Quality Manager Graduate Jobs in Navi Mumbai

We are looking for a dedicated Sales Administration Executive to join our team in New Panvel. The ideal candidate should have 1 to 2 years of experience in sales administration and be able to work from our office. This role is best suited for female candidates.**Key Responsibilities:**- **Order Processing:** Manage customer orders by entering data accurately into the system and ensuring all orders are tracked and fulfilled on time.- **Customer Interaction:** Communicate with clients through phone and email to address inquiries, provide information about products, and resolve any issues.- **Sales Reporting:** Prepare regular sales reports and analyze data to support the sales team in making informed decisions.- **Database Management:** Maintain and update customer databases to ensure that all information is current and accessible for the sales team.- **Sales Support:** Assist the sales team with administrative tasks, including preparing presentations, coordinating meetings, and compiling sales materials.**Required Skills and Expectations:**Candidates should possess excellent communication skills, both verbal and written, to interact effectively with clients and team members. Proficiency in Microsoft Office Suite, particularly Excel and Word, is essential for reporting and data management. Attention to detail and strong organizational skills are necessary for managing multiple tasks efficiently. The candidate should be a team player with a positive attitude and the ability to work in a fast-paced environment. Previous experience in a sales environment will be an advantage.

Quality Oversight & ApprovalApprove analytical results, reports, protocols, methods, specifications, and other quality-related documents.Ensure the integrity, accuracy, and regulatory compliance of analytical and laboratory data.Provide final quality approval for services and deliverables provided to clients.2. Quality Management System (QMS)Establish, maintain, and continuously improve the Quality Management System (QMS) in compliance with GMP, GLP, and applicable regulatory guidelines.Ensure effective management of SOPs, deviations, CAPAs, change controls, OOS/OOT investigations, complaints, and risk management activities.Ensure data integrity compliance in line with ALCOA+ principles across all systems and documentation.3. Regulatory ComplianceEnsure compliance with applicable global regulations and guidelines, including FDA, EMA, ICH, WHO, and ISO standards.Lead, support, and manage regulatory inspections, client audits, and third-party audits.Act as the primary quality point of contact for regulatory authorities, auditors, and customers.4. Systems & ValidationReview and approve validation activities including analytical method validation, equipment qualification (IQ/OQ/PQ), computer system validation (CSV), and process validation.Ensure laboratory instruments, electronic systems, and software meet regulatory and data integrity requirements.5. Training & Quality CultureEnsure appropriate training of personnel on GMP, GLP, SOPs, and quality best practices.Promote and sustain a strong quality culture and compliance mindset across the organization.6. Risk Management & Continuous ImprovementIdentify potential quality and compliance risks and implement effective mitigation strategies.Drive continuous improvement initiatives to enhance regulatory compliance, operational efficiency, and service quality.

Develop and match new color shades as per customer or sample references. Perform visual and instrumental color matching using tools like spectrophotometer, colorimeter, etc. Adjust formulations to achieve color accuracy in paints, plastics, textiles, inks, or cosmetics. Maintain shade standards and color records for all matched formulations. Conduct lab trials and prepare drawdowns for approvals. Coordinate with production and QC to ensure shade consistency in batch scale-up. Handle customer shade complaints or re-matches, providing timely solutions. Work with software like Color iMatch, Datacolor, X-Rite, or equivalent tools. Ensure adherence to *quality and color tolerance parameters Maintain safety, housekeeping, and compliance with company standards.

QC MANAGER

We are looking for 15 Quality manager Posts in Mahape, Navi Mumbai, Vashi, Navi Mumbai, Turbhe, Navi Mumbai, Navi Mumbai, with deep knowledge in testing and managing, Basic Computer Skills and Required Educational Qualification is : B.E, B.Tech, M.Tech

Urgent job opening for QA Officer. required fresher and experience candidate.job location - Navi Mumbai / Taloja / mahape / kopar khairne / Dombivali / Ambernath / Mumbai.experience - 0 to 5 years.salary - 15000 to 65000.interested candidate call on - 8850696229. or WhatsApp resume..

