562 Uv Jobs - Page 6

Role Description Work in the areas of water systems and treatment plant evaluation, modelling and design, master planning and project delivery. Design clean and water treatment plants, typical applications being data centres, medical water systems, municipal, industrial, Pharma, and reuse/recycling water systems with payback evaluations. Must have experience working with water treatment technologies such as Membranes, Ion Exchange, CDI, Filtration, Chemical Dosing Systems and UV. Coordinating and adjusting the work effort within the project team to ensure project work is completed on schedule and within allocated budget. Execution of project design (management of resources within constraints of project budget and schedule) and culminating with management of the bid and construction phase engineering service support. Maintain regular and constructive communication with clients and project team members. Simultaneously managing multiple projects and clients. Compiling pre and post project completion documentation to a very high standard Support business development activities Qualifications: Our ideal candidate will be self-motivated with a high level of energy. This individual must be capable of independent and teamwork environments. This position demands an individual with a strong detail-oriented work style, excellent oral and written communication skills, and an accommodating and proactive attitude. Additional qualifications required include: Will have a degree or equivalent qualification in Engineering, Chemical Engineering, Process Engineering, Manufacturing Engineering, Mechanical Engineering, Electrical Engineering or similar. Extensive experience in the design of water treatment systems is essential with design emphasis on the Data Centre, Industrial, Municipal and Pharma sectors being an advantage Excellent technical writing and communication skills. Fluent English speaker with strong speaking skills as the position will require presentations to clients. Must exhibit strong project management skills. Work in a multi-disciplinary team in developing conceptual, feasibility, and final designs for a wide variety of water treatment projects. Strong detail-oriented work style, and an accommodating and proactive attitude. IT literate and proficiency in the use of Microsoft Office including Word, Excel, Powerpoint, Outlook and MS Project Proficiency in the use of 2D/3D CAD and Revit is an advantage

The role of Executive - QC (Stability) at Piramal Pharma Solutions involves conducting stability studies, analyzing samples, preparing reports, and ensuring compliance with regulatory guidelines to maintain product quality throughout its shelf life. You will be working closely with Operations, R & D, QA, and Regulatory affairs teams under the supervision of the QC Supervisor. With a minimum of 3 years of experience in the stability section, you should be a quick learner with excellent communication skills. Punctuality, dedication, and reliability are essential qualities for this role, as well as the ability to work both independently and as part of a team. Proficiency in written and spoken English is required, along with knowledge or experience in peptides. Your responsibilities will include working in the stability section, handling instruments such as HPLC, UV, Culometer, KF-titrator, LCMS, conducting stability sample analysis, managing stability chamber, and utilizing software like Lab solutions, Empower, DMS, and Ensur. The ideal candidate for this position should hold an MSc in Chemistry and be committed to inclusive growth and ethical practices. Piramal Group values equal employment opportunities and makes decisions based on merit, ensuring that all applicants and employees are treated fairly and have equal access to recruitment, training, promotion, compensation, and working conditions. Piramal Pharma Solutions (PPS) is a Contract Development and Manufacturing Organization (CDMO) providing end-to-end solutions across the drug life cycle. As part of a global network with facilities in North America, Europe, and Asia, PPS offers a wide range of services including drug discovery, process development, clinical trial supplies, commercial supply of APIs, and finished dosage forms. Specialized services such as highly potent APIs, antibody-drug conjugations, and biologics are also offered, making PPS a trusted partner for innovators and generic companies worldwide. This full-time position is based in Piramal, Thane, Maharashtra, 400703, IN and requires a Master's Degree qualification. If you are passionate about maintaining product quality through stability studies and analysis while upholding ethical standards and values, we invite you to join our team at Piramal Pharma Solutions.,

