889 Freelance Reviewer jobs in India
Tax Reviewer
Posted 5 days ago
Job Viewed
Job Description
Anderson Global ( is an educational based leading provider of corporate services, supporting entrepreneurs and investors across key markets including the UAE (Dubai), India, Singapore, France, Switzerland, the USA, and the Cayman Islands. With over 600 professionals and a strong acquisition track record, we deliver expert corporate services such as bookkeeping, tax and legal solutions tailored to global business needs for SME's . Want to be part of a fast-growing, international team that’s shaping the future of corporate services? Join us!
Job Purpose:
The Tax Reviewer is responsible for performing detailed quality reviews of tax returns prepared by Associates and Senior Associates before submission to the U.S. for final review and signing. This role ensures the accuracy and compliance of individual and business tax returns while providing guidance and feedback to the preparation team. The Tax Reviewer also plays a key role in improving processes, supporting team development, and maintaining high standards of service delivery.
Key Responsibilities:
Tax Preparation and Review:
- Oversee the preparation and review of individual income tax returns (1040) and business income tax returns (1120, 1120S, 1065, 1041).
- Ensure the accuracy of tax returns and compliance with U.S. tax laws and regulations.
- Assist with more complex tax issues and provide support to team members as needed.
Communication:
- Communicate internally with the Ahmedabad tax team and coordinate with the U.S. tax team for workflow management and feedback on return corrections.
- Act as an intermediary between U.S. signing reviewers and the Ahmedabad preparation staff.
- Address and resolve any inquiries or issues from the U.S. team promptly.
Process Improvement:
- Identify opportunities for improving tax preparation and review processes to enhance efficiency.
- Implement best practices aimed at improving team performance and client satisfaction.
Training and Development:
- Provide constructive feedback and training to Associates and Senior Associates to improve the quality of tax returns.
- Encourage continuous learning and professional development within the team, sharing knowledge and resources to empower team members.
Administrative Tasks :
- Ensure all client documentation is accurately recorded, organized, and maintained in accordance with company policies.
- Perform any additional duties assigned by management to support the overall objectives of the organization.
Required Qualifications:
- Bachelor’s degree in accounting, Finance, or a related field.
- 5+ years of experience preparing and reviewing U.S. tax returns (1040, 1120, 1120S, 1065, 1041).
- Strong understanding of U.S. tax regulations and compliance standards.
- Experience in providing feedback and training to tax preparation teams.
- Excellent attention to detail and strong analytical skills.
- Proficiency with tax preparation software (e.g., CCH Axcess or ProSystem fx) and Google Suite or Microsoft Office tools.
Preferred Qualifications:
- CA certification or equivalent tax certification.
- Experience with complex tax return reviews and workflow management.
- Familiarity with U.S. tax concepts and business taxation.
Performance Metrics:
- Accuracy of Tax Returns: Measured by the reduction in errors or discrepancies in the tax returns reviewed before submission to the U.S. team.
- Timeliness of Review: Success in ensuring tax returns are reviewed within the established deadlines and sent for final review promptly.
- Training and Development Effectiveness: Improvement in team performance through the delivery of constructive feedback and training to junior team members.
- Process Improvement Contributions: Success in identifying and implementing process improvements that increase efficiency and service quality.
Tax Reviewer
Posted 5 days ago
Job Viewed
Job Description
We are seeking a skilled and detail-oriented US Tax associate with over 5 years of experience in reviewing US individual and business tax returns. The ideal candidate will be responsible for thoroughly reviewing tax returns prepared by junior staff for accuracy, completeness, and compliance with applicable tax laws.
Key Responsibilities:
- Review US federal and state tax returns for:
- Individuals (Form 1040)
- Corporations (1120, 1120S)
- Partnerships (1065)
- Check supporting documents, work papers, and schedules for accuracy.
- Identify errors, omissions, or inconsistencies and suggest corrections.
- Ensure tax compliance with current IRS and state tax laws.
- Communicate with tax preparers to clarify details or request revisions.
- Conduct basic tax research when required to resolve return-specific issues.
- Stay updated on changes in US tax codes and software practices.
- Meet internal deadlines and quality standards for reviewed returns.
Preferred Skills:
- Experience in an outsourced US tax process or CPA firm.
- Familiarity with tools like GoSystem Tax RS, CCH Axcess Tax, or similar platforms.
