Quality Manager Graduate Jobs in Vadodara

The Design Estimation Engineer is responsible for accurately estimating design projects within the engineering field. Key responsibilities include analyzing project specifications, creating cost estimates, developing design plans, and collaborating with the engineering team. The ideal candidate should have a strong background in engineering, proficiency in design software, attention to detail, and excellent communication skills. The candidate should also be able to work independently and meet project deadlines efficiently.

experiance HPLC/GC analysis like Assay, RS, ChiralPurity Residual solvent analysisCandidate must have experience in Pharmaceutical industry.

A. Production Planning:Develop and manage the Master Production Schedule (MPS) based on demand forecasts, sales trends, and inventory levels. - Coordinate with manufacturing, quality, and regulatory teams to ensure production plans align with compliance requirements. - Ensure proper capacity planning to avoid bottlenecks in production. B. Procurement & Vendor Management:- Source and procure raw materials (APIs, excipients), packaging materials, and consumables as per production needs. - Negotiate with vendors to get the best pricing, quality, and delivery timelines. - Develop and maintain relationships with approved suppliers and ensure compliance with procurement policies. C. Inventory Management & Materials Control:- Maintain optimum inventory levels to prevent shortages or overstocking. - Implement inventory tracking systems (SAP, ERP, or manual tracking) to ensure accurate stock records. - Conduct regular stock audits and reconciliations to prevent pilferage and wastage. D. Supply Chain Coordination:- Work closely with warehouse and logistics teams to ensure the timely dispatch of materials to production units. - Optimize supply chain workflows to reduce lead times and costs. - Address logistics issues such as import/export delays, supplier disruptions, and transportation bottlenecks. E. Compliance & Documentation:- Ensure all procurement and inventory management processes comply with GMP (Good Manufacturing Practices), FDA, and other regulatory guidelines. - Maintain accurate MRP (Material Requirements Planning) records, purchase orders, and vendor contracts. - Coordinate with the regulatory affairs team to ensure compliance with pharma industry norms.

with 2 - 5 years of experience in QC for review work.Must have good knowledge of GMP.

Responsible to maintain an optimum level of manpower and over timeResponsible to ensure all operation of production adherence to cGMP complianceResponsible on manpower development (training) for quality, productivity and cost consciousnessTo train the production personnel on cGMP Trend & regulatory requirement.Monitor the work of subordinates and ensure that the necessary assistance is provided to them for their timely, adequate and accurate completion of the assigned workAccountability to ensure production planning & timely delivery of high productivity and low cost products and with compliance to cGMP.Responsible for handling CAPA, Deviation, Change Control, URS, Contingency Plan and Investigation report.Responsible for Departmental Standard Operating Procedure update and revision execute within production in DCM.Responsible to carry out production operation as per production plan and delivery on time.Other instruction by superior.

Project Planning: Participate in project planning meetings to understand project goals, timelines, and resource requirements. Collaborate with project managers and other engineering disciplines to develop a comprehensive project plan.Site Inspections: Conduct regular inspections of the construction site to ensure that mechanical systems are installed correctly and according to designspecifications. Identify and address any issues that may affect the quality or progress of the project.Quality Assurance: Implement quality assurance processes to ensure that mechanical installations meet industry standards and project requirements. Perform inspections and tests to verify the quality of materials and workmanship.Coordination with Other Disciplines: Collaborate with civil, electrical, and other engineering disciplines to ensure seamless integration of mechanical systems with overall projectrequirements. Address interdisciplinary coordination challenges during construction.Safety Compliance: Enforce safety protocols and standards on the construction site to prevent accidents and ensure a safe working environment. Conduct safety audits and inspections regularly.Construction Management: Oversee the our mechanical service activities on site. Monitor activity progress and ensure it aligns with the project schedule.Material Procurement and Management: Coordinate with procurement teams to ensure timely delivery of mechanical equipment and materials. Manage the storage and distribution of materials on the construction site.Documentation: Maintain accurate and up-to-date documentation, including project plans, drawings, specifications, and change orders. Prepare daily reports on site activities and progress.Problem Resolution: Identify and address technical issues or conflicts that arise during construction. Collaborate with the design team and contractors to find effective solutions.Client Interaction: Communicate with clients,

Company Name: Global Gourmet Pvt LtdQualification : Food Technologist/B.Tech(Food technology)Experience : 5-7 Years (Must be in food industry)Job Location : Unit.1, G I D C Estate, 296, Makarpura Rd, Makarpura GIDC, Makarpura, Vadodara, Gujarat Assisting FSTL for documentation & record keeping Outside laboratory communication for the annual testing Daily traceability record keeping Daily Mass balance activity. Corrective action & preventive actions follow up to be taken from respective process owner Verification of daily records & Trend analysis of process deviations Training to workers with regards to Food safety, allergens, foreign body, CCPs etc. Assisting in Internal Audit documentation and effective NC closure Providing assistance in external audits Interdepartmental communication. Assisting QA Manager/HOD in staff planning and making shift schedule. Additional responsibility whenever required. Monitoring and controlling the allocated budget for the department.

