We are hiring candidates who are having Experience in Compounding , Aseptic , Filling Walk in date : 09/05/2025 Experience : 2-5 Years in Injectable only Qualification : Operator : B.SC / Diploma Chemist : B. Pharma/ M. Pharma / M. Sc Preferred candidate profile Should have Experience in Injectable Production Department

Role & responsibilities Aspetic areas and compounding areas operations Autoclave and DHS operations handling Automatic filter integrity machine handling Sterile API Production Planning and Execution QMS activities handling - Change controls, deviations, CAPAs & investigations Validations protocols preparation and reports generation Adherence to GMP Compliances Regulatory audits handling experience Preferred candidate profile Experience in Sterile API Production operations and QMS activities Perks and benefits As per norms

Role & responsibilities Exp : 4 to 8 years (Environmental Monitoring, MLT, Media Preparation & QMS activities etc.,) Qualification : B.Sc (Microbiology/ Biotechnology /Biology), M.Sc (Microbiology/Biotechnology) Preferred candidate profile Responsible for sampling, testing and documentation of MLT samples of finished and stability samples. Responsible for Handling of Instruments like LAF/BOD incubators/Autoclave/colony counter /Microscope/pH meter /Air sampler and Vitek etc. Responsible for monitoring and review of daily printouts of instruments like incubators, Autoclaves, refrigerators, hot air ovens and deep freezers. Responsible for ensuring the destruction of used media plates/tubes, product plates/tubes, monitoring plates, GPT plates/tubes and IND plates/tubes. Responsible for ensuring the handling, calibration of Instruments like pH meter and top pan balance. Responsible for ensuring external calibration review of standard weights used in Microbiology laboratory. Responsible for ensuring the receipt, storage and handling of ATCC cultures/cryovials/bio balls. Responsible for Preparation of SOPs and ensure that complies in microbiology laboratory. Responsible for ensuring verification of instrument preventive maintenance schedules for incubators, autoclaves, LAFs, air samplers, hot air oven, refrigerator and deep freezer, Colony counter and Vitek. Responsible for MLT, BET Analysis & method validations, and other validation studies. Responsible for Perform and verify Environmental monitoring at sterile and non-sterile production blocks. Responsible for QMS activities OOS, OOL, Deviations and incidents. Responsible for Data integrity compliance. Responsible to follow and implement the applicable Environment Health and safety procedures, practices in the plant premises Perks and benefits As Per the company Norms

Production Role & responsibilities :- Line Chemist: Experience on compounding, aseptic operations and aseptic behaviors equipment trouble shooting and solution oriented. •Ensuring online documentation, CFT co-ordination, etc. Packing Role & responsibilities :- Line Chemist :- Experience on Labelling and Packaging operations as per cGMP norms. •Ensure that equipment, processes, line cleaning and line clearances are completed /operated within SOP requirements. •Efficiently manage materials are stored prior and after use, received at line and promptly transfer finished goods. Operators: Operate labelling machines & Auto-cartonator equipments efficiently to meet production targets and timelines. •Troubleshoot and resolve machine malfunctions to minimize downtime. Ensure proper storage and handling of labelling materials to prevent damage or contamination.

Role & responsibilities Utility Executive : 1. Responsible for Operation, Maintenance of Block Utilities & Central Utilities.. 2. Responsible for ordering, maintain stock of spares, consumables required for the machines & facility. 3. Responsible for implementation of Preventive Maintenance activities as per schedule. 4. Execution of Qualification documents. 5. Preparation of SOPs and reviewing of daily log sheets. 6. Responsible for Change Controls & Deviations. 7. Responsible for breakdown analysis &CAPA. 8. Responsible for Energy conservation in Utilities. 9. Responsible for up gradation in utility systems. 10. Responsible for minimising break downs & Improving efficiency of utility systems & equipments. Instrumentation Executive : 1.Responsible for Operation of Lyophilizers. 2. Responsible for Preventive Maintenance of Lyophilizers. 3. Responsible for history records & service cards. 4. Responsible for breakdowns of Lyophilizers. 5. Planning & execution of Anticancer block all lines instrumentation electronics activities. 6 .Execution of Qualification documents. 7. Packing hall machinery Instrumentation Preventive, Breakdown & Major activities maintenance 8. Responsible for Preventive maintenance and breakdown of utilities equipments. 9. Responsible for data backup activitys for computerized systems (Engineering scope). 10. Responsible for preparation and Execution of IQ, OQ & IOQ documents. 11. Responsible for preparation VMP Annexures.

Roles and Responsibilities: Expertise in Compounding, Aseptic Operations, and Equipment Troubleshooting with a focus on solution-oriented approaches. Dry Powder Filling/Autoclave Operators/ Vial Sealing/ Line Chemist/ Compounding Chemist. Vial Washing, Ampoules, PFS, Bag & Filling & Sealing Operators. ANDA Projects & QMS activities (FCR, DCR, BPCR Preparation, SOP Preparation & Track-wise related knowledge). Compounding and filtration of the product as per batch manufacturing records & ensuring the cleanliness of the compounding area, personal entry and material pass of the component area, and APA & online documentation.

