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Collection Executive <ul><li>Hard collection 180+ Bucket Local region knowledge.</li><li>Litigation documents knowledge.</li><li>Micro finance field related candidate also apply.</li></ul> <ul><li>Department - Legal </li><li>Qualification: LLB or any other degree </li><li>Salary: Best in Industry</li><li>Experience: 0-3 years</li></ul> Share your updated resume now.

Namdev Finvest Pvt Ltd

Collections Executive

Manager-Liaisoning No. of Requirement - 2Qualification/Experience required - Graduate with 8+ years Land Acquisition through the following government departments. Handling the legal cases and compliances. Share your updated resume now with Subject Line: Position - Location (e.g., SAP Consultant - Gandhinagar)

MKC INFRASTRUCTURE LIMITED

Manager - Projects

Legal Officer Key Responsibilities: •	Handle legal matters pertaining to loan recovery, arbitration, litigation, and SARFAESI. •	Coordinate with external legal counsels and recovery teams. •	Draft and review legal documents, notices, and agreements. •	Ensure legal and regulatory compliance specific to NBFC operations. •	Appear for legal matters in DRT, Civil Courts, and other forums if required. Requirements: •	Bachelor’s degree in Law (LLB); LLM preferred. •	Strong understanding of NBFC-related laws, recovery process, and civil litigation. •	Proficiency in drafting legal documents and case follow-up. •	Willingness to travel locally as per business needs. •	Experience: 1-3 years in NBFC/Financial Services legal compliance preferred •	Immediate Joiners Preferred Share your updated resume now with subject line “Legal Officer – preferred location”

Legal Officer

Company Secretary-Infrastructure Debt Funding-DEFAULT<ul><li>Corporate Governance:<ul><li>Advising the board on corporate governance best practices. </li><li>Ensuring compliance with relevant laws, regulations, and the company's articles of association. </li><li>Developing and implementing governance frameworks. </li><li>Managing board and committee meetings, including preparing agendas, taking minutes, and ensuring proper follow-up. </li></ul></li><li>Compliance:<ul><li>Maintaining statutory registers (e.g., registers of members, directors). </li><li>Filing statutory documents (e.g., annual returns, accounts, director appointments). </li><li>Ensuring timely and accurate filing of all necessary documents with regulatory authorities. </li></ul></li><li>Administration:<ul><li>Managing company records, including minute books and other essential documents. </li><li>Handling communication with shareholders and stakeholders. </li><li>Organizing and coordinating annual general meetings (AGMs). </li></ul></li><li>Advisory:<ul><li>Providing guidance to the board and management on corporate governance matters. </li><li>Advising on legal and regulatory requirements related to corporate activities. </li><li>Supporting the board in its decision-making processes</li></ul></li></ul> <h4>Experience Level</h4>Mid Level

Kotak Mahindra Bank

Article Assistant

Contract Management PractitionerProject Role : Contract Management Practitioner Project Role Description : Counsel project teams on contract management and policy compliance matters. Document risks and issues with contract management processes and account delivery requirements. Must have skills : Microsoft 365 Good to have skills : NA Minimum 12 year(s) of experience is required Educational Qualification : 15 years full time education Summary: 
As a Contract Management Practitioner, you will provide guidance to project teams on contract management and policy compliance matters, documenting risks and issues with contract management processes and account delivery requirements. Your day will involve advising on contractual matters and ensuring compliance with policies and regulations.
 
