quality system manager

DyDo DRINCO Türkiye

<div>
 <p>
  We Are DyDo Drinco T&uuml;rkiye!
 </p>
 <p>
  <br/>
 </p>
 <p>
  We are owner of pioneer beverage brands such as Cola Turka, &Ccedil;aml&inodot;ca, Maltana, Saka, &Idot;&ccedil;im and Link.
 </p>
 <p>
  <br/>
 </p>
 <p>
  Working with us;
 </p>
 <ul>
  <li>
   People-oriented work environment based on open communication and trust
  </li>
  <li>
   Experience working with multinational company
  </li>
  <li>
   Opportunity to work in supportive and collaborative teams
  </li>
  <li>
   Digital learning opportunities to improve yourself
  </li>
  <li>
   Working environment that values diversity and is inclusive
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  We are looking for a &lsquo;
  <strong>
   <em>
    &rsquo;Assistant Quality System Management Manager&rsquo;&rsquo;
   </em>
  </strong>
  <em>
   to
  </em>
  be in
  <strong>
   <em>
    Akyaz&inodot;.
   </em>
  </strong>
  A brief job description of the position and preferred qualifications for the suitable candidates are defined below:
 </p>
 <ul>
  <li>
   Managing and developing the Quality/Food Safety/System Management system of 5 factories,dealer and warehouses,
  </li>
  <li>
   Acts in accordance with the policies, procedures and instructions published and implemented within the scope of Management Systems (KVKK, ISO 27001, ISO 9001, ISO 22000, BRCGS, Halal, YYS, Scan),
  </li>
  <li>
   Ensures the sustainability of management systems by following current standards. Monitoring and controlling the documantation,
  </li>
  <li>
   Establishing and managing systems that comply with international quality standards such as ISO 14001, ISO 45001 and etc.,
  </li>
  <li>
   Monitors the compliance of all locations' internal and external audits, hygiene audits, supplier audits, OEM company audits, dealer and warehouse audits with the plan,
  </li>
  <li>
   Prepares audit reports and ensures that actions are taken and followed up,
  </li>
  <li>
   Ensuring compliance with legal and regulatory requirements,
  </li>
  <li>
   Ensuring that all departments work inline with the principles of the quality assurance system,
  </li>
  <li>
   Carrying out Quality Risk Assesment studies,
  </li>
  <li>
   Examining and follow up the root cause, action planning and implementation of corrective-Improving Activities,
  </li>
  <li>
   Managing improvement projects about product efficiency,qaulity and food safety,
  </li>
  <li>
   Provides management of the team under his/her responsibility,
  </li>
  <li>
   Leading the team to establish quality management systems, prepare documents and ensure the continuity of their implementation,
  </li>
  <li>
   Preparing trainings for food safety and quality culture,
  </li>
  <li>
   Manages dealers' audit processes,
  </li>
  <li>
   Monitors audit performances and actions,
  </li>
  <li>
   Manages OEM processes,
  </li>
  <li>
   Preparing and presenting performance ,KPI,YGG reports.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   Qualifications
  </strong>
 </p>
 <ul>
  <li>
   Graduate from Food or Chemical Engineering departments of universities,
  </li>
  <li>
   Knowledge and experience with food safety management systems (TSE 22000, ISO 9001, BRC etc.),
  </li>
  <li>
   Preferably has ISO 9001 and 22000 auditor certification,
  </li>
  <li>
   Preferably with experience on auditing certification or equivalent experience,
  </li>
  <li>
   Preferably quality system management experience in FMCG manufacturing environment min. 5 years,
  </li>
  <li>
   Working in harmony and coordination with the team with strong communication skills,
  </li>
  <li>
   Effective communication and interpersonal skills and presence in meetings,
  </li>
  <li>
   Being solution-oriented with an innovative perspective, resolving complex problems,
  </li>
  <li>
   Acting proactively by taking responsibility with a system development perspective,
  </li>
  <li>
   Experience in team management,
  </li>
  <li>
   Have a good command of spoken and written English,
  </li>
  <li>
   Preferably have knowledge SAP,
  </li>
  <li>
   No restriction to travel.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <strong>
   What We offer you?
  </strong>
 </p>
 <ul>
  <li>
   Hybrid Working Model
  </li>
  <li>
   Company Car
  </li>
  <li>
   Fair Salary Policy Based on Gender Equality
  </li>
  <li>
   Cafeteria
  </li>
  <li>
   Private Health Insurance
  </li>
  <li>
   Annual Performance-based bonus system
  </li>
  <li>
   Birthday Leave
  </li>
  <li>
   Holiday Gift Packages
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  As the data controller DYDO DR&Idot;NCO TURKEY &Idot;&Ccedil;ECEK SATI&Scedil; VE PAZARLAMA ANON&Idot;M &Scedil;&Idot;RKET&Idot; and DELLA GIDA SAN VE T&Idot;C A&Scedil;. will process the identity, communication information and other personal information available in your resume for the purpose of recruitment. Your information may be processed pursuant to the provisions of 5/2 (c) and 5/2 (f) of the Law No. 6698 on the Protection of Personal Data and will not be transferred to third parties other than the platform on which you view this posting. You can find more detailed information about your rights under article 11 of KVKK and the processing of your personal data in the relevant data protection notice: https://www.dydodrinco.com.tr/kisisel-verilerin-korunmasi-kanunu
 </p>
</div>


