3970 Sampling Jobs - Page 14

Packaging- Junior Engineer - Technical Service - ( 250000Q8 ) Description Finish goods are checked as per sampling plan, as per customer requirement, specification. To check on line slitting samples & giving feed back to all operator & shift in charge. To inspect all slitting m/c parameter & control. To ensure 100% defect free material & maintain ALC to avoid mix-up. Check all in line & maintain all document & check list during audits. To attend customer complaints. Qualifications B.sc./Diploma with 5+ years of experience in Q.A/Q.C department of reputed flexible packaging industry. Primary Location : IN-IN-Jammu Work Locations : Packaging Jammu 1 Line-3,Phase-I SIDCO Industrial Complex, Unit-IJammu Jammu 181133 Job : Production Organization : Jammu (Packaging Div.) Regular Employee Status : Entry Level Job Level : Rotating Travel : No Job Posting : Jul 25, 2025, 11:30:59 PM

Position: QC Inward Executive (Food Industry) Role Summary The QC Inward Executive is responsible for inspecting, sampling, and testing all incoming raw materials and ingredients to ensure they meet defined quality, safety, and compliance standards. This role supports the seamless flow of the production line by verifying material quality at intake and flagging any deviations early. Key Responsibilities Raw Materials Inspection Conduct thorough visual inspections and quality checks on all incoming materials (ingredients, packaging) to ensure compliance with specifications. Measure parameters such as moisture, pH, purity, or contaminants. Sample Collection & Testing Collect random samples for testing (chemical, microbiological, physical) either in-house or via external labs. Compare against approved standards/specifications and document outcomes. Record Keeping & Reporting Maintain detailed logs of inspection results, test findings, and any deviations. Generate reports to inform higher QC levels, procurement, and production teams. Equipment Calibration & Maintenance Ensure measuring equipment (scales, moisture meters, pH meters, etc.) are calibrated regularly; coordinate repairs or replacements as needed. Supplier & Batch Verification Verify supplier credentials, batch compliance, certificates of analysis, and proper labeling. Work with procurement to update the approved supplier list. HACCP & GMP Adherence Follow critical control points (CCP) procedures as per HACCP standards. Ensure Good Manufacturing Practices and plant hygiene protocols for incoming materials are observed. Deviation Handling & Corrective Actions Highlight non-conformance issues, initiate corrective steps (quarantine, rejection, supplier feedback) and monitor resolution. Training & Awareness Educate warehouse and procurement staff on quality norms and best practices. Provide routine updates and training refreshers related to QC procedures. Continuous Improvement Recommend process enhancements to reduce defects or delays and improve efficiency in inbound QC workflows. Qualifications & Skills Bachelor’s degree (Food Technology, Microbiology, Chemistry, or related) Practical experience in QC/QC-inward roles within food manufacturing or FMCG Good knowledge of food safety systems: HACCP, ISO 22000, FSMS. Familiarity with GMP and relevant regulatory compliance Strong analytical skills; experience with lab testing and record-keeping Excellent communication abilities in delivering findings and collaborating with suppliers and internal teams Attention to detail and strong numerical/measurement proficiency Ability to work independently and maintain calm under production‑pressure conditions Job Type: Full-time Pay: ₹15,000.00 - ₹20,000.00 per month Schedule: Day shift

Service and solutions provider for water treatment chemicals used in Chillers, Boilers and cooling towers for our various clients. This dynamic position requires you to travel independently(By bike) daily, to perform on-site analysis. If interested please contact 6369804009 As a Cooling Tower and boiler Water treatment testing Technician, you will play a crucial role in safeguarding our clients' water systems and promoting optimum performance. You will be our eyes and ears on the ground, ensuring accurate data collection and contributing to effective water treatment recommendations. Experience: Experienced Location: Ennore, Chennai Salary: As per industrial norms Job Responsibilities: Travel independently : Navigate to assigned client locations by bike daily, efficiently managing your time and route. Sample collection : Safely and accurately collect cooling tower water samples following established protocols. Field testing : Utilize portable testing equipment to measure key water parameters like pH, conductivity, chlorine, and corrosion potential. Data recording : Document measurements and observations meticulously in designated forms and software. Basic maintenance : Perform minor equipment checks and calibrations as needed. Communication : Maintain clear communication with clients regarding sampling procedures and findings. Reporting : Generate accurate and timely reports for internal analysis and client communication. Qualifications: Knowledge and understanding of cooling tower, chiller, and boiler systems, as well as the associated chemical treatment requirements is advantageous. Strong technical aptitude and the ability to effectively communicate complex concepts to customers. Self-motivated with a results-oriented mindset. Ability to work independently and as part of a team. Willingness to travel within the assigned territory, as required. Candidates currently working as delivery partners and who have a keen interest in the field of chemistry and chemical testing can also apply. Job Types: Full-time, Permanent Pay: From ₹15,000.00 per month Benefits: Health insurance Provident Fund Application Question(s): Do you have a bike to commute?? Experience: total work: 1 year (Preferred) Work Location: In person

