140 Filtration Jobs - Page 4

Job Purpose: Contributes to planning and execution of chemical reactions to ensure that the R & D targets are met. Ensure efficient production of goods as per the defined quality and quantity while STRICTLY following all the safety protocols. Continuously improving efficiency, following good laboratory practices by proper planning and maintaining the lab notebook regularly are important. Role & responsibilities: Technology- Basic knowledge of organic chemistry, and analytical techniques such as NMR, IR, HPLC, and GC. Good understanding of purification techniques such as distillation, crystallization, precipitation and filtration. Identify and estimate impurities. Smart literature search using Reaxys, SciFinder-n, publication/patent sites and various search engines. Operation and Safety- Knowledge of setting up of a chemical reaction under anhydrous condition, distillation, crystallization, separation etc. Understanding reaction parameters, good observation and documenting the unit operations. Follow and implement safety measures. Documentation and Data Analysis - Coordinate with analytical chemists to access data, analyze and report to TL while recording in lab notebooks. Policies, Processes and Systems- Possess excellent organization, written, and verbal skills to convey project goals and inspire support from peers and senior management. Follow internal processes diligently. Organizational Capacity- Continuously improve processes to ensure quality and efficiency. Set goals and review performance. Identify development needs and take stake in the department performance. Preferred candidate profile: Minimum Education Qualification- M.Sc or PhD in Organic Chemistry Minimum Experience (in Years)- 4 - 6 years Shifts- Candidates willing to take second & night shifts Interested candidates are requested to share their updated profiles on shweta.chaskar@cohizon.com Regards, Shweta

Responsibility : 1. To ensure working in-line as per defined operational control and standard operation procedure. 2. To ensure effective housekeeping and safe work environment in surrounding area. 3. To awareness of EHS policy and EHS objective. 4. Establish, implement and maintain EHS management system pertaining to operation department. 5. To control and reduce wastages during performing operation activities. 6. To report unsafe conditions, unsafe act or near miss. 7. To Wear All PPE and refer MSDS before handling of material. 8. To First cheek Reactor. It should be clean & dry. MOISTURE FREE 9. To check out jacket of reactor it should be empty. 10. To check out side of reactor, it should be clean & dry. 11. To check wear & tear of gland of reactor, there should not be any particles. 12. TO check pipe used for charging. It should be clean & dry. 13. To check candle filter should be attached to charging line 14. All Liquid RAW materials to be charged through candle filter only 15. To check all line of reactor. All line should be closed. 16. To operate as per BMR instruction like 17. To Close all lines and apply water ring vacuumed in the reactor. 18. To Releasing of vacuum & starting of stirring of reactor. 19. To Purging of nitrogen as per BMR limit in kg in the reactor. 20. To applying slowly heating and temperature as per BMR instruction in the reactor. 21. To Applying of cooling /Chilling/Brine as per BMR instruction in the reactor. 22. To Release pressure from went line by jacket of reactor. 23. To Maintain rate of Distillation by slowly and increasing gradually in the reactor. 24. To Identify the EHS related corrective & preventive action. 25. Accountable for in process EHS of the product. 26. To stop working in unsafe area/ unsafe condition. 27. To report near-miss or accident observed. 28. Housekeeping in surrounding work area.

Dear Candidate , we are hiring for QC Jr Executive ,Down stream process executives & Operators. Open Positions-50 Down Stream Process Executives & Operators Required • Qualification: Bsc/Msc/ITI/B Pharmacy Experience in handling the following Equipment 1 Chromatography column and system handling. 2 Column Packing (BPG And Chromoflow) 3 TFF System 4 Centrifuge system 5 Filtration, Filter Integrity,Buffer Preparation,CIP_SIP PRODUCTION-DS M Pharmacy/Diploma/B tech/Any Degree 6 Expertise in documentation QMS/GMP Compliance / Process Awareness Biologics Company's only Preferable. • Experience: 2 to 6 years in Total Downstream CTC :up to 5.0 LPA. IMMEDIATE JOINERS ARE PREFERABLE" Interested candidates please reach out Manasa - 9502434725