Assistant Quality System Management Manager

Air India SATS Airport Services Private Limited (AISATS)

<div>
 <p>
  <strong>
   <u>
    JOB PURPOSE
   </u>
  </strong>
 </p>
 <p>
  Manager-QMS, reporting to the designated manager serves as a business partner to the AISATS &ndash; business unit leaders by managing and implementing processes in Operations and ensuring consistencies which support the Mission, Vision and Objectives of AISATS. She/he is also responsible for acquiring certifications for AISATS and thereby maintaining the standards for the same.
 </p>
 <p>
  <br/>
 </p>
 <p>
  Manager- QMS interacts with AISATS senior management and staff along with external agencies to define, acquire, measure, monitor and validate AISATS Quality Management System and service standards.
 </p>
 <p>
  <br/>
 </p>
 <p>
  Manager- QMS also manages a team of talents who are accountable for delivery of data and information about AISATS.
 </p>
 <p>
  <br/>
 </p>
 <p>
  SPECIFIC RESPONSIBILITIES
 </p>
 <ul>
  <li>
   Manage the department performance from a purely Operational aspect.
  </li>
  <li>
   Lead, manage and recommend feasible options to reporting manager to ensure that the services provided are consistent, fit for purpose and meet both external and internal requirements; this would include both legal compliance and customer expectations
  </li>
  <li>
   Maintain a set of AISATS data archives.
  </li>
  <li>
   Responsible for every aspect of the QMS/QC function from Audit Planning, Conduct of Audits, &amp; Implementation, Corrective Action &amp; Closure, Monitoring &amp; Verification, Feedback/follow up and re audit where necessary
  </li>
  <li>
   Converts data collected during internal audits into information and provide necessary statistics to Senior Management for Management Review.
  </li>
  <li>
   Responsible for strategizing and defining the Internal Audit Plan and review the implementation of the Annual Plan across the company while streamlining the Audits to minimize disruptions/duplications on operations.
  </li>
  <li>
   Assist the BU Head to implement the Quality Policy, Quality Manual and measureable Quality Targets in accordance to ISO 9001:2015 that is appropriate to AISATS goals and supports strategies devised by the senior management to achieve those policies.
  </li>
  <li>
   Implement and maintain the processes needed for seamless QMS functioning.
  </li>
  <li>
   Monitor measure and analyze the QMS within the organization and make continuous improvements to suit AISATS operations and changing environment/policies.
  </li>
  <li>
   Initiate and implement process/certification projects involving continual improvement and best industry standards.
  </li>
  <li>
   Ensure implementation of an effective system of document and record controls.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Ensure development of a system of identification and traceability of process and records.
  </li>
  <li>
   Implement the internal audit program to verify that the QMS conforms to planned arrangements.
  </li>
  <li>
   Coordinates audit follow-up and closure activities, to see that recommendations have been implemented or otherwise resolved.
  </li>
  <li>
   Perform Internal Audits at other stations as and when asked to.
  </li>
  <li>
   Analysis of the data collected on the effectiveness of the QMS and evaluate where the continuous improvement of the QMS can be made.
  </li>
  <li>
   Manage the Quality Management team in carrying out routine activities and persuading reluctant employees within AISATS to change their way of working to incorporate quality methods.
  </li>
  <li>
   Ensure that Quality Control mechanism is in place such that operation functions have an active process of conducting self-audits to ensure compliance/conformity to various standards.
  </li>
  <li>
   Overlooks the Safety Audits performed at the station and ensures that the Safety function is performing as required.
  </li>
  <li>
   Ensure the protection of data archives and the integrity, security, confidentiality and privacy of data, information and knowledge of AISATS.
  </li>
  <li>
   Support Senior Management- AISATS, in ensuring smooth functioning of the internal Audit department and document the Internal Audit monthly report for providing an update to the AISATS Senior management on Internal Audit activities and challenges.
  </li>
  <li>
   Responsible for managerial review and approval of the audit report, Discusses audit results with management to ensure recommendations are understood, accepted and appropriate corrective action is proposed. Assures that appropriate auditee responses to the audit report are received.
  </li>
  <li>
   Developing programs to support the effective implementation of QMS as stated in the Quality Manual and Process Manual.
  </li>
  <li>
   Translate documented requirements into functional specifications.
  </li>
  <li>
   Perform any other functions as required by the BU Head
  </li>
  <li>
   Responsible and accountable for overall quality, safety and security of operations.
  </li>
  <li>
   You will be responsible and accountable to make necessary operational decisions related to safety and security matters at all times whilst on duty.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <br/>
 </p>
 <p>
  EDUCATIONAL QUALIFICATIONS
 </p>
 <ul>
  <li>
   Master&rsquo;s/University Degree with minimum 10 years of working experience of which at least
  </li>
 </ul>
 <p>
  02 years in a managerial/supervisory capacity in the Aviation Industry
 </p>
 <ul>
  <li>
   Certified Internal Auditor with an in-depth knowledge of the auditing field.
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  RELEVANT EXPERIENCE
 </p>
 <p>
  Manager- QMS should possess the following experiences:
 </p>
 <p>
  <br/>
 </p>
 <p>
  <br/>
 </p>
 <ul>
  <li>
   Have extensive experience across all areas of operations namely Passenger Services, Flight Operations, Baggage and Ramp
  </li>
  <li>
   Have demonstrated ability in negotiations as well as presentations, budget preparations and execution
  </li>
  <li>
   Have the appropriate skill set to set and manage priorities at senior management level
  </li>
 </ul>
 <p>
  <br/>
 </p>
 <p>
  <br/>
 </p>
 <p>
  PERSONAL CHARACTERISTICS &amp; BEHAVIOURS
 </p>
 <p>
  For a successful role as Manager&ndash;QMS, he/she should have the following traits:
 </p>
 <ul>
  <li>
   Have management and leadership skills
  </li>
  <li>
   Effective communication skills and leadership traits to relate to all levels of employees and handling cross sectional teams
  </li>
  <li>
   Comprehend and translate complex data and its relationship to trends and observations
  </li>
 </ul>
 <p>
 </p>
</div>