To handle the proposed changes as per the change control procedure. To assess the risk / impact associated with proposed change and to verify the implementation of action plan as per approved change control form. To determine the investigation plan and carry out investigations using appropriate root cause analysis tools, assessing the risk associated with them, to perform the additional studies and to derive the appropriate CAPA. To handle the recommended CAPA and to verify the implementation of recommended actions as per CAPA system and to evaluate effectiveness checks of implemented CAPA. To perform the trend analysis of deviation, change control, complaints etc.. to identify any repetitive event for further evaluation and CAPA. To conduct or be part of team conducting risk assessment of various activities, equipment, systems, etc.. and responsible for assigning the QRM no. To review all labelling related artwork components for products. To prepare artwork information details for new / revised labelling components and submit to QA doc cell for issuance of artwork as per procedure. To review and verify the destruction of old printed packaging materials (vendor and Amneal site) in case of revision of artworks of labelling components. Tracking the actions, review of extensions, verification of documents and closure of actions. Responsible for document handling, issuance, distribution, and retrieval of document. Scanning of documents for regulatory submission To maintain master documents like Site Master File, Validation Master Plan, Quality Manual, SOPs, protocols, reports, Batch Records, specification, method of analysis, drawings, artworks, planners, etc.. Responsible for issuance, archival and retrieval of documents like SOPs, Validation / qualification protocols / reports, Batch records, Specifications, Drawings, Artworks, planners, etc.. To provide BMR/BPR numbering to exhibit, intended and media fill BMR. To provide Batch number to exhibit, commercial, feasibility and medial fill batches. To receive and distribute the product development documents like Master Formula Records, Master Packaging records, protocols (sampling, study, and stability protocols). Issuance of uncontrolled copy / reference copies of master document to user as and when requested by user. To provide requested documents to regulatory affairs department for regulatory submissions (AR or other submissions), whenever required. Artwork management that includes effective the Artwork information details, distribution, retrieval and archival of artwork and all labelling components. To retire the documents as per change control assessment / proposal. Activities other than defined in the Job responsibility are to be done as per the requirement of HOD, by following HODs instruction and guidance. Skills: Monitors production processes in real-time to ensure compliance with specifications and GMP, Batch record review, process monitoring, sampling, quality checks, real-time deviation management. M.Sc. / B. Pharm / M. Pharm

Role Summary: This is a full-time on-site role for a Phlebotomist at Genestring Lab , Haldwani. The role involves conducting blood collection of new born babies and adult, performing laboratory tasks, assisting with medical processes, delivering samples and ensuring accurate documentation and sample handling. Job Type: Full-time Schedule: Day shift Application Question(s): Do you have 2 wheeler? Education: Diploma (Required) Experience: New Born Baby - Blood Sampling: 1 year (Required) Location: Haldwani, Uttarakhand (Required) Willingness to travel: 100% (Required) Work Location: In person

clients' Requirements A Bachelor's degree in Mechanical Engineering Previous experience in product development. Good working knowledge of manufacturing processes, materials, and quality control protocols. Experience with 3D modeling software and report writing programs. Excellent math, creativity, and problem-solving skills Responsibility Performing market research to understand market requirements & determine the needs and goals of new products. Conceptualizing new product ideas by using CAD software & Team to design prototypes. Sampling different materials, manufacturing processes, design tolerances, and other factors to find the best ones that suit the new product brief. Testing products throughout the design process to troubleshoot any potential problems. Determine the budgeted product cost by analyzing the desired materials and operational processes. Analyze root causes for all fabrication issues and resolve same and implement new process tools according to required order. Delivering product specifications and procedures to the manufacturing team for production purposes. Developing quality control criteria and safety guidelines and ensuring that all team members adhere to them. About Spectra Overseas: We lead with innovation, offering top-tier products, including fabrication items, while delivering unwavering quality to our valued USA-based client. Join our journey of excellence today. Explore Our Client's World For a glimpse into the remarkable projects and partnerships we've forged over the years, we invite you to visit the link below to explore our clients' world. It's a testament to the trust they've placed in us and the innovative solutions we've consistently delivered. www.simondstore.com Job Types: Full-time, Permanent Pay: ₹20,000.00 - ₹25,000.00 per month Benefits: Provident Fund Ability to commute/relocate: Rajkot, Rajkot, Gujarat: Reliably commute or planning to relocate before starting work (Preferred) Work Location: In person

We are seeking a creative and detail-oriented Fashion Designer with prior experience working in Mumbai’s fast-paced fashion industry. The ideal candidate should be passionate about design, familiar with the latest trends, and enthusiastic about relocating or working in Surat’s growing textile and fashion sector . Key Responsibilities : Develop new designs for women’s wear (as per specialization), keeping current fashion trends in mind. Create mood boards, color palettes, fabric swatches, and sketches using CAD or manual illustration. Collaborate with the merchandising, sampling, and production teams. Supervise sample development and ensure design integrity is maintained through production. Coordinate with Mumbai buyers or brands if applicable, for custom design development. Participate in exhibitions, buyer meetings, and design presentations. Candidate Profile : Bachelor's Degree / Diploma in Fashion Design (NIFT, Pearl, INIFD, or equivalent). Minimum 3 years of industry experience, with exposure to Mumbai’s fashion/export industry. Strong knowledge of fabrics, printing techniques, embroidery, and garment construction. Proficient in Adobe Illustrator, Photoshop, and CorelDRAW. Open to relocation or long-term work in Surat. Excellent communication and team collaboration skills. Preferred Skills : Experience with Western or ethnic wear designing Vendor or factory coordination (especially with Surat textile ecosystem) Trend forecasting and design research abilities Knowledge of textile surface embellishment and value addition Job Type: Full-time Pay: ₹35,000.00 - ₹50,000.00 per month Schedule: Day shift Work Location: In person