Dear Candidate , we are hiring for the Position Jr Executive .(Instrumentation,Hematology,Activity,Potency Based Assays,Bio chemical group) 1.Candidate have good hands on experience in HPLC, electroscopic test methods. 2.should be able to handle liquid chromatography instrument and relevant 21 CFR softwares 3.should be able to handle ELISA Reader ,microscope,basic QC Instruments . 4.candidate should have good hands experience in colorimetric ,spectrophotometric. 5. should be have a idea on GLP compliance requirements. for more details please reach out Venkat -9381915043 /Manasa - 9502434725

Role & responsibilities We are seeking a dynamic and results-oriented professional to lead our Used Lubricant Oil Re-Refining Plant. The Plant Head will be responsible for overall operations, safety, regulatory compliance, team leadership, and driving profitability. This role holds full P&L responsibility and will ensure the plant operates efficiently, sustainably, and profitably in line with company goals and environmental standards. Strategic and P&L Management: Own the plants Profit & Loss, ensuring cost-effective operations and margin improvement. Drive strategic planning and budgeting for the plant. Implement business strategies that ensure plant profitability, efficiency, and sustainability. Monitor KPIs and operational metrics to achieve financial and production targets. Operations Management: Oversee daily plant operations including feedstock procurement through different channel partners and other stakeholders, refining processes, product quality, and dispatch. Optimize plant throughput, yield, and energy efficiency. Ensure maximum plant uptime through effective preventive and predictive maintenance. Team Leadership: Lead and mentor cross-functional teams including production, maintenance, quality, logistics, and safety. Develop team capabilities through training, performance management, and succession planning. Compliance and Safety: Ensure full compliance with environmental, health, and safety (EHS) standards. Liaise with environmental agencies and regulatory authorities. Promote a culture of safety and continuous improvement. Supply Chain and Procurement: Oversee procurement of used oil feedstock and other raw materials. Collaborate with logistics for inbound and outbound transportation. Stakeholder Management: Coordinate with senior leadership, customers, vendors, and government authorities. Support business development efforts to identify new markets or partners. Preferred candidate profile Qualifications: Bachelor's degree in Chemical/Mechanical Engineering or related field. MBA is a plus. Minimum 10-15 years of experience in used oil re-refining plant management, petroleum refining, chemical processing, or related industries, with at least 3 years in a leadership role. Strong understanding of used oil re-refining technologies (e.g., Filtration, vacuum distillation, polishing technologies, hydrotreating). Proven experience in managing P&L and driving operational excellence. Continuously developing through learning and competency building. Skills & Competencies: Leadership and people management Financial and analytical acumen Strong knowledge of process safety and compliance Strategic thinking with a hands-on approach Excellent communication and stakeholder management

Key Responsibilities: Lead all technical efforts related to industrial filtration and pressure vessel projects, from inquiry to final delivery. Serve as the principal application engineer , interpreting client specifications and translating them into effective filtration solutions. Guide and oversee all process calculations , including flow rate, pressure drop, sizing, and filtration element selection. Ensure accurate vessel sizing and mechanical design , meeting applicable standards such as ASME, PED, and DIN. Oversee and validate the creation of P&IDs, GA drawings, fabrication drawings , and complete design packages using AutoCAD and design tools. Engage directly with customers and consultants during the pre-sales and post-sales phases to clarify technical specifications, conduct meetings, and support the sales team in generating accurate technical proposals. Lead cross-functional coordination with sales, production, quality, procurement , and project management teams to ensure alignment across departments. Manage, mentor, and grow a team of process engineers and CAD designers, ensuring adherence to quality and project timelines. Provide final approval of engineering documentation, calculations, and deliverables before submission to clients or internal departments. Drive innovation in product and process design, continuously seeking improvements in cost, quality, and performance. Represent the company in client meetings, technical presentations, audits, and industry forums as a subject matter expert. Qualifications & Skills: Bachelors degree in Mechanical or Chemical Engineering (Masters preferred) Minimum 15 years of experience in filtration systems, pressure vessel design, or process engineering in related industries In-depth knowledge of industrial filters, strainers, coalescers, separators , and their engineering applications Strong expertise in AutoCAD , process simulation tools, and engineering documentation Familiar with ASME Section VIII, PED, U-Stamp, and other relevant codes and standards Proven experience in leading engineering teams and managing end-to-end technical responsibilities Excellent communication skills with the ability to engage professionally with senior stakeholders and clients Strategic thinker with high attention to detail, planning, and problem-solving abilities

