quality coordinator

Balchem Corporation

<div>
 
 Company Overview
 
 
 
 Balchem Corporation develops, manufactures and markets specialty ingredients that improve and enhance the health and well-being of life on the planet, providing state-of-the-art solutions and the finest quality products for a range of industries worldwide. Our corporate headquarters is located in New Hampton, New York, (Hudson Valley area) and we have a broad network of sales offices, manufacturing sites, and R&amp;D centers, primarily located in the US and Europe. Founded in 1967, Balchem is a publicly traded company (NASDAQ &ndash; &ldquo;BCPC&rdquo;) with annual revenues over $640 million and a market cap exceeding $3.0 billion. The company consists of three business segments: Human Nutrition &amp; Health; Animal Nutrition &amp; Health; and Specialty Products. Balchem employs over 1,400 people worldwide who are engaged in diverse activities, committed to developing the company into global market leadership positions. To learn more about our dynamic, stable and growing company, visit www.balchem.com
 
 
 
 POSITION SUMMARY
 
 : The QA Coordinator provides necessary support to Quality Team Members and customers in administering and completing essential duties and responsibilities for the department, while supporting all day-to-day activities of QA team members, QA processes and procedures. An important component of this position is the effective use of communication skills to keep customers, employees and vendors advised and updated with key quality information. This is a highly visible position with opportunities for growth.
 
 
 Directly reports to the Quality Assurance Manager for proper direction, interpretation, and evaluation. Maintains and guarantees Balchem Corporation&rsquo;s quality and safety standards.
 
 
 Position is for 2nd shift: M-F 3PM-11:30PM
 
 
 
 Pay Rate
 
 starts at $21/hr
 
 
 
 Essential Functions
 
 
 
 <ul>
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 Manages finished goods COA's and specs
 </li>
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 Assists with product specification sheets, sampling plans, and lab data sheets
 </li>
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 Manages testing and evaluation of all finished goods
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 Documents and manages retain finished products samples and sample requests
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 Manages finished goods COA's and specs
 </li>
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 Verifies compliance with SOPs, SSOP's and HACCP plan
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 Performs mock recalls
 </li>
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 Reviews finished product folders for positive release program, as needed
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 Manages ATP, Allergen, Organoleptic/Sensory, QA Training, and/or New Hire Orientation programs
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 Communicates with Operations and Quality Supervisor or Manager to resolve any quality issues
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 Identifies opportunities for improvement and coordinated QA Team efforts to address them
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 Arrives on time to work, meetings, and training sessions
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 Observes safety and security procedures, determines appropriate action beyond guidelines, and reports potentially unsafe conditions
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 Performs other duties as assigned by the Quality Assurance Manager
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 Reports to Manager any failure to adhere to Balchem&rsquo;s work ethics and standards
 
 
 
 </li>
 </ul>
 
 Requirements
 
 
 
 <ul>
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 Lab experience is required, and food-handling experience is desirable
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 HACCP knowledge and understanding required/PCQI preferred
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 Must have sound analytical and technical skills
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 Individual must be equipped with strong motivation, organization, time management, documentation, and communication skills (both orally and written)
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 Must have excellent attention to detail and the ability to multi-task and prioritize
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 Demonstration of strong work ethics (dependable, and trustworthy)
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 Must be able to communicate and handle conflict in a professional manner
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 Ability to give and welcome feedback and contribute to building a positive team spirit
 
 
 
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 </ul>
 
 Working Conditions
 
 
 
 <ul>
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 Individual will continually be required to stand, walk, use hands to finger, handle or feel, to talk and hear, and to utilize specific vision abilities including but not limited to close vision, distance vision, peripheral vision, depth perception and the ability to adjust focus
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 Regularly required to climb, balance, stoop, kneel, crouch, and crawl, using proper ergonomic principles, taste, smell, and lift up to 25 pounds
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 Periodically required to lift up to 60 pounds, utilizing safe and proper lift techniques and equipment
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 Individual will operate equipment, including but not limited to computers, lab equipment, instruments involving scientific meters and measuring devices, and a sit down and/or stand-up forklift
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 The ability to distinguish colors is required
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 Balchem Corporation requires anyone working in the plant or entering the plant to adhere to the personal protective equipment policies and procedures
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 Individual may rarely be exposed to wet or humid conditions, working near moving mechanical parts, work in extreme heat (non-weather), work in high noise levels and vibration
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 Individual may also be periodically working in high or precarious places, around fumes or airborne particles, and with caustic chemicals
 
 
 
 </li>
 </ul>
 Balchem is committed to a workplace culture that values and promotes diversity, inclusion, equal employment opportunities, and a work environment free of harassment and hostility.
</div>

Quality Assurance Coordinator

Michigan Sugar Company

<div>
 
 Safety First. Excellence. Pride. Integrity. Compassion. Trust.
 
