1,024 Diamond Processing jobs in India
Quality Control
Posted 20 days ago
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Qualifications and Skills
- Familiarity with statistical process control to foster continuous improvement in manufacturing processes and product quality.
- Understanding of quality management systems to maintain excellence in organizational processes and customer satisfaction.
- Knowledge of lean manufacturing concepts to enhance process efficiency and minimize waste effectively in the production environment.
- Ability to perform non-destructive testing techniques for ensuring product quality and reliability in compliance with industry standards.
- Experience or foundational knowledge in testing and evaluating rubber for distinct industry applications and product development.
- Proficiency in sample collection from factory environments to ensure quality compliance and adherence to predefined standards.
- Capable of conducting thorough quality control activities to verify product conformity and maintain high-quality benchmarks.
- Effective communication and problem-solving skills to address quality concerns with relevant stakeholders and facilitate improvements.
Roles and Responsibilities
- Conduct routine quality checks on raw materials and finished products to maintain standards and ensure customer satisfaction.
- Implement quality control procedures and processes aligned with QMS to uphold product quality and safety requirements.
- Collaborate with production teams to address quality issues and introduce corrective actions for continuous process improvements.
- Prepare detailed reports on quality findings and recommend strategic adjustments for superior production outcomes.
- Perform audits on production processes and quality management practices to identify areas for enhancement and operational efficiency.
- Monitor production environments to prevent defects and ensure adherence to established quality parameters.
- Identify root causes of quality deviations and work collaboratively with cross-functional teams to develop effective solutions.
- Keep abreast of industry best practices and technological advancements in quality control to drive innovation across operational functions.
Quality Control
Posted 20 days ago
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Company Overview
Kaiser Industries Limited is a prominent manufacturer of surfactants and specialty chemicals, serving the agro-chemical industry for over 30 years. With state-of-the-art plants in Haryana, J&K, and Gujarat, the company boasts a cutting-edge R&D facility and industry's best quality assurance systems. Besides agrochemical surfactants, it operates in paints, synthetic lubricants, cosmetics, oil field chemicals, textiles, and leather chemicals sectors. The company headquarters is located in Bahadurgarh, Haryana.
Job Overview
Kaiser Industries Limited is seeking a Mid-Level Quality Control professional, specializing in chemical quality control, to join our team in Samba (J&K). This full-time position requires a maximum of 3-6 years of work experience. The ideal candidate will ensure that our chemical manufacturing processes meet the highest quality standards. As a pivotal part of our operations, you will be responsible for maintaining the reliability and efficiency of our products.
Qualifications and Skills
- Proficient with Statistical Process Control (SPC) including data analysis and interpretation to maintain chemical processes (Mandatory skill).
- Thorough understanding and implementation of ISO 9001 Standards to enhance quality assurance (Mandatory skill).
- Strong experience with Quality Management Systems (QMS) to oversee quality throughout the production (Mandatory skill).
- Ability to use calipers and micrometers for precise measurements in quality assessments of manufactured chemicals.
- Knowledge of Non-Destructive Testing (NDT) methods to inspect materials without causing damage.
- Expertise in Root Cause Analysis to effectively identify and rectify issues impacting product quality.
- Familiarity with Lean Manufacturing Techniques for process optimization and waste reduction in the production line.
- Experience in Automated Inspection Systems to foster efficiency and accuracy in quality checks.
Roles and Responsibilities
- Conduct regular quality inspections and tests on raw materials and finished products to maintain high standards.
- Implement and monitor Statistical Process Control (SPC) methods to improve production efficiency.
- Ensure compliance with ISO 9001 and other quality management standards in all areas of manufacturing.
- Analyze quality test results and provide technical expertise for quality system improvements.
- Coordinate with production and R&D teams to ensure process and materials meet predefined specifications and standards.
- Investigate and document any product or process non-conformance, recommending corrective actions.
- Drive continuous improvement initiatives through effective root cause analysis and solution implementation.
- Maintain up-to-date documentation of quality control processes and improvement actions.
Quality Control Chemist
Posted today
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The Assistant Manager - QC will provide expertise with all daily operations in quality control laboratories. In this role, you will support the buildup and maintenance of the rapid technology platform by providing reliable accurate analytical figures as well as perform validation and troubleshooting of new analytical methods to ensure they meet the requirements and deadlines.
**Key Accountabilities**
+ Provide analytical support to Rapid Technology Application platform by releasing precise and accurate results and ensure scope of testing parameter is sufficient to build MPA module.
+ Provide ongoing technical support to stakeholders, investigate quality problems and deliver improvement actions with follow up.
+ Perform method validation and verification to roll out new testing method in the lab.
+ Document standard operating procedures, identify possible trends in testing results with data analysis software and provide input to team members to improve quality control system.
+ Organize and maintain accurate and pertinent data, including spreadsheets, graphs and reports.
