87 Media Preparation Jobs - Page 2

Job Description: We are looking for a dynamic and detail-oriented professional with hands-on experience in upstream processing for biologics, biosimilars, and monoclonal antibodies (mAbs) to join our R&D team. The ideal candidate will work in a fast-paced, innovation-driven environment and contribute significantly to upstream bioprocess development activities. Key Responsibilities: Work in a vibrant R&D setup focused on analytical research for mAbs/biosimilars/biologics. Operate bioreactors (1L, 10L and above) with strict adherence to sterile practices, ensuring zero contamination and batch failures. Prepare media, feeds, and buffers with precision, ensuring sterile conditions via filtration and/or autoclaving. Handle various filtration techniques and sterile transfer of media and feeds. Perform Cleaning-In-Place (CIP) and Sterilization-In-Place (SIP) of bioreactors and ensure equipment is ready for use at any time. Ensure timely calibration, maintenance, and troubleshooting of instruments and equipment to avoid workflow interruptions. Learn and handle gel electrophoresis techniques, aiming for accurate and reproducible results. Perform cleaning and sterilization of lab glassware and materials using autoclave and dry heat methods. Learn and execute protein expression analysis techniques such as SDS-PAGE, Western blotting, and ELISA. Understand both upstream and downstream processes and support cross-functional activities accordingly. Maintain sufficient stock of chemicals, glassware, consumables, and other lab essentials to ensure uninterrupted workflow. Raise material requisitions as needed and ensure timely procurement to avoid delays. Prepare daily work reports and submit documentation to the reporting manager as required. Collaborate effectively with internal teams (e.g., STBI, Purchase, IT, HR) to meet project goals without conflict.

Note ; Required only male candidates. 1. Microbiologist Position - Required Qualification : M.Sc.; B.Sc. in Microbiologist. Media preparation and daily monitoring. Ensure regular calibration of all quality measuring equipment. General lab hygiene check, Temperature charts, checklists, overall cleanliness Ensure activities of Microbiology and in- process trials etc. Documentation (customer wise) & SOP preparation. Representing Quality function in daily operation meetings. Ensuring environment safety by controlling pathogen in air, water, discard criteria and waste 12 disposed and regular auditing to avoid near miss. 13 Ensure that daily waste is discarded according to SOP of Microlab. Ensure Testing of incoming raw material, as per SOP /FSSR. Sign off to CoA/CoCs 2. Position: Officer/Sr. Officer (FG Analyst) 1. Good Analyst validation, RM verification 2. Analytical Approach 3. Accountability for Achievement 4. Sensory, Physical and Chemical Analysis 5. RM SOP, Specification, TAT 6. Good Knowledge of HACCP, QMS, GMP, GHP, GLP, GDP. 7. 1-3 Minimum Years of experience in FMCG/Manufacturing/Food processing etc. 3. Executive (FSMS) Qualification : - B.Sc./ M.Sc./B.Tech/ M- Tech/Diploma- Food Technology, Food Science & Microbiology 1. Good Knowlodage of HACCP,QMS, GHP, GMPVACCP & TACCP 2. Accountability for Achievement 3.Updated knowladage of Food Safety Management System Documents/SOP, manual, policies and amendments 4. Better Coordination for customer audits & GFSI audits 5.Drive Risk Assessment/ RCA/CAPA 6. Good Knowledge of FSSC, BRC, HALAL, KOASER

