1478 Jobs in Ankleshwar - Page 6

As a Project Engineer specializing in pharmaceutical machinery manufacturing at CoralPT Worldwide Pvt. Ltd., located in Ankleshwar, Gujarat, you will play a crucial role in managing projects from inception to completion with a focus on quality, efficiency, and adherence to industry standards. Your expertise in Blenders, Stainless steel reactors, fluid bed dryers, RMG/HSMG, Tray dryers, and other pharmaceutical equipment will be instrumental in ensuring the successful design, development, and execution of projects related to pharmaceutical machinery. Your key responsibilities will include overseeing the installation, commissioning, and validation of equipment, collaborating with cross-functional teams, utilizing AutoCAD for drafting technical drawings, monitoring project timelines and budgets, coordinating with vendors, troubleshooting technical issues, ensuring compliance with industry regulations, preparing technical reports, and mentoring junior engineers. To excel in this role, you should hold a Bachelor's Degree in Mechanical Engineering, Industrial Engineering, or a related field, along with at least 5 years of project management experience in pharmaceutical machinery manufacturing. Proficiency in AutoCAD, strong project management skills, excellent communication, leadership abilities, knowledge of GMP, FDA, and regulatory requirements, problem-solving capabilities, and willingness to travel for site visits are essential requirements. Preferred qualifications include experience in process automation, certification in Project Management, and familiarity with 3D modeling software. In return, we offer a competitive salary, performance-based incentives, opportunities to work on cutting-edge projects, professional development prospects, and health and wellness benefits. If you are ready to take on this challenging yet rewarding role, please submit your resume and cover letter to recruitment@coralpt.com with the subject line "Application for Project Engineer Pharma Machinery." Join us in our mission to provide sustainable and cost-effective solutions to various industries through innovative pharmaceutical machinery manufacturing.,

post : safety officer loct ; ahamadabad GJ Ankleshvar GJ construction site @ power plant accomadation free salary ; depending knowledge & exp

Process, Process Planning, PFD, P&ID, Must have exp. in Pharma, Male and female both required

1. Production: Coordinate and manage the activities of the production shift to ensure optimal productivity and efficiency. Supervise and provide guidance to a team of production operators, assigning tasks and monitoring their performance. Monitor production processes, troubleshoot issues, and implement corrective measures to minimize downtime and maximize output. Collaborate with other departments, such as Quality Control and Maintenance to address production-related issues and smooth operations. Maintain accurate records of production data, including output, downtime, and any deviations from quality standards. Conduct regular inspections of equipment and machinery, identifying maintenance needs and coordinating repairs or servicing as required. Implement and enforce company policies and procedures, including quality standards, safety guidelines, and operational protocols. 2. Quality: To ensure best quality products and produced without any batch failure and to ensure compliance. 3. Safety: To ensure Safest workplace and Safety in each operation of Plant and ensure compliance with safety regulations and promote a safe working environment for all employees. 4. Housekeeping & TQM: To ensure best housekeeping as per standards of 5S. Activity involved in driving the TQM culture in the plant. 5. Manpower: To manage manpower and ensure efficient work from them.Responsible for yield improvement projects, cost optimization, reduction in breakdown, capacity utilization improvement, batch cycle time reduction, improvement in planning and working. Participation in DWM, 5S, AM, ensure ZLD and other parameters pertaining to operational efficiency.

specialization engineering in costing, Expertise in material specifications, cost controlling, monitoring expenditures & identifying cost saving opportunities.

Responsible to Plan, Execute & Perform Maint Activities-Preventive, Predictive & BD maint, Utilities operation, Provide technical expertise to Maint team, ISO/ Safety norms Compliance, Project Work, Equipment selections, Energy Saving, manpower Mgt. Required Candidate profile BE/B.Tech(Mech) with 14 to 20 yrs relevant exp in Chemical industry. Should have handled Chemical Plant Maint & Utility O&M independently. Should be dynamic, result oriented with communication skill. Perks and benefits Negotiable

Responsible for instrumentation Dept. functions Maintenance/ Calibration of all process instrument related to Flow/Level/ Pressure & Temperature, Maintenance/troubleshooting of process plant instruments, control system of utilities, DCS / PLC etc. Required Candidate profile Diploma (Inst) with 4 to 8 yrs exp in chemical industry having DCS/PLC system. Working knowledge of Installation, Commissioning & Fault diagnosis of all process instruments, Foundation Field bus etc

