321 Injectables Jobs - Page 12

Job Overview: The PDL Scientist - Injectable will be responsible for the development, optimization, and scale-up of sterile injectable formulations and manufacturing processes. The role demands expertise in injectable formulation science, process engineering, and compliance with regulatory and quality standards. Role & responsibilities Formulation Development: Design and optimize sterile injectable formulations, including solutions, emulsions, and suspensions. Perform compatibility and stability studies of active pharmaceutical ingredients (APIs) with excipients. Process Optimization: Develop robust, scalable manufacturing processes for injectable formulations. Define and optimize critical process parameters (CPP) and quality attributes (CQA). Sterility Assurance: Establish aseptic processes and ensure compliance with sterility requirements. Perform filtration studies, autoclave cycle development, and validation. Analytical Support: Collaborate with the analytical team for the development and validation of testing methods. Conduct particle size analysis, pH, and osmolarity evaluations, and other critical tests. Regulatory Compliance and Documentation: Prepare technical reports, batch records, and regulatory submissions in compliance with GMP, ICH, and FDA guidelines. Support regulatory inspections and audits with comprehensive process documentation. Technology Transfer: Facilitate the transfer of processes from lab-scale to manufacturing-scale environments. Work closely with cross-functional teams, including production, quality assurance, and regulatory affairs. Preferred candidate profile 3 - 5 years of experience in injectable formulation and process development. Hands-on experience with lyophilization, sterilization techniques, and aseptic manufacturing processes. Strong knowledge of GMP, ICH, and regulatory guidelines. Proficiency in using laboratory equipment such as autoclaves, lyophilizes, and HPLC systems. Excellent technical writing and documentation skills.

Role & responsibilities To meet the production schedule both in quality and quantity. To maintain good discipline in the Packaging area and department. To ensure the implementation of EHS practices during the work To plan the activities of the area as per daily basis schedule To plan & allocate different jobs on daily basis to workmen/ machine operators of Packing area. To check and verify the transfer of Packing Material to the finished goods store in coordination with Section Manager - Production. To ensure implementation of Good Packaging Practices and SOP during work. To maintain and improve quality of the products as per standards. To ensure the effective control on usage of men, machine and material in the department. To participate and co-ordinate various ongoing validation activities of equipment and system. To supervise the Packing activities under the supervision of Packing Manager. To ensure training completion of all employees working in packing area activities. To conduct investigation of OOS, monitor CAPA and handle deviations. To ensure instruction of validation protocols, change controls, deviations, SOPs and specifications relating to packaging and ensure their strict implementations.. To maintain department and equipment in neat and tidy condition all the time. To control the rejection during packaging operations. To do counselling and grievance handling of the subordinates. To review the BPR after its completion. To perform any other related work allotted by the superior as per the production requirement. To work for the control of wastages during Packaging and to achieve higher yields of product. To perform all the trackwise and SAP related work. Any other responsibility to be completed that may be assigned for time to time. To perform investigation for Market Complaint and Deviations & handling of change controls. Completion of all the record work on daily basis.

WALK-IN INTERVIEW FOR EXPERIENCED PROFESSIONALS Job Location: Hyderabad Experience: 2 to 10 Years Qualification: ITI / Diploma / B.Sc / B.Pharmacy / M.Sc Designations: Operator Sr. Operator Jr. Executive Executive Sr. Executive Openings in the Following Areas: 1. Drug Substance (Bioprocess) Roles & Responsibilities: Upstream Process: Cell Culture Fermentation Autoclave Operation Downstream Process: Virus Culture Centrifugation Tangential Flow Filtration (TFF) Purification Chromatography 2. Drug Product (Formulation & Filling) Roles & Responsibilities: Formulation Activities Filling (Vials, BFS, PFS) Operating Equipment in: Closed RABS (C-RABS) Open RABS (O-RABS) Isolators Sealing and Capping Vial Washing & Autoclaving 3. Packing & Visual Inspection Roles & Responsibilities: Primary and Secondary Packing Operations Handling Track and Trace Systems Operating Labeling and Cartonator machine Documentation & SAP Entries Visual Inspection of Vials & Pre-Filled Syringes (PFS) Note: Candidates with relevant experience in regulatory and compliance environments (USFDA, EU GMP, etc.) will be preferred. Please bring: Updated resume, latest salary slips, passport-size photo, and original certificates.