Manager – Quality Management System Aviation

Coca-Cola Arena

<p>The Assistant Quality Systems Manager shall support the Head of Quality &amp; Business Standards on managing the coordination of the Arena s Business Management Framework (BMF) and its Integrated Management System (IMS), including the compilation, record-keeping and analysis of BMF/IMS to drive continual improvement activities.</p><p>The BMF/IMS facilitates to achieve sustainable business performance by assisting in the implementation of an effective management system and driving continuous process improvement. This role is on a freelancer agreement, and it requires the candidate to have their own visa / sponsorship.</p><p><b>Qualifications:</b></p><ul><li>Minimum Bachelor s degree in a business qualification or equivalent systems experience.</li></ul><p><b>Experience:</b></p><ul><li>Minimum 2 year s experience in similar role.</li><li>Minimum 2 years certified on latest ISO 9001 Lead Auditor.</li><li>Minimum 4 years auditing experience using the latest ISO 9001 standards (use of additional internationally recognized auditing standards is a plus).</li><li>Nebosh IGC certification or higher.</li><li>Previous experience in the UAE, preferably in the event industry.</li><li>Excellent oral and written communication skills.</li><li>Previous experience in events or hotel industry.</li><li>Experience in managing team and its initiatives.</li><li>Fluent in English.</li></ul>

Assistant Quality Systems Manager

Reventech Engineering Services

<p><b>Position:</b> Management Representative (MR)<br/><b>Experience:</b> 3 &ndash; 4 years<br/><b>Location:</b> Kumbalgodu, Bengaluru<br/><b>Industry:</b> Manufacturing</p><p><b>Key Responsibilities:</b></p><ul><li>Maintain and update all <b>quality system documentation</b>.</li><li>Plan and coordinate <b>internal audits</b> and assist in <b>external audits</b>.</li><li>Lead follow-up on <b>non-conformities</b> and ensure <b>corrective actions</b> are implemented.</li><li>Support process improvements and ensure teams comply with standard procedures.</li><li>Prepare reports for <b>management review meetings</b>.</li><li>Coordinate with auditors and customers on quality matters.</li></ul><p><b>Requirements:</b></p><ul><li>Bachelor&rsquo;s Degree or Diploma in <b>Mechanical, Electrical &amp; Electronics Engineering</b>, or related field.</li><li>3&ndash;4 years of experience in <b>ISO/IATF quality system management</b> in a manufacturing setup.</li><li>Good understanding of <b>audits, documentation, and quality processes</b>.</li><li>Strong coordination, communication, and problem-solving skills.</li></ul><p>Thank You</p><p>Job Types: Full-time, Permanent</p><p>Pay: &#8377;150,000.00 - &#8377;550,000.00 per year</p><p>Benefits:</p><ul><li>Health insurance</li></ul><p>Experience:</p><ul><li>MR &amp; Quality : 3 years (Required)</li></ul><p>Willingness to travel:</p><ul><li>25% (Required)</li></ul><p>Work Location: In person</p>

