1,197 Control Analyst jobs in India

Total Number of Openings
1
About the position:
The Project Control Analyst is part of a multi-functional Cost Engineering team and responsible to provide planning and scheduling support to brownfield projects. Typical role responsibilities include: develop, update and maintain integrated resources loaded project schedules; generate schedule reports; review, validate, and challenge contractors detailed schedules and integrate into the master schedule; works with Project Controls on schedule progress and performance reporting, monitoring, and analysis; present schedule updates to the projects leadership team; participates in project reviews, assurances and risk assessments; develop Schedule Plan and Basis of Schedule.
Key responsibilities:
+ Participate in developing Work Breakdown Structures (WBS) and Cost Breakdown Structures as basis for project budgeting, cost controls, planning, scheduling and forecasting.
+ Develop project controls plan, cost estimate and schedule as required by Chevron Cost Engineering Handbook for Chevron Project Development and Execution Process (CPDEP) project phases.
+ Support generation of quality project documents for project Funding Appropriation and Business Planning.
+ Configure, maintain and administer cost control system and ensure interfaces between the project cost control system and JDE accounting system and Ariba Procurement System is accurate.
+ Track project progress, earned value and project performance, and provide project performance analysis.
+ Develop project monthly cost and schedule status reports to support Facilities Engineering monthly program report.
+ Implement Project Management of Change process and procedures.
+ Support and participate in cost and schedule assurance process and risk management process.
+ Manage and control project changes for approved budgets. Ensure that cost and schedule impact of the change to be captured into budget recap and project cost and schedule forecasting.
+ Evaluate contingency to establish appropriate contingency drawdown strategy required to complete the project based on proper risk analysis.
Required Qualifications:
+ Bachelor's degree (B.E./B. Tech) in engineering or related field from a recognized (AICTE) university
+ Proactive, process and details oriented individual who can work with people and be able to recognize and work through hurdles, able to find resolutions to issues.
Preferred Qualifications:
+ 5+ years of experience in cost estimating, planning, scheduling, project control and project reporting
+ Experience working across interfaces between engineering, procurement, fabrication, and Hook-up and Commissioning
+ Experience working in complex process facilities, especially in refineries and/or LNG facilities.
+ Broad knowledge of industry and professional cost engineering trends, lessons learned and best practices.
Chevron ENGINE supports global operations, supporting business requirements across the world. Accordingly, the work hours for employees will be aligned to support business requirements. The standard work week will be Monday to Friday. Working hours are 8:00am to 5:00pm or 1.30pm to 10.30pm.
Chevron participates in E-Verify in certain locations as required by law.
Chevron Corporation is one of the world's leading integrated energy companies. Through its subsidiaries that conduct business worldwide, the company is involved in virtually every facet of the energy industry. Chevron explores for, produces and transports crude oil and natural gas; refines, markets and distributes transportation fuels and lubricants; manufactures and sells petrochemicals and additives; generates power; and develops and deploys technologies that enhance business value in every aspect of the company's operations. Chevron is based in Houston, Texas. More information about Chevron is available at .
Chevron is an Equal Opportunity / Affirmative Action employer. Qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status, or other status protected by law or regulation.

Bring more to life.
Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?
At Cepheid, one of Danaher's 15+ operating companies, our work saves lives-and we're all united by a shared commitment to innovate for tangible impact.
You'll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher's system of continuous improvement, you help turn ideas into impact - innovating at the speed of life.
At Cepheid, we are passionate about improving health care through fast, accurate, molecular diagnostic systems and tests. As a member of our team, you'll get to make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development. Our mission drives us to develop groundbreaking solutions for the world's most complex health challenges. Together, we bring MORE change to the world.
Learn about the Danaher Business System which makes everything possible.
The Quality Control Analyst is responsible for ensuring inspection process as per MDR 2017, European regulations, ISO 13485 and Cepheid corporate quality system requirements.
This position reports to the quality manager and is part of the quality and regularity compliance department located in Cepheid Manufacturing facility, Bengaluru and will be an on-site role.
In this role, you will be responsible for:
+ Perform inspections of incoming, in-process and finished products/stability testing and identify/troubleshoot product if non-conformance.
+ Performs/monitor the laboratory equipment validation/calibration/maintenance and ensure quality control lab as per safety standards/GLP.
+ Write/review SOP/WI, technical reports or documentation such as deviation reports, testing protocols, and trend analyses. Support for internal/external audit schedule, NC, CAPA for site.
The essential requirements of the job include:
+ Master's degree in Biochemistry, Molecular Biology, Microbiology, Biotechnology or related discipline and a minimum of 3+ years related to quality control experience.
+ 2+ years' experience in Vitro Diagnostics (IVD) is mandate. Need to act as competent technical staff for supervision the testing / analysis of diagnostic reagents & kits
Business Schedule Requirement
+ Must be flexible to work in shift-based time schedules (able to consistently maintain schedules and meet timelines).
It would be a plus if you also possess previous experience in:
+ Experience working with medical device quality systems in compliance with MDR and ISO 13485
+ Experience in leading continuous improvement efforts, in both quality systems and IVD products.
+ Required strong interpersonal skills, effective communication skills / micro-soft word and excel knowledge / strong multi-tasking skill.
Cepheid, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it's a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.
Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit .
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.
Operating Company: Cepheid

