10945 Qc Jobs - Page 7

Qualification : (B.Sc. from a recognized University) and minimum 5 years of experience of analysis & sample collection or similar work in the chemical plants & execution of the following types of jobs under the contract. a. Sample collection, preparation, analysis and preservation / recycling b. Classical Analysis - Acid-base titrations, Redox titrations / complexometric titrations, Argentometric titrations, Iodimetric and Iodometric titrations, Volumetric & Gravimetric Estimations, KF titrations, etc. c. Instrumental analysis using equipment / instruments as mentioned in this scope of work elsewhere d. Physical inspection or any other method required to be carried out. e. Calibration of Instruments, Preparation and Standardization of reagents and solution as per requirements and established frequency. Records and data will be submitted to GACL Lab authorities from time to time. f. Communication of Results, data entry in computer and related documentation. g. Special studies and plant trouble shooting. h. Maintaining Laboratory to meet any analysis requirements. i. Cleaning of Glass ware and any other item as directed j. Movement of lab equipment, laboratory chemicals, cylinder etc. from one lab to another lab or from store. k. Cleaning of analytical platform, table, lab equipment etc. l. Cross checking / verification of sampling & analysis methodology followed, equipment performance checking, etc. as per the requirements of the job. Interested profiles kindly contact on 9727779612 or drop email on info@kamakshifacilities with subject line "Applying for QC Chemist Vacany". Job Type: Full-time Pay: ₹11,901.16 - ₹22,000.00 per month Benefits: Provident Fund Experience: total work: 1 year (Preferred) Work Location: In person

Job Role: Pharma QA Head Experience Required: Minimum 10 years in Pharmaceutical Quality Assurance. Job Time: 9:00 AM to 6:00 PM Work Location: Kalol, Gujarat Key Responsibilities: Lead and manage the QA department to ensure compliance with GMP, GLP, and regulatory requirements. Oversee document control, batch record review, and product release activities. Ensure timely handling of deviations, change controls, CAPA, and OOS investigations. Coordinate internal and external audits, including regulatory inspections. Implement and monitor quality systems to maintain product safety, efficacy, and compliance. Train and mentor QA team members for continuous skill enhancement. Collaborate with Production, QC, and R&D for quality improvement initiatives. Job Types: Full-time, Permanent Pay: ₹50,000.00 - ₹100,000.00 per month Benefits: Provident Fund Work Location: In person

Post : Quality Line Inspector Experience : 01 to 03 Years Qualification : DME / BE Mechanical Industry : Automobile Manufacturing Industry Timing: 9 am to 7:30 pm and 9 pm to 7:30 am. Willing to do the night shift Accommodation facilities: The company will provide the same Job Description: On time Inspection Report preparation. Should have basic quality instruments knowledge like Vernier calipers, gauges & micrometers Should be able to do night shifts (Weekly) Should be good in Excel Coordinate all QA/QC activities with the QC Manager. Inspect, test or measure materials. Contact No : 8956289165 Job Type: Full-time Pay: ₹18,000.00 - ₹25,000.00 per month Benefits: Food provided Ability to commute/relocate: Jamnagar, Gujarat: Reliably commute or planning to relocate before starting work (Preferred) Shift availability: Day Shift (Preferred) Night Shift (Preferred) Work Location: In person

Job Summary: We are seeking an experienced and results-driven Production Manager to oversee manufacturing operations related to Core, Current Transformer (CT), and Potential Transformer (PT) production. The ideal candidate will have a strong background in electrical equipment manufacturing, proven leadership capabilities, and a commitment to maintaining high standards of quality, safety, and efficiency. Key Responsibilities:Production Management: Plan, coordinate, and supervise daily production activities for Core, CT, and PT units. Ensure timely delivery and execution of production targets as per monthly and quarterly plans. Monitor production KPIs including efficiency, downtime, yield, and manpower utilization. Technical Expertise: Interpret transformer designs and ensure correct execution of winding, core assembly, insulation, tanking, and testing processes. Optimize material usage and reduce wastage in core cutting, stacking, and assembly. Troubleshoot technical issues during production and provide timely solutions. Quality & Compliance: Ensure adherence to quality standards (IS/IEC) and internal QA/QC protocols. Coordinate with the quality team to resolve NCRs (Non-Conformance Reports). Implement continuous improvement processes (Kaizen, 5S, Lean Manufacturing). Team Management: Lead a team of supervisors, technicians, and shop floor workers. Train and develop staff for multi-skill development and safety awareness. Evaluate team performance and recommend improvements. Coordination & Reporting: Coordinate with the planning, purchase, design, and quality departments for smooth operations. Maintain daily production reports and MIS for senior management review. Participate in internal and external audits. Required Qualifications & Skills: Education: Diploma / B.E. / B.Tech in Electrical / Mechanical Engineering Experience: 8–15 years in a transformer manufacturing setup, with at least 5 years in CT/PT/Core production management. Technical Skills: Knowledge of CT/PT construction, testing standards (IEC/IS), and manufacturing processes Familiarity with production planning tools (ERP/SAP) Understanding of lean manufacturing, 5S, TPM principles Job Type: Full-time Pay: ₹35,000.00 - ₹45,000.00 per month Work Location: In person