Interested candidates can share the resume on
US Tax Reviewer
Posted 5 days ago
Job Viewed
Job Description
We are seeking a skilled and detail-oriented US Tax Reviewer with over 4 years of experience in reviewing US individual and business tax returns. The ideal candidate will be responsible for thoroughly reviewing tax returns prepared by junior staff for accuracy, completeness, and compliance with applicable tax laws.
Key Responsibilities:
- Review US federal and state tax returns for:
- Individuals (Form 1040)
- Corporations (1120, 1120S)
- Partnerships (1065)
- Check supporting documents, work papers, and schedules for accuracy.
- Identify errors, omissions, or inconsistencies and suggest corrections.
- Ensure tax compliance with current IRS and state tax laws.
- Communicate with tax preparers to clarify details or request revisions.
- Conduct basic tax research when required to resolve return-specific issues.
- Stay updated on changes in US tax codes and software practices.
- Meet internal deadlines and quality standards for reviewed returns.
Requirements:
- Bachelor’s degree in Accounting, Finance, or related field (EA preferred but not mandatory).
- Minimum 4 years of hands-on experience in US taxation, specifically in return review.
- Strong knowledge of US tax laws for individuals and businesses.
- Proficiency in US tax software like Lacerte, ProSeries, Drake, or similar.
- Attention to detail and strong analytical skills.
- Good written and verbal communication skills.
- Ability to work independently and meet deadlines in a high-volume environment.
Preferred Skills:
- Experience in an outsourced US tax process or CPA firm.
- Familiarity with tools like GoSystem Tax RS, CCH Axcess Tax, or similar platforms.
KYC Post Execution Quality Reviewer
Posted 2 days ago
Job Viewed
Job Description
**Responsibilities:**
+ Conduct client profile reviews for customer accounts
+ Review all information and documentation ensuring compliance with local regulation and Citi standards
+ Update KYC forms and client profiles according to policy requirements
+ Follow up with clients to ensure information is received before due dates
+ Perform KYC tasks, including monitoring and tracking of the KYC records and Appendix approval process, assisting with the development and execution of action planning for expiring records, and ensuring records are not past due
+ Appropriately assess risk when business decisions are made, demonstrating particular consideration for the firm's reputation and safeguarding Citigroup, its clients and assets, by driving compliance with applicable laws, rules and regulations, adhering to Policy, applying sound ethical judgment regarding personal behavior, conduct and business practices, and escalating, managing and reporting control issues with transparency.
**Qualifications:**
+ 0-2 years of relevant experience
+ Experience in banking operations, preferably in the client account opening and pre-requirements process
**Education:**
+ Bachelor's degree/University degree or equivalent experience
---
**Job Family Group:**
Operations - Services
---
**Job Family:**
Business KYC
---
**Time Type:**
Full time
---
**Most Relevant Skills**
Business Acumen, Credible Challenge, Laws and Regulations, Management Reporting, Policy and Procedure, Program Management, Referral and Escalation, Risk Controls and Monitors, Risk Identification and Assessment, Risk Remediation.
---
**Other Relevant Skills**
For complementary skills, please see above and/or contact the recruiter.
---
_Citi is an equal opportunity employer, and qualified candidates will receive consideration without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other characteristic protected by law._
_If you are a person with a disability and need a reasonable accommodation to use our search tools and/or apply for a career opportunity review_ _Accessibility at Citi ( _._
_View Citi's_ _EEO Policy Statement ( _and the_ _Know Your Rights ( _poster._
Citi is an equal opportunity and affirmative action employer.
Minority/Female/Veteran/Individuals with Disabilities/Sexual Orientation/Gender Identity.
Medical Reviewer MLR, Scientific Communications
Posted 2 days ago
Job Viewed
Job Description
The Scientific Communications MLR Technical Reviewer is responsible for checking all medical content for data and scientific accuracy, and reference appropriateness for materials submitted through the Medical, Legal, and Regulatory (MLR) process. This role ensures that all content adheres to Amgen's scientific and compliance standards, while supporting timely review and approval of assets that inform and engage healthcare providers, patients, and internal stakeholders.
Working closely with the US Scientific Communications MLR Reviewer, the Technical Reviewer brings scientific expertise, attention to detail, and compliance awareness to evaluate the submissions. This role contributes to the quality and consistency of Amgen's communications by safeguarding scientific integrity across materials.