 Are you ready to plant your career in a place where words like these serve as the foundation for doing business every day? At Michigan Sugar, our purpose is Making Life Sweeter, and our mission is Creating Growth and Opportunity.
 
 
 
 Michigan Sugar Company has an immediate, full-time opportunity for a Food Safety and Quality Assurance Coordinator
 
 
 , located at the Sebewaing facility, 947 E Pine St, Sebewaing, MI 48759
 
 
 
 
 Job Summary
 
 
 
 The Food Safety and Quality Assurance Coordinator (FSQA Coordinator) will act as the Preventive Controls Qualified Individual (PCQI) for Human Food and Animal Food and/or Safe Quality Foods (SQF) Practitioner for the site(s) and will manage overall development, implementation, review and maintenance of the Food &amp; Feed Safety Management Systems and the Quality Assurance Management System. This position will require travel to other Michigan Sugar Company facilities, as needed.
 
 
 
 Primary Responsibilities
 
 
 
 <ul>
 <li>
 Food &amp; Animal Feed Safety and Quality Assurance &ndash; Leads cross-functional team members, including site management, and other required personnel, in developing, implementing and reviewing site policies and procedures, related to the Food &amp; Feed Safety Systems and Quality Management Systems. Supports the establishment of corporate policies and procedures. Ensures products shipped from the facility meet all regulatory, internal, and customer specifications. Is the site point of contact for Food &amp; Feed Safety and Quality Assurance escalations.
 </li>
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 Food &amp; Feed Safety Plans and Site Management Reviews &ndash; Conducts review of plans and revises plans, as required. Leads/facilitates FSQA meetings and site management reviews.
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 Training - Develops and oversees the employee training program as it relates to Food &amp; Feed Safety. Provides annual orientation and refresher trainings, and ensures completion of specific job training. Maintains training skills registers and training records. Provides/facilitates trainings as necessary.
 </li>
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 Corrective Actions and Preventive Actions (CAPAs) - Documents CAPAs related to Food &amp; Feed Safety and Quality Assurance, works with team members to ensure that CAPAs are completed.
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 Customer Complaints &ndash; Works with appropriate Departments to investigate Customer Complaints. Works with Customer Service Representatives on providing solutions to the affected Customer.
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 Integrated Pest Management &ndash; Oversees the 3 rd party managed Integrated Pest Management Program. Reviews reports, issues work orders/corrective actions and monitors trends.
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 Management of Change &ndash; Conducts reviews for necessary changes to the Food &amp; Feed Safety System. Approves process or equipment changes (from a food safety standpoint) and performs/facilitates validation studies. Updates documentation, as necessary.
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 Document Control - Maintains documents for the Food &amp; Feed Safety Systems. Reviews documents, issues updates, tracks changes, and revises documents as necessary.
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 Crisis Management &ndash; Is a member of the Crisis Management Team. Schedules, conducts and /or facilitates mock crisis exercises.
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 Food Defense and Food Fraud - Oversees the development, review and maintenance of the Food Defense Plan. Supports Corporate FSQA Team with the Food Fraud Program.
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 Mock Recall and Traceability Program &ndash; Directs and reviews trace exercises. Documents findings, issues corrective actions and follows-up as needed.
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 Foreign Material Program &ndash;Manages the foreign material program. Reviews foreign material inspection logs, preventive control monitoring records, and ensures appropriate disposition for contaminated/ suspect product.
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 Non-conforming Product/Hold Program &ndash; Ensures the effectiveness of the Non-Conforming Product/Hold Program and has final disposition authority with consultation from Corporate FSQA, if needed.
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 Internal &amp; external audits and self-inspections &ndash; Manages the internal audit program. Facilitates and partners in internal audits and self-inspections to mitigate potential food or feed safety risks. Is the primary auditee during certification and customer audits, and regulatory inspections. Communicates audit/inspection results to management and ensures follow-up of audit non-conformances.
 </li>
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 Verification and Validation Programs &ndash; Oversees the overall validation, effectiveness review, and verification of program documents, forms, and records. Ensures verifications are accurate and complete.
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 Calibration &ndash; Manages the site calibration program and ensures timely completion of calibrations for equipment related to Food Safety.
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 Water and Air Quality &ndash; Obtains annual city water report. Ensures site samples are taken for analysis and reviews test results with Environmental to ensure compliance.
 