Essential Functions: Take regular plant rounds to monitor production activities and ensure cGMP compliance at the shop floor level. Review and approve Batch Manufacturing Records (BMR), Batch Cleaning Records (BCR), and related analytical records prior to release of API. Prepare and revise SOPs, BMRs, BCRs, BPRs, and other QA-related documents in line with regulatory and internal requirements. Perform sampling of APIs, maintain related records, and ensure proper cleaning and maintenance of sampling tools. Maintain records and storage of control samples of API as per defined procedures. Provide line clearance at every product changeover stage, ensuring readiness of area and equipment. Monitor dispatch process and review records related to finished goods dispatch to ensure compliance. Coordinate and support investigations of deviations, incidents, and non-conformances with QA Head/Designee. Participate in Product Quality Reviews (PQR) for all APIs, compiling relevant data and identifying improvement areas. Monitor process and cleaning validation activities on the shop floor to ensure compliance with protocols. Support data integrity, documentation practices, and readiness for internal/external audits. Coordinate with production, QC, engineering, and warehouse teams for day-to-day IPQA requirements. Additional Responsibilities: Participate in risk assessments (HIRA), change controls, and CAPA implementation related to IPQA. Support training of QA executives and production personnel in cGMP, documentation, and in-process control requirements. Assist in handling of quality events such as market complaints, recalls, and audit observations. Contribute to continuous improvement initiatives within QA and across departments. Ensure readiness and compliance for regulatory inspections and internal quality audits. Lead initiatives related to QMS enhancements and harmonization of documentation practices. Maintain logs, registers, and master data related to IPQA activities. Monitor and report compliance KPIs to QA management. Act as QA representative in daily production meetings and batch release discussions. Qualifications :- Education: B.Sc – Organic Chemistry – Required M.Sc – Organic Chemistry – Preferred B.Pharm / M.Pharm – Preferred Job Type: Full-time Pay: ₹50,000.00 - ₹100,000.00 per month Benefits: Health insurance Provident Fund Work Location: In person

Role Description This is a full-time (Mon - Saturday) on-site role for a Purchase Executive located in Kheda, Gujarat. (Approximately 40 kms from Ahmedabad). You will be reporting directly to the Assistant Manager (Operations) and the Chief Technical Director (CTO). Domestic Purchase Duties: Procurement of raw materials (Epoxy resin, hardeners, additives), packaging materials, consumables, and engineering items. Vendor development, quotation comparison, price negotiation. Raising Purchase Orders in ERP and tracking deliveries. Coordination with store, QC, and production for material planning and quality clearance. Import Procurement Duties: Handle import orders including communication with overseas suppliers. Get Proforma Invoice (PI), prepare and track advance payments / LC (if applicable). Coordination with freight forwarders and CHA for import shipment status. Check & verify Import documents (Invoice, Packing List, BL, COA, MSDS, etc.). Import Documentation & Bank Coordination: Preparation & submission of BOE (Bill of Entry) documents. Submission of import documents to the bank (for foreign remittance/payment release). Maintain import records as per DGFT / FEMA and audit requirements. Ensure timely clearance from customs with support of CHA. Other responsibilities: Provides general administrative duties, project support, special events and activities as requested. To undertake any other job / assignment given by management from time to time Qualifications & Skills required Bachelor’s degree in Commerce / International Trade / Science / Engineering. 1 to 3 years of experience in purchase and import handling in a manufacturing company. Knowledge of the chemical industry or epoxy resins is preferred. Experience in import documentation, CHA coordination, BOE, and FEMA compliance is must. Familiarity with ERP systems, MS Excel, email communication. Strong coordination and follow-up skills Good understanding of INCOTERMS, HS Codes, Customs process Effective communication in English (written & verbal) Basic knowledge of banking process for imports, LC, TT remittance ISO (9001, 14001, 45001) & 5S documentation awareness (preferred) Job Type: Full-time Pay: ₹250,000.00 - ₹400,000.00 per year Benefits: Provident Fund Ability to commute/relocate: Kheda, Gujarat: Reliably commute or planning to relocate before starting work (Preferred) Experience: total work: 1 year (Required) Language: English (Required) Work Location: In person

