23 Peptide Synthesis Jobs

As a Peptide/Peptidomimetic Purification and Analysis Specialist, your primary responsibility will be to purify complex peptides with a high level of purity using PREP HPLC techniques. You will also be involved in the purification of peptides for scale-up activities. Your productivity will be measured based on the number of purifications and analyses you perform. It will be essential to ensure the proper maintenance of instruments such as HPLC, MPLC, lyophilizer, peptide synthesizer, centrifuge, etc., and to adhere to SHE/regulatory guidelines. Collaboration with the peptide synthesis team will be crucial for successful project outcomes. Regular updates in the form of PowerPoint or Excel presentations will need to be prepared, and maintaining a detailed lab notebook is a key requirement. Key Competencies for this role include excellent communication and interpersonal skills, the ability to work effectively in cross-functional teams, a positive attitude, and strong problem-solving abilities. Additionally, having good analytical skills will be essential for carrying out peptide purification and analysis tasks efficiently.,

* Process development, scale up and technology transfer of products from R&D to Pilot plant upto commercial batches to production department as per regulatory requirement * Day to day lab experiment planning & to ensure execution Required Candidate profile * To ensure requirement of raw materials as per experiment planned in R&D and pilot plant. *Complete literature search with IPR status study, ROS finalization, lab experiment planning.

As a Peptides Production Executive at Piramal Pharma Solutions (PPS), your primary responsibility will be to learn and assist in the production of peptides following established protocols and quality standards. This role is designed to provide hands-on training in peptide synthesis, purification, and related processes. Your key responsibilities will include understanding and adhering to standard operating procedures (SOPs) for peptide synthesis, assisting in the preparation of reagents, solutions, and equipment, executing peptide synthesis under the guidance of experienced personnel, and learning and performing purification techniques such as HPLC, chromatography, and filtration. You will also be expected to maintain accurate records of production and testing activities, follow Good Manufacturing Practices (GMP) and safety guidelines, operate and maintain peptide production equipment, and report any equipment malfunctions promptly. Additionally, you will be required to maintain detailed records of all production activities, compile data, assist in preparing production reports, communicate effectively with team members and supervisors, contribute to process improvements, provide feedback on procedures to enhance efficiency and quality, attend training sessions to enhance knowledge and skills, and actively participate in professional development opportunities. The preferred candidate profile for this role includes a basic understanding of peptide synthesis principles, strong attention to detail, commitment to quality, ability to work in a team-oriented environment, good communication and interpersonal skills, and willingness to learn and adapt to new processes. To be considered for this position, you should have a minimum of 2 years of experience in peptides production. Piramal Group values inclusive growth and ethical practices, and as an equal employment opportunity employer, bases its decisions on merit, considering qualifications, skills, performance, and achievements. The organization strives to ensure that all applicants and employees receive equal opportunities in personnel matters, including recruitment, selection, training, placement, promotion, compensation, and benefits, among others.,

As a Team Member in Chemical Research & Development at the Research & Development department, specifically in the Peptide Synthesis sub-department, your primary role is to perform chemical synthesis of molecules. This involves process development, process validation, and transferring the processes to production units. Your responsibilities include conducting literature searches, collecting MSDS, performing lab experiments, documenting experimental results, and interpreting spectral data. You will also be responsible for maintaining various documents such as patents, literature, and analytical reports. Collaborating with analytical chemists and DQA on analytical results and methods is an essential part of the role. To ensure the smooth functioning of the lab, you will need to account for chemical usage, availability of raw materials, and perform calibration of lab equipment like weighing balance, pH meter, and driers. Keeping track of regular solvents, reagents, and managing effluent generation from lab experiments are also part of your duties. In addition, you will be required to perform Manual Solid Phase Peptide Synthesis of Peptides on various scales, ranging from medium to commercial scale with minimal supervision. This includes purification of solid phase products, CGMP activities, synthesis of impurities, and degradation impurity standards for analytical method development and validation. Safety awareness and implementation are crucial aspects of this role, and you must strictly adhere to Good Laboratory Practices and Laboratory Safety Norms. Continuous learning and staying updated with industry trends are essential for success in this position. To qualify for this role, you should have an M.Sc. in Organic Chemistry and a minimum of 2 years of experience in the R&D Department of an API manufacturing company. Preferred qualifications include 6 years of experience and knowledge of Process R&D and scale-up processes. In terms of competencies, you should have a strong understanding of coupling reagents, documentation, GLP, safety compliances, plant scale-up, solid phase synthesis, solution phase synthesis, and purification. Behavioral competencies such as results orientation, customer centricity, collaboration & teamwork, problem-solving, planning, and communication are also essential for this role. Continuous learning and professional development are encouraged to excel in this position.,