Responsible for line clearance activity before commencing the different operations like dispensing, manufacturing, filling, inspection, sealing, labelling, and packing. Responsible for Process validation, cleaning validation/verification, hold time study, media fill & routine batch sampling as per protocol/SOP. Responsible for review of executed BMRs and BPRs. Responsible to perform the in-process test at different stages as per batch document/SOP. Responsible to review the environment monitoring, water trends. Responsible to review the different type of planner and calibration certificates. Responsible to receive the required resources for EM monitoring e.g., plates, samplers, swabs etc.. from microbiology lab and after completion of EM monitoring plates, samplers, swabs etc.. should be handed over to microbiology lab for further process along with applicable formats which is filled in aseptic area. Responsible to monitor cGMP compliance at shop floor. Responsible to review the different type of print outs i.e CIP, SIP, autoclave, filter integrity etc.. To maintain the Issuance/reconciliation record of items / media for Environment monitoring material e.g., plates, swabs, etc.. Environmental monitoring of manufacturing clean room area as per the defined schedule. Responsible to participate in media fill simulation study. Responsible to participate in perform qualification activities of manufacturing area. Non-viable particle monitoring of manufacturing clean room area as per the defined schedule. Compressed air /nitrogen gas monitoring and Personnel monitoring. Review of Media fill CD. Review of Visual inspector qualification record. Activities other than defined in the Job responsibility are to be done, as per the requirement of HOD, by following HODs instruction and guidance. To perform aseptic behavior/practice monitoring of operators (while working inside aseptic process area) during each aseptic batch (GMP batch) as per SOP. Skills : Skills : Conducting sterility testing, endotoxin testing, and microbial contamination control. Monitoring and documenting environmental conditions (temperature, humidity, microbial contamination, airborne particulates).

About Blendonomics Blendonomics is a premium hot chocolate brand trusted by over 150+ cafes, QSRs, and beverage chains across India. With our café-style blends crafted from real chocolate chips and high-quality ingredients, we are redefining how India experiences hot chocolate – both in B2B and D2C markets. We are now expanding and seeking a dynamic Sales Representative / Management Trainee who can support our growth by onboarding new clients and building long-term relationships. Training & Probation Period Duration: 1 Month (Probation) Week 1: Product Training (Ingredients, USPs, Applications) Sales & Communication Training (Pitching, Objection Handling,Follow-ups) On successful completion of the probation period, the candidate may be offered a full-time position based on performance. Key Responsibilities Conduct outreach to cafes, restaurants, QSRs, and hospitality brands. Identify if they are seeking a better hot chocolate solution and introduce Blendonomics as the ideal option. Set up product trial sessions and coordinate sampling efforts. Engage and convince potential clients based on product merit and commercial value. Maintain strong follow-ups, manage leads, and drive conversions. Close orders and ensure proper documentation and coordination with the operations team. Desired Candidate Profile Recent graduates or up to 1 year of experience in Sales, Business Development, or Marketing (F&B industry preferred). Excellent communication and interpersonal skills (English & Hindi proficiency required). Strong persuasion and follow-up skills. Willingness to travel for client meetings and trials. Passion for the F&B industry and customer-centric mindset. Compensation & Benefits Monthly stipend during probation Performance-based incentives Travel & fuel expenses reimbursed Opportunity for full-time employment based on performance Exposure to one of India’s fastest-growing Artisanal beverage brand Work Culture & Values Fast-paced, high-growth startup environment Ownership and accountability encouraged Direct mentorship from the founders Hands-on learning across product, marketing, and sales functions