Position: Sampling Quality Assurance (QA) Location: Arsh Fashions (GIDC Vapi) Experience: 2 to 3 years Salary: ₹25,000 - ₹32,000 per month (As per candidature) Job Summary Should have 4-5 years’ experience of Garment Export house as a Sampling QA. Must be well versed with QA Process - Fabric knowledge, pattern auditing, Cutting, Stitching, finishing, washing and packing - Cut to Pack. Required experience in Men’s, Ladies and Kids Wear - Woven & Denim garments. Required experience in line Quality checking and Production of garments. Must have knowledge about different processes of Audit - Inline , Midline, Online Observations, Pre and Final. Required experience in SGS & ITS level checking. Must be skilled in making Audit Reports. Good at verbal and written communication. Must be experienced to handle a team of checkers and QC team. Reporting to the QA Manager. Job Type: Full-time Pay: ₹25,000.00 - ₹32,000.00 per month Work Location: In person Expected Start Date: 13/08/2025

We are looking for a QC Officer to join a reputed API / Intermediate Manufacturing Company. Position: QC Officer Location: Khambhat, Gujarat Experience: 2–4 years Qualification: B.Sc./M.Sc. (Chemistry) or B.Pharm/M.Pharm Salary: Up to ₹3.50 LPA Key Responsibilities: * Operate & maintain HPLC, GC, UV, and FTIR instruments * Calibrate lab instruments (HPLC & GC preferred) * Sample & analyze raw materials, packaging materials, intermediates, and finished products * Handle weighing instruments, lab chemicals, reagents, and solutions * Manage working & reference standards * Review in-process analysis data and maintain QC records * Ensure compliance with GDP, GLP, GMP, and audit requirements Apply Now: 9974253672 Job Type: Full-time Pay: Up to ₹350,000.00 per year Work Location: In person

Job Title: Head – Quality Control (QC) Location: Atlas Transformers India Limited (Por,GIDC) Experience: 12 to 15 Years in Transformers industry Job Type: Full-Time Job Summary: We are looking for a highly experienced and quality-driven QC Head to lead the Quality Control function in our transformer manufacturing facility. The ideal candidate will oversee and manage all aspects of quality inspection and control processes for incoming materials, in-process manufacturing stages, and final product testing. The role is vital to ensuring compliance with design specifications, international standards, and customer expectations for distribution and/or power transformers. Key Responsibilities:Strategic Quality Oversight: Develop and implement the quality control strategy and inspection procedures across all manufacturing stages (core, winding, assembly, tanking, and testing). Define and enforce quality standards in accordance with IEC, IS, ANSI, BIS, or customer-specific requirements . Inspection & Quality Control: Lead a team of QC inspectors to perform incoming, in-process, and final inspection of components and assemblies. Ensure thorough documentation of inspection results and maintain quality records . Oversee material testing (e.g., CRGO, copper, insulation, oil) and coordinate with suppliers for non-conformances. Implement root cause analysis and corrective/preventive actions (CAPA) for quality issues. Testing & Compliance: Ensure transformers are tested as per standard procedures in routine, type, and special tests . Review and approve test reports and ensure customer inspections are effectively managed. Collaborate with third-party labs or agencies for external quality audits or certifications. Quality System Management: Maintain and improve ISO 9001 or other quality management systems. Drive continuous improvement programs such as Kaizen, 5S, Lean Manufacturing, or Six Sigma . Team Management: Train, mentor, and manage QC staff to build a proactive and skilled quality team. Conduct internal audits and facilitate customer or regulatory audits. Qualifications and Experience: Bachelor’s degree in Electrical / Mechanical Engineering or a related field. 10+ years of experience in quality control within the transformer industry , with at least 3–5 years in a leadership role. Strong knowledge of power and distribution transformer manufacturing , including materials, winding, core assembly, tanking, and testing. Deep understanding of national and international quality standards (IEC, IS, ANSI, BIS, etc.) . Familiarity with routine and type testing in transformer test bays. Proficient in quality tools such as 7QC tools, RCA, FMEA, SPC, MSA, etc. Key Skills: Leadership and team management Problem-solving and analytical thinking Strong communication and documentation skills Attention to detail and compliance mindset Customer-facing experience in inspections and audits Working Conditions: Factory-based role with regular presence in shop floor, stores, and test bay. Must be willing to work under tight deadlines and respond quickly to quality incidents or escalations. Job Type: Full-time Pay: ₹1,200,000.00 - ₹1,500,000.00 per year Work Location: In person