**Roles & Responsibilities:**
+ Conducting a review of proactive materials for scientific accuracy and reference appropriateness
+ Reviewing the material and ensuring appropriate medical context, scientific balance, and compliance are maintained in submitted content
+ Ensuring the timely and high-quality review of MLR materials within established SLAs and agreed-upon timeframes
+ Collaborating with the US Scientific Communication MLR Reviewer to ensure clear guidance on action items
+ Working within Amgen's MLR systems to apply clear review comments per company process
+ Conducting and participating in knowledge-sharing sessions to align on therapeutic areas, products, and review best practices
+ Providing scientific guidance to cross-functional teams regarding appropriate interpretation and use of data in promotional and medical content
+ Supporting standardization of review practices, templates, and criteria to drive efficiency and consistency across reviews
+ Staying current on therapeutic area developments, industry guidelines, and regulatory requirements relevant to MLR reviews
+ Contributing to process improvement initiatives and adoption of new technologies that enhance review workflows
**Basic Qualifications and Experience:**
Doctorate degree & 2 years of directly related experience
OR
MBBS or Master's degree & 4 years of directly related industry experience
OR
Bachelor's degree & 4 years of directly related industry experience
OR
Associate's degree & 6 years of directly related industry experience
**Functional Skills:**
**Preferred Qualifications:**
+ Doctorate degree in life sciences, pharmacy, biomedical sciences, or a related field
+ 5+ years of experience in medical review, medical writing, scientific communications, publications, or related industry role
+ Familiarity with the MLR review process and regulatory requirements for medical and promotional materials
+ Strong ability to critically evaluate data, references, and claims for scientific accuracy and compliance
+ Prior experience with content management and MLR review systems (e.g., Veeva PromoMats or equivalent)
+ Excellent attention to detail and organizational skills to manage multiple, concurrent submissions under tight timelines
+ Strong written and verbal communication skills to interact effectively with cross-functional stakeholders
+ Knowledge of therapeutic areas such as oncology, cardiovascular, inflammation, bone, and rare diseases is a plus
+ Understanding of US compliance, copyright, and transfer-of-value requirements
**Competencies:**
+ **Scientific Integrity:** Upholds rigorous standards in data accuracy and interpretation
+ **Collaboration:** Works effectively with cross-functional global teams in MLR review cycles
+ **Attention to Detail:** Ensures consistency, accuracy, and compliance in content review
+ **Time Management:** Prioritizes high-volume review workload and meets critical deadlines
+ **Adaptability:** Adjusts to evolving review practices, systems, and regulatory expectations
+ **Compliance:** Demonstrates commitment to integrity in all aspects of review work
Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.
KYC Change Management Reviewer - Officer
Posted 2 days ago
Job Viewed
Job Description
**Responsibilities:**
+ Collaborate with Compliance and Operations to develop Ops procedures with clear guidance on completing APAC country variance requirements
+ Develop materials and deliver training to Operations covering key changes around completing APAC country variance requirements
+ Coordinate APAC country variance changes from Compliance and socialise with Operations
+ Responsible for various aspects of risk and control, include but are not limited to Information Security, Continuation of Business and Records Management
+ Conduct analysis of risk and associated controls to identify root cause and collaborate with peers and management to report findings with solutions to mitigate risk/control issues
+ Provide support to business managers and product staff
+ Partner with peers and management on various activities, including developing and executing business plans within area of responsibility, developing compliance guidelines and completing monthly, quarterly, and other periodic risk & control reporting to be used for various forums
+ Interface with internal and external teams to provide guidance and subject matter expertise, as needed
+ Interface with Internal Audit (IA) and external audit to provide input on situations that create risk and legal liabilities for Citi
+ Oversee situations that create risk and legal liabilities for Citi
+ Has the ability to operate with a limited level of direct supervision.
+ Can exercise independence of judgement and autonomy.
+ Acts as SME to senior stakeholders and /or other team members.
+ Appropriately assess risk when business decisions are made, demonstrating particular consideration for the firm's reputation and safeguarding Citigroup, its clients and assets, by driving compliance with applicable laws, rules and regulations, adhering to Policy, applying sound ethical judgment regarding personal behavior, conduct and business practices, and escalating, managing and reporting control issues with transparency.
**Qualifications:**
+ 2-5 years of relevant experience
+ Proven ability to make effective and timely decisions
+ Consistently able to anticipate and respond to customer/business needs
+ Demonstrated ability to build and cultivate partnerships across business regions
**Education:**
+ Bachelor's degree/University degree or equivalent experience
---
**Job Family Group:**
Operations - Services
---
**Job Family:**
Business KYC
---
**Time Type:**
Full time
---
**Most Relevant Skills**
Business Acumen, Credible Challenge, Laws and Regulations, Management Reporting, Policy and Procedure, Program Management, Referral and Escalation, Risk Controls and Monitors, Risk Identification and Assessment, Risk Remediation.
