261 Finished Products Jobs - Page 7

Assistant Manager - Sourcing - E commerce Brand of products including electronics, apparel, home goods, and more. Our Private Brands division is dedicated to creating high-quality, exclusive products that offer great value to our customers. Role Overview: We are seeking a dynamic and experienced professional to join our Private Brands Retail Sourcing and Business Development team. In this role, you will be responsible for sourcing and developing our private label products, working closely with suppliers, and driving growth through innovative strategies and partnerships. Key Responsibilities: Sourcing and Supplier Management: Identify and evaluate potential suppliers for private label products. Negotiate contracts and manage supplier relationships to ensure product quality and cost-effectiveness. Conduct regular supplier performance reviews and address any issues that arise. Product Development:Collaborate with internal teams to develop new private label products that meet market demands and customer preferences. Oversee the product development process from concept to launch, ensuring timely delivery and adherence to quality standards. Business Development: Develop and execute strategies to increase the market share of private label products. Analyze market trends and competitor activities to identify new opportunities for growth. Work closely with the marketing team to create promotional campaigns and drive sales. Market Analysis and Reporting: Monitor and analyze sales data, market trends, and customer feedback to inform sourcing and product development decisions. Prepare and present reports on key metrics and performance indicators to senior management. Cross-Functional Collaboration: Collaborate with merchandising, logistics, and quality assurance teams to ensure seamless product integration and delivery. Foster strong working relationships with internal stakeholders to support business objectives. Qualifications: Education: Bachelors degree in Business, Supply Chain Management, Marketing, or a related field. Advanced degrees or certifications are a plus. Experience: Minimum of 5-7 years of experience in retail sourcing, private label development, or business development within the e-commerce or retail industry. Skills: Strong negotiation and communication skills. Proven ability to manage supplier relationships and drive product development.Analytical mindset with the ability to interpret data and make strategic decisions. Proficiency in MS Office Suite (Excel, PowerPoint, Word) and familiarity with sourcing and procurement software. Personal Attributes: Strategic thinker with a proactive approach to problem-solving. Results-oriented with a track record of achieving targets and driving growth. Strong interpersonal skills and the ability to work effectively in a team environment. private label products. Dynamic and inclusive work environment with opportunities for career growth and development. Competitive salary and benefits package.

Urgent openings for Helpers Location : Naikpada, Vasai E Job Details : Finishing, Fitting, Box Packing, Assembly, Soldering , Material Movement etc. Job timings : 9am -7pm ( 10hr duty) Salary 500 per Day

Experience: 4-8 Year Experience in manufacturing (API) as per Pharma Manufacturing GMP requirements. Responsibilities for Internal Candidates Key Roles & Responsibilities 1. Capable to handle independent projects 2. Analytical testing support to PDG synthetic group. 3. Coordinate with QA regarding method transfer, CCF and investigation reports. 4. Experience of handling of HPLC, GC, Potentiometer, Polarimeter instruments. 5. API Stability knowledge. 6. Capable to handle analytical method development, Implementation, Validation as per requirement. 7. Should have experience of Analytical method transfer to QC. 8. Experience of making documents like method transfer protocol & report, method validation protocol & report, method development report, specification, standard test procedure etc. 9. Should aware about GLP practices and 21 CFR part-11. 10. Keep the work area clean and the laboratory under controlled temperature. 11. Calibrate the instruments according to the master calibration schedule and follow GLP and SOPs. 12. Understand the safety and environmental aspect. 13. Maintain the reagents and standardize the volumetric solutions as per schedule. 14. Maintain the laboratory journals and instrument log books online. 15. Ensure compliance to Hazardous waste and chemical management. Responsibilities Qualifications Qualification : M.Sc (Analytical Chemistry), (Chemistry) & (Organic Chemistry)