Roles &amp; Responsibilities: 
- Expected to be an SME
- Collaborate and manage the team to perform
- Responsible for team decisions
- Engage with multiple teams and contribute on key decisions
- Expected to provide solutions to problems that apply across multiple teams
- Develop and implement contract management strategies
- Review and analyze contract terms and conditions
- Provide guidance on contract negotiations
 
Professional &amp; Technical Skills: 
- Must To Have Skills: Proficiency in Microsoft 365
- Strong understanding of contract management principles
- Experience in risk assessment and mitigation
- Excellent communication and negotiation skills
- Good To Have Skills: Experience with legal contract drafting
 
Additional Information: 
- The candidate should have a minimum of 12 years of experience in Microsoft 365
- This position is based at our Kolkata office
- A 15 years full time education is required

Accenture India Private Limited

Vendor Compliance executive

Regulatory Affairs Senior Manager (CMC)<h4>Career Category</h4>Regulatory<h4>Job Description</h4>The RA CMC Senior Manager is responsible for execution and/ or coordination of global regulatory CMC activities, including providing leadership, guidance, and insight to oversee the successful execution and implementation of the regulatory strategy for an assigned set of commercial products. The RA CMC Senior Manager is responsible for communicating the regulatory strategy, risks and issues to Regulatory and Operations senior management. The RA CMC Senior Manager coordinates communication, collaboration, and coordination with the site and regional CMC representatives within the department to develop and execute global regulatory activities.  Key Activities Contributes to product teams and acts as Global RA-CMC lead or supervisor for one or more products. Provides strategic regulatory input and regulatory risk assessments for product teams; executes regulatory strategy with respect to preparation of submissions; complies with critical RA CMC processes; identifies need for process and strategy changes to meet internal Amgen initiatives and changes in external regulatory policy and guidance; reports needs for process changes to CMC systems and contributes to process improvements; incorporates changes in external regulatory guidance into CMC strategy and guidance for product teams; reports issues to RA CMC product team management.   Key Responsibilities Include:  <ul><li>Oversees deliverables for CMC strategy and submissions for an assigned portfolio of products at varying stages of development,  </li></ul><ul><li>Works with external stakeholders including regulatory agencies and influential professional bodies, and seeks to influence regulatory policy globally  </li></ul><ul><li>Identifies regulatory risks across products within the defined scope, communicates these risks, and ensures aligned plans for mitigation  </li></ul><ul><li>Provides coaching, mentoring, and supports development of junior CMC Regulatory Affairs staff   </li></ul><ul><li>Provide CMC regulatory strategy for assigned projects by defining minimal regulatory filing requirements, submission strategy, and regulatory risk assessments </li></ul><ul><li>Develop response strategy and respond to health authority questions  </li></ul><ul><li>Liaise with other functions in development, operations and commercial to ensure alignment of global regulatory strategies, timing, execution and supply plans  </li></ul><ul><li>Liaise with local regulatory teams to align on filing strategy  </li></ul><ul><li>Monitor and, as necessary, provide data to be entered into tracking systems for department deliverables and ensure information is current. Maintain submission information according to the Regulatory Information Management (RIM) system  </li></ul><ul><li>Follow established department regulatory processes to ensure cross-product alignment  </li></ul> Knowledge and Skills Regulatory CMC- specific regulatory knowledge &amp; experience Staff management and development Education &amp; Experience (Basic) Doctorate degree  OR  Master’s degree and 3 years of directly related experience  OR  Bachelor’s degree and 5 years of directly related experience  OR  Associate’s degree and10 years of directly related experience  Experience in manufacture, testing (QC/QA or clinical), or distribution Regulatory CMC experience  <h4>What you can expect of us </h4>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.<h4>Apply now</h4>for a career that defies imaginationObjects in your future are closer than they appear. Join us.<h4>careers.amgen.com</h4>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.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..<h4>Experience Level</h4>Senior Level

