Job Details :Organisation: Zydus GroupWebsite: zyduslife.comAbout Us:Zydus is a global healthcare leader dedicated to innovation. We discover, manufacture, and market a wide range of healthcare therapies. With over 27,000 employees worldwide, including 1,400+ scientists, we are committed to creating healthier communities globally.Position: CSV - ITLocation: Goa & AhmedabadQualification: BCA / MCA /B.EExperience: 3+ yearsKey Responsibilities:Administer user management activities as per SOP.Manage user access (activation, reset, change, deactivation) 24/7.Review, configure, and manage Privilege Right Matrix.Create and update User Access Matrix.Provide and review access for service engineers.Update application-wise process steps for user management.Prepare and implement site SOPs, ensuring periodic updates.Review qualification protocols and participate in instrument/software qualification activities.Handle IT-related QMS activities (change control, deviation, CAPA, incidents, qualification documents, SOPs).Manage backup and restoration activities.Support software assessments, maintenance, and network issues.Ensure compliance during periodic reviews.Verify GLP and desktop policies periodically.Conduct risk-based network failure tests.Communicate IT roles to auditors and regulators.Engage with middle/senior management.Lead and manage a team effectively.

Role & responsibilities Drug Product (Filling-Officer/Executive)Experienced in handling of O-RABS, Operation of Vial washing/Filling/Lyophilizers/Autoclave/Process vessels. Bacterial vaccine manufacturing- (Upstream/Downstream)Experience in execution of upstream process & of Downstream purification operations

Role & responsibilities Manage employee life cycle activities such as recruitment, onboarding, Induction training.Inputs and Executing on engagement strategiesAssisting with Day-to-day HR ActivitiesSupport for employees documentation work Handle Employee Grievances to give the best solutionsPreferred candidate profile Fresher from Educational Background of MBA- HR / MHRM / MSW Excellent Communication skills .

Role & responsibilities Reporting to Senior Management for EHS functions & as Safety Officer for the Vaccine PlantLiasoning with GPCB for all Zydus Units of Ahmedabad, Implementation of Zero Landfill waste for all Formulation units of Zydus, Implementation of Zydus Water shed project by constructing Rain water harvesting structures in Villages Implementation of ISO 14001 & ISO 45001Operation & Maintenance of ETP, RO and MEE, Fire Hydrant system, Conducting Monthly Environment Monitoring, Maintaining inventory of chemicals and consumablesIssuing of Daily work permit system, Conducting mock drills & fire drills, Conduct workplace monitoringImpart EHS trainings to Employees and Workmen, Daily Tool Box talk, EHS Induction training to new joineesCelebration of various EHS campaigns like Road Safety week, National Safety Week, World Environment Day and Any other developmental task assigned by managementEmptying of Rain water from VTC, Disposal of excess rainwater to CETP, Sending Rain water pumps for repairingEnsure regular servicing of Fire extinguishers, Smoke Detectors, First aid boxes, Safety Showers, Refilling and Hydro testing of Fire extinguishers, Refilling and Hydro testing of SCBA set, Time to time replacement of wind sock, Ensuring availability of Safety signages in the area Ensure checking of Lifts and Hoists, Lifting tools and Pressure vessels as per defined frequency, Yearly checking of Centrifuge and Lifts as per Annexure XXExecution of Fire Alarm system projects, Installation of ETP, Technical review of Fire Hydrant systemResponsible for maintaining medicine stock at Main Gate for Employees, Coordinating & Sending Employees to Hospital in case of illness or injury, Preparation of manual PO for hospital services, Maintaining inventory of First Aid itemsRegular Disposal of Biomedical waste & Hazardous waste, Disposal of Spent Solvent by selling to registered recyclers, Disposal of Waste Corn cobPreparation of Capital & Revenue BudgetPreparing Purchase requisition for procuring EHS materials, Generation of material code for procurement of EHS materials, Clearing the invoices of service availedResponsible for uniformization of PPEs across Zydus Units, Responsible for preparation of SOP and harmonizing it across all Zydus UnitsConducting Monthly Plant EHS committee meetings, Monthly Plant Head EHS round, Monthly EHS risk assessment, Recording Minutes of Meeting of EHS meetings in Zysafe, Tracking Open EHS observation and CAPA in Zysafe with responsible persons, Submission of Monthly EHS Report to CEHS for Monthly EHS index, Tracking Open EHS observation and CAPA in Zysafe with responsible personsImplementation of Monthly Department Score card systemConducting Safety Audit at every two years, Conducting Fire adequacy study, Preparation and Updation of Site Legal registerPreferred candidate profile Candidate should have lead team of employeesCandidate must have professional Qualification for EHS.