JD for Deputy General Manager-International Business Location : Dappar (near Chandigarh/Panchkula) Qualification : Candidate with MBA in Marketing/International Business will be preferred. Experience : 8 -15 Years in Pharma Industry. Reporting to : President-International Business. Role & Responsibilities: Job description: 1. To be responsible for marketing, sales, and distribution in the international markets. 2. To act as a first point of contact of the company in the assigned market. 3. To generate business by maintaining good relations with current distributors & appointing new distributors for increasing business & sales. To develop new markets. 4. Support existing distributors in commercialization, marketing, promotion, registrations. 5. Responsible for Tender Business. 6. Exp. in international sales/marketing in pharma industry is must. Candidate Profile: 1. Should have working exposure in the International market in B2B domain. 2. Should have worked for Injectables product line in the past. 3. Ready to relocate. 4. Minimum experience of 8+ years in pharmaceutical sales/business development in international markets for injectable products. Travel Requirements : Overseas travelling will be required as per need basis. The candidate has to remain open for travelling to meet the clients, coordination and support services.

JOB OPENING FOR INJECTABLES QC CHEMICAL 1. Experience: 6 to 7 years Education: M.Sc/B.Sc/M.Pharma Job Description: 1. Well versed knowledge of QC software (Chromeleon, Labsolution, Taimo etc). 2. Knowledge of QC documentation 3. Knowledge of analytical data review. 2. Experience: 3 to 5 years Education: M.Sc/B.Sc/M.Pharma Job Description: 1. Knowledge of laboratory instrument handling such as HPLC, GC, Autotitrator, UV, FTIR etc. 2. Well versed knowledge of GLP, GDP & Data Integrity PRODUCTION INJECTABLES 1. Lyo-Operator/ Officer Experience: 3 to 5 years Education: B.Pharma//M.Pharma Job Description: 1. Knowledge of Lyophilizer operation & troubleshooting 2. Handling of Automatic loading & unloading system 2. Aseptic Area Operator/Officer Experience: 3 to 5 years Education: B.Pharma//M.Pharma Job Description : 1. Knowledge of media fill & dry powder filing machine operation 2. Knowledge of aseptic area operation QC MICRO Experience: 3 to 5 years Education: B.Pharma//M.Pharma Job Description : 1. Preparation of trend data for water analysis & environment monitoring program. 2.Responsible for performing MLT of Water, Raw material and Bioburden Test of in process sample. 3.BET testing of finished products, raw material and stability sample. 4.Sterility Testing of finished products, raw material and stability sample. If interested, share your updated CV along with the below mentioned details on mail id: preeti.yadav@brookssteriscience.com 1. Current Organization 2. Total Experience: 3. Current Designation: 4. Current CTC: 5. Expected CTC: 6. Notice Period: 7. Availability for Interview: With Regards Team-HRA