💻 Position: National Head - Modern Trade 📍Location: Bangalore, HSR Layout 🗓️ Working Days: Monday- Friday 📌 Experience Required: 10-15 years in FMCG and 3-4 years in National Modern Trade (D-Mart) 🤝 Client: New age beverage brand 💸 Salary: 22-24 LPA Role Overview We are looking for a seasoned, driven, and entrepreneurial leader to helm our Modern Trade vertical nationally. The National Head – Modern Trade will be responsible for scaling footprint in modern retail, driving strategic partnerships, improving in-store execution, and unlocking growth across chains, formats, and regions. If you’re excited by high-growth environments and want to shape the future of a youth brand that breaks category stereotypes—this is your calling. Key Responsibilities 1. Strategy & Growth Leadership  Build and execute a national Modern Trade roadmap aligned with aggressive growth goals.  Own the annual and quarterly sales plan, category expansion targets, and retail partner strategies.  Identify new-age retail opportunities—especially those engaging Gen Z audiences. 2. Key Account Management & Business Development  Lead end-to-end partnerships with top national and regional accounts (D-Mart, Reliance Retail, etc.).  Drive listings, visibility, shelf-space negotiations, and in-store promotions with retailers.  Ensure the successful launch and scale-up of new products across modern trade partners. 3. Sales Execution & Performance Management  Deliver top-line revenue, volume, and distribution KPIs across modern trade channels.  Continuously track performance vs. plan and optimize pricing, promotions, and assortment strategies.  Leverage retail sales data and shopper insights to drive in-store conversions and repeat purchases. 4. Team Leadership & Capability Building  Hire, mentor, and develop a high-performing modern trade sales team across regions.  Set clear KPIs, coach for performance, and create a strong culture of accountability and ambition. 5. Trade Marketing & Activation Execution  Collaborate with brand and marketing teams to plan and execute trade marketing programs.  Ensure sharp execution of planograms, point-of-sale branding, sampling, and promotions.  Track ROI of trade spends and tweak activations based on data and feedback loops. 6. Cross-functional Collaboration & Ops Alignment  Work closely with Supply Chain and Finance teams to ensure seamless order fulfilment, inventory hygiene, and credit discipline.  Quickly resolve operational bottlenecks across geographies to ensure retail continuity. Candidate Profile Experience & Qualifications  MBA preferred; Bachelor's in Business, Marketing, or related fields.  12–15 years of FMCG experience, with at least 5 years in a national Modern Trade leadership role.  Strong preference for prior experience in the beverages, chocolate, snacking category. Skillset  Deep expertise in modern trade formats (National Chains, Regional Chains.)  Proven track record of double-digit sales growth, expanding retail reach, and brand activation.  Strategic mindset with tactical execution skills and data-led decision-making.  Exceptional communication, negotiation, and people leadership abilities.  Proficiency in Excel, PowerPoint, and retail analytics dashboards. Attitude & Cultural Fit  Startup-ready mindset: agile, solutions-focused, and high on initiative.  A love for youth brands, pop culture, and decoding what makes Gen Z tick.  Willingness to travel as required across the country. What You’ll Get  A front-row seat to build a national brand from the frontlines.  Autonomy, ownership, and a say in strategic decisions.  A passionate team and culture that values speed, boldness, and execution.  Competitive salary, performance-based incentives, and long-term wealth creation opportunities.

This job is with Pfizer, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ+ business community. Please do not contact the recruiter directly. Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard. What You Will Achieve In this role, you will: Assist in the preparation and maintenance of media stocks, including sterilization of accessories by autoclave cycles. Manage receipt, storage, and handling of Bio ball cultures, and assist in the maintenance of Master cultures and preparation of Cryo vials. Perform various microbiological tests such as water analysis, Microbial Limit Test, Sterility tests, Bacterial Endotoxin Test, CCIT, and micro challenge studies. Ensure training records are updated and correctly filed to reflect current testing capabilities. Perform sampling and labeling of materials as per defined procedures and verify all equipment and instruments. Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions. Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies. Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current. Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database, and generate EMS reports. Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on supervisor and working under their direction. Here Is What You Need (Minimum Requirements) Master's degree in microbiology with minimum of 3 year's experience Demonstrated technical skills in method validation and testing Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations Knowledge of Good Manufacturing Practices and its application standards, processes, and policies. Excellent organizational skills and strong ability to multi-task Strong written and verbal communication skills Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation Bonus Points If You Have (Preferred Requirements) Experience with laboratory work, particularly microbiological techniques Proven track record in leading continuous improvement projects Strong knowledge of lean manufacturing principles, six sigma methodologies, and statistical analysis Strong problem-solving skills and attention to detail Ability to manage multiple priorities and meet deadlines. Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels Adaptability and willingness to learn new techniques and procedures Work Location Assignment: On Premise Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Quality Assurance and Control

clients' Requirements A Bachelor's degree in Mechanical Engineering Previous experience in product development. Good working knowledge of manufacturing processes, materials, and quality control protocols. Experience with 3D modeling software and report writing programs. Excellent math, creativity, and problem-solving skills Responsibility Performing market research to understand market requirements & determine the needs and goals of new products. Conceptualizing new product ideas by using CAD software & Team to design prototypes. Sampling different materials, manufacturing processes, design tolerances, and other factors to find the best ones that suit the new product brief. Testing products throughout the design process to troubleshoot any potential problems. Determine the budgeted product cost by analyzing the desired materials and operational processes. Analyze root causes for all fabrication issues and resolve same and implement new process tools according to required order. Delivering product specifications and procedures to the manufacturing team for production purposes. Developing quality control criteria and safety guidelines and ensuring that all team members adhere to them. About Spectra Overseas: We lead with innovation, offering top-tier products, including fabrication items, while delivering unwavering quality to our valued USA-based client. Join our journey of excellence today. Explore Our Client's World For a glimpse into the remarkable projects and partnerships we've forged over the years, we invite you to visit the link below to explore our clients' world. It's a testament to the trust they've placed in us and the innovative solutions we've consistently delivered. www.simondstore.com Job Types: Full-time, Permanent Pay: ₹20,000.00 - ₹25,000.00 per month Benefits: Provident Fund Ability to commute/relocate: Rajkot, Rajkot, Gujarat: Reliably commute or planning to relocate before starting work (Preferred) Work Location: In person

Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard. What You Will Achieve In this role, you will: Assist in the preparation and maintenance of media stocks, including sterilization of accessories by autoclave cycles. Manage receipt, storage, and handling of Bio ball cultures, and assist in the maintenance of Master cultures and preparation of Cryo vials. Perform various microbiological tests such as water analysis, Microbial Limit Test, Sterility tests, Bacterial Endotoxin Test, CCIT, and micro challenge studies. Ensure training records are updated and correctly filed to reflect current testing capabilities. Perform sampling and labeling of materials as per defined procedures and verify all equipment and instruments. Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions. Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies. Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current. Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database, and generate EMS reports. Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on supervisor and working under their direction. Here Is What You Need (Minimum Requirements) Master's degree in microbiology with minimum of 3 year's experience Demonstrated technical skills in method validation and testing Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations Knowledge of Good Manufacturing Practices and its application standards, processes, and policies. Excellent organizational skills and strong ability to multi-task Strong written and verbal communication skills Proficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation Bonus Points If You Have (Preferred Requirements) Experience with laboratory work, particularly microbiological techniques Proven track record in leading continuous improvement projects Strong knowledge of lean manufacturing principles, six sigma methodologies, and statistical analysis Strong problem-solving skills and attention to detail Ability to manage multiple priorities and meet deadlines. Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels Adaptability and willingness to learn new techniques and procedures Work Location Assignment: On Premise Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Quality Assurance and Control

Job Description Responsible for line clearance activity before commencing the different operations like dispensing, manufacturing, filling, inspection, sealing, labelling, and packing. Responsible for Process validation, cleaning validation/verification, hold time study, media fill & routine batch sampling as per protocol/SOP. Responsible for review of executed BMRs and BPRs. Responsible to perform the in-process test at different stages as per batch document/SOP. Responsible to review the environment monitoring, water trends. Responsible to review the different type of planner and calibration certificates. Responsible to receive the required resources for EM monitoring e.g., plates, samplers, swabs etc.. from microbiology lab and after completion of EM monitoring plates, samplers, swabs etc.. should be handed over to microbiology lab for further process along with applicable formats which is filled in aseptic area. Responsible to monitor cGMP compliance at shop floor. Responsible to review the different type of print outs i.e CIP, SIP, autoclave, filter integrity etc.. To maintain the Issuance/reconciliation record of items / media for Environment monitoring material e.g., plates, swabs, etc.. Environmental monitoring of manufacturing clean room area as per the defined schedule. Responsible to participate in media fill simulation study. Responsible to participate in perform qualification activities of manufacturing area. Non-viable particle monitoring of manufacturing clean room area as per the defined schedule. Compressed air /nitrogen gas monitoring and Personnel monitoring. Review of Media fill CD. Review of Visual inspector qualification record. Activities other than defined in the Job responsibility are to be done, as per the requirement of HOD, by following HODs instruction and guidance. To perform aseptic behavior/practice monitoring of operators (while working inside aseptic process area) during each aseptic batch (GMP batch) as per SOP. Skills Skills : Conducting sterility testing, endotoxin testing, and microbial contamination control. Monitoring and documenting environmental conditions (temperature, humidity, microbial contamination, airborne particulates).

Job Description To handle the proposed changes as per the change control procedure. To assess the risk / impact associated with proposed change and to verify the implementation of action plan as per approved change control form. To determine the investigation plan and carry out investigations using appropriate root cause analysis tools, assessing the risk associated with them, to perform the additional studies and to derive the appropriate CAPA. To handle the recommended CAPA and to verify the implementation of recommended actions as per CAPA system and to evaluate effectiveness checks of implemented CAPA. To perform the trend analysis of deviation, change control, complaints etc.. to identify any repetitive event for further evaluation and CAPA. To conduct or be part of team conducting risk assessment of various activities, equipment, systems, etc.. and responsible for assigning the QRM no. To review all labelling related artwork components for products. To prepare artwork information details for new / revised labelling components and submit to QA doc cell for issuance of artwork as per procedure. To review and verify the destruction of old printed packaging materials (vendor and Amneal site) in case of revision of artworks of labelling components. Tracking the actions, review of extensions, verification of documents and closure of actions. Responsible for document handling, issuance, distribution, and retrieval of document. Scanning of documents for regulatory submission To maintain master documents like Site Master File, Validation Master Plan, Quality Manual, SOPs, protocols, reports, Batch Records, specification, method of analysis, drawings, artworks, planners, etc.. Responsible for issuance, archival and retrieval of documents like SOPs, Validation / qualification protocols / reports, Batch records, Specifications, Drawings, Artworks, planners, etc.. To provide BMR/BPR numbering to exhibit, intended and media fill BMR. To provide Batch number to exhibit, commercial, feasibility and medial fill batches. To receive and distribute the product development documents like Master Formula Records, Master Packaging records, protocols (sampling, study, and stability protocols). Issuance of uncontrolled copy / reference copies of master document to user as and when requested by user. To provide requested documents to regulatory affairs department for regulatory submissions (AR or other submissions), whenever required. Artwork management that includes effective the Artwork information details, distribution, retrieval and archival of artwork and all labelling components. To retire the documents as per change control assessment / proposal. Activities other than defined in the Job responsibility are to be done as per the requirement of HOD, by following HODs instruction and guidance. Skills Monitors production processes in real-time to ensure compliance with specifications and GMP, Batch record review, process monitoring, sampling, quality checks, real-time deviation management. Qualifications M.Sc. / B. Pharm / M. Pharm