Designation : QA ManagerLocation : MumbaiQualifications : Degree in a science-related field, chemistry or pharmacyExperience : 3+ years in R&D Pharmaceutical Industry from QA DepartmentResponsibility :* Review of Manufacturing Processes.* Knowledge of All regulated Guideline & Pharmacopoeia.* Preparation & implementation of SOPs related to the concerned department & Justification of Specification.* Nitrosamine Impurity, Elemental impurity, Genotoxic Impurity & their role related DMF Filing.* QA person collaborates with the Quality Control (QC) team to ensure that laboratory testing is conducted appropriately and meets the required specifications.* The QA person conducts regular internal audits of the manufacturing facility at R&D to ensure that the facility meets the required quality standards. Also handles the external audit cand its compliance.* QA person is responsible for ensuring that all necessary documentation is completed accurately, in a timely manner, and in compliance with regulatory requirements* The QA person is responsible for reviewing and approving deviation reports and ensuring that corrective and preventive actions (CAPA) are implemented.* The QA person is responsible for reviewing and investigating product complaints to ensure implementation of corrective and preventive actions (CAPA)* QA person is responsible for training of manufacturing and laboratory personnel on quality-related procedures and regulations.* Handling of out of specification (OOS) and out of trend (OOT) laboratory incidents and their closing.* Preparation & review the method of analysis (MOA), standard testing procedure (STP) and other documents related to QC.* Implementation & verification, in-process checks, online entries in BPR of product at Pilot plant manufacturing site.* Monitoring and ensuring the good manufacturing practice (GMP) at manufacturing site.Contact Person- Deepak - 7757087059ID- deepak.vijayamgmt@gmail.com

Job title QA Mgr.Department name Quality AssuranceExperience 12 To 15yrsIndustry Engineering services Reporting To PartnerReporter All QA /QC in place TeamSalary Range 7L To 7.2L/-PABased at Taloja, Navi Mumbai.Goals 1. Quality Management System review within 60days.2. Establish successfully a system for CAPA within 60days.3. Implementation of 5s in 24 zonal areas within the company in 90days.4. Develop and plan for presentation to management and drive the TQM best practices within the organization.5. Establish and Set Quality Objective according to departments.6. Establish and set KPI, KRA to achieve 8 departments quality and productivity.7. Identifying bottlenecks in Blasting, Machining department and streamline procedures. 8. Collecting and analyzing data to identify trends, detect variations, and make data-driven decisions through SPC in minimum of 2 departments to maintain quality standards.Key responsibilities and accountabilities 1. Conduct Systems Audits every first week in a month.2. Daily QA morning meeting to discuss & guide problems faced by QA/QC team.3. Qualification and evaluation of Suppliers and Subcontractors.4. Analysing customer complaints and Internal rejection on weekly basis. Actively involved in Troubleshooting of process problems and monitor the non-conformities.5. Plan, conduct and face internal and external quality audits to verify compliance with quality standards and identify improvement areas.6. Plan and review the annual training calendar. Arrange three department-wise trainings monthly. Check and verify the effectiveness of the training and share feedback with management on a monthly basis.7. Implement Work management practice for planning, execution, and monitoring of all tasks and activities required to accomplish jobs on time.Knowledge, skills, and abilities Education and experience Diploma / BE Should be Technically Sound.Work Days Friday Weekly offSunday Working

Job Description: Assist the sustainability lead to assess various plastic recycling technologies - Identify, understand, and evaluate plastic recycling technologies. To Identify opportunities in various biopolymer product/technology and bio composites. Assessment of various technology for sorting / segregation and cleaning of waste plastic for mechanical recycling Support for preparation of overview/prefeed documents for new projects Validate equipment data sheets prepared by consultant/ engineering contractor for various projects. Execute process design calculations for the various schemes. Assist to develop process design package using appropriate tools. Identify opportunities for product quality enhancement/ product upgradation. Participate in pilot / commercial plant trials. Understand and evaluate basic engineering design documents. Validate modifications to ensure specified standards and codes are followed in calculations. Participate in PHA/ HAZOP of new projects/ modifications. Contribute to derive value from technology network. Understand and be abreast with legislation/ regulation as and when mandated by CPCB/ MoEF, GoI.Skills and Competencies Sound knowledge regarding polymerization process and technology. Knowledge on polymer product, processing, and applications. Experience in polymer plant operation / technical service domain Knowledge of chemical engineering and process technology Ability to plan / discuss results and network under the guidance of senior colleagues. Process design calculations at Skill level Use of process calculation templates at Skill level Process simulation skills Use of Six sigma for problem solvingEducation RequiredBE/B Tech in Chemical Engineering from a reputed instituteMBA will be added advantage.Experience Required3 to 4 years of experience with at least 2 years in plant Operations / CTS