Note ; Required only male candidates for microbiologist. 1. Microbiologist Position - Required Qualification : M.Sc.; B.Sc. in Microbiologist. Media preparation and daily monitoring. Ensure regular calibration of all quality measuring equipment. General lab hygiene check, Temperature charts, checklists, overall cleanliness Ensure activities of Microbiology and in- process trials etc. Documentation (customer wise) & SOP preparation. Representing Quality function in daily operation meetings. Ensuring environment safety by controlling pathogen in air, water, discard criteria and waste 12 disposed and regular auditing to avoid near miss. 13 Ensure that daily waste is discarded according to SOP of Microlab. Ensure Testing of incoming raw material, as per SOP /FSSR. Sign off to CoA/CoCs 2. Position: Officer/Sr. Officer (FG Analyst) 1. Good Analyst validation, RM verification 2. Analytical Approach 3. Accountability for Achievement 4. Sensory, Physical and Chemical Analysis 5. RM SOP, Specification, TAT 6. Good Knowledge of HACCP, QMS, GMP, GHP, GLP, GDP. 7. 1-3 Minimum Years of experience in FMCG/Manufacturing/Food processing etc. 3. Executive (FSMS) Qualification : - B.Sc./ M.Sc./B.Tech/ M- Tech/Diploma- Food Technology, Food Science & Microbiology 1. Good Knowledge of HACCP,QMS, GHP, GMPVACCP & TACCP 2. Accountability for Achievement 3.Updated knowledge of Food Safety Management System Documents/SOP, manual, policies and amendments 4. Better Coordination for customer audits & GFSI audits 5.Drive Risk Assessment/ RCA/CAPA 6. Good Knowledge of FSSC, BRC, HALAL, KOASER

Role & responsibilities Responsible for cell revival, subculture, cell counting of MRC-5 cells. Preparation of MCB/WCB. Experience in Preparation of media and in process buffers in media mixing vessels. Experience in handling Roller bottles, Cell stacks, TCFs. Experience in working in GMP conditions / production department of viral vaccines. Preparation of SOP, BMR’s, Protocols related to cell culture / virus culture. Experience in virus infection, virus harvesting procedures. Experience in working with Chicken embryo fibroblast cells, pooling of embryos, seeding of RB’s . Preparation of Media, in process solutions using preparation vessels. Preferred candidate profile Candidate should have experience in Cell Culture vaccine 6 days work from office based at Ahmedabad

1. Microbial Testing MLT and Pathogens 2. Environmental Monitoring- Clean room viable and non-viable particle counts 3. Water Testing - specific pathogens. 4. Documentation and reporting as per GDP

Perform routine Environmental Monitoring activities: viable and non-viable monitoring, surface monitoring, personnel monitoring. Good knowledge of cleanroom classification (ISO 14644), Good Manufacting P and EM requirements Ability to prepare and execute validation protocols and summarize reports Skilled in microbial monitoring techniques and aseptic area behaviour. Strong documentation, audit readiness, and data integrity practices

Job Title: Proposal Engineer Location: Pune Department: Engineering Reporting To: Head of Office Pune Domain: Water and Wastewater Treatment Key Responsibilities: Design and prepare proposals for Sewage Treatment Plants (STPs) ranging from 5 KLD to 5 MLD , using technologies such as: Fixed Bed MBBR (Moving Bed Biofilm Reactor) MBR (Membrane Bioreactor) ASP (Activated Sludge Process) Design and cost estimation of Pre-treatment and Tertiary Treatment units including: Ultrafiltration (UF) Reverse Osmosis (RO) Chlorination systems Design of Sludge Handling and Dewatering Plants . Prepare technical and commercial proposals as per client requirements and tender specifications. Selection and sizing of equipment, preparation of P&ID, technical BOQ, and coordination with vendors. Maintain excellent knowledge and network with vendors for key components such as: Pumps, Blowers, RO/UF Membranes Media Suppliers Dosing Packages, Screw Presses Instrumentation and Automation components Candidate Requirements: Education: B.Tech / B.E in Chemical Engineering Experience: 5 to 8 years of relevant experience in design/proposal engineering in water and wastewater treatment projects. Skills: Strong knowledge of wastewater treatment technologies and systems Proficiency in MS Office , Excel , PowerPoint Good communication and documentation skills Ability to manage multiple proposals and deadlines Preferred Gender: Male CTC: Salary is not a constraint for deserving candidates

We are currently seeking an Assistant Manager to join our Digital Transformation team. Key Qualifications: Proficiency in Macros, Python, SQL and GPT technologies is essential. Familiarity with ERP systems and WordPress is a plus. Strong analytical skills and a willingness to learn new technologies. Understanding of Machine Learning, Alteryx, and related tools is advantageous. Excellent communication and interpersonal skills. Strong work ethic and ability to collaborate effectively within a team. If you are passionate about leveraging technology to drive innovation, we encourage you to apply. Educational Qualification Bachelors degree in Computer Science, Information Technology, Data Science, or a related field. Relevant certifications in programming or data analysis are a plus.

