106 Jobs in Dholka

Job Purpose This position is open with Bajaj finance limited Duties and Responsibilities Responsibilities: Responsible for overall branch operations,performance & profitability of the branch. Drive & participate in field-marketing activities of various financial products along with the team to improve brand visibility Plan,conduct & monitor the branch & field level marketing activities to ensure health pipeline of leads resulting into business conversion & branch growth Focus on customer engagement for new customer acquisitions & retainment of old customers Conducting error free valuation & appraisal of gold ornaments being pledged in branch with correct weight & purity assessment as per company policy and auditory compliance Joint custodian of the Vault with responsibility of safekeeping of of pledged securities as per company policies Responsible for keeping NPAs in control through strong follow-ups from the customers for interest collections Good planning abilities are required for smooth functioning of the branch & for developing cohesiveness within the company and co-workers. Hiring, coaching, mentoring and training employees and providing them with timely feedback on their performance Maintaining quality & performance of the business, preparing various reports of the same and take necessary actions for growth of business in branch Increase Gold Loan business, plus various other third-party products i.e., NCD's, Gold Coins sale etc. Responsible for keeping NPAs in control through strong follow-ups from the customers for interest collections. Responsible for correct valuation & maintenance of 100% process compliance at branch. Manage error free valuation & appraisal of gold ornaments being pledged in branch with correct weight & purity assessment as per company policy and auditory compliance. Required Qualifications and Experience Education & Skill Qualifications: 4-7 years of relevant experience required. Bachelors Degree/Post-graduation Degree preferred. Previous experience in gold loan banking, gold loan products, management or client service preferred. Consistently demonstrates clear and concise written and verbal communication skills.

Role: Pre-Clinical Pathology Lab Executive Job Location: Dholka (Near Ahmedabad), Gujarat Experience: 3-5 Years Job description: Core responsibility related to GLP:  Planning and execution of blood collection from various laboratory animals  Monitoring anesthesia / euthanasia of laboratory animals  Planning for necropsy examination.  Preparing and conduct of necropsy examination of laboratory animals.  Responsible for conducting and monitoring of tissue trimming, processing, block making, sectioning, slide staining of various studies.  Histopathological slide reading for toxicity and efficacy studies.  Responsible for monitoring Histopathological slide preparation  Slide reading and Histopathological report preparation of various Pre-clinical studies as a study pathologist.  Conduct and monitor various clinical chemistry, hematology, coagulation parameters & urine analysis.  Monitoring microscopic evaluation of urine samples  Implementation and maintenance of high standard quality control check external as well as internal for in house biochemical analysis.  Preparing SOPs related to pathology area.  Control and supervise the maintenance and operation of various histopathology related instruments.  Review of various in-house test results.  Involvement in planning and execution of pharmacological evaluation projects. Individual job responsibility/ description  Allied responsibility:  Responsible for availability of the required chemicals and other related material / facility for projects.  Responsible for RQA comments on SOPs, Protocols, Reports and study audits.  Responsible for planning and execution of health monitoring of animal and employee.  Collection of samples, analysis / dispatch of samples for various analyses.  Preparation and execution of calibration schedule for pathology related equipments.  Preparation and execution of preventive maintenance schedules for pathology lab related equipments.  Any additional responsibility / activity as and when assigned by management which would not arise any conflict of interest.

INDEL MONEY PVT. LTD is looking for Internal Auditor to join our dynamic team and embark on a rewarding career journey. Develop and execute audit programs to test the effectiveness of internal controls and compliance with policies and proceduresAssist in the preparation of audit reports for presentation to senior management and the Audit CommitteeStrong knowledge of internal auditing standards, accounting principles, and financial reportingExcellent analytical and problem-solving skillsStrong written and verbal communication skillsExperience with data analytics and visualization tools a plus Disclaimer: This job description has been sourced from a public domain and may have been modified by Naukri.com to improve clarity for our users. We encourage job seekers to verify all details directly with the employer via their official channels before applying.

