1478 Jobs in Ankleshwar - Page 4

Interview Scheduled for Below Position for MNC Engineering Company in Dahej on 09-09-2025, Tuesday on Permanent Role Fabrication Fitter Tube Filling & Fin Machine Operator Apply on sdpbharuch@gmail.com with Subject: MNC Dahej & Call on 7600033423 Required Candidate profile Interview Venue SDP HR SOLUTION 611, Golden Square Bs DMART, Near ABC Circle, Bholav, Bharuch Interview Time: 09:00 AM to 03:00 PM NO CHARGES !!! Share with your friends Perks and benefits Transportation Canteen Mediclaim Uniform

Job Description: Data Entry / Back Office Please call on the given number to apply 08375858125 Role: Accurately enter, update, and manage financial data in banking systems. Key Responsibilities: Ensure data accuracy, integrity, and confidentiality; verify and cross-check information. Qualifications: 10th, 12th, Graduation, Under Graduation and Any Diploma. Skills Required: Go od communication and basic knowledge. Experience: Freshers are welcome. Please call on the given number to apply 08375858125

As a Senior QA Officer, your role will involve various responsibilities to ensure quality assurance within the API pharma industry. You will be tasked with issuing Batch Manufacturing Records, equipment cleaning records, logbooks, and analytical reports for raw materials, finished products, and packing materials. Additionally, you will assist in the preparation of SOPs for different departments and conduct plant rounds to verify documents according to cGMP and GLP norms. Line clearance activities for manufacturing and packaging, issuing deviation forms, change control forms, and handling customer complaints will also be part of your duties. You will review and verify analytical and Batch Manufacturing Records, participate in audits and inspections, and ensure data integrity as per procedures. Maintaining documents and records, controlling SOPs and departmental documents, and preparing for internal and customer audits are crucial aspects of the role. You will also oversee activities related to manufacturing, store, and QC, as well as prepare vendor lists, conduct traceability activities, and manage CAPA logs. Ensuring compliance with equipment maintenance, calibration, and training on cGMP and GLP will be essential. Investigating deviations, product complaints, and environmental incidents, as well as conducting process validation and equipment qualification, will also fall under your responsibilities. Your role will involve preparing annual product reviews, handling waste disposal procedures, and supporting environmental management initiatives within the department. Additionally, any other assignments or tasks allocated by the Head of QA will be expected from you. If you are interested in this position or have a suitable reference, please contact Jyoti at 8657017223. This is a full-time job with day shift hours, based in Ankleshwar.,

Wanted Cardiologist for hospitals in Uttarakhand, Gujarat . fresher or experienced Education - DM, DNB. Salary 300000 to 500000 Rs Per month. Salary Negotiable.

Lead deviation and market complaint investigations, with timely CAPA execution Ensure effective implementation and tracking of CAPAs from deviations & complaints Review Batch Manufacturing & Packing Records, APQR, and SOPs Candidate stability Required Candidate profile Manage Change Controls Validations Qualifications, and QMS documentation Conduct regulatory gap assessments and support compliance plan execution Strong understanding of cGMP, investigation tools

Greetings from Kotak Life Insurance!!! Here is an excellent opportunity to get associated with the leading brand Interested candidates can email their resumes to kli.aarti-choudhary@kotak.com or Whatsapp on 9082268319 1. The incumbent will formulate and implement sales plan for the partner for achieving business targets of sales unit. Lead, motivate and train the partner. 2. Set and monitor clear objectives to achieve the agreed sales targets for the partners. 3. Help partners to generate and track leads, close sales. 4. Help partners to upsell and cross sell to customers basis need analysis 5. Help the partner facilitate their training on an ongoing basis to ensure a productive channel at all times 6. Take regular feedback from partners and customers on satisfaction on selling process and products 7. Review Sales plan of the partner and support their growth. 8. The candidate will be on the payroll of Kotak Life Insurance and will be sitting in Bandhan Bank Perks and Benefits: Attractive Incentives and Travelling allowance

