preferred.</li><li>
Basic knowledge of inspection and test equipment.</li><li>
Familiarity with drawings and blueprints, including GD&amp;T.</li><li>
Technical math skills including trigonometry.</li><li>
Knowledge of materials associated with typical products.</li><li>
Basic knowledge of standard inspector duties such as sampling, sorting, and containment actions.</li><li>
Ideal candidates will have good verbal and written communication skills, be organized, industrious, and hard-working, and will possess above average problem-solving skills.</li><li>
Must be able to to adapt to daily changes in priority and take direction from leadership.</li><li>
A strong desire to increase knowledge and skills in quality and inspection is critical to this role.</li></ul><p></p><p><b><br>
EEO STATEMENT</b></p><p>
KEEL is an Equal Opportunity Employer. We are committed to creating an inclusive environment for all employees and applicants. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity, sexual orientation, national origin, genetics, disability, age, veteran status, or any other legally protected status. We believe in fostering a workplace that values diversity and promotes equity and respect for all. The job requirements are subject to change to reasonably accommodate qualified disabled individuals.</p></div>

Quality Inspector I

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