38 Inprocess Jobs

You are invited to join our team at AIM EXCELLENCY HR SOLUTIONS PVT. LTD for the position of Quality Supervisor. With 3 to 4 years of experience in the Sheet Metal/Fabrication industry, you will play a key role in ensuring quality standards are maintained. As a Quality Supervisor, your responsibilities will include process inspection, material inspection, managing ecksheets, data entry, and conducting incoming, in-process, and final inspection of DG sets. To qualify for this role, you should hold a Diploma/BE in Mechanical Engineering. The ideal candidate will have a keen eye for detail and a strong understanding of quality control processes within the manufacturing sector. This is a permanent position with benefits such as health insurance and provident fund. If you are interested in this opportunity, please contact HR Prachi at 8237944555 or email aim8237944555@gmail.com. The work location will be in person. Join us at AIM EXCELLENCY HR SOLUTIONS PVT. LTD and be a part of a dynamic team dedicated to maintaining excellence in quality standards.,

As a Factory Manager specializing in waterproofing chemical products, you will be responsible for overseeing and optimizing the production processes to ensure high-quality end products. Your role will involve conducting thorough quality assurance checks at various stages of manufacturing, from testing raw materials upon arrival to verifying final batch quality before market release. Your ability to make prompt decisions based on data-driven insights will be crucial in maintaining the standard of excellence in product quality. You will be expected to implement and uphold comprehensive quality systems and protocols throughout the manufacturing process. Your expertise in raw material testing, in-process quality checks, and final product inspections will be essential in ensuring that only top-tier products meet the market standards. Furthermore, your proficiency in coordinating with research and development teams, as well as procurement departments, will be instrumental in aligning specifications and driving continuous quality improvements. Your experience should demonstrate a track record of successfully conducting routine and specialized tests on raw materials, intermediates, and finished goods. Additionally, your ability to lead root cause analysis and implement corrective/preventive actions for quality deviations will be highly valued. Your role will also involve collaborating with suppliers to enhance raw material quality and align specifications to meet the desired standards. This position requires a full-time commitment and will involve working during day shifts at the designated manufacturing facility. Your dedication to compliance with ISO and other quality certifications will be necessary to uphold industry standards and ensure regulatory adherence. Your familiarity with waterproofing chemicals and standards, as well as your experience in production decision-making based on quality parameters, will play a significant role in your success as a Factory Manager in this specialized field.,

Overview Analyzes, develops, designs, and maintains software for the organization's products and systems. Performs system integration of software and hardware to maintain throughput and program consistency. Develops, validates, and tests: structures and user documentation. Work may be reviewed for accuracy and overall adequacy. Follows established processes and directions. Responsibilities Establishes requirements for less complex design projects Works on Completing all phases of Software engineering design projects Works on analysis of processes and delivers results to necessary stakeholders Analyzes results and recommends solutions Works on developing expected results on a variety of products Develops documentation for new projects and reviews previous results Works with latest technologies and new approaches Reviews changes or upgrades to existing designs or test Exercises judgment in selecting methods and techniques for obtaining solutions on assignments Qualifications All other Regions: Bachelor's Degree 1 to 2 years of experience Quantitative and problem solving skills

Role & responsibilities Lead the team in new product development and translocation model qualification, ensuring timely customer PPAP (Production Part Approval Process) approval. Proactively coordinate and participate in meetings with the R&D team and OEM customers to define and establish product and process specifications during the development phase Conduct new layout audits and perform troubleshooting analysis using quality tools and statistical techniques; implement robust Root Cause and Corrective Action (RCCA) measures to reduce scrap costs in the respective production cells. Lead quality initiatives within the respective production cells, validating quality objectives and monitoring results to ensure compliance and continuous improvement. Ensure compliance with IPC 610 and IPC 620 standards to maintain high product quality, with a specific focus on soldering, assembly, and associated processes. Enhance customer satisfaction by delivering zero-defect products and ensuring timely resolution and closure of customer claims. Drive continuous improvement initiatives aligned with Integrated Quality Management Systems (IATF & ISO), and ensure readiness for customer and internal audits. Specialized in failure analysis of PCBA and electronic products, leveraging technical expertise to identify root causes and implement corrective actions. Preferred candidate profile Preferred candidates from EMS industry

Dear candidates , Pl join us whatsapp group no 9356395439 Post- Incoming Quality Engineer Industry - Automotive / Plastics Education - BE / DME Experience - 01-03 yrs Immediate Skills - Incoming quality , Inward quality , quality inspection , RFQ Own bike must

Dear candidates , Pl join us whatsapp group no 9356395439 Post- Receiving / Incoming Quality Engineer Industry - Automotive / Plastics Education - BE / DME Experience - 01-03 yrs Immediate Skills - Incoming quality , Inward quality , quality inspection , RFQ Own bike must

Roles and Responsibilities Conduct In-Process Quality Assurance (IPQA) activities to ensure compliance with regulatory requirements and company standards. Monitor and control production processes to identify deviations, implement corrective actions, and maintain product quality. Collaborate with cross-functional teams to resolve issues related to formulation, processing, packaging, labeling, and release of products. Develop and maintain documentation for IPQA procedures, protocols, reports, and records. Ensure timely completion of tasks assigned by supervisors or managers within specified deadlines.