Roles and Responsibilities Operate and maintain equipment such as centrifuges, reactors, distillation columns, filters (RO & DM Plant), dryers, bulk drugs handling systems, CGMP compliance systems. Ensure adherence to BMR guidelines during API manufacturing processes. Monitor and control process parameters to ensure quality production of APIs. Perform routine maintenance tasks on equipment and facilities to prevent breakdowns and optimize performance. Collaborate with cross-functional teams to resolve issues related to production operations. Desired Candidate Profile 3-7 years of experience in API manufacturing or pharmaceutical industry. Diploma/B.Sc degree in Chemistry or relevant field. Strong understanding of batch manufacturing records (BMR) principles and practices. Proficiency in operating various types of equipment including centrifuges, reactors, distillation columns, filters etc.

ITI with 3 to 4 years of work experience as RO Operator. Experience in the pharmaceutical (excipients) & food industry. Operation of DM Plant, RO Plant, maintaining log book and its related documents, etc. Age - 22 to 30 years age limit preferred. Required Candidate profile Operate & maintain the RO plant to produce high-quality water. Operating & controlling filtration, pumps & valves. Perform preventive maintenance, such as cleaning & greasing machinery. Perks and benefits Negotiable - Depending Upon Candidate & Experience

ITI with 3 to 4 years of work experience as RO Operator. Experience in the pharmaceutical (excipients) & food industry. Operation of DM Plant, RO Plant, maintaining log book and its related documents, etc. Age - 22 to 30 years age limit preferred. Required Candidate profile Operate & maintain the RO plant to produce high-quality water. Operating & controlling filtration, pumps & valves. Perform preventive maintenance, such as cleaning & greasing machinery. Perks and benefits Negotiable - Depending Upon Candidate & Experience

ITI with 3 to 4 years of work experience as RO Operator. Experience in the pharmaceutical (excipients) & food industry. Operation of DM Plant, RO Plant, maintaining log book and its related documents, etc. Age - 22 to 30 years age limit preferred. Required Candidate profile Operate & maintain the RO plant to produce high-quality water. Operating & controlling filtration, pumps & valves. Perform preventive maintenance, such as cleaning & greasing machinery. Perks and benefits Negotiable - Depending Upon Candidate & Experience

ITI with 3 to 4 years of work experience as RO Operator. Experience in the pharmaceutical (excipients) & food industry. Operation of DM Plant, RO Plant, maintaining log book and its related documents, etc. Age - 22 to 30 years age limit preferred. Required Candidate profile Operate & maintain the RO plant to produce high-quality water. Operating & controlling filtration, pumps & valves. Perform preventive maintenance, such as cleaning & greasing machinery. Perks and benefits Negotiable - Depending Upon Candidate & Experience

ITI with 3 to 4 years of work experience as RO Operator. Experience in the pharmaceutical (excipients) & food industry. Operation of DM Plant, RO Plant, maintaining log book and its related documents, etc. Age - 22 to 30 years age limit preferred. Required Candidate profile Operate & maintain the RO plant to produce high-quality water. Operating & controlling filtration, pumps & valves. Perform preventive maintenance, such as cleaning & greasing machinery. Perks and benefits Negotiable - Depending Upon Candidate & Experience