Role : Senior Manager Regulatory Affairs Job Description: Handling submissions in Sugam & NSWS Portal Preparation & Submission of o New Drug applications, Subsequent New Drug Applications Clinical trial application - Phase I, II, III, IV (Form CT-04) BA/BE Export application (Form CT-05) Test License application (Form CT-10, Form CT-13, Form CT-14, Form CT-16, Form-11) Manufacturing new drug & Marketing (MA) application (Form CT-21) Import new drug & Marketing application (Form CT-18) Form-40 & Form-10 application Post approval changes RCGM Submission o for R&D activities o Pre-clinical toxicity study of vaccines (Form C-1, Form C-3b) Dual use NOC application Import and export application of Narcotic & Psychotropic substance Submission of Quarterly returns to CBN, Gwalior [Note: Local Candidate required from Ahmedabad ]

Machine Operation & Maintenance:- Operate assigned machines independently as per SOPs. Perform basic troubleshooting and routine maintenance of machinery. Ensure machines run efficiently to meet production timelines and reduce downtime. Monitor machine parameters and take corrective actions proactively. Quality Control:- Ensure pouches are sealed and printed (text/barcode) as per defined quality standards. Conduct visual and functional checks on output to maintain consistency. Report any defects, quality deviations, or equipment issues immediately. Team Handling :- Manage a small team of 56 labourers. Allocate tasks based on team members’ skills and capabilities. Supervise and support labourers during shift operations. Production Execution :- Execute the production plan as provided by the production supervisor. Record shift production output, machine downtimes, and material consumption. Coordinate with maintenance and quality teams when required. Documentation & Reporting:- Maintain shift-wise logs for machine operation, breakdowns, and preventive actions. Ensure accurate reporting of shift performance to the Production Supervisor.

Shift Supervisor – Brick Production Department Location: Plot No. 282/9, Nr. Jai Parmeshwar Petrol Pump, Dholka Road, Badarkha, Ahmedabad-382260 (GUJ) Shift Timing: Night Shift (9:30 PM – 9:30 AM, 11–12 hours) Job Summary: We are looking for an energetic and responsible Shift Supervisor (Fresher to 2 years of experience) to oversee night shift operations in our Brick Production Department. The role involves supervising production activities, dispatch operations, and loading/unloading work while ensuring safety and quality standards. Key Responsibilities: Monitor and supervise daily shift activities in brick production. Oversee dispatch, loading, and unloading of raw materials and finished goods. Ensure production targets are achieved within quality standards. Allocate tasks to workers and monitor performance. Maintain shift-wise records of production and dispatch. Coordinate with maintenance/production teams for smooth operations. Follow safety protocols and ensure compliance during the shift. Report daily shift updates to the Production/Factory Manager. Requirements: Qualification: Diploma/ITI/Graduate (any stream). Experience: Fresher to 2 years (factory/production/logistics experience preferred). Basic knowledge of dispatch and material handling is an advantage. Willingness to work in night shifts (9:30 PM – 9:30 AM) . Good communication and team-handling ability. Skills: Leadership potential Team coordination Basic knowledge of dispatch & logistics Safety awareness Record-keeping & reporting Job Type: Full-time Pay: ₹22,000.00 - ₹26,000.00 per month Benefits: Provident Fund Work Location: In person

Role 1. Segment the market and identify potential direct clients, approach them and generate business through customized loan structure offerings that meet client requirements and also generate good margins for business 2. Deliver on sales targets for Business by building strong relationships in the DSA/ DST / Connector network 3. Carry out meetings and sales calls with prospective clients on a regular basis to source business 4. Drive faster TATs through effective loan sanctioning by building strong relationships with internal stakeholders in order to expand channel presence and customer base 5. Track and report on sales operations and productivity metrics, and work towards building a highperformance sales culture 6. Actively participate in initiatives and contests driven by business team 7. Customer centric approach to liasion better with customer

Position description: Acquisition of new Unsecured loans customersfrom open market Identification of quality leads fromunsecured loans & liabilities customers for Unsecured loans Assessment/evaluation of the leadsgenerated which include analyzing credit histories & simple financialanalysis by adhering to internal and external regulations Monitor installment payments andcollections of his/her customers Enhancement of relationshipwith the existing customers by cross-selling Ujjivans products as per theprofile & need of the customers Primary Responsibilities: Business/ Financials Achieve the set targets on Unsecured loans in terms of open market acquisition and existing customer conversion Work with liabilities team to focus on cross selling unsecured Location - Bharuch,Chikhli,Dholka,Kheda,Patan,Petlad,Valsad

Position: Sales Coordinator Location :- HO-Ahmadabad- Dholka Highway, - Bachelor’s degree in Business Administration, Sales & Marketing, Commerce, related field. Required Candidate profile - Experience in handling customer relations, order processing, and supporting a sales team is preferred.

