952 Quality Control Analyst jobs in India

This is an exciting role and would entail you to

· Perform comprehensive quality checks on medical writing deliverables (manuscripts, abstracts, HCP materials, regulatory documents, publication content).

· Review creative assets (emails, videos, images, HTML banners, and digital content) to ensure medical content is accurately and consistently represented.

· Ensure compliance with client-specific style guides, medical writing standards, and regulatory requirements (ICH, GPP, FDA/EMA).

· Check for accuracy in medical terminology, grammar, spelling, referencing, and data consistency across both written and visual deliverables.

· Verify alignment of content between text and creative assets (copy, callouts, disclaimers, references).

· Identify discrepancies, raise queries, follow up on corrections, and ensure updates are implemented.

· Maintain version control and audit trails for all reviewed documents and creative assets.

· Prepare Daily/Weekly/Monthly quality reports using manual tracking, QMS, and project overview tools.

You will be working closely with

Our global creative agency teams. You will also be closely collaborating with our team of talented and designers to deliver high-quality services.

This may be the right role for you if you have

· 3–5 years’ experience in Medical Writing Quality Control/Review, with additional exposure to creative/digital assets QC.

· Bachelor’s degree is a must.

· Strong background in reviewing medical content and ensuring its correct integration into creative outputs.

· Experience with proofreading, copy editing, and QC for both text-based and creative materials.

· Familiarity with referencing tools (e.G., EndNote, Mendeley)

Experienced in project management tool (Jira/ Hive /Adobe Workfront)

· Good understanding of creative asset formats (email templates, videos, static images, HTML banners).

· Proficiency in basic QC of creative assets—checking layout, alignment, copy placement, and regulatory footnotes.

· Good communication skills and ability to collaborate with cross-functional teams to meet deadlines.

· Ensuring timely completion of project, understanding process requirements and providing use cases for the business, functional & technical requirements

· Able to review and annotate 3-5 assets per day with first time right from the agency/brand.

EOE:

Our client is an Equal Opportunity Employer and Prohibits Discrimination and Harassment of Any Kind: We are committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at our client are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion or belief, national, social or ethnic origin, sex (including pregnancy), age, physical, mental or sensory disability, HIV Status, sexual orientation, gender identity and/or expression, marital, civil union or domestic partnership status, past or present military service, family medical history or genetic information, family or parental status, or any other status protected by the laws or regulations in the locations where we operate. We will not tolerate discrimination or harassment based on any of these characteristics

Fulkrum is a global leader in inspection, expediting, auditing, and technical staffing services, delivering exceptional solutions to the energy, engineering, and construction industries for over 14 years. Headquartered in the UK, we have established a strong presence across six continents, serving more than 300 clients worldwide.

Our commitment to excellence has been recognised with prestigious awards, including the King's Award for Enterprise in International Trade (2023), the People and Competency Award at the EIC Awards (2023), and the Scale-Up Award at the WESCA North America Awards (2024).

Our Mumbai office is currently seeking a highly motivated and experienced QC Coordinator to join our dynamic team.

Key Responsibilities

• Respond to client requests for QA/QC, engineering, and project support personnel across various locations.
• Source, screen, and prepare candidates for client interviews, ensuring alignment with project requirements.
• Coordinate the full placement process, including proposals, interviews, onboarding, and documentation.
• Liaise with candidates regarding contractual terms, task-related documents, and performance expectations.
• Review, screen, and submit inspection reports and site documentation to clients promptly.
• Monitor candidate performance, timekeeping, and reporting quality, providing feedback and support.
• Maintain strong relationships with candidates through regular care calls and assignment follow-ups.
• Ensure compliance with ISO/IEC 17020:2012 and Fulkrum’s internal quality procedures and policies.
• Support the accounts team by ensuring timely submission of timesheets and purchase orders for invoicing.
• Participate in internal audits, identify process improvements, and report any conflicts of interest or HSE concerns.

What We’re Looking For

• Strong knowledge of onshore and offshore oil & gas projects.
• Proficiency in MS Office and documentation management.
• Excellent communication, organisational, and multitasking skills.
• Ability to work independently and collaboratively.
• Familiarity with QA/QC processes and ISO/IEC 17020:2012 standards.

HSE Awareness:

All personnel are informed of Fulkrum's Health and Safety policy and procedures during the onboarding process. Any HSE incidents must be reported and logged with the QHSE Manager, who will oversee and support any subsequent investigations.

Provide site-specific HSE instructions to Inspectors prior to mobilisation.

Why Join Us?

This is an exciting opportunity for a driven QC Coordinator to showcase their expertise in a supportive and collaborative environment. At Fulkrum, you’ll make a tangible impact while advancing your career in the thriving global business sector.