The CSSD Technician is responsible for the effective sterilization and disinfection of surgical instruments and medical equipment. This role involves preparing, sterilizing, and ensuring the safe handling of instruments to maintain the highest standards of hygiene and safety within the hospital environment. The technician will also be responsible for the quality control of sterilization processes and will work closely with various departments to support surgical procedures. Roles and Responsibilities - Clean, decontaminate, and sterilize instruments and medical equipment using appropriate methods and technologies. - Ensure the proper functioning of sterilization equipment and report any malfunctions. - Monitor and maintain sterilization logs and quality assurance records. - Prepare and package instruments for surgery, following established protocols. - Collaborate with surgical teams to meet instrument and equipment needs during procedures. - Follow infection control standards and safety protocols to prevent contamination. - Conduct routine checks and maintenance of CSSD supplies and inventory management. - Participate in ongoing training and professional development related to sterilization techniques and infection control practices. Skills Required: - Knowledge of sterilization techniques, principles of infection control, and safety standards. - Familiarity with surgical instruments and medical equipment. - Attention to detail and strong organizational skills. - Ability to work under pressure and manage time effectively. - Excellent communication and teamwork skills. - Analytical skills to monitor sterilization processes and troubleshoot issues. Tools and Equipment: - Autoclaves and sterilization equipment. - Decontamination tools and instruments. - Personal protective equipment (PPE). - Inventory management software. - Quality control systems and logging tools.

Responsibilities: * Manage budget & resources effectively * Ensure compliance with safety protocols * Oversee laboratory operations & staff development * Collaborate with R&D team on project planning & execution

Job Title: Research Assistant Quality Control (QC) Department: Quality Control Location: Noida Company: Advancells Group Salary Range: 25,000 - 40,000 per month Preference : Male Candidate, Immediate Joiner About Advancells Group: Advancells is a pioneering leader in stem cell manufacturing and regenerative medicine. Our mission is to bring cutting-edge biomedical science into practical application for patient well-being and healthcare innovation. As part of our growth, we are hiring passionate professionals to join our Quality Control team. Role Overview: We are looking for a committed and detail-oriented Research Assistant QC to support on-site quality control operations, microbiological testing, and packaging inspection activities. The role will involve hands-on testing, documentation, and collaboration with the production team to uphold product quality and GMP compliance. Key Responsibilities: Perform microbiological testing on raw materials, in-process samples, and finished goods. Conduct Sterility Testing and Bacterial Endotoxin Testing (BET) as per pharmacopeial and SOP standards. Execute and record Quality Control checks for product packaging and labeling. Support in-process quality checks on production floor to ensure hygiene and GMP adherence. Conduct visual and physical inspections for finished product quality parameters. Perform routine environmental monitoring , cleanroom checks, and personnel hygiene audits. Assist in line clearance activities before and after batch production. Participate in root cause analysis of non-conformities, especially related to packaging or contamination issues. Ensure Good Documentation Practices (GDP) while recording observations and test results. Be available for on-site physical tasks such as sampling, validations, and quality checks during production. Support field activities such as transporting samples, overseeing external testing, and maintaining sample integrity. Candidate Requirements: Qualification: M.Sc. in Microbiology / Biotechnology / Life Sciences (preferred) Experience: 13 years in QC/QA roles within pharmaceutical, biotech, or stem cell environments. Strong understanding of GMP, GDP, and QC protocols . Hands-on experience in microbiological testing and working in cleanroom environments . Good interpersonal skills and ability to coordinate with production and documentation teams. Immediate joiners will be given preference. Why Join Us? Be part of India's leading organization in regenerative medicine. Work in a GMP-certified lab environment with world-class QC standards. Growth opportunities in a fast-evolving biomedical industry. How to Apply: Send your updated resume to hr@advancells.com with the subject line: Application for Research Assistant QC . Immediate joiners will be prioritized.