Company : Cadila Pharmaceutical Ltd. About Us : Cadila Pharmaceuticals Ltd, is one of the Largest Privately- held Pharmaceuticals companies in India. Over the past seven decades, We have been developing and manufacturing affordable medicines for the patients around the world. About the Role A Regulatory Affairs Executive for the Africa market plays a critical role in ensuring products comply with regional regulations and maintaining market access across diverse countries. This position requires a blend of technical expertise, communication, project management, and analytical skills to navigate the complex regulatory landscape in Africa Responsibilities Preparation and submission of registration and re-registration dossiers as per country requirements i.e. African countries, FWA countries and Nepal Submission of various original documents for notarization, chamberization and legalization which forms an important part of dossier. Arrangement for Indent of Samples, Packing Material specimen, Impurities, Reference Standards as per MOH requirement. Establish Coordination with other departments like QA/QC, R&D, Marketing and Purchase for ensuring the filings and query response within time frame. Post approval activities: Submission of variations to the terms of marketing authorizations for finished products as per respective variation guideline. Preparation of COPP's (Certificate of Pharmaceutical Product) and FSC to be submitted to Local FDA approvals. Preparation of Tender documents. Enhance self-awareness about changing regulatory requirements. Qualifications M. Pharma/B.Pharma Required Skills Having experience in Pharmaceutical Industries in African Market

Assist Factory Manager in planning and executing daily production activities. Ensure production targets are met with optimal use of resources. Maintain daily machine-wise production and performance records. Maintenance & Downtime Reduction :- Conduct preventive maintenance of machines to minimize breakdowns. Monitor machine efficiency and coordinate with technicians for timely repairs. Maintain logs of preventive and corrective actions. Productivity Improvement:- Identify and implement process improvements to enhance productivity per person. Suggest changes in layout, processes, or materials for better efficiency. Monitor KPIs like machine uptime, output, and waste percentage. Documentation & Reporting :- Maintain accurate records of production metrics and machine-wise data. Share regular performance updates and suggest corrective actions where needed. Team Development:- Analyze and develop team members (operators and supervisors) based on skills and potential. Allocate tasks effectively and follow up on performance. Conduct on-the-job training and motivate team members continuously. Training & Continuous Improvement:- Deliver training sessions on 5S, safety practices, and process improvements. Encourage active participation of team members in problem-solving and idea generation."

