quality control head

D.P. Jewellers

<div>
 
 
 About the Company
 
 
 
 
 
 
 D.P. Abhushan Ltd. is a trusted and renowned name in the Indian gems and jewellery industry, known for its exquisite craftsmanship, legacy of trust, and commitment to delivering timeless designs. With a strong presence in Central India, we are expanding our retail footprint and seeking passionate professionals to join our growing team.
 
 
 
 
 
 
 About the Role
 
 
 
 
 
 
 Job Title: Quality Control Head
 
 
 Job Type: Regular, Full-time
 
 
 Location: Mumbai, Maharashtra, India
 
 
 
 
 
 
 Job Summary:
 
 
 
 
 
 
 We are seeking a highly skilled and experienced Quality Control Head to join our team. The ideal candidate will be responsible for overseeing the quality control processes and procedures for our jewelry products. This role will be based at our Sourcing Office in Mumbai, Maharashtra, India.
 
 
 
 
 
 
 Key Responsibilities:
 
 
 
 - Develop and implement quality control processes and procedures for jewelry products.
 
 
 - Conduct regular quality audits to ensure compliance with company standards and industry regulations.
 
 
 - Collaborate with cross-functional teams to identify and resolve quality issues.
 
 
 - Train and mentor quality control team members to ensure consistent and accurate execution of quality control processes.
 
 
 - Monitor and analyze quality control data to identify trends and areas for improvement.
 
 
 - Develop and maintain relationships with suppliers to ensure quality standards are met.
 
 
 - Stay updated on industry trends and advancements in quality control practices.
 
 
 
 
 
 
 Qualifications:
 
 
 
 - Bachelor's degree in a relevant field (e.g. engineering, quality management, etc.).
 
 
 - Minimum of 10 years of experience in quality control, preferably in the jewelry industry.
 
 
 - Strong knowledge of quality control processes and procedures.
 
 
 - Experience in conducting quality audits and analyzing data.
 
 
 - Excellent communication and interpersonal skills.
 
 
 - Ability to work in a fast-paced and dynamic environment.
 
 
 - Strong leadership and team management skills.
 
 
 - Attention to detail and a commitment to delivering high-quality products.
 
 
 
 
 
 
 Equal Opportunity Statement
 
 
 
 
 
 
 At D.P. Abhushan Ltd., we are committed to fostering a diverse and inclusive workplace. We believe that every individual deserves equal respect, opportunities, and fair treatment&mdash;regardless of gender, age, caste, religion, ethnicity, disability, marital status, or background.
 
 
 
 
 
 We are proud to be an
 
 Equal Opportunity Employer
 
 , and we strive to create an environment where talent thrives purely on the basis of merit, dedication, and performance.
 
 
 
 
 
 Join us in building a workplace that reflects the values of respect, integrity, and equality.
 
</div>

Head of Quality Control

BSES India private limited

Job Description: Competence HeadThe Competence Head is responsible for overseeing technical training, competency development, and service excellence.Key Responsibilities:Lead competency-based training programs and skill development initiatives.Provide technical guidance and support to trainers and field service teams.Ensure high-quality service delivery, including troubleshooting, installation, and commissioning.Monitor and maintain training records, time logs, and resource utilization.Prepare reports and feedback for management to improve technical operations.Collaborate with supervisors to enhance workforce competency and efficiency.Qualifications &amp; Requirements:Degree: Preferred in Mechanical or Electrical Engineering.Experience: Minimum 4 years in a related field.Technical Skills: Proven knowledge and hands-on experience with construction equipment.Other Skills: Strong leadership, problem-solving, and communication abilities.How to apply-hrsupport@bsesindia.com9116920435Job Type: Full-timeWork Location: In person

Competence Head

Arcera

<div>
 
 
 The position may be located either in Turkey or Egypt
 
 
 
 
 
 
 Arcera is a global life sciences company headquartered in Abu Dhabi, United Arab Emirates. Our purpose is to enable longer and healthier lives while creating sustainable growth. We develop, manufacture, and commercialize a broad range of high-quality innovative and proven medicines in key international markets. With an operational footprint spanning over 90 countries across four continents, and manufacturing sites in eight countries, we offer more than 2,000 medicines across various therapeutic areas worldwide.
 
