486 Injectables Jobs

We are seeking an experienced Plant/Site Head with expertise in Injectable manufacturing at the leading pharma formulation facility in Tada, Andhra Pradesh. The successful candidate will be responsible for overseeing the entire plant operation, ensuring adherence to industry standards, and driving operational excellence within a fast-paced environment. Key Responsibilities: Oversee daily plant operations, ensuring smooth functioning across production, quality, and supply chain. Manage and lead a multidisciplinary team, including production, quality control, maintenance, and other support functions. Ensure compliance with Good Manufacturing Practices (GMP), regulatory standards, and safety regulations. Drive process improvements to enhance efficiency, reduce costs, and improve product quality. Lead the implementation of strategic initiatives to meet production targets and ensure timely delivery. Collaborate with cross-functional teams, including R&D, to improve product formulations and production processes. Report and liaise with senior management regarding plant performance, operational challenges, and opportunities for growth. Manage budgets, resources, and facilities to ensure operational efficiency and cost-effectiveness. Qualifications: Educational Requirements: B.Pharm or M.Pharm Experience: Minimum 19 years of experience in the pharmaceutical industry , with Injectable manufacturing experience Skills and Competencies: In-depth knowledge of Injectable formulations and manufacturing processes. Strong leadership and team management skills, with the ability to inspire and develop teams. Experience in handling plant operations, including production, quality assurance, and compliance. Strong problem-solving and decision-making skills with a focus on continuous improvement. Excellent communication skills for effective interaction with internal and external stakeholders. Familiarity with industry standards and regulatory requirements in the pharmaceutical sector. Regards, Ila Rajput Utkarsh Placement Pvt. Ltd. Baroda Mob-9824059611 Phone: 0265 - 2601938 ila@uppl.in

IND/NDA/ANDAs/Amendments and Biologics to the FDA within company timelines and in accordance with regulatory guidelines and applicable federal laws The Manager, Regulatory Affairs CMC is responsible for developing and implementing regulatory strategies related to Chemistry, Manufacturing, and Controls (CMC) for pharmaceutical or biologic products Having prior experience of handling pre-approval and post-approval regulatory activities for multiple dosage form including Sterile, Sterile (Injectables/Ophthalmic/Otic/IV Bags) dosage forms in US market either for Aseptic sterilization or Terminal sterilization or both

TEAM LEADER - FORMULATION AND DEVELOPMENT INJECTABLE Activities and Responsibilities :- Coordinate with formulation scientists for day-to-day activities, designing formulation strategies, execution of laboratory trials and preparation of technical documents for sterile dosage forms. Coordinate with other technical staff responsible for testing new drug substances, excipients, pre-formulation samples, and formulation development samples. Ensure the timely completion of new product development of sterile dosage form. Interact with Manufacturing, Validation, and Materials Management teams to ensure smooth drug product development and transition to commercial-scale manufacturing. Manage all activities associated with registration batch manufacturing, including authoring, reviewing, and approving technical documents. To perform, review and interpret literature related to drug products, including patents, research articles, reference product details, drug substance information, and excipient details. Provide support in troubleshooting formulation and process-related issues for both sterile and sterile dosage forms. To perform various studies such as pre-formulation studies, API characterization study, excipient characterization study, excipient optimization studies, filter compatibility studies, tubing compatibility studies, bulk hold in SS vessels / SS compatibility studies, pH optimization studies, nitrogen requirement studies, photo stability studies, freeze-thaw studies, in-use studies, dilution compatibility studies, selection of sterilization methods, selection of packaging materials, stress studies, and scale-up operations. To perform all required activities, i.e., procurement of raw materials, packaging materials, and processing aids etc. for the initiation and execution of development batches, process validation/ exhibit batches and commercial batches of the drug product. To prepare and review product-specific risk assessments, QQ, Master Formulation Records (MFR), development batch Stability Protocols, Scale-up BMRs, Scale-up reports, Product Development Reports (PDR), etc. To propose and review finished product specifications to the Analytical Development Laboratory (ADL) based on dosage form requirements. To prepare and review of technical documents based on CTD required for dossier submission and handling all technical queries raised by all respected regulatory authority. Percolate the instruction and work assigned by Head R & D to Team members for timely completion of activities. To prepare and review Standard Operating Procedures (SOPs) and related documents, ensuring work is performed according to SOPs, Good Manufacturing Practices (GMP), and safety guidelines in the R&D department. To assist and support in the preparation and review of qualification and validation documents, change controls, deviations, investigations, and CAPAs. To visit LL sites and third-party sites for development batch trials or batch execution as required. To be responsible for coordination, execution, monitoring, and troubleshooting of scale-up batches, exhibit batches, process validation batches, and commercial batches at in-house manufacturing sites, CMO sites, TT sites, and LL sites. To co-ordination with Cross Functional Team to ensure timely completion of assigned activities. To perform any other task assigned by HOD / Management. THANKS YOU REGARDS MILAP RATHOD (7486829377) HR DEPARTMENT OPES HEALTHCARE PRIVATE LIMITED

