Work Experience 1-5 years Job Description Visiting to Quality Control Labs to ensure that activities are being carried out by following GMP requirements and as per approved procedures. To ensure that labs are maintained to be GMP ready always. Follow-up to close the findings as per established procedures. Handling of QC Lab incidents, Deviations, change controls, OOS, OOT, OOL, QRM, CAPA management and related investigations throughout the year. Verification of analytical test results and approval through SAP. (In-process, Intermediate, DS, FB, DP and additional study reports if any). Batch Release activity for intermediates and In-process (i.e.: Media, buffers and so on). Review of SOPs/ STPs/ Specifications and any other documents as per GMP requirements for QC/QA department. Ensure that stability studies/ testing of samples are being carried out by following approved procedure/protocols. Education Masters in Life Science Competencies 1. Strategic Agility 2. Innovation & Creativity 5. Result Orientation Quality Technical Skills

May support in the development, review and approval of sterilization process and equipment validation/qualifications (IQ, OQ & PQ). Be the point of contact for suppliers/development engineers for new process development, quality issues and process improvements for assigned projects. Participate in the development and improvement of the manufacturing processes for existing and new products. Support product transfers to other plants/facilities. Review/approve nonconforming material and system documentation. Review/approve product and process change control documentation and specifications. Actively participate on teams to support new product development activities. Support design verification and validation test requirements that ensure appropriate objective evidence is available to support acceptance criteria. Specific Job Skills: Must understand the fundamentals of at least one of the following sterilization techniquesgamma irradiation, ethylene oxide (preferred), hydrogen peroxide gas plasma, moist heat, or dry heat and be an expert in one of the techniques. Demonstrated knowledge about a variety of microbiological concepts, practices, and procedures. Ability to use ISO, AAMI, USP, ANSI, EPA, EU and related guidelines toward the design, manufacturing, development, and launch of initiatives. Experience with ISO 17025, Lab Quality Management System. Desired Profile EducationM.Sc. in Microbiology ExperienceMin 5 years of experience in applied device or pharmaceutical microbiological or biological testing, research and development, or sterility assurance experience.

Candidate must have experience from chemical manufacturing industry.

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

Walk-in Drive @ Chennai on 15th June 2025 (Sunday) Strides Pharma is hosting a Walk-In Drive for multiple roles across our Manufacturing facilities in Chennai & Pondicherry. Venue: Days Hotel by Wyndham Chennai OMR, 245/1, Rajiv Gandhi Salai, Chennai, Padur, Tamil Nadu-603103 Open Positions Department: Production Experience: 2-7 years Qualification: B.Pharm/M.Pharm Job Location: Chennai Key Skills: Granulation, Compression, Coating, Capsule Filling, OSD Production Department: Packing Experience: 2-7 years Qualification: B.Pharm/M.Pharm Job Location: Chennai Key Skills: OSD Packing, Bottle Packing, Blister Packing, BQS, CVC, BPR Department: Quality Control Experience: 2-7 years Qualification: B.Pharm/M.Pharm/M.Sc. Job Location: Chennai/Pondicherry Key Skills: HPLC, GC, UV, IR, KF, FTIR, Dissolution, LIMS, GLP Department: Quality Assurance Experience: 2-7 years Qualification: B.Pharm/M.Pharm Job Location: Chennai Key Skills: IPQA, QMS, BMR Review, BPR Review, Line Clearance, Change Control, Deviation, CAPA Department: Engineering Process Maintenance Experience: 2-7 years Qualification: Diploma/B.Tech. (Electrical, Mechanical, Instrumentation) Job Location: Chennai Key Skills: Maintenance of RMG, FBD, Compression, Coating, Capsule filling, Blister Packing, Bottle Packing Machines Department: Engineering Utility & Instrumentation Experience: 2-7 years Qualification: Diploma/B.Tech. (Electrical, Mechanical, Instrumentation) Job Location: Chennai Key Skills: Utility, Water System, HVAC, Chillers, AHU, Air Compressors, Cooling Tower, DG, LT & HT Panel, PLC, SCADA, HMI Best Regards, Talent Acquisition Team, STRIDES PHARMA SCIENCE LTD

Quality Control – Session Auditor: 1:1 tutoring Prior EDTECH Experience Mandatory Are you passionate about maintaining high-quality online education? Mentor Match is looking for a Performach support Specialist (QC) professional to audit and elevate our 1:1 tutoring sessions. Role: Performach support Specialist (QC) - EdTech ( Quality Control – Session Auditor) Compensation: ₹30,000/month Timings: 11 PM – 8 AM IST (US Shift) Location: Remote Key Responsibilities: Audit 15 live/recorded 1:1 sessions per day Evaluate session delivery, engagement, and adherence to quality standards Provide constructive and Live feedback to tutors Requirements: Prior experience in EdTech/online tutoring evaluation Strong subject knowledge in Math (Grades 9–12, US Common Core) Excellent attention to detail and communication skills Show more Show less