Job Title: QC Analyst I
At Cepheid, we are passionate about improving health care through fast, accurate diagnostic testing. Our mission drives us, every moment of every day, as we develop scalable, groundbreaking solutions to solve the world's most complex health challenges. Our associates are involved in every stage of molecular diagnostics, from ideation to development and delivery of testing advancements that improve patient outcomes across a range of settings. As a member of our team, you can make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development.
Cepheid is proud to work alongside a community of six fellow Danaher Diagnostics companies. Together, we're working at the pace of change on diagnostic tools that address the world's biggest health challenges, driven by knowing that behind every test there is a patient waiting.
Learn about the Danaher Business System ( which makes everything possible.
+ This position is part of the Quality Organization and will be in India. Reporting directly to the Quality Control lead or site lead, the Quality Control Analyst is responsible for managing the day today activities quality control function at Cepheid India Private Ltd.
+ Ensure compliance of quality control procedures as per MDR 2017, European regulations, ISO 13485, Cepheid corporate quality system requirements.
In this role, you will have the opportunity to:
+ Conducts routine and non-routine analysis of raw materials, in-process and finished formulations under supervision and according to Standard Operating Procedures (SOPs).
+ Competent technical staff for supervision the Testing/ analysis of diagnostic reagents & kits.
+ Perform inspections of incoming, in-process and finished products.
+ Performs and calibration and maintenance of lab equipment as per requirements.
+ May perform special projects on analytical and instrument problem solving.
+ Ensure that lab cleanliness and safety standards are maintained.
+ Qualify test methods as part of new product development activities.
+ Serve as a technical liaison between quality control and other departments
+ Write technical reports or documentation such as deviation reports, testing protocols, and trend analyses & Write or revise standard quality control operating procedures.
+ Perform validations or transfers of analytical methods in accordance with applicable policies or guidelines.
+ Follow documentation procedure (filling out Data History Records (DHRs), reading and understanding instructions from Work Release (WR), Planned Deviation Report (PDR) or Non-Conformance Report (NCR). Read and follow Standard Operating Procedures (SOPs) and Manufacturing Work Instructions.
+ Review records and documents for completeness and compliance with company policies and procedures.
+ Support for internal audit schedule, NC, CAPA for site.
+ Review production batch records, QC test results and release product.
Education and Experience:
+ Master's degree in Biochemistry, Molecular Biology, Microbiology or related discipline and a minimum of 3+ years related Quality Control experience.
+ 2+ years' experience with in Vitro Diagnostics (IVD) is mandate
+ Experience with in Vitro Diagnostics (IVD) is very beneficial and highly desirable
+ Quality competent technical person approved as per D&C act if any
Knowledge and skills:
+ Hands on Experience on IVD product testing.
+ Working Knowledge of current GxP regulations for Invitro Medical Devices and ISO 13485 QMS.
+ Must be flexible to work off-shifts and weekends as per production Schedule.
+ Schedule orientated (able to consistently maintains schedules and meet timelines)
+ Strong interpersonal skills, Effective organization and Communication skills are essential.
+ Good skills in English language
+ Knowledge of Microsoft Word and Excel
+ Strong multi-tasking and attention to details skills.
It would be a plus if you also possess previous experience in:
+ Experience working with medical device quality systems in compliance with MDR and ISO 13485
+ Able to interpret quality problem and establish practical solutions within a dynamic business environment.
+ Experience in leading continuous improvement efforts, in both quality systems and products.
+ Knowledge of the process of establishing facility QMS certifications.
+ Cross functional experience with products and manufacturing processes to influence change at all levels within the organization Visio and Project knowledge desirable.
When you join us, you'll also be joining Danaher's global organization, where 69,000 people wake up every day determined to help our customers win. As an associate, you'll try new things, work hard, and advance your skills with guidance from dedicated leaders, all with the support of powerful Danaher Business System ( tools and the stability of a tested organization.
Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law. We value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.The EEO posters are available here ( .We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform crucial job functions, and to receive other benefits and privileges of employment. Please contact us at to request accommodation.If you've ever wondered what's within you, there's no better time to find out.
Join our winning team today. Together, we'll accelerate the real-life impact of tomorrow's science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.
For more information, visit .
At Danaher, we value diversity and the existence of similarities and differences, both visible and not, found in our workforce, workplace and throughout the markets we serve. Our associates, customers and shareholders contribute unique and different perspectives as a result of these diverse attributes.
Operating Company: Cepheid

Job description

Job Description: HPLC Analyst - Pharma Background only.

