What Jobs are available for Manufacturing Processes in Mumbai?
Showing 453 Manufacturing Processes jobs in Mumbai
Remote Senior Industrial Engineering Consultant
Posted 2 days ago
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Job Description
Key Responsibilities:
- Lead and manage industrial engineering consulting projects for clients, from assessment to implementation.
- Conduct comprehensive analysis of client operations, including workflow, supply chain, production processes, and resource allocation.
- Identify opportunities for efficiency gains, cost reductions, and quality improvements using methodologies like Lean, Six Sigma, and Theory of Constraints.
- Develop and present detailed recommendations and strategic roadmaps to senior client leadership.
- Design and implement optimized operational processes, systems, and organizational structures.
- Utilize advanced data analytics, modeling, and simulation tools to support recommendations and solutions.
- Facilitate workshops and training sessions for client teams on process improvement techniques.
- Manage project timelines, budgets, and resources effectively.
- Build and maintain strong client relationships, acting as a trusted advisor.
- Mentor junior consultants and contribute to the firm's knowledge base.
- Stay abreast of emerging trends and best practices in industrial engineering and operations management.
- Develop proposals and contribute to business development efforts.
- Ensure successful knowledge transfer and sustainability of implemented solutions.
Qualifications:
- Master's or Ph.D. in Industrial Engineering, Operations Research, or a related quantitative field. MBA is a plus.
- A minimum of 8-12 years of progressive experience in industrial engineering, operations consulting, or a similar role.
- Proven track record of successfully delivering complex operational improvement projects for diverse clients.
- Expertise in Lean Manufacturing, Six Sigma (Black Belt certification preferred), and other process optimization methodologies.
- Strong analytical and quantitative skills, with proficiency in statistical analysis and modeling software (e.g., Minitab, SPSS, Arena).
- Excellent problem-solving, critical thinking, and strategic planning abilities.
- Exceptional communication, presentation, and interpersonal skills, with the ability to influence stakeholders at all levels.
- Experience with data visualization tools (e.g., Tableau, Power BI).
- Proven ability to work independently, manage multiple projects simultaneously, and deliver high-quality results in a remote setting.
- Demonstrated leadership and team collaboration capabilities.
- Willingness to travel as required (though primary role is remote).
This is an unparalleled opportunity for a senior-level industrial engineer to impact major organizations, working remotely and contributing to cutting-edge operational strategies.
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Quality Control Executive
Posted 4 days ago
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Job Description
Standard (Mon-Fri)
**Environmental Conditions**
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials
**Job Description**
**About the Company**
Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $44 billion. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Whether our customers are accelerating life sciences research, solving analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to support them. Our distributed team delivers an outstanding combination of innovative technologies, purchasing convenience, and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD. Our Innovative Laboratory technologies & Services makes it easier for customers.
**Responsibilities:**
+ Responsible to carry out analysis on analytical instruments like HPLC, GC, ICP, GCMS etc.
+ Responsible to analyse and interpretate the analytical data basis customer requirement on Window based tools
+ Process knowledge of chemical testing, Analytical work, basic trouble shooting, method preparation/validation, handling and calibration of instrument like HPLC, GC, ICP, GCMS etc.
+ Responsible to maintain and carry out chemical analysis basis ISO/NABL standards 17025 and 17034.
+ Responsible for good laboratory practice in Quality control lab.
+ Perform analysis and reporting of raw materials, packing materials, Finished products, in-process and routine analysis.
+ Preparation of volumetric solutions, reagents, buffer solutions, indicator and maintain its records.
+ Perform standardization of volumetric solutions.
+ Preparation of Quality control SOP's.
+ Responsible to be self aware of Safety and Quality compliance and adhere to set compliance norms.
**Experience and Skill Sets:**
+ B.Sc. Chemistry with five years experience
+ M.Sc in Analytical / Inorganic chemistry with three years experience
+ The role needs good communication, presentation skill & solution-oriented approach.
**Benefits:**
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!
At Thermo Fisher Scientific, each one of our 100,000 extraordinary minds have a unique story to tell.
ThermoFisher is committed to crafting a diverse work environment that values and respects individuals.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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Senior Quality Control Analyst
Posted 2 days ago
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Job Description
Responsibilities:
- Perform routine and non-routine analytical tests on raw materials, intermediates, and finished products.
- Operate and maintain laboratory equipment such as HPLC, GC, FTIR, UV-Vis, and dissolution apparatus.