 
 </li>
 </ul>
 
 Position Qualifications
 
 
 
 <ul>
 <li>
 BS degree in Chemistry, Biology, Food Science or related field preferred.
 </li>
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 Food &amp; beverage, animal food, or pharmaceutical experience is preferred.
 </li>
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 2 years Food Safety or Quality Management Systems experience preferred.
 
 
 </li>
 </ul>
 
 KEY COMPETENCIES
 
 
 
 <ul>
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 Ability to deliver results working within collective bargaining agreement
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 Self-starter and motivated to implement change
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 Working knowledge of Microsoft office software programs (Outlook, Word, Excel, Power point)
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 Ability to solve problems and make decisions
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 Flexible and able to work in fast paced and varying environments
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 Ability to work well with others and in a team environment
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 Leading by demonstrating ethics and integrity, displaying drive and purpose, demonstrated capability to learn, managing self, increasing self-awareness
 </li>
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 Provides model behavior to demonstrate corporate values
 </li>
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 Demonstrates excellence in oral and written communication
 
 
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 </ul>
 
 Training
 
 
 
 <ul>
 <li>
 HACCP certification
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 Completion of SQF course and successfully pass the SQF exam
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 General factory safety requirements (right to know)
 </li>
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 Good Manufacturing Practices (GMPs)
 </li>
 <li>
 Food Safety Modernization Act (FSMA)
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 Food Defense
 </li>
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 Integrated Pest Management
 </li>
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 Internal Auditing
 
 
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 </ul>
 
 NOTE: The above statements are intended to describe the general nature and level of work being performed by staff assigned to this position. The above statements are not to be construed as an exhaustive list of all responsibilities, duties and skills that may be required. All staff may be required to perform duties outside their normal responsibilities as needed.
 
 
 
 Michigan Sugar Company offers competitive market wages for both hourly and salaried employees, opportunity for professional growth and development, and comprehensive benefit packages that may include medical, dental, 401(k) and paid time off. To learn more visit www.michigansugar.com .
 
 
 
 Michigan Sugar Company
 
 was founded in 1906 when six smaller sugar companies merged their operations. In 2002, Michigan Sugar Company became a grower-owned cooperative and in 2004, it merged with Monitor Sugar Company to form the company that exists today.
 
 
 Michigan Sugar Company is headquartered in Bay City and has sugar beet processing facilities in Bay City, Caro, Croswell and Sebewaing. Its nearly 900 grower-owners plant and harvest up to 140,000 acres of sugar beets each year in 17 Michigan counties, as well as Ontario, Canada. Those beets are sliced at the factories and turned into about 1.3 billion pounds of sugar annually.
 
 
 That sugar is sold to industrial, commercial, and retail customers under the Pioneer and Big Chief brands.
 
 
 Michigan Sugar Company has approximately 1,000 year-round employees and an additional 1,100 seasonal workers. It is the No. 1 employer in Huron County, the No. 2 employer in Bay and Sanilac counties and the No. 3 employer in Tuscola County. The company&rsquo;s annual payroll is more than $90 million and its annual local economic impact is about $700 million.
 
 
 Michigan Sugar Company is the third largest of eight sugar beet processing companies in the United States and Michigan is one of 11 states where sugar beets are grown in the country.
 
 
 
 Michigan Sugar Company is an Equal Opportunity Employer
 
 
 
</div>

Food Safety and Quality Assurance Coordinator

Penspen

<div></div><div>Penspen is a leading energy services company, providing engineering, project management, asset management and integrity services to the energy industry worldwide for over 70+ years. Originally founded in the UK in 1954 as Spencer &amp; Partners, the company has now grown to include almost 1,000 members of staff, with major offices in London, Mexico, Colombia Houston and Abu Dhabi, Saudi Arabia, Kuwait. (https://www.penspen.com)
Job Description
Ensure the effective implementation of the project Quality Management System (QMS) across engineering, procurement, and construction phases. Review and approve EPC contractor quality plans, ITPs, and procedures. Monitor inspection, testing, and documentation for compliance with project specifications, codes, and standards. Conduct surveillance and audits to verify EPC quality performance and adherence to ISO 9001 requirements. Coordinate NCRs, corrective actions, and lessons learned. Interface with client representatives for quality-related matters and ensure timely close-out of quality issues. Support turnover and documentation compilation for mechanical completion.
Required Experience Criteria in years
Alternative (I): Ten (10) years of experience in coordinating QA/QC engineering and construction activities of which at least five (5) years in performing project quality control/quality assurance activities for Oil and Gas/ Petrochemical projects. Alternative (II): Fourteen (14) years of experience in coordinating QA/QC engineering and construction activities of which at least Seven (7) years in performing project quality control/quality assurance activities for Oil and Gas/ Petrochemical projects.
Minimum Education Qualification Required
Alternative (I): Bachelor's Degree in Engineering Alternative (II): Diploma or equivalent with a certificate from a recognized agency in QA/QC. 
The job location will be based on Alkhafji , Saudi Arabia.
If you have the skills and are interested, please apply on the link below - https://careers.penspen.com/vacancy/qaqc-coordinator-613386.html#hs_show_apply_popup=true
#LI-BA1</div>