Responsible for formulation development for OSD, external preparations, oral liquids, and injectables. Responsible for pre-formulation studies, prototype development, and scale-up activities. Ensure compliance with regulatory guidelines (ICH, WHO, USFDA, etc.). Collaborate with cross-functional teams (A, C, RA, Production) for tech transfer. Mentor junior scientists and manage project timelines and documentation.

Job Description: Position : Area Sales Manager-Team handling (IC role) Segment: Bio logics/ Bio Similar- Derma segment Please find below the JD. B. Pharma. / B.Sc. / B. Tech. -Biotechnology graduates 30 years of age with 4+ years of Experience in Derma Biologics / Biosimilar industry. Dynamic Individuals : Energetic, self-motivated, and goal-oriented professionals. Excellent Communicators : Strong interpersonal and communication skills. Healthcare Enthusiasts : Passion for the pharmaceutical industry and a commitment to excellence. Team Players : Ability to work collaboratively in a fast-paced environment. Roles & Responsibilities: Build and maintain strong Customer relationships. Ensure effective Rx product detailing in the assigned territory. Ensure targeted brand wise coverage and penetration . Stay updated with the latest industry trends and product and therapy knowledge. Interested candidates are can apply on Darpana: 9978604075 OR can email me on darpana@upman.in

Were looking for a skilled Shopify Developer to create and maintain e-commerce solutions on the Shopify platform. Key Responsibilities: Develop and maintain Shopify stores with focus on front-end features Customize Shopify themes to meet client requirements Collaborate with designers and project managers Implement responsive designs for mobile and desktop Requirements: Minimum 1 year of Shopify development experience Strong knowledge of Liquid, HTML, CSS, and JavaScript Understanding of e-commerce best practices and SEO Excellent problem-solving skills and attention to detail

Walk In drive for Formulation Research & Development - Department FR&D - MSN R&D Center Pashamylaram on 20.09.2025 (Saturday ) Formulation R&D Department ( Formulations R&D) in Formulation Division - R&D Center. Key Responsibilities: Formulation Development : Lead the formulation development process for new pharmaceutical products, including solid oral dosage forms, liquids, and semisolids. Experimental Design : Plan and execute formulation experiments, optimizing product composition, excipients, and processes for efficacy and stability. Documentation : Maintain comprehensive records of experimental procedures, results, and regulatory documents, ensuring compliance with industry standards and protocols. Regulatory Compliance : Collaborate with regulatory affairs to ensure that all formulations adhere to applicable regulatory guidelines and quality standards. Analytical Techniques : Employ a variety of analytical techniques, such as HPLC, dissolution testing, and spectroscopy, to evaluate formulation properties. Scale-up and Tech Transfer : Assist in the scale-up of successful formulations from laboratory to pilot plant and full-scale manufacturing, facilitating technology transfer. Team Collaboration : Work closely with cross-functional teams, including analytical, regulatory, and quality control, to drive projects to completion. Position : Executive / Senior Executive / Junior Manager Qualification : M Pharma (Pharmaceutics) Work Location : MSN R&D Center, Pashamylaram. Department : Formulation Research & Development - ( FR&D ) Experience : 2 to 10 Years Date of Interview : 20.09.2025 ( Saturday) Interview Time : 9.00 AM to 3.00 PM Note : Preferable Male Candidates only Interview Venue Details : MSN Laboratories Pvt Ltd, MSN R&D center, Pashamylaram, Isnapur,Patancheru,Sangareddy,040-30438786