Quality Control (QC) Officer required for reputed organisation in Vadodara (Gujarat) location Dear Professionals,, I am Sindhura C , from the Pharma Vertical of Masadir HR Services , an International Recruitment Firm. We have been retained by professionally managed organisation to recruit Quality Control (QC) Officer for them. The job location is in Vadodara (Gujarat). Qualification: Bsc/Msc Experience: Min 2 yrs Must experience in HPLC instrument like- Agilent HPLC, Shimadzu HPLC, Agilent GC,UV) If you are interested in exploring the above opportunity, kindly share your updated resume with me please. In case, if you are not interested, kindly feel free to refer your friends who may be interested in this. Looking forward to hearing from you soon. Thank you! Have a great day! Warm Regards, Sindhura C Associate| Global Talent Acquisition Operations | India Mobile/ WhatsApp : +91 6282564376 Email Id: sindhura.c@masadirservices.com www.masadirservices.com

Candidate should have knowledge of handling and troubleshooting the sophisticated Analytical Instruments like HPLC, GC, IR, UV, KF ETC . Also He should be able to work, adopt and guide subordinates in following Good Laboratory Practices. He should be well versed with various regulatory & Statutory requirements. Candidate Profile: Should have minimum Four years experience. He should be able to work with the team and be willing to take initiative & challenge for completing the task assigned.

Candidate should be from API industry having knowledge of handling & troubleshooting of sophisticated Analytical Instruments. like HPLC, GC, IR, UV, KF ETC He should be able to work, adopt and guide subordinates and juniors in following Good Laboratory Practices. He should be well versed with various regulatory & Statutory requirements should be able to face regulatory and customer audits independently. Candidate Profile: Should have minimum 10 years experience including minimum 3 years as Deputy Manager. He should be able to guide the team for completing the task assigned. Also should be able to complete task timely assigned by the management

The ideal candidate should possess strong communication skills and be well-versed in analytical techniques such as HPLC, GC, IR, UV, and Wet analysis.,

Long Description 1. Perform characterization of peptides , nucleic acids-based (oligonucleotides) or other injectable drug products using High Resolution Mass Spectrometry (LC-HRMS) . Experience with QToF/Orbitrap instruments and Ion Mobility will be preferred. Additional experience in Fluorescence, particle size analysis (DLS), and other relevant techniques (e.g. SEC-MALS) are desirable. 2. Analyze and interpret LC-MS and MS/MS data for impurity profiling and characterization. Solve problems and implement new research methods through literature search, coordinate with cross-functional teams (formulation, QA, QC, regulatory, etc.), application specialists, etc. to complete analytical tasks. 3. Prepare, review and share LC-MS data and documentation (SOP, STP, Test Reports, etc.) in a timely manner for regulatory submissions. Follow good laboratory practices (GLP) , manage samples (collection, storage, and disposal), deviations and incidences as per established procedures. 4. Undertake routine maintenance & calibration of the analytical instruments, troubleshoot equipment malfunction often in coordination with service engineers, etc. Assist in the maintenance of the laboratory, inventory of R&D consumables, & other lab management activities from time to time Competencies Education Masters in Pharmacy or Applied Chemistry Doctorate in Pharmaceutical Technology or Analytical Chemistry Work Experience 5 – 7 years (with MPharm) or NIL (with PhD)

Job Requirements TITAN COMPANY LTD Watch Division \u2013 ISCM Job Title Trainee MED lab Education Bsc -Chemistry Fresher Location Watches Division ISCM - Hosur Department Material engineering department Reports To Head \u2013 Material engineering department 1. Scope of the role 1)Role primarily involves handling basic chemical techniques, preparing samples and reagents, conducting routine quality checks, and ensuring that all tests comply with regulatory and company standards. 2)Providing necessary support in the day-to-day operations of the laboratory. 2. Job Profile Testing Assist in conducting routine chemical tests on raw materials, electroplated and Ion plated products. Prepare reagents, standard solutions, and samples for analysis. Operate basic laboratory instruments such as pH meters, titration setups and analytical balances. Record and maintain test results and ensure accurate documentation. Maintain 5S and orderliness in the lab. Precious metal recovery Assist in chemical leaching, filtration, and metal precipitation processes. Collect, weigh, and label samples for lab analysis. Operate basic equipment such as furnaces, fume hoods, filtration units, and balances. 3. Key Deliverables Execution of routine analytical tests and reporting. Support in maintaining test records, logs, and calibration reports. Effective collaboration with QA/QC teams. 4. Skills required Strong knowledge in chemistry & attention to detail. Ability to work in chemical-handling environments. Proficiency in MS Office (Word, Excel) is an advantage.