Junior Management Representative

BridgeBio

<div><div><h3 class="jobSectionHeader"><b>Mavericks Wanted</b></h3><br>
<p>
When was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here, but if it sparks excitement...read on<br>
<br>
In 2015, we pioneered a &ldquo;moneyball for biotech&rdquo; approach, pooling projects and promising early-stage research from academia together under one financial umbrella to reduce risk and unleash innovation. This model allows science and small teams of experts to lead the way. We build bridges to groundbreaking advancements in rare disease, and develop life-changing medicines for patients with unmet needs as fast as humanly possible.<br>
<br>
Together we define white space, push boundaries and empower people to solve problems. If you're someone who defies convention, join us and work alongside some of the most respected minds in the industry. Together, we'll ask &quot;why not?&quot; and help reengineer the future of biopharma.</p>
<h3 class="jobSectionHeader"><b>
Affiliate Overview</b></h3>
<p>
Eidos Therapeutics, an affiliate within BridgeBio Pharma, is a commercial-stage biopharmaceutical company focused on Transthyretin Amyloid Cardiomyopathy (ATTR-CM).</p>
<h3 class="jobSectionHeader"><b>
What You'll Do</b></h3>
<p>
The Manager, Computer System Validation (CSV), QA will report to the Associate Director, Quality Assurance (QA). This position will provide quality oversight of the computer system validation lifecycle from design and implementation to retirement, ensuring compliance of GxP applications. This role will ensure that all GxP computerized systems, including Veeva, Argus, SAP, Tracelink, etc., are implemented, validated, and maintained in compliance with FDA, EMA, ICH, GAMP 5, and other Health Authority requirements. The ideal candidate will combine technical expertise in CSV, strong quality systems acumen, and exceptional cross-functional communication skills.</p>
<h3 class="jobSectionHeader"><b>
Responsibilities</b></h3>
<ul><li>Provide QA oversight of the GxP computer system validation lifecycle, ensuring ongoing compliance and validated state through design, configuration, updates, and maintenance</li>
<li>Review and approve IT change control and validation deliverables, including protocols, test scripts, and reports of the GxP validated system</li>
<li>Evaluate risk assessments and determine the impact of changes/updates on user experience, system performance, and compliance</li>
<li>Participate, review, and approve periodic system reviews and release management activities, identifying and remediating compliance gaps</li>
<li>Collaborate with IT, cross-functional stakeholders such as business owners, to establish and enforce requirements for system validation, data integrity, and ongoing system maintenance</li>
<li>Drive continuous improvement initiatives for QMS and validated GxP systems</li>
<li>Support regulatory inspections and audits, ensuring adherence to 21 CFR Part 11, EU Annex 11, GxP, and other regulatory frameworks</li>
<li>Support inspection remediation activities and CAPA management through timely resolution and closure</li>
<li>Collaborate with cross-functional teams to optimize workflows, reporting capabilities, and system usability for business and compliance needs</li>
<li>Review and approve GxP-computer system SOPs, and support end-user training to ensure proper adoption and compliance</li>
<li>Serve as QA CSV subject matter expert (SME) and provide guidance on risk-based validation strategies (CSV/CSA)</li>
</ul><h3 class="jobSectionHeader"><b>Where You'll Work</b></h3>
<p>
This position can be a hybrid role which requires in-office collaboration 2-3x per week in our San Francisco Office. This position can also be considered for U.S-based remote role, that will require quarterly, or as needed visits to our San Francisco Office.</p>