Trending Job Description Business: Piramal Pharma Solutions Department: Engineering Location: Digwal, Hyderabad Travel: Medium Job Overview This is to upkeep the manufacturing assets to ensure availability and reliability,ensuring the smooth operation and reliability of equipment and facilities for the API plant Key Stakeholders: Internal Cross - functional teams at Digwal site like Production, QA, QC, HR, TSD, SCM , EHS, Administration etc Key Stakeholders: External Statutory and Regulatory agencies, External Suppliers, Engineering Contractors, Service providers & Customers (on need basis) Reporting Structure Role reports to: General Manager – Engineering Experience 15-20 Years experience preferably in API plants’ Engineering and Maintenance (E&M) function. The incumbent should have exposure to managing Breakdown, Preventive maintenance, troubleshooting related API manufacturing. Blocks, Clean Rooms, HVAC, Utilities, Boiler, Electricals, Instrumentation and managing CAPAs. Should have academics understanding, operational know-how of Utilities, Electricals, Instrumentation, HVAC to maximize performance and optimizing OPEX into these areas. Should understand the KPIs of E&M function, working in matrix reporting environment to manage Corporate initiatives and Compliances. Have a passion and past exposure to drive for high standard of Safety and Compliance standard into day-to-day work, meeting EHS & statutory compliances and realizing zero incident performance Competencies Ability to manage a large team and guide them to achieve functional objectives Stakeholder management – internal and external Structured approach to manage overall E&M work and quick learning attitude to adapt cultural changes. High analytical abilities to spot on actual reasons for gaps in asset performance, energy performance and other E&M performances. Good level of understanding on Process oriented approach to designing and managing the work. Inter-personnel skills to work in matrix reporting, managing stake holders, working with Piramal Corporate Engineering. Multitask master to work in highly dynamic CMO Business environment. Key Role & Responsibilities Responsible for Maintenance of API Plant with exposure to Mechanical, Electrical, Utilities and Instrumentation areas . Responsible for the complete E & M function to act as HOD in absence of HOD. Exposure to Utilities and Electrical efficiencies and to contribute into Energy efficiencies and ESG program. Jobs assigned time to time by HOD (E&M). He has been trained to perform Qualified Auditor. Responsible for internal Audits on time action closures as per the date & Agenda Circulated by QA & EHS. Develop & prepare work procedures to minimize OHS risks and Adverse environment effect. Comply with SHE Guidelines, SHE Rules and Regulations. Implement emergency control plan. Maintain all relevant records under OHSAS & EMS Systems. Ensure compliance to Hazardous waste and chemical management. Managing to complete observed unsafe acts and conditions and take corrective & preventive actions as per plan. Responsible for on time completion of all the maintenance work as per the satisfaction of end user. Responsible for in time payment of maintenance work carried out by fabricators & Contractors. Responsible for quality of maintenance work carried out by fabricators and contractors as per the specifications in timely manner. Responsible for carrying out breakdown investigation for any incident / accident/ near miss / illness and report if his superiors in two working days Responsibilities BE - Mechanical About Us In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices. Equal employment opportunity Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics. We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice. About The Team Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited’s investment in Yapan Bio Private Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide. Job Info Job Identification 5564 Job Category Engineering Posting Date 06/09/2025, 08:03 AM Apply Before 09/30/2025, 08:03 AM Degree Level Bachelor's Degree Job Schedule Full time Locations Piramal Enterprises Limited. Factory: Digwal, Medak, Telangana, 502321, IN Show more Show less

Be the First to Apply 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 SOP’s , 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 COA’s 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. Qualifications Bachelors degree Required Skills LCMS/MS, HPLC About Us In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices. Equal employment opportunity Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetics, or other applicable legally protected characteristics. We base our employment decisions on merit considering qualifications, skills, performance, and achievements. We endeavor to ensure that all applicants and employees receive equal opportunity in personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions, including reasonable accommodation for qualified individuals with disabilities as well as individuals with needs related to their religious observance or practice. About The Team Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our customers through a globally integrated network of facilities in North America, Europe, and Asia. This enables us to offer a comprehensive range of services including drug discovery solutions, process & pharmaceutical development services, clinical trial supplies, commercial supply of APIs, and finished dosage forms. We also offer specialized services such as the development and manufacture of highly potent APIs, antibody-drug conjugations, sterile fill/finish, peptide products & services, and potent solid oral drug products. PPS also offers development and manufacturing services for biologics including vaccines, gene therapies, and monoclonal antibodies, made possible through Piramal Pharma Limited’s investment in Yapan Bio Private Limited. Our track record as a trusted service provider with experience across varied technologies makes us a partner of choice for innovators and generic companies worldwide. Job Info Job Identification 8645 Job Category Quality Control Posting Date 06/09/2025, 10:36 AM Degree Level Bachelor's Degree Job Schedule Full time Locations Piramal Enterprises Limited. Factory: Digwal, Medak, Telangana, 502321, IN Show more Show less