Work with Us. Change the World. At AECOM, we're delivering a better world. Whether improving your commute, keeping the lights on, providing access to clean water, or transforming skylines, our work helps people and communities thrive. We are the world's trusted infrastructure consulting firm, partnering with clients to solve the world’s most complex challenges and build legacies for future generations. There has never been a better time to be at AECOM. With accelerating infrastructure investment worldwide, our services are in great demand. We invite you to bring your bold ideas and big dreams and become part of a global team of over 50,000 planners, designers, engineers, scientists, digital innovators, program and construction managers and other professionals delivering projects that create a positive and tangible impact around the world. We're one global team driven by our common purpose to deliver a better world. Join us. Serves as lead engineer on mid- to large size projects. Provides specialized technical input to studies and design for staff's specific area of expertise. Approves and signs off on work. Provides technical expertise for studies and design efforts. Presents complex technical solutions to clients. Performs quality control reviews of work developed by others. Participates in development of technical proposals. Provides estimates for the engineering budget and schedule to meet requirements on large projects. Additional Information

As a Fortune 50 company with more than 400,000 team members worldwide, Target is an iconic brand and one of America's leading retailers. Joining Target means promoting a culture of mutual care and respect and striving to make the most meaningful and positive impact. Becoming a Target team member means joining a community that values different voices and lifts each other up . Here, we believe your unique perspective is important, and you'll build relationships by being authentic and respectful. Overview about TII At Target, we have a timeless purpose and a proven strategy. And that hasnt happened by accident. Some of the best minds from different backgrounds come together at Target to redefine retail in an inclusive learning environment that values people and delivers world-class outcomes. That winning formula is especially apparent in Bengaluru, where Target in India operates as a fully integrated part of Targets global team and has more than 4,000 team members supporting the companys global strategy and operations. Digital Strategy & Platform Right along with Targets distinctive retail brand, we are constantly improving and innovating our digital shopping experience. Are you ready to excel in the fast-changing retail environmentAre you a customer service enthusiast whos curious about the guest and can see the shopping journey through their eyesThen youll have success on the Digital Strategy & Platform team, whose goal is to offer guests a seamless online shopping experience across our platformsincluding Target.com and the store networks fulfillment capabilities. Here, youll collaborate to create and implement the digital strategies that enrich the online experience through the right mix of personalization, simplicity and intuitiveness. Your ideas will support Target in complementing the beloved in-store shopping interaction with a convenient, reliable and instantly gratifying digital experience. The Category Site Merchandising team focuses on increasing digital topline sales by optimizing conversion and the overall site experience. The team plays a crucial role in ensuring findability and discoverability of products, making it easy for guests to locate and discover items. By partnering with various teams within and outside of the Digital organization, the team drives the right experience for each category. Additionally, the team is responsible for delivering financial outcomes and plans for the digital business, ensuring that financial goals are met and sustained. As Senior Manager, Site Merchandising Category you will develop and lead teams to drive digital business growth through the development of effective site merchandising strategies for your categories. Your focus will be on leading your team to optimize the site experience to maximize guest engagement and sales. You will collaborate closely with cross-functional teams to ensure seamless execution of category strategies and alignment with business goals. Your leadership will be crucial in translating business objectives into actionable site merchandising tactics that enhance the digital shopping experience. Core Responsibilities: Category Digital Strategic Planning and Execution . Develop cohesive digital strategies for several categories and mobilize the team to execute those strategies, in close partnership with Merchandising, Marketing, Product/Technology, Operations, and Item partners. Key responsibilities included but are not limited to: Category Digital StrategyResponsible for partnering with merchant leaders to develop and prioritize initiatives to best drive category goals. Core Site MerchandisingImplement and optimize site merchandising strategies that focus on conversion, findability, maximizing guest engagement, and frictionless shopping. Senior Managers both set the vision for the category and work with the team to operationalize that vision within their team and by influencing across multiple partner teams. Analytics: Monitor, understand, and utilize data and key metrics from multiple and varied sources (devices and platforms, guest behavior, market trends, and competitive insights) to optimize short-term performance and to inform long-term strategies. Provide in-depth reporting and insights to partner teams and identify & highlight performance opportunities. Results & Financial Accountability: Maintain a strong sense of accountability for delivering financial results, ensuring strategies drive topline sales, profitability, and guest engagement. Team Leadership: Lead, mentor, and develop a team of site merchandisers, providing development, coaching, motivation, support, and feedback. Promote and model key Target behaviors. Champion diversity and inclusion. Create an atmosphere of teamwork, collaboration, agility, attention to detail, and drive. Cross-Functional Leadership: Establish strong cross-functional and cross-channel partnerships across Target. Influence and leverage other teams within the broader organization to advance digital objectives. Quarterly Planning and Activation Own & drive cross-functional category roadmap based on guest insights & business needs. Streamline processes, manage project timelines, and resolve operational challenges to improve task execution and efficiency. Core responsibilities of this job are described within this job description. Job duties may change at any time due to business needs. About You: 4 year college degree or equivalent experience 8+ years e-commerce experience Deep business acumen with an entrepreneurial, revenue-generating mindset Must have both strong technical acumen and a passion for customer experience Excellent understanding of mass merchandising, retail, e-commerce and multi-channel retailing Demonstrated experience in strategic and cross-functional influence, planning and execution High level of initiative and organization, with the ability to manage ambiguity, risk, uncertainty and changing directions Demonstrated experience in team leadership, with a personal interest in development Strong analytical and quantitative skills, including financial and business metrics Strong written and verbal communication skills with the ability to present to varying levels of leadership Demonstrate a deep understanding of e-commerce principles and the full customer journey funnel, to optimize site performance and enhance the digital shopping experience Experience in leading large-scale projects, track deliverables, allocate resources, and ensure alignment with strategic objectives Useful Links- Life at Target- https://india.target.com/ Benefits- https://india.target.com/life-at-target/workplace/benefits Culture- https://india.target.com/life-at-target/belonging

