24 Purification Jobs

Execute process development activities for pharmaceutical products at laboratory scale Design and implement experiments to optimize manufacturing processes for increased efficiency and product quality Conduct and analyze data from characterization and optimization studies Prepare the documents like PIS, sampling plan and risk matrix for pilot scale batches (Confirmatory batch and exhibit batch manufacturing) Troubleshoot process issues and implement corrective actions Collaborate with cross-functional teams including manufacturing, quality assurance, and regulatory affairs Author and review technical reports, batch records, and standard operating procedures Ensure compliance with cGMP regulations and company policies Participate in technology transfer activities to support scale-up and exhibit batches. Stay current with industry trends and emerging technologies in pharmaceutical process development Present findings and recommendations to group leader. Contribute to continuous improvement initiatives within the department Qualification M. Pharmacy Additional Information

Experience in Organic Synthesis / Multi-step Synthesis State-of-the-art scientific knowledge in technical background for synthesis and purification methods Handling reactions from milligram to gram scale Sound knowledge of isolation, separation, and purification techniques Positive and confident individual with strong work ethics Team player with good communication skills Good in English written and spoken (recommendable) Candidates are expected to work for Mithros, with the flexibility to quickly move to work in Taros if required Sr. Chemist Research Associate with MSc. Organic Chemistry (2 to 5 years experience only) Good in English written and spoken (recommendable)

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.

Optimize yield, quality, cost Run trials (pH, temp, solvents) Ensure IP/USP quality (HPLC, FTIR) Scale up with consistency Source materials/equipment Update SOPs, train team Cut waste, save resources Ensure regulatory compliance Required Candidate profile Skilled in biopolymer process optimization & scale-up Knowledge of food/pharma quality standards & testing Experienced in HPLC, FTIR, and viscosity testing Knowledge of sustainable manufacturing

Hi, Greetings from Biophore India Pharmaceuticals!! We are hiring for Synthesis R&D /Process R&D/CRO Experience: 3 to 6 Years Qualification: M. Sc ( Organic Chemistry) Walk In date : 19th November 2024, Tuesday . Timings : From 10:00 AM to 02:00 PM . Preferable Male Candidates only If any one not able to attend the interviews , share your CV to " recruitments@biophore.com "

Skills Description Proficiency Level (General Awareness; Working Knowledge; Functional Expert, Mastery ) Functional Skills Organic Chemistry, Purification skills, Inert Reactions, Named Reactions Ability to self-design synthetic schemes, plan and order chemicals and deliver the targets in the stipulated time-line. Excellent trouble-shooting skills Responsible for laboratory maintenance on day to day basis. Functional Expert Behavioral Skills Strong communication skills are essential so as to individually procure chemicals, taking care of laboratory maintenance. Working Knowledge

Skills Description Proficiency Level (General Awareness; Working Knowledge; Functional Expert, Mastery ) Functional Skills Organic Chemistry, Purification skills, Inert Reactions, Named Reactions Ability to self-design synthetic schemes, plan and order chemicals and deliver the targets in the stipulated time-line. Excellent trouble-shooting skills Responsible for laboratory maintenance on day to day basis. Functional Expert Behavioral Skills Strong communication skills are essential so as to individually procure chemicals, taking care of laboratory maintenance. Working Knowledge

