33 Quality Control jobs in Vadodara

• Quality Control based in Waghodia, Vadodara
• The ideal candidate brings 4-7 Years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments
• Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety
• The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen)
• Additional info:
• Role: Chemist & Analysts (For RM/PM, AMV/IPFP, Report Preparation)
• Experience: 4-7 YearsEducation: B.Sc/M.Sc
• in Chemistry with sterile USFDA experience Must demonstrate strong ownership, attention to detail, and the ability to work in a fast-paced, inspection-ready environment
• Familiarity with ICH, WHO TRS, ISPE, and data integrity principles is expected; hands-on with spreadsheets/ERP/LIMS is a plus

Job Title: Quality Control Chemist

Company: Ambrosia Remedies Pvt. Ltd.

Location: Waghodia GIDC, Vadodara

Experience Required: 13 Years

CTC: 3.0 – 4.0 LPA

About the Company

Ambrosia Remedies Pvt. Ltd. is a fast-growing pharmaceutical company dedicated to delivering safe, effective, and high-quality healthcare solutions. We are committed to maintaining global quality standards while ensuring compliance with regulatory norms.

Job Responsibilities

• Conduct quality control testing of raw materials, Packing materials, intermediates, and finished products as per defined specifications.
• Perform analysis using analytical instruments such as HPLC, UV, and other relevant techniques/Instruments.
• Monitor and test purified water, effluent water, and other utilities as per regulatory requirements.
• Prepare and maintain accurate documentation, analytical reports, and test records in line with WHO and GMP guidelines.
• Ensure adherence to Standard Operating Procedures (SOPs) and Good Laboratory Practices (GLP).
• Participate in audits, validations, and continuous improvement activities in the QC department.
• Collaborate with production and QA teams to ensure consistent product quality.

Key Skills & Competencies

• Proficiency in analytical techniques (HPLC, UV, Titrations, etc.).
• Strong knowledge of regulatory guidelines (WHO, GMP, GLP).
• Good documentation and reporting skills.
• Problem-solving mindset with attention to detail.
• Ability to work under timelines and in a team environment.

Educational Qualification

• B.Sc. / M.Sc. in Chemistry / Pharmaceutical Chemistry / Industrial Chemistry

Why Join Us?

• Opportunity to work with advanced analytical instruments and techniques.
• Exposure to international quality standards and compliance requirements.
• Career growth in a professional and supportive work environment.

Role & responsibilities

• Conduct in-process inspection of fabricated parts as per drawing and Standard Operating Procedures (SOP).
• Perform inspection of sub-assemblies and final assemblies as per General Arrangement Drawings (GAD) and P&ID.
• Apply quality tools such as 7 QC tools, Why-Why analysis, and 8D for effective problem-solving.
• Carry out final inspection and testing of systems in accordance with customer requirements.
• Prepare and implement control plans and ensure adherence throughout the process.
• Maintain proper documentation and records of inspections and tests conducted.
• Assist in vendor assessment and vendor development in coordination with the purchase department.
• Participate in and support implementation of 5S, KAIZEN, and other continuous improvement activities.
• Monitor and verify surface preparation, blasting, painting, and powder coating quality, and maintain DFT check records.
• Conduct supplier inspections to verify capability and compliance with requirements.
• Coordinate with Production and Design teams to resolve quality concerns during manufacturing and contribute to continual improvement.
• Possess working knowledge of Quality Management System (QMS) as per ISO 9001:2015 and be capable of facing audits. (Internal auditor certification will be an added advantage.

Preferred candidate profile

• Achieve Zero Defect (Inspection accuracy no defect in inspected parts)
• Process improvements (Continuous improvement – KAIZEN)
• Problem Solving – CAPA (Avoid recurrence of problems)
• Systematic Documentation & Record Keeping

• The BK QC Associate plays a critical role in reviewing and ensuring quality standards, processing accuracy and compliance as per predefined checklist.
• This position requires an understanding of legal documentation, including but not limited to court orders, retainer agreement, affidavits, and BK filings, which are essential for ARCHER to deliver its services.
• The BK QC Associate will collaborate closely with the BK Coordinators from both US and IND businesses to execute daily responsibilities.