Regional Head – Operations Job type : Full time Reporting Manager : India Operations Director / Account Director No of staff managed : 200 Job profile Qualification Bachelor’s Degree / Master Degree Industry Type FM Services, Hotels, Projects, Overall Experience : 12 -14 years Industry Experience 10-12 years of relevant / equivalent experience Technical Skills Building Services Generic Skills Leadership, Communication, Vendor/people management, Strategies Behaviors Team work, Learning attitude, Innovation mindset Job Aim: To take complete ownership for all client deliverables for all the facilities in the city. The person will be responsible to provide comprehensive facility management services, as per the contractual terms with a focus on continuous improvement for the respective facilities. Will also be responsible to achieve financial and other Key Performance Indicators ( KPIs) established by the Client. The Regional Head must be a team player and work with other functions within JLL and also the client stakeholders to achieve outcomes. Competencies Interpersonal skills with a strong client focus. Team Leader with line management skills and the ability to delegate Client /Supplier relationship management Technical comprehension and experience with performance based service contracts and vendor management Knowledge of occupational safety requirements Strong budget management and financial analysis skills Excellent written and oral communication skills. Strong analytical skills. Responsibilities Operations delivery Overall service delivery of the region KPI / Compliance Scores and management Manage escalations with closure in a timely manner People Management Ensure right expectation setting for the team, ability to maximise performance of the team. Training for the team Growth Plan for the team Employee assessment, identify shortcomings and plan development Technology Ensure optimum utilization of all technology tools that are implemented from time to time. Innovation/ Initiative Keep a track and updates on Energy savings project for the region. Focus / Thrust on improvements/ initiatives Financial Acumen Keep a track one Office services / R&M /Capex Budgets /work closure Understanding of the facility / City spend Track FM Operational Expenses CRM / SRM Client/employee engagement, Leadership connects Service partner’s engagement Vendor management Vendor engagement /Identification and evaluation on larger aspects Expansion/Go live Overall planning / Cost proposal & approval Approval/transition/Go live Ensure/oversee closure on project snag BCP /Risk management Oversee, assess risk, plan and handle any BCP situation. Certification/Internal Audit Ensure/oversee preparation end to end for all audits Business Reviews Responsible for Quarterly Business Reviews Publish timely and relevant reports for client and senior management Location On-site –Bengaluru, KA Scheduled Weekly Hours: 40 If this job description resonates with you, we encourage you to apply even if you don’t meet all of the requirements. We’re interested in getting to know you and what you bring to the table! JLL Privacy Notice Jones Lang LaSalle (JLL), together with its subsidiaries and affiliates, is a leading global provider of real estate and investment management services. We take our responsibility to protect the personal information provided to us seriously. Generally the personal information we collect from you are for the purposes of processing in connection with JLL’s recruitment process. We endeavour to keep your personal information secure with appropriate level of security and keep for as long as we need it for legitimate business or legal reasons. We will then delete it safely and securely. Candidate Privacy Statement . For candidates in the United States, please see a full copy of our Equal Employment Opportunity and Affirmative Action policy here. Jones Lang LaSalle (“JLL”) is an Equal Opportunity Employer and is committed to working with and providing reasonable accommodations to individuals with disabilities. If you need a reasonable accommodation because of a disability for any part of the employment process – including the online application and/or overall selection process – you may contact us at Accommodation Requests . This email is only to request an accommodation. Please direct any other general recruiting inquiries to our Contact Us page I want to work for JLL.

Role & responsibilities Keen Knowledge on Regulatory guidelines for finished product registration. Dossier compilation as per guidelines. Compilation and review the product dossiers for submission in CTD, ACTD . Gap analysis of the dossier and addressing the gaps before submission to MOH. Handling the customer and MOH queries . Life cycle management of the product. Development report, scale up report , specification, COA, stability protocol and Process validation protocol. Documents review (Specification, STP, Analytical method validations, Development report and validation reports, BMR, BPR, PVP/R and stability). Post approval experience to file the applicable variations timely. Knowledge on EAEU, ICH and EMEA guidelines. Re-registration (Renewal) procedures. Administrative documents requirements (COPP, Mfg. License and Import License) . Registration information management system updates on regular basis.

Desired Experience : 3-7 years Job Location : Genome Valley, Shameerpet, Hyderabad Preferred Industry : Vaccines / Biotech Designation: Deputy Manager/ Assistant Manager/ Senior Executive/ Executive Qualification: M. Pharmacy/ M. Sc/ B. Pharmacy Main purpose of the Job: Responsible for Preparation of Regulatory Documents for submission to Indian NRA, WHO and other Regulatory Authorities. Job Responsibilities: 1. Preparation of following Regulatory Submission Packages related to NRA submissions but not limited to. a. Application for Post Approval Change(s) b. Marketing Authorization Applications c. Clinical trial applications d. Support the submission of Import licenses/ export NoC e. Support the preparation, review and submission of applications/ response to RCGM vide IBSC f. Support in handling of SUGAM, IBKP, NSWS & ONDLS/ ODLS sites 2. Assisting in Responding Queries to various regulatory authorities. 3. Preparation of dossiers / submission packages for NRA submissions. 4. Preparation of dossiers for registration in ROW countries. 5. Maintenance of Documentation Data base available with RA. 6. Coordination with cross functional departments like QA, QC, Production, Warehouse, Distribution and Marketing. 7. Routine Interaction with QA-documentation for updating Master Files. 8. Review of Pack Profiles. 9. Review of Artworks (Labels and Package Insert). 10. Preparation / compilation of technical documents related to tenders / queries. 11. Arranging Samples required for registration. 12. Any other support required by the other members of RA. Interested Candidates having relevant experience can send in their CVs to HR.Intern4@biologicale.com by mention the subject as Applying for Department Name

"Hiring Event Announcement" MFG Production Operators (ITI): 3 to 8 Experience in Injectable production, filling, dispensing, sterilization, autoclave, batch record review etc., activity MFG Packing Operators ( ITI): 3 to 8 Experience in Injectable packing activity. Date & Time : 31st May 2025 || 09 AM to 3 PM IST Venue : Ahmedabad (Invites will be shared based on your shortlisting) Registration Link copy : https://talentcommunity.baxter.com/flows/manufacturing-packing-operators-31st-may-25-gqengvlfs EEO (Equal Employment Opportunity) This is where Baxter International Inc. is an equal opportunity employer. Baxter evaluates qualified applicants without regard to race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, protected veteran status, disability/handicap status, or any other legally protected characteristic.