Sunrise Remedies Job Opening for Quality Control Executive Experience: 01 To 02 Year in years of experience in QC in an Ayurvedic / herbal / pharmaceutical company. Education Qualification: B.Sc | M.Sc | B.Pharm |M.Pharm Department: Quality Control – Ayurvedic Location: Santej Ahmedabad. Transportation Facility Available (As Per Circumference Of Sunrise Remedies) Mediclaim and Food Facility provide By Company. Key Responsibilities: – Conduct routine quality checks and testing of raw materials, packaging materials, in-process samples, and finished Ayurvedic products. – Ensure compliance with AYUSH regulations, GMP, and ISO standards where applicable. – Maintain and calibrate lab instruments such as HPTLC, UV-Vis Spectrophotometer, pH meters, etc. – Prepare and maintain Standard Operating Procedures (SOPs), test reports, COAs, and specifications for materials and products. – Conduct microbiological testing and stability studies as required. – Collaborate with the production, and QA departments for troubleshooting and quality-related investigations. – Handle non-conformance reports (NCRs) and support in CAPA implementation. – Review batch manufacturing records (BMRs) and ensure quality documentation is in place. – Support in regulatory audits (AYUSH, FSSAI, WHO-GMP, etc.) and third-party inspections. Please drop your CV or Resume to info@sunriseremedies.in Our HR Department will get in touch with you.

Key Responsibilities: Supervise and coordinate the activities of production workers and technicians. Ensure daily production targets are met with quality and efficiency. Monitor production schedules and allocate resources effectively. Oversee the assembly of filling, capping, labeling, and packaging machinery. Ensure adherence to standard operating procedures (SOPs) and quality standards. Maintain 5S, safety, and housekeeping practices in the production area. Coordinate with the Quality Control (QC), Design, and Purchase departments to resolve production issues. Maintain daily production reports and update management on progress and challenges. Train and guide team members on machinery, safety protocols, and work discipline. Identify bottlenecks in the process and suggest improvements for optimization. Ensure timely maintenance of tools, equipment, and production machinery. Qualifications and Skills: Education: Diploma / B.E. / B.Tech in Mechanical / Production / Industrial Engineering. Experience: 2–6 years in a manufacturing or machinery assembly environment, preferably in the packaging or automation industry. Technical Skills: Strong understanding of mechanical assembly and production processes. Ability to read mechanical drawings and interpret BOMs. Familiarity with lean manufacturing practices is a plus. Soft Skills: Leadership and team management. Good communication and problem-solving skills. Attention to detail and time management. Other Requirements: Willing to work in shifts, if required. Hands-on approach and readiness to work on the shop floor. Job Type: Full-time Pay: ₹20,000.00 - ₹40,000.00 per month Benefits: Cell phone reimbursement Internet reimbursement Leave encashment Application Question(s): Current CTC Expected CTC Notice Period Work Location: In person

Department : Quality Control Location : Vadsar, Gandhinagar Experience : 0-2 years (Preferably in Cosmetics or Pharma Industry) Salary Range : ₹2-2.8 LPA Education : B.Sc. / M.Sc. in Chemistry, Organic Chemistry, or related field Job Summary: We are looking for a QC Inspector with strong analytical skills and hands-on experience in laboratory operations. The ideal candidate will ensure product quality by performing chemical analysis on raw materials, in-process samples, and finished goods in compliance with industry and regulatory standards. Key Responsibilities: Perform routine and non-routine chemical testing on raw materials, in-process samples, and finished products as per SOPs. Conduct stability studies and document observations and test results with accuracy and traceability. Maintain proper documentation and logs to ensure full traceability and compliance with GLP. Follow internal quality procedures and ensure adherence to ISO, GMP, and regulatory requirements. Identify, report, and escalate deviations or out-of-spec results; support in root cause analysis and CAPA implementation. Participate in internal and external audits, ensuring lab readiness and compliance. Support continuous improvement initiatives in lab practices and documentation. Skills & Competencies: Strong analytical and observation skills. Proficiency in laboratory equipment operation and troubleshooting. Excellent documentation and record-keeping abilities. Proficiency in MS Office (Word, Excel, Outlook). Ability to work independently and collaboratively in a team. Detail-oriented with a proactive approach to quality. Job Types: Full-time, Permanent Pay: ₹200,000.00 - ₹280,000.00 per year Benefits: Leave encashment Work Location: In person