---
**Other Relevant Skills**
For complementary skills, please see above and/or contact the recruiter.
---
_Citi is an equal opportunity employer, and qualified candidates will receive consideration without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other characteristic protected by law._
_If you are a person with a disability and need a reasonable accommodation to use our search tools and/or apply for a career opportunity review_ _Accessibility at Citi ( _._
_View Citi's_ _EEO Policy Statement ( _and the_ _Know Your Rights ( _poster._
Citi is an equal opportunity and affirmative action employer.
Minority/Female/Veteran/Individuals with Disabilities/Sexual Orientation/Gender Identity.
Periodic Report Safety QC Reviewer
Posted 2 days ago
Job Viewed
Job Description
Key Responsibilities:
- Conduct thorough quality control reviews of PBRER/PSURs, DSURs, PADER/PAERs, and other aggregate safety reports to ensure content accuracy, data integrity, formatting consistency, and adherence to regulatory and internal requirements.
- Verify correct incorporation of safety data, narratives, tables, and appendices, ensuring alignment with source documents and databases.
- Collaborate with Periodic Report Specialists to address discrepancies and ensure timely resolution of quality issues.
- Maintain up-to-date knowledge of global regulatory requirements and industry best practices for periodic safety reporting.
- Contribute to the development and refinement of QC checklists, templates, and SOPs to ensure consistent review practices.
- Track QC metrics and support continuous improvement initiatives related to safety report quality and delivery.
Basic Qualifications and Experience:
+ Total experience: 5-9 years
+ At least 2-3 years in QC
+ Bachelor's or Master's degree in Life Sciences or Pharmacy
Be The First To Know
About the latest Freelance reviewer Jobs in India !
Medical Reviewer-Drug Safety Physician
Posted 5 days ago
Job Viewed
Job Description
We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations to be future ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship, and is guided by passion, innovation, collaboration and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out Looking to jump-start your career? We understand how important the first few years of your career are, which create the foundation of your entire professional journey. At Indegene, we promise you a differentiated career experience. You will not only work at the exciting intersection of healthcare and technology but also will be mentored by some of the most brilliant minds in the industry. We are offering a global fast track career where you can grow along with Indegene’s high-speed growth. We are purpose-driven. We enable healthcare organizations be future ready and our customer obsession is our driving force. We ensure that our customers achieve what they truly want. We are bold in our actions, nimble in our decision-making, and industrious in the way we work. If this excites you, then apply below:
Job Title: Medical Reviewer – Pharmacovigilance
Location:
Work from office: Bangalore, Hyderabad, Mumbai, Pune, Delhi
Willingness to relocate to one of the above locations is mandatory.
Education Requirements:
- MBBS and MD (mandatory)
- Candidates without both qualifications will not be considered.
Job Title: Medical Reviewer – Pharmacovigilance
Location:
Work from office: Bangalore, Hyderabad, Mumbai, Pune, Delhi
Willingness to relocate to one of the above locations is mandatory.
Education Requirements:
- MBBS, MD(mandatory)
- Medical council of India registration ( Mandatory)
Job Description:
As a Medical Reviewer – Pharmacovigilance , you will be responsible for the comprehensive medical review of individual case safety reports (ICSRs) and ensuring compliance with regulatory and client-specific requirements. You will play a critical role in safeguarding patient safety through high-quality medical evaluation and regulatory reporting.
Key Responsibilities:
- Perform medical review of ICSRs for accuracy , medical relevance , and consistency with the source documents and safety database entries, in alignment with client requirements.
- Conduct second-level triaging of non-serious cases to identify any potential serious adverse events (SAEs), as per client-specific conventions.
- Review and validate:
- Suspect product coding
- Event selection and MedDRA coding (current version)
- Grouping/subsuming and event ordering
- Confirm and correct:
- Event coding and classification
- Ranking of events, seriousness criteria, and listedness/expectedness
- Perform comprehensive medical evaluation of adverse event reports including serious/expedited cases and pregnancy-related reports.
- Assess adverse events for seriousness , listedness , and causality , ensuring all medically relevant data from source documents is accurately reflected.
- Review and enhance narratives in compliance with client conventions.
- Provide or verify company pharmacovigilance (PV) comments as needed.
- Initiate appropriate follow-up queries based on the clinical context of the case.