JOB RESPONSIBILITIES : -

• Collaborate with onshore and offshore teams to ensure quality compliances and processing accuracy for daily operations.
• Independently audit population/sample proportion of the processed tickets basis the predefined checklist for the tickets assigned via email, Salesforce, Jit Bit, RAGIC, ARCHER Connect and other data sources, at a set frequency as defined by the business.
• Ensure random audits, at least twice or thrice per month, to check documentation around the BK Claimants.
• Perform random sample checks on the communication sent/received to/from Trustees
• Accurately review and interpret legal especially court motions/orders, affidavits, PACER reports, and legal heirship documents.
• Build up a quick learning curve to ensure an in-depth understanding of the Standard Operating Procedures (SOPs) and training materials. Setup weekly connect with business for TNI in collaboration with trainers for SOP updates & PKT requirements.
• Create weekly/monthly reports for the audits performed on the set frequency and report out to supervisor and business with requisite analytics & inferences. The report should be inclusive of root cause and CAPA (Corrective Action/Preventive Action) for the defects/deficiencies identified during quality audits.

KNOWLEDGE AND SKILLS : -

• Bachelors degree in any field (preferably in Law/ BBA or commerce).
• 2 - 4 Years of experience in a US-based multinational corporation.
• Project management experience or certifications are highly desirable.
• ISO 9001 onwards any such certification is preferrable.

Technical Skills:

• Advanced proficiency in MS Office, including Excel & PowerPoint, MS Teams and Outlook.
• Experience in quality audits of legal documents/ email communications. Should have the ability to comprehend legal terminologies and scope of work required during quality audits.
• To have understanding and maintain checklist of requisite state/district wise requirements if any
• Strong data analysis capabilities, with an eye for detail to identify errors.
• Exceptional written and verbal communication skills, with the ability to derive insights from information provided.
• Analytical problem-solving skills for addressing complex issues.
• Basic understanding of tools and techniques such as CAPA, RCA, FMEA, SPC & 7 QC tools.

Behavioral Skills:

• Strong problem-solving skills, with a solution-oriented mindset.
• Ability to handle confidential information with discretion.
• Strong interpersonal and customer service skills.
• Keen attention to detail, anticipating potential challenges and addressing them proactively.

PREFFERED KNOWLEDGE:

• Familiarity with US legal laws or bankruptcy processes is an advantage.
• Experience in operations or business analysis

Drop us your CV or reach out directly or

Role Description

This is a full-time on-site role for a Quality Control Investigator located in Vadodara. The Quality Control Investigator will be responsible for conducting investigations, analyzing data, and documenting findings related to quality control issues. The role involves ensuring compliance with regulatory standards, implementing corrective and preventive actions, and collaborating with other departments to maintain product quality. The investigator will also monitor and continuously improve quality control processes.

Qualifications

• Strong analytical and investigative skills
• Experience in data analysis and documentation
• Knowledge of regulatory standards and compliance
• Skills in implementing corrective and preventive actions
• Proficiency in quality control processes and continuous improvement
• Excellent written and verbal communication skills
• Ability to work collaboratively with cross-functional teams
• Bachelor's degree in Chemistry, Pharmacy, or related field
• Experience in the pharmaceutical industry is a plus

* Conduct quality assurance and quality control activities in compliance with company standards.

* Perform testing on products and processes to ensure adherence to quality standards.

PYG Lifesciences Private Limited is hiring for Quality Control Officer Role

Role Description

This is a full-time on-site role for a Quality Control Officer located in Vagra. The Quality Control Officer will be responsible for ensuring the consistently high quality of the company's products and will be involved in the testing, analysis, and documentation of products throughout their development.

Experience:

• 02 to 03 years of experience in Quality Control for synthetic Organic Manufacturing Industries.
• Experience working in a Quality Control role in the pharmaceutical or chemical industry.

Qualifications

• Bachelor's degree in Chemistry, Biochemistry, or a related field.
• Or Master's Degree in analytical chemistry.
• Experience with analytical techniques such as HPLC, GC, and UV-Vis spectroscopy.
• Familiarity with regulatory requirements such as GMP, GLP, and ICH guidelines.
• Ability to work well in a team environment and communicate effectively with colleagues.