1. Inventory Management: Conduct physical inventory verification in an effective and efficient manner. 2. Material Handling: Receive, check, and verify incoming materials against purchase orders. Ensure timely posting of Goods Receipt Notes (GRNs) and issues in ERP. 3. Documentation: Maintain proper documentation of incoming materials, stock registers, and manage strong records of PO, SO, invoicing, billing, and discrepancies. 4. Stores Maintenance: Keep the store area organized, clean, and compliant with ISO standards. 5. Team Leadership: Supervise, train, and develop the stores team to ensure effective daily and periodic task management. 6. Stock Optimization: Monitor and reduce non-moving stock regularly by implementing best practices. Generate indent for regular consumable and B&C class items. 7. Coordination: Liaise with transporters/couriers for smooth inbound and outbound logistics. 8. Internal Co-ordination: Co-ordinate with internal Depts like Purchase, Accounts, Mfg & QC for effective stores management as well as support proactively Mfg for fulfilling the material requirements. 9. Continuous Improvement: Drive process improvements in store functions through new initiatives and industry best practices. Implementation of 5S. 10. Reporting & Reviews: Submit regular MIS reports on stock and inventory to management (weekly, monthly, quarterly) and participate in review/planning meetings (WPRM, MRM, Project Kick-offs, etc.) 11. Issue Resolution: Address and escalate material-related issues promptly to the concerned authority for timely resolution. Job Types: Full-time, Permanent Pay: ₹40,000.00 - ₹60,000.00 per month Benefits: Health insurance Leave encashment Paid sick time Provident Fund Work Location: In person

BSC or MSC - can work independently. Job Types: Full-time, Permanent Pay: ₹12,000.00 - ₹20,000.00 per month Benefits: Leave encashment Paid sick time Provident Fund Work Location: In person

INFINIUM PHARMACHEM LIMITED is an NSE Listed, well known Pharmaceutical Intermediates & APIs manufacturing company since 2003. We are looking for enthusiastic and well experienced candidate for post of QA Officer for the Company. Post : QA Officer Experience : 0 to 2 Year Qualification: M. Pharm (QA) / M.Sc Job profile: - Knowledge of Basic Chemistry - Knowledge of Documentation - Knowledge of importance of API & Intermediates - Knowledge of basic reactions - Fill daily records like temp. And humidity record - Give line clearance in store as well in production dept. - Take samples from In Process as well as from FP Quarantine and send them to QC . - Knowledge of basic of computer and their applications. Job Type: Full-time Benefits: Health insurance Provident Fund Work Location: In person

Purpose and objectives: A Quality Control Engineer evaluates materials and products to determine if there are any deviations or defects. They work to ensure that the industry standards and specifications are met on the Customer end. Key Responsibilities/Accountabilities: Candidate having basic knowledge of Instruments e.g. Vernier Caliper, Micrometer, Bore gauge, Height gauge & Comparator, etc. Able to read and understand drawings. Education Qualifications: B.E. (Mech) / Diploma (Mech) / ITI Job Types: Full-time, Fresher Pay: ₹25,000.00 - ₹35,000.00 per month Benefits: Health insurance Work Location: In person