- Identify and escalate potential safety signals or concerns in line with client procedures.
- Ensure completeness and medical soundness of cases before providing final medical sign-off .
- Assess malfunctions and serious injury/death outcomes in relation to combination products.
- Participate in literature surveillance and aggregate report medical review, ensuring compliance with regulatory timelines and SOPs.
- Track and document inconsistencies in data entry and provide feedback for continuous improvement.
- Collaborate closely with cross-functional teams to maintain scientific accuracy , clarity , and regulatory compliance in all case documentation.
- Stay updated with international pharmacovigilance regulations and follow all applicable SOPs , guidelines , and best practices .
- Attend mandatory internal and client-specific trainings to ensure continuous compliance.
Required Skills and Competencies:
- Strong analytical and critical thinking abilities
- High attention to detail and scientific accuracy
- Sound medical judgment and decision-making in line with pharmacovigilance standards
- Proficiency in medical terminology , disease pathology, pharmacology, and therapeutics
- Ability to analyze and interpret adverse event data
- Strong written and verbal communication skills
- Good comprehension and the ability to summarize complex medical data
- Team player with effective interpersonal and collaboration skills
- Familiarity with pharmaceutical industry practices and drug development processes (preferred)
Additional Requirements:
- Willing to relocate to any of the listed office locations.
- Ready to work from the office with hybrid options
- Must possess MBBS and MD degrees (non-negotiable)
EQUAL OPPORTUNITY:
Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, candidate’s merit and qualification. We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.
Senior Scientist I, Documentary Standards (Reviewer)
Posted 2 days ago
Job Viewed
Job Description
At USP, we value inclusivity for all. We recognize the importance of building an organizational culture with meaningful opportunities for mentorship and professional growth. From the standards we create, the partnerships we build, and the conversations we foster, we affirm the value of Diversity, Equity, Inclusion, and Belonging in building a world where everyone can be confident of quality in health and healthcare.
USP is proud to be an equal employment opportunity employer (EEOE) and affirmative action employer. We are committed to creating an inclusive environment in all aspects of our work-an environment where every employee feels fully empowered and valued irrespective of, but not limited to, race, ethnicity, physical and mental abilities, education, religion, gender identity, and expression, life experience, sexual orientation, country of origin, regional differences, work experience, and family status. We are committed to working with and providing reasonable accommodation to individuals with disabilities.
**Brief Job Overview**
This is a hands-on, non-supervisory scientific position the Global Biologics department. The incumbent is responsible for providing support for the development of USP documentary standards and reference standards for biological products such as peptides, Oligonucleotides, protein, carbohydrates, Complex Biologics, Vaccines, Antibiotics, and advanced therapies. The incumbent will provide quality and technical review of scientific documents for accuracy, clarity and compliance, manage and track reference standard stability program and organize efforts for continuous process improvements. The incumbent will also focus on supporting the reference standard suitability program, including preparing and reviewing CSU testing protocols, providing technical assistance to testing labs, reviewing analytical data and preparing summary reports for confirming the continued suitability of USP Reference Standards (RS). The incumbent need to be excellent team player with good collaboration/Liaising skills to complete assigned projects in time-bound manner.
**How will YOU create impact here at USP?**
In this role at USP, you contribute to USP's public health mission of increasing equitable access to high-quality, safe medicine and improving global health through public standards and related programs. In addition, as part of our commitment to our employees, Global, People, and Culture, in partnership with the Equity Office, regularly invests in the professional development of all people managers. This includes training in inclusive management styles and other competencies necessary to ensure engaged and productive work environments.
**The Sr. Scientist -I (RSS-Review) has the following responsibilities:**
Roles and Responsibilities
+ Performs technical and quality reviews of documents to ensure a high level of document quality and compliance before QA review
+ Manages and tracks efforts for continuous process improvements.
+ Develops and reviews SOP's, Operation Manuals, and training documents.
+ Assists in investigations of quality related issues resulting from customer complaints to include root cause analysis, corrective action identification, action planning, and implementation monitoring.
+ Supports the day to day operation of the reference standard stability program.
+ Works with internal stakeholders to develop new and innovative standards for analytical analysis of biological products.
+ Communicates and maintains working relationships with cross functional USP departments regarding assigned projects
+ Supports day to day operations of the RS Stability (CSU) program covering the USP Biologics RS catalog inventory.
+ Reviews RS testing history and drafts test protocols for CSU studies and submits to labs based on designated testing requirements and schedules.