Role & responsibilities : 1) Having from OSD background. 2) Responsible for analysis of RM/IP/FG/Stability on HPLC. 3) Responsible for Calibration of HPLC 4)Having the Knowledge of the Pharmacopeia.IP/BP/Ph.Eur/USP Skill Required: 1) Handling of the HPLC, 2) Calibration Management. 3)Knowledge of the GLP Environment 4) Handling of the HPLC, 5) Calibration Management. 6)Working Standard, Ref. Standard, Imp Standard, Primary Standard Management Additional Remark: Required candidates background should be in Regulatory environments

Greetings from Avani Consulting. We are hiring QC Officer / Trainee and QC Associates for a leading Pharma API Company in Mysore. Positions: 1. QC Officer / Trainee : EXP: 2 to 3 year exp in Pharma Company. Salary : Up to 4LPA ( Take way home only . NO Parks & Benefits ) 2. Quality Control Associates - API : EXP: 5 to 9 year exp in Pharma API Industry. Salary : Up to 7.5LPA ( Including Parks & Benefits ) Preferred candidate profile Qualification : M.Sc. Chemistry Experience : Pharma -API Quality Control Role & responsibilities : Handling and troubleshooting of Analytical Equipment's like HPLC, GC-HS, FT-IR, UV, Potentiometry, Polarimeter, ICP and KF. Handling of Analytical Method development and Method Validations. Qualification of Equipments as per GLP requirements. Analysis of Inprocess, Stability and FG Samples as per the Specification. Operation, Maintenance and Calibration of HPLC and GC as per the schedule. Review of results and release of Analytical test report or Certificate of Analysis. Maintenance of minimum consumables in the Laboratory. Planning and coordination to release on time results delivery. Investigation of OOT/OOS in the laboratory. Sampling of Raw Material, Inprocess and Finished product samples. Basic knowledge on LIMS/SAP. Handling 21 CFR compliance. ***NOTE :: NO CHARGES Looking forward to know about your interest. Thanks & Regards Priyanka Palit [9518220852 | priyanka@avaniconsulting.com]

Role & responsibilities : -Operation of pH meter, Conductivity meter, Karl Fischer, Halogen Moister analyser, Balance, UV- cabinet , Melting Point apparatus, UV spectrometer, Particle size analyser, Polari meter, Bulk Density, Sieve-Shaker, FT-IR, Potentiometer etc. -To perform analysis of in process, Intermediate, raw material, stability sample, holding time study sample & Finished products on HPLC & to maintain record accordingly. - To plan and perform analysis and reporting for column performance & to maintain vial destruction record.

School : WITTY Campus : Witty International School, Malad Country : India Qualification : Bachelor in Education,BA (Hons) ,BA+MA OverView : TGT English - ICSE Responsibility : Organize classroom lectures and coursework Prepare materials and activities Assign homework and interesting exercises Determine exam and assignment grades Provide feedback based on workload and classroom behavior Keep a record of students’ attendance and grades Manage classroom crises and resolve conflict Collaborate with teaching staff and administrators to foster a good student experience SkillsDescription : Knowledge of various teaching methods Exceptional organizational and communication skills A patient and resilient personality Dedication to students and education Disclaimer : Our company is an equal opportunity employer committed to creating a diverse and inclusive workplace. We encourage applications from individuals of all backgrounds and experiences.

Conduct routine and in-process testing of sterile products according to SOPs and GLP. Support Central Lab operations including sample preparation, testing, and documentation. Perform microbiological and physicochemical tests under sterile conditions. Record and report test data accurately in compliance with GLP and GMP standards. Maintain lab equipment, clean work areas, and follow aseptic techniques. Assist in investigations related to product quality deviations as needed. Follow safety, hygiene, and contamination control procedures strictly.

Perform routine and non-routine QC testing in the Central Laboratory according to SOPs and regulatory requirements. Lead or support investigations related to out-of-specification (OOS), out-of-trend (OOT), and other quality deviations. Collect and analyze data to identify root causes and recommend corrective and preventive actions (CAPA). Collaborate with cross-functional teams (Quality Assurance, Production, R&D) during investigations and product release. Prepare and maintain accurate investigation reports, lab records, and documentation in compliance with GMP and corporate policies. Support stability studies, method validations, and lab audits. Ensure lab equipment calibration, maintenance, and compliance with safety standards.