Job Title: Production Machine Operators (6 Positions) Nourish Pharmaceutical Pvt Ltd is a leading manufacturer of finish dosage formulations, including tablets, capsules, and oral liquids. We are seeking skilled Production Machine Operators to join our team. Positions: 1. Granulation Operator 2. Compression Machine Operator 3. Primary Packing Operator 4. Coating Operator 5. Capsule Operator 6. Oral Liquid Packing Operator Job Descriptions: 1. Granulation Operator - Key Responsibilities: - Operate and maintain RMG (Rapid Mixer Granulator), FBD (Fluid Bed Dryer), and Paste Cattle Blender equipment - Ensure smooth granulation process and maintain product quality - Monitor and control process parameters, such as temperature, humidity, and mixing time - Perform routine cleaning and maintenance of equipment - Collaborate with production team to meet production targets - Core Skills: - Basic knowledge of granulation process and equipment operation - Attention to detail and ability to follow SOPs - Good communication and teamwork skills - Experience & Qualification: - 1-2 years of experience in a similar role within the pharmaceutical industry - Diploma or certificate in Pharmacy, Chemical Engineering, or a related field 2. Compression Machine Operator - Key Responsibilities: - Operate and maintain Fluidpack 39 station tablet compression machine - Ensure smooth compression process and maintain product quality - Monitor and control process parameters, such as compression force, tablet weight, and hardness - Perform routine cleaning and maintenance of equipment - Collaborate with production team to meet production targets - Core Skills: - Basic knowledge of tablet compression process and equipment operation - Attention to detail and ability to follow SOPs - Good communication and teamwork skills - Experience & Qualification: - 1-2 years of experience in a similar role within the pharmaceutical industry - Diploma or certificate in Pharmacy, Mechanical Engineering, or a related field 3. Blister, Alu-Alu, Strip Packing Operator - Key Responsibilities: - Operate and maintain Alu-Alu, Blister, Strip machine - Ensure smooth packaging process and maintain product quality - Monitor and control process parameters, such as blister sealing, cutting, and packaging - Perform routine cleaning and maintenance of equipment - Collaborate with production team to meet production targets - Core Skills: - Basic knowledge of packaging process and equipment operation - Attention to detail and ability to follow SOPs - Good communication and teamwork skills - Experience & Qualification: - 1-2 years of experience in a similar role within the pharmaceutical industry - Diploma or certificate in Pharmacy, Packaging Technology, or a related field 4. Coating Operator - Key Responsibilities: - Operate and maintain Auto Coater equipment - Ensure smooth coating process and maintain product quality - Monitor and control process parameters, such as coating thickness, temperature, and humidity - Perform routine cleaning and maintenance of equipment - Collaborate with production team to meet production targets - Core Skills: - Basic knowledge of coating process and equipment operation - Attention to detail and ability to follow SOPs - Good communication and teamwork skills - Experience & Qualification: - 1-2 years of experience in a similar role within the pharmaceutical industry - Diploma or certificate in Pharmacy, Chemical Engineering, or a related field 5. Capsule Operator - Key Responsibilities: - Operate and maintain ACG F9 fully automatic capsule filling machine - Ensure smooth capsule filling process and maintain product quality - Monitor and control process parameters, such as fill weight, capsule quality, and machine speed - Perform routine cleaning and maintenance of equipment - Collaborate with production team to meet production targets - Core Skills: - Basic knowledge of capsule filling process and equipment operation - Attention to detail and ability to follow SOPs - Good communication and teamwork skills - Experience & Qualification: - 1-2 years of experience in a similar role within the pharmaceutical industry - Diploma or certificate in Pharmacy, Mechanical Engineering, or a related field 6. Oral Liquid Packing Operator - Key Responsibilities: - Operate and maintain four header filling and one sealing liquid line equipment - Ensure smooth packaging process and maintain product quality - Monitor and control process parameters, such as filling volume, sealing quality, and machine speed - Perform routine cleaning and maintenance of equipment - Collaborate with production team to meet production targets - Core Skills: - Basic knowledge of capsule filling process and equipment operation - Attention to detail and ability to follow SOPs - Good communication and teamwork skills - Experience & Qualification: - 1-2 years of experience in a similar role within the pharmaceutical industry - Diploma or certificate in Pharmacy, Mechanical Engineering, or a related field Shift Time 1: 06.30 AM to 03:00 PM Shift Time 2: 03:00 PM to 11:30 PM How to Apply: If you're a motivated and skilled individual with a passion for production operations, please submit your resume to info@nourishpharma.com

