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1476 Capa Jobs - Page 46

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0.0 - 2.0 years

1 - 5 Lacs

Hyderabad

Work from Office

Chemveda is hiring for Quality Assurance Executive Position Experience - 2-6 years Qualification - M.Sc Chemistry /M.Pharma Designation - Executive Job Responsibilities :- 1. Involves in daily QA activities for SOP compliance. 2. Equipment and Software qualifications Review of USR & SRS, Review of IQ, OQ, PQ document inhouse softwares and maintenance of Equipment and software related back up coordination with other departments. 3. Preparation of refresh and QMS Training presentation and circulating training links to all employees based on training schedules and follow ups. 4. Review of Risk assessments related to change control, CAPA, Deviation, OOS, OOT. 5. Review of Analyst Qualifications ...

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12.0 - 16.0 years

12 - 16 Lacs

Nalagarh

Work from Office

Role & responsibilities Key deliverables Supervise compliance of cGMP and any other applicable regulatory requirement, including EH&S requirements. Complete self-training and monitor training of team members on the relevant SOPs. Report any quality concern or suggestion for improvement to managers. Execute and supervise all tasks and activities as per the applicable SOPs. To lead and guide site investigation teams to investigate the reported OOS, repeat OOT, deviations and market complaints by working closely with site CFT and operating personnel, to arrive at appropriate RCA and CAPA. To personally lead major/critical/repeat investigations and ensure proper closures. To review and share wee...

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12.0 - 22.0 years

12 - 22 Lacs

Bilaspur, Uttar Pradesh, Uttar Pradesh, India

On-site

To ensure plaining and scheduling for annual preventive maintenance of all utilities installed in the plant to attend and timely response for all emergency breakdowns of utility equipment in the plant To ensure and implement GMP requirements in function. Aligning SOP corporate SOP and guideline and to ensure spare part inventory of the utility equipment items in Engineering Stores To evaluate new utility equipment and ETP equipment proposals for Capex modification and its procurement with timely execution support site project team for evaluation and timely completion for utility project To ensure renewal of registrations and licenses related to Utility equipment for concerned Government Depa...

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7.0 - 15.0 years

7 - 15 Lacs

Bilaspur, Madhya Pradesh, , India

On-site

Overhauling & replacing faulty parts of process & utility equipment. Trouble shooting in case of any abnormality/breakdown & diagnosing the troubles. Responsible for undertaking maintenance, repairs, minor improvement works across the site Recording all maintenance records & reports for future reference Execute preventative and corrective maintenance of equipment s. Ensure work compliance as per job orders/work permits. Responsible for getting the material from Engineering Store for the respective work to be carried out. Ensure preventive maintenance has been carried out within schedule date. Ensure compliance of job order and closure of work permits. Responsible to check the breakdown/maint...

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3.0 - 7.0 years

4 - 6 Lacs

Rajkot, Gujarat, India

On-site

This role is for one of the Weekday's clients Salary range: Rs 400000 - Rs 600000 (ie INR 4-6 LPA) Min Experience: 3 years Location: Rajkot JobType: full-time Seeking an experienced quality professional responsible for conducting 100% inspection and ensuring the quality of raw and machined castings. The role involves verifying compliance with customer specifications, engineering drawings, internal SOPs, and relevant industry standards. The Senior Quality Engineer plays a key role in identifying non-conformities, supporting root cause analysis, and driving corrective and preventive actions to maintain product quality and integrity. Requirements Key Responsibilities: Perform 100% visual inspec...

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8.0 - 12.0 years

8 - 12 Lacs

Bilaspur, Madhya Pradesh, , India

On-site

Overall responsible for New Project, Modification jobs activity in the plant as per requirement of site. Project management and execution of new and expansion project from Design to till handing over to plant. Also closing of project with capitalization. Responsible for execution of project with given time line. Compliance of all statutory & GMP requirement in new project. Design & compliance of safety practices at site and to ensure zero reportable incidents. Coordination with consultant for technical aspect. Evaluation of Design, drawing, technical specification as per Teva Standards. Procurement assistance to SCM for project. Installation and commissioning of project as per standard/ Teva...