ITI with 3 to 4 years of work experience as RO Operator. Experience in the pharmaceutical (excipients) & food industry. Operation of DM Plant, RO Plant, maintaining log book and its related documents, etc. Age - 22 to 30 years age limit preferred. Required Candidate profile Operate & maintain the RO plant to produce high-quality water. Operating & controlling filtration, pumps & valves. Perform preventive maintenance, such as cleaning & greasing machinery. Perks and benefits Negotiable - Depending Upon Candidate & Experience

Role & responsibilities : Chemical Researcher & Development Udyog Vihar, Ecotech-II, Udyog Vihar, Greater Noida, Uttar Pradesh 201306, India Full-time Company Description At TAPI, were not just a companywere a community committed to advancing health from the core. As the world’s leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we’re shaping the future of health worldwide. Our strength lies in our people—a team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that transforms lives. Job Description Are you a passionate scientist with a strong background in organic chemistry. process development? Join our innovative team at our state-of-the art Global R&D Centre , where your expertise will contribute to the development of life-changing therapies. Key Responsibilities – What You’ll Be Doing: Literature & Patent Research Diving deep into scientific literature and patents—gathering insights on specific molecules or synthetic steps to support Lead Selection and Route Scouting (LSR) . Synthesis & Characterization Using both Solid and Liquid Phase Synthesis (SPPS) techniques, develop and synthesize . Then characterizing them using LC-MS , NMR , and HPLC to ensure purity and sequence accuracy. Analytical Techniques & Quality Control From MALDI-TOF to spectroscopy , a range of analytical tools to identify compounds and maintain strict quality control and to make sure it’s all documented with precision. Strategic Chemistry Designing and executing synthetic strategies for complex molecules is both a challenge and a passion. It involves a deep understanding of protecting groups , coupling agents , and the core principles of chemistry. Compliance & Clean Lab Practices To follow GLP and GMP standards to the letter, ensuring a clean, safe, and organized lab environment that supports high-quality research. Technical Competencies: Focus on synthesis , literature search , developing and analyzing , and its characterization . Must have handled Synthesizers (Manual/Automatic), Purification Using Preparative HPLC, Lyophilizer and must be aware about Membrane filtration process. Broader scope including technology development , cross-functional collaboration , and process optimization . Qualifications We’re looking for candidates with a strong academic background and hands-on industry experience in organic chemistry and process development. The ideal candidate will have: M.Sc. in Organic Chemistry with a minimum of 3-5 years of relevant industrial experience OR Ph.D. in Chemistry with at least 1-2 years of experience in process development and scale-up. In addition to academic credentials, we value: Sound knowledge of organic chemistry, Spectroscopy, Drug Regulatory Affairs & Quality Assurance ICH Guidelines and IP understanding Good experimental hand & Scale-up knowledge Innovative thinking & excellent observance Problem Solving Ability Excellent teamwork and collaboration within & with other functions Effective communication & Presentation skills Planning & Organization Additional Information Make Your Mark with TAPI Your journey with TAPI is more than a job—it’s an opportunity to make a lasting impact on global health. If you’re ready to lead, innovate, and inspire, we’re excited to welcome you to our team. Together, let’s shape the future of pharmaceuticals. Apply on top of this page and our talent acquisition team will be in touch soon! "API experience is required" Interested candidate can connect on 8076954558 or else share your profile on *jasleen.kaur@tapi.com*

AFTER MARKET SALES, AFTMARKET SALES, FILTERS, FILTRATION, FUEL SYSTEMS, AIR ITNAKE SYSTEMS, ENGINE SYSTEM PARTS, AUTO PARTS AFTERMARKET SALES, BUSINESS DEVELOPMENT CHANNEL SALES, DEALER & DISTRIBUTOR MANAGEMENT, NEW BUSINESS CRM, MIS, TEAM,