Role & responsibilities Experience: 9-14 years Specialization: Injectable Drug Formulation & Development Key Responsibilities: 1. Formulation Development: Lead the design and optimization of injectable drug formulations, ensuring stability, efficacy, and manufacturability. 2. Pre-Formulation Studies: Conduct compatibility assessments, stability testing, and excipient selection to enhance product quality. 3. Scale-Up & Technology Transfer: Oversee successful scale-up from lab-scale development to pilot and commercial manufacturing, ensuring reproducibility. 4. Sterile Manufacturing Expertise: Manage aspects of sterile formulation processes, including aseptic techniques, lyophilization, and parenteral drug delivery innovations. 5. Regulatory Documentation: Prepare and review CMC documentation for regulatory submissions, ensuring alignment with global health authority requirements (FDA, EMA, etc.). 6. Process Development & Optimization: Implement Quality by Design (QbD) and Design of Experiments (DoE) principles to refine injectable formulation strategies. 7. Cross-Functional Collaboration: Work closely with analytical, manufacturing, and regulatory teams to ensure seamless product development. 8. Troubleshooting & Problem-Solving: Address formulation challenges related to stability, compatibility, and manufacturing scale-up. 9. Innovation in Drug Delivery: Explore novel injectable delivery mechanisms, including depot injections, nanoparticle-based formulations, and biopharmaceuticals. 10. Leadership & Mentorship: Guide junior scientists, fostering innovation and technical excellence in formulation research. Qualifications: PhD/Masters in Pharmaceutical Sciences Extensive experience in sterile injectable formulation development with a strong track record of successful product launches. Expertise in aseptic processing, lyophilization, and excipient compatibility for injectables. Strong knowledge of scale-up processes, technology transfer, and industrial manufacturing practices. Proven ability to develop and optimize parenteral drug formulations, ensuring quality and regulatory compliance. Experience with regulatory pathways, and ANDA submissions. Understanding of bio pharmaceutical characterization for injectable products. Preferred candidate profile Candidate with exp of Pre-Formulation Studies and research Candidate with experience of successful scale-up from lab-scale development to pilot and commercial manufacturing, ensuring reproducibility candidate with Sterile Manufacturing Expertise. candidate with experience in Innovation in Drug Delivery: novel injectable delivery mechanisms, including depot injections, nanoparticle-based formulations, and biopharmaceuticals.

MS Dynamics prefer, and generic Testing skills CRM will be good to have Ensure successful test case execution maintaining the organizations quality standards Maintain work allocation and reporting structure Maintain document repository of all test results and project level changes Maintain workplace discipline and adhere to organization standards Provide status updates on daily, weekly, monthly basis to test manager and Project Manager