Amgen Technology Private Limited

Chemical Analyst

Legal Negotiator<h4>Job Description:</h4>Job Title: Legal NegotiatorCorporate Title: Senior Analyst or Associate Location: Mumbai, IndiaShift Timing: APAC region / Regular shift Role Description<ul><li>The Regional Office Legal team (“RO Legal”) in Mumbai is a team of around thirty lawyers providing expertise in derivative documentation and transaction legal support to various businesses of Deutsche Bank Group across the APAC, EU and US regions.</li><li>RO Legal is looking for legal negotiators in India to support with respect to the derivative and financial product transactions undertaken by the Deutsche Bank Group globally by drafting and negotiating mid and high complexity contracts and other ancillary legal documentation.</li><li>You will spend a significant amount of your time drafting, reviewing and negotiating agreements, relating to derivative transactions and your role will involve liaising directly with the front office, internal stakeholders and the Deutsche Bank Group’s diverse client base.  In your role, you would be responsible for delivery, process and client management.</li></ul>What we’ll offer youAs part of our flexible scheme, here are just some of the benefits that you’ll enjoy,<ul><li>Best in class leave policy.</li><li>Gender neutral parental leaves</li><li>100% reimbursement under childcare assistance benefit (gender neutral)</li><li>Sponsorship for Industry relevant certifications and education</li><li>Employee Assistance Program for you and your family members</li><li>Comprehensive Hospitalization Insurance for you and your dependents</li><li>Accident and Term life Insurance</li><li>Complementary Health screening for 35 yrs. and above</li></ul>Your key responsibilities <ul><li>Drafting reviewing and negotiating wide range of master agreements amongst others, ISDA Master Agreements, Credit Support documents (CSA, CSDs), Global Master Repurchase Agreements (GMRA), Master Repurchase Agreement (MRA), Global Master Securities Lending Agreement (GMSLA), Master Securities Lending Agreement (MSLA), Prime Brokerage Agreements and all other relevant documentation and subsequent amendments.</li><li>Reviewing constitutional documents and ensuring that all requisite corporate consents and approvals are in place prior to finalization of agreements and subsequent trading.</li><li>Liaising and coordinating with the various internal stakeholders / teams and business divisions on risk and deviations and responding to queries in relation to the master agreements.</li><li>Building a strong relationship with both the internal and external clients of Deutsche Bank Group, understanding their needs and business operations and working closely with them.</li><li>Understanding business and regulatory requirements and ensuring functions are being performed taking into consideration those requirements.</li><li>Staying abreast on all legal and regulatory matters affecting your area of work.</li><li>Participating in various documentation and process improvement initiatives.</li></ul>Your skills and experience<ul><li>Law Degree or Commonwealth qualified lawyer or solicitor with 2 to 5 years of PQE for Senior Analyst level and 6 to 8 years of PQE for Associate level in financial products or commercial contract drafting and negotiations.</li><li>Having prior experience in derivative documentation will be an advantage.</li><li>Excellent legal drafting ability and eye for detail.</li><li>Strong problem solving and/or analytical skills with solution-based approach.</li><li>Excellent interpersonal skills and ability to communicate and build working relationships both internally and externally.</li><li>Excellent communication skills, both oral and written.</li><li>Ability to work independently, as well as in a team environment.</li><li>Ability to read complex legal documents with confidence, ease and understanding.</li><li>Ability to multi-task and work in a fast-paced environment.</li></ul>How we’ll support you<ul><li>Training and development to help you excel in your career.</li><li>Coaching and support from experts in your team.</li><li>A culture of continuous learning to aid progression.</li><li>A range of flexible benefits that you can tailor to suit your needs.</li></ul>About us and our teamsPlease visit our company website for further information:<a href="https://www.db.com/company/company.htm" rel="noopener noreferrer" target="_blank">https://www.db.com/company/company.htm</a>We strive for a <a href="https://careers.db.com/inside-deutsche-bank/our-culture" rel="noopener noreferrer" target="_blank">culture </a>in which we are empowered to excel together every day. This includes acting responsibly, thinking commercially, taking initiative and working collaboratively.Together we share and celebrate the successes of our people. Together we are Deutsche Bank Group.We welcome applications from all people and promote a positive, fair and inclusive work environment.<h4>Experience Level</h4>Senior Level