- Analyze samples using validated methods and ensure compliance with pharmacopoeial standards.
- Document all laboratory activities, results, and observations accurately and contemporaneously.
- Investigate out-of-specification (OOS) results and deviations, and implement corrective and preventive actions (CAPA).
- Prepare certificates of analysis (CoA) and other quality control reports.
- Ensure adherence to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
- Participate in method validation and transfer activities.
- Maintain laboratory inventory and ensure proper storage of reagents and samples.
- Collaborate with Quality Assurance and Production teams on quality-related issues.
- Stay updated with the latest regulatory guidelines and scientific advancements in pharmaceutical quality control.
- Contribute to continuous improvement initiatives within the QC department.
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a related life science field.
- Minimum of 4-6 years of experience in a pharmaceutical Quality Control laboratory setting.
- Hands-on experience with analytical instrumentation (HPLC, GC, etc.).
- Thorough understanding of GMP, GLP, and regulatory requirements.
- Proficiency in data analysis and interpretation.
- Strong attention to detail and accuracy.
- Excellent problem-solving and investigative skills.
- Good written and verbal communication skills.
- Ability to work effectively in a team environment.
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Senior Quality Control Analyst
Posted 2 days ago
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Job Description
Responsibilities:
- Develop, implement, and manage comprehensive quality control strategies.
- Perform advanced analytical testing on raw materials, in-process samples, and finished products.
- Interpret and analyze complex analytical data, ensuring accuracy and reliability.
- Validate analytical methods and instrumentation according to regulatory guidelines.
- Oversee and manage stability study programs.
- Investigate deviations, out-of-specification (OOS) results, and out-of-trend (OOT) data.
- Implement and track Corrective and Preventive Actions (CAPA).
- Collaborate with manufacturing and R&D teams to resolve quality issues.
- Ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulations.
- Prepare and review quality control reports, specifications, and procedures.
- Contribute to the improvement of the overall Quality Management System (QMS).
- Bachelor's or Master's degree in Pharmacy, Chemistry, Analytical Chemistry, or a related life science discipline.
- Minimum of 6 years of experience in pharmaceutical quality control or quality assurance.
- Extensive hands-on experience with analytical instrumentation (HPLC, GC, KF, UV-Vis, dissolution).
- Thorough understanding of GMP, ICH guidelines, and regulatory submission requirements.
- Proven experience in method validation, stability studies, and OOS investigations.
- Strong analytical, problem-solving, and critical thinking skills.
- Excellent written and verbal communication skills for technical reporting and collaboration.
- Ability to work independently and manage workload effectively in a remote setting.
- Detail-oriented with a strong commitment to quality and compliance.
- Experience with quality management software systems is a plus.
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Pharmaceutical Quality Control Analyst
Posted 2 days ago
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Senior Quality Control Manager (Manufacturing)
Posted today
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Job Description
Key Responsibilities:
- Develop, implement, and maintain comprehensive quality control policies, procedures, and standards across all manufacturing operations.
- Lead and manage the quality control team, providing direction, training, and performance evaluations.
- Oversee all quality assurance activities, including incoming material inspection, in-process quality checks, and final product testing.
- Establish and monitor key quality metrics (KPIs) such as defect rates, customer complaints, and first-pass yield, reporting findings to senior management.
- Conduct root cause analysis for quality deviations and implement effective corrective and preventive actions (CAPA).
- Ensure compliance with relevant industry standards (e.g., ISO 9001, industry-specific certifications) and regulatory requirements.
- Collaborate with production, engineering, and R&D teams to address quality issues and improve product design and manufacturability.
- Manage the calibration and maintenance of quality control equipment and instrumentation.
- Develop and deliver quality training programs for manufacturing personnel.
- Conduct internal audits and support external audits by customers or regulatory bodies.
- Drive continuous improvement initiatives to enhance product quality, reduce waste, and increase overall operational efficiency.
- Maintain accurate quality records and documentation.
Qualifications:
- Bachelor's degree in Engineering (Mechanical, Industrial, or related field) or a related scientific discipline.
- Minimum of 7 years of experience in quality control or quality assurance within a manufacturing environment, with at least 3 years in a leadership or management role.
- Strong knowledge of quality management systems (QMS), such as ISO 9001, and quality control methodologies (e.g., Six Sigma, SPC).
- Proven experience in root cause analysis and CAPA implementation.