Production Manager position. Looking after daily production of medical devices and following SOP and maintaining QMS as per required. Looking after waste management, production management, raw material management and quality assurance in production. Looking after production time frame for dispatch

Key Responsibilities :Good Knowledge in (products)- (Management and Quality assurance work) as per ISO 17025:2017,Required experience in our material testing as per REQUIRED scope.To establish quality policy and objectives.Assist with laboratory administrative duties.Follow all quality assurance and quality system procedures(QSP).Issuance of all quality system documents.Monitoring to control of non-conforming work and initiate corrective & preventive actions to forestall the recurrence of non-conformities.To maintain training records for all laboratory staff.Implementing internal quality checks.Coordinate customer complaints and interacts with customers for giving feedback etc.To prepare internal audit plan & conduct ainternal audit.To prepare agenda for management review meetings.Officiate Management Review Meeting.Record the minutes of management review meeting for the outcome of the review meeting.Issuance of all quality system documents.Promote good relations with all customers.To maintain smooth laboratory work flow.Provision of resources.Responsible for the safe storage, supervision and use of equipment by suitably trained persons.To plan, schedule, conduct and record the findings of internal audit, conduct verification audit and present summary report to management about audit findings and corrective actions initiated for closure of audit non-conformities.Monitoring to control of non-conforming work and initiate corrective & preventive actions to forestall the recurrence of non-conformities.To control log book and maintenance of equipment.To supervise and perform the site testing activities.Reports to Lab Director/Technical Manager.To ensure safety and security of all office recordsEnsure proper maintenance of personal files, service registers etc., of all the staff.To deal with the matters relating to telephone, housekeeping, security, upkeep of the building etc.To initiate proposals for procurement of stores like computers, furn

Required Skills:No degree/qualification requiredStrong Java programming skills and OOPS conceptsBasic knowledge on QA testing methodology and toolsBasic knowledge of Selenium web driver.Decent understanding of QA automation on web, mobile and APIBasic knowledge of using git and shell scripting.Decent understanding of performance testingRoles and responsibilities:Will be working as a freelancer and should be able to devote atleast 25 hours/weekFlexible working hoursWill be required to do both manual and automation QAAnalysing/preparing test cases and debugging defects.Automation responsibility - developing test scripts/framework using Java for web/mobile/APIs.Performance testing of web based applicationsDecent understanding of performance testingSince this is a freelancing role - no laptop/machine will be provided for the same.Highest qualificationYears of experience into QA/Dev if any?Expected salary/monthLink to github or any open source contribution (if any)Configuration of the machine/laptop which you will be using to workLatest CV

KEY JOB RESPONSIBILITIES (Deliverables):1. Authenticating & collecting Daily production reports.2. Follow-up of prod. Dept. Emails/phone calls.3. Managing & deputing activities in case of Leaves of any supervisors.4. Keeping accountability of all deputed activities to responsible persons on shop floor.5. Keep coordination with sales for Local orders samples.6. Managing Manpower utilization.7 Managing Online samples to Qc/parties as and when required. 8 Activities as and when Required by Management.9 Keeping Vigilance/record on each material movement in plant.10. Conducting Trainings as per calendar.11. Checking and authenticating of stocks entries on system.12. Entering Production data in system as per Guidelines.13. Adherence to the standards as per management guidelines.14. Data feeding in system as per production reports.

Need a candidate who has good amount of production management knowledge with minimum 5 to 6 years of experience in the same field. He should have qualities like Production control, quality control, stock management waste management, error control, costing control, QMS, SOP, 5 P of production. production staff management. We looking for candidate for long term for at least 5 years.