We are L.J.Purani and Associates, we are searching for Candidates who is localized in Gujarat for the Position of Civil site Engineer Please contact or update on this post ASAP

Designation / Title : Regional Bisiness Manager : Equivalent to second line team leader in sales & BD.Job Location: Gujarat, MumbaiReporting to: Company Director and other senior managersQualification: Any Graduate with relevant experience in the Pharma industryGender: Male and Female both are ok (Preferred Male)Criteria: Minimum 3 years of man management experience in pharma salesCardio-Diabetic segment exposure is preferredAge Limit: 25 35 yearsSalary Package: Negotiable on present CTCOther Benefits PF, ESIC, Medical insurance, Sales Incentives, Monthly Expense reimbursements,Travelling allowances, Daily allowances, CUG plan, performances based rewards.Industry Preference: Pharmaceutical IndustryFunctional Area : Sales and Business DevelopmentJob Profile:1. Achieving sales target for the assigned area and team2. Ensuring the basic work form subordinates like customer coverage, visitfrequencies, programs, reporting, collaboration etc.3. Doing field work with subordinates for customer visits and ensuringperfect implementation of company designed strategies4. Responsible for ROI.5. Supervising the engagement activities executed by the sales team andtaking follow ups with customers and team to ensure the desired results6. Rapport building with key customers to improve sales volumes and brandadvocacy of the organization7. Inventory management and ensuring smooth distribution channel8. Motivation to the subordinates for sales target achievementsSkills Required1. Leadership Qualities2. Excellent Communication skill3. Ability to meet deadlinesComputer Literacy: Should be conversant with MS Office applications, Internet etcPhysical status: Normal and Physically fit for field work

Gaining an understanding of the client's needs and requirements and communicating them and the quality standards to the production teams.Devising ways to improve the manufacturing process to ensure higher-quality goods.Devising, improving, and reviewing new specifications and procedures for products or processes, and training staff to use them.Setting the requirements for raw materials from suppliers and monitoring their compliance.Supervising inspectors, technicians, and other staff members and providing guidance.Ensuring legal obligations are followed and ensuring compliance with regulatory bodies and with health and safety guidelines.Overseeing product development procedures to identify any deviations from quality standards.Inspecting the final output, comparing it to the requirements, and approving or rejecting the final products.Keeping accurate documentation and performing statistical analysis.Gaining feedback from the clients, attending meetings, submitting reports, and assisting external auditors and inspectors.

Candidate has to work in pharma formulation (OSD) Manufacturing plant.

Production Manager : MNC Chemical in Ahmedabad, VadodaraDesired Candidate profile:Should have experience in a Chemical Manufacture unit. ((NO FROM PHARMA) Reaction handle :- Sulfonation, Reduction , Ethoxylation , Acetylation,Condensation, Nitration, Benzoylation, Diazotisation, Polymerization, Bromination,Estrification, Propoxylaition, Chlorination, Chlorosulfonation, Hydrolysis Unit Operations:- Distillations, Pressure Reactions, Dryings, Filtrations, Equipment Handled : S.F.D (Spin Flash Dryer), ANF (Agitate Nuch filters) RVPD( Rotary Vacuum Paddle Dryers ) Knowledge in S.A.P or any Equivalent ERPJob Description: Being accountable for production in accordance with company targets with the help ofShift Engineers Managing quality standards as per benchmark / standards set by the company Managing yield ratio for various products. Managing wellbeing, Training & Development of team members Proactively plan and suggest enhancements/ maintenance for production infrastructure Managing PPC functions [Production Planning and Control] Taking corrective steps for customer complaints Conducting trial for new products / custom synthesis and make sure it reaches tocommercial production Taking initiatives for CI, reducing waste and energy consumption Train and validate plant operators and engineers (as per need) Responsible for Reports of PPC [Routing, estimating, scheduling, despatching, followup, inspecting, and evaluating in given formats] and MIS of Daily production reports.Material management reports. By-products reports Responsible For Manpower Management

Formulation Company Shaimil laboratoriesTime : 9 to 5: 30BonusPF also Available

Full Time jobBenefitPFsick LeavePaid LeaveCasuala Leave

Assistant Manager Production : MNC Chemical in AhmedabadDesired Candidate profile:Should have experience in a Chemical Manufacture unit.Should have hands of experience in Ethoxylation, Surfactant.Job Description: Managing day to day production in accordance with company targets/ goals Plan and manage production (Master Production Schedule) and get it approved bydepartment head Managing quality standards and yield ratio for various products as per standards set Proactively plan and suggest enhancements/ maintenance for production infrastructure Generate requirement and BOM for procurement of raw and packing materials Schedule dispatch activities and coordinate with logistics team Keeping track of physical stoke of RM, FG and PM Managing shifts of workers and schedule their duties Managing wellbeing, Training & Development of team members Review of audit report of plant and proactively suggest areas of improvements Troubleshooting of quality issues and take corrective actions to satisfy client needs Managing customer complaints and take corrective actions Manage and assist in audit of SOPs [managing cost, quality, time and people Manage compliance to EHS norms and training Coordinate with other dept. like ETP, Lab, and Maintenance Department for smoothoperation. SAP knowledge is preferred. Knowledge of ISO , CAPA, HAZOP

Must have good knowledge of GMP and Documentation.