Aforeserve Technologies Pvt Ltd (XtraCover) is looking for Quality Control Executive (QC) to join our dynamic team and embark on a rewarding career journey Assist in quality control tasks and activities. Develop and implement quality control policies and procedures. Monitor and report on quality control performance metrics. Collaborate with quality control teams and stakeholders. Ensure compliance with quality control standards and regulations.

NOTE: Only Male & Candidates from AP & Telangana Preferred. Kindly Understand the JD It's not for the Clinical Trails Department 2Years Bond & Need to Submit your 10th Original Mark list with us during the Bond Period. Qualifications required: Bachelors / Masters in Pharmacy, Msc Chemistry/Organic Chemistry Role and responsibility: In process quality control of ongoing studies. Review of raw data, chromatograms and reports of the method validations and studies. Checking of all the instruments and equipments for the calibration status and appropriate labeling. Checking and monitoring of the day-to-day activities in the lab for compliance to SOPs and GLP principles. Checking of the concentration data of subject samples before releasing to PK department. Generation, control and distribution of method SOPs. Logbook handling and archival of the completed logbooks. Performing the routine glassware validations and monitoring of the temperature and humidity in the Bio-analytical lab. Calibration of pipettes and multipedes. Coordinating for training programs on SOPs. Ensure cleanliness of laboratory and disposal of non-bio-waste & Bio-waste.