Job Title: Peptide synthesis Team members; No. of positions: 1 The ideal candidates will possess background and experience in peptide synthesis, process optimization and isolation techniques. Job Description Strong background and hands-on experience in synthetic organic and/or peptide chemistry Independently perform Solid/Solution phase peptide synthesize of complex peptide active pharmaceutical ingredients (APIs) Knowledge in handling of diverse resins for peptide synthesis and associated process Hands on experience on automatic peptide synthesizers such as Biotage MW, Symphony X, Sonata etc is desirable Familiarity with peptide purification techniques is desirable. Able to work in mg to higher scale along with excellent problem solving skills To follow safety rules in all operations in the lab, lab chemicals management, maintain lab instruments and their proper use. Required Qualification : MSc in Chemistry Experience: > 3 to 5 Years in Peptide-API Industry Regards Srinidhi S srinidhi@bvrpc.com

Position : Product Manager Centrifugal Partition Chromatography (CPC) Systems Location : Hyderabad (Nacharam) – Head Office About Inkarp Inkarp is a 40-year-old scientific instrumentation company, with strong roots in analytical and life science technologies. We work closely with global brands and serve customers across pharma, biotech, research, and academia. Our approach is technical, honest, and relationship driven. What This Role Is About We are looking for someone to take full ownership of CPC Systems across India. This is not just about selling. It is about understanding where the product fits, building the market patiently, and supporting our teams and customers with the right knowledge and direction. This is a niche technology. The number of customers may be small, but the value they bring is very high. Most of them will be from peptide manufacturing, natural product extraction, and advanced process chemistry. They will expect clarity, honesty, and expertise, not just presentations and brochures. You will have full freedom to run this product line the way it should be. We will support you, but you will lead it. What You Will Be Doing Build and drive the complete product strategy for CPC Systems across India Identify where this technology fits – industries, customer types, problem areas Work closely with the sales team to support lead generation and closure Guide feasibility studies, sample discussions, and customer demos Coordinate with technical teams – both local and international – for quotations, training, and application support Own the funnel, monthly reports, forecasting, and competitive positioning Drive post-sale engagement and ensure systems are used successfully What We Are Looking For Bachelors or Masters in Chemistry, Biotech, or Pharma Minimum 4 to 6 year’s experience in chromatography, purification workflows, or preparative systems Experience in handling peptide synthesizers will be a strong advantage Ability to explain complex concepts in simple terms – both to scientists and business heads Prior experience handling a technical product independently is a strong plus Willingness to travel 10 to 15 days a month for customer visits, demos, and follow-ups Someone who takes ownership, follows through, and works without reminders What You Will Get A rare opportunity to manage and scale a truly differentiated product The space to build something long-term and be known for it Strong internal support, but the independence to take your own calls Direct access to global experts, modern purification technology, and a focused customer segment If you are looking for a meaningful role with space to grow, learn, and lead, and not just meet monthly numbers, then this could be the right place for you.