Company Overview Global Calcium Pvt Ltd is a leading company in the calcium carbonate industry, committed to providing high-quality products to our customers. Our mission is to deliver exceptional value through innovative solutions and superior service. We foster a culture of integrity, teamwork, and sustainability, ensuring a positive environment for both our employees and clients. Position: Executive - QC (ICP - MS) Location: Hosur, Tamil Nadu Workplace Type: On-site Role Responsibilities Conduct regular quality control tests and inspections on raw materials and finished products. Implement and maintain quality management systems and protocols. Prepare detailed reports on quality control findings and recommend improvements. Monitor equipment calibration and maintenance schedules to ensure operational efficiency. Collaborate with production teams to identify areas of quality concern. Ensure compliance with industry standards and regulations. Train and mentor junior quality control staff on laboratory procedures. Manage non-conformities and implement corrective actions effectively. Perform data analysis to track quality trends and execute process improvements. Work closely with research and development to support new product testing. Participate in internal audits and improve audit responses. Assist with the development of quality-related training programs for staff. Evaluate and enhance testing methods to improve efficiency. Maintain accurate records in accordance with ISO standards. Support the investigation of customer complaints related to product quality. Qualifications Required: Bachelor’s degree in Chemistry, or related field. 2+ years of experience in quality control or laboratory environment. Strong understanding of quality assurance and quality control principles. Proficiency in using laboratory equipment and software. Excellent written and verbal communication skills. Ability to work independently and in a team setting. Familiarity with regulatory requirements (ISO, GMP). Strong analytical and problem-solving abilities. Attention to detail and precision in lab work. Ability to manage multiple tasks and deadlines. Proficient in Microsoft Office Suite (Excel, Word, PowerPoint). A proactive approach to quality improvement. Demonstrated ability to adhere to safety protocols. Strong organizational skills and time management. Willingness to adapt to changing priorities. Preferred Master’s degree in a relevant scientific field. Certification in Quality Control or related disciplines. Experience with statistical process control (SPC). Knowledge of chromatography (ICP-MS) techniques. Previous experience in the manufacturing sector. If you are passionate about quality control and want to contribute to a dynamic team at Global Calcium Pvt Ltd, we encourage you to apply. Skills: regulatory compliance,iso standards,technical writing,laboratory techniques,problem solving,laboratory procedures,chromatography (icp-ms),problem-solving,team collaboration,quality management systems,analytical skills,data analysis,quality control,microsoft office suite,time management Show more Show less

Job Description To follow safety rules in the premises according to the company norms. To maintain the BMRs and other log books in the aseptic processing area as per cGMP and SOP. Preparation and periodic revision of SOPs related to aseptic processing area. Monitoring of DP, RH and temperature in aseptic processing area. Responsible to perform the in process checks during filling. To ensure aseptic area cleaning and fogging to coordinating with engineering department as per the schedule. Operation and Cleaning of heating cooling skid, CIP & SIP skid. Responsible for environmental monitoring of (Viable) aseptic processing area. Timely completion of SOPs training and on the job trainings related to aseptic processing area. To ensure all equipments cleaning activity like CIP / SIP for vessels before starting of the batch process and after completion of the batch process related to filling and filtration. To ensure all aseptic processing area equipment's change parts cleaning and storage as per the procedure. Responsible for cleaning verification and preparation of filling parts for autoclaving Responsible for operation and cleaning of area equipment present in the filling area like filling machine, Rubber stoppering, sealing machines, Isolators, Pass boxes, Glove cleaning and integrity testers including VHP. Responsible to carry out the filling, stoppering, lyophilization and sealing operations as per the SOP and BMR. Responsible for the co-ordination with cross functional departments like QA, QC, warehouse Engineering, HR and administration for day to day activities. Responsible for timely completion of calibrations and validations in coordination with engineering and QA related to aseptic processing area. Activities other than defined in the job responsibility are to be done, as per the requirement of HOD, by following HODs instructions and guidance. Qualifications Qualification - B. Pharma, M.Pharma, B Tech, Diploma About Us Amneal is an equal opportunity employer. We do not discriminate based on caste, religion, gender, disability, or any other legally protected status. We believe in fostering a workplace that values diversity and inclusion. About The Team The Human Resources team partners with all aspects of the organization, driving success through the effective and innovative management of people for both current and future business needs. Key Roles That The Human Resources Team Performs Executive Role: Specialists in all aspects of people management. High-level input at strategic level into all key business decisions. Audit Role: Ensures all areas of the organization are compliant with legal requirements AND best practice employment policies and procedures. Facilitator Role: Close partnership to support, advise and extend the ability of all areas of the organization to meet their objectives through implementation of highly effective employment practices in areas such as Talent Acquisition, Learning and Development, Reward systems, Performance Management, Health and Wellbeing. Consultancy Role: Provide expert advice to the organization and it’s managers on any aspect of workforce management and employee relations and performance. Service Role: Ensure the organization is fully aware of and is equipped to deal with developments impacting employment matters, such as changes in legislation, changes in the characteristics of the labor market. Show more Show less

Improve production quality Process improvement and control Continuous improvement of process quality Process quality control Continuously improve the production process with Lean Implement Cost Saving strategies Quality Improvement reports Required Candidate profile Vacancy for both male and female. Any graduate can apply.