Deutsche Bank

Legal Executive

Regulatory Affairs Manager (CMC)<h4>Career Category</h4>Regulatory<h4>Job Description</h4>The RA CMC Manager is responsible for execution and/ or coordination of global regulatory CMC activities, including providing leadership, guidance, and insight to oversee the successful execution and implementation of the regulatory strategy for an assigned set of commercial products. The RA CMC Manager is responsible for communicating the regulatory strategy, risks and issues to Regulatory and Operations senior management. The RA CMC manager coordinates communication, collaboration, and coordination with the site and regional CMC representatives within the department to develop and execute global regulatory activities. Key Activities Contributes to product teams and acts as product lead or principal for one or more products. Provides strategic regulatory input and regulatory risk assessments for product teams; executes regulatory strategy with respect to preparation of submissions; complies with critical RA CMC processes; identifies need for process and strategy changes to meet internal Amgen initiatives and changes in external regulatory policy and guidance; reports needs for process changes to CMC systems and contributes to process improvements; incorporates changes in external regulatory guidance into CMC strategy and guidance for product teams; reports issues to RA CMC product team management. Key Responsibilities Include:  <ul><li>Generate and execute of global and country-specific regulatory strategies </li></ul><ul><li>Provide CMC regulatory strategy for assigned projects by defining minimal regulatory filing requirements, submission strategy, and regulatory risk assessments  </li></ul><ul><li>Develop global dossiers for CMC content for initial submissions, variations and amendments </li></ul><ul><li>Support change management activities  </li></ul><ul><li>Develop response strategy and respond to health authority questions </li></ul><ul><li>Liaise with other functions in development, operations and commercial to ensure alignment of global regulatory strategies, timing, execution and supply plans </li></ul><ul><li>Liaise with local regulatory teams to align on filing strategy </li></ul><ul><li>Monitor and, as necessary, provide data to be entered into tracking systems for department deliverables and ensure information is current. Maintain submission information according to the Regulatory Information Management (RIM) system </li></ul><ul><li>Follow established department regulatory processes to ensure cross-product alignment </li></ul>Knowledge and Skills CMC- specific regulatory knowledge &amp; experience Education &amp; Experience (Basic) Doctorate degree  OR  Master’s degree and 3 years of directly related experience  OR  Bachelor’s degree and 5 years of directly related experience Experience in manufacture, testing (QC/QA or clinical), or distribution Regulatory CMC experience  .<h4>Experience Level</h4>Mid Level

Regulatory Affairs Manager (Site)<h4>Career Category</h4>Regulatory<h4>Job Description</h4>Regulatory Affairs, Chemistry, Manufacturing and Controls (RA CMC) facilitates product development and global registration by developing and executing regulatory strategies and managing effective regulatory agency interactions for product manufacturing and quality programs throughout product lifecycle. The Regulatory Compliance team is a part of RA CMC and is seeking to expand its capacity in India.  The Regulatory Compliance team performs assessment of operational changes for regulatory reportability and maintains state and federal licenses for Amgen products across phases of development, modality, and countries.    The team member will be responsible for maintaining U.S. state and federal commercial product licenses and will collaborate with Global CMC, Site CMC, Device Regulatory, Operations, Quality, and Supply Chain teams on strategies and activities impacting licensed products. <h4>Roles &amp; Responsibilities:</h4>Key responsibilities of the Regulatory Affairs Manager include:<ul><li><ul><li>Conducts periodic assessments of licenses / facilities and ensures business practices comply with current regulations and statutes. </li><li>Evaluates new and existing regulations to maintain up-to-date compliance.</li></ul><ul><li>Communicates requirements to internal Amgen functional teams.  </li></ul><ul><li>Obtains supplemental documentation from internal and external partners.  </li></ul><ul><li>Prepares, reviews, and submits license applications and renewals.  </li></ul><ul><li>Maintains all State Licensing documentation, submissions, and interactions with State Authorities.  </li></ul><ul><li>Interfaces with State Board of Pharmacy (BoP) and/or Department of Health (DoH).  </li></ul><ul><li>Completes required annual notifications to U.S. FDA  </li></ul><ul><li>Obtains DUNS and FEI numbers for new U.S. sites, as required </li></ul><ul><li>Processes Financial obligations relating to fee payment. </li></ul><ul><li>Identifies and implements process improvements for the state licensing process </li></ul><ul><li>Coaches and supports junior regulatory staff’s career development </li></ul></li></ul><h4>What we expect of you</h4>We are all different, yet we all use our unique contributions to serve patients. The successful candidate will have the following qualifications:Basic Qualifications:<ul><li>Doctorate degree OR</li><li>Master’s degree and 3 years of manufacture, QA/QC, or regulatory CMC in the Pharmaceutical/Biotechnology industry OR</li><li>Bachelor’s degree and 5 years of manufacture, QA/QC, or regulatory CMC in the Pharmaceutical/Biotechnology industry</li></ul>Preferred Qualifications:<ul><li>Degree in Life Science discipline</li><li>Regulatory CMC specific knowledge &amp; experience</li><li>Experience in manufacture, testing (QC/QA or clinical), or distribution in Pharmaceutical/Biotech industry </li><li>Working knowledge of US state and/or federal licensing requirements </li></ul><h4>What you can expect of us</h4>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.<h4>Apply now</h4>for a career that defies imaginationObjects in your future are closer than they appear. Join us.<h4>careers.amgen.com</h4> .<h4>Experience Level</h4>Mid Level