<h3 class="jobSectionHeader"><b>
Who You Are</b></h3>
<ul><li>Bachelor&rsquo;s or Master&rsquo;s degree in software, computer engineering, or technical field</li>
<li>8+ years of experience in quality systems development and maintenance within clinical and commercial-stage pharmaceutical or biotech companies</li>
<li>Excellent attention to detail and strong organizational skills</li>
<li>Effective communication skills both written and verbal</li>
<li>Demonstrated expertise in GxP computerized system validation (CSV/CSA) and system lifecycle management</li>
<li>Strong working knowledge of regulatory requirements, including:
<ul><li>21 CFR Part 11</li>
<li>EU Annex 11</li>
<li>ICH Q10</li>
<li>GAMP 5</li>
</ul></li><li>Hands-on experience with computer system validated platforms (Veeva eTMF, Quality, QMS, RIM; SAP; Argus; Tracelink)</li>
<li>Experience developing GxP SOPs and training personnel on compliance requirements</li>
<li>Ability to work independently and collaboratively within a team</li>
<li>Ability to influence and drive cross-functional teams</li>
<li>Familiarity with risk-based validation methodologies (CSV/CSA)</li>
</ul><h3 class="jobSectionHeader"><b>Rewarding Those Who Make the Mission Possible</b></h3>
<p>
We have high expectations for our team members. We make sure those working hard for patients are rewarded and cared for in return.</p>
<p><b>
Financial Benefits:</b></p>
<ul>
<li>Market leading compensation</li>
<li>401K with 100% employer match on first 3% &amp; 50% on the next 2%</li>
<li>Employee stock purchase program</li>
<li>Pre-tax commuter benefits</li>
<li>Referral program with $2,500 award for hired referrals</li>
</ul>
<p><b>Health &amp; Wellbeing:</b></p>
<ul>
<li>Comprehensive health care with 100% premiums covered - no cost to you and dependents</li>
<li>Mental health support via Spring Health (6 therapy sessions &amp; 6 coaching sessions)</li>
<li>Hybrid work model - employees have the autonomy in where and how they do their work</li>
<li>Unlimited flexible paid time off - take the time that you need</li>
<li>Paid parental leave - 4 months for birthing parents &amp; 2 months for non-birthing parents</li>
<li>Flex spending accounts &amp; company-provided group term life &amp; disability</li>
<li>Subsidized lunch via Forkable on days worked from our office</li>
</ul>
<p><b>Skill Development &amp; Career Paths:</b></p>
<ul>
<li>People are part of our growth and success story - from discovery to active drug trials and FDA pipelines, there are endless opportunities for skill development and internal mobility</li>
<li>We provide career pathing through regular feedback, continuous education and professional development programs via LinkedIn Learning, LifeLabs, Spring Health &amp; BetterUp Coaching</li>
<li>We celebrate strong performance with financial rewards, peer-to-peer recognition, and growth opportunities</li>
</ul></div><div><div><div><div><div><div>At BridgeBio, we strive to provide a market-competitive total rewards package, including base pay, an annual performance bonus, company equity, and generous health benefits. Below is the anticipated salary range for candidates for this role who will work in California. The final salary offered to a successful candidate will depend on several factors that may include but are not limited to the type and length of experience within the job, type, and length of experience within the industry, educational background, location of residence and performance during the interview process. BridgeBio is a multi-state employer, and this salary range may not reflect positions based in other states.</div>
</div></div></div><p>
Salary</p><p>
$130,000 - $160,000 USD</p></div></div></div>