BD & provide technical support. Handle Multistep Synthesis. Peptides Synthesis using Solid Phase Peptide Synthesis. Design & synthesis of small molecules in API. Handling synthesis of organic chemical reactions.Knowledge on Instrumentation is a must. Annual bonus Provident fund Health insurance

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. Roles & 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 opportunitie Experience 4 to 6 Yrs experience in Peptides Manufacturing 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.

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.

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. Roles & 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 opportunitie Experience 4 to 6 Yrs experience in Peptides Manufacturing 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 4 to 6 Yrs experience in Peptides Manufacturing

Develop and implement strategic plans for peptide research and development in alignment with organizational goals and objectives. Lead and manage peptide synthesis projects from inception to completion, ensuring timelines, budgets, and quality standards are met. Collaborate with process development and purification teams to ensure seamless integration of peptide synthesis into downstream processes. Drive innovation by exploring new techniques and technologies for peptide synthesis. Create the Innovative Research and Development Environment Train and guide the research teams to improve on developing/ adopting new chemical technologies. Support in driving positive & major EHS Cultural transformation Initiatives Take ownership of solvent recovery and yields improvement. Ensure compliance with regulatory guidelines and requirements governing peptide drug development and help the teams in successful regulatory inspection with no critical observations

Role and Responsibilities Do literature search for a given step(s) / molecules and support in LSR Organize for relevant patents and papers from literature Developing, synthesizing, and analyzing peptides using various techniques like Solid & Liquid Phase Peptide Synthesis (SPPS), LC-MS, and NMR Researcher will be responsible for characterizing peptides, ensuring quality control, and contributing to research projects by designing experiments and analyzing data Developing and executing synthetic strategies for complex molecules. Purifying and analyzing synthesized peptides to assess sequence and purity. Understanding and applying principles of peptide chemistry, including the use of protecting groups and coupling agents Acquiring and interpreting data from analytical techniques like HPLC, LC-MS, and MALDI-TOF. Using spectroscopic techniques to analyze and identify compounds. Maintaining accurate records and reports of analytical data Adhering to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). Maintaining a clean and organized laboratory environment. Competencies required Sound knowledge of Organic Chemistry & Spectroscopy ICH Guidelines and basic IP understanding Good experimental hand & Scale-up knowledge Critical Thinking & excellent observance Problem Solving Ability Excellent teamwork and collaboration within & with other functions Good communication Qualifications, Education and skill Requirements M.Sc. Organic Chemistry with 3-5 years industrial experience Ph.D. Chemistry with 12-year Industrial experience Interested candidate can share their profile on jasleen.kaur@tapi.com or connect on 8076954558.

Role & responsibilities 1. Candidate should be B-tech (chemical) preferably. 2. Candidate should have minimum 3 to 10 years work experience in Peptide R & D, PD, MS & T, Tech transfer. 3. Candidate should have work experience on peptide SPPS/LPPS upstream (Synthesis) and Downstream (Purification) process. 4. Candidate should have hands on SPPS peptide synthesizer, Preparative HPLC, Column packing/ unpacking, HETP, Lyophilizer etc. 5. Candidate should have involves with R & D team for what if studies / to identify process requirements and to ensure the process can be execute smoothly at manufacturing scale. 6. Candidate should enough competent for technology adsorption, scale up and validation support for the peptide API. 7. Candidate should have able to Monitoring peptide upstream and downstream process and ability to demonstrate to operators. 8. Candidate is responsible Ensure we make scalable, robust and competitive peptide APIs. 9. Support the CFTs with continuous process and projects improvement, implementation of new technologies and products, scale-up and troubleshooting. 10. Responsible to prepare/review technical documents and other allied activities. 11. Train and support team adequately to accomplish the day to day tasks. 12. Ensure self and team members safety at all time. Coordinate with CFTs to meet the same. 13. Any other relevant activities assigned by reporting manager to be taken up on priority basis. 14. Operation of softwares like SAP, LIMS, WMS, GxP Digitize and Documentum as per applicability

