234 Sterile Jobs - Page 9

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.

Greetings! We are looking for Formulation Research & Development Scientist - Injectables for a leading Pharmaceutical company based at Hosur location. Responsibility: 1. Develop robust formulations and processes for general products to various markets such as Regulatory, Semi-regulatory, ROW, and Domestic with application on QbD as needed. 2. Monitoring and supporting the formulation team for the completion of allocated projects within the timelines by trouble shooting the concerns involved. 3. Scale-up and optimization of manufacturing process; execution of pre-exhibit and exhibit batches; scale up and technology transfer from R&D to production to meet timeIines. 4. Plan and contribute to project-related scientific/technical activities (e.g., interpret results, critical assessment of data, draw relevant conclusions, and write reports). 5. Author technical documents including Product Development Report, Quality Overall Summary and other relevant documents for filing purpose. 6 Interaction with API/Excipient manufacturers, CROs and CMOs as needed. 7. Interaction with external testing laboratories as needed. 8. Work proactively with other cross-functional groups to execute all product related activities such as Manuticturing and Packaging master records, SOPs and protocols etc. 9. Co-ordination with other Dept. like Purchase. QC/QA, RA, ADD, Production Eng. etc. related to product development activity. 10. Review SOPs, as well as appropriate documentation and test results for accuracy and coin pleteness and coinpl iance with SOPs/GM P requirement. 11 . Coordinate with RA for fiI ing AN DAs and addressing deficiencies; provide relevant documents to Regulatory Affairs in a timely man ner for ANDA fil ings and Supplements filing. 1 2. Review of batch records, process characteri xation reports, validation reports and investigation reports. Interested Candidates Kindly share your updated cv to khyati@bvrpc.com

Walk-in at Matoda We are hiring multiple positions for our manufacturing facility at Matoda as mentioned below. Please find our current job requirements and venue details mentioned. If any of the requirements match your current job profile, kindly walk in with your latest resume. Role & responsibilities QUALITY ASSURANCE IPQA (Injectable), IPQA (OSD) & QMS / Documentation / Validation and Qualification (Officer / Senior Officer / Executive/Senior Executive) Experience - 02 to 09 Years Qualification - B. Pharmacy/ M Pharmacy / M.Sc. Injectable Manufacturing Aseptic operations/ QMS / SKID / Multi-vessel / SVP / Visual Inspector (Senior Officer / Officer / Associate) Experience - 01 to 05 Years Qualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma / ITI OSD Manufacturing / Dispensing / QMS (Senior Officer / Officer / Associate) Experience - 01 to 05 Years Qualification B Sc / M Sc / B. Pharmacy/ M Pharmacy / Diploma Time and Venue : 17th May 2025, 09:30 Hrs to 14:00 Hrs SATURDAY ______________________________________________________ INTAS, Matoda facility Plot No. 457, 458 Sarkhej Bavla Highway, Matoda Village, Sanand, Taluka, Ahmedabad, Gujarat 382210 ______________________________________________________ We would be pleased if you forward or refer any of your colleagues matching the desired job roles. Preferred candidate profile *Having relevant qualification as mentioned above can attend the scheduled walk-in.

Roles & responsibilities: Media preparation, media suitability test, growth promotion test. Water sampling and testing. Maintenance of stock cultures, sub culturing and culture suspension preparation. Environment monitoring program (passive air sampling, Active air sampling and surface sampling). Sterility Testing, Bacterial endotoxin test, bioburden testing. Testing of Total organic carbon (TOC) in water samples. Endotoxin testing through KTA method and Gel Clot method. Testing of media fill samples. Enumeration of biological indicators. Preparation of trends and compilation summery for water and environmental monitoring. Establishment of alert and action limits for water and environmental monitoring. Establishment of Limit for bioburden samples. Identification or microorganisms by Vitek 2 Identification system. Container closure integrity test. Preservative efficacy test. Disinfectant Validation. Handling of Change controls, deviation, Out of Specification and writing of audit justification reports. Preparation of sops, protocols and reports aligning as per quality standards, cGMP documents as per pharmacopeias. Audits faced USFDA,WHO, MHRA, ANVISA,customer audits, etc.. Training of team members in SOP, Analyst qualification, Quality documents Preferred candidate profile: Posses the quality of good Team Leader. Believe in team work. • Should have exposure to day-to-day routine microbiological activities like media preparation, culture handling, Plating etc. *Relevant experience must be for working in microbiology lab. *Must have experience of working into sterile area.