Role Summary We are seeking a highly motivated Assistant Category Manager to support the growth and management of the Home category on our platform. The role involves owning business targets, working cross-functionally, managing brand relationships, ensuring site merchandising hygiene, and driving operational efficiency. Key Responsibilities: Target Achievement & Growth Drive topline and bottom-line sales for the category. Monitor and improve conversion rates. Regularly track performance against targets and identify growth opportunities. Marketing Income Ensure achievement of monthly marketing income targets. Track brand contributions (e.g., coupons, offers) and align with internal marketing initiatives. Brand Relationship Management Maintain consistent communication with partner brands. Share data-driven insights and performance updates. Coordinate for brand queries, catalog updates, launches, and events. Site Merchandising Conduct continuous QC of site listings. Ensure timely and accurate corrections. Optimize navigation and visibility by creating and refreshing key landing pages. Collaboration Liaise with cross-functional teams (Marketing, Ops, Finance, Tech, Content, etc.) to execute tasks effectively. Ensure timely communication and follow-ups for business execution. Daily Seller Operations Monitor order fulfilment and delivery timelines. Troubleshoot price/listing issues and coordinate with seller/warehouse teams to ensure smooth operations. Key Skills Required: Strong analytical and problem-solving skills Excellent communication and stakeholder management Detail-oriented with an eye for site hygiene and merchandising Proficiency in Excel, data dashboards, and e-commerce tools Ability to multitask and work in a fast-paced environment Qualification: Graduate/Postgraduate in Business, Marketing, or related field 2–4 years of relevant experience in category management/e-commerce/retail Show more Show less

Urgent Hiring || QA Head || Ankleshwar -Gujarat Designation : QA - Head Experience : Minimum 15 to 19 years’ experience in pharma from QA Department. Salary : upto 15 lpa (Depend on the interview) Location: Ankleshwar -Gujarat Essential Duties and Responsibilities : Knowledge of all regulated Guideline & Pharmacopoeia. Preparation & implementation of SOPs related to the concerned department & Justification of Specification. Nitrosamine Impurity, Elemental impurity, Genotoxic Impurity & their role related DMF Filing. collaborates with the Quality Control (QC) team to ensure that laboratory testing is conducted appropriately and meets the required specifications. The conducts regular internal audits of the manufacturing facility to ensure that the facility meets the required quality standards. handles the Regulatory and Customer audit and its compliance. Responsible for ensuring that all necessary documentation is completed accurately, in a timely manner, and in compliance with regulatory requirements Responsible for reviewing and approving deviation reports and ensuring that corrective and preventive actions (CAPA) are implemented. Responsible for reviewing and investigating product complaints to ensure implementation of corrective and preventive actions (CAPA). Responsible for training of manufacturing and laboratory personnel on quality-related procedures and regulations. Handling of out of specification (OOS) and out of trend (OOT) laboratory incidents and their closing. Preparation & review the method of analysis (MOA), standard testing procedure (STP) and other documents related to QC. Implementation & verification, in-process checks, online entries in BPR Review of Manufacturing Processes. Monitoring and ensuring the good manufacturing practice (GMP) at manufacturing site. Monitoring and ensuring the good laboratory practice (GLP) by laboratory personal during the routine analysis and instrument operation ensure adherence to procedure Preparation & review of Quality Risk Assessment. Preparation & review of process validation, cleaning validation, equipment qualification To prepare/review the Validation Master Plan, Site Master File, Drug Master File, Annual Product Quality Review, Plant Layout and other documents related to QA Show more Show less

· Responsible for overall functionality of Production department · Management Representative for all audits · Production planning · Determine amount of necessary resources (workforce, raw materials etc.) · Organize workflow to meet specifications and deadlines · Monitor production to resolve issues · Monitoring performance of production engineers & operators and managing their day-to-day responsibilities · Coordinating with maintenance & quality department · Reviewing & monitoring performance of quality objectives related to production department · Co-ordination with QA & QC regarding issues related to rejections, rework, customer complaints, and second- & third-party audits. · Ensuring the stock of critical spares and other production requirements are maintained as necessary · Reviewing production related formats at planned frequencies · Ensuring issues raised during second- & third-party audits are resolved · Ensuring non-conforming product is handled as per procedure defined for the same. · Reviewing work & safety instructions for suitability to actual operations · Conducting, approving & measuring effectiveness of trainings related to production department · Participate in management review meetings and suggest opportunities for improvements · Ensure all production activities comply with ISO 9001 and other applicable standards. · Overall functionality of the department Job Type: Full-time Benefits: Cell phone reimbursement Health insurance Internet reimbursement Leave encashment Paid sick time Provident Fund Schedule: Day shift Supplemental Pay: Yearly bonus Work Location: In person Expected Start Date: 25/06/2025