Job Area: Engineering Group, Engineering Group > Hardware Engineering General Summary: As a leading technology innovator, Qualcomm pushes the boundaries of what's possible to enable next-generation experiences and drives digital transformation to help create a smarter, connected future for all. As a Qualcomm Hardware Engineer, you will plan, design, optimize, verify, and test electronic systems, bring-up yield, circuits, mechanical systems, Digital/Analog/RF/optical systems, equipment and packaging, test systems, FPGA, and/or DSP systems that launch cutting-edge, world class products. Qualcomm Hardware Engineers collaborate with cross-functional teams to develop solutions and meet performance requirements. Minimum Qualifications: Bachelor's degree in Computer Science, Electrical/Electronics Engineering, Engineering, or related field and 3+ years of Hardware Engineering or related work experience. OR Master's degree in Computer Science, Electrical/Electronics Engineering, Engineering, or related field and 2+ years of Hardware Engineering or related work experience. OR PhD in Computer Science, Electrical/Electronics Engineering, Engineering, or related field and 1+ year of Hardware Engineering or related work experience. Key Technical skills requirement: Candidate should have deep and sound understating of: Memory basic design understating for different architectures Memory measurement parameters Memory timing/power characterization and compiler engine building with all accuracy parameters involved Memory power views All the LVF/different forms of variation parameter Memory lib w.r.t. parameters/arcs/SDF conditions/variation parameters/QA steps/different formats Different Simulator tools Should have thorough understanding of release process to customers Knowledge of scripting languages such as Shell, Perl Good working knowledge of MS excel, PPT Mentoring skills to Juniors Applicants Qualcomm is an equal opportunity employer. If you are an individual with a disability and need an accommodation during the application/hiring process, rest assured that Qualcomm is committed to providing an accessible process. You may e-mail disability-accomodations@qualcomm.com or call Qualcomm's toll-free number found here. Upon request, Qualcomm will provide reasonable accommodations to support individuals with disabilities to be able participate in the hiring process. Qualcomm is also committed to making our workplace accessible for individuals with disabilities. (Keep in mind that this email address is used to provide reasonable accommodations for individuals with disabilities. We will not respond here to requests for updates on applications or resume inquiries). Qualcomm expects its employees to abide by all applicable policies and procedures, including but not limited to security and other requirements regarding protection of Company confidential information and other confidential and/or proprietary information, to the extent those requirements are permissible under applicable law. To all Staffing and Recruiting Agencies Please do not forward resumes to our jobs alias, Qualcomm employees or any other company location. Qualcomm is not responsible for any fees related to unsolicited resumes/applications. If you would like more information about this role, please contact Qualcomm Careers.

Job Responsibilities : 1. Coordinate and drive activities under guidance of Group Leader/ Head Of Department. 2. Conduct Literature survey of assigned projects. 3. Plan 7 Execute experiments as instructed and discussed. 4. Discuss reaction observations with GL/HOD 5. Records Experiments in the Laboratory note book as per SOP, update and get checked by seniors. 6. Follow up for analysis and collect analytical reports from ADL, interpret the results. 7. Record analyses results like chromatograms, chemical analysis etc. in the lab note book. 8.Maintain experimental and analysis reports. 9. Evaluate costing of the product to achieve target RMC 10. Support to QA and RA for necessary documentation and queries. Following are some of the Job Responsibilities.

Role & responsibilities Synthesize novel target molecules according to client specifications, working independently and efficiently. Utilize your broad knowledge of modern organic chemistry and synthetic methods, including: Heterocyclic chemistry, Metal-catalyzed reactions, Handling air/moisture sensitive reagents, Hydrogenations, Multi-step synthesis Apply a wide range of techniques in synthesis and purification like Chromatographic methods (including expertise in MPLCs) Spectroscopic characterization of novel compounds (NMR, LCMS, HPLC, IR) Preferred candidate profile M.Sc. in Organic Chemistry with 4to 10years of relevant experience. Strong knowledge of modern organic chemistry principles and synthetic methods. Expertise in various techniques for organic synthesis, purification, and characterization. Excellent problem-solving and critical thinking skills.

Production: Execute production batches, ensure GMP, manage documentation QA: Ensure cGMP, Issuance and retrievals and manage records. QC: Analyze biopharma samples & maintain Documentation R&D: Prepare stocks and buffers, extract proteins & analyze.

Roles & Responsibilities: The Research Scientist will contribute to research work focused on designing lab scale experiments for microbial fermentation products developed through recombinant microbes and subsequent purification as per project timelines and objectives. This position also supports the Team Leader / Group Leader in the fermentation function's daily operations. Key Responsibilities: Contributing strategically to the overall success of Biotechnology R&D by driving innovation and enhancing team performance, aligning with departmental/organizational goals. Ensuring the security of intellectual property for R&D. Carrying out literature search by use of all available analytical tools. Conducting fermentation/ purification process development of enzymes/protein & small molecules from different microbial platforms and carrying out subsequent. Executing POC studies and manage scale-up methodologies from lab scale to pilot scale. Preparing technical reports and document all research results obtained in form of presentations. Collaborating effectively with cross-functional teams as per requirement. Constructive and active participations in all technical and functional meetings of the group. Adhere to all safety protocols and proactively participate in laboratory maintenance. Attention to details in experimental design, execution and data analysis and interpretation. Education Qualification: Ph.D./ M.Sc./ M.Tech. in Biotechnology from a reputed university with excellent academic credentials, and peer-reviewed papers/patents. Knowledge of fermentation / purification and biotransformation process development & scale up for microbial platforms for small molecules, Enzymes & Proteins Good experimentalist with experience in industry/ academia Worked with Biotechnology, Biopharmaceuticals, Agrochemical Industry.

