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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

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

Assistant CS We are looking for passionate and experienced professionals to join our growing team in Water Sector / Solar Infra Projects.Department - CSQualification - Company Secretary (CS) QualifiedExperience - 1-3 years Share your updated resume now.

LCC Projects Pvt Ltd

Corporate Controller

SLA – Internal Contract (IC) Coordinator We're looking for a Service Level Agreement (SLA) – Internal Contract (IC) Coordinator to join our dynamic team!Experience : 9 - 12 Years&nbsp; What You'll Do:As the SLA – IC Coordinator, you'll play a key role in managing internal service agreements and ensuring all contract-related processes are aligned with project deliveries and legal requirements. Your day-to-day will include:<ul><li> Coordinating the drafting, review, and signing of internal service agreements</li><li> Working with IT teams, project managers, legal, and compliance</li><li> Ensuring contract timelines match project delivery dates</li><li> Preparing and leading committee meetings and service review sessions</li><li> Producing KPIs and performance reports</li><li> Managing controls and compliance checks related to internal contracts</li><li> Collaborating in an international and cross-functional environment</li></ul> Who You Are:<ul><li> You bring 10+ years of experience working with Service Level Agreements or Internal Contracts</li><li> You’re fluent in English (written and spoken)</li><li> You have a good understanding of legal documents, GDPR, and IT security</li><li> You’re organized, collaborative, and detail-oriented</li><li> Proficiency in Excel, PowerPoint — Power BI is a plus!</li></ul> Nice to Have:<ul><li> Background or experience working with legal teams or contract governance</li><li> Comfortable managing multiple stakeholders and priorities</li><li> Experience working in global or multicultural teams</li></ul> If you're passionate about legal coordination, project alignment, and delivering operational excellence, share your updated CV.

Teamware Solutions

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

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 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

Company Secretary Experience - 1 to 2 years of experience in Corporate Governance &amp; Legal ComplianceLocation: Ahmedabad Share your updated resume now.

Communities Heritage 

Article Assistant

Legal Advisory Officer Description:<ul><li>Vendor Management, Client Negotiations, Contract Management,</li><li>Document Review, Legal agreements, Statement of Work (SOW),</li><li>Master Service Agreement (MSA).,</li><li>Experience into ‘Legal &amp; Contract Management’ for U.S. process &amp; Hands on, Vendor contracts, Contract Management , Client Contracts.</li><li>Negotiating with tire one IT companies and different vendors of manpower solution.</li><li>Maintaining client contract database and experience of using CLM tools, Draft review, and negotiate Non-Compete/Non-Disclosure/Master Service agreements and contracts from Client and Vendors in compliance with the Company’s policies.</li><li>Setting up basic legal processes and systems to manage all legal documents relevant to the company from time to time.</li><li>Co-coordinating, with external lawyers of the company, various contractors, vendors etc., to negotiate and solve different legal and operational issues.</li><li>Handling all domestic legal issues for the organization.</li><li>Handle the Contractual Issues and negotiate via emails or phone call with Vendors and Clients.</li><li>Provide status updates of contract negotiations to the Management.</li></ul> Experience: 4+ years Share your resume now.

Miracle Software Systems India Pvt Ltd

Legal Advisor

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”

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Legal & Regulatory Jobs - 323 Verified Vacancies

Manager - Projects

Collections Executive

Collections Executive

Collections Executive

Corporate Controller

Vendor Compliance executive

Chemical Analyst

Chemical Analyst

Chemical Analyst

Article Assistant

Collections Executive

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Legal Officer

Collections Executive

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