Job Description Responsible for performing the chemical and instrumentation analysis for In-process, raw materials, packing materials, intermediates and finished products to meet the dispatch timeline as per the monthly schedule received from PPL. Responsible for performing the instrumentation like ICP-MS and LC-MS analysis for In-process, raw materials, intermediates and finished products to meet the dispatch timeline as per the monthly schedule. Responsible for performing the analytical method developments, analytical method validations, analytical method transfers and analytical method verifications by ICP-MS and LC-MS/MS. Responsible to prepare and review the protocols, work sheets and reports for method developments, method validations verifications and transfers Responsible for allotting the work to the chemist within the section. Responsible for performing the calibrations of all instruments in section as per the schedule. Responsible for maintaining all the documentation online. Responsible for maintaining the minimum stock for working standards, reference standards and impurity standards and ordering as and when required. Responsible for maintaining the minimum stocks for chemicals, reagents, glass wares and solvents required for analysis. Responsible for keeping instruments neat and clean and overall housekeeping in the section. Responsible for review of analytical data, calibration data, qualification data Responsible for keeping all instruments within the calibrated status. Responsible to do the analysis, review and release on time to support the production Responsible for reducing the lab incidences, repeat analysis and no Data Integrity issues. Responsible for real time data monitoring. Responsible for reviewing the analytical data received from external laboratory. Responsible for maintaining all the calibration certificates, qualification certificates, standard weight certificates and working/reference standard certificates. Responsible for maintaining the consumption records and traceability of working/reference standards. Responsible for OOS investigations, OOT, OOC and deviations investigations and CAPA implementations Responsible for review of SOPs , test procedures and specifications Responsible for providing the training on GLP/GMP to the employees working the section. Responsible for releasing the batches timely manner to achieve the site requirement. Responsible for preparing the COAs as per the customer requirement Responsible for approving/rejecting the batches in SAP Responsible for Controlling the cost and operate within the approved budget. Responsible for maintaining the instruments in working condition and reduce the breakdown time of instruments. Responsible for carrying out the analytical method transfers. Responsible for keeping the critical spare parts of the instruments. Responsible for Safe working conditions and clean environmental practices. Responsible for usages of required safety appliances in the section. Responsible for SFTI. Responsible for coordination with QA/Production/PPIC/Warehouse/TSD for smooth dispatches Responsible for training the contract persons and helpers on glassware cleaning. Responsibilities Qualifications Bachelors degree

The QA Executive is responsible for ensuring compliance with GMP, ISO, and regulatory guidelines by conducting audits, inspections, and documentation reviews The role involves overseeing batch record reviews, deviations, CAPA, and change control processes, ensuring adherence to quality standards for raw materials, in-process, and finished products The candidate will also implement quality improvements, handle customer complaints, and support regulatory audits to maintain product integrity and compliance : B Sc / M Sc

Job Purpose: Perform routine medical laboratory tests for the diagnosistreatmentand prevention of disease. May work under the supervision of a medical technologist Job Responsibilities: Conduct chemical analyses of body fluidssuch as blood or urineusing microscope or automatic analyzer to detect abnormalities or diseases and enter findings into computer. Analyze the results of tests or experiments to ensure conformity to specificationsusing special mechanical or electrical devices. Prepare standard volumetric solutions or reagents to be combined with samplesfollowing standardized formulas or experimental procedures. Supervise or instruct other technicians or laboratory assistants. Collect blood or tissue samples from patientsobserving principles of asepsis to obtain blood sample. Analyze and record test data to issue reports that use chartsgraphsor narratives. Test raw materialsprocessesor finished products to determine quality or quantity of materials or characteristics of a substance. Examine cells stained with dye to locate abnormalities. Conduct blood tests for transfusion purposes and perform blood counts. Perform medical research to further control or cure disease. Consult with a pathologist to determine a final diagnosis when abnormal cells are found. Inoculate fertilized eggsbrothsor other bacteriological media with organisms. Cutstainand mount tissue samples for examination by pathologists. Candidate Requirements: Able to work accurately and with minimal supervision. Ability to comprehend written instructions given by the related departmental personnel. Ability to plan & organize ones work schedule effectively. Speaking and listening are essential requirements to understand and carry out the instructions given by the supervisors and other related departmental personnel. Affinity to work in team. Enthusiasm.

Max Life Insurance Company Limited is looking for Assistant Manager to join our dynamic team and embark on a rewarding career journey Ensuring company policies are followed. Optimizing profits by controlling costs. Hiring, training and developing new employees. Resolving customer issues to their overall satisfaction. Maintaining an overall management style that follows company best practices. Providing leadership and direction to all employees. Ensuring product quality and availability. Preparing and presenting employee reviews. Working closely with the store manager to lead staff. Overseeing retail inventory. Assisting customers whenever necessary. Organizing employee schedule. Ensuring that health, safety, and security rules are followed. Ensuring a consistent standard of customer service. Motivating employees and ensuring a focus on the mission. Maintaining merchandise and a visual plan. Maintaining stores to standards, including stocking and cleaning. Completing tasks assigned by the general manager accurately and efficiently. Supporting store manager as needed.

