62 Inprocess Jobs - Page 3

Roles and Responsibilities Conduct quality control tests on raw materials, intermediates, and finished products using techniques such as HPLC, GC, FP, IP, Stability studies. Ensure compliance with cGMP guidelines and maintain accurate records of testing results. Investigate market complaints and perform microbiological analysis to identify root causes. Develop and implement quality assurance procedures for OSD formulations. Collaborate with cross-functional teams to resolve issues related to dissolution testing.

Roles and Responsibilities Ensure compliance with GMP guidelines, BMRs, OSD requirements, and WHO standards for IPQA activities. Develop and implement effective quality control processes to ensure product quality and regulatory compliance. Conduct regular audits, inspections, and investigations to identify areas of improvement in batch manufacturing operations. Collaborate with cross-functional teams to resolve quality issues related to formulations, tablets, capsules, etc. Provide training on Good Manufacturing Practices (GMP) and other relevant regulations to employees.

Exciting opportunity for IPQA Executive at our EU approved OSD Manufacturing faculity (UNIT 1) @ Moraiya, Ahmedabad!! Company : Unison Pharmaceuticals Pvt Ltd Website : www.unisonpharmaceuticals.com Location : UNIT 1 , Moraiya, Ahmedabad Experience : 4 - 9 Years Dept. & Sub Dept. : QA - IPQA - OSD MFG Designation : Executive Job description (Not limited to): Collect in-process and Finished sample as per Specifications and Protocol. Check documents like equipment log books, temperature & humidity records. Line clearance of machine & manufacturing area . Checking of batch manufacturing record. Perks & Benefits Dynamic work environment Career development opportunities Work-life balance Free transportation Canteen facility Free insurance coverage for self, spouse, and kids Range of learning opportunities to help employees grow and thrive If you are passionate about continuing to work in the pharmaceutical industry and possess the required skills, we encourage you to apply for this position. Please submit your resume to career@unisonpharmaceuticals.com to be considered for this role. Join our team at Unison Pharmaceuticals and take the first step towards a rewarding career.

School : WITTY Campus : Witty International School, Malad Country : India Qualification : B.Sc+B.Ed ,M.Sc ,Subject Expert Qualification OverView : PGT Teacher - Chemistry - CAIE 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 organisational 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.

Role & responsibilities We are looking for candidate on below criteria at our Nalagarh Plant Himachal Pradesh location. Candidate must have completed Pharma, M.Sc. or B.Sc. in Chemistry. Experience of regulatory industry would be preferred. Candidate should have 1-3 years of working experience Preferred candidate profile Responsible for Line clearance in Warehouse and Production area during dispensing, MFG, Filling and Packing & review of log books and status label of each equipments before start of activity. Responsible to carry out in-process checks as per respective Batch Production Record in Manufacturing, packing and warehouse. To ensure that the manufacturing and packing operations are carried out as per the instructions given in the Batch Production Record. Responsible for collection of in-process samples, FP sample, control samples, validation & stability samples. Responsible to make SAP entries, Release of inspection lot of SFG & FG, Physical sampling confirmation, Approval of Batch Production Records for printing and additional page issuance. Responsible for online review of Batch Production record and make entry of data required for trending in maintained excel sheet for preparation of APQR. Responsible for Line clearance in Warehouse and Production area during dispensing, MFG, Filling and Packing & review of log books and status label of each equipment’s before start of activity. Responsible to carry out in-process checks as per respective Batch Production Record in Manufacturing, packing and warehouse. To ensure that the manufacturing and packing operations are carried out as per the instructions given in the Batch Production Record. Responsible for collection of in-process samples, FP sample, control samples, validation & stability samples. Responsible to make SAP entries, Release of inspection lot of SFG & FG, Physical sampling confirmation, Approval of Batch Production Records for printing and additional page issuance. Responsible for online review of Batch Production record and make entry of data required for trending in maintained excel sheet for preparation of APQR. Perks and benefits

Role & responsibilities 1) Responsible for in process quality respective line. 2) To take in-charge of quality control activities. 3) Responsible for reduction of line rejection and rework. 4) Monitoring of re-work & rejections 5) Final inspectors training & development 6) Preparation of CAPA at particular line. 7) TPM circle activities. 8) Updating of respective documents and records on time. 9) Monitoring of First, Middle and Last Inspection. 10) Maintain 5S & 3C in the respective area 11) Ensure F/M/L reports to be reviewed Knowledge (Technical / Functional) Process knowledge in Welding & Sheet metal Analytical knowledge by using Quality core tools TPM QM module *Welding process knowledge must (MIG/TIG) Skills Good Communication Skill Presentation Skill Team Handling Skill Analytical Skill Qualifications B. E, Mech or Automobile Experience 5 to 7 years min. Contact: 9789092178 Email: arun.prasad@shardamotor.com

Post- Junior Engineer Quality Assurance Email - jobpune12@gmail.com Contact - 9356395439 Experience - 04-08 yrs Edu - DME / BE Mechanical Location - Pune Pirangut Industry - Automotive JD Conduct in-process inspection of machined parts Manufacturing QA to ensure in-process quality, maintain compliance . Maintain IATF 16949, ISO 9001 & PPAP documentation and support audits. Prepare PDIR, 8D/RCA methodology QC tools, gauges, control plans, PPAP, ERP, and machining component Handle customer quality interactions .

