ResponsibilitiesConduct routine environmental monitoring and assessments in various locations Collect, analyze, and interpret environmental data using specialized equipment and software Maintain accurate records and documentation of environmental conditions Communicate findings and recommendations to stakeholders and management Participate in environmental remediation and restoration projects Ensure compliance with environmental regulations and standards Growth promotion test, Media preparation, Autoclave operation, Cleaning and disinfectant preparation. Calibration of instruments. Qualification & ExperienceQualification: M.Sc (Microbiology) Experience: 2-7 years

ResponsibilitiesLead the team of Vial Line Responsible for preparation, review, revision, control and implementation of standard operating procedures. Responsible for preparation & review of the master documents. Responsible for preparation and review of Protocols and reports based on the requirements. Responsible for Document management like BMR’s, BPR’s, Master SOP’s etc. Responsible for the handling of Change Control, Deviations, CAPA, Investigation etc. Responsible for line clearance activity before commencing the operations like manufacturing, filling, capping & packing operatTo generate general purchase indent for departmental general items. Responsible for preparation of production planning on monthly and also daily as per the requirement and availability of material. To generate general purchase indent for departmental general items. Responsible to prepare daily production report as per the production achieved. Responsible to ensure that all equipment’s and lines are in validated and calibrated status. Responsible to follow cGMP, GDP and discipline in the department and to ensure that all employees follow the same. Responsible to give training to all the subordinates, technicians and operators of the department. Activities other than defined in the Job responsibility are to be done, as per the requirement of HOD, by following HOD’s instruction and guidance,, Responsible to attend the training as per training schedule and to ensure training as per16 Ensure the compliance & discipline on floor. Responsible to make shift schedule. Responsible to check that all the records and log books related to manufacturing, filling and sterilization of equipment’s.

Responsibilities Salesforce Administration Serve as the global administrator for the Salesforce platform, ensuring system stability, performance and security Manage users, roles, profiles, permission sets and access controls in line with governance policies Act as the primary point of contact for all Salesforce-related queries and issues Configuration & Development Design, build and maintain Salesforce configurations, including: Custom objects and fields Page layouts and Lightning record pages Validation rules and flows Workflow automation and business rules Deliver enhancements and new functionality in line with commercial priorities and the release cycle Stakeholder Partnership & Sales Enablement Work closely with Commercial teams to understand business processes and translate them into effective Salesforce solutions Improve sales force effectiveness through optimised pipelines, activity tracking and reporting Drive user adoption through usability improvements and regular engagement with stakeholders Data Quality, Governance & Reporting Define and maintain Salesforce data standards, validation rules and governance processes Proactively monitor and resolve data quality issues Support the creation and maintenance of reports and dashboards for commercial performance tracking Partner with Data teams to ensure Salesforce data is trusted and integrated into enterprise reporting platforms Integrations & Platform Ecosystem Collaborate with Data & Engineering teams to support integrations between Salesforce and other enterprise systems Ensure changes to Salesforce are aligned with downstream data models, analytics and data warehouse requirements Support testing and validation of integrations during releases and system updatesQualification & ExpeirneceRelevant degree (Mathematics, Economics, Business, Life Sciences, or related field) Minimum 3 years in a CRM Administrator role Proven hands-on experience as a Salesforce Administrator in a global or multi-region organisation Knowledge of the pharmaceutical industry and how it relates to CRM & Sales Force Effectiveness Experience working directly with commercial teams

Responsibilities Provides strategic and operational regulatory support to project management on new divestment projects, technical transfer, CMOs, quality assurance and commercial departments. Leads the preparation of core dossiers and submissions for global rollout. Authors, reviews, and approve M3 dossier sections, justification documents, and Product Information as necessary. In collaboration with global partners, consultancies, and distributors, we outline global regulatory intelligence and develop a global regulatory strategy. In collaboration with senior management and project strategy teams, develops and reviews global cross-functional regulatory strategies. Ensures diligent reporting and progress updates on regulatory workload at weekly/bi-weekly internal regulatory meeting. Negotiates and makes agreements on behalf of the department. Interprets applicable regulations and guidelines for the project team’s use. Keeps the project team abreast of regulatory decisions, evolving regulatory requirements, risks and mitigation plans. Serves as a primary contact to the local health authority (HA(s), local consultancies/ distributors and internal stakeholders, to ensure timely and accurate submissions. Facilitates communication between the HA(s) and the project team. Attends and generally leads agency meetings, if required. Coordinates and solicits components of the submission from various functional areas, distributors and CMOs. Proactively identifies project issues to the project team and supports mitigation plans. Attends cross-functional, vendor, and kick-off meetings as required. Mentors and/or manages other Regulatory Managers, Regulatory Associates and other junior-level or administrative Regulatory staff. Qualification & ExperienceBachelor’s degree in a scientific/health field. Required Skills Excellent IT skills across all MS packages, including Excel, Word, PowerPoint, Project, Outlook, and Teams. Experience in compliance and maintenance of product life cycle databases and RIM systems.

Qualification & Experience                        Qualification: B.Pharm / D.Pharm   Experience: Fresher's Can Also Apply                            Gender: Male / Female                     

Qualification & Expeirence Only MBBS candidates Minimum 2 years of relevant experience required

Qualification & ExperienceOnly MBBS candidates Minimum 2 years of relevant experience required

Qualification & ExperienceSection: Qualification & Validation (CV/PV) Experience: 5-7 Years Position: Executive Qualification: B.Pharm

Qualification & ExperienceSection: US/EU Market (Sterile) Experience: 4-8 Years - Position: Executive / Sr. Executive Qualification: M.Pharm

Qualification & ExperienceQualification - Diploma in CSSD Experience- 2 to 4 years