 
 
 
 
 The Regional QA Head META is responsible for overseeing and directing all Quality Assurance (QA) activities and initiatives across the META region. This includes the implementation and continuous improvement of the Quality Management System (QMS), ensuring compliance with company standards, local and international regulations (GMP, GDP, GLP), and fostering a culture of quality, data integrity, and operational excellence. The role involves developing and leading regional and local QA teams, ensuring effective training, documentation, and archiving practices, and acting as the primary interface with regulatory authorities and external partners. The Regional QA Head META also leads escalation processes, supports audits and inspections, and drives initiatives to enhance quality performance and compliance across the region.
 
 
 
 
 
 
 Key Responsibilities
 
 
 
 
 1. Release and Distribution:
 
 
 <ul>
 <li>
 Lead batch release and certification for products where Arcera is the Marketing Authorization Holder (MAH), exercising independent decision-making authority for batch release or rejection
 </li>
 </ul>
 
 
 2. Quality Management System (QMS) Implementation:
 
 
 <ul>
 <li>
 Oversee the implementation, maintenance, and continuous improvement of the QMS, including Technical Quality Agreements (TQAs) and all quality-related documentation, ensuring compliance with company, local, and international regulations.
 </li>
 </ul>
 
 
 3. Compliance and Regulatory Affairs:
 
 
 <ul>
 <li>
 Ensure all products and processes comply with market authorization, GMP, GDP, and GLP requirements. Act as the primary interface with regulatory authorities for GxP-related activities, including pharmacovigilance and regulatory submissions.
 </li>
 </ul>
 
 
 4. Quality Culture and Data Integrity:
 
 
 <ul>
 <li>
 Establish and promote a culture of quality and data integrity across the META region, acting as a data integrity ambassador and driving DI best practices.
 </li>
 </ul>
 
 
 5. Escalation and Issue Management:
 
 
 <ul>
 <li>
 Lead the escalation process for quality-related matters in the META region, track investigations, and consolidate findings to ensure timely and effective resolution.
 </li>
 </ul>
 
 
 6. Audit and Inspection Support:
 
 
 <ul>
 <li>
 Support and coordinate internal and external audits and inspections, ensuring readiness and effective follow-up on findings.
 </li>
 </ul>
 
 
 7. Performance Monitoring and Reporting:
 
 
 <ul>
 <li>
 Monitor the effectiveness of quality systems, including self-inspections, KPI tracking, and participation in management reviews. Track and report on site quality KPIs and manage hot topic issues.
 </li>
 </ul>
 
 
 8. People Leadership and Talent Management:
 
 
 <ul>
 <li>
 Develop and lead regional and local QA teams, fostering talent management and organizational development. Conduct regular performance reviews of direct reports against agreed goals and KPIs.
 </li>
 </ul>
 
 
 9. Cross-Functional Collaboration:
 
 
 <ul>
 <li>
 Work collaboratively with cross-functional teams to ensure alignment with global quality KPIs, annual quality plans, and business objectives.
 </li>
 </ul>
 
 
 10. Continuous Improvement:
 
 
 <ul>
 <li>
 Drive initiatives to enhance quality performance, process efficiency, and compliance, fostering a culture of continuous improvement throughout the region
 </li>
 </ul>
 
 
 
 
 
 Key Competencies
 
 
 <ul>
 <li>
 
 Quality Assurance Expertise
 
 : Deep understanding of QA, pharmaceutical manufacturing, and quality control.
 </li>
 <li>
 
 Auditing &amp; Compliance
 
 : Experience in auditing and ensuring compliance with international GMP, GDP, and GLP requirements with focus on Out of Specification, Transport Validations etc...
 </li>
 <li>
 
 Leadership &amp; People Development
 
 : Proven ability to lead, coach, and develop teams across diverse cultures.
 </li>
 <li>
 
 Analytical Thinking
 
 : Ability to analyze training data, audit findings, and quality metrics to drive improvements.
 </li>
 <li>
 