Role & responsibilities Has Experience of Validation process .Experience of Process ValidationExperience of Cleaning Validation Hands on experience of Creating and reviewing Protocol for ValidationPreferred candidate profile Profile - Validation Total Experience - 3+ to 5 YrsQualification - Msc Chemistry

Role & responsibilities Operation and Maintenance of Chilled water plants.Operation and Maintenance of Chilled Brine plants.Operation and Maintenance of Natural gas fired boilerOperation and Maintenance of Nitrogen generation plantOperation and maintenance of Air compressors.Operation and maintenance of Air dryers.Operation and Maintenance of cooling towers.Potable water storage and distribution.Process water Operation, Generation, and distribution including schedule activities.Schedule Preventive maintenance of Utility equipment.To ensure efficient operation of Utility equipment.Efficiency monitoring and ensure for utility equipment.Preferred candidate profile Qualification - BE Mechaical Experience - 2 - 5 Yrs

Role & responsibilities Responsible for Regular Plan visits Should be keen with observation in plant visits to point out any observations .Preferred candidate profile Total Experience - 2+ to 5 YrsQualification - Msc Chemistry

Role & responsibilities Operate and maintain pharmaceutical manufacturing equipment.Monitor and control the production process to ensure quality.Maintain accurate production records and documentation.Adhere to GMP guidelines and safety protocols.Collaborate with team members to ensure efficient production.Preferred candidate profile D.PharmPerks and benefits TransportationCanteen

Profile - To review the documents and improve the same grammatically and technically. Qualifications:Bachelor's (B.Sc.) or Master's (M.Sc.) degree in a relevant field.Excellent English communication skills (reading, writing, comprehension).Attention to detail and ability to understand and convey the intent of documentation.Responsibilities:Prepare, review, and manage QA documentation.Ensure all documents are clear, concise, and accurately reflect the intended purpose.Collaborate with team members to maintain high standards of documentation quality.Requirements:Fresh graduates (2023 onwards) are welcome to apply.Strong command of the English language.Ability to work independently and as part of a team.

Designation : Fix Term Associate Role & responsibilities Recruitment & SelectionInduction & OnboardingTime Office ManagementPreferred candidate profile MSW/MLW/MBA fresher or Graduate with 1 to 3 years experience in HRPerks and benefits Transportation & Subsidised Canteen

Role Project Execution (Pharmaceutical Greenfield/Brownfield Projects)Designation - Below Manager (Deputy Manager/Associate Manager)Dept – Engineering Projects Reporting to – Team Lead Projects JOB RESPONSIBILITIESPerson should have Project execution skills for - Process eqp , HVAC, BMS execution validation Bachelor’s degree in engineering with excellent aptitude for pharmaceutical project execution work for production equipment. Incumbent should have hands on Regulatory guidelines such as USFDA, MHRA, ISO ASTM, BIS, ISPE, USP etc. Should have good working hands on MS office, Internet, SAP etc.JOB RESPONSIBILITIESResponsible for Timely Site Execution of Production Equipment along with Installation, Testing, Commissioning and hand over to user.Process Equipment documentation coordination with CFT team & Vendor.Provide support to CFT team for Process equipment DQ/IQ/OQ Execution.Analyzing, understanding project drawings.Estimate of quantity (BOQ) required at site for the planned work.Purchase request and co-ordination with SCM department to ensuring material availability. Technical discussion with vendors and cross functional team. Location at site for technical discussion with project team and advice/assist contractor’s project in charge also inspect work quality and progress at site.Intra Service coordination with CFT team.Preparing bar chart/schedule for work to be executed.FAT of Process Equipment & Compliance ;Co-ordination with local plant team for the work progress, documents for validation.Forward planning for manpower, material to ensure timely action. Ensure quality is as per requirement & agreed specifications.Actions/improvements in planning as per the site conditions.As built drawings after execution of project.Analyzing, understanding project drawings with respect to HVAC and BMS. Understanding of HVAC system for cleanroom application and comfort applications.Good understanding of Psychometric chart and Air properties.Understanding of Control logic/Philosophy of BMS System.Good troubleshooting experience related to HVAC and BMS.Site co-ordination with back office team, User, Consultants, Contractors and other concern agencies etc.Installation, testing and commissioning of HVAC Equipment, i.e. Chiller, Chilled water pumps, Cooling tower, Cooling water pumps, PRS, Hot water generator, Hot water pumps for HVACAir Handling units, Dehumidifiers, Air distribution duct, Ducting insulation, Chilled water and hot water piping, Manifolds, drain piping, Piping insulation, Terminal heating units HEPA Filters, electrical panel, VFDs, Fire dampers, DX Units etc.Installation, testing and commissioning of BMS system and field instruments, i.e. Operating software, I/O summary, DDC Panel, DPT, DPS, CAV/VAV, T&RH sensors and displays, Fire/Smoke sensor, Cable tray, Cabling (Power and control), BMS Screen development etc.Material receiving, loading/ unloading and proper storage of incoming material. Ensuring timely GRN from store and processing of bills.