Job Description : - Department - Injectable Mfg & Packing Position - Technician / Officer / Sr. Officer Exp - 2 to 6 Education - ITI / Diploma Eng / D.Pharma / B.Pharma / M.Pharma Skill Set - Require good knowledge in Complex Skid / NDDS / Aseptic (PFS / Vials Liquid) / Autoclave/ Lyopholizer / Batch Manufacturing, Sterile Secondary Packing and track and trace activity + visual inspection activity. Department - QC ( QC FG / Stability / AMV ) Position - Officer to Executive Exp - 2 to 7 Education - M.Sc / B.Pahrma / M.Pharma Skill Set - Analyst : Finished, AMV & Stability Section. knowledge of Instrument - HPLC / GC. Preferably know-how of Chromeleon Software Department - Engineering ( Plant Maintenance Sterile / Instrumentation Sterile ) Exp - 2 to 15 Position - Technician / Executive / Assistant Manager / Manager Education - Diploma Eng / ITI / B.Tech Skill Set - Have good exposure in Plant Maintenance & Instrumentation related work in sterile facility Department - QA ( IPQA / Qualification (Sterile Background Only) Position - Officer to Executive Exp - 2 to 7 Education - B. Pharmacy / M.Pahrma / M.Sc Skill Set - Have good exposure in Sterile IPQA & Sterile Qualification Related activity Department - Lab QA Position - Officer to Sr. Executive Exp - 2 to 9 Education - B. Pharmacy / M.Pahrma / M.Sc Skill Set - Having good exposure of QC QMS handling , Lab instrumentation & audit trails. Have strong background of Lab QA activity. Department - Solid Oral Packing Position - Technician / Officer / Sr. Officer Exp - 2 to 5 Education - ITI / Diploma Eng / D.Pharma / B.Pharma Skill Set - Require good knowledge in Primary & Secondary Packing, Track & Trace, Carton Packing Machine (CAM HV1 Model), Online Documentation BPCR / Logbook etc.

Key Responsibilities: Oversee end-to-end manufacturing operations for Nasal formulations (sprays, drops, etc.). Ensure adherence to production schedules, batch planning, and resource allocation. Monitor and enforce cGMP, safety, and hygiene practices across the Nasal production area. Review and maintain production documentation including BMRs, BPRs, and SOPs. Coordinate with Quality Assurance, Quality Control, Engineering, and Warehouse for seamless operations. Identify and troubleshoot production issues to minimize downtime and rejections. Lead a team of operators and supervisors, ensuring proper training and performance monitoring. Participate in internal and external audits; ensure timely CAPA implementation. Drive process improvement initiatives to increase productivity and reduce waste. Ensure proper maintenance and calibration of production equipment used in Nasal manufacturing.

Help in Day To Day Production Of Pharmaceutical Products Manpower Allocation For Smooth Working In Shift Supervision Of Production Activity BMR And BPR Report Preparation Data Preparation For Internal And External Audit -IE. US FDA - EU GMP Etc Required Candidate profile B. Pharm - M. Pharm - B.Sc - M. Sc Experience In Production Or Packaging Working Experience US FDA Approved Plant is Desirable FDA Approval in Tablet - Capsule Or Any will be an added advantage

Help in Day To Day Production Of Pharmaceutical Products Manpower Allocation For Smooth Working In Shift Supervision Of Production Activity BMR And BPR Report Preparation Data Preparation For Internal And External Audit -IE. US FDA - EU GMP Etc Required Candidate profile B. Pharm - M. Pharm - B.Sc - M. Sc Experience In Production Or Packaging Working Experience US FDA Approved Plant is Desirable FDA Approval in Tablet - Capsule Or Any will be an added advantage