Division Department Sub Department 1 Job Purpose Support R&D and manufacturing unit by on time provision of specifications, preparation of standards, Pharmacoepeial collaboration and Toxicity predictions for time bound development of the project Key Accountabilities (1/6) Review development specifications in order to provide support to Unit QC for finalization of CCDC specifications and submission of competent qualitative monographs to Local and International pharmacopoeias to monopolise Cipla's products in regions under the jurisdiction of the corresponding pharmacopoeia Develop specifications for APIs, RMs and Intermediates Method of Analysis and Certificate of Analysis Review monographs to ensure that it fulfils all the criteria’s required for submission Key Accountabilities (2/6) Predict Genotoxic impurities for API R&D molecules and interaction with the Vendor for Genotoxic prediction of molecules in order to support R&D and Unit ADL for method development. Predict and interpret Genotoxic impurities for easier understanding Arrange structures from R&D and Unit ADL to Vendors for Toxicity prediction Key Accountabilities (3/6) Prepare and maintain Laboratory standards and review data for providing compliance to regulatory and FDA norms which entails checking and monitoring Laboratory, safety and documentation practise Prepare and maintain Laboratory standards such as Test Standards, Volumetric standards, GC standards which also includes reference standards like USPRS and EPCRS Review Lab notebooks, IQ, OQ, PQ, Stability reports, deficiency reports, Characterization data Key Accountabilities (4/6) Prepare SOPs/ EOPs/ IOPs for maintaining GLP and GDP timely with data integrity Take Approval on the change requests Prepare SOPs/ EOPs/ IOP’s for existing quality systems Collate all the comments received from other units and the R&D team Plan and incorporate innovative ideas to implement new SOPs Impart training on SOPs and electronic systems Prepare and maintain in-house, external calibration schedule and preventive maintenance schedule Review of external and internal calibration reports. Maintain breakdown records of instruments and equipment Prepare and finalise the qualification documents and URS Prepare internal quality related audits and finance audits and provide compliance for the same Handle change controls, deviations, incidence Prepare job responsibilities and updates on organogram Issue project code Check and maintain the logs, Eg. R&D log book issuance log, MPG issuance log, pilot requisition forms, analytical method validation checklists, batch number, PDS issuance and submission. Check R & D record books, training files Key Accountabilities (5/6) Execute on time technology transfer of projects to transferring unit which entails co-ordination with the cross-functional teams of other units and relevant documentation of product life cycle Prepare the Master Process Guidelines and related documents for TT Acquire data from R & D and ADL team to prepare the documents Collate all the comments received from pilot and unit on the process Co-ordinate with cross-functional teams after the technology transfer of the projects Prepare the Strategy documents and QbD documents, Project closure forms and development reports Prepare and compile TT file for Audits Prepare, maintain and archive PDS for API process Key Accountabilities (6/6) Major Challenges Time taken from the cross-functional teams for getting approval on change requests To overcome frequent follow-ups taken to get approval Getting prompt compliance from R & D team,To overcomecommunicate and take follow –ups. Key Interactions (1/2) Internal stakeholders for data required by Formulation department for strategy preparation (need basis) Manufacturing units by providing development specifications, standards, data and compendial updates (need basis) DQA/ CQA for approval on change requests (need basis) Accounts for accounts related queries (need basis) Safety Auditors for audits and giving compliance (need basis) Key Interactions (2/2) Outsourcing partners for on time deliverables such as V life for toxicity prediction (need basis) Pharmacopoeial authorities for collaboration across the globe (need basis) External Calibration Parties and Instrument/equipment service Providers for the qualification and calibration related activities (need basis) External finance auditors for asset related audits (need basis) Dimensions (1/2) TAT for review of Unit ADL development specifications: 2 days TAT for preparation of development specifications/ MoAs: 2 days TAT for compliance review of characterization report : 2 days TAT for compliance review of deficiency report : 2 days TAT for preparation of Test standards: 2 days. TAT for sending pharmacopoeial queries: 2 days. TAT for Non-chromeleon Data integrity :1 Day TAT for Compendial updates:1 Day TAT for review of Laboratory Notebooks: 1 Day TAT for Analytical strategy review: 1 Day Rework for Monograph preparation : less than 3 rectifications per Monograph Rework for preparation of specification/ MoA: less than 3 rectifications per specification/ MoA Technology related Documentation ( range 5-10 ) Development Reports(1-5) Strategy documents(5-10) SOP’s, EOP’s, IOP’s(10-15) PDS(1-5) Change requests ( 15-20) Dimensions (2/2) Key Decisions (1/2) Critical decisions required for inclusion and exclusion of tests in the development specification Selection of monographs with ANDA approval for pharmacopoeial submission Finalization of specification and Test Standards Key Decisions (2/2) Approval on Unit ADL specification (to reporting manager) Final monograph submission (to pharmacopoeial Authority) Education Qualification M.Sc. (Analytical or Organic or Inorganic) Relevant Work Experience Minimum 5-6 years of ADL experience. Good communication and co-ordination skills with Analytical knowledge

Unicor Pharmatech was incorporated in the year 2020. Our manufacturing plant is built as per FDA norms and cGMP requirements. The company has state of the art export oriented facility to manufacture Tablets, Capsules, Ointments, Liquids and Sachets. Roles & Responsibilities:-. 1. Responsible for timely delivery of products as per the Rolling Forecast (RFC). 2. To ensure the delivery of quality products to market. 3. Review and approval of QMS (Quality Management System) documents such as Change controls, Events, Market complaints, Annual Product Quality reviews. 4. To ensure up-keep of building facilities, equipment's through regular preventive maintenance calibration and requalification. 5. To ensure that the required initial and continuous training of personnel are carried out. 6. Participation in manufacturing and packing operations of Scale up, Clinical trial batches with FDD. 7. Co-ordinate with Warehouse, EHS, Engineering, QA and QC in implementation of policies and guidelines. 8. Review of SOP's and Qualification documents. 9. To ensure the implementation of Environment, Health and Safety policy requirements in plant operations. 10. To ensure the compliance of internal/ external audit and to ensure timely adequate response of audit finding from the department to the auditor to close the issue. 11. Involvement in New Project with right to production. 12. To develop team member to take up responsibility in absence. 13. To meet the production targets 14. To ensure Accuracy, Reliability, validity, integrity and completeness of the cGxP data/records. 15. To plan the department activities as per weekly delivery schedule for OSD and Liquid orals. 16. To control the rejection during manufacturing and packing operations. Education, Experience and Skills Required:- 1. M.Sc. / B. Pharma / M. Pharma 2. 8-10 years of experience as production manager in finished pharma formulation plant. 3. Excellent communication skills required. Note: - Candidates willing to relocate to Anjar [Kutch, Gujarat] only needs to apply. Job Types: Full-time, Permanent Pay: ₹900,000.00 - ₹1,000,000.00 per year Benefits: Cell phone reimbursement Paid sick time Paid time off Provident Fund Work Location: In person