1. Production Planning Develop and maintain monthly, weekly, and daily production plans based on: Sales forecasts Customer orders Inventory levels Capacity constraints (equipment, labor, shift availability) Coordinate with manufacturing, QA/QC, and maintenance to ensure realistic and achievable schedules. Optimize plant capacity utilization and minimize downtime. 2. Material Requirements Planning (MRP) Calculate and plan for raw materials, packaging materials, and consumables based on the production plan. Monitor stock levels and lead times to avoid shortages or overstocking. Generate material requisitions/purchase requests in coordination with the procurement team. 3. Inventory Control Track inventory of raw materials, intermediates, packaging, and finished goods. Implement FIFO/FEFO principles and ensure GMP-compliant warehousing . Prevent material expiry, obsolescence, or deviations by managing inventory accuracy. Conduct cycle counts and physical inventory reconciliations . 4. Coordination Across Departments Act as a liaison between: Production Quality Assurance (QA) & Quality Control (QC) Procurement Sales & Marketing Warehouse & Logistics Ensure alignment between supply and demand to meet customer and market needs. 5. Monitoring & Reporting Track production vs. plan and provide daily/weekly/monthly reports on: Line efficiency Inventory status Schedule adherence Material variances Identify bottlenecks and propose corrective actions. 6. Demand Forecasting & Sales Coordination Collaborate with sales and business development teams to: Forecast product demand accurately Adjust plans for urgent market needs or product launches Manage Make-to-Stock (MTS) or Make-to-Order (MTO) strategies based on product category. 7. GMP & Documentation Compliance Ensure all planning and inventory documents are: Properly recorded Aligned with GMP guidelines Ready for internal/external audits Maintain batch-wise traceability of materials used and products manufactured. 8. Change Management & New Product Planning Plan for scale-up, validation, or launch of new products. Adjust production and material planning to accommodate formula or process changes. 9. Supply Chain Risk Management Identify and mitigate risks in supply and production (e.g., supplier delays, equipment breakdowns). Develop contingency plans for critical materials and SKUs. 10. Continuous Improvement Use Lean, Six Sigma, or other tools to: Improve planning accuracy Reduce waste Enhance production flow Implement ERP/MRP software solutions effectively (e.g., SAP, Oracle, or Pharma-specific tools). Immidiate Joiner Preffered Salary Upto 40k Job Type: Full-time Pay: ₹35,000.00 - ₹40,000.00 per month Benefits: Cell phone reimbursement Health insurance Schedule: Day shift Work Location: In person

Wings Biotech LLP is steadfast in creating drugs in the Prescriptions and Branded Formulations segments with solutions to counter the problems. We are on a constant hunt for talented professionals. If you are an experienced healthcare professional who is skilled, qualified, and innovative. If you are one of those who redeem challenges to meet success with cutting-edge creative ideas and growth in life, Wings is the place for you. Walk in to explore a world of change that assures bright career and growth prospects. Profile Requirements: Company Name: Wings Biotech LLP Profile : QC chemist Vacancy : 1 Position Location : Baddi CTC : Best in market, Negotiable as per current package Exp : 1 to 2 years in Chemical Analysis RM Qualification: B Pharma, B.sc or M.Sc Email ID : amhr.plant@wingsbiotech.com (*If interested share updated CVs on the provided email address )* Job Types: Full-time, Permanent Pay: ₹180,000.00 - ₹220,000.00 per year Benefits: Leave encashment Paid sick time Paid time off Provident Fund Schedule: Day shift Night shift Rotational shift Supplemental Pay: Overtime pay Performance bonus Yearly bonus Education: Bachelor's (Preferred) Location: Baddi, Himachal Pradesh (Preferred)

CANDIDATES FROM PRINTING & PACKAGING INDUSTRY NEED TO APPLY ONLY DIPLOMA IN PRINTING PREFERRED AWARENESS ON ISO 9001:2015 & BRCGS REQUIREMENTS KNOWLEDGE ABOUT MANUFACTURING PROCESS AND PRODUCTS. KNOWLEDGE ABOUT KAIZEN , 5S, FIFO KNOWLEDGE ABOUT DRAWING RELIABILITY, INSPECTION METHOD AND TOLERANCE CLARITY KNOWLEDGE OF HANDLING CUSTOMER COMPLAINTS SHOULD HAVE GOOD COMMUNICATION SKILLS AWARENESS ABOUT THE 7 QC TOOL ANALYSIS OF REJECTION & CAPA Job Type: Permanent Pay: ₹40,000.00 - ₹60,000.00 per month Benefits: Provident Fund Schedule: Morning shift Supplemental Pay: Yearly bonus Work Location: In person

*Job Title* : Oil and Gas QA/QC NDT Faculty *Eligibility* : A minimum Post Graduation/Bachelors Degree in Mechanical Engineering Experienced Candidates are preferred *Roles and Responsibilities* # Develop and Deliver lectures in Quality Assurance/Quality Control courses and NDT # Conduct practical and lab sessions that facilitate students to acquire deeper understanding in Mechanical QC principles # Contribute to curriculum development and program assessment Job Type: Permanent Pay: ₹25,000.00 - ₹40,000.00 per month Schedule: Day shift Fixed shift Experience: Teaching: 2 years (Preferred) Work Location: In person