Sterilization and Decontamination: Cleaning, decontaminating, and sterilizing medical instruments, equipment, and supplies using various methods like autoclaving. Equipment Operation and Maintenance: Operating and maintaining autoclaves, low-temperature sterilizers, and other sterilization equipment, ensuring proper functioning and adherence to safety protocols. Instrument Inspection: Inspecting instruments and supplies for cleanliness, proper function, and any defects before they are sterilized. Assembly and Packaging: Assembling and packaging sterile instruments and supplies in appropriate containers or trays for storage and distribution. Inventory Management: Maintaining accurate inventory records of sterile supplies and instruments, ensuring adequate stock levels. Distribution: Providing sterile supplies and instruments to various departments within the hospital or healthcare facility as needed. Documentation: Maintaining detailed records of sterilization processes and quality control measures, ensuring compliance with regulations. Collaboration: Collaborating with other healthcare staff, such as surgeons and nurses, to ensure timely availability of sterile supplies and address any needs.

Roles and Responsibilities Review of technical regulatory documents for drug substance and drug products Compilation of CMC data for submission to regulatory authorities Review and approval of master documents for CMC segments Preparation and review of annual reports, amendments, supplements etc. Assist with CMC responses to regulatory authorities queries during development, registration, and product lifecycle. Evaluation and co-ordination of change controls Liaison with various departments like R&D, QC, QA, Production, stability departments for obtaining documents. Prepare response to regulatory deficiencies letters according to US regulatory requirements. Desired Candidate Profile The candidate should have adequate knowledge in regulatory affairs (Injectable or Ophthalmic formulations) for US market. He/ She should have 3 - 5 years of experience with B. Pharm./ M. Pharm./ M. Sc. as a educational qualification. Candidate should possess excellent verbal and communicational skills.

Walk In Drive For Production Injectables In Formulation Division @ Kothur Department:- Production Injectables Qualification :- Diploma | ITI | B Tech | B Pharmacy | BSc | MSc | M Pharmacy Experience :- 2 to 8 Years Skills :- Labelling Machine Operator | Filling Operator Division :- Formulation Interview Date:-10-05-2025 Interview Time :- 9.00AM TO 2.00PM Work Location:- Unit-II, Kothur & MSNF-V, RK Puram Venue Location :- Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) 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.

Walk In Drive For Production Injectables In Formulation Division @ Corporate Office Department:- Production Injectables Qualification :- Diploma | ITI | B Tech | B Pharmacy | BSc | MSc | M Pharmacy Experience :- 2 to 8 Years Division :- Formulation Interview Date:-10-05-2025 Interview Time :- 9.00AM TO 2.00PM Work Location:- Unit-II, Kothur & MSNF-V, RK Puram Venue Location :- MSN Corporate, H. No. 2-91/10 & 11 /MSN, Whitefields, Kondapur, 500084 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.

Multiple positions open for various operators who are responsible to operator vial filling/ sealing machine, autoclave, ampoule filling machine, manufacturing of injectable.

Spearheading the Production Department Production Yield Planning and calculation Manpower Mangement Breakdown Analysis Cost vs Production Analysis Required Candidate profile Should have handled multiple lines, candidate from aseptic background will be prefered

Role & responsibilities : Candidate should have experience in Injectable plant (Parenteral) Candidate should have experience in Vial line (Liquid/Lyophilizer), PFS Line, Bag Line, Cartridge line, Ampoule Line. Candidate should have experience in Imported Equipments like Groninger, B+S, Bosch, Pluemat, SFM, Steriline (Vial/PFS/Cartoridge/Bag/Ampoule Lines), IMA/GEA/Tofflon (Lyophilizer), Fedegari (Autoclave), Bonfiglioli (Leak test), Caser (X ray). Candidate should be capable of handling the Team and Block/Plant. Candidate should have experience in HVAC/Water system Candidate should have hold on Documentation line QMS/Qualifications. Candidate should have experience in Energy Conservation projects. Candidate should have experience in Handling the Brownfield Projects. Educational Qualification : B.E (Electrical/Instrumentation/Mechanical/ Electronics and Telecommunication) Experience : 15+ Years