Responsible for instrumentation Dept. functions Maintenance/ Calibration of all process instrument related to Flow/Level/ Pressure & Temperature, Maintenance/troubleshooting of process plant instruments, control system of utilities, DCS / PLC etc. Required Candidate profile Diploma(Inst) with 4 to 8 yrs exp in DCS/PLC based chemical industry. Should have working exposure of Fault diagnosis of process instrumentation, Foundation Field bus, Smart positioner & project work. Perks and benefits Negotiable

Responsible for complete monitoring production related activities in PLC based plant in shift, planning & execution of jobs, manpower management, compliance of safety, Environment & ISO standards, Co-ordination with service departments etc. Required Candidate profile BE(Chem) with 2 to 4 yrs relevant working exp in Chemical industry. Should have working exposure of continuous process, distillation, Solvents handling. excellent communication & leadership skill. Perks and benefits Negotiable

Responsible for Product Costing, Budgeting & MIS, Performance & Variance report, Budget Analysis, Stock Valuation & Inventory Mgt, BOOT information systems, Legal compliance, Internal & Statutory Audit, Cost reduction /Savings, SAP etc. Required Candidate profile Should be CMA/ ICWA with 6 to 9 yrs exp in reputed chemical industry. Should have Sound knowledge in Cost Analysis, MIS & budgeting and excellent analytical & communication skill Perks and benefits Negotiable

Responsible for entire packing process, Timely sampling & Inspection of packaging Matl, FG & Export container, compliance of SAP, HSE & NABL norms, Design & development of new packaging system, NC intimation to prodn, Packaging Quality Manual, MIS.. Required Candidate profile B.Sc/M.Sc & Dip Packaging with 10 to 15 yrs exp In packing dept of Chemical/Pharma industry. Capable to participate in controlling emergency situation in plant. Knowledge of QMS/ EMS/ISO/SAP is must Perks and benefits Negotiable

Responsible for the Safety functions like compliances of Safety standards, accident investigation & Analysis,Safety Training/ inspection/ documents, Work Permit, Plant Round, Safety Preventive Measures, Risk Assessments, EHS committee meetings etc.. Required Candidate profile M.Sc/B.Sc with Diploma in industrial Safety & having 4-8 yrs experience in reputed Chemical/Bulk Drug industry. He should be dynamic & result–oriented with excellent communication & leadership skill. Perks and benefits Negotiable

Responsible for sourcing of Raw Materials, chemicals, lab chemicals & accessories, getting price quotes, provide costings for key RM & initiate procurement strategies/schedules, Vendor Development, techno-commercial negotiations, Maintain ARC/AMC etc Required Candidate profile B.Sc/M.Sc/BE(Chem) with 3 to 6 yrs exp of chemical procurement in chemical/pharma industry. Should have sound exposure of ISO/NABL & GLP compliance documentation & modern sourcing tools/information. Perks and benefits Negotiable

About The Role JOB ROLE Develops new and expands existing High Net worth Customer relationships for liabilities by sourcing customers. Sources new bank customers through external individual efforts and acquisition channel. Cross sells bank products to existing set of Branch customers which are mapped. Informs customers of new products or product enhancements to further expand the banking relationship. Plans and conducts special sales initiatives and events for prospective and existing clients. Coordinates with other group companies to provide seamless access to other products. Maintains complete relationship record for assigned customer accounts. Tracks customer complaints/queries and turnaround times for customer satisfaction JOB REQUIREMENT Graduate - 3 -5 years of experience Post Graduate - 2 -3 years of experience Customer orientation High energy and drive AMFI / IRDA certified is preferred

• Responsible for shift planning. • Responsible for smooth running of operation as per SOP, troubleshooting during emergency. • Responsible for handling day to day operations and knowledge of maintenance. • Ensure smooth running of all machineries. • Responsible for handling control room operations. • Should posses excellent co-ordination skills with maintenance, QC, waste preparation, stores and other departments. • Ensure preparation of work permit. • Responsible for training of operators and labour and work place safety.