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 1 year experience in peptides Production Competencies Masters/Bachelors degree in Chemistry or a related field. 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. Qualifications Masters/Bachelors degree in Chemistry or a related field

Role and Responsibilities Literature search review, segregation, compilation and ROS proposals for a given step(s) / molecules Coordinate and arranging raw materials / chemicals from different vendors / plants To review the processes for potential impurities in the beginning itself and planning for their preparation. To review RMC sheet and process operations to identify areas of cost improvement, operational ease and recovery and recycling to have most cost-effective processes To prepare and review reports such as safety, vendor qualification reports, process development, ACMI report, Nitrosamine assessment for customers Contribute novel ideas by way of participation during technical discussion & motivating the team members To meet EHS and compliance expectation and guiding other members Preparation and sharing presentations for various reviews with internal and external customers. Management of Laboratory and equipment, Ensuring Maintenance of inventory with the support of other team members The candidate will participate and/or lead project teams associated with process development and characterization for peptides and other modalities. Develop and characterize peptide (or other modalities) processes in the laboratory and translate them to scalable processes. Proactively advise and share knowledge and expert opinions with subordinates, peers, and senior management. Mentor staff in troubleshooting strategic and experimental issues. The position involves multi-disciplinary interactions with organic chemists, analytical chemists, engineers, IP, Regulatory and program management. The candidate will identify and nurture ideas for continuous improvement activities and initiatives within the department. The candidate will be responsible for setting project strategies, defining project responsibilities and timelines, developing control strategies, providing leadership in a matrixed team setting and developing robust processes for cGMP manufacturing. Competencies required 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 Interested candidate can share their profile on jasleen.kaur@tapi.com or else share on 8076954558

Position: Senior Manager - Peptide Production Grade: G9B / G9A Job Location: Ahmednagar Qualification: M.Sc. (Chemistry) / B.E. (Chemical) / B.Tech (Chemical) Experience: 13-18 yrs experience in Peptide API plant Job Profile 1. To plan and execute peptide manufacturing activities as per the schedule and Budget by optimum utilization of plant capacity 2. To ensure the sustainable quality production with optimum utilization of plant capacity. 3. Monitoring and reduction in process TRT, Cleaning TRT, number of preps per batch on Prep HPLC, Improve yields. Improve the process of Synthesis & Analytical Section. 4. Co-ordinate with Purchase, Planning department to deliver the goods in time. 5. To ensure every day interaction with each department for smooth functioning 6. Compliance of waste water disposal as per IN-HOUSE policy 7. To ensure grooming of disciplined workforce and staff to meet the planned growth charts. 8. Developing different innovative practices to increase productivities and up gradation of work culture. 9. To maintain Good Documentation Practices and Good Laboratory Practices 10. Review of batch process record, Standard Operating procedure and cGMP documents 11. Investigation of Deviation, Change Control & OOS 12. Implementation & follow all safety instruction & practices

Role & responsibilities Incumbent should possess design development know-how of peptide APIs Should have hands on experience in synthesis and purification of peptides and complex generics. Exposure on scale-up, technology transfer and manufacturing of peptide APIs Experience of impurity profiling (process and product related) Must have experience of technical documents preparation and to support regulatory filing Preferred candidate profile M.Tech/M.Sc./Chemical Engineering/Biotechnology degree or equivalent. 15+ years of post-qualification experience in the Peptides field, with a focus on new technologies and PAT (Process Analytical Technology) tools. Experience in operational excellence and Six Sigma methodology will be an added advantage.