Role & responsibilities As a research associate / Assistant, the candidate must play a leading role in ongoing pilot scale testing and research projects. The candidate will be responsible for ensuring the current pilot plant is successfully scaled up. The candidate is expected to vary process parameters and optimize the manufacturing process of fabricating membranes. Conduct lab scale trials and implement them successfully on pilot plant. Responsibilities include simulating processes, getting quotes, estimating total job / project cost and preparing proposals. Keep leads and supervisor informed of project status and work progress, required project material and equipment. Prepare and maintain accurate laboratory records. Having good knowledge of testing all types of chemicals for industrial applications. Should have good experience in handling all lab equipments. Would be responsible for testing of product sampling, incoming sampling & R&D testing. Generate and maintain accurate documentations of process specification, standard operating procedures (SOPs), equipment requirement and quality control standards throughout the technology transfer lifecycle. Preferred candidate profile Should be graduate, M.Sc., B.Sc. Chemistry, BE Chemical from reputed university. Minimum 2+ years of experience in the field of research and development, technology transfer work within Speciality chemical manufacturing industries. Excellent communication and interpersonal skills with the ability of effectively collaborate with both technical and non-technical team. Female candidate preferred. Research experience from environment analysis or membrane analysis . Sound knowledge of Material science, membrane technology is plus. Should be able to work individually. Strong understanding of processing, chemical manufacturing associated with analytical technique. Recent graduates / Fresher can also apply. Immediate joiners preferred. Work location Andheri West Mumbai. Week Off Alternate Saturday are off & Sunday. Contact hr@vipulorganics.com

1.Design clean & water treatment plants evaluation, modelling & design, master planning & project delivery. 2. Technologies such as Membranes, Ion Exchange, CDI, Filtration, Chemical Dosing Systems & UV. 3.AutoCAD 4. Project Management Provident fund Annual bonus

As a Peptides Production Executive, you will be responsible for learning and assisting in the production of peptides according to established protocols and quality standards. This position is designed to provide hands-on training in peptide synthesis, purification, and related processes. Key Responsibilities: Understand and follow standard operating procedures (SOPs) for peptide synthesis. Assist in the preparation of reagents, solutions, and equipment for peptide production. Execute peptide synthesis under the guidance of experienced personnel Learn and perform purification techniques such as HPLC, chromatography, and filtration. Assist in maintaining accurate records of production and testing activities. Follow Good Manufacturing Practices (GMP) and safety guidelines. Learn to operate and maintain peptide production equipment. Report equipment malfunctions or abnormalities promptly. Maintain accurate and detailed records of all production activities. Compile data and assist in preparing production reports. Communicate effectively with team members and supervisors. Contribute to the identification and implementation of process improvements. Provide feedback on procedures to enhance efficiency and quality Attend training sessions to enhance knowledge and skills. Actively participate in professional development opportunities. Experience Min 1 Year experience in Peptides manufacturing Competencies Basic understanding of peptide synthesis principles is a plus. Strong attention to detail and commitment to quality. Ability to work in a team-oriented environment. Good communication and interpersonal skills. Willingness to learn and adapt to new processes. Responsibilities Qualifications Masters/Bachelors degree in Chemistry or a related field.

Job Description Job Overview As a Peptides Production Executive, you will be responsible for learning and assisting in the production of peptides according to established protocols and quality standards. This position is designed to provide hands-on training in peptide synthesis, purification, and related processes. Key Responsibilities: Understand and follow standard operating procedures (SOPs) for peptide synthesis. Assist in the preparation of reagents, solutions, and equipment for peptide production. Execute peptide synthesis under the guidance of experienced personnel Learn and perform purification techniques such as HPLC, chromatography, and filtration. Assist in maintaining accurate records of production and testing activities. Follow Good Manufacturing Practices (GMP) and safety guidelines. Learn to operate and maintain peptide production equipment. Report equipment malfunctions or abnormalities promptly. Maintain accurate and detailed records of all production activities. Compile data and assist in preparing production reports. Communicate effectively with team members and supervisors. Contribute to the identification and implementation of process improvements. Provide feedback on procedures to enhance efficiency and quality Attend training sessions to enhance knowledge and skills. Actively participate in professional development opportunities. Experience: Min 2 to 3 Yrs experience in Peptides production department. Preferred candidate profile: Basic understanding of peptide synthesis principles is a plus. Strong attention to detail and commitment to quality. Ability to work in a team-oriented environment. Good communication and interpersonal skills. Willingness to learn and adapt to new processes. Responsibilities Qualifications Masters/Bachelors degree in Chemistry or a related field.

