101 Inprocess Jobs - Page 3

Location: Mysore, KA, IN Areas of Work: Supply Chain Job Id: 13499 External Job Description Logging into & understanding the DCS and MES system Taking batches through MES as per the planning Preparing shift reports,Monitoring the inventory level in Silo, IBC pumping area, Day tanks, day bins and inform it to the materials technician,Performing stock taking activities with the help of apprentices,Timely calibration of equipments by coordinating with the other stakeholders,Co-Ordinate with engineers for any breakdown,Performing the inprocess checks and doing the necessary adjustments in TSD/Mixer,Ensure running of UV units/scrubber/dust collection system and other auxiliary equipments,Maintain...

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 produ...

Must Have Exp of Bearing Industry only as Quality Manager. Exp of In-process Quality, Final Quality, Customer Quality , Supplier Quality etc. Exp of Customer audit, Customer Handling, IATF, ISO audit Exp of Turning, grinding, CNC , Heat treatment Required Candidate profile Ensure compliance of QA processes & Quality Management Systems (QMS) Monitor & resolve non-conformances, customer complaints & audits daily Lead APQP, PPAP, IATF 16949:2016 documentation & compliance

Job Description Receipt and Storage of Raw and Packing Materials. Dispensing of Raw and Packing materials. Should have knowledge of SAP . Should have good communication skills. Exposure to regulatory enviornment. Work Experience Should have experience of 2 to 5 years in dispensing of raw and packing materials. Education Diploma in Pharmacy Competencies

Improve production quality Process improvement and control Continuous improvement of process quality Process quality control Continuously improve the production process with Lean Implement Cost Saving strategies Quality Improvement reports Required Candidate profile Vacancy for both male and female. Only ITI, B.Sc, B.Com,B.A candidates are prefered

Post - In Process Quality Engineer mail - jobpune22@gmail.com Contact - 9356395439 Experience - 02-05 yrs Bus and Canteen Requirement: Sheet Metal Industry Education: Diploma Automobile/Mechanical Location Pune Khed City Industrial Park Skills Quality Inspection Documentation In Process inspection Part checking Drawing Redding QMS IATF Press Shop or BIW Car Body manufacturing will be advantage.

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 permane...

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, i...

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 produ...

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 r...

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...

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 resili...

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...

•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 temperat...

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 i...

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 Requiremen...

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: Coll...

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"