Manager, Computer System Validation (CSV), QA

Kraft Heinz

<p></p><div><div><div><div><div><div><div><div><div><ul><div><b>All Posting Locations:</b> Susurluk, Balikesir, TR
</div><div><b>Job Functions:</b> Quality</div>
<div><b>Date Published:</b> November 7, 2025</div>
<div><b>Ref#:</b> R-97935</div></ul><div></div><div><br>
</div></div></div></div></div></div></div></div></div><p></p><div><div><div><div><div><div>ABOUT THE ROLE</div></div><p></p><div>
<div>Job Description</div>
<p>We are looking for Quality Management System Lead to strengthen our Kraft Heinz family.</p>
<p>Quality Management Lead position is within our FSQ Department. This is a field-based position located in Susurluk, Bal&#305;kesir.</p>
<p><b>Qualifications</b></p>
<ul><li>Bachelor&rsquo;s degree in food engineering or a related engineering field</li>
<li>Preferably min intermediate level of English</li>
<li>Preferably with at least 2 years of experience in the food industry,</li>
<li>Preferably experienced in SAP Quality Management module</li>
<li>Proficient in MS Office programs</li>
<li>Knowledge of Food Safety Management Systems, ISO 9001, BRCGS, IFS, Food Legislation</li>
<li>Knowledge of Continuous Improvement tools and methodologies</li>
</ul><ul><li>Theoretical and practical knowledge about laboratory equipment and laboratory rules</li>
<li>Strong analytical skills, result-oriented, and a team player</li>
<li>Able to adapt to shift and flexible working systems,</li>
<li>Residing in or willing to relocate to Bal&#305;kesir Susurluk, Bursa (Karacabey-Mustafakemalpa&#351;a) areas</li>
</ul><p><b>Job Description
</b></p><ul><li>To support activities to ensure compliance with the Kraft Heinz Quality Management System requirements and other applicable instructions and standards</li>
<li>To ensure that the implementation of quality procedures, instructions and plans is followed.</li>
<li>Verification of the conformity of the analyses performed within the plan with the values specified in the product and/or material specifications</li>
<li>To monitor GMP activities, to ensure the improvement and verification of standards</li>
<li>To monitor 5S activities in the laboratories to ensure the improvement and verification of standards</li>
<li>To monitor corrective and preventive activities and ensure verification (internal audit,3rd party audits)</li>
<li>Lead/participate in projects to analyze and eliminate recurring errors in processes by working with production teams</li>
<li>Supporting the standardization of processes, instructions and documentation by identifying improvement potentials,</li>
<li>Ensuring that calibrations are implemented according to plan and their results are monitored</li>
<li>To comply with the occupational health and safety rules required by the job in the area in which he/she is assigned and to work on improving the working environment</li>
</ul><p><b>About Us</b></p><p><b><br>
</b></p><p>The Kraft Heinz Company is one of the largest food and beverage companies in the world, with eight $1 billion+ brands and global sales of approximately $25 billion. We&rsquo;re a globally trusted producer of high-quality, great-tasting, and nutritious foods for over 150 years. Our brands are truly global, with products produced and marketed in over 40 countries. These beloved products include condiments and sauces, cheese and dairy, meals, meats, refreshment beverages, coffee, infant and nutrition products, and numerous other grocery products in a portfolio of more than 200 legacy and emerging brands.</p>