 Collaboration
 
 : Works effectively across functions and with diverse teams.
 </li>
 <li>
 
 Change Management
 
 : Supports and drives change initiatives in the META region.
 </li>
 <li>
 
 Regulatory Knowledge
 
 : Expertise in regulatory requirements for target markets.
 </li>
 <li>
 
 Communication
 
 : Strong communication and interpersonal skills.
 </li>
 <li>
 
 Problem Solving
 
 : Able to solve complex situations and problems.
 </li>
 <li>
 
 Cultural Awareness
 
 : Understanding and adapting to different cultural behaviors.
 </li>
 <li>
 
 Result- and Process-Oriented
 
 : Focused on achieving results and optimizing processes.
 </li>
 <li>
 
 Service/Customer Orientation
 
 : Committed to internal and external customer satisfaction.
 </li>
 </ul>
 
 
 
 
 
 Qualifications &amp; Experience
 
 
 <ul>
 <li>
 Degree in Life Sciences, Pharmacy, Chemistry, or related field; advanced degree preferred.
 </li>
 <li>
 5+ years&rsquo; experience in pharmaceutical quality management systems, with a focus on QA leadership, training, documentation, or data integrity.
 </li>
 <li>
 Experience in developing and delivering training programs.
 </li>
 <li>
 Strong knowledge of GMP, GDP, GLP, and QC requirements.
 </li>
 <li>
 Experience with electronic documentation and learning management systems.
 </li>
 <li>
 Audit support and regulatory inspection experience.
 </li>
 <li>
 Excellent organizational and communication skills.
 </li>
 <li>
 Proven ability to drive process improvements and foster a culture of quality and compliance.
 </li>
 <li>
 Business fluent English; additional languages are an asset
 </li>
 </ul>
 
 
 
 
 In connection with your application, Arcera will collect, process and store personal data about you. Our
 
 Privacy Notice for Prospective Employees
 
 , also available in
 
 German
 
 , provides an overview of the personal data that Arcera processes during the application process.
 
 
 Note: This Privacy Notice may be updated by Arcera, we therefore invite you to consult the latest versions via the above links. In the event of any conflict between the English and German versions of this Privacy Notice, the English version shall prevail.
 
</div>

Region META Quality Head 100%(m/f/d)

SAINATH HOSPITAL

Urgently Required Quality Head at Sainath Hospital, Moshi.1. Generally responsible for complying with all the requirements given in NABH hospital accreditation standards and ISO 9001: 2015 standards.2. Coordination with all department heads for implementation of Quality Improvement Program3. Provide guidance in understanding requirements of standards, assist in solving difficulties.4. Prepare program for development of system, sensitization of people, implementation of policies, procedures programs.5. Responsible for all Quality related activities in the hospital.6.Review of documentation once in a year for all NABH documents.7. Prepare and follow Quality Calendar of activities prescribed in NABH standards. Make others to follow the calendar8. Conduct Internal Audits and MRMs for NABH and ISO standards.9. Analysis of NCs and closure of NCs in Internal as well as external audits10.Prepare annual budget for Quality Improvement activities and utilize the budgeted amounts to bring about necessary improvements.11.Monitor Quality Indicator data mapping and analysis activities. Prepare Dash Board and publish.12.Validate data mapped for Quality Indicators.13.Define targets for Quality Indicator Performance and take improvement actions on non-performing Quality Indicators14.Ensure that all OSPR happen as per the frequencies defined.15.Conduct QA reviews planned and take improvement actions.16.Encourage Incidence reporting in the hospital. Investigate &amp; analyze received incidence reports and take corrective preventive actions.17.Review complaints received through complaint registers, feedback forms, through floor coordinators etc. Closure of actions on complaints received.18.Ensure conduction of mock drills as per the plan.19.Monitor Risk assessment and risk mitigations in all departments of the hospital.20.Conduct reviews of progress made/ not made, identify bottle-necks, and provide solutions.21.Liaise with Accreditation Consultants, external agencies involved, External trainers, External auditors, NABH &amp; ISO etc.22.Be responsible for conduction of meetings of various committees, Various surveys, Audits, Management Reviews, Data tracking of Quality/ Safety/ Performance indicators etc.23.Be responsible for use of modern management tools and statistical techniques24.Be responsible for making improvement action plans and bringing about improvements in identified areas.25.Handle Patient satisfaction feedback and patient complaints.26.Be responsible for preparation of budget to support quality and safety programmers, get the budgets sanctioned and monitor that timely and appropriate utilization takes place.27.Shall coordinate harmonious working among Consultants, Doctors, Nurses, Management and other staff toward successful accreditation of the hospitals.28.Implementation of Policies and Procedures of the hospital. Participation in mock drills.29.Monitor and manage performance of Quality coordinators and floor coordinators.30.Assign work to quality coordinators and floor coordinatorsDesired Candidate Profile<ul><li>Any Medical Graduate (BAMS/BHMS/Nursing/ with MHA or MBA in Healthcare.</li><li>Knowledgeable with computers &amp; quality management systems</li><li>Experienced (1 o 3 yrs) candidate from hospital domain preferable.</li><li>Interested can send CV to hrdsainathhospital(at)gmail(dot)com</li></ul>Job Type: Full-timePay: &#8377;25,000.00 - &#8377;30,000.00 per monthEducation:<ul><li>Bachelor's (Preferred)</li></ul>Experience:<ul><li>total work: 1 year (Preferred)</li></ul>Work Location: In person