Date Posted: 2025-06-06 Country: India Location: Phase-II, 7th Floor, Block-III, DLF Commercial Developer Ltd., Plot No. 129 to 132, APHB Colony, Gachibowli, Hyderabad, Telengana, India Position Role Type: Unspecified Job Summary: We're seeking a skilled Software Tester to join our QA CoE team. As a Manual and Automation Tester, you'll be responsible for ensuring high-quality software products with thorough testing processes for complex Mobile, API, SAP, Web-based applications. Your expertise in both manual testing techniques and automation using Tosca will be crucial in identifying bugs, improving efficiency, and collaborating effectively with cross-functional teams. OPERATIONS AND SUPPORT Design, develop and execute manual test scripts for e-com applications Ensure the developed components meets the application requirement specifications and regression tested before passed on for final acceptance testing Report defects and execute defect lifecycle to ensure defects are closed Support RCA, RRCA and other QC activities Consult with product development to evaluate system interfaces, operational requirements, and performance requirements of overall system Define test methods and create test plans for new or updated software projects to determine if the software will perform accurately and reliably according to documented requirements as well as established standards under both normal and abnormal conditions Execute test plans and create test reports. Escalate repeated or critical issues to the management timely for their action Create test tools that facilitate data gathering and test method execution Automation – Selenium with Java Develop the automation scripts for web applications using Selenium Framework with java. Automating the E2E scripts involves multiple web applications and other applications. Handling or maintaining complex frame works, Maintain existing frameworks and build new automation from scratch using Selenium with Java. Creates and maintains automated framework using standard coding methodologies. Designing and executing Selenium (Java) automated scripts to support our testing needs. Sets up and automates test development, testing on System, Integration, E2E and UAT environments for smoke and regression testing. Performs necessary testing of assigned systems and applications, including the generation of test data, writing test scripts/execution sequences, examining test results, debugging detected errors, etc. Develops test scripts that are clearly stated, complete, and executable with high degree of quality. Provides Status Reports and works collaboratively with Test Lead and Manager Collaborates with other team members to understand the scope of test cases that will be used for automated scripts. Experience with automated and test management tools, developing test strategies and plans. Performs moderately complex to complex test data conditioning, regression testing and testing validation. TECHNICAL SKILLS 3+ years of experience in the following areas: Should have good knowledge of working with SAP, Mobile, Web and API Testing Should be very strong at design and developing functional test cases Must possess very good analytical and problem-solving skills. Proficient and Hands on experience on Tricentis - Tosca for automation testing. Strong knowledge of software testing methodologies, tools, and processes. Proficiency in REST/SOAP API testing using tools like Postman, SoapUI, or Rest Assured. Familiarity with bug tracking and version control systems. Experience with Agile/Scrum methodologies. Knowledge with CI/CD pipelines and continuous integration practices. PROCESS AND TOOLS Should be adaptable to the frequent changes and have worked in a highly dynamic agile development environment in at least one end-to-end large implementation Should be process oriented and contribute to the continuous process improvements by identifying its inefficiencies and provide improvement recommendation and work towards successful implementation of the same. Should have worked extensively with tools such as JIRA INTERPERSONAL & COMMUNICATION SKILLS This role involves application ownership and the individual MUST be flexible to provide support during off hours, holidays and weekends to meet the project critical needs This position involves direct interaction with the customers and technical team at US on a regular basis, candidate should have very good verbal and technical writing skills MUST be adaptable and embrace to the frequent changes from each development iteration and be able to support continuously evolving requirements. MUST be adaptable in working with a highly dynamic team with constant change in priorities Should be good at multitasking and be able to maintain balance between production support requests and development activities in parallel Demonstrated ability to be a team player and willingness to lend a hand to others in team, assist them with challenges and be able to coach, guide and mentor junior members in the team. Position may involve short term international travels. Must be able to support the same with short notice DESIRED SKILLS Exposure to writing, executing and maintaining automated test scripts QUALIFICATION / CERTIFICATION Candidate should have BE/ME/MS/M Tech degree in Computer Science, Information Technology, Engineering or equivalent. KEY WORDS Automation, selenium with Java, Tricentis Tosca, Mobile Testing, API Testing, SAP Testing. About Collins Aerospace: Collins Aerospace, a Raytheon Technologies company, is a leader in technologically advanced and intelligent solutions for the global aerospace and defense industry. Collins Aerospace has the capabilities, comprehensive portfolio and expertise to solve customers’ toughest challenges and to meet the demands of a rapidly evolving global market. Digital Technology Do you want to be part of a new, exciting initiative to combine foundational IT with new digital technologies? Our Digital Technology team is driving business efficiencies and a better customer experience by connecting technologies, people, information and processes. From making aircraft more electric, intelligent and integrated to building new software platforms such as Internet of Things, big data, artificial intelligence, and blockchain, there’s no better place to be right now than in digital. If you’re an agile thinker who enjoys utilizing modern technology to make big improvements, then you’re a perfect fit for this team. Join Collins Aerospace to help us revolutionize the aerospace industry today! WE ARE REDEFINING AEROSPACE. Some of our competitive benefits package includes: Transportation facility. Meal coupons Group Term Life Insurance. Group Health Insurance. Group Personal Accident Insurance. Entitled for 18 days of vacation and 12 days of contingency leave annually. Employee scholar programme. Work life balance. Car lease programme. National Pension Scheme LTA Fuel & Maintenance /Driver wages Meal vouchers And more! Nothing matters more to Collins Aerospace than our strong ethical and safety commitments. As such, all India positions require a background check, which may include a drug screen. Note: Background check and drug screen required (every external new hire in the India) Drug Screen only performed for Operations Positions At Collins, the paths we pave together lead to limitless possibility. And the bonds we form – with our customers and with each other - propel us all higher, again and again. Apply now and be part of the team that’s redefining aerospace, every day. RTX adheres to the principles of equal employment. All qualified applications will be given careful consideration without regard to ethnicity, color, religion, gender, sexual orientation or identity, national origin, disability, protected veteran status or any other characteristic protected by law. Privacy Policy and Terms: Click on this link to read the Policy and Terms RTX adheres to the principles of equal employment. All qualified applications will be given careful consideration without regard to ethnicity, color, religion, gender, sexual orientation or identity, national origin, age, disability, protected veteran status or any other characteristic protected by law. Privacy Policy and Terms: Click on this link to read the Policy and Terms