Responsible for Collection, compilation, analysis, and review of all data for APQR Responsible for Processing and oversight of changes through the generation, justification, impact assessment, modification, review, approval, and implementation workflow Responsible for Review/approval of all documentation associated with the process validation, CPV & cleaning validation Must have experince in Peptide Synthesis. Responsible for processing of documents through the generation, modification, review, and approval and archival of records Responsible for review/approval of all documentation associated with the GMP equipment. This includes any Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) documents Responsible for tracking, trending, and reporting of Quality Metrics for site, regional, and global review. Trending as required by SOP, Corp. Standards, and/or regulations Responsible for Review/approval of all documentation associated with the establishment and configuration of a GMP computerized system. This includes all lifecycle documents Responsible for Review of regulatory and quality compliance requirements and divisional policy, performance of gap assessments, and establishment or improvement of SOPs covering all areas of applicability Quality support to Regulatory Affairs as it relates to updates/changes to Market Authorizations Responsible for Management, tracking, and/or performance of GMP type training supporting plant performance and Quality Departmental training and hands on qualification Responsible for Review/approval of the Validation Master Plan and all documentation associated with the validation or qualification of a process, system, equipment, facility and/or the utilities associated with the site

Role & responsibilities The Senior Principal Scientist Peptide Synthesis will lead the design, development, and optimization of peptide synthesis processes, driving innovation and contributing to the strategic direction of the peptides R&D program. Develop and implement strategic plans for peptide research and development in alignment with organizational goals and objectives. Lead and manage peptide synthesis projects from inception to completion, ensuring timelines, budgets, and quality standards are met. Collaborate with process development and purification teams to ensure seamless integration of peptide synthesis into downstream processes. Preferred candidate profile M.Sc./ PhD in Chemistry, Biochemistry, Pharmaceutical Chemistry or any related field. Minimum 10+ years of hands-on experience in peptide purification.

The Senior Principal Scientist Peptide Synthesis will lead the design, development, and optimization of peptide synthesis processes, driving innovation and contributing to the strategic direction of the peptides R&D program. Key Stakeholders: Internal Operations, Marketing, Quality, Finance, Sr. leaders Key Stakeholders: External Vendors and Customers on need basis Reporting Structure Functional reporting to Associate Director R&D Experience Minimum 10+ years of hands-on experience in peptide purification. Competencies Leadership skills Ability to connect the dots in various situations, seeing the risk and keep the mitigation plans. Clear communication. Analytical mindset. Quick and effective decision making. Stakeholder management. Roles & Responsibilities Develop and implement strategic plans for peptide research and development in alignment with organizational goals and objectives. Lead and manage peptide synthesis projects from inception to completion, ensuring timelines, budgets, and quality standards are met. Collaborate with process development and purification teams to ensure seamless integration of peptide synthesis into downstream processes. Drive innovation by exploring new techniques and technologies for peptide synthesis. Create the Innovative Research and Development Environment Train and guide the research teams to improve on developing/ adopting new chemical technologies. Support in driving positive & major EHS Cultural transformation Initiatives Take ownership of solvent recovery and yields improvement. Ensure compliance with regulatory guidelines and requirements governing peptide drug development and help the teams in successful regulatory inspection with no critical observations Responsibilities Qualifications M.Sc./ PhD in Chemistry, Biochemistry, Pharmaceutical Chemistry or any related field.

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. 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. Experience: Minimum 2 Yrs in peptides production Responsibilities Qualifications Masters/Bachelors degree in Chemistry or a related field.

Role: Scientist Peptide Chemistry. Qualification: M.Sc. Organic Chemistry with 2 to 6 years of experience on Synthetic and Analytical knowledge and experience of Peptide molecules. Areas Of Responsibility: Synthesis and Characterization of peptides Plan and execute the synthesis of peptide molecules with adequate purity and quantity as per project requirements. Develop good trouble shooting skills and comply with IPM and Safety norms. Developing appropriate methods for special functionalized peptides. Preparing key intermediates by solution phase synthesis which would be used as building blocks for synthesis of final target molecules. IN ORDER TO: successfully synthesize and deliver target compounds as per project specifications. Data Interpretation: To interpret the analytical data in identifying the synthesized targets and key intermediates. IN ORDER TO: successfully characterize the synthesized targets. Safety Compliance To follow the lab safety and industrial hygiene practices.