Set up maintain calibratecleanand test sterility of medical laboratory equipment. Conduct chemical analyses of body fluidssuch as blood or urineusing microscope or automatic analyzer to detect abnormalities or diseases and enter findings into computer. Analyze the results of tests or experiments to ensure conformity to specification susing special mechanical or electrical devices. Prepare standard volumetric solutions or reagents to be combined with samplesfollowing standardized formulas or experimental procedures. Supervise or instruct other technicians or laboratory assistants. Collect blood or tissue samples from patientsobserving principles of asepsis to obtain blood sample. Analyze and record test data to issue reports that use chartsgraphsor narratives. Test raw materials processesor finished products to determine quality or quantity of materials or characteristics of a substance. Obtain specimens cultivating isolatingand identifying microorganisms for analysis. Examine cells stained with dye to locate abnormalities. Conduct blood tests for transfusion purposes and perform blood counts. Perform medical research to further control or cure disease. Consult with a pathologist to determine a final diagnosis when abnormal cells are found. Inoculate fertilized eggsbrothsor other bacteriological media with organisms. Cutstainand mount tissue samples for examination by pathologists. Candidate Requirements: Able to work accurately and with minimal supervision. Ability to comprehend written instructions given by the related departmental personnel. Ability to plan & organize ones work schedule effectively. Speaking and listening are essential requirements to understand and carry out the instructions given by the supervisors and other related departmental personnel. Affinity to work in team.

Find a Career With Purpose at Teva Keyword Location Select how often (in days) to receive an alert: Analytical Researcher Date: Jun 12, 2025 Location: Ambernath, India, 421506 Company: Teva Pharmaceuticals Job Id: 62374 Who we are How you ll spend your day To analyze samples received from Formulation department (samples include in-process, finished product, pre-formulation study samples and stability samples etc.). To carry out analytical method development for API, in-process samples and finished products including the methods for cleaning studies. To carry out analytical method transfer activity. Calibration and maintenance of analytical instruments. Maintenance includes activities such as Qualification, keeping track of AMC, History, Spares, Usage records etc. To ensure that all activities undertaken are executed in the framework of good laboratory and documentation practices and the existing quality systems are adhered to. To ensure safety practices are followed during the execution of activities and strict adherence to the EHS systems of the site. Any other activity assigned but the line manager Trouble shooting of analytical instruments for difficulties faced during day-to-day operations Your experience and qualifications PhD with 1 plus years of experience/ Masters degree in Pharmaceutical sciences/Msc 3 to 5 years relevant experience

Develops, evaluates, revises, and applies technical quality assurance protocols/methods to inspect and test in-process raw materials, production equipment, and finished products Ensures activities and items are in compliance with both company quality assurance standards and applicable government regulations Performs analysis and identifies trends in the inspection of finished products, in-process materials and bulk raw materials, and recommends corrective actions when necessary Ensures that established manufacturing inspection, sampling and statistical process control procedures are followe'd May assure compliance to in-house and/or external specifications and standards, such as GMPs and ISO regulations Evaluates and analyzes the efforts in organizing, documenting, and interpreting inspection support documents and records

Develops, evaluates, revises, and applies technical quality assurance protocols/methods to inspect and test in-process raw materials, production equipment, and finished products Ensures activities and items are in compliance with both company quality assurance standards and applicable government regulations Performs analysis and identifies trends in the inspection of finished products, in-process materials and bulk raw materials, and recommends corrective actions when necessary Ensures that established manufacturing inspection, sampling and statistical process control procedures are followe'd May assure compliance to in-house and/or external specifications and standards, such as GMPs and ISO regulations Evaluates and analyzes the efforts in organizing, documenting, and interpreting inspection support documents and records