Job Title: Quality Assurance Officers (4 Positions) Company: Nourish Pharmaceutical Pvt Ltd Location: Kheda, Gujarat Job Type: Full-time Nourish Pharmaceutical Pvt Ltd is a leading pharmaceutical company committed to delivering high-quality products. We're expanding our Quality Assurance team and looking for talented professionals to join us. Positions: 1. Quality Assurance Officer - Production 2. Quality Assurance Officer - QMS 3. Quality Assurance Officer - Validation & Qualification 4. Quality Assurance Document Control Officer Job Descriptions: 1. Quality Assurance Officer - Production - Key Responsibilities: - Ensure cGMP compliance in production areas - Manage and review Batch Manufacturing Records (BMRs), Batch Packaging Records (BPRs), and Master Formula Records (MFRs) in Pharma Cloud - Conduct in-process quality checks and documentation - Verify dispensing activities and line clearance - Collaborate with production team to ensure quality and compliance - Core Skills: - Attention to detail and analytical skills - Strong knowledge of cGMP, SOPs, and quality control procedures - Excellent communication and interpersonal skills - Experience & Qualification: - 0-3 years of experience in a similar role within the pharmaceutical industry - B.Pharm or M.Pharm degree in Pharmacy or a related field - Certification in quality assurance or a related field is an added advantage 2. Quality Assurance Officer - QMS - Key Responsibilities: - Manage deviations, CAPAs, and document handling - Ensure compliance with Quality Management System (QMS) standards - Conduct internal audits and facilitate external audits - Review and update SOPs, policies, and procedures - Collaborate with departments to ensure quality and compliance - Core Skills: - Strong analytical and problem-solving skills - Excellent communication and interpersonal skills - Ability to work independently and prioritize tasks - Experience & Qualification: - 1-3 years of experience in a similar role within the pharmaceutical industry - B.Pharm or M.Pharm degree in Pharmacy or a related field - Certification in quality assurance or a related field is an added advantage 3. Quality Assurance Officer - Validation & Qualification - Key Responsibilities: - Plan, coordinate, and execute validation and qualification activities - Ensure compliance with validation and qualification protocols - Review and approve validation reports and documentation - Collaborate with departments to ensure quality and compliance - Identify and mitigate risks associated with validation and qualification - Core Skills: - Strong knowledge of validation and qualification procedures - Excellent analytical and problem-solving skills - Ability to work independently and prioritize tasks - Experience & Qualification: - 1-5 years of experience in a similar role within the pharmaceutical industry - B.Pharm or M.Pharm degree in Pharmacy or a related field - Certification in validation and qualification or a related field is an added advantage 4. Quality Assurance Document Control Officer - Key Responsibilities: - Manage and maintain document control system - Implement and maintain change control system - Issue and maintain logbooks and records - Ensure plant and product documentation is accurate and compliant - Collaborate with QA team to ensure document accuracy and compliance - Core Skills: - Attention to detail and organizational skills - Basic knowledge of cGMP and quality control procedures - Excellent communication and interpersonal skills - Experience & Qualification: - 0-2 years of experience in a similar role within the pharmaceutical industry - B.Pharm, B.Sc or M.Pharm degree in Pharmacy or a related field - Certification in validation and qualification or a related field is an added advantage - All positions open for Fresher B.Pharm or M.Pharm degree in Pharmacy, Willingness to learn and grow in a quality assurance role How to Apply: If you're a motivated and detail-oriented individual with a passion for quality assurance, please submit your resume to info@nourishpharma.com

We are seeking a highly skilled and motivated Lab Assistant / Executive Research Assistant to join our materials research and procurement division focused on electronic waste (e-waste) recovery. The ideal candidate will play a crucial role in sourcing recyclable e-waste materials and supporting the recovery of precious metals like gold, silver, and other valuable components. Key Responsibilities: Procure recyclable electronic waste materials such as RAM, hard drives, motherboards , and similar items Manage and document procurement data and recovery output for analysis and reporting Assist in chemical formulation processes involving organic and inorganic substances Operate or support metal extraction and recovery processes for precious metals from e-waste Ensure lab safety standards and maintain detailed experimental and inventory records Collaborate with R&D and procurement teams for sourcing strategies and process improvements Must-Have Skills: E-Waste Management and recycling expertise Strong understanding of Organic & Inorganic Chemistry Hands-on experience in precious and base metal recovery from electronic components Technical knowledge of chemical extraction and purification methods Familiarity with components like RAM, PCBs, hard disks, and motherboards Additional Skills (Preferred): Procurement, purchase operations, and vendor development Strategic sourcing and supply chain planning in the recycling sector Experience with lab equipment, testing procedures, and chemical safety protocols Knowledge of compliance and environmental standards in waste management Job Type: Full-time Pay: ₹20,000.00 - ₹50,000.00 per month Work Location: In person