The QA/QC Engineer will be responsible for ensuring that all construction activities, materials, and workmanship meet the required quality standards and project specifications. The role involves implementing and monitoring the Quality Management System (QMS), conducting inspections, reviewing documentation, and coordinating with contractors, consultants, and clients to ensure compliance with contractual and regulatory requirements. Key Responsibilities: Implement and monitor the project’s QA/QC plan. Review method statements, ITPs, and material submittals. Conduct inspections for materials, equipment, and site activities. Ensure compliance with approved drawings, specifications, and standards. Issue and follow up on Non-Conformance Reports (NCRs). Coordinate with contractors, consultants, and clients on quality matters. Maintain quality logs, reports, and documentation. Qualifications: Bachelor’s/Diploma in Civil Engineering or related field. 6–8 years of QA/QC experience in construction/project management. Knowledge of ISO 9001:2015 and relevant codes/standards. Strong communication, problem-solving, and documentation skills. Job Types: Full-time, Permanent Pay: ₹60,000.00 - ₹80,000.00 per month Benefits: Commuter assistance Health insurance Leave encashment Life insurance Paid time off Provident Fund Work Location: In person Expected Start Date: 01/09/2025

Key Responsibilities Quality Assurance & Control Review project specifications, drawings, and standards related to façade works. Prepare and implement QA/QC plans, ITPs (Inspection & Test Plans), and checklists for façade installation. Monitor all façade works (structural glazing, ACP cladding, curtain walls, spider glazing, skylights, etc.) to ensure compliance with quality standards. Inspections & Testing Conduct and witness inspections for incoming materials, fabrication, and installation. Coordinate with third-party labs for testing façade materials (glass, sealants, aluminum, fasteners, etc.). Ensure all mock-up and site testing (water leakage, air infiltration, structural load tests) are carried out. Documentation & Reporting Maintain inspection reports, NCRs (Non-Conformance Reports), corrective action plans, and quality records. Prepare daily, weekly, and monthly QA/QC progress reports. Coordination Liaise with project managers, site engineers, design teams, and contractors for quality-related matters. Coordinate with suppliers for material approvals and ensure they meet required standards. Compliance & Safety Ensure façade works comply with project specifications, IS codes, ASTM, and BS standards. Monitor adherence to HSE (Health, Safety & Environment) guidelines during façade installation. Job Type: Full-time Pay: ₹50,000.00 - ₹60,000.00 per year

Company Description At TAPI, we’re not just a company—we’re a community committed to advancing health from the core. As the world’s leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we’re shaping the future of health worldwide. Our strength lies in our people—a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that transforms lives. Job Description Key Responsibilities: 1. 24 × 7 audit readiness. 2. Responsible to work in different shifts. 3. Participation in internal, external, regulatory audits. 4. Ensure 100% participation in training’s against CAPA’s. 5. Responsible for initiation and investigation on LIR, OOS, OOT & boarder line results and reporting them to the in-charge. 6. Supporting to share required documents from QC to RA/ other requirement. 7. Determining team priorities in accordance with the plant’s needs, while coordinating with the team leader / Manger. 8. Follow up the housekeeping, cGMP, GLP and Safety Guideline in laboratory. 9. Sampling and analysis of RM / FG / intermediates / cleaning samples based on requirement and result entry in analytical sheet, QA form, LIMS and online documentation as per data integrity norms. 10. Perform analytical test according to the monograph and SOP. 11. Responsible for calibration and verification of instruments. 12. Maintaining of reserved samples room and chambers / autoclaves / incubators. 13. Help to in charge in preparation of documents related to department (like STP’s, SOP’s and etc.) 14. Ensure the sampling of finished products, Raw material, Intermediate and sending sample to outside laboratory for analysis. 15. Must be ensured sampled, approved and rejected labels timely as require. 16. Responsible to maintain the stock record of chemicals and reconciliation of standards. 17. Any other job assigned by the Manger -QC Manger or group leader-QC Qualifications The ideal candidate will have: Education: B.Sc. / M.Sc. in Chemistry . Experience: Minimum 5 years of industrial experience. Preferred Industries: API / Pharma. Additional Information Make Your Mark with TAPI Your journey with TAPI is more than a job—it’s an opportunity to make a lasting impact on global health. If you’re ready to lead, innovate, and inspire, we’re excited to welcome you to our team. Together, let’s shape the future of pharmaceuticals. Apply on top of this page and our talent acquisition team will be in touch soon!