Walk-In Drive for Development Quality Assurance - Formulation Department @ MSN R&D Center Pashamylaram on 20.09.2025 (Saturday ) Roles & Responsibilities 1. Issuing of Batch Manufacturing Records, Analytical Raw datas and maintaining the respective log books. 2. Issuing of registers and formats for all departments and maintaining of records for issuance and reconciliation. 3. Issuance approval, Issuance and Retrieval of the documents in eDMS. 4. Receiving, Issuing and reviewing the bio batches related executed Batch Manufacturing Records, Analytical raw datas and archiving. 5. Responsible for review of product development documents and analytical documents related to technology transfer. 6. Preparation and review of departmental SOPs 7. Reviewing of Equipment qualification protocols and Reports. 8. Review of supplier qualification documents. 9. Review of calibration documents 10. Receiving and reviewing of executed raw datas & ATRs and archiving for bio batches. 11. Reviewing of analytical method validation protocols & reports. 12. Maintenance, Retrieval and Archiving of all GMP related documents and records. 13. Preparation & review of department Schedules 14. Responsible for document distribution to the user departments. 15. Responsible for Document control activities. 16. Responsible for preparation, review and submitting License Applications. 17. Handling of Change controls (Permanent and Temporary), OOS and Incidents. 18. Responsible for approval of documents in absence of Head FDQA. 19. Responsible for performing job assigned by Head FDQA or his authorized designee. Note : Formulation R&D, API R&D Candidates also eligible for this positions Position : Executive / Senior Executive Qualification : M.Sc, M Pharma / B Pharma Only. Work Location : MSN R&D Center, Pashamylaram. Department : Development Quality Assurance - Formulation Department. Experience : 2 to 8 Years Date of Interview : 20.09.2025 (Saturday ) Interview Time : 9.00 AM to 3.00 PM Venue Details : MSN Laboratories Pvt Ltd. MSN R&D center, Pashamylaram , Isnapur, Patancheru, Sangareddy - 040-30438786

1. Head QC ( 1 position vacant) QC Head Pharmaceuticals | Expertise in USFDA, EUGMP, MHRA, and WHO Compliance 2. Plant/Site Head ( 1 position vacant) Site Head Injectable Plant | Driving USFDA, EUGMP, MHRA & Global Compliance 3. Production Head ( 1 position vacant) Production Head Pharma Injectables | USFDA, EUGMP, MHRA & WHO-GMP Compliance

Key Responsibilities Lead and manage the Quality Assurance department, ensuring compliance with GMP norms and regulatory requirements of WHO, EU GMP, PICS, TGA, MHRA, USFDA, and other global agencies . Develop, implement, and monitor Quality Management Systems (QMS) across all QA functions. Ensure strict adherence to SOPs and continuous improvement practices in line with regulatory expectations. Oversee handling of rejected materials, market complaints, product recalls, deviations, change controls, CAPA, and CCF . Manage end-to-end Validation and Qualification activities (process validation, cleaning validation, equipment qualification, analytical method validation, etc.). Ensure audit readiness at all times and lead regulatory/customer audits and inspections. Review, approve, and monitor the control of documents, records, and quality risk management systems . Provide leadership and guidance to QA teams, including training, mentoring, and performance monitoring. Collaborate with cross-functional teams (Production, QC, R&D, Regulatory Affairs) to maintain high-quality standards. Drive initiatives for continuous quality improvement and compliance to ensure products meet global regulatory expectations. Desired Candidate Profile B.Pharm / M.Pharm with 1520 years of proven experience in Quality Assurance of Pharma Formulation Units . Strong command over WHO GMP, EU GMP, PICS, TGA, MHRA, and USFDA regulatory guidelines . Expertise in handling market complaints, investigations, and product recalls . Thorough knowledge of CAPA, deviations, and change control processes . In-depth experience in validation & qualification activities . Excellent leadership, decision-making, and cross-functional coordination skills. Strong communication skills with the ability to face regulatory and customer audits confidently. Willingness to relocate to Gandhidham . Candidates who can join immediately will be given preference. Compensation & Benefits Competitive salary aligned with industry standards. Relocation support for suitable candidates. Opportunity to head the QA function and drive strategic quality initiatives for a regulated market facility. Role & responsibilities