QC Role & responsibilities : Handling of QC instruments, Such as HPLC, GC, UV, FTIR, Dissolution Apparatus, Melting point, Karl Fischer apparatus, Auto titration, Analytical weighing Balance, Polari meter, Disintegration Apparatus, pH Meter etc. Analysis of In process, validation, Hold time study, finished products and stability samples according to related specifications Daily as well as monthly calibration of analytical balance of instrumentation section To maintain the daily logs adhering to the Good Laboratory Practices. Daily standardization of Karl Fischer reagent. Daily temp recording of instrumentation room, chemical room & refrigerator. Daily preparation of 0.4% NaoH for discarded penicillin sample deactivation. Regular, online analysis of cleaning (Rinse & swab) samples. QA Role & responsibilities : Execute and review Equipment Qualification protocols (IQ, OQ, PQ) in compliance with regulatory requirements. Prepare, execute, and review Cleaning Validation protocols and reports. Participate in the design, execution, and documentation of Computer System Validation (CSV) as per GAMP 5 guidelines. Coordinate and support Process Validation activities, including preparation and review of protocols, execution, and final reporting. Ensure that all validation activities are compliant with cGMP, regulatory guidelines, and internal SOPs. Perform gap assessments, risk assessments, and deviation handling related to validation. Collaborate with cross-functional teams including production, engineering, QC, and IT for validation planning and execution. Assist in internal audits, regulatory inspections, and prepare responses to audit observations. Maintain and update validation master plans and SOPs regularly.

Role & responsibilities Operate and maintain QC instruments, including HPLC, GC, UV, FTIR, Dissolution Apparatus, Melting Point Apparatus, Karl Fischer Apparatus, Auto Titration, Analytical Weighing Balance, Polarimeter, Disintegration Apparatus, pH Meter, etc. Perform analysis of in-process samples, validation, hold-time study, finished products, and stability samples as per relevant specifications. Conduct daily and monthly calibration of analytical balances in the instrumentation section. Maintain daily logs and ensure adherence to Good Laboratory Practices (GLP). Perform daily standardization of Karl Fischer reagent. Monitor and record daily temperature readings of the instrumentation room, chemical room, and refrigerator. Prepare 0.4% NaOH solution daily for the deactivation of discarded penicillin samples. Conduct regular and online analysis of cleaning (rinse & swab) samples Preferred candidate profile Hands-on experience with laboratory instruments and analytical techniques. Knowledge of GLP, GMP, and regulatory guidelines. Strong documentation and record-keeping skills. Ability to work in a fast-paced, compliance-driven environment. Attention to detail and problem-solving skills.

Role & responsibilities 1. Knowledge of calibration and operation of HPLC with empower software. 2. Sound knowledge of analytical method development and Analytical method validation of OVI, purity, and assay method by HPLC as per pharma guidelines. 3. Knowledge of caliberation and operations of all equipments like balance, ph meter, in analytical opeartion. 4. good knowledge of sample preperation as per GLP. 5. Knowledge of retreival and storage working standards and columns. 6. Handling of final compilation of raw data, chromatographic data complying with GLP requirements. 7. Recording all analytical activities, approximately in respective raw data forms. 8. knowledge of preperation of general lab SOPs and instrument sops. Desired candidate profile: 1. Must have worked analytical lab. 2, Knowledge of HPLC,

Role & responsibilities Preferred candidate profile Perks and benefits

Job Track Description: Performs tasks based on established procedures. Uses data organizing and coordination skills to perform business support or technical work. Requires vocational training, certifications, licensures, or equivalent experience. General Profile Requires limited prior training or licenses and training certifications. Has basic operational or analytical skills to perform tasks. Works within clearly defined standard operating procedures and adheres to quality guidelines. Work is completed with close supervision and under clearly defined procedures. Functional Knowledge Requires a basic understanding of theories, practices, and procedures. Business Expertise Understanding of how best teams integrate and work together to achieve company goals. Impact Responsible for the accuracy of own work. Receives close supervision and duties are clearly defined. Methods and tasks are described in detail. Leadership Has no supervisory responsibilities. Problem Solving Uses existing procedures to solve standard problems. Has limited opportunity to exercise discretion. Interpersonal Skills Exchanges information and ideas effectively. Responsibility Statements Maintains employee records through data entry. Performs calculations for outstanding payments due on termination or leave of absence. Coordinates termination details to ensure assets are returned/access is revoked on the employee\u2019s last day. Compiles data for review and reporting. May perform routine analysis for internal review. Performs other duties as assigned. Complies with all policies and standards. Conduent is an Equal Opportunity Employer and considers applicants for all positions without regard to race, color, creed, religion, ancestry, national origin, age, gender identity, gender expression, sex/gender, marital status, sexual orientation, physical or mental disability, medical condition, use of a guide dog or service animal, military/veteran status, citizenship status, basis of genetic information, or any other group protected by law. People with disabilities who need a reasonable accommodation to apply for or compete for employment with Conduent may request such accommodation(s) by submitting their request through this form that must be downloaded:click here to access or download the form. Complete the form and then email it as an attachment toFTADAAA@conduent.com.You may alsoclick here to access Conduent's ADAAA Accommodation Policy. At Conduent we value the health and safety of our associates, their families and our community. For US applicants while we DO NOT require vaccination for most of our jobs, we DO require that you provide us with your vaccination status, where legally permissible. Providing this information is a requirement of your employment at Conduent.