+ Liaisons and Assists laboratories to ensure CSU testing is completed as per protocol and in timely manner.
+ Reviews laboratory reports, evaluates results and compares to previous data and RS attributes to assess and conclude on RS suitability for use.
+ Compiles, assess current and historical stability testing data and prepare stability trend reports in a time-bound manner.
+ Support the maintenance and updation of various databases documenting laboratory data and program determinations on suitability and Stability interval updates.
+ Filing and closure of QMS elements as per QMS system when required and supports the RS Laboratory, Supporting Quality Assurance and Reference Standard Evaluation in the investigation of unexpected stability testing results
+ Works collaboratively with various USP departments as needed on test planning, data impact assessments and appropriate determination of next steps.
+ Prepare, present and discuss regular work updates with Team Lead and other team members
**Who is USP Looking For?**
The successful candidate will have a demonstrated understanding of our mission, commitment to excellence through inclusive and equitable behaviors and practices, ability to quickly build credibility with stakeholders, along with the following competencies and experience:
+ PhD. degree in Biochemistry/Biology/Pharmacy, or a related field Minimum of 7 to 10 years, or Masters degree in Biochemistry/Biology/Pharmacy or a related field with 11 to13 years of years of commensurate industrial experience.
+ Demonstrated experience in Techical review of analytical documents in Quality Assurance.
+ Hands-on experience with state-of-the-art analytical techniques for the characterization of recombinant therapeutic proteins, peptides, gene therapy, vaccines and carbohydrates, such as UPLC/HPLC, LC-MS, CD, Fluorescence spectroscopy, FTIR, DSC, SEC-MALS, CE-SDS (Reducing and Non-reducing), icIEF, ELISA, SPR, ddPCR/qPCR etc.
+ Strong ability to evaluate and compile analytical testing data, ability to write technical reports related to material characterization, references standard evaluations, and method development.
+ Demonstrated experience in analytical method development, method qualification/validation and characterization of biological products and impurities using a variety of physicochemical techniques and biological assays.
+ Excellent technical writing, presentation and oral communication skills are required.
+ Must be excellent team player and able to work amicably and communicate effectively with both internal and external stakeholders.
**Additional Desired Preferences**
+ Knowledge of USP products and services is highly desirable.
+ Operates collaboratively at all levels of the organization in a highly technical environment.
+ Must be able to work in a fast-paced environment and respond to shifting priorities.
+ Well-developed interpersonal, negotiation, conflict-resolution and listening skills.
+ Must possess the ability to multi-task and to work effectively with a team.
+ Takes ownership and personal responsibility to ensure work is delivered on time and is of the highest possible quality.
+ Experience working in the compendial, pharmaceutical and/or biotechnology industry strongly preferred.
**Supervisory Responsibilities**
No
**Benefits**
USP provides the benefits to protect yourself and your family today and tomorrow. From company-paid time off and comprehensive healthcare options to retirement savings, you can have peace of mind that your personal and financial well-being is protected.
Note: USP does not accept unsolicited resumes from 3rd party recruitment agencies and is not responsible for fees from recruiters or other agencies except under specific written agreement with USP.
**Job Category** Chemistry & Scientific Standards
**Job Type** Full-Time
NEET Content Reviewer – Physics/Chemistry/Biology
Posted 23 days ago
Job Viewed
Job Description
Job Summary:
Matrix Smart Learning is launching a next-gen learning app dedicated to NEET aspirants. We are currently hiring Academic Content Verifiers for Physics, Chemistry, and Biology to review and validate our in-app question bank, ensuring accuracy, alignment with NEET/NCERT standards, and tagging for silly, conceptual, or minor errors
Key Responsibilities:
Verify and proofread NEET-level multiple-choice questions for the subject you specialize in (Physics, Chemistry, or Biology).
Cross-check solutions and explanations for accuracy and clarity.
Tag errors as Silly / Conceptual / Minor, and provide feedback for corrections.
Ensure alignment with the latest NEET syllabus and NCERT curriculum.
Collaborate with the in-house academic and technical team to maintain quality standards.
Required Qualifications:
M.Sc / M.Phil / Ph.D. in Physics, Chemistry, or Biology OR MBBS / BDS / BAMS for Biology domain.
1+ years of experience in NEET content creation, validation, or teaching.
In-depth understanding of NEET-level exam pattern and question design.
Excellent attention to detail and subject matter accuracy.
Preferred Skills:
Familiarity with NCERT Books & NEET Exam Trends
Strong grammar and editing ability
Team collaboration and time management