You will be responsible to review of journals and patents. You will be responsible for feasibility study of the Process, Process Optimization,Lab Validations, Technology Transfer to plant and identify and evaluate the reaction parameters You will be responsible for staying up to date with relevant scientific and technical developments. Execute experiments efficiently with high reproducibility. You will be responsible for interpretation of analytical and spectral data to ensure quality and regulatory compliance. You will be responsible to write technical development reports, Quality by Design (QbD) reports, justification reports and Drug Master Filing (DMF) filing related documents. You will be responsible to provide support in scale up batches execution and ensure process reproducibility at scale. You will be responsible for ensuring lab safety and process safety. Qualification M.Sc Organic chemistry with 3-5 years of Experience in API process R&D. 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/#!/

Role & responsibilities Execute daily production operations and ensure the efficient functioning of the department. Supervise and monitor manufacturing processes to ensure compliance with quality standards. Review and maintain production-related QMS elements, including Change Control, Deviation, Event Investigation, and Corrective and Preventive Actions (CAPA). Prepare and review Standard Operating Procedures (SOPs), Batch Manufacturing Records (BMRs), and Batch Packing Records (BPRs). Address and resolve production issues promptly to minimize downtime and ensure continuous production. Respond to challenges or bottlenecks and implement mitigation strategies within defined timelines. Ensure that all processes and documentation comply with SOPs and protocols. Maintain and review all production-related records, including batch records, equipment logs, and production output reports. Prepare regular reports on production output, efficiency, and quality metrics for management review. Coordinate with the maintenance department to resolve equipment breakdowns and ensure smooth production activities. Oversee the document control system to ensure the availability and integrity of quality documents. Preferred candidate profile Bachelor's or Masters degree in Pharmacy, Life Sciences, Biotechnology, or a related field. Minimum of 1 year of experience in a production/QMS-related role within the pharmaceutical, biotechnology, or manufacturing industry. Strong understanding of QMS principles, regulatory compliance, and production processes. Ability to analyze and resolve production-related challenges effectively. Proficiency in documentation, report preparation, and adherence to SOPs.

Walk In Drive For Production Injectables In Formulation Division @ RK Puram Department:- Production Injectables Qualification :- ITI | Diploma | B Sc | B. Tech | B Pharmacy | M Sc | M Pharmacy Experience :- 2 to 8 Years Skills :- Operators :- Filling | Production Injectables Packing / Blister | Lyo | PFS Operators | QMS | ALUS | Vial filling | Stoppering | Sealing Machine | Autoclave Division :- Formulation Interview Date: 13-09-2025 (Saturday) Interview Time :- 9.00AM TO 2.00PM Work Location:- Unit-II, Kothur| MSNF-V, RK Puram Venue Location :- Unit-5, RK Puram, 25GX+XHX, Solipur, RK Puram,Telangana 509216 Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Pay slips, Bank Statement, Certificates, Aadhar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

Your Day-to-Day Tasks Include: 1. Initiating first level contact with Inbound and Outreach leads. 2. Creating and executing an outreach strategy in collaboration with the PDR Managers and PDR team leads.

Job Purpose: To operate, monitor, and maintain filling machines and related equipment in compliance with cGMP, safety, and quality standards, ensuring smooth and efficient production of sterile / non-sterile products.