Roles & Responsibilities You will be responsible for end to end Formulation development of Injectable including development, execution, filing and approval. You will be responsible to co-ordinate closely with analytical team to devise effective Proof of Concept (POC) for developing generic equivalent of Reference Listed Drug (RLD)/generic Injections. You will be responsible to support in scale-up to pilot/plant scales for Injectable Products. You will be responsible to monitor the development for robust, effective and bioequivalent drug product in timely manner adhering to safety and quality standards. Also provide support in documentation for regulatory submissions. You will be responsible for technology transfer and execution of the batches. You will be responsible for performing pre-formulation studies for material characterization, drug-excipient compatibility and Reference Listed Drug (RLD) characterization (including reverse engineering, formulation designing and optimization, processes designing and scale up). You will be responsible for preparation of risk evaluation and risk mitigation documents, Scale-up batch documents, and filing documents for drug product at every stage of development. You will be responsible to review data generated and participate in discussions with experts to conclude on prototype(s). Participate in strategizing the sourcing of Active Pharmaceutical Ingredient (API), raw materials and ensure development studies are performed related to regulatory and internal system requirements. You will be responsible for designing and implementing stability studies for injectable formulations to ensure product quality and shelf life. You will be accountable for troubleshooting formulation and process-related issues during development and manufacturing stages. You will collaborate with cross-functional teams to ensure alignment of formulation development with regulatory requirements and commercial objectives. You will be responsible for staying current with emerging technologies and regulatory guidelines in injectable drug development and incorporating them into your work. You will mentor junior scientists and contribute to the continuous improvement of the formulation development process. Qualification Educational qualification: Masters in Pharmaceutical/M.Tech in Chemical Engineering Minimum work experience: 5 to 8 years of experience in pharmaceutical company in Injectable products. Skills & attributes: Technical Skills Have work experience on Formulation Development and expertise in inhalation/injectable dosage form. Experience in areas of product development for Generic Injectable Experience in Quality by Design (QbD). Experience in Process Optimization and scale up. Experience in Operational Excellence. Knowledge on Good Manufacturing Practice and Good Laboratory Practice. Experience in Technology Transfer. Behavioral Skills Excellent communication and interpersonal skills. Strong analytical and problem-solving abilities. Ability to work collaboratively with own team and cross-functional teams. Additional Information About the Department Integrated Product Development Organisation We integrate our deep science capabilities and cutting-edge technology to develop innovative, accessible and affordable therapies for patients worldwide. We are a science-driven, innovation-focused pharmaceutical company committed to accelerating access to healthcare solutions to patients around the world. We have End to end capabilities in API, Formulations, Clinical, Intellectual Property and Regulatory Affairs. We are serving 55+ markets including USA, Canada, Europe, China, LATAM, ASEAN and all Emerging Markets with innovative and generic products ranging from Active pharmaceutical ingredients (API), Oral formulations, Parenteral (Injectables, Opthalmics) & Other dosages Our product development efforts drive a portfolio of more than 1,000 products Enabled by our robust R&D team consisting of more 200 scientists and functional experts and more than 150 doctorates, we have filed 1,071 patents and also published over 1,000 papers for peer review over the years. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/

Dear Candidates, Greetings from KEYBIZ DASHBOARDS, We are looking for Production Executive & operators injectables for one of our reputed pharmaceutical client, based at Hyderabad & Vizag location. Please find below openings list. 1. Vial Washing 2. Filling 3. Compounding 4. Lyophilization 5. Autoclave 6. Sealing 7. Monitoring of aseptic area / Environmental \ Media Fill \ Lyophilization operation The above positions we are looking for Hyderabad & Vizag locations, interested please share us updated cv to krishna_veni@mydashboards.in Thanks and Regards Krishnaveni - Dashboards Team HR

Walk-in-Interview Biological E. Limited invites experienced, dynamic, and self-motivated professionals with 2 to 10 years of experience to apply for the following positions in its Vaccine and Pharma SGI businesses, located in Shamirpet, Hyderabad. Production (Injectables): Designation: Sr. Executive/ Executive/Sr. Officer/Officer Qualification: M Pharmacy/ B Pharmacy/ M Sc/ Diploma / B. Sc. Job role: Experience in Manufacturing, Compounding, filtration, Filling, Washing, Lyophilization, Sealing, Pre & Post Manufacturing activities. Isolators experience will be preferable. QA - In Process Quality Assurance (IPQA): Designation: Dy. Manager/Asst. Manager/Sr. Executive/Executive Qualification: M. Pharmacy/ B. Pharmacy/ M.Sc. (Lifesciences) / B. Tech/M. Tech (Biotechnology) Job Roles: Drug Product: To execute Fill-Finish activities. review of SOPs, batch records, validations and media fills; line clearance for filling operations; change controls, deviations, OOS investigations, and trend analysis. Drug Substance: To execute activities for Bulk Viral Antigen production, line clearance, dispensing. review and approval of batch records, SOPs, PV, CV, and APS documents; QMS management; trending and batch release activities; control and reconciliation of Master and Working Cell Banks. Quality Assurance (Validation): Designation: Sr.Executive/Executive Qualification: M. Pharmacy/ B. Pharmacy/ M.Sc. / B. Tech Job Roles: Experience in Preparation and review and Execution of Qualification/Validation protocols and reports for its compliance, Responsible for review of Engineering related Preventive maintenance schedules, Calibration schedules, Calibration certificates, Validation protocols and log books. Quality Control (Biologics/Vaccines): Designation: Asst. Manager/Sr. Executive/Executive Qualification: M.Sc. (Lifesciences) / B. Tech/M. Tech (Biotechnology) Job Roles: Biochemical Assays: - Estimation of components in polysaccharides, along with biochemical analyses such as protein, nucleic acid, aluminium content, and composition analysis. Analytical method validation, adherence to ALCOA principles,OOS and OOT investigations. Instrumentation Testing: - Analytical instruments such as HPLC and IC, along with performing instrument-based assays including molecular size, aggregates, purity, and composition analysis. Basic troubleshooting, 21 CFR Part 11 and Audit trial review practices, ALCOA principles, OOS, OOT systems and investigations. Virology: Experience in in-vitro viral testing of Starting material, Raw material, In-process, Final bulk, Final lot and Stability samples for Viral vaccines. review testing for QC release of products/RM/stability studies of Viral Vaccines/New projects/Products. Interested candidates may walk-in with an updated CV, latest increment letter and the last 3 months payslips on 25th May, 2025 i.e., Sunday from 09:30 am to 03:00 pm at Hotel Vivanta, 147, 53, SG Highway, opposite Bhagwat Vidhya Peeth, Sola, Ahmedabad, Gujarat - 380061. PS: Candidates who are unable to walk-in may send in their CVs by mention subject as Applying for Department Name to careers@biologicale.com . If an individual has already attended the interview in the past 6 months or has already been offered a position with us, please do not share the profiles. - Human Resources