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15.0 - 25.0 years

15 - 25 Lacs

Bilaspur, Uttar Pradesh, Uttar Pradesh, India

On-site

To do planning and scheduling for annual preventive maintenance and calibration of all electrical and instrument installations in the Plant To attend and timely response for all emergency breakdowns of electrical and instrument installations in the plant. To ensure tentative schedule for earthing audit of all electrical installations and its execution, also scheduling & implementations of other GMP requirements. To ensure implementing compliances of computer validation as per 21CFR part 11, GAMP-5 and other relevant guidelines. Ensure the GMP compliance in calibration lab and instrument function. To inspect and approve the electrical and instrumentation items received in Engineering Stores. ...

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10.0 - 12.0 years

5 - 12 Lacs

Noida, Uttar Pradesh, India

On-site

Job Description JOB DESCRIPTION Position Title: Quality Manager Reports to: Operations Location: Noida Experience: At least 10 years related working experience in a manufacturing environment with at least 5 years in management position. Working experience in automotive industry is a must. Academic: B-Tech / BE Overview: The Quality Manager at IMI Transport plays a crucial role in maintaining and enhancing the highest standards of product quality and regulatory compliance. This position leads the implementation and maintenance of effective quality management systems, driving continuous improvement to enhance customer satisfaction and organizational efficiency. Key Responsibilities: ? Maintain...

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5.0 - 7.0 years

6 - 12 Lacs

Pune

Work from Office

Role & responsibilities: Experience on Mechanical design. Experience of delivering on Design change management , Design documentation , Risk management, DFEMA. Medical Device industry experience will be preferred . Skill Set: Must have - Medical Domain & Process Mechanical Design and Design Documentations Risk Management , Understanding of Product design cycle DFMA , GDnT , Medical domain Quality process Medical Regulatory Keywords & Tools: Medical Device industry experience Design Documentations. Solidwork , PLM Windchill, CAPA

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2.0 - 5.0 years

3 - 4 Lacs

Bengaluru

Work from Office

Position: Contract Engineer Project portfolio and Quality Key Purpose of the Job: As a member of the Project Management team, the Contract Engineer will facilitate project gate reviews, act as a project scheduler, and consolidate gate meeting outcomes (GO/NO GO). The role involves monitoring risk assessments, advising project teams on gate outcomes, and ensuring adherence to quality standards at each project stage. The engineer will also support project quality initiatives, certification processes, and problem-solving methodologies such as 8D and ISO standards Key Responsibilities: Facilitate project gate reviews and consolidate outcomes. Act as a project scheduler and ensure alignment with ...

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5.0 - 8.0 years

4 - 5 Lacs

Nalagarh, Faridabad

Work from Office

To Maintain documentation as per ISO-9001:2015 in plant To make PPAP of all part which is produced in other Plant To carry out doc audit as per the doc audit process Responsible for Instrument and gauges Required Candidate profile To conduct daily training of operator Auditee for Internal Quality Audit To maintain 5S at work place To initiate the corrective action for any non conformity

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8.0 - 13.0 years

8 - 10 Lacs

Baddi

Work from Office

Role & responsibilities :- Lead the development, implementation, and continuous improvement of our Quality Management System (QMS). Ensure adherence to industry standards and regulatory requirements (e.g., EMA, WHO). Collaborate with cross-functional teams to drive quality initiatives and foster a culture of quality. Oversee audits and inspections, ensuring timely resolution of findings and implementation of corrective actions. Analyze quality metrics to identify trends and recommend improvements to enhance product quality and safety. Develop and implement quality management system policies and procedures. Identify, analyze, document and report on system deficiencies. Monitor and evaluate th...

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12.0 - 15.0 years

20 - 25 Lacs

Pune

Work from Office

Role & responsibilities Lead and manage the Quality Assurance and Quality Control teams across the plant. Develop and implement quality strategies aligned with organizational goals and customer requirements. Drive continuous improvement initiatives using Six Sigma, Lean, and other quality methodologies. Oversee the deployment and optimization of Automatic Optical Inspection (AOI) systems. Analyze quality data using advanced analytical tools (e.g. Minitab, SPC, DOE, FMEA, Root Cause Analysis). Ensure compliance with ISO/TS standards and customer-specific requirements. Lead internal and external audits, and manage corrective/preventive actions (CAPA). Collaborate with cross-functional teams in...