Job Summary Roles & Responsibilities Review and approval of all analytical test data of Quality control. Review and usage decision of analytical reports in LIMS, Empower and SAP. Electronic signatures level-2 for chromatography data station (CDS) and standalone instruments. Review the Analytical test report in LIMS. Review the reported results against specification and trends. Review the method validation and method transfer documents. Review the instrument calibrations and working standard qualification records. Handling the Incidents/ Deviations, Out of Trends, Out of Specification including investigations, Corrective and Preventive actions follow up and closure. Monitoring of analytical activities in Quality control laboratory. Verification of Specifications/standard test Procedures/Worksheets/Analytical Reports before Approval. Verification and review of the audit trails for Standalone, Empower and LIMS. Ensure cGMP / cGLP compliance. To follow Safety, Health and Environmental procedures and practices. Review and approval of excel sheet validations. Review results acceptance for API and Excipients and Packing material. Review of compiled of Stability Data and its verification/ Exhibit batch sampling protocols. Handling of Robotic Process Automation of Chromatography Data review (RPACD) To carry any other activities assigned by upward reporting staff. Qualification Educational qualification: A Bachelor’s/Master's degree in Pharmacy, Chemistry, Chemical Engineering, or a related field Minimum work experience : 3 to 7 years of experience in QC or AQA department is mandatory. Additional Information About the Department Global Manufacturing Organisation (GMO) At Dr. Reddy's Laboratories, we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence, we are a leading force in the pharmaceutical industry. We operate 19 state-of-the-art manufacturing plants across Hyderabad, Vizag, Baddi, Mexico, Shreveport, and Mirfield, comprising 8 OSD facilities, 3 Injectables facilities, and 8 API facilities. Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1,150+ drug master files across key therapy areas such as Oncology, Cardio-vascular, Central Nervous System and Anti-Diabetes. he World Economic Forum has recognised our largest manufacturing facility in Bachupally, Hyderabad, as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive, meeting business imperatives, and meeting our ambitious ESG goals. Building such ‘factories of the future’ is integral to innovation and to build healthcare of the future. 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/#!/

Job profile Qualification : Bachelors 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 partners 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

Job profile Qualification : Bachelors 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 partners 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

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.

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.

Greetings From Immacule Lifesciences Pvt Ltd! We are looking for an Injectable Production QMS experienced professionals. Position : Executive / Sr. Executive Department : Production QMS Qualification : B. Pharma / M. Pharma Experience : 4 - 9 Years Key Skills : Prepare and maintain QMS documents Manage Change Control, Deviations, and CAPA with timely closure and effectiveness check. Coordinate with QA, Engineering, QC and other departments, etc.. To Apply: Email ID : Eswar.reddy@immacule.in Mobile : 9490101534

BUILD YOUR CAREER WITH CHIRON! Hiring Fresher's & Experience (1 to 5) WALK IN INTERVIEW FOR FITTERS On 13 Sep 2025, Saturday TIME: 09:30 AM to 01:00 PM Department Engineering Fitter (* Shift applicable) Lyophilizer Autoclave Vial Filling Vial washing Depyrogenation tunnel Qualification: ITI (Fitter)

Role & responsibilities: Job Summary: We are seeking a skilled and detail-oriented Production Officer with hands-on experience in autoclave operations within a parenteral pharmaceutical manufacturing environment. The ideal candidate will be responsible for ensuring sterile production processes, maintaining equipment, and adhering to GMP standards. Key Responsibilities: Operate and monitor autoclave machines for sterilization of equipment, garments, and components. Ensure compliance with aseptic processing and cleanroom protocols. Maintain accurate documentation of sterilization cycles and batch records. Perform routine checks and preventive maintenance of autoclave and related equipment. Coordinate with QA/QC for validation and calibration activities. Support production planning and execution of parenteral dosage forms (e.g., injectables). Adhere strictly to cGMP, SOPs, and safety guidelines. Participate in audits and assist in regulatory compliance activities. Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications. Send Cv at Rashmi.kulkarni1@Fresenius-kabi.com

Role & responsibilities To perform operation and changeover of the equipments like Vial Filling & Stoppering Machine, Vial Cap Sealing Machine, Vial Washing Machine, Sterilizing and Depyrogenation tunnel, Lyophilizer, Autoclave, Pasteurizer, Incubator, Fogger and Filter integrity tester. Actively involve in fill finish operation and media fills. Preparation and review of general and equipment operation SOP’s. Involve in preparation and reviewing of BMR, MFR & Validation protocol etc. Compilation of all critical process attribute to analyze yield variation and investigation of low yield batches or OOS routed through change control or deviation. To get involve in external and internal regulatory audits and ensuring audit compliances.

Role & responsibilities Sr. Executive Visual Inspection (and Packing) : JD : Preferably with 5 to 10 Years of experience in handling visual inspection activities @ reputed Pharma / Biotech companies ( preferably in Small volume injectables ) Should be expert in KIT preparation and Qualification of Visual inspector. Should be ready to work in A/B shifts regularly. Should have GMP Audit Exposures. Handling of Packing activities and will be an advantage.