+ Maintain systems and techniques for reporting data across functional areas.
+ Organize and participate ring tests with the goal to check and control methods and equipment.
+ Handle basic issues and problems under direct supervision, while escalating more complex issues to appropriate staff.
+ Other duties as assigned
**Qualifications**
**Minimum Qualifications**
+ Bachelor's degree in a related field or equivalent experience
**Preferred Qualifications**
+ "Able to work independently, possess positive working attitude with high initiative level, and communicate effectively"
+ Necessary English reading capacity
+ Experience with chemical analysis (preferable)- oils and fats, starch, sweeteners, etc.
+ Knowledge in calibrate, maintain and troubleshoot various analytical instruments such as GC, HPLC, AAS, ICP, NIR etc
+ Able to demonstrate sound understanding of Statistical Process Control (SPC), method validation and report writing
+ Minimum of Three years of working experience in the Food industry Lab
Officer - Quality Control
Posted today
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Officer -QC
**Business Unit:**
Global Global Quality And Compliance
**Job Grade**
G12C
**Location :**
Gangtok
At Sun Pharma, we commit to helping you **Create your own sunshine** by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.
**Are You Ready to Create Your Own Sunshine?**
As you enter the Sun Pharma world, youll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each others journeys.
**Key responsibilities:**
To follow the SOP/ATP/STP and protocols.
To follow good working bench practices while performing the analysis
To follow good documentation practices and to perform online documentation.
To maintain the data integrity and to plan the work such as to give maximum productivity within stipulated time.
To help in maintaining the laboratory neat and clean.
To operate, maintain and clean the instruments as per the SOP.
To perform analysis of analytical samples e.g. Stability, FP, in-process, hold time, validation and other miscellaneous samples.
To analyze raw material, wash water and miscellaneous analytical samples as and when required.
To calculate the analytical results on time and to do its LIMS entry.
To follow the proper safety precautions while working in the lab.
To immediately report any odd observations/ noncompliance/ Failures and errors to section head or designee.
To coordinate with GLP while facing problem related to instrument breakdown and to communicate in case any odd observations found in laboratory (i.e. temperature/ humidity, purified/ Mill Q water, any spillage etc.)
To keep documents, records, chemicals, reagents, working standards and all miscellaneous items to its designated place after their usage.
Responsible for handling software like empower, EWS etc.
Responsible for completion of training and to provide pending signature in LMS.
To perform analysis in any other section of quality control as when required.
To perform any additional job responsibility assigned by Quality Control Head.
**Travel Estimate**
**Job Requirements**
**Educational Qualification**
B.SC, M.SC. B.Pharm
**Experience**
_2 to 4 yrs Exp_
**Your Success Matters to Us**
At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. _Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Lets create a brighter future together!_
**_Disclaimer:_** _The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification. It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities, and qualifications required of employees as assigned to this job. Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent(s)._
We provide equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, military or veteran status, generic predisposing characteristics or any other basis prohibited by law.
Quality Control Executive
Posted today
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Standard (Mon-Fri)
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials
**Job Description**
**About the Company**
Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $44 billion. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Whether our customers are accelerating life sciences research, solving analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to support them. Our distributed team delivers an outstanding combination of innovative technologies, purchasing convenience, and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD. Our Innovative Laboratory technologies & Services makes it easier for customers.
**Responsibilities:**
+ Responsible to carry out analysis on analytical instruments like HPLC, GC, ICP, GCMS etc.
+ Responsible to analyse and interpretate the analytical data basis customer requirement on Window based tools
+ Process knowledge of chemical testing, Analytical work, basic trouble shooting, method preparation/validation, handling and calibration of instrument like HPLC, GC, ICP, GCMS etc.
+ Responsible to maintain and carry out chemical analysis basis ISO/NABL standards 17025 and 17034.
+ Responsible for good laboratory practice in Quality control lab.
+ Perform analysis and reporting of raw materials, packing materials, Finished products, in-process and routine analysis.
+ Preparation of volumetric solutions, reagents, buffer solutions, indicator and maintain its records.
+ Perform standardization of volumetric solutions.
+ Preparation of Quality control SOP's.
+ Responsible to be self aware of Safety and Quality compliance and adhere to set compliance norms.
**Experience and Skill Sets:**
+ B.Sc. Chemistry with five years experience
+ M.Sc in Analytical / Inorganic chemistry with three years experience
+ The role needs good communication, presentation skill & solution-oriented approach.
**Benefits:**
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!
At Thermo Fisher Scientific, each one of our 100,000 extraordinary minds have a unique story to tell.
ThermoFisher is committed to crafting a diverse work environment that values and respects individuals.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Mgr, Quality Control
Posted today
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To manage 12-member team of analysts, senior analysts in QC - microbiology laboratory.