- Responsible for the availability of raw materials as per lab requirements -To analyse quality results and discuss the experimentation plan with Research Incharge. - Understand the safety aspects of all reactions and chemicals to be used - Ensure the setup ( reaction assembly, distillation, filtration, reaction work-up, crystallization) as planned - Carry out reaction process as per the provided plan, get the analysis done of raw material , in process reaction intermediate and product - Record all observations and give suggestions for improvement - 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) - Stack of all the chemicals & glassware as per 5S (sort, set-in-order, shine, standardize, sustain) - After reaction completion, decontaminate the glass apparatus

- Responsible for the availability of raw materials as per lab requirements -To analyse quality results and discuss the experimentation plan with Research Incharge. - Understand the safety aspects of all reactions and chemicals to be used - Ensure the setup ( reaction assembly, distillation, filtration, reaction work-up, crystallization) as planned - Carry out reaction process as per the provided plan, get the analysis done of raw material , in process reaction intermediate and product - Record all observations and give suggestions for improvement - 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) - Stack of all the chemicals & glassware as per 5S (sort, set-in-order, shine, standardize, sustain) - After reaction completion, decontaminate the glass apparatus and give for further cleaning. - Segregate effluents as per the lab system

Benefits: Transportation Facilities Subsidized Canteen Facilities Job Location: Intas Plasma Fractionation Centre

We are seeking a detail-oriented and experienced QA/QC Engineer to join our manufacturing team. The ideal candidate will be responsible for ensuring that our products meet the highest quality standards and comply with industry regulations. Key Responsibilities : Develop and implement quality control procedures and processes. Develop QAP / ITP with required procedures and get customer approvals for projects Conduct inspections and tests throughout the manufacturing process. Manage inspections with customers and TPI Manage quality team to ensure meeting orders CDD while ensuring all quality requirements are met with the highest standard Co-ordinate and expedite materials to ensure timely delivery of jobs, ensure receiving timely dispatch clearance from customers Prepare final documents and dossier sets and ensure customer approvals for final submissions Analyze data and prepare reports on quality metrics and trends. Identify areas for improvement in the production process and implement corrective actions. Collaborate with production teams to resolve quality issues and enhance product reliability. Ensure compliance with industry standards and regulatory requirements. Maintain documentation of quality assurance activities and audits like WPS PQR, calibration, etc. Managing audits by customers and various TPI agencies. Qualifications : Bachelors Degree in Mechanical Engineering or Diploma in Mechanical Engineering. Minimum of 10 years of experience in QA/QC within a manufacturing environment for pressure vessels or filters and strainers Experience in managing teams to ensure smooth work of the Quality department Strong knowledge of quality control methodologies and tools. Experience in working with customers such as IOCL, EIL, NTPC, NPCIL, BHEL, etc Proficient in using measuring and testing equipment. Familiarity with ISO standards and other relevant quality frameworks. Knowledge of ASME codes, material grades, welding process, painting & its testing requirement. NDT Level II in RT, DPT, MPT & UT. Able to review MTC with respective standard & specification. Strong communication and interpersonal skills. Ability to work effectively in a team environment.

handling Chemcial Plant Operation, knowledge of ETP process, BMR Filling , ISO Documentation , knowledge of Hydrogenation , Handling of Distillation, knowledge of chemicals

Role & responsibilities 1. Should be familiar in operating - Unit operations like Distillation, Evaporation, Filtration, Extraction, crystallization & Reactions 2. Should be aware of PLC Operations 3. Should be familiar in operating ERP 4. Should be aware of cGMP practices & should be capable of facing audits Preferred candidate profile Candidate must have experience in the Solvent Recovery department ( API Industry ) .