Quality Head

GHV Infra FZ LLC

Role &amp; responsibilities Responsible for overseeing all quality assurance and control activities, ensuring projects meet company, customer, and regulatory standards. Developing and implementing quality management systems, leading QA/QC teams, conducting audits, managing documentation, and ensuring compliance throughout the project lifecycle. Ensure compliance with company, customer, and regulatory standards, codes, and specifications. Conduct internal and external audits, and coordinate with site personnel for inspections and corrective actions. Manage quality documentation, including the Quality Management Plan (QMP), non-conformance reports (NCRs), and final handover documentation. Liaise with vendors and clients on quality matters, and review vendor documentation submittals. Preferred candidate profile B.E. or B.Tech in a relevant field like Civil Engineering Experience of years in Quality Assurance and Quality Control, ideally within the construction and infrastructure sector <div>Role: Construction Engineering - Other</div><div>Industry Type: Engineering &amp; Construction</div><div>Department: Construction &amp; Site Engineering</div><div>Employment Type: Full Time, Permanent</div><div>Role Category: Construction Engineering</div><div>Education</div><div>UG: B.Tech/B.E. in Civil</div>

Head (QA/QC)

Immacule Lifesciences

<div>
 
 
 About the Company
 
 
 
 
 
 
 Founded in 2012, today, Immacule Lifesciences has become a renowned name in the pharmaceutical industry. At Immacule, our dedicated team of scientists is here to provide you with customized services, supported by our extensive network of capabilities and resources. No matter where you are, as an end-to-end pharmaceutical service provider and partner we offer quality, speed and value by combining our technical competencies and cost-effective solutions.
 
 
 We are backward integrated in pharmaceutical research and development and our focus ranges from the classification and development, to the commercialization of complex liquid (aqueous/non aqueous) and lyophilized injectables in vials and ampoules, with robust capabilities for terminal sterilization as well as aseptically filled injectables.
 
 
 As a CDMO we are rapidly capturing the highly competitive sterile US market, in collaboration with our partners we have received 37 ANDAs approvals, have 18 ANDAs under review and a filing target of 50+ by 2025.
 
 
 Immacule is focusing on First to File 505(b)(2) submissions, NCEs &amp; complex generics niche products scale-up, exhibit batches &amp; commercial manufacturing support services to its global clients.
 