Job Team Lead - Quality Control Description About the Company As the world’s leading multidisciplinary service provider, Deluxe underpins the media and entertainment industry, servicing content creators and distributors including Netflix, WarnerMedia, The Walt Disney Company, Amazon, Apple, Viacom, NBCU, Google, AT&T and many others, by providing Global Content Distribution, Localization, Accessibility and Mastering while leading end-to-end innovation with unparalleled scale and agility across the Streaming, Theatrical, Broadcast and Mobile landscapes. With headquarters in Los Angeles and offices around the globe, the company employs over 3,200 of the most talented and experienced industry individuals worldwide. For more information, please visit www.bydeluxe.com Position Summary Responsible for functioning of the shift and conveying information across all shifts, thereby ensuring the team is equipped with the latest updates. Should work closely with the QC management, Team Leads and editors to ensure smooth day to day functionality along with proper time and resource management. Implementing existing and new processes with the team and making certain that the team is aware and trained on the latest software updates. Outcomes and Accomplishments As a Team Lead, You Are Required To Be directly responsible for 10 to 15 QC editors Oversee the daily work schedule. This is accomplished by: o Ensuring all client cores have adequate resources to complete daily deliverables Hand over to the following shift on pending task when necessary Making sure all mails, queries pertaining to QC are actioned in a timely manner Taking over scheduling when required o Taking assistance from sister departments when workload cannot be accommodated internally Tracking work schedules during rush periods, holidays and weekends and informing counterpart departments across offices for assistance and coverage, if required Conduct daily huddles with the team and core client group to discuss day to day work and updates Conduct refreshers when required Ensure core groups are always adequately staffed and audits are performed regularly Ensure proper training and mentoring is focused towards new recruits Required to track changes and updates in other departments that may impact QC, and regularly communicate the same to team Process internal and external feedback in the following ways: o Ensure external feedback to other departments and translator is logged in a regular and timely manner Ensure internal feedback is provided within the team and assuring this is done in a positive approach which allows the team to perform better Ensure the team has adequate training to effectively perform their daily task and improve; and work with management to address any loopholes Maintain metrics for the team and present the same monthly, highlighting achievements and areas of improvement Liaise with Assistant Managers to maintain a monthly quality profile data and organize refresher based on feedback trends as needed Ensure overall adherence of protocol Maintaining discipline within the team with respect to schedule adherence Maintain a healthy work relationship with the team members and understand their challenges and help them overcome Act as a mentor to the team and help them improve their performances Alert team management about any non-compliance issue with editors Conduct 1-3-6-month probation reviews and annual appraisals, with input from reporting managers Recognize and reward team members’ accomplishments, through nominations for awards like performance premiums, Oscars, GPAs, etc. What You Bring Will be managing the day-to-day activities of the team Motivate the team to achieve organizational goals Empowering team members with skills to improve their confidence, product knowledge, and communication skills Contributing to the growth of the company through a successful team Creating a pleasant working environment that inspires the team Ability to multitask and think critically Conflict resolution skills You are a team player Willing to learn and take on new tasks Benefits You will be part of a large international and culturally diverse team You will have opportunities to upskill and grow You will have the opportunity to expand your professional network You will be part of a career driven and competitive work environment Equal Employment Deluxe is committed to inclusivity, fostering an environment where every employee feels comfortable bringing their full selves to work. It is our policy to provide equal employment opportunities to all applicants and employees. Applicants will receive fair consideration for employment without regard to, and will not be discriminated against, based on race, colour, religion, creed, national origin or ancestry, sex, age, or any other discriminations. Show more Show less

JOB POSITION : QC Control – Inspector Qualification : Diploma in Plastic/Polymer Tech, or Diploma in Mechanical Experience : 0-6 Months Job Description : Ø To Inspect the Raw Materials and Consumables in Incoming Inspection Quality Control. Ø To Inspect raw materials and products during Processing as In Process Inspection Quality Control. Ø To ensure the Finished Goods as Product Specifications and Packaging Process. Ø Should have knowledge about the Plastic Materials and its Properties Ø Should have Exposure in ISO 9001:2015 QMS Ø Have exposure in Plastic Processing would be an advantage. Ø Have Exposure in Printing Process would be an advantage. Ø To Prepare the IQC, IPI, FQC Documents as per ISO 9001 : 2015 . Ø Able to Work in Both Shifts ( Day & Night ) ( 9 Hour Shift). Job Type: Internship Contract length: 6 months Pay: ₹7,000.00 - ₹10,000.00 per month Schedule: Day shift Work Location: In person