We offer a fantastic working environment with a highly engaged team and consistently high eNPS scores. Fulkrum's success in attracting new clients and expanding our global footprint is a testament to our excellence and dedication. We have regular reward and recognition initiatives, a social budget, and a refer-a-friend scheme to ensure our team feels valued and motivated.

Join us to be part of a high-performing team with ample opportunities for skill enhancement and development. Be a part of our success story and contribute to our continued growth and innovation.

Apply now and become a valued part of our growing team!

Fulkrum

About Us:

MUFG Bank, Ltd. is Japans premier bank, with a global network spanning in more than 40 markets. Outside of Japan, the bank offers an extensive scope of commercial and investment banking products and services to businesses, governments, and individuals worldwide. MUFG Banks parent, Mitsubishi UFJ Financial Group, Inc. (MUFG) is one of the worlds leading financial groups. Headquartered in Tokyo and with over 360 years of history, the Group has about 120,000 employees and offers services including commercial banking, trust banking, securities, credit cards, consumer finance, asset management, and leasing. The Group aims to be the worlds most trusted financial group through close collaboration among our operating companies and flexibly respond to all the financial needs of our customers, serving society, and fostering shared and sustainable growth for a better world. MUFGs shares trade on the Tokyo, Nagoya, and New York stock exchanges.

MUFG Global Service Private Limited:

Established in 2020, MUFG Global Service Private Limited (MGS) is 100% subsidiary of MUFG having offices in Bengaluru and Mumbai. MGS India has been set up as a Global Capability Centre / Centre of Excellence to provide support services across various functions such as IT, KYC/ AML, Credit, Operations etc. to MUFG Bank offices globally. MGS India has plans to significantly ramp-up its growth over the next 18-24 months while servicing MUFGs global network across Americas, EMEA and Asia Pacific.

Position Title: Documentation Quality Control Analyst

Corporate Title: Analyst

Job Profile:

Position details:

The use of models presents model risk, which is the potential for adverse consequences from decisions based on incorrect or misused model outputs and reports. Model risk can lead to financial loss, poor business and strategic decision-making, or damage to a banking organizations reputation. Model validation is the set of processes and activities intended to verify that models are performing as expected, in line with their design objectives and business uses.The candidate will report to the Head of Model and EUCC Risk Management in MGS India as a part of the Model and End User Computing Calculator (EUCC) Risk Center of Excellence. This team works to support the Model and EUCC Risk Management team of the Americas which is responsible for the enterprise-wide model validation and control function to ensure the continued safety and soundness of models used across the bank. Americas Model Risk Management touches models across all lines of businesses in the Americas.

The requirement of the role may evolve depending on the future target operating model of the Model and EUCC Risk Center of Excellence. Maintaining a willingness to learn and a can-do attitude are important elements for success. The ideal candidate is one who is able to adapt to and assist in different responsibilities.

Roles and Responsibilities:

The Quality Control role is responsible for ensuring the quality of the Model Validation Report which is the primary deliverable coming out of the independent model validation. The validation is a critical work product for the organization and is subject to regulatory and audit scrutiny.

Quality Control is the final step in the model validation process to ensure the validation report is fully compliant to the standard. The candidate will perform Quality Control verification following all Model Validation Reports, document comments on observed gaps, review remediation and publish the validation report. The candidate will work with the validators and governance team to conclude on any outstanding gaps. The candidate will work with the governance team to identify efficiencies or process improvements or other projects as needed.

Job Requirements:

• 2 - 4 years of experience, preferably within the financial services industry or risk management.
• Experience with risk and controls assessment processes or other quality control functions. Experience in at least one of the following areas is ideal: Model Risk Management, EUCC Risk Management, Internal Control, Quality Control, Third Party Risk Management, Operational Risk Management, Compliance, Internal Audit, or other Regulatory-related supervision.
• Good verbal / written communication and people management skills.
• Knowledgeable model risk management and associated US regulatory requirements such as OCC , FRB SR 11-7 is a plus.
• Experience working with offshore partners is preferred.

Equal Opportunity Employer:

The MUFG Group is committed to providing equal employment opportunities to all applicants and employees and does not discriminate on the basis of race, colour, national origin, physical appearance, religion, gender expression, gender identity, sex, age, ancestry, marital status, disability, medical condition, sexual orientation, genetic information, or any other protected status of an individual or that individual's associates or relatives, or any other classification protected by the applicable laws.