Position Title: Executive : Manufacturing Science and Technology (MST) Qualification And Experience POST GRADUATE IN CHEMISTRY/PHARMACY Experience: 0-7 years of Experience as an analyst/Development technologist in the Pharmaceuticals / API industry. GMP & GLP knowledge Job Overview Providing analytical support for Chemistry activities ensuring compliance to regulatory, group directives, quality requirements, safety standards to fulfill the organization’s objective, living Group’s Values and Code of Ethics Responsibilities Responsibilities: Analytical method validation: Analytical method Development Analytical method transfer, Analytical method validation CMC Activity Sampling & testing of Process water, Raw materials, Intermediates, APIs, stability samples, hold time study samples & Cleaning validation samples Sending samples to third party/customer, Preparation and approval of CoA, Generation and archival of GMP documents Preparation of system & operational SOPs using eDMS Maintaining inventory of laboratory reagents and chemicals Providing analytical support to pilot plant in case of deviation investigation Co-ordination with pilot plant & PRD to provide analytical support Investigation in case of OOS/OOT, laboratory incidence, deviation & customer complaint Impurity & reference standard qualification, Management of change control, OOS/OOT, deviation CGMP Compliance to current GMP guidelines, Follow ALCOA principal maintaining GMP data Compliance to local and international norms (Quality/HSE) Knowledge of change control and deviation management Regulatory compliance Regular Pharmacopoeia and regulatory requirement review Training of self on quality and HSE systems. Instrumentation Operation & calibration of HPLC, GC, HSGC, UPLC, UV, FITR, DSC & other laboratory instruments, Trouble shooting for said instrument Co-ordination with service provider for repairing and preventive maintenance Qualification of laboratory instruments Management of logbooks Other Complying to HSE Requirements Identifying and correcting unsafe conditions or behaviours and promptly reporting other potentially hazardous situations. Carrying out any other assignments or projects as per the instruction of the Dept. Head to meet with the organizational objectives and priorities. Requirements GMP & GLP knowledge, Good coordination & communication skills. Analytical ability, Knowledge on LIMS & QMS What makes this position unique? This position will provide good exposure to work in Analytical Method Development and validation, GMP/ GLP environment. Location Information: Ankleshwar, Gujarat, India

A bench scale chemist leads a team of chemists working on Biocides, production chemicals, intermediate chemicals and its application as scale inhibitor & corrosion inhibitor for oil and gas and industries. Required Candidate profile Practical experience of electrochemistry with experience of organic reactions by using electrochemistry technique

Lead and manage our US company’s regulatory portfolio, with a focus on biocides and other regulated products. Work directly with EPA, PMRA, and other regulatory agencies to obtain new product registrations and maintain existing ones. Required Candidate profile Partner with manufacturing teams to ensure full regulatory compliance of EPA-registered products, including labeling and production.