Synthesis, purification,characterization of Nucleoside and Nucleotide to develop efficient processes for production,quality,safety,qulity.Use HPLC/NMR/Mass spectrometry.Analyze and interpret data to assess the purity, structure, and identity. Required Candidate profile Ph.D(Organic Chemistry). Process Development Chemist (API), Nucleic Acid Chemist, Peptide Chemist. Hands on experience in synthesis, purification, and characterization of nucleosides and nucleotides.

Role & responsibilities Lead and manage peptide R&D Purification projects from inception to completion, ensuring timelines, budgets, and quality standards are met. Design and implement advanced purification strategies for peptide molecules Develop and implement strategic plans for peptide research and development in alignment with organizational goals and objectives. Purification of Peptide impurities by using solution & solid phase technique. Create the Innovative Research and Development Environment Train and guide the research teams to improve on developing/ adopting new chemical technologies. Drive positive & major EHS Cultural transformation Initiatives Take ownership of solvent recovery and yields improvement. Mentor and manage a team of scientists and research associates working in peptide purification. Ensure compliance with regulatory guidelines and requirements governing peptide drug development and help the teams in successful regulatory inspection with no critical observations

Job Responsibilities: A) Project Management Undertake on-going referencing and literature reviews and provide strategic inputs to projects at all stages Evaluate methods under consideration by conducting literature survey (incl. regulatory guidelines, pharmacopeia guidelines, publicly available research, etc.) Identify initial cell-lines/ anti-body requirement based on method(s) identified Conduct lab experiments for bio-assay/ immuno-assay development and optimization Conduct lab experiments to qualify the method for reproducibility Prepare/provide inputs for the preparation of necessary documents like Method development report, Method qualification protocol and report. Method validation protocol and report, Standard Analytical Procedures (SAP), Method transfer protocol and report. Ensure tech-transfer by demonstrating process to plant operators (in lab premises) Observe process in plant and resolve any queries that may arise (post-transfer) B) Bio-assay/Impurity assay (HCP and HCDNA) /Binding ELISA assay/SPR assay/BET Method development, qualification and transfer Conduct regular analysis for non-GMP and non- release batches (not transferred to plant) - support other labs by stability testing samples provided by them Prepare and share detailed reports with the relevant labs upon completion of the tests Conduct Bioassay, HCP, HCDNA, Protein A ELISA, SPR, Binding assay and BET method development/qualification and routine analysis (C) Other tests and routine processes Conduct / guide RAs for conduct of regular analysis for non-GMP and non-release batches (not transferred to plant) - Support other labs by stability testing samples provided by them tests as requested. Prepare/review and share detailed reports with the relevant labs upon completion of the tests Conduct/ guide RAs for conduct of method development/qualification and routine analysis Review protocols and reports provided by CRO (based on expertise) Coordinate CRO with ADA assays, Antibody generation, purification and biotinylating activity for in-house HCP method. (D) Materials and equipment management Procure and maintain inventory of cell-lines/anti-bodies/ consumables/ equipment: Share details of requirements with purchase team Engage in technical discussions with vendors to identify and recommend suitable ones to lab head and Supply Chain Raise PR for purchase Oversee Check materials upon receipt and store them as per set-norms (freeze in case of cell-lines) Track and maintain inventory in order to control and manage short-falls and damage Maintain inventory-logs and intimate superiors in case of short-falls and damage Manage cell-culturing and sub-culturing process: Prepare cell-banks (by freezing cell-lines) for storage Passage cells (remove vials from these banks) as per testing need Calibrate select lab-equipment on regular basis to facilitate use Ensure scheduled and break-down maintenance by coordinating with vendors/ maintenance team ( E) Regulatory and compliance Accurately capture all lab experiments in raw- data and lab-notebooks (incl. electronic data- capture) in real-time on an on-going basis. Adhere to regulatory, SOPs and safety guidelines for all processes. Ensure timely closure of regulatory queries by conducting and documenting lab experiments. Ensure data integrity in all respects Compile and Review all project-related documents created during lab activity on a regular basis Prepare/ modify SOPs by gauging work ability of the processes/practices in timely manner (F ) Business (people & budgets) planning, continuity and improvement Conduct SOP and induction trainings for subordinates Provide timely and relevant inputs for the preparation of capex budget Identify and implement continuous improvement initiatives to enhance process efficiency Take initiative to provide time and inputs (based on expertise/interest) to other on-going projects (G) Learning and improvement Attend all mandatory trainings Take initiative to provide inputs (based on expertise/interest) to other on-going projects Take initiatives for self-development and update self on recent developments in own area of work Take initiative to train fresh RAs upon induction or guide them with select lab processes (basis expertise) (F) Quality Compliance Initiate change control for New instrument IQ/OQ/PQ/CSV of new instrument. GDP Compliance Compliance related to internal and external audits