 
 
 
 
 
 Responsibilities
 
 
 <ul>
 <li>
 Responsible for overall activities performed in the Quality Control Department.
 </li>
 <li>
 Implementing and monitoring of cGLP norms in the Quality Control Department.
 </li>
 <li>
 Responsible for internal/Customer/Regulatory Audits and Preparation of Reports.
 </li>
 <li>
 Implementation, Compliance and Maintenance of Quality Control SOPs.
 </li>
 <li>
 Responsible for Document Management System for Raw Material, In-Process Samples, Packing Material, Finished Product and Stability Samples.
 </li>
 <li>
 Managing Deviations, Change Control, Incidences with Investigations and associated CAPA.
 </li>
 <li>
 Investigation of OOS, OOT &amp; OOE in the Quality Control Department and associated CAPA.
 </li>
 <li>
 To review and approve the Validation/Qualification protocol and report of the equipment installed in the Quality Control Department.
 </li>
 <li>
 Arrangements of Analytical Method Transfer, Analytical Method Validation of Chemical and Micro sections.
 </li>
 <li>
 Accomplishing QC Human Resources objectives by Recurring, Selecting, Training, assigning, counseling and discipline employees.
 </li>
 <li>
 Meet QC financial objectives by estimating requirements.
 </li>
 <li>
 Involving in self inspection, CFT meeting and functional review meeting.
 </li>
 <li>
 Achieving QC operational objectives by contributing information and analysis to strategic plans and review.
 </li>
 <li>
 Review and approval of analytical documents w.r.t. Data Integrity.
 </li>
 <li>
 Release/ reject of Raw Materials, Packing Materials, Stability, In-Process and Finished Products.
 </li>
 <li>
 To impart trainings to the subordinated and participate in the training programs organized by the company.
 </li>
 <li>
 To ensure that prescribed safety precautions are being taken by the subordinates while performing analysis.
 </li>
 </ul>
 
 
 
 
 Qualifications
 
 
 
 M.sc/M.pharma in Chemistry
 
 
 
 
 
 
 Preferred Skills
 
 
 
 18+ Years experience in sterile facility
 
 
 
</div>

Deputy General Manager - Quality Control

Confidential Company

Interested candidates can call us or drop their resumes at +91 8657487961. Job Description Job TitleManager - QualityJob LocationDubai Brief Summary The Manager Quality will play a critical role in ensuring the highest standards of quality control and assurance across operations. The ideal candidate will have a strong background in jewellery quality testing, excellent analytical skills, and the ability to drive continuous improvement. This role involves managing overall jewellery quality processes, including coloured jewellery quality control at store level. The position reports directly to the Head of Quality and requires close collaboration with the Quality Control Team and vendors. Brief Job Description (just an indicative list and not limited to the following) <ol type="1"><li>Conduct surprise visits to sites alongside the Quality Control Team to perform random checks and ensure alignment with the quality control module. </li><li>Prepare quarterly quality control reports with findings, observations, and recommendations, and share them with vendors to promote transparency. </li><li>Analyze trends in quality control rejections, identify recurring issues, and provide actionable insights to vendors. </li><li>Collaborate with the Head of Quality to develop and implement vendor scorecards and performance reports. </li><li>Assist in establishing and maintaining a robust quality management system including SOPs and guidelines. </li><li>Conduct regular audits of vendor processes and QC procedures to ensure compliance. </li><li>Train and educate the QC Team and vendors on QA practices and product specifications. </li><li>Drive quality initiatives, identify process bottlenecks, and implement solutions to enhance product quality and customer satisfaction. </li><li>Stay updated with industry trends and advancements in jewellery QA practices. </li><li>Collaborate cross-functionally with Production, Design, and Procurement teams to resolve quality-related issues. </li><li>Manage coloured jewellery quality control at store level, ensuring consistency and adherence to defined standards. </li></ol>Skill Required <ol type="1"><li>8 years of experience in jewellery quality testing (diamonds, colored diamonds, precious stones etc.) </li><li>Strong knowledge of jewellery manufacturing processes, materials, and QC techniques. </li><li>Experience in conducting audits, preparing reports, and analyzing quality data. </li><li>Excellent analytical skills with the ability to interpret complex data. </li><li>Strong communication and interpersonal skills for internal and external collaboration. </li><li>Detail-oriented with a focus on accuracy in assessments. </li><li>Proficiency in quality control tools and software. </li><li>Gems Certificate is mandatory, candidates must hold a valid certification in gemology or equivalent.</li></ol> Interested candidates can call us or drop their resumes at +91 8657487961.

Hiring QC Manager for a Jewellery Boutique in Dubai

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