QA/QC Coordinator

Zoetis

<div>Quality Liaison
Louisville Lab
Summary:
The Quality Liaison is responsible for driving Non-Conforming Event (NCE) management and conformance to ZRL Quality checklists and policies for their location, as well as providing coordination for local Document Control. The primary focus is on investigating NCEs and Opportunities for Improvement (OFIs), developing and implementing Corrective/Preventative Actions (CAPAs), and supporting the quality team in driving continuous improvement. This role serves as a subject matter expert in quality systems, supports staff training of quality requirements, tools and initiatives, and collaborates with Lab Operations, Medical, Operations Support, and other supporting department teams. Additionally, this position will be responsible for project managing the quality assessment activities, participating as an auditor in Quality Assessments, and leading the lab in OFI resolution. The Quality Liaison utilizes the MediaLab web-based Quality Management System platform for daily operations and serves an administrator for this software. This role is also responsible for compiling and analyzing quality metrics for quality scorecards for their location.
Job Duties:
&middot; Oversee and project manage Non-Conforming Event Management for site. Collaborate with local management and subject matter experts to investigate and resolve Quality Improvement Tickets (QITs). Apply structured root cause analysis techniques (such as 5 Whys, Fishbone Diagram, etc.) to accurately identify underlying issues, work with departmental and local leaders to develop and implement corrective/preventive actions (CAPAs), and, when appropriate, include Return on Investment (ROI) analysis using the Cost of Poor Quality calculator.
&middot; Conduct periodic comprehensive and weekly focused audits to maintain continuous quality conformance to ZRL checklist requirements for patient safety and assessment readiness. Coordinate onsite audits for location, participate in other ZRL Quality Assessments as required, and project manage and participate in the resolution of findings through Opportunity for Improvement (OFI) QITs.
&middot; Act as the site&rsquo;s Document Control specialist, ensuring all documents are properly managed and compliant, and maintaining an up-to-date local SOP manual for use during system downtime.
&middot; Deliver training to staff on Quality related programs, tools, philosophies and processes. Serve as subject matter expert to answer questions around document control, NCEs, good documentation practices, temperature monitoring, quality assessment program and quality related topics to ensure consistent compliance and excellence.
&middot; Manage the Man Overboard (MoB) program for location by overseeing the Man Overboard program. Coordinate the searches for missing samples using MoB form, ensuring each incident is documented as a Quality Improvement Ticket (QIT) to facilitate tracking through resolution, remediation and corrective action development.
&middot; Generate and communicate local quality metrics to inform Management Review KPI feedback.
&middot; Contribute to other quality improvement projects and fulfill other duties as assigned. 
Education/Experience: 
Minimum Requirements:
&middot; Requires an Associate&rsquo;s degree in science or related discipline or equivalent combination of experience and/or education.
&middot; Minimum of two (2) years on the bench in a veterinary or clinical laboratory. Must possess an understanding of most service lines and departments offered by the ZRL network to include accessioning, chemistry, hematology, histology, microbiology, parasitology, urinalysis and cytology.
Preferred Experience:
&middot; Previous experience in laboratory Quality Management.
&middot; Experience with Non-conforming Event Management, Internal Auditing, and/or Document Control.
&middot; Experience with MediaLab.
&middot; MLS/MT/MLS/CLS and/or Relevant ASQ Certification. 
Technical Skills Required:
&middot; Proficient in the use of the Microsoft Office suite, including Excel, Outlook, Word and Powerpoint.
&middot; Strong analytical and troubleshooting abilities, and a flexible, adaptable approach to shifting priorities and new challenges
&middot; Ability to apply established organizational policies to make decisions with minimal supervision.
&middot; Excellent written and oral communication skills.
&middot; Ability to work within a team and as an individual contributor in a fast-paced, demanding, and changing environment.
&middot; Candidate must possess flexibility to respond to constantly changing conditions and priorities.
&middot; Self-directed - can work with little supervision on most tasks.
&middot; Excellent organization, prioritization, and time management skills &ndash; can work effectively under pressure.
&middot; Exceptional attention to detail.
&middot; (Preferred) Advanced skills utilizing Excel, Power BI and/or other software to generate and analyzer reports pertaining to metrics, raw data, and other role related tasks. 
Physical Position Requirements:
&middot; Able to work hours on a computer and tolerate computer screens
&middot; Ability to travel domestically up to 5%.
&middot; Some irregular hours as needed to collaborate with Lab Operations teams.
Routine responsibilities may include standing and/or walking for extended periods of time. 
Full time 
Regular 
Colleague 
Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume.
Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search. 
Notice: Zoetis Recruiters will contact candidates via email from an address ending in @zoetis.com and may also initially connect with candidates through LinkedIn , including LinkedIn InMail. Zoetis does not use Gmail, Outlook, Yahoo, or other web-based/generic email domains to communicate about job opportunities, interviews, or offers of employment. If you receive a recruitment-related email message claiming to be from Zoetis that does not come from @zoetis.com , please treat it as suspicious. For your security, do not reply, click links, open attachments, share personal or financial information, or send money in response to unexpected or questionable recruitment communications. 
Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at zoetiscolleagueservices@zoetis.com to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at www.Zoetis.com/careers site, or (2) via email to/from addresses using only the Zoetis domain of &ldquo;@zoetis.com&rdquo;. In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.</div>