• Perform routine and non-routine analytical testing using a variety of laboratory techniques (e.g., HPLC, GC, UV-Vis Spectroscopy, Titration).
• Analyze samples of raw materials, intermediates, and finished pharmaceutical products.
• Document all laboratory activities, results, and observations accurately and in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
• Prepare reagents, standards, and samples for testing.
• Calibrate and maintain laboratory equipment, ensuring proper functioning and calibration records.
• Investigate out-of-specification (OOS) results and deviations, participating in root cause analysis.
• Assist in the validation and qualification of analytical methods and equipment.
• Review and approve test results and associated documentation.
• Maintain a clean and organized laboratory environment.
• Stay updated on pharmacopoeial standards (e.g., IP, BP, USP) and regulatory guidelines.
• Contribute to the continuous improvement of quality control processes.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Microbiology, or a related life science discipline.
• Minimum of 3-5 years of experience in a pharmaceutical Quality Control laboratory.
• Proficiency in analytical techniques such as HPLC, GC, and wet chemistry.
• Thorough understanding of GLP, GMP, and relevant regulatory guidelines.
• Experience with laboratory information management systems (LIMS) is a plus.
• Strong attention to detail and accuracy in data recording and analysis.
• Excellent organizational and time management skills.
• Ability to work independently and as part of a team.
• Good written and verbal communication skills.
• Proficiency in Microsoft Office Suite.

• Performing analytical tests on raw materials, intermediates, and finished pharmaceutical products using various laboratory techniques (e.g., HPLC, GC, UV-Vis Spectroscopy, Titration).
• Analyzing test results and comparing them against established specifications and regulatory standards.
• Documenting all testing procedures, results, and observations accurately in laboratory notebooks and electronic systems.
• Identifying and investigating any deviations from established specifications or procedures.
• Participating in method validation and transfer activities.
• Preparing and standardizing reagents and solutions for analytical testing.
• Calibrating and maintaining laboratory equipment to ensure accurate and reliable results.
• Ensuring compliance with all safety regulations and environmental policies.
• Assisting in the investigation of out-of-specification (OOS) results.
• Contributing to the continuous improvement of quality control processes.
• Collaborating with production and R&D teams to resolve quality-related issues.
• Maintaining a clean and organized laboratory environment.

• Perform routine and advanced analytical testing of raw materials, in-process samples, and finished products using various laboratory techniques (e.g., HPLC, GC, UV-Vis, FTIR).
• Develop, validate, and transfer analytical methods according to established protocols and regulatory guidelines.
• Analyze test results, interpret data, and prepare accurate and comprehensive reports.
• Investigate out-of-specification (OOS) results and deviations, documenting findings and recommending corrective and preventive actions (CAPA).
• Maintain laboratory equipment, ensuring calibration, qualification, and routine maintenance are performed.
• Ensure adherence to Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and other relevant regulatory standards.
• Prepare and review standard operating procedures (SOPs) for analytical testing and laboratory operations.
• Collaborate with R&D, Manufacturing, and Regulatory Affairs departments to resolve quality issues and support product development.
• Manage laboratory inventory, including chemicals, reagents, and consumables.
• Participate in internal and external audits as required.
• Stay updated with the latest advancements in pharmaceutical analysis and quality control techniques.
• Contribute to continuous improvement initiatives within the Quality Control department.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a related life science field.
• Minimum of 3-5 years of experience in pharmaceutical quality control or analytical development.
• Extensive hands-on experience with analytical instrumentation such as HPLC, GC, dissolution testers, and spectrophotometers.
• Proficiency in wet chemistry techniques and compendial testing (USP/EP/BP/IP).
• Strong understanding of GMP, GLP, and ICH guidelines.
• Excellent analytical, problem-solving, and critical thinking skills.
• Meticulous attention to detail and accuracy in data recording and reporting.
• Ability to work independently and as part of a team in a fast-paced laboratory environment.
• Proficient in Microsoft Office Suite and LIMS (Laboratory Information Management System) software.
• Strong written and verbal communication skills.
• Experience with method validation and transfer is highly desirable.

• Perform analytical testing on raw materials, intermediates, and finished pharmaceutical products.
• Operate and maintain various laboratory instruments (e.g., HPLC, GC, UV-Vis).
• Document all testing procedures, results, and observations accurately.
• Investigate out-of-specification (OOS) results and deviations.
• Ensure compliance with GMP, SOPs, and regulatory guidelines.
• Participate in equipment calibration and validation activities.
• Collaborate with cross-functional teams to resolve quality issues.
• Contribute to continuous improvement of quality control processes.

• Bachelor's or Master's degree in Pharmacy, Chemistry, or a related life science field.
• Hands-on experience with pharmaceutical quality control testing methods and instrumentation.
• Familiarity with GMP and regulatory requirements for pharmaceuticals.
• Strong analytical and problem-solving abilities.
• Excellent documentation and record-keeping skills.
• Proficiency in data analysis and interpretation.
• Ability to work effectively in a team and independently.
• Good communication skills.