Role & responsibilities Actively engage with multiple stakeholders in order to foster gathering of insights. Support implementation of Marketing-led initiatives including supporting and coordinating for appropriate campaign content, support for kick-off or cycle meeting and digital campaigns. Share in-field best practices and support field teams in their tactical execution for activities. Supporting marketing colleagues in development of Marketing materials and other marketing inputs. Providing the sales team with necessary technical expertise, promotional materials, product training, and relevant clinical papers Reviewing product data to keep the field force updated on new developments and competitor products Serving as the primary point of contact for all product-related inquiries Conducting market research to assess customer attitudes and guide new product introductions Developing annual marketing plans and controlling advertising, promotion, and sales aids Preparing product forecasts and monitoring inventory levels to ensure supply chain efficiency

Role & responsibilities Aspetic areas and compounding areas operations Autoclave and DHS operations handling Automatic filter integrity machine handling Sterile API Production Execution Adherence to GMP Compliances Regulatory audits handling experience Preferred candidate profile Experience in Sterile API Production operations and QMS activities Perks and benefits As per norms

Role & responsibilities Responsible for driving Business development for all ROW and Institutional tender business with end-to-end tender management responsibilities Identify collaboration opportunities, Analysing markets and appointing distributers in the assigned territory Tender Participation in UNICEF/PAHO/WHO/IDA and other institutional agencies Tender management- tender preparation / documentation accuracy / timely submission of EOIs, RFPs and RFQ’s. Coordination with Alliance Management/ Regulatory / IP/ production teams for supply and documentation related needs Stock planning and inventory management in co-ordination with internal teams Ensuring OTIF (on time in full) delivery and documentation accuracy for tenders. Market research / sales data analysis/ analysing various tender related data sets to understand market trends and identifying the new portfolio opportunities for the organisation. Participate in stakeholder engagement meetings and weekly BRM’s. Visit trade fairs and countries as and when necessary If you interested, please share your updated resume to jagadees.komiri@glandpharma.com

Quality Assurance B. Pharma / M. Sc / M. Pharma 2 to 5 Years Ensure implementation and compliance of site-wide Quality Management Systems (QMS) in line with regulatory and internal requirements. • Review and approve validation protocols/reports related to equipment, processes, cleaning & CSV. • Conduct Analytical Quality Assurance (AQA) review of laboratory documents and data. • Lead and support investigations for deviations, OOS, OOT, and other quality events. Ensure timely and effective CAPA implementation. Quality Control-Microbiology M. Sc 0 to 5 Years Routine microbiological testing and environmental monitoring to ensure compliance with regulatory standards and cGMP guidelines. Quality Control B. Pharma / M. Sc 0 to 5 Years Wet Analysis by using IR, UV, pH, etc. •Quality Control Documentation. IPQA M. Sc / B. Pharma / M. Pharma 2 to 4 Years Line clearances for the manufacturing of the drug product •In- process checks during compounding as per the instruction mentioned in the BPCR and confirmed to the specification, etc.

Role & responsibilities JOB SUMMARY In line with business strategy, develop and introduce new packaging solutions that satisfy the consumer, customer • Work closely with the cross-functional teams in order to effectively deliver new, fit for use packaging solutions to the business. • To support the Product Development and Process Managers throughout the launch procedure. KEY ACCOUNTIBILITIES % OF TIME Packaging Development Awareness of new briefs and critical path requirements. Assist with internal feasibility assessment. Provide packaging solutions for new products, range re-launches and range extensions/Alternate vendor developments. Generate and manage the packaging critical path in conjunction with the Development and Process Managers. Be involved in the appropriate phases to ensure the correct management of the packaging process as the product moves from Concept to Launch. Provision of all information in order for concept team to finalise product costings. Work with the Process team on pre-production runs, ensuring customer approval of packaging. Where appropriate conduct alternative supplier evaluation trials Follow risk management procedures. Review of transit trials with the process team Basic packaging specification management, including checking the quality of information. Ensure that all packaging for new products meets with customer and business expectations whilst adhering to legislative, quality, safety, and environmental standards. Ensure all packaging for new products achieves manufacturing performance by providing cost effective solutions. Management of packaging samples throughout the process for the new development products. Strongly influence and shape the customers perception of the company as a forward thinking innovator with regards to packaging. Proactively investigate innovative and new packaging solutions for new and existing product. Take the lead in developing and promoting new packaging innovation. Identify and visit new potential suppliers that can help us achieve our goals of excellence in packaging innovation. Sourcing and finalization of Primary packing materials for R&D and commercial in a regulated market. Knowledge of sourcing of Vials, stoppers, PFS, auto injectors, pens, bags, tubes and films, primary filters and secondary filters, ophthalmic 3-piece containers, Tubing for filling lines , seals, Labels, cartons aluminum pouches Vendor related documents to ensure the vendor qualification and their manufacturing facility audits. Business continuity plan/derisking plan for the complex development products. KEY ACCOUNTIBILITIES % OF TIME KSM/Raw material procurement/Advance intermediate/Chemicals . The person should have minimum understanding in procuring of the API related raw materials like : KSM/Raw material procurement/Advance intermediate/Chemicals. . should have understanding about regulatory requirement of KSM/Raw material procurement/Advance intermediate/Chemicals vendors to manufacturer an API and its regulatory filing requirements.