Description: Manager QC, is responsible for Managing the activities of the quality control laboratory to ensure timely delivery of materials for use in production and releases of finished products from the laboratory as committed, ensure testing of stability samples within structure of timelines identified in relevant SOP, ensure laboratory activities on par with compliance expectations, and provide top notch inter- and intra-department customer service. Essential Functions: Manage the day-to-day operations of the Quality Control laboratory including setting and communicating priorities based on the production schedule. Maintain knowledge of the potential impact of Quality Control activities on activities in other departments and effectively communicate this information to the appropriate personnel in a timely manner. Manage/Enforce laboratory GMP systems and ensure that they are adequate, sustainable and are being followed. Update Laboratory Procedures (SOPs) and Policies. Interpret SOPs/Methods/Specifications and provide clarity as needed Manage and perform investigation of out-of-specification laboratory results ensuring that all investigations proceed in a logical, orderly and timely manner and that appropriate corrective and preventive actions are identified when necessary, review and approve investigation reports. Review and signoff process validation/cleaning validation protocols/reports, method verification/validation reports, annual product review reports. Review certificate of analysis to ensure compliance with the specifications. Develop and implement systems to improve laboratory GMP compliance and/or productivity. Make decisions and implement solutions where deficiencies are found. Provide formal and informal performance feedback to direct and indirect reports including disciplinary action when necessary. Provide input on yearly departmental headcount and turnover of tested samples. Provide input on employee development including promotion and salary increase recommendations. Research and propose capital projects for the laboratory. Additional Responsibilities:

Perform and review method validation of Assay, Dissolution, Related compound and Residual solvents etc. for new projects using instruments like HPLC, IC and GC etc. Preparation of method validation/verification protocol (API and finish product) like HPLC, GC, IC, and ICP-MS etc. Check and perform the method transfer protocol/report and methods and resolve the query of Assay, Dissolution, Related compound and Residual solvents etc. To coordination with ARD-Development, QA and QC Ensure timely completion of validation/verification and method transfer as per timeline To be able to perform the Daily calibration all instruments/equipments as per respective schedule. To be able to perform the periodic calibration, Maintenance of all instruments/equipments as per respective schedule. To be able to perform the daily temperature monitoring of Freeze and Freezer To be able to maintain and review the qualifications, preventive maintenance and calibration of instruments/equipment s and their records To be able to review stability chambers data and print outs.

CALDERYS INDIA REFRACTORIES LIMITED is looking for Plant Associate - Production to join our dynamic team and embark on a rewarding career journey. Assembly : Performing tasks related to the assembly of products or components according to standard operating procedures. Quality Control : Inspecting products for defects or irregularities and ensuring that they meet quality standards. Packaging : Packaging finished products according to specifications, which may involve labeling, boxing, or palletizing items. Machine Operation : Operating machinery or equipment used in the production process, such as conveyor belts, assembly line machines, or packaging equipment. Inventory Management : Keeping track of inventory levels and reporting shortages or discrepancies to supervisors. Safety Compliance : Following safety protocols and guidelines to maintain a safe working environment for themselves and their colleagues. Cleaning and Maintenance : Performing routine cleaning and maintenance tasks on machinery and work areas to ensure optimal functioning and cleanliness.

JOB DESCRIPTION Quality Control Manager Designation: Manager 1 Location: Panoli, Gujarat Department: Quality Control Group/Area: GC section and Working standard section Experience: 10+ years Education: M.Sc. in Chemistry Work planning, distribution and monitoring of GC section and working standard section. LIMS template preview and Instrument method preparation and updation in Empower. To initiate Laboratory event/out of specification /out of trend /Deviations/change control in the Track Wise and perform investigation as per the SOP. To ensure working standard qualification activity. To ensure procurement activity and availability of Reference standards/Impurity Standard/GC standards/GC columns. To ensure cleaning of Instrument, work place and Laboratory Training given to subordinates To ensure PPEs as per work requirement and maintain safety in laboratory Other activities instructed from time to time.

Ensure the quality of incoming materials, in-process production, and finished products meets defined standards. Manage PPAP activities for new parts, engineering changes, and improvement projects to ensure compliance with design and industry requirements. Investigate root causes of internal defects, customer complaints, and rework using quality tools, and implement effective corrective and preventive actions (CAPA). Conduct regular internal and supplier audits to ensure compliance and drive quality improvements. Support continuous improvement initiatives to reduce defects and increase operational efficiency. Ensure all quality activities align with the requirements of the Integrated Management System (IMS). Qualification: B.E. in Mechanical Engineering Experience: 12 years of experience in the manufacturing industry Skills Required: Proficiency in relevant software and tools used in quality management, data analysis, and documentation In-depth knowledge in SAP QM module Knowledge in Microsoft Excel and PowerPoint are preferred