Regulatory Affairs Sr Associate (Site)<h4>Career Category</h4>Regulatory<h4>Job Description</h4>Regulatory Affairs, Chemistry, Manufacturing and Controls (RA CMC) facilitates product development and global registration by developing and executing regulatory strategies and managing effective regulatory agency interactions for product manufacturing and quality programs throughout product lifecycle. The Regulatory Compliance team is a part of RA CMC and is seeking to expand its capacity in India.  The Regulatory Compliance team performs assessment of operational changes for regulatory reportability and maintenance of state and federal licenses for Amgen products across phases of development, modality, and countries.      The team member will be responsible for maintaining U.S. state and federal commercial product licenses and will collaborate with Global CMC, Site CMC, and Device Regulatory, Operations, Quality, and Supply Chain teams on strategies and activities impacting licensed products. <h4>Roles &amp; Responsibilities:</h4>Key responsibilities of the Regulatory Affairs Sr Associate include:<ul><li><ul><li>Tracks license status to ensure all are current and effective.  </li></ul><ul><li>Communicates requirements to internal Amgen functional teams.  </li></ul><ul><li>Obtains supplemental documentation from internal and external partners.  </li></ul><ul><li>Prepares, reviews, and submits license applications and renewals.  </li></ul><ul><li>Maintains all State Licensing documentation, submissions, and interactions with State Authorities.  </li></ul><ul><li>Interfaces with State Board of Pharmacy (BoP) and/or Department of Health (DoH).  </li></ul><ul><li>Completes required annual notifications to FDA  </li></ul></li></ul><h4>What we expect of you</h4>We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a type of person with these qualifications.Basic Qualifications:<ul><li>Master’s degree OR</li><li>Bachelor’s degree and 2 years of manufacture, QA/QC, or regulatory CMC in the Pharmaceutical/Biotechnology industry OR</li><li>Associate’s degree and 6 years of manufacture, QA/QC, or regulatory CMC in the Pharmaceutical/Biotechnology industry</li></ul>Preferred Qualifications:<ul><li>Degree in Life Science discipline</li><li>Regulatory CMC specific knowledge &amp; experience</li><li>Experience in manufacture, testing (QC/QA or clinical), or distribution in Pharmaceutical/Biotech industry</li><li>Working knowledge of US state and/or federal licensing requirements </li></ul><h4>What you can expect of us </h4>As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards.<h4>Apply now</h4>for a career that defies imaginationObjects in your future are closer than they appear. Join us.<h4>careers.amgen.com</h4>As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.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..<h4>Experience Level</h4>Mid Level

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Legal & Regulatory Jobs - 327 Verified Vacancies

Collections Executive

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Vendor Compliance executive

Collections Executive

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