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2.0 - 6.0 years

1 - 5 Lacs

Hyderabad

Work from Office

Chemveda is hiring for Quality Assurance Executive Position Experience - 2-6 years Qualification - M.Sc Chemistry /M.Pharma Designation - Executive Job Responsibilities :- 1. Involves in daily QA activities for SOP compliance. 2. Equipment and Software qualifications Review of USR & SRS, Review of IQ, OQ, PQ document inhouse softwares and maintenance of Equipment and software related back up coordination with other departments. 3. Preparation of refresh and QMS Training presentation and circulating training links to all employees based on training schedules and follow ups. 4. Review of Risk assessments related to change control, CAPA, Deviation, OOS, OOT. 5. Review of Analyst Qualifications ...

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3.0 - 8.0 years

5 - 10 Lacs

Hyderabad

Work from Office

Job Area: Finance & Accounting Group, Finance & Accounting Group > Internal Audit General Summary: Job Overview Qualcomm is a company of inventors that unlocked 5G - ushering in an age of rapid acceleration in connectivity and new possibilities that will transform industries, create jobs, and enrich lives. But this is just the beginning. It takes inventive minds with diverse skills, backgrounds, and cultures to transform 5Gs potential into world-changing technologies and products. This is the Invention Age - and this is where you come in. This is a unique opportunity to join Qualcomms finance and accounting organization based in Hyderabad in the Corporate Internal Audit & Advisory Services (...

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3.0 - 5.0 years

3 - 6 Lacs

Tirupati, Jharsuguda, Vallam

Work from Office

Sr. Executive AM- Hot Refining: CMR GreenTechnologies Limited CMR Group is India's largest producer ofAluminium and zinc die-casting alloys. With 13 state-of-the-art manufacturingplants across the country, CMR has become the preferred supplier for many ofIndias largest automotive industry leaders. Since its inception in 2006, CMRhas consistently outpaced competition by focusing on delivering superior valueto its stakeholders. This value is driven by a strong commitment to technicaladvancements, quality enhancement, sustainability, and people-centric practices.We believe in an " Employee First " philosophy, ensuring that our people are at the core of our success. Our dedication tofostering an...

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2.0 - 6.0 years

4 - 7 Lacs

Mumbai, Delhi / NCR, Bengaluru

Work from Office

Job Summary: We are seeking a highly skilled and detail-oriented Quality Control (QC) Engineer with 35 years of experience in quality inspection, process validation, and compliance monitoring. The ideal candidate will ensure that our products meet internal and external standards and comply with regulatory and customer requirements. You will work closely with cross-functional teams, including Production, R&D, and Supply Chain, to drive continuous quality improvements in a high-performing, fast-paced environment. Key Responsibilities: Perform inspections of incoming materials, in-process items, and finished products to ensure compliance with specifications and industry standards. Develop and i...

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10.0 - 15.0 years

15 - 28 Lacs

Remote, , India

On-site

Bachelor's degree with over 10 years of experience in designing and developing solutions in Trackwise. Experience working in a GMP environment, 7+ years in an IT Systems Role. Expert knowledge of GMP Quality Management to include CAPA/Deviation, Lab Exception, Product Complaint, Audit, and Supplier Management. SDLC/GAMP, Business Analysis, and Enterprise Systems Management. General knowledge of GxP Quality Processes and Systems (GMP, GLP, GCP, GVP, GDP) Demonstrated experience leading teams in the implementation of Trackwise and QMS solutions, ensuring alignment with business objectives and compliance requirements. Comprehensive understanding of Quality Management processes, regulatory compl...