Designation : Plant OperatorRole & responsibilities - Preventive maintenance of plant and utility equipment-Break down maintenance of plant and utility equipment-To provide back up power in case of power failure-Utility Maintenance-Pharmaceutical industry plant maintenancePreferred candidate profile Qualification : ITI/DiplomaExperience : 1 year to 5 yearsPerks and benefits Transportation & Canteen FacilityInterested candidate may share their resume to : yashpalgiri.v.gosai@zyduslife.comCompany Name : Zydus Animal Health & Investments Ltd. Plot No. 12/13, Pharmez, Matoda, Ahmedabad, Gujarat

Job responsibilities:To achieve market share objectives of the brands.To develop marketing plans.To enhance prescription base and prescriber base.Aligning strategies to divisional business plan for medium and long term.

Operate Manufacturing/Production Equipment: Efficiently operate ointment production machinery, including mixers, filling machines.Batch Preparation: Accurately measure and mix raw materials according to batch records and standard operating procedures (SOPs).Maintenance and Troubleshooting: Perform routine maintenance on equipment, troubleshoot issues, and coordinate with the maintenance team for repairs.Documentation: Maintain accurate production records, including batch records, logbooks, and other required documentation.Safety Compliance: Adhere to all safety protocols and guidelines to maintain a safe working environment.cGMP Adherence: Follow cGMP guidelines and SOPs to ensure the integrity and quality of the products.

Department : EngineeringRole & responsibilities -QMS-Trackwise management-Change Control-Deviation -CAPA-QualificationPreferred candidate profile Qualification : BE/BTechExperience : 4 to 8 Years in Pharmaceutical IndustryPerks and benefits Transportation and Canteen FacilityJob Location : Zydus Animal Health & Investments Ltd Pharmez, Matoda, Ahmedabad - Bavla Highway Ahmedabad, GujaratEmail Id : Yashpalgiri.v.gosai@zyduslife.com

Role & responsibilities : Good Communication and presentation skill.To ensure target achievement and growth.To improve performance of key focus brands and new products.implementation of company strategies.Good Team management.Building new business in the region.Preferred candidate profile : Candidates must be from Cardio- Diabetic segment Perks and benefits

Role & responsibilities:Responsible for all Deficiency management of US MarketSkill to compile & review ANDAs & their Deficiency responses.Experience of working on IND / 505(b)(2) / Innovations projects for US market.Good analytical and formulation understandings of various dosage forms. Sound knowledge of Regulatory Science and Regulatory Intelligence. Thorough understanding of US ANDAs / GDUFA / ICH guidance.To provide support to cross functional teams to ensure quality and timely submission of the NDA/ANDA/Def. responses.Preferred candidate profile :Must have experience of IRA US market more than 2 years.Critical thinking ability, problem solving skill, regulatory writing skill, and communication skills are very much desiredReady to work at Ahmedabad location. Work from Office only.