Hiring for multiple sub-functions of engineering department. Candidate should have worked for sterile formulations company of pharmaceutical industry

Biological E. Limited invites dynamic & self-motivated fresher candidates for Production department at its Pharma SGI - Injectables USFDA Approved plant, Shamirpet, Hyderabad: Desired Candidate Requirements: Good communication skills Able to work in shift operations (A,B & C) B.Sc & Diploma passed in 2024 & 2025 with > 60% marks Learning apatite Confidence Prepared male candidates

Greetings! We are looking for Formulation Research & Development Scientist - Injectables for a leading Pharmaceutical company based at Chennai location. Interested Candidates Kindly share your updated cv to srinidhi@bvrpc.com

Role & responsibilities > Should have experience on injectables process maintenance. > Preventive maintenance and breakdown maintenance on Vial Filling, Tunnel, Vial Washing, Lyophillizer, Autoclave, Capping. > Must be from Injectable plant.

Basic Section No. Of Openings 1 External Title Tele Collections Lead - Cards & PL Employment Type Permanent Employment Category Field Closing Date 06 Jun 2025 Organisational Entity Equitas Small Finance Bank Business Unit Assets Division/Function (SBU) Credit Cards Department Receivables Sub-Department Receivables Generic Role Unit Manager External Title (Job Role) Tele Collections Lead - Cards & PL Division Credit Cards Zone South State Tamil Nadu Region Tamil Nadu Area Chennai Cluster Chennai PT Location Chennai Branch Code 9999 Branch Name Head Office Skills Skill Sales Highest Education Bachelor of Science Working Language English Urdu About The Role Lead and manage a team of collection agents. Set and monitor performance targets for the team. Provide training, support, and guidance to team members. Ensure compliance with company policies and regulatory requirements. Handle escalated customer issues and resolve in a timely manner. Analyze collection data to identify areas for improvement. Develop and implement strategies to improve collection efficiency. Prepare and present regular reports on team performance.

Basic Section No. Of Openings 1 External Title Area Risk Manager Employment Type Permanent Employment Category Field Closing Date 06 Jun 2025 Organisational Entity Equitas Small Finance Bank Business Unit Assets Division/Function (SBU) Risk Containment Unit Department RCU - IB Sub-Department RCU - IB Generic Role Area Risk Manager External Title (Job Role) Area Risk Manager Division Risk Containment Unit Zone North State Rajasthan Region Rajasthan Area Jodhpur Cluster Jodhpur PT Location RAJASTHAN Branch Code 16052 Branch Name Jodhpur Skills Skill Post-conflict Highest Education Other Qualification Type Working Language Hindi English About The Role Area Risk Manager Area Risk Manager Area Risk Manager Area Risk Manager Area Risk Manager Area Risk Manager Area Risk Manager Area Risk Manager Area Risk Manager