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10.0 - 15.0 years

10 - 12 Lacs

Amroha, Moradabad

Work from Office

Ensure Quality of products, processes & services r established,monitored & maintained & against defined Goals.Establish Strong Customer Base while performing Internal/External Audits & Plant Improvements.Ensure people/process adhere 2 Co's norms Required Candidate profile Develop & maintain Quality Standards/check procedures throughout.Analyzing rejections/rework/statistical data to take CAPA to eliminate root cause of problems in order to prevent recurrence of problem

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2.0 - 7.0 years

3 - 6 Lacs

Hyderabad, Chennai, Bengaluru

Work from Office

Raw Material Inspection. Like Boards, Kraft, Liner, Adhesive, Coating, Film, Etc (Sampling, Testing, Reporting & Recording) In-Process Checking (Printing & Post printing) COA (Certificate of Analysis) making. Lab Instruments Calibration Required Candidate profile Customer Specification Analysis & Comparison Against Actual. Job Traceability (Forward & Backward) Creating Job file like Artwork, KLD, shade card, approved Dummy and Inspected incoming raw materials. Perks and benefits Accommodation, PF, ESI, Bonus

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8.0 - 10.0 years

6 - 10 Lacs

Noida, Hyderabad, Bengaluru

Work from Office

Req ID: 309049 We are currently seeking a QA - Core Banking Data migration to join our team in Noida, Uttar Pradesh (IN-UP), India (IN). Job TitleQA Data Migration "“ Core Banking (Transact) : We are looking for a highly skilled Quality Analyst with expertise in the banking sector, specifically in Core Banking (Transact) along with migration experience. The successful candidate will be responsible for ensuring the quality and integrity of data during migration from legacy systems to new platforms. Key Responsibilities: Develop and execute test plans, test cases and test scripts to ensure data integrity, accuracy and completeness during migration. Work across multiple functional projects to u...

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0.0 - 5.0 years

4 - 5 Lacs

Coimbatore

Work from Office

SUMMARY Ensure the quality of incoming materials, in-process production, and finished products meets defined standards. Manage PPAP activities for new parts, engineering changes, and improvement projects to ensure compliance with design and industry requirements. Investigate root causes of internal defects, customer complaints, and rework using quality tools, and implement effective corrective and preventive actions (CAPA). Conduct regular internal and supplier audits to ensure compliance and drive quality improvements. Support continuous improvement initiatives to reduce defects and increase operational efficiency. Ensure all quality activities align with the requirements of the Integrated ...

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2.0 - 7.0 years

2 - 7 Lacs

Jhagadia, Ankleshwar

Work from Office

JD: 1) To be prepared document related to audit as per audit agenda. 2) Filled vendor questionnaires & prepared related documents. 3) Keeping record of key Customer. 4) To be prepared process validation protocol and report as per seniors guidance. 5) To be prepare cleaning validation protocol and report as per seniors guidance. 7) To be prepared master, controlled, uncontrolled, reference, obsolete & distribute documents as per SOPs and formats requirement. 8) To help the senior for preparation of CAPA according to audit report. 9) Issuance of Change control, OOS, deviation & other QMS formats whenever required from respective department and retained record in logbook. 10) To be prepared BPC...

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2.0 - 7.0 years

3 - 8 Lacs

Ahmedabad

Work from Office

Walk-in at Matoda We are hiring multiple positions for our manufacturing facility at Matoda as mentioned below. Please find our current job requirements and venue details mentioned. If any of the requirements match your current job profile, kindly walk in with your latest resume. Role & responsibilities Injectable Manufacturing & Visual Inspection Aseptic operations/ QMS / SKID / Multi-vessel / SVP / Visual Inspector (Senior Officer / Officer / Associate) Experience - 01 to 05 Years Qualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma / ITI OSD – Manufacturing / QMS (Senior Officer / Officer / Executive) Experience - 02 to 07 Years Qualification – B. Pharmacy/ M Pharmacy Engineering ...

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5.0 - 10.0 years

5 - 9 Lacs

Ahmedabad

Work from Office

Maintain QMS & ensure compliance with GMP standards across the plant Conduct audits, compile reports, approve vendors for RM & packaging Review documentation like SOP, BMR, BPR, APQR, etc Handle deviations, complaints, OOS reviews, and implement CAPA Required Candidate profile Experience facing audits in the pharma intermediates/API/bulk drug industry only; formulation experience not relevant Excellent communication skills for audits. Fluency in English & MS Office.

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