Sterile Operations Trainer Grade: G9 Designation: Senior Manager Location: Halol 1 Job Description: Education: B. Pharm / M. Pharm Overall responsibility of Aseptic Training Academy (ATA), Baska To plan, develop, and execute training at Aseptic Training Academy (ATA) - Sterile Operations for Sun Global Operations (SGO) Training. Creation of simplified training modules for technicians, scheduling and execution of training Creation of training evaluation and/or feedback systems Course creation according to levels (Level 1 - Technicians, Level 2 - Supervisors and above, Level 3 - Managers and above) pertaining to sterile operations Planning, scheduling & execution of technical training program relevant to sterile operations for new recruits/for existing employee by self/internal or external facility Identification of Certified trainer at various locations (sterile operations) based on additional training need of respective location Coordination with location head and Subject Matter Expert (SME) for conducting the additional training program according to training calendar on monthly basis pertaining to sterile operations To prepare and submit SGO training score card for sterile operations on monthly basis after plant review to Corporate Quality Policy and Training department (CQPT) To maintain the training records of training Periodical review of technical courses along with business units for site specific course and the head of course for suitable course content / design and pedagogy up gradation To coordinate in technical course scheduling and publishing of calendars and facilitate visiting faculty/guest faculty in course delivery Any other work assigned by superiors from time to time

Role & responsibilities Operate and manage freeze drying and lyophilization equipment , including Freeze Dryer, Palltronic Integrity Tester, and CLU. Ensure smooth functioning of computerized systems such as eBMR, PLC, SCADA , and manage data integrity, audit trails, and system backups. Participate in equipment and area qualification/requalification activities, including LAF (Laminar Air Flow) systems. Ensure adherence to and documentation of Change Controls , Risk Assessments (RA) , Corrective and Preventive Actions (CAPA) , and EHS (Environment, Health, and Safety) protocols. Ensure compliance with regulatory standards and assist during audits and inspections . Maintain accurate and timely documentation as per GMP guidelines. Preferred candidate profile Bachelors degree in Pharmacy (B. Pharma) – Mandatory 4 to 7 years of experience in a sterile pharmaceutical manufacturing environment , specifically in Lyophilizer operations . Strong understanding of pharmaceutical regulatory standards , including GMP, FDA, MHRA, etc. Familiarity with automation and computerized systems like eBMR, SCADA, PLC. Sound knowledge of qualification protocols , equipment handling , and process controls . Excellent documentation and communication skills. Proactive, team-oriented mindset with the ability to handle audits and cross-functional coordination.

- Sterile Injectables Handling dealing with liquid ampoules, vials, lyophilized products - FIFO / FEFO Implementation - ERP Inventory Management - Inward & Outward Material Management - Warehouse Housekeeping - Pharmaceutical industry - Compliance

- Sterile Injectable Manufacturing (Core) - Liquid ampoules, vials, lyophilized products - BMR/BPR Documentation - cGMP - Production Line Operation - Pharmaceutical Equipment Handling - Cleaning/Sterilization - Internal Audit/Validation - Maintenance

- 8+ yrs in Sterile Injectable Manufacturing - 3+ yrs as Production Manager in Injectable Plant - Handling Liquid Ampoule, Vial, and Lyophilized Vial Lines, BMR/BPR Documentation - Leadership & People Management - cGMP; WHO-GMP; FDA Guidelines, SOP

Must have Exp in Injectable & Parenteral formulations. Lead and optimize end-to-end sterile injectable production, ensuring cGMP compliance, on-time delivery and continuous process improvement.