Position Title: Executive : Manufacturing Science and Technology (MST) Qualification and Experience: POST GRADUATE IN CHEMISTRY/PHARMACY Experience: 0-7 years of Experience as an analyst/Development technologist in the Pharmaceuticals / API industry. GMP & GLP knowledge Job overview: Providing analytical support for Chemistry activities ensuring compliance to regulatory, group directives, quality requirements, safety standards to fulfill the organization’s objective, living Group’s Values and Code of Ethics Responsibilities: Analytical method validation: Analytical method Development Analytical method transfer, Analytical method validation CMC activity: Sampling & testing of Process water, Raw materials, Intermediates, APIs, stability samples, hold time study samples & Cleaning validation samples Sending samples to third party/customer, Preparation and approval of CoA, Generation and archival of GMP documents Preparation of system & operational SOPs using eDMS Maintaining inventory of laboratory reagents and chemicals Providing analytical support to pilot plant in case of deviation investigation Co-ordination with pilot plant & PRD to provide analytical support Investigation in case of OOS/OOT, laboratory incidence, deviation & customer complaint Impurity & reference standard qualification, Management of change control, OOS/OOT, deviation cGMP: Compliance to current GMP guidelines, Follow ALCOA principal maintaining GMP data Compliance to local and international norms (Quality/HSE) Knowledge of change control and deviation management Regulatory compliance Regular Pharmacopoeia and regulatory requirement review Training of self on quality and HSE systems. Instrumentation: Operation & calibration of HPLC, GC, HSGC, UPLC, UV, FITR, DSC & other laboratory instruments, Trouble shooting for said instrument Co-ordination with service provider for repairing and preventive maintenance Qualification of laboratory instruments Management of logbooks Other Complying to HSE Requirements Identifying and correcting unsafe conditions or behaviours and promptly reporting other potentially hazardous situations. Carrying out any other assignments or projects as per the instruction of the Dept. Head to meet with the organizational objectives and priorities. Requirements GMP & GLP knowledge, Good coordination & communication skills. Analytical ability, Knowledge on LIMS & QMS What makes this position unique? This position will provide good exposure to work in Analytical Method Development and validation, GMP/ GLP environment. Location Information: Ankleshwar, Gujarat, India

Should Know how to use Corel Draw Software perfectly Job Type: Full-time Pay: ₹10,000.00 - ₹20,000.00 per month Work Location: In person

**Objective:** Install, maintain, and repair electrical systems, motors, panels, and instrumentation in a PHARMA API Manufacturing and Chemical plant environment. **Key Responsibilities:**- Troubleshoot and repair faults in MCC panels, motors, VFDs, and lighting circuits.- Conduct preventive maintenance of electrical infrastructure.- Install new plant equipment, ensuring compliance with electrical safety norms.- Collaborate with maintenance and production for equipment upgrades and shutdowns. - Maintain electrical documentation and support audit requirements. SOP etc.. **Requirements:** - ITI/Diploma in Electrical Engineering.- Minimum 7 years’ experience in PHARMA API Manufacturing /industrial/chemical plant electrical, ERP systems. - Strong problem-solving, equipment diagnostic, and safety skills. - Knowledge of hazardous area electrical requirements (ATEX/IEC preferred). - Knowledge of instrument calibration or automation integration etc.. Minimum 7+ years of experience in pharma industry Job Types: Full-time, Permanent Pay: ₹15,000.00 - ₹60,000.00 per month Benefits: Food provided Health insurance Life insurance Provident Fund Experience: Electrician: 7 years (Preferred) Work Location: In person

**Objective:** Oversee and optimize Batch and Continuous chemical processes for PHARMA API and specialty chemical manufacturing, ensuring compliance with quality, safety, and environmental standards. **Key Responsibilities:**- Plan, execute, and optimize chemical reactions and processes for production of PHARMA API and specialty chemical manufacturing, - Scale up laboratory processes to commercial production. - Troubleshoot process bottlenecks and investigate non-conformances. - Collaborate with R&D, QC, and production teams on product and process improvements. - Ensure compliance with EHS (Environment, Health, Safety) and statutory regulations. - Maintain accurate production records, reports, and batch documentation. **Requirements:** - Master’s/Bachelor’s degree in Chemistry or Chemical Engineering. - 7+ years of production experience in PHARMA API and specialty chemical manufacturing - Strong understanding of process chemistry, scale-up, and safety. - Problem-solving, analytical, and team leadership skills. - Person should be able to handle entire production activities. - He has knowledge about GMP documentation & able to maintain all documents as per SOPs. - He has good exposure to handle all trouble shoot related to plant operation. - He is able to closely coordinate with QC on quality related aspects. - He has good experience to handle team & manage shift & production planning. - He is able to work based on given timeline of sales & marketing. - He is able to closely coordinate with QA team on all documentation & deviation if any happened in Plant. - He has exposure & experience to give training to plant & operational people. - He has good exposure to face audit of customer & regulatory. - He is able to work as per given management timeline of production & planning. Job Types: Full-time, Permanent Pay: ₹25,000.00 - ₹75,000.00 per month Benefits: Food provided Health insurance Provident Fund Education: Bachelor's (Preferred) Experience: total work: 5 years (Preferred) Work Location: In person Application Deadline: 24/07/2024