We are looking for a dynamic and strategic leader to head our Modern Trade channel for a fast-growing D2C brand in the wellness and nutrition space. The ideal candidate will bring deep experience in driving revenue, expanding footprint across key modern trade accounts (national & regional chains), and leading high-performance sales teams. This is a leadership role that requires a strong understanding of category development, trade marketing, P&L management, and strategic partnerships with retail chains. Key Responsibilities: Modern Trade Strategy: Own and drive the national modern trade strategy aligned with business growth goals Key Account Management: Build, negotiate, and grow partnerships with major MT chains like Reliance Retail, Wellness Forever, Apollo, Star Bazaar, Nature’s Basket, etc. Team Leadership: Lead, mentor, and scale the modern trade team (KAMs, merchandisers, promoters) Business Development: Identify and onboard new accounts and distribution opportunities within modern retail formats Trade Marketing: Plan and execute consumer promotions, visibility drives, sampling activities, and store-level activation Forecasting & Inventory: Work closely with supply chain and finance teams to manage demand planning and minimize stock-outs Category Insights: Leverage data to track performance, market trends, and consumer behavior within modern trade Cross-functional Collaboration: Work with marketing, finance, and product teams to ensure brand consistency and promotional alignment Qualifications & Experience: 10–15 years of sales and key account experience in Modern Trade Prior experience in wellness, nutrition, healthcare, or pharma categories is a must Strong understanding of MT dynamics, trade spends, and category management Proven experience in leading and scaling modern trade businesses Excellent negotiation, communication, and leadership skills

The ideal candidate will own the process for leather bag production . They will strategize with other internal teams to ensure operational excellence. The will also run quality assessment to ensure customer satisfaction. Key Responsibilities: · Coordinate with internal teams to ensure seamless production and operational excellence. · Develop and execute production plans, scheduling, and monitoring to meet targets and deadlines. · Prepare and review production documents for new products in line with QA guidelines. · Oversee the execution of approved manufacturing processes and ensure compliance with Standard Operating Procedures (SOPs). · Lead quality assessments and address customer complaints to ensure satisfaction. · Supervise and train production personnel, fostering a disciplined and safe working environment. · Manage the complete production cycle, including resource allocation, productivity, and cost control. · Collaborate with warehouse, quality control, and procurement teams for efficient workflow. · Communicate with external vendors and manage outsourced production to ensure timely delivery. · Maintain and monitor inventory of raw materials and manage stock procurement. · Prepare and analyze production reports, cycle times, and capacity utilization. · Ensure adherence to safety protocols and maintain operational harmony on the production floor. · Support production planning, budgeting, and contribute to continuous process improvement. · Report operational challenges and progress to management, assisting with special projects as needed. Qualifications Bachelor's degree or equivalent experience Minimum 3 years of core production experience in leather accessories within an export house environment. Strong exposure to sampling, merchandising, and timely manufacturing/production processes. Strong organizational and managerial skills

Be the First to Apply Job Description Business: Pharma Solution Department: Analytical Quality Control (AQC) Location: Lexington Job Overview The Chemist I performs testing of raw materials, in-process and finished products, and maintains and calibrates analytical instruments in compliance with cGMP standards. Reporting Structure Directly reports to AQC Group Lead Key Responsibilities Perform routine/non-routine testing, both wet chemistry and instrumental analysis, according to SOPs, testing methods, protocols, compendia (USP EP/JP) etc. with minimum supervision Testing of raw materials, APIs, finished products, stability samples, and cleaning verification samples, etc. Document laboratory work according to, GDP, cGMPs, and SOPs Troubleshoot, calibrate and maintain instruments as required Prepare and label laboratory reagents, reference standards, or solutions according to SOPs. Write SOP's, laboratory protocols and reports, memos and/or other interdepartmental correspondence Participate in laboratory investigations Perform peer review of analytical documentation Follow safety procedures when working in laboratory. Understand and comply with cGMPs and other regulations Maintain the laboratory in an organized and neat manner Act as backup for Material sampling activities. Purchasing of laboratory reagents and consumables Education Requirements Bachelor of Science in Chemistry, Pharmaceutical Science, or other closely related scientific field Experience Minimum 1-year hands-on experience performing quality control work within a laboratory, proficiency with HPLC/GC analysis strongly preferred Experience working with potent, cytotoxic materials and parenteral drug products preferred Competencies High level of proficiency operating all Microsoft Office applications Excellent communication skills, both verbally and in writing Detail oriented and organized Demonstrated ability to work within a team environment, supporting a continuous operation manufacturing facility Excellent problem solving, communication, and interpersonal skills Ability to follow written instructions 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 9085 Job Category Analytical QC Posting Date 07/25/2025, 08:17 PM Job Schedule Full time Locations 1500 BULL LEA ROAD,, Lexington, KY, 40511, US