To prepare plans, protocols, reports and to execute day to day operations in microbiology laboratory.
**Job Description**
To manage a team of analysts, senior analysts, trainees in QC - microbiology laboratory.
To prepare plans, protocols, reports and to execute day to day operations in microbiology laboratory.
**Commitment to Diversity, Equity, and Inclusion:**
At Endo, our diversity unites and empowers us as One Team, and we are committed to cultivating, and valuing, each person's unique perspective. We actively promote a culture of inclusion that draws strength from our broad spectrums of diversity, including race, ethnicity, religion, gender identity or expression, national origin, color, sexual orientation, disability status, age, and all our other unique characteristics, qualifications, demonstrated skills, achievements, and contributions, backgrounds, experiences, cultures, styles, and talents.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
Quality Control Analyst
Posted today
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Essential Qualification :
M.Pharm/ MSc./ MTech/Bsc./B.Pharm
Experience :
- 6-10 years experience quality assurance/ quality control with Candidature with solid dosage forms preferrable in herbal field with Juice processing or liquid orals formulation process who had responsibility for routine QA activities and to ensure GMP in the plant.
- Excellent communication and leadership skills
Job Summary & Responsibilities :
- Candidature with solid dosage forms preferrable in herbal field with Juice processing or liquid orals formulation process who had responsibility for routine QA activities and to ensure GMP in the plant.
- Responsible to monitor the quality products are produced and documentation is ensured for onlinity. Should have strong knowledge on the raw materials quality checks, in-process, equipment’s knowledge, FG release process, implementation of standards, documentation and approach to ensure defects free products.
- To ensure that actively involved in review of analytical data and to ensure that the sampling, coordinating with external lab. and release shall be effective with reporting of OOS, Deviations and incidents on needy basis.
- Capable of handling quality at site with complete controls over system enhancing quality standards, strong knowledge on vendor management, Packing materials, packing trials and reporting it in effective manner.
- Responsible to ensure that actively involve in process standardization, Optimization, regular batch monitoring and release of product.
- Responsible for effective implementation of quality assurance system in accordance with the company’s quality policies and procedures.
- To maintain high degree of discipline in daily working which are directly related to the quality of the product.
- To co-ordinate with site on water testing, equipment qualification, complaint management, implementing new system, coordinating with R & D and ensuring for smooth implementation.
- To review and approve technology transfer documents and ensuring the smooth commercialization and validation.
- To review and approve SMF/Quality Manual records.
- To instruct and guide all respective site QA Executives/Officers for strict implementation of quality assurance procedures.
- To work for constant up-gradation in the existing quality assurance systems through innovative ideas as per current regulatory guidelines
- To undertake quality review of systems, products and furnish quality audit reports to the management on annual basis
- Responsible to co-ordinate for continuous improvement programme
- To see periodically the quality assurance operations at the plant and create confidence in site quality assurance organization
- Responsible in devising schedule and execution of internal quality audit/self-inspection by identifying cross functional team. To review audit report and recommend action plan for the non-compliances
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Quality Control Executive
Posted 2 days ago
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About us
We are Light Tree Ventures, a company specialized in Research, Development and Manufacturing of LED Light Therapy products for beauty and health. We have offices in the Netherlands, China, the US and India, with our headquarters in Rijswijk.
Our team of professionals are the heart of our company and encompass a wide variety of cultures, skills and competences. We love our work and share the ambition to be the best at what we do: create meaningful, well-designed products for LED Light therapy markets worldwide.
Light Tree Ventures (LTV) works with brands from all over the world. We develop custom light therapy devices that are being sold online and offline (in Sephora e.g.). This development is often a R&D sprint, designing a prototype and getting it ready for production. A fast and creative process, realizing the next generation product for a brand. LTV also owns several brands for which we develop our own innovative light therapy products.
In our India team we are looking for a new firmware developer that create and implement firmware on our LED light therapy devices. You will work together with our team to create new, innovative and exciting light therapy products. So what will you do?
Job description
We are looking for a Quality Control Engineer.
Your main tasks will include:
- Set detailed guidelines on what needs to be checked and what the quality standards are
- Update our Quality Management System (QMS) with incidents, fixes and improvements.
- Audit our systems based on ISO 9001:2015 requirements
- Determine quality metrics for all manufacturing procedures
- Monitor the entire production cycle and perform regular tests to identify potential malfunctions as early as possible
- Inspect product materials(which includes PCB, Components, SMT, etc) and electrical systems for defects and durability
- Identify the root of technical issues and recommend fixes
- Prepare reports on malfunctions and corrective actions (e.g. number of defective raw materials per order)
- Review current blueprints and quality documentation
- Set and track quality assurance goals (e.g. reduce average turnaround time for quality checks by 20%)
- Coordinate with external quality assurance auditors and technicians to ensure legal compliance
- Work with internal teams to increase customer satisfaction by improving the quality of the products
- Provision of records proving conformity of produced product to specifications.