<p>No matter the brand, we&rsquo;re united under one vision: To sustainably grow by delighting more consumers globally. Bringing this vision to life is our team of 39,000+ food lovers, creative thinkers, and high performers worldwide. Together, we help provide meals to those in need through our global partnership with Rise Against Hunger. We also stand committed to responsible, sustainable practices that extend to every facet of our business, our consumers, and our communities. Every day, we&rsquo;re transforming the food industry with bold thinking and unprecedented results. If you share our passion &ndash; and are ready to create the future, build a legacy, and lead as a global citizen &ndash; there&rsquo;s only one thing to do: join our table and let&rsquo;s make life delicious!</p>
<p>Our Culture of Ownership, Meritocracy &amp; Collaboration</p>
<p>We're not afraid to think differently. Embrace new ideas. Dream big. We empower our people at every level &ndash; from entry-level intern to senior leader &ndash; to own their work. We share a responsibility to think like Owners &ndash; to be mindful of the collective and sustained success of Kraft Heinz &ndash; which we apply to every situation, every day. As part of Kraft Heinz, you're supported to grow and achieve. You&rsquo;re expected to bring your authentic self to work every day, to lead with humility, and drive outstanding performance at every level &ndash; and you&rsquo;ll be rewarded. You&rsquo;re given opportunities to leave a mark and build a legacy. But you won&rsquo;t do it alone. You&rsquo;re supported by passionate teammates along the way, and our collective, collaborative spirit fuels our incredible progress.</p>
<p></p><div>Location(s)</div>
<p>Bal&#305;kesir-Susurluk</p>
<p><b>Kraft Heinz is an Equal Opportunity Employer &ndash; Underrepresented Ethnic Minority Groups/Women/Veterans/Individuals with Disabilities/Sexual Orientation/Gender Identity and other protected classes</b><b>.</b></p></div></div></div></div></div></div>

Quality Management System Lead

UNITED TOWEL EXPORTERS PRIVATE LIMITED

<p>We are hiring <b>Deputy Manager QMS</b></p><p><b>Location: </b>Korangi Industrial Area, Karachi.</p><p><b>Experience:</b> Minimum 5-8 years of relevant experience (Terry Towel industry experience will be preferred).</p><p><b>Education: </b>B.E/Masters/MPA/MBA or equivalent from any reputable HEC recognized University/Institute .</p><p><b>Responsibilities:</b></p><ul><li><i>Strengthen QMS team to drive in overall with QMS methodologies and system.</i></li><li><i>Hands on continuous improvement process excellence and cost enhancement.</i></li><li><i>Hands on experience in lean six sigma, value stream mapping and other statistical models.</i></li><li><i>Lead developing sections of QMS for development of different levels of documents.</i></li><li><i>Train upper &amp; middle management regarding importance of audits and systems.</i></li></ul><p><i><b>Skills and Traits: </b></i></p><ul><li><i>Proficient in MS Office &amp; SAP application.</i></li><li><i>Strong organizational, Analytical, Multi tasking and problem solving skills.</i></li></ul><p>Job Type: Full-time</p><p>Work Location: In person</p>

Deputy Manager QMS

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