Company: Sain Medicaments Pvt Ltd, UPPAL, HYDERABAD.

Location: Uppal, Hyderabad

Industry: Pharmaceutical (Pharma Experience Required)

We are seeking a skilled and experienced HPLC Analyst to join our Quality Control (QC) team. The ideal candidate should have a strong background in the pharmaceutical industry and hands-on experience in laboratory analysis.

Job Responsibilities:

• Perform analysis of raw materials and finished products.
• Operate and maintain HPLC (High-Performance Liquid Chromatography) equipment.
• Conduct UV, pH, and Karl Fischer (KF) titration analyses.
• Ensure accurate and reliable testing results in line with industry standards.
• Follow Good Laboratory Practices (GLP) and ensure compliance with quality protocols.

Experience:

• Minimum of 2 to 3 years of experience in a clinical, industrial, or pharmaceutical laboratory.

Qualifications:

• M.Sc. / B.Sc. / M.Pharm / B.Pharm in a scientific or related field.

If you have the required experience and are passionate about working in a dynamic pharmaceutical environment, we invite you to apply!

Industry

• Pharmaceutical Manufacturing
  

Are you a detail-driven professional with experience in product inspections and manufacturing quality ? Do you thrive on the factory floor and have a passion for catching even the smallest deviations? If so, we want you on our team!
We’re hiring a Quality Control Analyst to be based on-site at a partner factory in Kanpur, India . This role will focus primarily on quality control , with a supporting role in process-based quality assurance — ensuring our products not only meet standards but that the systems behind them are solid too.

What You'll Do: Perform regular inspections of incoming materials, in-process production, and final products.
Identify defects, deviations, or inconsistencies and report findings to relevant teams.
Document all QC activities , maintain inspection logs, and compile detailed quality reports.
Ensure that production processes comply with defined QA protocols and internal standards .
Collaborate with the factory’s production team to implement corrective actions when quality issues arise.
Assist in refining and maintaining standard operating procedures (SOPs) and inspection checklists.
Support periodic audits and client visits , showcasing product quality and process discipline.

What We’re Looking For: 2–5 years of hands-on experience in Quality Control within a manufacturing environment .
Familiarity with visual, dimensional, and functional inspections .
Understanding of QA principles , including documentation and process checks.
Ability to read and interpret technical drawings, tolerances, and specifications .
Detail-oriented with strong reporting, communication, and problem-solving skills.
Proficient in Hindi and English .
Comfortable working full-time, on-site at a factory location in Kanpur.

Nice to Have: Experience working with metal or engineered products
Familiarity with manufacturing processes , production flow, and factory-floor coordination.
Knowledge of ISO standards or factory compliance protocols .
Degree or diploma in Engineering , Manufacturing , or a related technical field.

If you’re ready to take your career to the next level and join an amazing team, we’d love to hear from you!
Send your resume to:

Job description

Job Description: HPLC Analyst - Pharma Background only.
Company: Sain Medicaments Pvt Ltd, UPPAL, HYDERABAD.
Location: Uppal, Hyderabad
Industry: Pharmaceutical (Pharma Experience Required)

We are seeking a skilled and experienced HPLC Analyst to join our Quality Control (QC) team. The ideal candidate should have a strong background in the pharmaceutical industry and hands-on experience in laboratory analysis.

Job Responsibilities:
Perform analysis of raw materials and finished products.
Operate and maintain HPLC (High-Performance Liquid Chromatography) equipment.
Conduct UV, pH, and Karl Fischer (KF) titration analyses.
Ensure accurate and reliable testing results in line with industry standards.
Follow Good Laboratory Practices (GLP) and ensure compliance with quality protocols.

Experience:
Minimum of 2 to 3 years of experience in a clinical, industrial, or pharmaceutical laboratory.

Qualifications:
M.Sc. / B.Sc. / M.Pharm / B.Pharm in a scientific or related field.

If you have the required experience and are passionate about working in a dynamic pharmaceutical environment, we invite you to apply!
Industry Pharmaceutical Manufacturing

This job description outlines the role of someone on an Agile internal control team at Ford Motor Company. The core responsibilities revolve around identifying and mitigating risks, ensuring compliance, and improving internal processes. This involves a blend of hands-on control testing, analysis, communication, and project management. The individual will use "Smart reviews" (likely a proprietary methodology) to assess processes, pinpoint weaknesses, and suggest improvements. They'll work across different departments and globally, collaborating to implement solutions and keep documentation (process narratives and risk control matrices) up-to-date

CA, ICWA, CIA with 2-5 years of experience

Should have experience in performing control testing

Ability to work with cross functional teams at different time zones

Quick learner with curious mind

Good in presentation skills, communication/ Coordination skills

Have continuous improvement mind set

Independently coordinate and lead initiative

Ability to meet tight deadlines

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