Organica Water is looking for Project Engineer to join our dynamic team and embark on a rewarding career journeyPrepare, schedule, coordinate, monitor and control the assigned engineering projects.Monitor compliance to applicable codes, practices, QA/QC policies, performance standards and specifications.Cooperate and communicate effectively with the client and project team.Functional planning and execution of particular work packages within the given parameters.Implementing Project driven changes and requests.Evaluation of customers specifications.Ability to lead multiple projects and partner with management / functional managers to resolve conflicts and obtain resources for project.Excellent interpersonal, leadership and negotiation skills

SUMMARY Job Title: UV Printing Machine Technician Job Summary: We are seeking a skilled UV Printing Machine Technician with a minimum of 5 years of hands-on experience in the Gulf region . The ideal candidate will have a strong background in operating and maintaining UV printing equipment and a solid understanding of graphic design principles. Practical experience is valued more than formal qualifications. Key Responsibilities: Operate and maintain UV printing machines with precision. Troubleshoot and resolve mechanical and printing-related issues. Collaborate with the design team to ensure high-quality output. Execute printing tasks for various materials as per design requirements. Ensure timely delivery and quality standards are consistently met. Requirements Minimum 5 years of Gulf experience in UV printing or related field (mandatory). Strong understanding of graphic design principles. Hands - on experience with UV printing technology and equipment. Experience preferred over formal degrees. Ability to work independently and meet tight deadlines. Benefits Accommodation provided. Weekly working hours: 78 hours. Weekly day off: 1 day. Languages required: English and Arabic. Salary: Based on experience and qualifications.

As a Senior Executive - Chemistry in the Quality Control department at Zydus Pfizer located in Ahmedabad, your role will require you to have a Bachelor's degree in Pharmacy or a Master's degree in Chemistry along with 2 to 4 years of relevant experience. Additionally, experience within Zydus for a minimum of 12 to 24 months is preferred. Your responsibilities will include hands-on experience with GMP/GLP/GDP/Data integrity ALCOA+ practices and the operation and calibration of various Wet chemistry techniques such as IR, UV, pH, KF, Polarimeter, and LPC. You will also be expected to handle operations, sample analysis, method validation, calibration, and troubleshooting of HPLC systems from Agilent and Shimadzu. Proficiency in basic computer applications like Word, Excel, and PowerPoint is essential for this role. In terms of behavioral skills, you should be self-motivated with basic problem-solving abilities. Your administrative skills should encompass being proactive, effective time management, and a collaborative approach towards working with team members. Excellent communication skills, both written and verbal, are crucial for this position to ensure seamless coordination within the team and across departments.,

Role & responsibilities Regular & development Analytical support for R&D projects Method development using HPLC & GC Should Handle Instruments (HPLC, GC, IR, UV, KF & Potentiometer) independently. Preferred candidate profile Exposure to handle analytical equipments like GC, HPLC, KF, Potentiometer, IR & UV. Basic knowledge on ICH guidelines. Good Development Knowledge Awareness of Industry practices in Analytical domain. Basic regulatory knowledge.

