130 Inprocess Jobs

Role & responsibilities Lead and manage all QC activities in accordance with approved SOPs and regulatory requirements. Approve job descriptions, assign responsibilities, and develop QC team members through training. Review and approve analytical documentation ensuring cGMP, cGLP, ALCOA++ compliance, and data integrity. Prepare, review, and approve QMS activities including OOS, OOT, Deviations, Change Control, CAPA, and Incidents. Ensure proper sample receipt, testing, review, approval/rejection, and timely batch release to meet SLAs and dispatch plans. Plan and allocate resources for testing of RM, IP, Bulk, FG, Validation, Stability, and external lab samples. Ensure specifications, STPs, w...

Preferred candidate profile Diploma in pharmacy/mechanical/electrical with minimum 1 year experience in OSD production. Recruiter Mohaneswara https://www.linkedin.com/in/mohaneswarareddy Role & responsibilities Operate Fluid Bed Equipment and Spheroniser as per SOP, including cleaning and line clearance activities to ensure readiness for production. Strict adherence to safety, health and environment. Carry out Manufacturing activities by following and monitoring standard operating procedure (SOP) and current Good Manufacturing Practice (cGMP). To ensure effective implementation of RFT and Data integrity policy. Maintenance, upkeep of the department, premises, and equipment. To maintain disci...

Greetings from Immacule Lifesciences Pvt. Ltd. We are hiring Quality Control professionals (all sections) for our new Injectable Manufacturing Plant located at Nalagarh . Qualifications: M.Sc. B. Pharma M. Pharma Requirements: 3 to 9 years Strong experience in HPLC analysis Exposure to USFDA-approved facilities is mandatory Job Location: Nalagarh Interested candidates may share their updated resume at: eswar.reddy@immacule.in

Position - Jr QC / Sr QC / Asst Manager QC Exp - 1 to 10 yrs Salary - As per Cmpy Norms Location - Chennai

Preferred candidate profile Diploma in pharmacy/mechanical/electrical with minimum 1 year experience in pellets production. Recruiter Mohaneswara https://www.linkedin.com/in/mohaneswarareddy Role & responsibilities Operate Fluid Bed Equipment and Spheroniser as per SOP, including cleaning and line clearance activities to ensure readiness for production. Strict adherence to safety, health and environment. Carry out Manufacturing activities by following and monitoring standard operating procedure (SOP) and current Good Manufacturing Practice (cGMP). To ensure effective implementation of RFT and Data integrity policy. Maintenance, upkeep of the department, premises, and equipment. To maintain d...

Purpose/Objective The Shift Engineer - Cluster - IPQA conducts in-process quality inspections during shifts, monitoring production processes and identifying quality deviations. This role records and analyzes quality data, assists in implementing corrective actions, provides training on in-process quality procedures, and supports continuous improvement initiatives to enhance process quality. Key Responsibilities of Role Safety: - Follow and promote safety guidelines during inspections and quality checks, contributing to a safe work environment. In-Process Inspections: - Conduct in-process quality inspections during assigned shifts to ensure compliance with quality standards at stages like tex...

Opening for Pharma Lifescience. Role & responsibilities : Candidate is having knowledge of OSD Formulation Plant. Depth knowledge of In Process Quality Assurance . Third Party Manufacturing Knowledge. Candidate is Ready for Within City Travelling for who are Manufacturing our Medicine. Qualification:-M-Pharma-QA or B-Pharma. Interested candidates shared resume on snehal@topgearconsultants.com

SUMMARY Responsible for ensuring incoming materials, production processes, and finished products meet the required specifications and quality standards. Handle PPAP activities for new parts, design changes, and improvement projects, including casting, machining, plastic, and fabricated components. Perform root cause analysis for customer complaints and implement CAPA. Perform regular internal and supplier audits to check compliance and improve quality. Support improvement activities to reduce defects and increase efficiency. Ensure all quality tasks follow IMS (Integrated Management System) requirements. Requirements Qualification: Bachelor’s Degree in Mechanical Engineering (BE Mechanical) ...

D.M.E. / D.A.E. Minimum 7+ yrs of work experience in any Automobile Manufacturing company as In-process inspection / Q.C. Need to do final inspection before despatch. IAFT 16949:2016 / Cost / Safety Location: Vellore Good Salary with other befits

Role & responsibilities Has an excellent attitude to ensure with Zero Defect outflow Disciplined, diligent and quality conscious mindset. Good communication skills Good eye hand coordination Good 2D drawing reading skill Good GD&T and Quality Core tools knowledge Good knowledge on the 7QC tools Good knowledge on all measuring instruments Ability to follow instructions and diagrams as delivered for each parts Diploma in Mech or Electrical or Automobile with 1 to 2 year experience SAP, Odoo knowledge is added advantages Preferred candidate profile

We are looking for Quality Officers with hands on experience of chemical industry.

Hiring experienced IPQA professionals (48 years) for OSD formulation unit. Job Responsibilities: Line clearance, in-process checks, documentation (BPRs / Logbooks), Empower-3, Analytical Data Review, and QMS activities. Perform in-process checks during granulation, blending, compression, encapsulation & coating. Monitor IPC parameters: LOD, bulk density, blend uniformity, we Provide line clearance for manufacturing & packing operations Review BMR/BPR and ensure real-time documentation as per GMP/GDP . Verify equipment cleaning and ensure absence of cross-contamination . Conduct online sampling and coordinate with QC for testing. Support process validation & cleaning validation for OSD equipm...