Principal Tasks & Responsibilities: Experience in handling Audit trails, User management for application like LIMS,DMS,QMS and QC lab equipment’s, manufacturing equipment’s in pharma industry Ensure smooth working & maximum uptime of Networks, Servers, various Services (like Mail, Antivirus, Backup, etc.), QC & manufacturing and Security Systems. Monitoring server performance to ensure that it meets the organization’s standards Monitoring network traffic to ensure it is secure and operating efficiently Monitor and manage Disaster Recovery activities for all critical applications. Installing and configuring new network components such as switches, routers, firewalls, intrusion detection systems (IDS), load balancers, VoIP phones, wireless access points (APs), and other networking hardware devices Handling security issues such as server failures, computer viruses, and unauthorized access attempts Providing technical support for users who have questions about their accounts or who have technical problems with their computers Administration and monitoring firewall, servers and network devices, monitoring and analyzing device/server logs for any suspicious activities. Desired Skillset: Hands-on knowledge on technologies related to QC & Manufacturing equipment with CSV knowledge in Pharma industry Hands-on knowledge on technologies related to network (active & passive) activities, security activities (network level and server level) Working knowledge on server management and SAP setup. Working knowledge on systems like EDS, SIEM, EDR/XDR, IAM, SDWAN, Microsoft AD, DNS, DHCP, Segmentation, VLAN, LAN, WAN etc., Working knowledge on administration activities related to systems like Email, O365, SharePoint, Power-BI, Audio/Video, Collaboration tools.

Procurement & Buying Cycle: Manage the entire buying process from vendors (manufacturers/distributors) to the DCs. Raise purchase orders in SAP and track timely receipt of goods. Ensure quick turnaround time from order placement to goods receipt. Stock Planning : Implement the process for stock planning: Monitor opening stock, sales trends, and required reorder quantity. Ensure optimal inventory levels to meet demand without overstocking. Maintain appropriate stock levels in line with FMCG norms. SAP Operations: Process and rectify issues related to barcodes, MRP, case lots, offers, etc in SAP. Ensure all transactions are recorded and traceable within the system. Vendor Sourcing & Management: Source reliable and cost-effective grocery vendors. Maintain and enhance relationships with suppliers for cost, quality, and delivery efficiency. Ensure vendor compliance with company policies and service expectations. Category Coordination: Coordinate with the category team at HO and store integration team for alignment of product demand and supply. Ensure the fill rate at DC meets operational standards and supports sales goals. Market & Product Knowledge: Keep up to date with grocery pricing trends, quality benchmarks, and local consumer preferences. Support the growth of DC-attached manufacturers and suppliers. MIS & Reporting: Prepare regular reports including: Company growth reports Stock & discount reports Debit note summaries Share performance updates with seniors regarding vendor discounts, stock growth plans, and inventory.

Review and verify batch manufacturing records (BMR), batch packaging records (BPR), and other GMP documents. Perform line clearance activities during manufacturing and packaging to ensure readiness and compliance. Support the QA team in root cause analysis and implementation of corrective and preventive actions. Assist in issuance, retrieval, and archival of quality documents in accordance with document control procedures. Perform routine GMP audits and hygiene inspections in production, warehouse, and QC areas. Job Types: Full-time, Permanent, Fresher Pay: ₹15,000.00 - ₹20,000.00 per month Benefits: Paid sick time Provident Fund Work Location: In person

Role & responsibilities Finishing/ processing report data Sheet Management Manage all the products Quality related data throughout the Process from start to End ( From Calendaring to inspection of Goods) SAP System (Report records) Maintaining Physical Record of Finished material Quality reports of semi-goods material use for manufacturing final product with qualitative results. Man power handling and their allocation Assure About Quality Manage Consistency of the Product at individual Stage of Manufacturing by comparing physical parameters against standard Parameters. Matching specified product with last supply for same customers to satisfy and maintain quality for consistency Decision making Pass or Fail the Semi-goods material which is using for manufacturing the product Evaluate the product at every phase from starting to end related to quality. Analysis physical parameters of the product, through the record and resolve problems related to quality of product. Improvement the product quality Analysis the customer complaint due to quality and take corrective action in next production Try to overcome regular occurring defects in to regular product by attending it and analysis that.