Key Responsibilities of a QC Manager: · Ensuring Quality Standards: QC Managers ensure that products or services consistently meet specified quality standards. · Developing and Implementing QC Procedures: They create and implement quality control procedures, inspections, and testing methods. · Monitoring and Evaluation: They continuously monitor and evaluate the quality of products and processes. · Identifying and Resolving Issues: QC Managers identify defects and implement corrective actions to address quality issues. · Compliance and Regulations: They ensure compliance with industry and regulatory standards. · Team Leadership: In many roles, QC Managers lead and manage a quality control team. · Collaboration: They work with other departments to improve processes and quality. Skills and Qualifications : · Education: A bachelor's degree in a relevant field (e.g., engineering, science, and manufacturing) is often required. · Experience : Relevant experience in quality control, quality assurance, or manufacturing is typically needed. · Skills: Strong analytical, problem-solving, and communication skills are essential. · Certifications: Industry-recognized certifications (e.g., ASQ certifications) can be beneficial. Key Performance Indicators (KPIs): Cycle Time: Measures the time taken to complete a process from start to finish. Process Efficiency: Assesses how efficiently production processes operate, often measured by resource utilization or cycle time. Inspection Coverage: The percentage of the total project area or length that has been inspected. Response Time to NCRs: The average time taken to address and resolve non-compliance issues Job Types: Full-time, Permanent Pay: ₹15,000.00 - ₹30,000.00 per month Schedule: Day shift Work Location: In person

Location: Kundli, Sonipat Industry: Plastic/Electronic Toy Manufacturing Job Type: Full-Time | Shift-Based Experience Required: Minimum 4–5 years in Injection Moulding/Plastic Moulding Job Summary: We are seeking an experienced Moulding Shift Supervisor to manage and oversee daily operations of the plastic injection moulding department. The candidate must have hands-on experience with moulding machines, production planning, manpower handling, and quality assurance during their shift. Key Responsibilities: Machine Supervision: Operate and monitor plastic injection moulding machines during assigned shift. Shift Planning: Ensure proper manpower allocation and smooth execution of shift production targets. Tool Changeovers: Supervise and guide team on quick and safe mould/tool changeovers. Quality Control: Monitor part quality and ensure rejection levels remain under control. Troubleshooting: Identify technical issues in machines or moulds and coordinate with maintenance. Team Handling: Manage and guide operators, helpers, and QC during the shift. Reporting: Maintain shift-wise production reports, downtime logs, and rejection data. Safety Compliance: Ensure all safety protocols are followed on the shop floor. Skills & Qualifications: Minimum 4 years of experience in injection moulding or toy moulding industry. Hands-on experience with moulding machines like Haitian, Windsor, etc. Strong knowledge of moulding parameters, cycle time control, and troubleshooting. Team management and shift handling experience. Ability to work in rotational shifts and under pressure. Understanding of basic quality standards and rejection analysis. Job Types: Full-time, Permanent Pay: ₹25,000.00 - ₹27,000.00 per month Benefits: Health insurance Leave encashment Schedule: Day shift Supplemental Pay: Yearly bonus Ability to commute/relocate: Sonipat, Haryana: Reliably commute or planning to relocate before starting work (Preferred) Education: Bachelor's (Preferred) Experience: Plastics injection molding: 5 years (Preferred) Location: Sonipat, Haryana (Preferred) Work Location: In person

Dear All, Greetings From M.M.K Enterprises!!! Hiring For E&I QA/QC Engineer for location Kakinada and Panipat It's a 1 year of contract and further extendable candidate will be on our payroll i.e on M.M.K payroll. You have confirmed the following criteria as for consideration Name Position E&I QA/QC Engineer Status Contract Current Salary per month Expected Salary per month D.O. J _Days Other Facilities Bachelor Accommodation & Local Transport is provided and Food is included in the Salary Duty Hours 12 hours If ok can reply on Mob: 89561 04316 or Email: recruiter2@kushalengineers.com Job Type: Full-time Pay: ₹13,483.23 - ₹52,623.25 per month Schedule: Day shift Work Location: In person

Responsibilities: · Develop SOPs and infrastructure requirements for laboratories and optimal calibration standards in line with good laboratory practice (GLP) requirements. · Develop inspection and testing protocols for materials, products and packaging. · Develop methods for the testing quality of materials, products and packaging · Establish SOPs and conditions for handling, storage and preservation of samples. · Implement plans and strategies to support provision of safe food products. · Review reports and develop guidelines and standard practices for data documentations and analysis. · Specify the protocols and laboratory infrastructure and equipment to be inspected and tested. · Verify alignment of sampling documentation, testing activities and procedures with established protocols to identify issues. · Verify quality control (QC) records, test results and reports for regulatory authorities. · Inspecting final products. · Reporting faulty packaging or problems on the machines to the relevant managers. Requirements: · Having Minimum Experience of 8 Years at any Food Industry with Lab & QA Head profile. · Bachelor's degree in food science, microbiology, chemistry, or a related field. · A master's degree (Food Technology) preferred for advanced positions. · Proven experience in quality assurance and quality control within the food industry, preferably in a managerial role. · A clear understanding of health and safety standards and protocols. · Good communication and interpersonal skill. · Ability to work well individually and as part of a team. (Having experience of Snacks Industry will be preferred) Job Types: Full-time, Permanent Pay: ₹80,000.00 - ₹120,000.00 per month Benefits: Health insurance Provident Fund Schedule: Day shift Work Location: In person