ArisInfra is a new age material procurement & smart financing platform for infrastructure and construction companies. We are a full stack solution for the customers providing best pricing, reliable supply and flexible credits. Customers can buy the full range of unfinished and finished products from us -Cement, Steel, RMC, Aggregates, Construction Chemicals, Electricals, Paints etc. Our mission is to make material procurement and financing smart, convenient, and simple for everyone. Role Description: We are seeking a highly motivated individual to join our team at Aris Infa as a Assistant Manager of Sales & Marketing in the building materials industry. This is a unique opportunity to contribute to a dynamic and rapidly growing company, and play a key role in achieving our ambitious business goals. Responsibilities: Identify and evaluate potential business opportunities, including analysing market trends, competitive landscape, and customer needs. Develop and implement effective strategies to penetrate new markets and increase market share. Build and maintain strong relationships with key customers and partners, ensuring a high level of customer satisfaction and retention. Manage the entire sales cycle from lead generation to closing deals, including conducting negotiations and preparing sales proposals. Collaborate with cross-functional teams, including marketing, product development, and operations, to ensure successful execution of business initiatives. Conduct market research and analysis to identify new trends and opportunities in the building materials industry. Stay up-to-date with industry developments and competitor activities to proactively identify and address challenges. Requirements: Bachelors degree in Business Administration, Marketing, or any related field. Minimum of 6 years of experience in business development, sales, or related roles, preferably in the building materials industry. To engage and pitch with all Retailers/IHBs/Contractors and do a complete opportunity mapping. Proven track record of successfully identifying and closing new business opportunities. Should have a strong team handling experience and managing team targets. Should have a strong geography territory knowledge. Strong analytical skills and ability to translate data into actionable insights. Excellent communication and presentation skills, both verbal and written. Ability to build and maintain strong client relationships. Proactive and self-motivated with a strong sense of accountability and ownership. Ability to thrive in a fast-paced and dynamic work environment. Were looking for you to be a part of our team Choosing a selection results in a full page refresh.

1. Plan and Perform activity : Incoming raw materials & finished goods testing as per WSL QAP. Preparing List of resource requirement. Collation of relevant information to be shared with the HOD. Maintaining all records as required as per documentation as per organizational defined process and SOP 2. Testing : Analysis and prepare necessary QC test reports and submission of the same to concerned person. Proper Testing of Incoming & finished goods in respective shift 3. Tools Knowledge & Maintenance : Should have detailed knowledge of tools and machines used for QC testing of Raw material and finished goods. Ensuring timely maintenance and calibration of testing tools as per industry standards 4. Industrial Safety : Ensure Safe Working Condition ,Safe work practices and Safety culture, Initiate the action to prevent occurrence of nonconformity relating to safety , Comply EMS ,OHSAS and statutory requirements.

SUMMARY Ensure the quality of incoming materials, in-process production, and finished products meets defined standards. Manage PPAP activities for new parts, engineering changes, and improvement projects to ensure compliance with design and industry requirements. Investigate root causes of internal defects, customer complaints, and rework using quality tools, and implement effective corrective and preventive actions (CAPA). Conduct regular internal and supplier audits to ensure compliance and drive quality improvements. Support continuous improvement initiatives to reduce defects and increase operational efficiency. Ensure all quality activities align with the requirements of the Integrated Management System (IMS). Requirements Qualification: B.E. in Mechanical Engineering Experience: 12 years of experience in the manufacturing industry Skills Required: Proficiency in relevant software and tools used in quality management, data analysis, and documentation In-depth knowledge in SAP QM module Knowledge in Microsoft Excel and PowerPoint are preferred

Vibonum Technologies Private Limted conducting a Walk-in interview in Hyderabad for Quality Control Executives and Officers for its OSD Plant at Mysore. Date of Walk-in: 14th & 15th Jun 2025 Responsibilities Hands-on experience on QC instruments such as HPLC, GC, UV-Vis Spectrophotometer, FTIR, Dissolution Tester, TOC Analyzer, etc. Exposure to stability testing, raw material and finished product, In-process and stability analysis, documentation as per cGMP, and regulatory compliance (WHO, USFDA, MHRA, etc.) Analytical data review and QMS Knowledge of Good Laboratory Practices and analytical method validation/verification is preferred. Quality Control Executive Total Vacancies - 20, Education: B. Pharm / M. Pharm / M.Sc Exp: 6-8 Years Quality Control Officer Total Vacancies - 20, Education: B. Pharm / M. Pharm / M.Sc Exp: 2-5 Years Work Location: Nanjangud Mysore Note: Immediate joiners or candidates with a notice period of up to 1 month will be given preference. Candidates must bring their updated resume, latest salary slip, passport size photograph, and copies of educational & experience certificates. Walking Address: Kinara Grand Hotel, 8-3-949/5, Ameerpet Road, Near Indian Overseas Bank, Nagarjuna Nagar colony, Ameerpet, Hyderabad, Telangana - 500073 Phone: 092468 20520 Google Map: https://maps.app.goo.gl/ohQWhu1RKMDbp2X78