Ensure efficient operation and maintenance of Utility (Boiler, chilling plant, Air compressor, cooling tower and N2 System). • To ensure strict compliance of cGMP requirements & Good Engineering Practice requirements besides other statutory laws, rules and regulations. • To implement Cost reduction measures in the operation of the Utility. • To prepare and maintain SOP and documents related to machine operation and maintenance. • To identify probable cause/potential non-conformity to any breakdown/abnormal condition. • To perform breakdown maintenance activity as and when applicable. • Review machine operation related documents and equipment log books. • To prepare schedule for planned activities like preventive maintenance, filter replacement, pump changeover, and to ensure execution as per defined schedule. • To help QA team in equipment validation/qualification, and review of concerned documents. • To ensure effective engineering support to help all the production facilities located at Dholka.To maintain safety practice during plant operation and maintenance.

HPLC Analyst Job Description (QC Department) 🧪 An HPLC Analyst in a Quality Control (QC) department is responsible for performing high-performance liquid chromatography (HPLC) testing on raw materials, in-process samples, and finished products to ensure they meet quality and purity standards. This role is crucial for maintaining the integrity and safety of pharmaceutical, food, or chemical products. Key Responsibilities Sample Analysis: Perform routine and non-routine analysis of samples using HPLC systems. This includes sample preparation, method execution, and data acquisition. Method Development & Validation: Develop and validate new HPLC analytical methods or optimize existing ones for new products or processes. This involves creating and executing protocols to demonstrate the method's accuracy, precision, and robustness. Instrument Maintenance: Conduct routine maintenance, calibration, and troubleshooting of HPLC equipment and other lab instruments to ensure their proper functioning and data accuracy. Documentation & Reporting: Meticulously document all analytical work, including raw data, results, and observations, in lab notebooks or LIMS (Laboratory Information Management System). Prepare and review reports, certificates of analysis (CoAs), and other quality documents. Compliance & Audits: Ensure all work is performed in compliance with Good Manufacturing Practices (GMP) , Good Laboratory Practices (GLP) , and standard operating procedures (SOPs). Participate in internal and external audits to demonstrate compliance. Data Integrity: Maintain the integrity of all data generated. Review and approve data from junior analysts and ensure that all records are complete, accurate, and traceable. Troubleshooting & Investigation: Investigate out-of-specification (OOS) or out-of-trend (OOT) results, identify the root cause, and implement corrective and preventive actions (CAPA). Required Qualifications Education: A bachelor's or master's degree in Chemistry, Biochemistry, or a related scientific field. Experience: 2-5 years of experience working with HPLC and other analytical techniques in a QC, R&D, or manufacturing environment. Experience in a cGMP-regulated industry is highly preferred.

Verify Receipt of Raw Material & Packaging Material for stores. • Verify SAP data entries like GRN, Issuance, Transfer posting, reservations, SAP report generation etc. • Verify the environmental parameters like Temperature, RH, pressure difference etc. • Verify Daily verification of weighing balance and daily documentation. • Verify Reconciliation of materials. Stock verification with internal and external auditors. • Verify to Maintain of Rack location in SAP as per physical. • Verify Preparation of packing list and keep ready the material for Ethiopia. • Verify timely dispatch of material to Loan license and Ethiopia plant. • Verify handling of retest, rejected, expired materials. • Co-ordinate with quality control / production / maintenance /QA / SCM/ Purchase / Contract Mfg etc. departments. For smooth functioning of stores activities. • Compliance to cGMP with respect to regulatory standards. • Maintaining & verify the proper housekeeping in Stores area. • Training attends as per schedule. • Revise or change the Store SOP for comply to any Audit/ for as per time schedule. • Ensure receipt and on-line documentation of the materials received as per SOP. • Ensure all the operating systems are maintained as per the SOP. • To receive the materials as per the amended approved vendor list. • Ensure no loss of production due to non-availability of dispensed materials. • Ensure clearance of obsolete, rejected and Artwork change materials on timely basis with coordination with Planner. • Ensure to carry out GMP self-inspection within the department once in a month and compliance on the observed deviations. • Ensure no major observation during internal as well as external audits • Ensure 100% compliance to the existing and no unplanned deviation on the shop floor • To review and correct gaps between SOP and policies and implement the audit (internal & external) findings.