QC

QA

QA

Job Title: Assistant Manager - Quality Compliance (Supplier Quality Assurance) Department: Quality Compliance Reports to: Quality Compliance Manager Location: Ankleshwar Position Type: Full-time Qualifications And Experience Education: B.Pharm / M.Pharm / M.Sc in Chemistry, Biotechnology, or related field. Experience: Minimum 6–8 years of experience in Quality Assurance / Quality Compliance within the pharmaceutical industry, with at least 2 years in a Supplier Quality Assurance role. Preferred: Exposure to regulatory inspections (e.g., USFDA, MHRA, TGA), and experience in working with global suppliers. Job Purpose To lead and manage Supplier Quality Assurance (SQA) activities ensuring all third-party suppliers, vendors, and contract manufacturers comply with applicable regulatory requirements, company quality standards, and Good Manufacturing Practices (GMP). The role involves oversight of supplier qualification, audits, risk assessment, and continuous quality improvement initiatives within the pharmaceutical supply chain. Key Responsibilities Supplier Quality Management: Develop, implement, and maintain a robust supplier quality assurance system aligned with cGMP and regulatory requirements (e.g., USFDA, EMA, WHO). Lead supplier qualification, requalification, and performance monitoring programs. Conduct risk-based assessments and ensure supplier categorization based on product and service criticality. Auditing & Compliance Plan, conduct, and follow up on supplier audits (on-site and remote) for API, excipient, packaging, and service providers. Evaluate audit findings, identify gaps, and oversee closure of CAPAs with suppliers. Maintain audit schedules, records, and ensure timely reporting. Maintenance of Approved Supplier List / GMP documents / Supplier files Quality Agreements & Documentation Coordinate the drafting, negotiation, and maintenance of Quality Agreements with suppliers. Review supplier documentation such as CoAs, TSE/BSE statements, stability data, and regulatory filings for compliance. Ensure all supplier documentation is up to date and archived as per data integrity principles. Regulatory Support Support regulatory inspections and provide supplier-related documentation during audits. Monitor regulatory changes and ensure suppliers are aligned with evolving GMP expectations. Cross-Functional Collaboration Work closely with Procurement, R&D, Manufacturing, and Regulatory Affairs to ensure supplier issues are identified, communicated, and resolved efficiently. Participate in cross-functional quality risk assessments and supplier development programs. Continuous Improvement Drive quality improvement initiatives with suppliers to enhance performance and reduce quality-related risks. Track and report quality KPIs related to suppliers and initiate corrective actions when targets are not met. Key Skills & Competencies Strong knowledge of cGMP, ICH Q7/Q10, WHO, and global regulatory requirements. Experience in conducting and managing supplier audits. Excellent communication and negotiation skills. Strong documentation and analytical skills. Proficiency in MS Office tools and electronic QMS ,SAP ERP systems. Ability to work independently and manage multiple priorities under tight timelines. Key Performance Indicators (KPIs) % of on-time completion of supplier audits and qualification activities. % of CAPA closures within agreed timelines. Supplier non-conformance rate (trend analysis and reduction). Compliance score during internal and regulatory audits.

Interview For BE Mechancial Fresher Candidates on 10th Sept Ankleshwar Location Contact Urvi Madam on 9712914207 & Visit Our Office Share with yr friends Golden opportunity to Start career with SDP HR Solution

Interview For BE Chemical Fresher Candidates on 10th Sept Ankleshwar Location Contact Urvi Madam on 9712914207 & Visit Our Office Share with yr friends Golden opportunity to Start career with SDP HR Solution