JOB DESCRIPTION 1) Technical Skills: a. In depth knowledge of Transmission / Gear Box manufacturing and Process specific knowhow b. Hands on experience on handling of Torque measuring and monitoring equipments. c. Experienced in Gear Manufacturing processes like Hobbing, Shaping, Shaving, Profile grinding, Gear Honing etc. d. Proficient in understanding Transmission EOL (End of line) testing, Analysis and able to drive improvement programs e. In depth knowledge of critical parts like Hydraulic Control Unit, Clutch assembly, Transmission Control unit and other critical electrical and electronic accessories associated with Transmission f. Proficient in Process Audit inline with AIAG/VDI/VDA guidelines. g. Proficient in latest data analysis, SPC and MSA techniques. e. Proficient in Project Management inline with APQP/PPAP requirements. 2) Quality Management System (QMS): a. Develop, implement, and maintain a comprehensive Quality Management System (QMS) in compliance with relevant industry standards and regulations. b. Ensure QMS documentation is up-to-date, accessible, and effectively communicated to relevant stakeholders. 3) Quality Assurance and Control: a. Establish and enforce quality control procedures, standards, and inspection processes to monitor and maintain product and service quality. b. Conduct audits and assessments to identify non-conformities and areas for improvement. c. Develop and implement corrective and preventive action plans to address quality issues. d. New Project development activities with effective usage of APQP/PPAP process. 4) Leadership and Team Management: a. Lead a team of quality professionals, providing guidance, coaching, and training as necessary. b. Foster a culture of quality excellence within the organization. 5) Quality Metrics and Reporting: a. Define key quality performance indicators (KPIs) and metrics to track and report on quality performance. b. Regularly analyse data and generate reports to assess the effectiveness of quality initiatives. c. Handle in process audit & analysis function with timely closure of issues. 6) Continuous Improvement: a. Drive continuous improvement initiatives by identifying opportunities to enhance processes, reduce defects, and improve overall quality. b. Implement lean and Six Sigma methodologies to optimize operations. 7) Regulatory Compliance: a. Stay up to date with relevant industry regulations and standards, ensuring the organization's compliance. b. Prepare for and participate in quality-related audits and inspections. Qualifications and Education Requirements a) B.E. in Mechanical Engineering orAutomobile Engineering. b) More than 10 years of professional experience. c) Current Role- Process QA Role in last 5 years with companies having TO of 500 Cr. d) Person who has worked for customers like TML, M&M, Maruti Suzuki, Daimler, GM, Stellantis etc. Preferred Skills / Competencies a) Quality Management System (QMS) b) Quality Assurance and Control c) Leadership and Team Management d) Quality Metrics and Reporting e) Continuous Improvement f) Regulatory Compliance g) Hi Tech product supplied to passenger cars consisting of Mechanical/Electrical/Hydraulics. h) New Product Development

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+ years of experience Quantitative and problem solving skills

Roles and Responsibilities Conduct quality control tests on raw materials, in-process samples, finished products, and stability studies using HPLC, GC, UV, Dissolution, LIMS, Microbiology techniques. Ensure compliance with GLP guidelines for laboratory operations and maintain accurate records of test results. Collaborate with cross-functional teams to resolve quality issues and implement corrective actions. Develop and execute protocols for wet analysis testing of pharmaceutical products. Participate in audits conducted by regulatory authorities or internal stakeholders.

Role & responsibilities Expert in Dimensional Layout Inspection of all Commodity Parts (Casting, Forging, Sheet Metal, Electrical, Proprietary, Rubber, Plastic, Barstock & Hardware) Incoming Sampling Inspection, Layout Inspection (With Ballooning) & 3D Scanning of Casting and/OR Cast Machining Parts for Dimensional Conformance in-line with DRG Accountable for New Part PPM Monitoring and Reduction- Inhouse, Zero-Hr & Field Failures- Root Cause Analysis and Corrective Actions Correction of New/Modified/Alternate Source Parts & PPAP Requirements Compliance before 100% Introduction in Regular Production Fitment & Functional Trials of New/Modified/Alternate Source Parts Quality Planning (QM View Generation) of New/Modified/Alternate Source Parts in SAP Daily & Monthly New Parts- MIS Generation and Communication to all Stakeholders Periodical Supplier Process Audit for Repetitive Failures & Supplier Assessment during Development Stage Capable of All Mechanical & Electrical Drgs Understanding- GD & T Parameters and Interpretation All Commodity- New Parts: Critical Inspection Gauges Planning & Procurement for In-house Inspection Core Quality Tools (APQP, PPAP, FMEA, SPC and MSA) Knowledge and Hands on Experience Preferred candidate profile Candidates - B.E. Mechanical with 9+ Years of experience in New Parts Quality Inspection with having experience in Engine Manufacturing Company Interested candidates may share their resume on sv21@svmanagement.com or may contact on 9893191553

Experience of FG/RM/Stability Analysis, validation samples and method validation . Must have handled HPLC ,GC,UV & other related QC instruments. Exposure of analysis in Formulations: Tablets/capsules