Company: Leeford Healthcare Ltd. https://www.leeford.in/ https://www.linkedin.com/company/1464125/admin/dashboard/ Role: Production Manager Sterile Prep (Eye/Ear Drops) Experience: Minimum 8-12 years Location: Baddi Education: Graduation; Post Graduation: BSC/B.Pharma Desired Candidate Profile: Required experience of 8-12 years, Exposure to work with one or more reputed organization. Knowledge of Sterile manufacturing like Eye Drops & Ear Drops i.e. Manufacturing, Filling, Sealing and packing of products. Job Description: Designation: Production Manager Sterile Prep (Eye/Ear Drops) Work Profile: 1. Responsible for Batch Manufacturing in SVP line, aqueous line. 2. Responsible for operating of Autoclave. 3. Responsible for filling operation In SVP line- Vial /Ampoule. 4. Responsible for Trend Data entry of Filling Rejection, Filling Yield, Packing Yield & Batch Yield. 5. Responsible for Product sterilization with Rotary Sterilizer for Emulsion and Steam air Sterilization for Aqueous product. 6. Responsible for maintaining the all record according to gmp compliance. 7. Must have experience of handle Ampoule leak test machine. 8. Must have working experience of aseptic filling area. Interested one can share resume to talent@leeford.in or can whatsapp to 9875961129

Novo Nordisk Global Business Services (GBS) India Department: GCM DP RoW Location Hyderabad, India Are you an experienced aseptic manufacturing project manager with a strong technical background and a passion for making a direct impact on patients'' livesDo you thrive in an international environment where cultural awareness is key to your successIf so, this could be your dream role! ApplyNow! The Position As a Project Manager in Aseptic Manufacturing, you will lead and mentor cross-functional teams, including both Novo Nordisk and our Contract Manufacturing Organisation (CMO) partners. It includes, Ensure the seamless Technology Transfer and manufacturing of our commercial products, always upholding Novo Nordisk''s stringent quality standards and adhering to cGMP and regulatory requirements. Lead and manage aseptic manufacturing projects, specifically leveraging your expertise in areas like Formulation/Compounding, Filling, Washing & Sterilisation, Environmental Monitoring, or Clean Utilities. Developing and managing detailed project plans and timelines and communicating effectively with steering groups and key stakeholders. Monitoring progress and proactively securing necessary resources. Developing project risk grids and identifying mitigation strategies with both Novo Nordisk and our Contract Manufacturing Organisation (CMOs). Qualifications Bachelors or Masters degree in engineering. Possess experience of 5-12Years of project management experience with a proven track record of successful project delivery in a highly regulated environment, especially internationally. Aseptic manufacturing experience is a must, and experience with Technology Transfer of biologics is a significant advantage. Professional experience balancing individual drive with effective stakeholder involvement. Proficiency in project management software (e.g., MS Project, Smartsheet, Jira, or equivalent). Demonstrated fluency in written and spoken English is essential. About the Department GCM DP RoW Projects is a dedicated team committed to providing life-saving insulin and GLP-1 to patients in regions such as Africa, India, the Middle East, and Asia. By partnering with CMOs in these areas, the department strives to make a meaningful impact on the quality of life for patients living with diabetes and obesity. Our projects are tailored to meet the unique requirements of each country, offering exciting growth opportunities. With a steadfast commitment to innovation and problem-solving, we work to overcome challenges and navigate complex regulatory landscapes to deliver insulin and GLP-1 on a global scale. Join us in making a difference.