•Knowledge of CNC machine •Hands on experience in incoming inspection & in process •Work exposure as a QA with a metal/steel manufacturing company

Qualification : B.Pharma Experience : 3 to 10 yrs. Designation : Officer Salary Range : 6 to 7 Lacs PA. Unit : Injectable Kindly Find the JD. Management of Aseptic Process Simulation (Media Fill) Program. Review of quality systems such as Change Control, Deviations, CAPA, OOS, OOT, LIR, Market Complaint, FAR, Product Recall and other QAMS documents. Preparation and Review of APQR. Nitrosamine Risk Assessment of Drug Product Preparation and review of site QA SOP and review of cross-functional department SOP. Review of Batch Manufacturing Record and Batch Packing Record. Preparation, review and execution of hold time study of drug product. Preparation and review of thermal cycling and temperature excursion study If interested mail cv at :- neetij@selectsourceintl.com

Roles and Responsibilities Conduct BMR reviews, CAPAs, GMP audits, and IPQC activities to ensure compliance with quality standards. Perform incoming inspection, process validation, and equipment qualification tasks as per SOPs. Identify and report deviations/OOS/OOT events during production runs. Collaborate with cross-functional teams to resolve quality issues and implement corrective actions. Maintain accurate records of QMS documentation and participate in training programs. Desired Candidate Profile 3-8 years of experience in pharmaceutical industry with expertise in IPQA (In Process Quality Assurance). Strong understanding of Good Manufacturing Practices (GMP) regulations. Proficiency in performing BMR reviews, CAPAs, GMP audits, IPQC activities. Experience with Incoming Inspection, Process Validation, Equipment Qualification processes.

Role & responsibilities APLHC Unit IV (Naidupeta, Tirupati Dist., Andhra Pradesh) Open Functions: Quality Control (GMP / GC / LCMS / HPLC) Experience Required: 1 - 6 years in USFDA Approved pharmaceutical manufacturing facility Quality Control Job Titles & Grades: Executive / Sr. Executive (based on experience) Job Description: Routine & stability testing of RM / IP / FP samples on HPLC, GC, LCMS, UV, etc. Prepare/standardize analytical methods, calibration & instrument qualification (IQ/OQ/PQ) Adhere to GDP, ALCOA+ and cGMP guidelines; ensure timely LIMS/SAP data entry Investigate OOS/OOT results and implement effective CAPA Support regulatory, customer and internal audits Common Requirements: Qualification: B.Pharm / M.Pharm / M.Sc. (Chemistry or related) Sound knowledge of current GMP guidelines (US-FDA, MHRA, EU, WHO) Good documentation, investigation and communication skills Willingness to work in shifts and collaborate with cross-functional teams How to Apply Subject Line: Immediate Joiner Send you updated resume : naidupetahr@aurobindo.com

Sanmina is seeking a highly motivated and experienced Quality Manager to lead our In-Process Quality Assurance (IPQA) activities. In this role, you'll be instrumental in ensuring product and process quality, fostering strong customer relationships, and driving continuous improvement initiatives. If you're a proactive leader with a passion for quality excellence and a proven track record in manufacturing environments, we encourage you to apply! Role & responsibilities Lead and Coordinate IPQA: Lead and coordinate the In-Process Quality Assurance (IPQA) team and Cross-Functional Teams (CFTs) to ensure robust quality control throughout the manufacturing process. Strategic Quality Planning: Collaborate with management to define and achieve IPQA goals and objectives aligned with overall business strategies. Customer Focus: Understand, review, and ensure adherence to customer quality requirements. Act as a primary point of contact for customers on quality-related topics, leading meetings and addressing concerns. Process and Product Quality Improvement: Drive continuous improvement in process and product quality, ensuring adherence to defined processes and standards. Quality Record Management: Oversee the maintenance of accurate and comprehensive quality records. Audits and Corrective Actions: Lead process audits to identify areas for improvement. Drive corrective actions for customer and internal major defects, working collaboratively with cross-functional teams. Performance Improvement: Partner with cross-functional teams to improve DPPM (Defective Parts Per Million) and RTY (Rolled Throughput Yield). EHS Participation: Actively participate in Environmental, Health, and Safety (EHS) activities, including identifying aspects and impacts, conducting Hazard Identification and Risk Assessment (HIRA), emergency preparedness, and continuous improvements. Proven experience in leading and mentoring quality teams. Strong understanding of quality management systems and methodologies. Excellent communication, interpersonal, and leadership skills. Ability to work effectively with cross-functional teams and external stakeholders. Knowledge of EHS principles and practices. To Apply: Interested candidates are invited to apply directly through recruitment.india@sanmina.com Preferred candidate profile 1. BE with Electronics & Communication / Electrical and Electronics Engineering with 12 Experience 2. Diploma with Electronics & Communication / Electrical and Electronics Engineering with 14 Experience