- Excellent analytical, problem-solving, and decision-making skills.
- Strong leadership, team management, and communication skills.
- Proficiency in quality control tools and techniques, including statistical process control (SPC).
- Familiarity with relevant manufacturing processes and standards.
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Senior Pharmaceutical Quality Control Analyst
Posted 4 days ago
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Senior Quality Control Inspector - Manufacturing
Posted 2 days ago
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Job Description
Responsibilities:
- Perform comprehensive quality inspections on materials and products.
- Utilize measurement and testing equipment to verify specifications.
- Identify and document product defects and non-conformities.
- Analyze quality data and trends to identify root causes of issues.
- Collaborate with production and engineering to implement corrective actions.
- Ensure compliance with quality standards and regulatory requirements.
- Develop and update inspection procedures and work instructions.
- Conduct internal quality audits.
- Train and mentor junior quality control personnel.
- High school diploma or equivalent; technical certification in Quality Assurance or a related field is preferred.
- Minimum of 4-6 years of experience in quality control inspection within a manufacturing setting.
- Proficiency with various measurement and testing instruments (calipers, micrometers, CMM, etc.).
- Strong understanding of quality control principles and methodologies (e.g., Six Sigma, Lean).
- Ability to read and interpret technical drawings and specifications.
- Excellent attention to detail and accuracy.
- Good analytical and problem-solving skills.
- Effective communication and interpersonal skills.
- Experience with documentation and reporting.
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Senior Quality Control Inspector (Manufacturing)
Posted 2 days ago
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Job Description
Key responsibilities include developing and executing comprehensive quality control plans and procedures. You will perform visual and dimensional inspections of raw materials, in-process materials, and finished goods using various measuring instruments and testing equipment. The Senior QC Inspector will also be tasked with documenting inspection results, analyzing quality data to identify trends and areas for improvement, and collaborating with production and engineering teams to resolve quality issues promptly.
Furthermore, this role involves training and mentoring junior quality inspectors, ensuring consistency and adherence to standards across the team. You will contribute to the continuous improvement of quality management systems and participate in internal audits. A thorough understanding of quality control methodologies, statistical process control (SPC), and relevant industry standards is essential. The ability to interpret technical drawings and specifications accurately is crucial.
Qualifications include a minimum of 5 years of experience in quality control or assurance within a manufacturing environment. A strong technical background, preferably with a diploma or degree in a related engineering field, is required. Excellent analytical, problem-solving, and communication skills are necessary for effective collaboration and reporting. Proficiency with measurement tools and quality management software is expected. This is an excellent opportunity for a detail-oriented professional to play a key role in maintaining the highest quality standards in a leading manufacturing operation.
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Senior Pharmaceutical Quality Control Analyst
Posted 2 days ago
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Job Description
Responsibilities:
- Perform a variety of analytical tests on raw materials, intermediates, and finished products using techniques such as HPLC, GC, UV-Vis spectrophotometry, and titrations.
- Ensure all testing is conducted in accordance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and relevant pharmacopoeial standards (e.g., USP, EP, BP).
- Prepare reagents, standards, and samples for analytical testing.
- Calibrate and maintain laboratory equipment, ensuring proper functioning and accuracy.
- Document all testing procedures, results, and observations meticulously in laboratory notebooks and reports.
- Investigate and troubleshoot out-of-specification (OOS) results, deviations, and laboratory investigations.
- Participate in method development and validation activities.
- Review and approve analytical data and reports generated by other QC analysts.
- Collaborate with production, R&D, and quality assurance departments to resolve quality issues.
- Maintain a safe and organized laboratory environment.
- Contribute to regulatory inspections and audits.
- Train and mentor junior QC analysts.
- Bachelor's or Master's degree in Pharmacy, Chemistry, Analytical Chemistry, or a related life science field.
- Minimum of 5-7 years of hands-on experience in a pharmaceutical Quality Control laboratory.
- Proficiency in a wide range of analytical techniques, particularly HPLC and GC.
- Strong understanding of GMP, GLP, and regulatory requirements in the pharmaceutical industry.
- Excellent attention to detail and accuracy in data recording and reporting.
- Strong problem-solving skills and the ability to investigate OOS results effectively.
- Proficiency in using laboratory information management systems (LIMS) and data analysis software.
- Good written and verbal communication skills.
- Ability to work independently and as part of a team.
- Experience with method validation is a significant advantage.
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