- Responsible for product release based on manufacturing and QC records and/or reports.
Requirements and skills
- Bachelor degree in electronic is preferred with 2+ year of Experience.
- Previous work experience as a Quality Engineer or similar role in any EMS or medical electrical device manufacturing company.
- Hands-on experience with Quality Management Systems (QMS) and testing methodologies.
- In-depth understanding of technical documentation
- Great attention to detail and problem-solving abilities
- Team spirit, Good analytical skills.
- Additional certification in Quality Control is a plus.
- Knowledge of IPC-A-610 for electronics products assembly inspection.
- Knowledge of ISO13485 preferred.
- Hands on experience of Risk Management process as per ISO 14971
- Good understanding of FDA 21CFR Part 822 / 820 (Good to have)
- Familiar with tools like Monday.com, Office 365, etc.
What we offer:
• A highly motivated, young and hardworking team.
• Fast growing company with a lot of opportunities to develop yourself.
• Awesome products and international clients to work with.
• Proper salary, holiday allowance, vacation days.
• Your work contributes to the health of the general public.
• Opportunities to travel the world.
Quality Control Specialist
Posted 2 days ago
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Job Title: Quality Control (QC) Executive / Officer
Location: Meerut, Uttar Pradesh
Department: Quality Control & Assurance
Company: Golden Bird Healthcare Pvt. Ltd.– Dental Materials Division
About the Company
We are a rapidly growing dental materials startup engaged in the manufacturing, trading, and export of premium-quality dental consumables and equipment. Our product portfolio includes acrylic teeth & denture bases, waxes, sodium alginate, silicone-based impression materials, dental cements, endodontic medicaments, and dental plasters.
We are driven by innovation, quality, and clinical reliability — and are now looking for a passionate Quality Control Executive to join our team and support our vision of delivering world-class dental solutions.
Quality Control Coordinator
Posted today
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Fulkrum is a global leader in inspection, expediting, auditing, and technical staffing services, delivering exceptional solutions to the energy, engineering, and construction industries for over 14 years. Headquartered in the UK, we have established a strong presence across six continents, serving more than 300 clients worldwide.
Our commitment to excellence has been recognised with prestigious awards, including the King's Award for Enterprise in International Trade (2023), the People and Competency Award at the EIC Awards (2023), and the Scale-Up Award at the WESCA North America Awards (2024). Most recently, Fulkrum was named the 2025 winner in the People, Culture & Optimisation category at the EIC North & Central America Regional Awards.
Our Mumbai office is currently seeking a highly motivated and experienced QC Coordinator to join our dynamic team.
Key Responsibilities
- Respond to client requests for QA/QC, engineering, and project support personnel across various locations.
- Source, screen, and prepare candidates for client interviews, ensuring alignment with project requirements.
- Coordinate the full placement process, including proposals, interviews, onboarding, and documentation.
- Liaise with candidates regarding contractual terms, task-related documents, and performance expectations.
- Review, screen, and submit inspection reports and site documentation to clients promptly.
- Monitor candidate performance, timekeeping, and reporting quality, providing feedback and support.
- Maintain strong relationships with candidates through regular care calls and assignment follow-ups.
- Ensure compliance with ISO/IEC 17020:2012 and Fulkrum’s internal quality procedures and policies.
- Support the accounts team by ensuring timely submission of timesheets and purchase orders for invoicing.
- Participate in internal audits, identify process improvements, and report any conflicts of interest or HSE concerns.
What We’re Looking For
- Strong knowledge of onshore and offshore oil & gas projects.
- Proficiency in MS Office and documentation management.
- Excellent communication, organisational, and multitasking skills.
- Ability to work independently and collaboratively.
- Familiarity with QA/QC processes and ISO/IEC 17020:2012 standards.
HSE Awareness:
All personnel are informed of Fulkrum's Health and Safety policy and procedures during the onboarding process. Any HSE incidents must be reported and logged with the QHSE Manager, who will oversee and support any subsequent investigations.
Provide site-specific HSE instructions to Inspectors prior to mobilisation.
Why Join Us?
This is an exciting opportunity for a driven QC Coordinator to showcase their expertise in a supportive and collaborative environment. At Fulkrum, you’ll make a tangible impact while advancing your career in the thriving global business sector.
We offer a fantastic working environment with a highly engaged team and consistently high eNPS scores. Fulkrum's success in attracting new clients and expanding our global footprint is a testament to our excellence and dedication. We have regular reward and recognition initiatives, a social budget, and a refer-a-friend scheme to ensure our team feels valued and motivated.
Join us to be part of a high-performing team with ample opportunities for skill enhancement and development. Be a part of our success story and contribute to our continued growth and innovation.
Apply now and become a valued part of our growing team!