Company - Sahajanand Laser Technology Ltd. Designation - Fresher - IPQC/R and D/QA/Production Work Location - Sector 25, Gandhinagar Interested please Mail your CV at placement@SLTL.com/7490055612 (Only WhatsApp) with Subject - "Your Name - Qualification - Location - Position Applying For"

Overview Analyzes, develops, designs, and maintains software for the organization's products and systems. Performs system integration of software and hardware to maintain throughput and program consistency. Develops, validates, and tests: structures and user documentation. Work may be reviewed for accuracy and overall adequacy. Follows established processes and directions. Responsibilities Establishes requirements for less complex design projects Works on Completing all phases of Software engineering design projects Works on analysis of processes and delivers results to necessary stakeholders Analyzes results and recommends solutions Works on developing expected results on a variety of products Develops documentation for new projects and reviews previous results Works with latest technologies and new approaches Reviews changes or upgrades to existing designs or test Exercises judgment in selecting methods and techniques for obtaining solutions on assignments Qualifications All other Regions: Bachelor's Degree 0 to 2 years of experience Quantitative and problem solving skills

To ensure calibration system, functioning as per written procedure and schedule To review the executed BMR, ECRS, analytical data and archieval Batch allocation for dispatch, product label review, monitoring of activities and maintain related records

Role & responsibilities a. Perform routine testing of raw materials, in-process, and finished products as per approved methods. b. Operate analytical instruments like HPLC, GC, UV, FTIR, and dissolution apparatus. c. Maintain and document all test results accurately in compliance with cGMP and GLP guidelines. d. Support stability studies, method validation, and method transfer under supervision. e. Assist in investigation of OOS/OOT results and follow SOPs strictly. f. Ensure proper calibration and maintenance of laboratory instruments. g. Maintain lab safety, cleanliness, and participate in regular training programs. h. Coordinate with other team members to ensure timely completion of lab activities. Preferred candidate profile Candidates having experiences in Pharma formulation(OSD) in EU/USFDA units will be preferred

1. Monitoring and Inspection: In-process inspection: 2. Regularly checking products at various stages of production to verify they meet quality standards and specifications. 4. Documenting findings: Creating detailed reports on inspection Required Candidate profile 3. Process monitoring: Observing and analyzing production processes to identify potential deviations or issues that could affect product quality.

Position Executive / Sr. Executive- QC Grade : A3 A4 Business Unit / Function Department - Quality Control Location Bharuch; SEZ;;;; Reports to Lab In charge-QC; Summary of Job (Purpose/ objective of the job Department Organogram to be enclosed) candidate is required having complete experience in API/Bulk/ Intermediates industries as per global regulatory requirements and responsible for implementation and compliances of ICH-Q7A, cGMP, WHO-GMP, ISO9001, FSSC, HACCP / global QMS requirements at SEZ site. Key Responsibilities (Performance Indicators) Knowledge about IMS system (ISO 9001:2015, ISO 14001:2015 OHSAS 18001:2007, and cGMP, USFDA, FSSC - 22000, NABL. Analytical skill for QC instrument, i.e. GLC, HPLC, UV-Visible, FTIR, ICP, K/F, Melting point etc. Regularize the QC activities as per cGMP requirements. RM, PKG, In-process and FG sampling and Analysis. Co-ordination with QC staff, R and D, Commercial and production for quality and dispatch related activities for on time dispatches. Day to day monitoring and execution online all IPQC and FG analysis activities. Resolve the trouble shooting related to QC activities.; Knowledge about 21 CFR Part 211, 111 with data integrity (Part-11) Awareness about responsible care (Environment, Health, Safety and Security) No. of Reportees Qualification and Experience M.Sc. (Chemistry) with 2 - 6 yrs. Key Competencies; (Technical, Functional and Behavioral) Handling, Calibration and Hand-on experience of all QC instruments. Compliance of 21 CFR Part-11. Troubleshooting related to QC analytical instrument

Monitor & control in-process quality to ensure compliance with product specifications Drive reduction in PPM levels through proactive process improvements &quality checks Identify &implement Poka-Yoke systems at critical process &customer touchpoints Required Candidate profile Support internal & external audits and ensure timely closure of NCRs Maintain up-to-date quality documentation, control plans & FMEA Maintain & report quality KPIs including PPM, COPQ & audit results