Greetings from Apitoria Pharma Private Limited (100% Subsidiary of Aurobindo Pharma Limited) Hiring for QC(Microbiology) - API Division - Visakhapatnam, Andhra Pradesh. Exp: 2 - 4 Yrs Qualification: M.Sc. (Microbiology / Biotechnology) Roles and Responsibilities Conduct microbiological testing of raw materials, in-process samples, and finished products to ensure compliance with quality standards. Perform environmental monitoring in clean rooms and controlled environments to detect potential contamination. Prepare media for culturing microorganisms, perform plate counting, and analyze results to identify trends and patterns. Participate in validation activities such as water system qualification, equipment qualification, and process validation. Maintain accurate records of test data, reports, and certificates of analysis.

The Senior Nurse - OT at Manipal Hospitals will be responsible for providing high-quality patient care in the operating theatre. This role involves assisting surgeons during procedures, ensuring a sterile environment, and monitoring patients' vital signs preoperatively and postoperatively. The Senior Nurse will also oversee and mentor junior nursing staff, collaborate with healthcare professionals to implement patient care plans, and maintain accurate patient records. The ideal candidate should be proactive in educating patients and their families about surgical procedures and aftercare. Roles and Responsibilities About the Role: As a Senior Nurse-OT at Manipal Hospitals, you will play a crucial role in ensuring the smooth operation of the operating theatre. Your expertise will be vital in delivering high-quality care to patients undergoing surgical procedures. You will work closely with surgeons and other healthcare professionals to maintain a safe and efficient environment. About the team: You will be part of a dedicated team of healthcare professionals committed to providing exceptional perioperative care. The team consists of skilled surgeons, anesthetists, and fellow nursing staff who collaborate to deliver the best patient outcomes. A supportive culture encourages continuous learning and professional development. You are Responsible for: - Preparing the operating room and ensuring all necessary equipment and instruments are sterile and ready for use. - Assisting the surgical team during procedures, providing necessary support and anticipating needs. - Monitoring patients' vital signs and providing post-operative care to ensure their comfort and safety. - Maintaining accurate and detailed records of patient information and surgical procedures. To succeed in this role – you should have the following: - A valid nursing degree with specialization in operating theatre nursing. - Strong communication and interpersonal skills to effectively interact with patients and healthcare colleagues. - A thorough understanding of surgical instruments and sterilization processes. - The ability to work efficiently in a fast-paced environment and manage multiple tasks simultaneously.

Role & responsibilities Assisted senior microbiologists in performing various microbiological tests, including sterility testing, bioburden testing, and environmental monitoring. Maintained accurate records and ensured compliance with GMP and SOP guidelines. Prepared and sterilized microbiological media and reagents. Performed routine equipment maintenance and calibration. Contributed to the development and improvement of laboratory procedures. Preferred candidate profile

M.Sc. (specialization in any Life sciences) with 4- 10 years relevant experience Experience in aseptic processing in GMP Classification and cell culture is (at least in mammalian cell culture) required; experience in the automated T-cell culturing process, washing, harvesting, and Cryopreservation is preferred. Hands-on experience or understanding in developing, manufacturing CAR-T cell therapy products is preferred. Experienced/Participated in aseptic process simulation, proficient in aseptic techniques, especially in aseptic filling of drug products, Biosafety cabinet operations, clean room behaviors, sterile welding, sealing, sterile transfer, etc. Good exposure or understanding of QMS aspects (Change control, Risk Assessment, Deviation, Preparation of Investigation report, and CAPA). In-depth understanding of Cell & Gene Therapy Manufacturing/development and associated regulatory guidelines. Roles & Responsibilities: Responsible for optimization of CAR cells manufacturing processes using normal human or patient-derived primary blood components, following ethical practices and QMS as per GMP guidelines Actively manufacture CAR-T cell therapy products by diligently prioritizing the lab functions to meet critical deadlines Establish and carefully execute transduction by viral vector and non-viral vector-based approaches, activation, and expansion of immune cells (T cells, NK cells, etc) isolated from clinical specimens without compromising sterility and quality parameters as per the guidelines and defined criteria by maintaining highest standards Able to communicate effectively in a highly matrixed team environment to advance the company's cell therapy pipeline Participate and assist in technical transfer and core R&D activities To review and prepare document SOPs, protocols, and reports pertaining to the program requirements Work closely with cross-functional teams to design and implement cell therapy processes and workflow for cell therapy platforms Provide critical technical/scientific recommendations for the manufacturing process improvements Work with vendors to evaluate raw materials and consumables for compatibility with the Manufacturing process Coordinate very closely with quality control, quality assurance, supply chain teams, etc, and strictly adhere to the project timelines by preserving integrity, accuracy, safety, and quality Prepare and participate in compliance monitoring inspections / regulatory agency interactions Able to troubleshoot experiments, record, analyze, interpret, and present the data in scientific meetings Understanding of systems and processes regarding sterile practices, work ethics, safety, health, and environment Ability to work off-shift and irregular hours as required Competencies: CAR-T manufacture under GMP settings Proficient in Aseptic Operations Culture of T cells/NK cells and handling of viral vectors Statistical analysis, Presentation & Communication Skills Documentation and Report Writing Interpersonal Skills Team Player / Team Management