As an Intern at our company, your day-to-day responsibilities will include designing soft luggage across various product categories such as Backpacks, Trolley bags, Duffels, and Travel accessories. We are looking for a Designer who can create trendy, fashionable, and user-friendly bags with innovative features and unique selling points. Your tasks will involve understanding design briefs, conducting user and market research, exploring concepts through sketching and rendering, and collecting feedback and approvals from the design, marketing, and sales teams. You will be responsible for suggesting and applying materials, ensuring the optimum use of raw materials, sampling, and planning for pre-production. Additionally, you will be involved in product photography, creative shoots, graphic design, and marketing projects including Hangtags, posters, catalogues, packaging design, and other marketing materials. About the Company: Established in 1959, Harissons offers a wide range of products including luggage bags, travel totes, sports bags, duffel bags, backpacks, school bags, college bags, messenger bags, office bags, handbags, pouches, and various accessories. Our company designs and manufactures bags using durable fabrics like nylons and polyesters, coated with special chemicals for added strength and waterproof properties. Our bags are designed to be user-friendly, functional, stylish, and comfortable.,

You will be responsible for performing sampling and testing of raw materials, feed ingredients, and finished products. This includes conducting routine chemical and physical analyses such as moisture, protein, fiber, ash, fat content, and adulteration detection. It is crucial to maintain accurate laboratory records and test reports for documentation and audits. Additionally, you will ensure the calibration and proper functioning of laboratory instruments and equipment. Your role will also involve assisting in preparing standard solutions, reagents, and sample preparations. As part of the team, you will support senior chemists and quality assurance teams in root cause analysis and troubleshooting. Compliance with GMP, HACCP, and safety protocols during lab activities is essential. You will monitor quality deviations and escalate issues as required. Participation in internal audits, inspections, and sample collection as per SOPs will be expected from you. The ideal candidate should possess a B.Sc. / M.Sc. in Chemistry or Biochemistry. A minimum of 2 years of experience in a feed mill, food processing unit, or analytical laboratory is required. Freshers with academic lab experience and good technical understanding are also encouraged to apply. This is a full-time, permanent position with opportunities for fresher candidates. The benefits include Provident Fund, a rotational shift schedule, and a yearly bonus. The work location is in person. (Note: Job Types, Benefits, Schedule, and Work Location details are included for your reference but will not be a part of the final Job Description),

NPS Prism Title: Quality Engineer – Software Development Engineer in Test (SDET) Company Profile: NPS Prism is a market-leading, cloud-based CX benchmarking and operational improvement platform owned by Bain & Company. NPS Prism provides its customers with actionable insights and analysis that guide the creation of game-changing customer experiences. Based on rock-solid sampling, research, and analytic methodology, it lets customers see how they compare to their competitors on overall NPS®, and on every step of the customer journey. With NPS Prism you can see where you’re strong, where you lag, and how customers feel about doing business with you and your competitors, in their own words. The result: Prioritize the customer interactions that matter most. NPS Prism customers use our customer experience benchmarks and insights to propel their growth and outpace the competition. Launched in 2019, NPS Prism has rapidly grown to a team of over 200, serving dozens of clients around the world. NPS Prism is 100% owned by Bain & Company, one of the top management consulting firms in the world and a company consistently recognized as one of the world’s best places to work. We believe that diversity, inclusion, and collaboration is key to building extraordinary teams. We hire people with exceptional talents, abilities and potential, then create an environment where you can become the best version of yourself and thrive both professionally and personally. Position Summary: NPS Prism has experienced tremendous growth as a standalone software and data business over the past few years and is making the leap from being a consulting-led business to a technology-led business. Given that shift, we are looking to build our team with world-class team members to help drive business growth to its full potential in this next phase. This is a great opportunity to help build the largest startup owned by Bain & Company and take NPS Prism into the future. We are seeking a Quality Engineering (QE) Software Development Engineer in Test (SDET) to join our dynamic team. As a QE SDET, you will be responsible for designing, developing, and executing automated test frameworks to ensure the reliability, scalability, and performance of our software products. You will collaborate closely with developers, product managers, and other stakeholders to drive high-quality software releases. Key Responsibilities: Reading logs to analyse the root cause of the issue Design, develop, and maintain automated test frameworks, scripts, and tools to improve test coverage and efficiency. Develop and execute unit, integration, functional, performance, and regression tests to ensure product quality. Collaborate with software engineers to integrate test automation into CI/CD pipelines . Identify, document, and track defects, ensuring timely resolution through collaboration with development teams. Perform code reviews, API testing, end to end testing, and white-box testing to improve product stability and reliability. Continuously enhance and improve test strategies, tools, and best practices in software testing. TEST CASE CREATION Work closely with DevOps and SRE teams to improve test environments and deployment processes. Participate in design and architecture discussion s, ensuring testability and quality are considered from the beginning. Monitor and analyze test results, providing reports and insights to improve software performance and reliability. Required Qualifications, Experience & Skills Education: Bachelor’s degree in computer science, information technology, or a related field. (BCS, B.Tech, BE, BCA, etc.) Experience: min 2 year full time and max 4 years of experience in manual and automation testing (Selenium preferred) min 2 year full time and max 4 years of experience in any programming language (Java or Python are preferred) ​Skills: Profic iency in coding with languages like Java, Python, JavaScript, C#, typescript or Kotlin. Expe ri ence in automation testing using tools such as Seleni um, Appium, Cypress, Playwright, or TestNG. Hands - on experience with API te sting tools (Post man, RestAssured, SoapUI). Knowle dge of CI/CD pipelines using Jenkins, GitHub Actions, GitLab CI/CD, or similar. Experi ence with cloud environments (AWS, Azure, GCP) and containerization tools like Docker and Kubernetes. Famili arity with perfor mance testing tools such as JMeter , Gatling, or k6. Unders tanding of softw are development methodologies (Agil e, Scrum, Kanban) and QA processes. Strong analytical and problem-solving skills with the ability to debug complex issues. Prefer red Qualifications:Experi ence with AI/ML- based testing tools. Know le dge of securi ty testing practices. Expe ri ence in databa se testing with SQL and NoSQL databases. Famili arity with behavior-driven development (BDD) ​