Department - Quality Control Experience - 2 to 5 years Qualification - M.Sc chemistry (Full time) Section - HPLC / GC / Wet lab To ensure that training is acquired for each activity/instrument prior to its execution/operation and that it is as per respective TNI. To perform Analysis (Chemical)of raw material/packaging material/in-process samples /intermediate /bulk & finished products/ process validation samples/ stability samples/ cleaning validation/method transfer sample, PD lab sample etc. To ensure that all tests carried out in the laboratory are documented contemporaneously in an appropriate authorized and controlled worksheet/ bound book. To make entries in the sample inward register / LIMS as required for assigning analytical reference number and to store at recommended storage condition until completion of the analysis. To operate and maintain laboratory equipment/instrument as per analyst qualification program. To ensure that entries in log books are made where ever instruments are used in the analysis. To perform all associated activities (bench reagents, indicators, volumetric solution preparation, factor determination etc.) required for sample testing by following the approved procedures. To perform analysis (Chemical) to qualify working standards against reference standard /certified standard/ primary standards. To ensure all primary standards/working standards/certified standards/reference standards are stored as per the storage conditions specified and documented. To check the availability of analytical resources like chemicals/reagents / standards etc. before start of the analysis. To take online print and perform data punching in the LIMS. To monitor temperature of laboratory daily. To send those samples to outside laboratory for analysis for tests not able to be carried out in laboratory. To maintain and ensure controlled laboratory practice in the quality control department. To document the raw data as per current GDP. To follow the SOPs of Quality control department and related area. To follow Specification, STP, GTP and protocol during analysis. To use applicable PPEs (personal protective equipment) while performing testing in the laboratory / during handling hazardous solvents/chemicals. To keep himself updated with current regulatory requirements and train the subordinates and colleagues for day to day activities as well as regulatory. To keep the things and his work area clean and tidy and get involved for the routine trouble shooting (if any). To ensure up-keeping of the instrument/equipment. To ensure laboratory inventory management. To inform section head any incident/ OOS/ OOT/ OOC on its immediate occurrence and for day to day activities. To investigate incident/ OOS/ OOT/ OOC (if any) under consultation with the department head/section head. To perform the analysis of stability samples as per the analyst qualification, requirements and respective procedure. To perform the calibration of instrument as per the planner and / or as and when required. To manage all standards for issuance and its usage. To co-ordinate with in-house service engineers and / or external service engineers as and when required. To ensure the destruction of remnant samples after analysis as per applicable procedure. To perform analysis at CHL inter locations whenever required. Responsible for implementing company quality ethics policy for data integrity and inform management and responsible data integrity compliance head on any data integrity issues as per corporate data governance policy. To escalate any issues related to discipline, availability of manpower, hygiene, contamination, cross contamination, Incidents or deviations, malfunctioning of equipments, any unusual observations, any safety risk or quality risk to next level or in absence further up. To perform any other activities as assigned by HOD after completion of the necessary trainings as applicable.

Bsc or Msc in chemical fresher to 2 year experience skills: communication Job Types: Full-time, Permanent, Fresher Work Location: In person

Job Title: Assistant Manager - Quality Compliance (Supplier Quality Assurance) Department: Quality Compliance Reports to: Quality Compliance Manager Location: Ankleshwar Position Type: Full-time Qualifications and Experience: Education: B.Pharm / M.Pharm / M.Sc in Chemistry, Biotechnology, or related field. Experience: Minimum 6–8 years of experience in Quality Assurance / Quality Compliance within the pharmaceutical industry, with at least 2 years in a Supplier Quality Assurance role. Preferred: Exposure to regulatory inspections (e.g., USFDA, MHRA, TGA), and experience in working with global suppliers. Job Purpose: To lead and manage Supplier Quality Assurance (SQA) activities ensuring all third-party suppliers, vendors, and contract manufacturers comply with applicable regulatory requirements, company quality standards, and Good Manufacturing Practices (GMP). The role involves oversight of supplier qualification, audits, risk assessment, and continuous quality improvement initiatives within the pharmaceutical supply chain. Key Responsibilities: Supplier Quality Management: Develop, implement, and maintain a robust supplier quality assurance system aligned with cGMP and regulatory requirements (e.g., USFDA, EMA, WHO). Lead supplier qualification, requalification, and performance monitoring programs. Conduct risk-based assessments and ensure supplier categorization based on product and service criticality. Auditing & Compliance: Plan, conduct, and follow up on supplier audits (on-site and remote) for API, excipient, packaging, and service providers. Evaluate audit findings, identify gaps, and oversee closure of CAPAs with suppliers. Maintain audit schedules, records, and ensure timely reporting. Maintenance of Approved Supplier List / GMP documents / Supplier files Quality Agreements & Documentation: Coordinate the drafting, negotiation, and maintenance of Quality Agreements with suppliers. Review supplier documentation such as CoAs, TSE/BSE statements, stability data, and regulatory filings for compliance. Ensure all supplier documentation is up to date and archived as per data integrity principles. Regulatory Support: Support regulatory inspections and provide supplier-related documentation during audits. Monitor regulatory changes and ensure suppliers are aligned with evolving GMP expectations. Cross-Functional Collaboration: Work closely with Procurement, R&D, Manufacturing, and Regulatory Affairs to ensure supplier issues are identified, communicated, and resolved efficiently. Participate in cross-functional quality risk assessments and supplier development programs. Continuous Improvement: Drive quality improvement initiatives with suppliers to enhance performance and reduce quality-related risks. Track and report quality KPIs related to suppliers and initiate corrective actions when targets are not met. Qualifications and Experience: Education: B.Pharm / M.Pharm / M.Sc in Chemistry, Biotechnology, or related field. Experience: Minimum 6–8 years of experience in Quality Assurance / Quality Compliance within the pharmaceutical industry, with at least 2 years in a Supplier Quality Assurance role. Preferred: Exposure to regulatory inspections (e.g., USFDA, MHRA, TGA), and experience in working with global suppliers. Key Skills & Competencies: Strong knowledge of cGMP, ICH Q7/Q10, WHO, and global regulatory requirements. Experience in conducting and managing supplier audits. Excellent communication and negotiation skills. Strong documentation and analytical skills. Proficiency in MS Office tools and electronic QMS ,SAP ERP systems. Ability to work independently and manage multiple priorities under tight timelines. Key Performance Indicators (KPIs): % of on-time completion of supplier audits and qualification activities. % of CAPA closures within agreed timelines. Supplier non-conformance rate (trend analysis and reduction). Compliance score during internal and regulatory audits.