Location Name: Morbi Job Purpose “This position is open with Bajaj Finance ltd.” Duties And Responsibilities Duties and Responsibilities: Understand financial loan products and disbursement process for BLSE/PLSE/SALPL/PSBL/PRO/LAP/UCF business lines Responsible for file disbursement of Secured/Unsecured products Deliver disbursement quality Maintain File Hold as per agreed SLA Know loan documentation pre sanction and post sanction Responsible for coordination with verification agencies and tracking verification reports on a day to day basis Ability to learn and apply learning quickly Know collateral documents for LAP product Same day file dispatch and QDP for files logged in within agreed Cut Off time Responsible for Disbursement, DM Preparation & QDP Processing Perform QC audit of allocated cases timely Required Qualifications And Experience: Graduate with 1 - 2 year of experience in Loan Operations Computer proficiency Flexible in terms of office timings Mortgage/Personal/Business loan disbursement experience is must Required Qualifications And Experience Required Qualifications and Experience : Graduate with 1 - 2 year of experience in Loan Operations Computer proficiency Flexible in terms of office timings Mortgage/Personal/Business loan disbursement experience is must

Location Name: Agra Job Purpose Sale of repo assets within TAT days Stockyard process management/Yard Audits-Visits To ensure zero deviation in pre-repo/parking process Empanelment of new buyer for repo sale process Co-Ordination with internal & external stake holders related to data & other activities Release of repo vehicle to Customer/Buyer Document Handling ( all documentation) related to the sale of vehicles. Repo QC Duties And Responsibilities Stock Yard Management Repo QC Pre and Post sale documentation Customer and Buyer release Sale of assets Required Qualifications And Experience Skill & Knowledge Relationship Building Negotiation Skills Education Min Graduation with relevant experience in the industry. Experience Industry Experience like – Two-wheeler three wheeler and four wheeler industry should be enough.

We are looking of a Assistant Manager QC for a pharmaceutical company located in Dera basi (Punjab) Qualification: M.Sc (Chemistry) /B pharma Experience : 7 years to 10 years Interested candidate may call@7888488054 Job Type: Permanent Pay: ₹55,000.00 - ₹60,000.00 per month Benefits: Provident Fund

Title Quality Assurance & NDE Engineer 10-15 years of relevant Experience with more than 8 years in a major EPC organization in a similar role. Should be conversant with ISO 9001 Quality Systems Requirements. Expertise in performing Internal and external audits, Shop surveys, New vendor evaluation surveys. Investigating and documenting non-conformances (NCRs), developing corrective and preventive actions, and tracking their closure. Verifying that all project activities comply with relevant standards, codes, and regulations. Maintaining accurate records of quality inspections, audits, and non-conformances, and reporting on quality performance to project management. Experience with EPC quality documentation like Project Quality Plan, ITPs, identify key procedures and monitor implementation Exposure to Rotary equipments, instrumentation items and package items is a must. In-depth knowledge of fabrication practices, QC methodologies, witnessing equipment pressure testing and final inspection. Exposure in inspecting ASME Code Stamped equipment. In-depth knowledge and experience in Quality Control aspects of Raw Materials, Receiving Inspection, Fabrication Inspection, Final Inspection and Documentation. Creating and maintaining the project's quality management system, including quality plans, procedures, and work processes. Developing and Implementing NDT Procedures Performing and/or overseeing NDT inspections, analyzing results, and ensuring accurate reporting. Providing expert advice and support to engineering, construction, and other teams on NDT-related matters. Evaluating and qualifying NDT vendors and subcontractors. Assisting in resolving technical issues related to NDT processes Certifications Certifications in Lead Auditor is must. Level III Certification in PT, MT, RT and UT under ASNT are desirable Certification in Refractory / Painting is desirable CSWIP or equivalent welding certification is preferred R2110581