Role & responsibilities Aurobindo Pharma Ltd. Unit IV (Naidupeta, Tirupati Dist., Andhra Pradesh) Open Functions: Quality Assurance (Market Complaints / QMS / Validation / IPQA) Quality Control (GMP / GC / LCMS / HPLC) 3 Experience Required: 2 7 years (pharmaceutical manufacturing) Job Titles & Grades: Executive / Sr. Executive (based on experience) Job Description: Quality Assurance Key Scope • Handle Market Complaint investigations, trend analysis and regulatory responses • Maintain site QMS: Deviations, CAPA, Change Control, Audit readiness • Execute and review Equipment / Process / Cleaning Validation documentation • Perform IPQA activities: line clearance, in-process checks, batch record review • Conduct GMP & Data-Integrity training for shop-floor teams Quality Control Key Scope • Routine & stability testing of RM / IP / FP samples on HPLC, GC, LCMS, UV, etc. • Prepare/standardise analytical methods, calibration & instrument qualification (IQ/OQ/PQ) • Adhere to GDP, ALCOA+ and cGMP guidelines; ensure timely LIMS/SAP data entry • Investigate OOS/OOT results and implement effective CAPA • Support regulatory, customer and internal audits Common Requirements: • Qualification: B.Pharm / M.Pharm / B.Sc. / M.Sc. (Chemistry or related) • Sound knowledge of current GMP guidelines (US-FDA, MHRA, EU, WHO) • Good documentation, investigation and communication skills • Willingness to work in shifts and collaborate with cross-functional teams How to Apply • Send you updated resume : naidupetahr@aurobindo.com • WhatsApp : 9851444337

To manage all Store, Inventory and Warehouse operations including Finished goods and RM etc.

Hog Projects is looking for QA / QC Engineer to join our dynamic team and embark on a rewarding career journey. A QA/QC Engineer is responsible for ensuring that products, projects, and processes meet established quality standards and specifications This role involves monitoring and evaluating the production or construction processes to identify and address issues that could affect product quality Additionally, the QA/QC Engineer plays a crucial role in creating and implementing quality control procedures and documentation Key Responsibilities:Quality Assurance:Develop and implement quality assurance policies, procedures, and standards Ensure that products or projects meet or exceed customer and regulatory requirements Conduct audits and inspections to identify areas for improvement in quality processes Quality Control:Establish and maintain quality control procedures to monitor and measure product or project performance Inspect materials, components, and finished products to verify their compliance with quality standards Implement testing protocols and document test results Documentation:Maintain comprehensive records of quality control activities, including test results, inspection reports, and corrective actions taken Prepare quality documentation and reports for internal and external stakeholders Process Improvement:Collaborate with other departments to identify and resolve quality-related issues Continuously assess and improve quality control processes to enhance overall efficiency and product quality Training and Compliance:Train personnel on quality control procedures and standards Ensure compliance with relevant industry standards, regulations, and certifications Problem Solving:Investigate and address non-conformities, defects, and quality-related incidents Identify the root causes of quality issues and recommend corrective and preventive actions Risk Assessment:Evaluate potential risks and hazards that could impact quality and safety Develop risk assessment strategies and mitigation plans Data Analysis:Utilize statistical analysis and data-driven techniques to monitor and improve quality control processes

Develop & implement quality control process Conduct regular inspections & tests of products & material Analyze quality control data Work closely with the production team to ensure quality standard Maintain accurate records of quality control activity Required Candidate profile Knowledge of quality control standards and regulations Strong analytical and problem-solving skills Interested candidates can share their resume on +91 6354377703 or marcom.vhr@gmail.com

• Analysis of Semi-finished , finished products, Raw material and packing material • Physical & chemical analysis of Semi-finished /Finished/in process /RM and PM samples and documentation. • Should have experience working on HPLC & GC