Novo Nordisk Global Business Services (GBS) India Department GCM DP RoW Job Location Hyderabad Are you an expert in aseptic manufacturing with a strong quality mindset and a desire to make a tangible impact on global healthNovo Nordisk is seeking a dedicated Manufacturing Specialist to join our Global Contract Manufacturing Drug Product (GCM DP) team in Hyderabad, India. In this role, you''ll be crucial in ensuring the high-quality production of life-saving insulin and GLP-1 products through our Contract Manufacturing Organizations (CMOs). ! The Position As a Manufacturing Specialist (SME), you''ll be the go-to expert driving Technology Transfer projects for commercial products, ensuring top-tier quality with our Contract Manufacturing Organizations (CMO) partners. Your key responsibilities will include: Lead cross-functional teams, ensuring seamless collaboration between Novo Nordisk as the sending Unit and Contract Manufacturing Organizations (CMOs) partners as the receiving Unit. Act as a mentor and support Contract Manufacturing Organizations (CMOs) to ensure Novo Nordisk products are manufactured to the highest quality standards. Provide training, share best practices, and review and approve validation documents to safeguard compliance. Offer oversight and support during the planning and execution of validation and qualification activities. Define, manage, and deliver on complex projects in collaboration with CMOs, Quality Assurance, and project managers. Drive problem-solving initiatives and provide scientific and technical solutions within tight project timelines. Qualifications Bachelors /Masters degree in engineering. Possess 10+Years experience and relevant 5 years of manufacturing experience, especially in an international, multicultural environment. Expertise in aseptic manufacturing processes is non-negotiable. Capable of communicating naturally and effectively with stakeholders at all levels with adept at finding solutions and motivating stakeholders to achieve ambitious goals. Possessing a strong mindset, a focus on continuous improvement, and keen attention to detail. Demonstrates the ability to work independently with minimal supervision, a strong willingness to learn new skills, and the motivation and flexibility to thrive in a fast-paced, dynamic environment. About the Department GCM DP RoW Projects is dedicated to delivering life-saving insulin and GLP-1 to patients in regions such as Africa, India, the Middle East, and Asia. By partnering with CMOs in these areas, the department plays a pivotal role in improving the quality of life for patients living with diabetes and obesity. With a focus on Market Access initiatives, the team tailors projects to meet the unique requirements of each country, offering exciting growth opportunities. The department thrives on innovation and problem-solving, overcoming challenges and navigating complex regulatory landscapes to deliver insulin and GLP-1 on a global scale. Based in Hyderabad, India, youll join a diverse and dynamic team committed to making a difference.

Job Role : Block Head (Engineering) Grade : Senior Manager Location : Guwahati Experience : 15+ Years (experience in lyophilizer ) Qualification : BE. Instrumentation Overseeing the engineering functions of parenteral block. Coordination with production personnel, contractors & machine manufactures to sort out machine related problems, major and minor modifications for smooth running in process. Tracking and maintaining the critical spares required for preventive and routine maintenance Planning various maintenance schedules and lead the team of engineering to ensure implementation of the schedules with the help of junior sub-ordinates for improving the overall reliability of the equipments. Inspect equipment and components to identify hazards, defects and the need for adjustment or repair to improve overall efficiency of the system and equipment. Provide safe working environment for staff & systems with zero accident. Responsible for sourcing of machine tools consumable parts and related services and interacting with user departments for analyzing the required material. Facing customer audits and taking corrective actions as per audit requirements. Preparing reports on maintenance performance and technical data of various equipments, spare parts, labour and machines for resources planning, budgeting, scheduling & execution of operation and maintenance activities. Executing cost saving and energy saving techniques & modifications to achieve substantial reduction in expenditures and work within the budget. Monitoring & Maintenance of EMS, BMS, Fire Detection and Door Interlock System, Process equipment and machine. Diagnose malfunctioning systems, apparatus and components using test equipment and hand tools to locate the cause of a breakdown and correct the problem. Provide prompt response to user whenever there is a breakdown and resolve the issue as quickly as possible. Ensure that equipments are in good working order so as to prevent disruption of activities during process/production. Keep record of all stock and supplies of all spares, items, instruments and assist the management in forecasting requirements and scheduling expenses to maintain the consumables. Working in collaboration with the production team to formulate the best cost-effective manufacturing process. Attend new training programs in order to increase knowledge of trends and best practices in industry. Support the company in increasing profitability by managing resources efficiently and making necessary recommendations. Handling QMS tools and support team to complete all the action within timeline. Participate in all EHS programs and share all EHS activity to make awareness into sub-ordinates and technicians. Follow GEP in daily work culture in build enhance performance and efficiency of equipment, system and organization Follow GMP practices, schedule and SOPs. Responsible for Calibration, Validation, Qualification Protocol & Reports.