Basic Section No. Of Openings 1 External Title Cluster Manager - MF Employment Type Permanent Employment Category Field Closing Date 13 Jun 2025 Organisational Entity Equitas Small Finance Bank Business Unit Assets Division/Function (SBU) Inclusive Banking - MF Department Micro Finance Sub-Department Business Generic Role Cluster Manager External Title (Job Role) Cluster Manager - MF Division Inclusive Banking - MF Zone West State Maharashtra Region Pune Area Kolhapur Cluster Datta Nagar PT Location Maharashtra Branch Code 9064 Branch Name Datta Nagar Skills Skill Sales Highest Education Bachelor of Arts Working Language Marathi About The Role anage the Branch in terms of achieving defined member target for the branch , Branch operations and administration. 2.Build a high Quality Loan portfolio 3.Track and Ensure Repayments of the Loan disbursed 4. Maintain Manage Acquit ion of micro finance member and collection of the branch 5.Enable sales team to high performance and be a team player 6.To Build and Nurture team & enable them to achieve high performance as per the branch capacity & budget. 7. Manage Administrative smooth functioning of the branch 8. Conversion of Micro finance eligible member to enroll recurring deposit of the bank 9.Lead generation for existing micro finance members who require MICRO LAP or MICRO Housing 10. Ensure consistent delivery of Equitas products and services and prompt repayment in an efficient and cost effective mann

Basic Section No. Of Openings 1 External Title Sales Manager Employment Type Permanent Employment Category Field Closing Date 28 May 2025 Organisational Entity Equitas Small Finance Bank Business Unit Small & Medium Enterprises Banking Division/Function (SBU) Sales Department Sales Sub-Department Sales Generic Role Sales Manager External Title (Job Role) Sales Manager Division Sales Zone West State Maharashtra Region Maharashtra Area Nashik Cluster Nashik PT Location Maharashtra Branch Code 9087 Branch Name Nashik II Skills Skill Highest Education No data available Working Language No data available About The Role To achieve the allocated Business Targets in DisbursementMaintain portfolio qualityPortfolio Pendencies at a minimum i.e for post disbursement 1. Non submission of stock (where applicable 2. Non Submission of applicable insurance 3. Closure of Bank account 4. Perfection of Security

Basic Section No. Of Openings 1 External Title Territory Risk Manager Employment Type Permanent Employment Category Field Closing Date 30 May 2025 Organisational Entity Equitas Small Finance Bank Business Unit Assets Division/Function (SBU) Risk Containment Unit Department RCU - EEB Sub-Department RCU - EEB Generic Role Territory Risk Manager External Title (Job Role) Territory Risk Manager Division Risk Containment Unit Zone North State Haryana Region Haryana Area Haryana Cluster Haryana PT Location Haryana Branch Code 11009 Branch Name Hisar Skills Skill Highest Education Bachelor of Arts Working Language English About The Role SNO.OBJECTIVE1Field Visits as per FCU plan and effective implementation, tracking and monitoring2Number of incident reports raised3Identify internal Business process gaps4Quality and Effectiveness of assigned task5Team Management6Training Development7Completing the investigation for all incident within defined timelines.8Bench marking best industry risk practices9Collaboration

Injectables Manufacturing Officer

Handling and set up for new laboratory project management which includes maintaining a safe and well-equipped laboratory environment that meets regulatory requirements. Procurement of new equipment or instrument from reputable manufacturers who meet regulatory standards along with validation and calibration certificates. Must be a technical expertise in selection and handling of new equipment procurement. Procurement of new potential vendors based on criteria regarding installation and qualifications of QC equipment including quality agreements. Ensuring compliance with relevant industry standards and regulations. Handling of IQ, OQ and PQ of the equipment in QC laboratory in a systematic framework to ensure compliance, reliability and efficacy. Relevant experience on Qualification documents i.e. IQ/OQ/PQ Protocols and summary reports for the new equipments/instruments. Familiarity with quality assurance methodologies (e.g., ISO standards, Good laboratory Practices) Relevant experience in procurement and handling of resources like chemicals, standards and materials. Efficiently organizing lab operations, managing schedules, and prioritizing tasks are essential for maintaining a smooth workflow. Investigations and closing the change controls, Deviations, OOS, OOT, CAPA and incident reports etc. Candidate should have key skills including project management, budget management, communication, problem-solving, leadership, and the ability to ensure compliance and maintain quality. Candidate should have interpersonal and soft skills regarding a team work. Effective communication is essential for interacting with internal teams (researchers, engineers, etc.) and external suppliers. This includes strong written and verbal skills, as well as the ability to clearly articulate needs and negotiate effectively