**Objective:** Assemble, install, maintain, and repair pipelines, pumps, filters, reactors, and other plant machinery essential for Pharma API and chemical production. **Key Responsibilities:** - Align and fit mechanical equipment (pumps, valves, pipelines) as per technical drawings. - Perform maintenance, repair, and overhauling of plant machinery. - Diagnose and rectify equipment faults or leaks in piping systems. - Collaborate with electricians and operators on plant shutdowns and installs.- Comply with safety standards and complete job documentation. **Requirements:** - ITI/Diploma in Mechanical Fitting or related field. - 7+ years’ experience in process plant fitting, preferably pharma api and chemical production manufacturing. - Knowledge of preventive/predictive maintenance and use of tools/measurement instruments. - Strong focus on safety and teamwork. fill maintenance sop, etc.. Job Type: Full-time Pay: ₹15,000.00 - ₹50,000.00 per month Benefits: Food provided Health insurance Life insurance Provident Fund Work Location: In person

Minimum 7+ Years experience in Pharma Company Production , knowledge of Fill BMR and Plant SOP Knowledge Of All Raw Material Handling knowledge Of SAP / ERP Software **Objective:** Operate Chemical process equipment for the manufacturing of Pharma API specialty chemicals, ensuring safety, quality, and efficiency. **Key Responsibilities:** Start-up, monitor, and shut down reactors, blenders, filters, dryers, and associated utilities. - Weigh, measure, and load raw materials as per batch instructions. - Monitor process parameters and log deviations, responding to alarms and process changes. - Sample intermediates and finished goods for QC testing. - Conduct equipment checks, basic maintenance, and cleaning. - Adhere to safety regulations and use of PPE. **Requirements:**- ITI/AOCP/Diploma in Chemical Engineering or related field. - 7+ years’ plant operation experience, ideally in PHARMA API PRODUCTION PLANT or Chemical Manufacturing. - Sound knowledge of DCS/PLC/ERP Systems, batch operations, and handling hazardous chemicals. - Safety-conscious and Physically fit. Job Type: Permanent Job Type: Full-time Pay: ₹20,000.00 - ₹50,000.00 per month Benefits: Food provided Health insurance Life insurance Provident Fund Work Location: In person

End-to-end recruitment & onboarding Employee lifecycle management Maintain HR records & database Payroll, attendance & leave management Performance reviews & engagement Compliance with laws & policies Handle employee queries & grievances Required Candidate profile Bachelor’s in HR / Business Administration 1–2 years of HR experience Strong communication & interpersonal skills Proficient in MS Office & HR software Detail-oriented & people-focused

Experince in process engineering. Experience of handling multiple vendors for outsourced processes Management of functions at the assigned vendor site with respect to jobs being outsourced to vendors- in order to ensure the job outsourced is in lines with required quality within the projected cost and timelines Overall Project Management of assigned off loaded Jobs to ensure time, cost and quality parameters are met. Offloading of job after consultation with reporting Manager. Ensuring stage wise inspection of job by QC inspector and on site pre FAT/FAT wherever applicable. Clearify priorities in case of multiple jobs to vendor. Ensure scope of material supply is on time, timely follow-up with materials. Ensure Soft copy archiving of Job data. Ensure job status is updated and forwarded to PMO for further information to the client. Ensure assigned jobs are reviewed with reporting Managers, deviation in target dates and action plan to bring the job on track

Role & responsibilities Position : Service Engineer Qualification : Diploma / BE Mechanical Experience : 3 to 7 Years Location: Jaipur / Kota / Ankleshwar / Nagpur Reporting to : Manager Have Experience in to bag filters Have Experience in to Air pollution control Have Experience in to Pneumatic Conveying Have Experience in to Industrial Grinding Best regards Mamta Mevada Recruitment consultant Mobile: +91 9904900177 Email: bdq5@uhr.co.in