Functional:- • Takes care of the entire store team & lead them to make the store profitable • Elevates coffee culture by educating customers; selling coffee and coffee grinding and brewing equipment; preparing and serving a quality coffee beverage, introducing seasonal beverages along with food offerings. • Welcome customers by assessing their coffee interests and needs. • Invite customers for tastings of manual brew & for sampling of food • Prepare beverages & food by adhering to the defined recipes • Helps in generating revenue through driving suggestive selling based on customer’s preferences. • Maintains stock on merch rack, FDU & other display units through timely replenishment. • Follow SOPs while handling equipment; adheres to PM schedule & call for timely repairs Behavioral:- • Maintains secured, safe, clean and healthy workplace by following SOP • Takes feedback from the customers about product & place; responds appropriately & if required than conveys it to Area Manager • Takes ownership of self-development & learning, shares skill & knowledge with fellow TMs

Call and follow up with event managers, caterers, and shopkeepers to promote our water bottle products Visit local vendors and clients for product demo and order discussion Handle basic office work like maintaining client records and follow-up lists in Excel Coordinate with delivery and operations team for smooth order fulfillment Help plan and run local promotional activities or sampling drives Collect feedback from customers and report it to management Build strong long-term relationships with regular clients

Job Title: B2B Sales Executive – Brand Partnerships Location: Sector 9, Noida | On-site | Full-Time Experience: 1–3 Years CTC: Up to ₹4 LPA Key Responsibilities: 1. Sales & Closures Pitch in-gym advertising, product sampling, and digital collaborations to potential brand partners Lead pricing discussions, campaign scope, and finalize deals 2. Client Onboarding Manage contracts, product uploads, and campaign logistics Coordinate with internal teams for smooth execution 3. Campaign Performance & Reporting Share bi-weekly campaign reports with performance metrics Maintain active client communication via WhatsApp, CRM tools, and email Requirements: 1–3 years of experience in B2B sales or brand partnerships Strong communication, negotiation, and storytelling skills Proficiency in CRM tools, LinkedIn lead generation, and structured documentation Interest in fitness and brand marketing is an added advantage How to Apply: Interested candidates can share their CV at recruitment@wtfgyms.com

Job Description Analyst with having the knowledge of Instrument HPLC, UV, FTIR, GC ,Polarimeter , KF, Auto titrator e.t.c. Responsible for sampling, testing and release of Raw material, packing material and miscellaneous material samples and maintain reserve sample as per SOP. Responsible for review of instruments logbooks, raw data of raw materials, packing materials, miscellaneous materials, in-process, finished products and water analysis. Analysis related to qualification of Instrument/Equipment and Standards Qualification of Standards and Instruments Knowledge and Skill on Sophisticated instruments like UV, HPLC, GC, UPLC, FTIR, Polarimeter and KFtitrator. Knowledge of Chemical analysis. Knowledge of LIMS/QMS Knowledge of current pharmaceuticals guidelines (eg. ICH, cGMP etc.) Troubleshooting and decision skills for analytical problems. Responsible to perform activities with respective TNI . To ensure the timeline for initiation and completion of testing. Responsible to maintain quality standards that apply to product Analysis, ensuring proper implementation. To maintain the cleaning in quality control department Skills And Proficiency Analytical Instrumentation Handling – Expert Particulate Matter Testing – Practitioner Good Laboratory Practices (GLP) & Documentation Accuracy – Practitioner Data Integrity & Documentation – Practitioner Regulatory Compliance – Practitioner SOP Preparation & Revision – Practitioner Analytical testing expertise and evaluation skills – Expert Handling of Analytical Instruments and Interpretation of Resulting Data – Practitioner Laboratory Instrument qualification, Calibration & Maintenance – Practitioner Quality Control & Compliance – Practitioner LIMS Operation & Data Management – Practitioner QMS Documentation (OOS, OOT, Deviation & Incident) – Beginner CAPA, Deviation, and Change Control Management – Beginner Qualifications Qualification : Bachelor or Master's degree in science Experience: Minimum 4 to 6 years of relevant experience in QCC Department Note: Candidate who want to apply for internal job posting must have completed at least 2 years in his current job role.