Role Overview Function Overview Assist in the production of Screening Memos for the Originations Team As part of the loan origination process, the Origination Team produces a screening memo that details property level information (photos, maps, property description, rent roll and cash flows), market information (comparable property metrics and location) and financing information (capital stack, debt yield and loan information). The initial goal is for company to participate in the production of screening memos with the potential to participate in the underwriting and approval process for deals that Client elects to finance and refinance as well. Focus is to work on all the asset classes such multifamily, retail, storage, Industrial etc. loans originated by the Insurance. The Candidate would be supporting on the different workflows as mentioned below Agency Pre-screening and ICM Screening/underwriting of Agency Loans (Fannie Mae), deriving Underwriting Value, using financial spreading, rent roll analysis and creation of Investment Committee Memo. Non-Agency/Deal Pre-screening and ICM Screening/underwriting of Non-Agency Loans, deriving Underwriting Value, using financial spreading, rent roll analysis and creation of ICM. Loan Portfolio Stratification and ICM Stratification of portfolio of loans belonging to various asset classes, assessing their risk exposure using their property level, loan level and performance metrices. Draw Review Process Reviewing draw related Invoices, Proof of Payments, Construction Budget, TI/LC, etc. and updating the Draw Review Trackers accordingly. On Boarding the delas on AI Based platform with the help of various closing documents, Offering Memorandum, Loan Agreement etc. Extracting market and asset specific statistics from various data sources (for egCoStar or similar platforms) for the pipeline deals which are shortlisted for screening or underwriting Comparing the key deal metrics which includes Occupancy, Cap Rates, Debt Yield, Cash Flow, NOI etc. of the pipeline deals with existing portfolio Analyzing property pictures & map for location-based insights, preparing the capital stack (i.e., Equity vs. Debt) and presenting them in an excel and ppt format Collecting and preparing sales and rent comparable of the target originations with the market data sourced through broker reports or web-based applications. Studying the demographics to understand the unit mixes, interpreting all sources of incomes & expenses through review of cash flows, ascertaining vacancy rates & rental income using rent rolls and using NOI to calculate key liquidity ratios i.e., DSCR, DY etc. Creating investment memorandums with the deal team ahead of investment committee. Conducting due diligence prior to closing of deal as per closing checklist. Data input in pipeline tool (i.e., DealPath, Loan Tapes) as and when required. Essential Skills & Experience Must have a good knowledge of US Real Estate Industry and Market in underwriting the CML/CRE loans across all the sectors; along with hand on experience in underwriting the Multifamily agency (Freddie & Fannie) loans. Should be aware of the US taxes for different States and Counties; along with knowledge of various rent/sales comparable to be used in accordance with subject properties. Must be well versed with concepts of Cap Rate/Index rate/ LTC/LTV/Spreads/Cap Stack, Implied vs Cash Equity and various loan specific terminologies. In addition, should know the implications and effect of UW In-place and Mark to Market assumptions using property financials and its demographics through broker provided offering memorandum. Candidate should have the knowledge of US Market and Sub-Market to understand the deals demographics and its impact on the subject property. Hand on experience and proficient in preparing the dynamic financial models in MS excel. Masters degree Major in Finance or Banking and Capital Markets, CFA designation a plus. Exceptional quantitative aptitude and skill set with a mastery of Microsoft Office applications. Ability to manage multiple priorities in a fast paced, fluid environment. Previous background with real estate lending required with Debt Underwriting in real estate preferable. Rigorous analytical mindset with a high level of intellectual curiosity and excellent problem-solving skills. Acute focus on attention to detail, accuracy, and data validation. Effective communication skills (listening, verbal, and written). Excellent interpersonal and teamwork skills. Sound judgment and discretion. Strong initiative, energy and confidence completing assignments with limited supervision.