Candidate must have experience Min. of 4 to 5 years of experience in chemical synthesis, process development. Experience in designing complex reactions, optimizing conditions, scaling up, & ensuring safety & involving organic synthesis, purification Required Candidate profile Experience in organic reaction mechanism, transformations & functional group chemistry. Proficient in optimizing reactions for scale-up with expertise in safety, catalytic processes & green chemistry.

Lead and manage peptide R&D Purification projects from inception to completion, ensuring timelines, budgets, and quality standards are met. Design and implement advanced purification strategies for peptide molecules Develop and implement strategic plans for peptide research and development in alignment with organizational goals and objectives. Purification of Peptide impurities by using solution & solid phase technique. Create the Innovative Research and Development Environment Train and guide the research teams to improve on developing/ adopting new chemical technologies. Drive positive & major EHS Cultural transformation Initiatives Take ownership of solvent recovery and yields improvement. Mentor and manage a team of scientists and research associates working in peptide purification. Ensure compliance with regulatory guidelines and requirements governing peptide drug development and help the teams in successful regulatory inspection with no critical observations

SUMMARY Job Opening: DC LAN Admin Professional Location: Navi Mumbai/Jaipur Experience: 3+ years Mode of Interview: L1: Virtual L2: F2F Job Description: Responsible for 24X7 operations of the Data Centre (DC) Operations team. Manage day-to-day operations of the Customer's Data Centre with a focus on COLO service Providers, Vendors, and Technology Infrastructure Group teams. Work in a team environment with high individual productivity and a can-do attitude. Flexibility to work in 24 X 7 shifts. Proficient in Data Centre passive infrastructure, cooling, electrical power, air purification, firefighting safety, etc. Experience in Data Centre structured cabling and labeling standards. Efficiently manage partners/outsourcing vendors to ensure high-quality and well-utilized resources. Introduce new processes/systems and/or redefine existing processes to align with changing business/technology needs. Ability to set processes to manage the high transactional-oriented environment for seamless operations. Comfortable leading in a fast-paced team environment and possess very good communications skills. Vendor management and negotiation skills. Rack mounting, commissioning/decommissioning of IT hardware. Manage day-to-day operations using the DCIM tools & preventive checks, temp, cooling, safety/security, and maintain hygiene. Coordinate with COLO service provider to manage electrical/UPS PDUs, HVAC, and other Data Centre performance parameters. Plan and coordinate maintenance/other support activities (UPS/electrical/HVAC etc.). Compile, maintain, and share performance reports and metrics with various stakeholders at regular intervals. Possess certifications such as ITIL, CDCP, and other IT infra professional certifications. Proven understanding of Data Centre Best practices and TIA-942/Uptime and other standards. Awareness and working knowledge of DCIM tools. Requirements Requirements: 3+ years of relevant experience in DC (Data Centre) Admin Certifications ITIL, CDCP, other IT infra professional certifications