Role & responsibilities : ITI/ Diploma Electrical or Instrumentation with valid license. Minimum 4+ years of experience Handling machines involved in Manufacturing and packing of FMCG ie. Tube filling machines, encapsulation & soft gel , tablets & capsules . Knowledge in reading P&ID , Datasheets , wiring drawing of Electrical and Instrumentation circuits . Experience on induction motors , servo motors and stepper motors Trouble shooting and installation of VFD , Servo drives and conventional starters. Experience on control valves and ON/OFF valves involved in PID loops. Hands on experience in UV and Inkjet printers involved in coding . Experience on PLC and servo drives. Basic instrumentation knowledge with respect to transmitters , sensors and measuring devices. Preferably work experience is required in Pharmaceutical formulation plants / FMCG plants / Food packing industries. Able to carry Scheduled / breakdown maintenance with documentation. Strictly adhering to company GMP , GDP and safety policies.

Long Description 1 Exposure of execution of planning of Inprocess, Finished product, stability and cleaning validation samples of MDI / DPI formulation. 2 Exposure of compliance to all cGMP, GxP or any other regulatory requirements, including EHS requirements. 3 Maintenance of GLP in the Laboratory. 4 Having knowledge of Analytical Instruments like HPLC, GC, GCMS, LCMS, UV, IR, KF, ACI, NGI, DUSA, Spray Pattern etc. 5 Exposure of Laboratory investigation like OOS, OOT, Incidence, Deviation, CAPA, Change control etc. 6 Exposure of Stability sample management & Regulatory Audits. 7 Exposure of Analytical method transfer, Analytical method validation / Verification activity. 8 Exposure of Calibration of Analytical Instruments & Equipment’s 9 Compliance to observation noted during internal and external audits. Competencies Strategic Agility Process Excellence Collaboration Innovation & Creativity Result Orientation Stakeholder Management Customer Centricity Developing Talent Education Graduation in Pharmacy Work Experience 10 to 15 years.

Long Description Annual maintenance contract preparation and preventive maintenance of QC instrument as per approved procedure. Breakdown handling of QC instrument as per approved procedure. Upkeep the records for preventive maintenance and breakdown in SAP. Qualification of New instruments with complete documentation. To participate in failure investigations related to instrument malfunctions. To impart training to the analysts for instrument maintenance and troubleshooting. Co-ordination with service engineer for service/ breakdown related activities To maintain good laboratory practices and discipline in respective work area. Actively taking part in cGMP, training and SOP training as and when required. Supporting for calibration and validation activity of Thermolab Make instruments. Competencies Innovation & Creativity Result Orientation Collaboration Customer Centricity Developing Talent Stakeholder Management Strategic Agility Process Excellence Education Graduation in Instrumentation Work Experience 5 to 7 years

To follow safety rules in the premises according to the company norms. Operation and Cleaning of glove integrity and filter integrity testers. Responsible to perform the in process checks during operation. Responsible for Dispensing, checking and receiving of PPM from warehouse on need basis. To ensure cleaning and storage of change parts as per the procedures. To maintain the BMRs and other log books in the compounding area as per cGMP and SOP Cleaning and maintenance of compounding area as per GMP and SOP Operation and cleaning of dynamic pass box in compounding area Responsible for Cleaning and sanitization of drain points in compounding area Responsible for manufacturing and supervising of Media fill and Drug products batches as per BMR To carry out CIP & SIP of the vessels related to compounding and flitration area. Responsible for operation, calibration and cleaning of weighing balance, pH meter, DO meter and conductivity meter, Compounding isolator, Manufacturing and filtration vessels, Heating & cooling skid, Air shower. Table mounted LAF and ceiling mounted LAF, Filter integrity tester, Sonicator , TFF, Homogenizer, Lipid extruder, Fogger, Heating magnetic stirrer with thermometer, SART system, Strip chart recorder Preparation and periodic revision of SOPs related to compounding area. Responsible for the co-ordination with cross functional departments like QA,QC, warehouse Engineering, HR and administration for the day to day activities. Activities other than defined in the job responsibility are to be done, as per the requirement of HOD, by following HODs instructions and guidance.