Role & responsibilities : 1 to 2 years experience in Manufacturing group with Regular B.Tech Qualification. Candidates have to comfortable to relocate to our Dholera, Gujarat Solar Manufacturing Plant.

Ensure the effective implementation of the Quality Management System in the production operations. Increase the Level of Customer Satisfaction, compliance with customer, regulatory and company requirements and achieve the company business objectives

Role & responsibilities 1) Sampling and testing of Raw material, Packaging material, in process samples and finished products as per specification and standard testing procedure. Testing of water samples as per defined sampling frequency. 2) Preparation of laboratory reagents and volumetric solutions required for chemical analysis in the laboratory. 3) Preparation of SOP (standard operating procedures), EOP (equipment operating procedures), protocols, STP (standard testing procedures) and specifications for the in-process samples and finished products as per customer requirement. 4) Calibration of the laboratory instruments as per the equipment operating procedures. 5) Appropriate record kee...

Job Title: Officer Business Unit: Sun Global Operation Job Grade G12C Location : Gangtok At Sun Pharma, we commit to helping you “Create your own sunshine” — by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Key responsibilities: o Ensure completion of all SOP as Training need matrix...

1. Job Purpose To lead and manage quality assurance activities within the manufacturing plant by ensuring product compliance with customer specifications, national/international standards, and internal quality systems. Responsible for process control, supplier quality, in-process inspection, customer complaint resolution, and continual improvement initiatives. 2. Key Responsibilities A. Quality Planning & System Management Implement and maintain documents for IMS as per ISO 9001 / ISO 14001 /ISO 45001 Prepare and maintain quality documents: Control Plans, FMEA, SOPs, Work Instructions, Manufacturing Quality Plans . Support internal and external audits (Customer, ISO, Regulatory). Drive corre...

Roles and Responsibilities - Electronics Experience perferable Review the Quality targets - CLR, warrenty claim, Inprocess rejection analysis, Incoming rejection, scrap monitoring status Review the Quality assurance plan and monitoring Review the Internal audit plan, Calibraion plan, MSA plan and adherence Review the Document control through SAP, MIS and WEB VAN Presenting the MRM with top management and team Review, verify and approve the Quality Assurance section Management of staff in Quality Assurance section Ensuring that processes needed for Quality management system are etablished, implemented and maintained Performance management of Quality Management system Management of PM Meeting ...

Job Title: QC Analyst Business Unit: Global Quality And Compliance Job Grade G12C/G12B Location : Jammu At Sun Pharma, we commit to helping you “Create your own sunshine” — by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you will find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Key responsibilities: 1) To perform analysis of samples all...

Role & responsibilities Monitor manufacturing processes to ensure adherence to quality standards and specifications. Analyze process data to identify trends, deviations, and areas for improvement. Develop and implement process control plans and procedures. Lead root cause analysis and problem-solving initiatives for quality-related issues. Work with production teams to implement corrective and preventive actions (CAPA). Collaborate with engineering teams to optimize processes for quality and efficiency. Maintain accurate and up-to-date records of quality performance metrics. Ensure all quality documentation complies with industry standards and regulations. Address customer complaints and con...

Role & responsibilities The In-Process Quality Engineer/Sr. Engineer is responsible for ensuring product and process quality during manufacturing operations. The role focuses on monitoring in-process inspection activities, driving defect reduction, maintaining compliance with ISO standards, analyzing quality trends, and supporting continuous improvement initiatives across the production floor. Duties & Responsibilities Monitor and control in-process quality through routine inspections, audits, and process checks. Establish and maintain in-process inspection plans, sampling plans, check sheets, and control charts. Work with production operators, line leaders, and supervisors to ensure process...

Ensure safety and quality compliance, support audits, manage customer complaints, track and reduce PPM, conduct process/product audits, enable defect-free launches, implement SPC/Kaizen/Poka-Yoke, maintain calibration, and train/engage teams. Required Candidate profile B. E/ B.Tech in Mechanical 3–7 years in automotive manufacturing quality

Handling of in-process and final inspection. Hands-on with inspection instruments i.e. Vernier Caliper, Height Gauge, VMM, attribute gauges, micrometer. Knowledge of Control Charts, SPC Hands-on with inspection methods for precision products. Required Candidate profile Diploma- Mechanical Engineering, Min. 1+ year exp as a Quality Executive/ Engineer for in-process and final inspection in Medical Devices or Automotive Industry.

Post: In-Process Engineer / Senior Engineer for Medical Devices Manufacturing Job Location: Faridabad Company: Aktive Technologies Pvt. Ltd. Whatsapp/Mobile: 9899546490 Experience with SPC, MSA, Control Plans, FMEA, and process audits. Required Candidate profile Ensures product/process quality during manufacturing of Medical Device System. IPQC, audits, defect analysis (5 Why, 8D), SOP validation, SPC, ISO 9001/13485 compliance,

Patrol Inspection / Line Inspection / In process Inspection for machined parts,dock audit, Check for process capabilities, Monitor tool life