Interview for ETP / MEE Chemist for Dahej Chemical Co on 08-09-2025, Monday Qualification: ITI LACP / BSC Chemistry Experience: 1 to 6 Years CTC: Up to 5 LPA Send CV on sdpbharuch@gmail.com with Sub : ETP QC Dahej & Call on 7600033423 No Charges Required Candidate profile Interview Venue: SDP HR SOLUTION, Sixth Floor, 611, Golden Square, Beside DMART, Near ABC Circle, Bholav, Bharuch - 392001 FREE JOB SHARE IN YOUR FRIENDS

As a passionate and experienced Speech and Drama Trainer, you will play a crucial role in developing students" communication, performance, and public speaking skills. Your responsibilities will include creating engaging and creative lessons to enhance voice modulation, articulation, expression, body language, and stage presence for both individuals and groups. You will be instrumental in preparing students for competitions, exams, and performances, all while fostering a supportive and motivating learning environment. Your key responsibilities will involve developing and implementing structured curricula for speech and drama classes, conducting individual and group lessons focusing on voice, speech, and performance skills, designing activities that promote confidence, creativity, and effective communication, providing constructive feedback and personalized coaching to students, and preparing students for exams, competitions, and public performances. To excel in this role, you should possess a Bachelor's or Masters (preferred) degree in English, Performing Arts, Drama, Education, or a related field. Additionally, a minimum of 6 months of experience in teaching drama, speech, or related subjects in schools/colleges is required. A strong understanding of theatre arts, public speaking, and creative expression is essential, along with experience in curriculum design and educational pedagogy. Excellent communication and storytelling abilities will further aid you in successfully fulfilling the responsibilities of this position.,

The job is located in Ankleshwar and is of a contract type. It was posted on 20th February 2025 with the reference number JPC - 105397. The ideal candidate should have 1-2 years of experience and a BE in Instrumentation & Control Engineering. They will be responsible for conducting routine preventative maintenance on instrumentation systems, which includes calibration checks and component replacements. Additionally, diagnosing and troubleshooting malfunctions in instrumentation systems, identifying root causes, and implementing corrective actions will be part of the job role. It is crucial to adhere to safety procedures during installation, maintenance, and troubleshooting activities. The candidate should possess a strong understanding of instrumentation principles and technologies, particularly in pressure, temperature, flow, and level measurement devices. Familiarity with control system architecture such as DCS (Emersons, Honeywell, Yokogawa) and PLC (Allen Bradley) along with programming skills is required. Knowledge of relevant industrial communication protocols like Modbus and Profibus is also necessary. Ideally, the candidate should have a total of 3 years of experience in the field.,

The ideal candidate for this position should possess the following qualifications: - Excellent communication skills to effectively interact with team members and clients. - Willingness to travel and work in the field as required. - Proficiency in routing protocols to ensure optimal network performance. - Hands-on experience in LAN/WAN management, VLAN creation, and configuration. - Practical skills in router and switch configuration and troubleshooting. - Ability to configure and troubleshoot VLANs and Interswitch connections. - Knowledge and experience in backup and restore of device configurations. - Familiarity with Cisco IOS upgrades and recovery procedures. - Clear understanding of CCNA concepts and certification. - Strong grasp of IP addressing and subnetting principles. - Practical experience with wireless Access Points and controller configuration. - Expertise in firewall monitoring and wireless networking. - Knowledge of server network monitoring. - Understanding of hardware such as printers and scanners. This is a full-time, permanent position with benefits including health insurance and Provident Fund. The work schedule is during day shift hours. The preferred education level is a Bachelor's degree, and candidates with at least 1 year of relevant work experience will be given preference. The work location is on-site.,