Skills Required

• Instrument Handling of GC, HPLC, Karl Fischer, pH meter, Auto Titrator apparatus, Malvern Partial size analysis etc.
• Performing as per ISO/IEC 17025:2017 NABL Document & relevant testing and calibration GC, HPLC, weight balance, pH meter, Karl Fischer instrument, melting point apparatus.
• Perform analysis of the raw materials, wet lab analysis, solution preparation, In-process sample.
• Hands of experience on SAP & COA.
• Analysis of COD sample.
• Good understanding of ISO 9001:2015 Quality Management System.
• GC calibration, HPLC calibration, Analytical balance calibration as per ISO/IEC 17025:2017.
• Preparation of table top SOP's and detailed manual on Start-up and Shut-down of the equipment

Basic Computer Skills

• Email Management
• MS Office Suite
• File Management
• Internet Browsing

Company Description

PYG Lifesciences, formerly known as PY GENRONE INTERMEDIATES PRIVATE LIMITED, is a leading chemical manufacturer dedicated to empowering Indian businesses and contributing to Atmanirbhar Bharat. Their expertise in specialty chemicals serves Indian API manufacturers and Pharma Marketing companies, with a global vision for sustainability and advancement. PYG Lifesciences focuses on local talent and innovation to boost the Indian economy and drive advancements in therapeutic areas.

The opportunity
Manufacturing Quality Control work includes Auditing, monitoring, and determining the quality of manufacturing processes and/or outputs against defined internal and regulatory standards. Testing random samples of finished goods. Reporting manufacturing process deviations and defects in finished goods and liaising with Quality Assurance to troubleshoot and resolve problems An Experienced Professional (P2) applies practical knowledge of job area typically obtained through advanced education and work experience. May require the following proficiency: Works independently with general supervision. Problems faced are difficult but typically not complex. May influence others within the job area through explanation of facts, policies and practices.

How You'll Make An Impact

• Conduct thorough material inspections in accordance with approved drawings, technical specifications, and review test certificates.
• Prepare and maintain comprehensive documentation related to quality, including inspection reports, calibration reports, NCR (Non-Conformance Reports), rejection data, QAP, and work instructions.
• Perform Incoming Inspection of NPD part and provide the feedback to SQ &SCM.
• Develop checking fixtures, templates, and gauges to streamline the inspection process for parts.
• Ensured quality clearance through SAP (QM Module), improving efficiency and consistency in product quality.
• Conduct root cause analysis of non-conformance using problem reports and tools such as 4Q, DMAIC, 7QC, and 8D.
• Preparing necessary IIPs (incoming inspection plan), checklist and CTQ (Critical to Quality) parameters to ensure best quality of material from supplier. Training quality third party employees in basic quality test routines to ensure quality process are followed as per standard.
• Ensuring all quality tools and instruments are timely calibrated. Performing first article inspection (first out turn sample inspection) for new development.
• Regular Quality Observation Tour (QOT) and drive improvement actions
• Regularly monitor production FPY data, identify repetitive failure modes and drive improvement actions
• Review and monitor manufacturing non-conformance, deploy right problem-solving tool to drive improvement action. Ensure sustainable solution. Outgoing inspection.
• Responsible to ensure compliance with applicable external and internal regulations, procedures, and guidelines.
• Living Hitachi Energy's core values of safety and integrity, which means taking responsibility for your own actions while caring for your colleagues and the business

Your background

• Degree/diploma in mechanical engineering with Lean Six Sigma certification.
• Minimum 3 year of experience in quality background at IQC of mechanical / electrical components and related products.
• Knowledge of Switchgear/Automotive Products and components manufacturing.
• Deep understanding of various national and international standards such as ASME, ANSI, IS, DIN, ISO etc.
• knowledge of SAP QM module. Should be capable of SAP transactions like create inspection plan (IIP), create quality plan .
• Handling and usage of quality tools and precise instruments such as CMM, bore gauge, surface roughness tester, etc. Basic knowledge of manufacturing process like casting, forging, welding & machining parts would be added advantage.
• Excellent collaboration and work within team skills will help you to succeed in this position. Willing to travel at supplier place.
• Proficiency in both spoken & written English language is required

Hitachi Energy is a global technology leader in electrification, powering a sustainable energy future through innovative power grid technologies with digital at the core. Over three billion people depend on our technologies to power their daily lives.

With over a century in pioneering mission-critical technologies like high-voltage, transformers, automation, and power electronics, we are addressing the most urgent energy challenge of our time – balancing soaring electricity demand, while decarbonizing the power system.

Headquartered in Switzerland, we employ over 50,000 people in 60 countries and generate revenues of around $16 billion USD. We welcome you to apply today.

We are urgently hiring for a QC Engineer 1 to 3 years of experience Candidate at Vadodara Location for a Pipe Manufacturing Company

Interested candidates can apply here or contact us below

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