Role & responsibilities To perform the microbial limit test & validation of samples as per GLP and other different types of samples. To perform Sterility test, BET test & Preservative Efficacy testing of different samples & to perform their validation activity. To monitor the environment of the Microbiology lab. To perform the sterilization of glassware's by autoclave and dry heat sterilizer. To prepare the microbiological media and chemical reagent as and when required and perform the necessary microbial tests. Preparation of disinfectant solution Daily, quarterly and yearly calibration of the balance, pH meter and other instruments as per the master schedule. To check the performance of all instruments as per the master schedule. To review the microbiological documents. To approve the microbiological test related TRF. Documentation and writing journals related to the microbiological test and there validation. To represent the Microbiological lab during audits . Preferred candidate profile M.Sc (Micro) with 02-07 Yrs of relent experience. Interested Candidate may share their Cvs on vilshashah@torrentpharma.com

1. Calibration of Instrument and equipment 2. Media preparation room MLT/BET area, 3. Recording Daily and weekly cleaning activities of microbiology department. 4.Ensure good Laboratory practices in Micro department.

Walk In Drive For Microbiology Department In Formulation Division @ Corporate Office Department:- Microbiology Qualification :-BSC Microbiology | MSC Microbiology Experience :- 2 - 8 Years Skills :- * MLT * BET * Media Preparation * EM * Sterility Test. Division :- Formulation Interview Date:- 28-06-2025 Interview Time :- 9.00AM TO 2.00PM Work Location:- MSNF-II , Kothur | MSNF-V, Rk Puram Venue Location:- MSN Corporate, H. No. 2-91/10 & 11 /MSN, Whitefield's, Kondapur, 500084 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 Microbiology Department In Formulation Division @ Corporate Office Department:- Microbiology Qualification :- B Sc | M Sc (Microbiology | Bio-Technology | Biochemistry) Division :- Formulation Fresher's :- 2023 | 2024 | 2025 Passed outs only. Interview Date:- 28-06-2025 Work Location :- MSNF Unit-II, Kothur & MSNF Unit-V, RK Puram Interview Location :- MSN Corporate, H. No. 2-91/10 & 11 /MSN, Whitefields, Kondapur, 500084 Contact No:- 040-30438701 | 8785 Note:- Candidate should bring Update Resume , Offer Letter, Increment Letter, CTC, Pay slips ,Bank Statement, Certificates, Aadhaar Card & Pan Card We are looking for candidates those who have experience in Production OSD Department.(Coating Operator & Compression Operator) 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.

Purpose Statement: Handle high pressure reactions at R&D lab operations, compile data and ensure adherence to safety and incorporate best laboratory housekeeping practices. - Responsible for the availability of raw materials, catalysts and instrument spares as per high pressure lab requirements. -To analyze quality results and discuss the experimentation plan and parameters with Research Incharge. - Understand the safety aspects of all reactions, chemicals and catalysts to be used in high pressure reactions. - Ensure the proper setup ( compatibility of autoclave, high pressure addition pumps, thermostats etc) as planned. - Carry out reaction process as per the provided plan, get the analysis done for raw materials, catalysts , in process reaction intermediates and product. - Record all observations and give suggestions for improvement. - Report any breakdown, abnormal functioning of instruments in high pressure lab. - Ensure proper housekeeping of the lab. - Maintain highest safety practices while working by using required PPEs (Personal protective equipment). - Maintain the log sheets of all the experiments regularly with critical observations and feed the data into Electronic Lab Notebook (ELN). - Ensure working in lab as per SOP's provided. - Maintain stock of all the chemicals, catalysts and instrument spares required as per 5'S' (sort, set-in-order, shine, standardize, sustain) - After reaction completion, decontaminate the autoclave/instruments properly. - To ensure proper and complete recovery/quenching of catalysts after reaction. - To ensure proper and safe storage of catalysts and maintain its record. - Segregate effluents as per the lab system. - To undergo trainings as per schedule. Experience 2-7 Years. Qualification M.Sc Organic Chemistry or equivalent. Certifications/Trainings Analytical & Waste Treatment, Process Safety training, Process Development training preferred