Quality Liaison

AL HIDAYA HEALTH CARE SERVICES

* Degree in Nursing with more than 4 years of experience *Valid QCHP/MOPH License (preferred)*Experience in quality assurance/control or clinical nursing(preferred)*Strong communication and documentation skills*Ability to conduct audits, staff evaluations, and compliance monitoring *Responsibilities* :*Monitor and improve quality of nursing services*Conduct clinical audits and competency assessments*Ensure compliance with healthcare standards and policies*Support staff training and performance improvement*Prepare quality reports and follow-up actions We Offer:*Competitive salary*Professional work environment*Career growth opportunitiesPay: From QAR3,000.00 per monthWork Location: In person

Quality Control Nurse

Propharma Medical Supplies

Key Responsibilities:<ul><li>Implement and maintain clinical quality and patient safety standards across healthcare operations</li><li>Ensure compliance with Abu Dhabi healthcare regulations and accreditation standards (DOH, JCI or equivalent)</li><li>Monitor, evaluate, and improve clinical governance systems and quality indicators</li><li>Conduct audits, risk assessments, and incident investigations, ensuring timely corrective and preventive actions (CAPA)</li><li>Support policy development, documentation control, and continuous quality improvement initiatives</li><li>Collaborate with clinical and non-clinical teams to enhance service quality and patient outcomes</li></ul>Requirements:<ul><li>Previous experience working in Abu Dhabi healthcare sector is mandatory</li><li>Strong knowledge of healthcare quality standards, clinical governance, and patient safety frameworks</li><li>Experience with DOH regulations, JCI accreditation, and audit processes</li><li>Background in medicine, nursing, pharmacy, or healthcare quality management</li><li>Excellent analytical, communication, and reporting skills</li><li>Ability to work effectively with multidisciplinary healthcare teams</li></ul>Work Location: In person

Medical Quality Officer (Abu Dhabi Experience Required)

Dubai Corporation for Ambulance Services

<div><div>Perform the Analysis of critical clinical quality risks related to compliance that arises from quality audits. 
Assist in the evaluation and analyses of the quality events &amp; incidents. 
Provide technical assistants for all clinical accreditations and inspections including JCIA accreditation activities. 
Assisting in the Implementation of emergency clinical quality management systems and quality improvement programs across multidisciplinary teams of DCAS. 
Assisting in conducting clinical quality internal audits for all clinical processes contributing to the performance of DCAS. 
Assist in Conducting clinical quality &amp; patient safety training for DCAS medical staff. 
Assist in Compile and prepare clinical quality materials for submission to regulatory agencies &amp; Document internal regulatory processes. 
Assist in Conducting day-to-day coordination for quality &amp; Patient safety related activities.
Comply with the information security system, policies, processes and programs, and report to the direct manager any security breaches or suspicious incidents. 
Perform any other duties related to the work of the section or as directed.<div> 
</div></div><div>
Qualifications<div></div> 
Bachelor/Diploma in Health Science or equivalent. 
Qualifications: Bachelor&rsquo;s degree with 2 years of experience in clinical quality. 
Diploma degree with 8 years of experience in clinical quality.</div></div><div></div>

Senior Clinical Quality Officer

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