Role & responsibilities Operate and monitor bioreactors, fermenters, and processing equipment. Handle upstream processing (fermentation, cell culture, media preparation). Perform downstream processing (filtration, centrifugation, chromatography). Troubleshoot and resolve issues in bioprocess operations. Maintain GMP compliance and proper documentation. Collaborate with other teams like Quality and Engineering. Assist in equipment maintenance and calibration. Follow Standard Operating Procedures (SOPs). Support process optimization for better yields and efficiency. Report on production activities and suggest improvements. Skills Required: Hands-on experience in bioprocessing operations. Knowledge of GMP guidelines. Basic troubleshooting skills for process equipment. Teamwork and communication abilities. Interested candidates can send their resumes to "rajiv5653@bharatbiotech.com" with the subject line "Production Bioprocess Application." Regards, Rajiv Pradhan HR Department

Synthesis, purification,characterization of Nucleoside and Nucleotide to develop efficient processes for production,quality,safety,qulity.Use HPLC/NMR/Mass spectrometry.Analyze and interpret data to assess the purity, structure, and identity. Required Candidate profile PhD Fresher/Post Doc/MSc Organic/Medicinal Chemistry with 5-7 years relevant experience.in Nucleoside/ Nucleotide Chemistry.

Job Area: Engineering Group, Engineering Group > Hardware Engineering General Summary: As a leading technology innovator, Qualcomm pushes the boundaries of what's possible to enable next-generation experiences and drives digital transformation to help create a smarter, connected future for all. As a Qualcomm Hardware Engineer, you will plan, design, optimize, verify, and test electronic systems, bring-up yield, circuits, mechanical systems, Digital/Analog/RF/optical systems, equipment and packaging, test systems, FPGA, and/or DSP systems that launch cutting-edge, world class products. Qualcomm Hardware Engineers collaborate with cross-functional teams to develop solutions and meet performance requirements. Minimum Qualifications: "¢ Bachelor's degree in Computer Science, Electrical/Electronics Engineering, Engineering, or related field and 3+ years of Hardware Engineering or related work experience. OR Master's degree in Computer Science, Electrical/Electronics Engineering, Engineering, or related field and 2+ years of Hardware Engineering or related work experience. OR PhD in Computer Science, Electrical/Electronics Engineering, Engineering, or related field and 1+ year of Hardware Engineering or related work experience. Key Technical skills requirement: Candidate should have deep and sound understating of: Memory basic design understating for different architectures Memory measurement parameters Memory timing/power characterization and compiler engine building with all accuracy parameters involved Memory power views All the LVF/different forms of variation parameter Memory lib w.r.t. parameters/arcs/SDF conditions/variation parameters/QA steps/different formats Different Simulator tools Should have thorough understanding of release process to customers Knowledge of scripting languages such as Shell, Perl Good working knowledge of MS excel, PPT Mentoring skills to Juniors

Role & responsibilities 1. To work on the new process development for the ongoing and new products at bench level. 1. Arranging of raw materials required for the Process development and R & D work from store. 2. To support the Sr. Chemist on the process development work. 3. Monitoring of reactions in R & D lab by TLC or other available methods. 4. Carry out reactions, isolation and purification as per process requirements. 5. Preparation of Batch summary record and daily lab records in R & D Journal. 6. To manage Lab cleaning, Equipment cleaning with the help of Lab assistants. 7. To arrange Glasswares and Raw materials in separate racks with the help of Lab assistants. 8. To arrange RBF setup as per reaction requirements. 9. Sending samples for the required test in the ADL and observing its results. 10. Purification of materials by Column chromatography as per project requirements.

Dear Candidate, WE ARE HIRING Department: - Production- DS Designation: - Dy Manager / Manager Qualification: - Preferably Post Graduation in Science Experience: - 15+ Years Age: - Between 35- 40Years Mandatory: - Should come in all shifts, including Night shifts Role: Shift-in-charge for entire DS floor Job Description: > Strong Functional knowledge of DS Biologics (Chromatography and related purification experience protein/ Insulin handling experience preferable). Capable of handling large teams as we have around 45 members in each shift, around 50% of contractual staff. Strong administration / team management capabilities to streamline GMP across the floor. Monitoring the efficiency of employee performance on the job. > Coordinating with other departments to ensure that production runs smoothly Ensuring that all safety regulations are followed in the production area. Managing all aspects of production, including hiring workers, ordering supplies, maintaining production schedules, and overseeing equipment maintenance. Reviewing production schedules and work orders to ensure that production goals are being met in handling QMS activities. for more details please reach out Venkat -9381915043 or please share your CV to venkateswara.k@talent21.in