Role & responsibilities Utilities, Water System, HVAC Preferred candidate profile Education Qualification : Diploma Pass Out : 2022,2023,2024,2025only Note : Only fresher candidates are eligible for graduate apprentice. Candidates who is having PF and ESI are not eligible.

Role & responsibilities Sterile API Production Preferred candidate profile Experience in Sterile API Production operations and QMS activities Perks and benefits As per norms

Role & responsibilities Responsible for end-to-end Recruitment cycle. Handling On-boarding process and joining formalities. Responsible for maintaining hiring trackers, organization charts, and MIS reports. Taking initiatives and launching various Employee Engagement activities. Responsible for maintaining 100% compliance and statutory requirements w.r.t all the HR Processes & handling employee grievances. Preferred candidate profile

Role & responsibilities Responsible for driving Business development for all ROW and Institutional tender business with end-to-end tender management responsibilities Identify collaboration opportunities, Analysing markets and appointing distributers in the assigned territory Tender Participation in UNICEF/PAHO/WHO/IDA and other institutional agencies Tender management- tender preparation / documentation accuracy / timely submission of EOIs, RFP’s and RFQ’s. Coordination with Alliance Management/ Regulatory / IP/ production teams for supply and documentation related needs Stock planning and inventory management in co-ordination with internal teams Ensuring OTIF (on time in full) delivery and documentation accuracy for tenders. Market research / sales data analysis/ analysing various tender related data sets to understand market trends and identifying the new portfolio opportunities for the organisation. Participate in stakeholder engagement meetings and weekly BRM’s. Visit trade fairs and countries as and when necessary

Job description Role & responsibilities Aseptic Operators 1.Operation of filling machines, sealing machines, cRABs, VHP Generators, and GLT machines. 2.Unloading of sterilized items, assembling, VHP sterilization, filling, stoppering (partial/ full), filled vials loading into lyophilizer, unloading of lyophilized vials and sealing of full stoppered vials. 3.Cleaning, inspection, integrity testing & replacement of APA RABs gloves as per frequency mentioned in respective SOPs. 4.Participation in Disinfectant filtration, APA area cleaning and documentation. 5.Participation in filtration activities and integrity testing of filters. Compounding operator 1. CIP and SIP of mixing vessels and holding vessels. 2. Operation of steam sterilizers, Filter integrity Machine. 3. Pre activities for batch compounding like water collection, cooling, pH meter calibration, DO meter calibration, weighing balance calibration, and Load cell calibration of mixing vessels. 4. Compounding and filtration of the products as per batch manufacturing record. 5. Operation and cleaning of compounding cRABs, LAFs, weighing balances, DO meter, vessels and pH meter etc. Ensuring Cleanliness of Non APA. Preferred candidate profile Education Qualifications: Diploma B.Sc B.Pharmacy M.Sc M.Pharmacy Experience : 3 to 5 Years Only Injectable/Formulation Experience required Immediate Joiner will be preferable

1. Expected to Launch Products in Regulated Markets in a Timely Manner, in line with Regulatory Approvals & Commitments shared with Customers 2. Close co-ordination with Regulatory Team on project updates (Products under review/ Fling/ Ready for approval) for suitable project initiation & movement 3. Co-ordination with internal CFTs (R&D, RA, QA, QC, Production, SCM) for timely preparation & sharing necessary documents with customers. 4. Understand Customers’ Launch Requirements, including Launch & Forecast Volumes and arrive at the right Batch Size, post suitable discussion with BD & Customer 5. Pro-actively work on Material Procurement with CFTs based on regulatory filings & expected approvals . 6. Co-ordinate between Customer & Packaging Development for Timely Artwork completion & clearance for all Secondary Packing material procurement 7. Facilitate smooth Indenting / PR & P.O Follow-up/ Spec Verification/STP Check/ GRN Coordination/ Timely Testing & Release of the materials. 8. Sharing P.Os for Licence Application & follow-up for timely availability 9. Liaison with R&D / MS&T 10. Conduct & drive weekly TCs/Meetings with cross functional teams for updates & conflict resolution where necessary 11. Conduct Weekly TCs / Meetings with Customers and exchange updates via MoM 12. Co-ordinate with PPIC to secure Slots for production of Launch SKU Interested Candidates share profiles to saranya.ramesan@glandpharma.com