Shift Leader - Process Job Id: 11600 City: Ankleshwar, Gujarat, India Department: Acephate Function: Manufacturing Employee Type: Permanent Full Time Seniority Level: Executive Description: UPL Limited (NSE: UPL & BSE: 512070, LSE: UPLL) is a global provider of sustainable agriculture products and solutions, with annual revenue exceeding $6bn. We are a purpose-led company. Through OpenAg®, UPL is focused on accelerating progress for the food system. We are building a network that is reimagining sustainability, redefining the way an entire industry thinks and works – open to fresh ideas, innovation, and new answers as we strive towards our mission to make every single food product more sustainable. As one of the largest agriculture solutions companies worldwide, our robust portfolio consists of biologicals and traditional crop protection solutions with more than 14,000 registrations. We are present in more than 130 countries, represented by more than 10,000 colleagues globally. For more information about our integrated portfolio of solutions across the food value chain including seeds, post-harvest, as well as physical and digital services, please visit upl-ltd.com and follow us on LinkedIn, Twitter, Instagram and Facebook. 1. Production: Coordinate and manage the activities of the production shift to ensure optimal productivity and efficiency. Supervise and provide guidance to a team of production operators, assigning tasks and monitoring their performance. Monitor production processes, troubleshoot issues, and implement corrective measures to minimize downtime and maximize output. Collaborate with other departments, such as Quality Control and Maintenance to address production-related issues and smooth operations. Maintain accurate records of production data, including output, downtime, and any deviations from quality standards. Conduct regular inspections of equipment and machinery, identifying maintenance needs and coordinating repairs or servicing as required. Implement and enforce company policies and procedures, including quality standards, safety guidelines, and operational protocols. 2. Quality: To ensure best quality products and produced without any batch failure and to ensure compliance. 3. Safety: To ensure Safest workplace and Safety in each operation of Plant and ensure compliance with safety regulations and promote a safe working environment for all employees. 4. Housekeeping & TQM: To ensure best housekeeping as per standards of 5S. Activity involved in driving the TQM culture in the plant. 5. Manpower: To manage manpower and ensure efficient work from them.Responsible for yield improvement projects, cost optimization, reduction in breakdown, capacity utilization improvement, batch cycle time reduction, improvement in planning and working. Participation in DWM, 5S, AM, ensure ZLD and other parameters pertaining to operational efficiency. We are one team, for maximum impact. One team with shared goals. We all play for the team and no one plays against the team. We have a laser-like focus on what our customers need and want, on anticipating their future needs and on how we can create innovative solutions and experiences for them. #UPLJobs