The role of Corporate QMS Manager at Zentiva involves the creation, development, and lifecycle management of the corporate Quality Management System (QMS) across the entire company. The primary responsibility is to ensure compliance with international pharmaceutical regulations, local requirements, and company operational standards in the GxP area. This position plays a crucial role in maintaining and monitoring Zentiva's QMS, driving continuous improvement, and supporting the organization's strategic objectives. Key Responsibilities And Activities: - Actively contribute to the development and implementation of a robust QMS aligned with international standards such as ICH and ISO. - Ensure compliance across all operations and drive the evolution of the QMS to support strategic objectives and business processes. - Standardize processes within the QMS to ensure consistency and efficiency across corporate operations. - Support the preparation of Zentiva Quality Manual, quality strategy, and operational principles for GxP teams. - Stay updated on international regulatory requirements and collaborate with regulatory affairs to address changes. - Write, review, comment, and approve corporate policies within the GxP scope. - Perform regular Quality Reviews between Corporate Quality and Zentiva's QMS sites. - Contribute to developing a learning platform for quality-related topics and continuous improvement. - Establish a framework for implementing Zentiva's QMS at sites, enforce local implementation, and ensure appropriate training. - Participate in internal audits at Zentiva manufacturing sites and affiliates. - Develop and deploy the Data Integrity Prevention Master Plan. - Contribute to implementing risk management practices within the QMS. Other activities: - Assure qualification and validation of all centralized GxP computerized systems in cooperation with IT. - Act as a business quality responsible for corporate IT GxP related projects. - Serve as a quality focal point/back-up for electronic document management systems and the eQMS tool. Qualifications & Required Skills: - Technical University Degree (health, pharma, technical, chemical areas are advantageous). - Minimum 8 years of experience in pharma quality, with knowledge of GxP regulations, process management, and auditing. - Proficiency in English language (written and spoken). - Ability to learn quickly, adapt, analyze, organize, and communicate effectively. - Ability to collaborate with transversal teams effectively. Join Zentiva as a Corporate QMS Manager to play a vital role in ensuring high-quality and affordable medicines reach those who depend on them every day. Your contribution will be instrumental in maintaining compliance, driving continuous improvement, and fostering a culture of excellence within the organization.,

B.Sc. or M.sc Chemist / Chemical / MIcro. Location :Surat / Navsari / Bharuch / Ahmedabad/ Vadodara Salary : 15000 to 25000 Living + Travel Free Chemical handling and disposal Analyze retrieved data and prepare reports for laboratory management Required Candidate profile Lab work to develop and improve both new and existing chemical product Mo No : +91 90816 99400 / +91 90816 88100 / 90816 99600

Main Responsibilities: Ensure timely reporting of the consolidated actual performance, forecasts and targets whilst supporting the operations with analysis, advice and tools to optimize performance. Ensuring internal finance control and processes are maintained and followed in accordance with the statutory practices. Standard cost (PK) calculation and upload, Variance analysis monthly, Support in profitability, Support in profitability, Variance analysis monthly Preparation and validation of business cases and investment proposals Cost Centre/ Product wise Profitability Reporting & Monitoring CWIP Analysis & CAPEX Monitoring Analysis of Net Working Capital (improving DIP, Obsolete Slow moving etc. ) Conduct and communicate financial analysis and reporting with relevant stakeholders to increase awareness leading to relevant actions and comments (monthly, quarterly, ad- hoc) Inventory Aging & analysis Country Finance Statutory, Internal & Group Audits Ensuring timely submission of data and Analysis for Group Audit , Hard close Responsible for Cost Audit Compliances Driving improvements related to internal Audit observations. Coordination with Corporate Finance Validating and monitoring various cost allocations Conducting Physical verification of Fixed Assets (once in a year) and stock take (once in a year) Follow up with the finance to ensure the cost are properly allocated among profit center Experience and required competencies: Minimum 03- 07 Years of relevant experience, SAP exposure is required Education CA /CMA/ Inter CA /Inter CMA/MBA (Finance)