To perform temperature monitoring of equipment and micro area. To check the calibration tags or external calibration of instrument. To carryout operation and calibration of instrument and maintain usage record. To prepare and maintain records of media preparation, sterilization and disposal. To perform water sampling and testing as suggested in SOP. To perform the Bacterial Endotoxin Test as per SOP. To carryout microbiological testing of raw materials, finished product, hold time study sample, stability samples and packing material. To carryout microbiological testing of cleaning validation samples (swab and rinse). To perform and maintain record of environmental monitoring of controlled areas by settle plate method and air sampler. To maintain and preserve microbial cultures. To enter all the analysis details in job allocation register. To arrange SOP training as per monthly schedule. To monitor the activity and ensure its compliance as per SOP. To check microbiological documents. To carryout qualification of equipment. To adhere to good laboratory practices, good manufacturing practice and good documentation practice. To prepare trends of water analysis and environmental monitoring. To handle the QAMS, DMS, E complain, LIMS, ICDAS Software. To manage all micro related documented activities (Handling of OOS, Lab. Incidence etc.) Immediate joiners will be prefered. Share your resume on dipika.parmar@milanlabs.com

Role & responsibilities Physicochemical characterization, Media preparation, Buffer preparation etc. Preferred candidate profile Experience in working in lab set up and good basic knowledge on physical/chemical techniques. Dilligent and accuracy driven.

About Intas Recruitment Fraud Disclaimer: Intas Pharmaceuticals does not request or accept any fees during recruitment If someone asks for payment on our behalf, it is a scam Please report the incident to the local police or cybercrime unit Your trust and safety are important to us, Intas is a leading global pharmaceutical company specializing in the development, manufacturing, and marketing of pharmaceutical formulations The mission of the company is to address unmet medical and societal needs through a fully integrated pharmaceutical value chain spanning across the world, Through its subsidiaries, the International presence of Intas includes the following countries: over 85 worldwide, with some of the more important global markets like North America, Europe, Latin America, and the Asia-Pacific under the well-known brand name Accord Healthcare The rapid expansion has been due to organic growth and strategic acquisitions alone, vindicating its position in some of the important major pharmaceutical markets across the world, Intas follows high standards of quality, as reflected by products approved for leading global regulatory agencies including USFDA, MHRA, and EMA Substantial in-house R&D capability, along with the beginning of a focus on highly advanced areas like Biosimilars and New Chemical Entities-Intas continues to push the frontiers of excellence in healthcare, At Intas, our success is fundamentally built on the strength of our people Our ongoing commitment is to attract and retain the best talent in the industry while fostering an empowering environment that encourages innovation and excellence This approach ensures that every employee plays a meaningful role in driving both the companys growth and advancements in global healthcare, Job Title: Officer QC Micro Job Requisitions No : 13760 Job Description Purpose of Job To perform Microbiological analysis, Skill Required Microbiological skill require to perform the microbiological analysis, Roles and Responsibilites Role of microbiologist and responsibilities to perform the microbial analysis, Qualification Required Sc Relevant Skills / Industry Experience Microbiological skills required and having experience related to pharma industries, Relevant professional / Educational background Master of Science in microbiology field and having two to three years of experience, Any Other Requirements (If Any) Compensation / Reward Location: SEZ, Ahmedabad, GJ, IN, 382213 Travel: 0% Life at Intas Pharmaceuticals For over three decades, Intas has thrived due to the exceptional talent of its people Our growth is fueled by a dynamic environment that nurtures individual potential while fostering collaboration and collective success We believe that when diverse skills and perspectives unite under a shared purpose and value system, we can achieve remarkable outcomes, driving innovation and excellence across the pharmaceutical landscape, Date: 26 May 2025

Daily Calibration pH ad weighing balance,Water sampling&testing,Raw&finished product sampling&analysis,Pckng material analy,Subculturing,Envrnment Monitoring&fumigation in control areas,Media Preparation,Grwth Promotion Test Maintanace of log records