Job Title : Senior General Manager - RA (DCGI) Location : Dholka, Near Ahmedabad, Gujarat Job Profile: •Liaison with regulatory authorities/government bodies, coordination with customers/consultants - DGCI and India Regulatory bodies •Provide regulatory advice to cross-functional departments right from the development stage leading to a scientifically sound regulatory submission within committed project timelines •Provide regulatory inputs and frame up strategy of regulatory submission during business development discussions with international customers and the International Marketing Division •Guidance to the regulatory/quality team to perform their respective functions efficiently and accurately. Identify team member's capabilities to perform and assign additional responsibilities accordingly. Adopt the role of a mentor to team members both personally and professionally. •Facilitate in preparing compliance to GMP audit observations for own facilities •Guide cross-functional departments on the implementation of systems for regulatory expectations and compliance •Review of technical and investigation reports, summaries for adherence to regulatory guidelines and to provide guidance to cross functional technical teams for the requirement and content of regulatory documentation •Evaluation of Day to Day operational issues w.r.t regulatory implications and providing short term and long term mitigation measures

Job Title: Research Associate – Analytical Development Laboratory (ADL) Department: Research & Development (API Manufacturing) Location: Dholka, Ahmedabad, Gujarat Position Summary: We are seeking a highly skilled and detail-oriented Research Associate – ADL to join our API R&D team. The selected candidate will be responsible for the development, validation, and transfer of analytical methods for Active Pharmaceutical Ingredients (APIs). The role plays a critical part in ensuring product quality, supporting process development, and facilitating regulatory compliance across the API lifecycle. Key Responsibilities: Develop and validate analytical methods for raw materials, intermediates, and APIs using techniques such as HPLC, GC, UV, IR, KF, and titration. Support API process development teams by analyzing in-process samples, final products, and impurities. Characterize degradation products and impurities using advanced analytical tools (e.g., LC-MS, GC-MS, NMR – if available). Perform routine and non-routine analysis to support R&D, stability studies, and method transfer activities. Conduct analytical method transfers to QC and manufacturing sites (internal or external). Prepare and review analytical documentation, including method validation protocols, reports, SOPs, and COAs. Ensure adherence to GLP, cGMP, and data integrity standards during all analytical activities. Maintain laboratory instruments and troubleshoot minor issues to minimize downtime. Participate in OOS investigations, deviations, and CAPA implementations. Collaborate closely with cross-functional teams including process chemistry, regulatory affairs, and quality assurance. Qualifications: M.Sc. in Analytical Chemistry / Organic Chemistry / Pharmaceutical Chemistry or related discipline. 2 to 5 years of experience in ADL for API R&D.

Responsible for operating ampoule filling and capping machine at Dholka premises. • Should have knowledge of Operating and maintenance of ampoule filling • To do aseptic and processing area entry exit procedure properly with proper gowning. • Should have knowledge of working in aseptic and processing area. • Repair and maintenance of all machines of parenteral manufacturing area. • To check and ensure that differential pressure and Temperature of the aseptic area and processing area are within limit and record it properly. • To check and ensure that pressure differential of all Laminar Air Flow are within limit and record it properly. • To check on line in process parameters like temperature, RH, DP, fill volume, quality of sealing at specific interval as mentioned in respective MMDI and SOPs. • To ensure proper inter personal relationships (IPR) in the section. • To ensure proper cleaning of the working areas. • To ensure proper status labeling as per Sop. • To ensure the all required documents to comply cGMP. • Reporting to Shift In charge for routine activities & special assignment given by seniors. Submit reports on performance and progress • To ensure calibration certificates of all measuring instruments comply with norms. • To review daily production and to discuss other issues."

📢 We’re Hiring – Quality Inspection Engineer Shree Hans Alloys Ltd. is looking for a Quality Inspection Engineer to join our team. Location: Ahmedabad / Dholka Department: Quality Assurance / Inspection Engineer 🔹 Responsibilities: Conduct dimensional and visual inspection of castings and components Ensure compliance with applicable standards and client specifications Prepare inspection reports, maintain documentation, and support audits Coordinate with production and QA teams for corrective actions 🔹 Requirements: Diploma/Degree in Mechanical/Metallurgy/Production Engineering 2–5 years of relevant experience in quality inspection (preferably in foundry/valves industry) Knowledge of NDT methods, ISO/QMS standards will be an advantage 📧 Interested candidates may apply by sending their resume to hr@hansalloys.com