Role & responsibilities Preferred candidate profile 1. Responsible for the Change control Handling through Track wise related to Spec & STP & CAPA 2. Prepare the Specification & Standard testing procedure of API Site. 3. Review of Method of analysis (MOA), Specification, STP of RM, IM, PM, INP, API & Cleaning generated by R&D Analytical. 4. Review of Standard qualification COA. 5. Review of Method comparison & MOA with Pre-validation data 6. Review of Validation Protocol & validation Report with respect to analytical data and Journal. 7. Review of R&D batches Stability data. 8. Issuance, login and closing of Incidence and change control of DQA/R&D-synthesis/R&D-Analytical. 9. Issuance of format, Logbooks, BMR and uncontrolled copy of MOA and/or Spec & STP. 10. Document and data control i.e. Receiving, Issuance/Distribution, Archival, Control, Storage and destruction of documents. 11. Assigning analytical method validation protocol and Report Numbering. 12. Responsible for sample management activity (i.e. Receiving, Issuance and Discard)

Zydus Lifesciences Limited, formerly known as Cadila Healthcare Limited, is an Indian multinational pharmaceutical company headquartered in Ahmedabad, which is primarily engaged in the manufacture of generic drugsName Of the Company Zydus Life SciencesIndustry PharmaceuticalsWebsite of the company - https://www.zyduslife.com/zyduslife/Location Zydus Life Science . Position - Sr. Executive/Assistant Manager No. Of Working Day in Week : 6 DaysExperience Required Between 2-6 Years Of Experience Role- Contract Manufacturing Department EMO (External Manufacturing Operations)Job Description : We are seeking a Quality Specialist to manage quality-related activities at our Contract Manufacturing Organization (CMO) sites in Haridwar. The ideal candidate will have at least 10 years of experience in In-Process Quality Assurance (IPQA) and exposure to multiple dosage forms including Injectable, Oral Solid Dosage (OSD), Liquid Oral, and Topical formulations.Key Responsibilities:Oversee quality operations across 17 CMO sites.Ensure compliance with regulatory standards and company policies.Conduct routine quality checks and audits.Implement and monitor IPQA activities.Visit remote locations in Uttarakhand as required.

Role & responsibilities: B.Sc. Chemistry /Diploma Chemical Freshers or less than 10 months Experience 1-To ensure smooth operations with optimum efficiency in adherence to cGMP requirements.2-ensure the safest workplace and safety in every operation of the plant.3-Manage manpower and ensure efficient work from them4-Troubleshooting (within Plant to take problem ahead and channel for the solution) / Critical Decision Maker of Shift (for breakdown) Aspiring applicants should be:Basics such as1) Operational Skills (production / adopting new technologies / troubleshooting)2) Ability to handle documents pertaining to quality systems (as per cGMP requirements)3) Essential knowledge of safety during the manufacturing4) In-depth understanding and awareness of the current and changing compliance and regulatory requirements.If Intrested mail on Karishma.r.kadu@zyduslife.com or connect on 02646660560

Role & responsibilities Responsible for Preparation of Basic Design Package for detail Engineering and CAPEX Preparation for Civil related Capex Preparation of construction schedule with various contractors. Preparation estimating time and contract manpower strength at various stage of construction. Coordination with purchase and detail engineering for timely availability of material, drawing and any other information. Coordinate with Civil/structural/Architect for expedite the Engineering Drawing and review comment w.r.t. to GA drawing and site conditions. Checking of GA, and RCC/Steel drawings. Coordinate with Unit, local safety, security, personnel for smooth functioning Construction progress review with contractors and concerned engineer. Checking of quality of civil works & Bill checking.

The job requires review of documents related to DMF submission against predefined checklists and submission to various agencies globally. Should keep the all the regulatory database up to date. Candidate must possess do it right the first-time approach with proven track record. Assessment of change controls (QMS) with reference to regulatory impact as part of life cycle management to meet business requirement. Should keep knowledge up to date with regard to regulatory guidelines and requirements in all global regions as well as for new technical trends. Candidate should have good communication skills, email etiquettes. Should be energetic, determined to be successful, and able to deal with new or difficult situations easily.