4 Capillary Electrophoresis Jobs

At USP, inclusive scientific collaboration is highly valued as it is believed that diverse expertise enhances the development of trusted public health standards. The organizational culture at USP promotes equitable access to mentorship, professional development, and leadership opportunities to ensure broad participation in scientific leadership for stronger and more impactful outcomes in global health. As an equal employment opportunity employer (EEOE), USP is committed to fair, merit-based selection processes that allow the best scientific minds, regardless of background, to contribute to advancing public health solutions worldwide. Accommodations are provided to individuals with disabilities, and policies are upheld to create an inclusive and collaborative work environment. The U.S. Pharmacopeial Convention (USP) is a scientific nonprofit organization that sets standards for medicines, food ingredients, and dietary supplements worldwide. USP's drug standards are enforceable in the United States by the Food and Drug Administration and are utilized in over 140 countries. The position offered is a hands-on, non-supervisory role where the incumbent will apply their knowledge and practical experience in executing bioanalytical projects on collaborative testing of reference standards, documentary standards, and characterization of biological products. The individual will also engage in verification, international and national reference standard development programs as assigned. In this role, you will have the opportunity to contribute significantly to increasing global access to high-quality medicines through public standards and related programs. USP prioritizes scientific integrity, regulatory excellence, and evidence-based decision-making to ensure health systems worldwide can rely on strong, tested, and globally relevant quality standards. The ideal candidate for this position will possess a postgraduate degree in a relevant stream of Biological Sciences along with 3-6 years of industry experience in Analytical R&D and QC departments of the Biopharmaceutical industry. Experience in method development, validation, and technology transfer, along with analytical characterization for biomolecules, will be advantageous. A strong background in cGLP/cGMP environments and expertise in specific analytical techniques are desired. Key responsibilities include aligning with USP's mission, demonstrating laboratory skills in various analytical techniques, executing experiments, analyzing data, contributing to projects, engaging in project coordination, preparing reports and documents, and continuously improving laboratory/project management methods and processes. USP is looking for a candidate who not only meets the technical requirements but also demonstrates excellent communication, presentation, and technical writing skills. Proficiency in using an Electronic Laboratory Notebook (ELN) is preferred along with strong written and verbal communication abilities. As an organization, USP provides comprehensive benefits to ensure the personal and financial well-being of its employees and their families. The company values inclusivity, diversity, and equity, and is dedicated to creating a work environment that fosters growth, mentorship, and professional opportunities for all its employees.,

Role & responsibilities : Person would be team leader. Person would be responsible for managing 6-10 people from sr. scientist to interns. Candidate would be responsible for planning of work for direct reportees, reviewing of their timesheets. Candidate would be responsible for coordination with cross functional team and AAT team. Person would be responsible for representing AAT in internal meetings Person should be experienced for HPLC, CE, SoloVPE related techniques, trouble shooting , data review and data interpretation Knowledge in characterization methods such as Mass analysis, CD, Flr, DSC, MALS would be an additional advantage. Person should know method qualification for HPLC, CE, SoloVPE related techniques Person would be involved in document preparation and review of MQP, MOA, MQR, Specification, analytical similairty studies Experience in analytical section related sourced document preparation for EMA and USFDA would be an additional advantage Person would be responsible for preparaing client query response and timely communication to cross functional team Technical Skill Requirement: Knowledge for HPLC based methods such as SE HPLC, CEX HPLC, Poly 20 measurement, RP HPLC, Capillary Electrophoresis related based techniques such as CE SDS R & NR, cIEF. CE analysis on Maurice system would be an added advantage SoloVPE analysis Soft Skill Requirement: Fluent in English, Should be approachable Able to present technical data in internal meeting Able to faciliate required work by coordinating with cross funcational team Technical review of the the data and ensuring timely communication to cross funcational team Able to resolve/disucss with manager if any conflicts within team is oberved

As an Analytical Scientist in our team, you will be responsible for developing and validating robust HPLC methods for the characterization and quantification of biological products such as monoclonal antibodies and recombinant proteins. Your role will involve performing method optimization, robustness studies, and transfer protocols following ICH guidelines. You will also be conducting routine and stability testing by analyzing in-process, release, and stability samples using various techniques including HPLC/UPLC, Capillary and Gel Electrophoresis, UV spectrophotometric methods, Host Cell DNA quantification, and immunoassays like HCP ELISA. In addition, you will be in charge of operating and maintaining analytical instruments such as HPLC, electrophoresis systems, spectrophotometers, and ELISA readers, ensuring their proper calibration, troubleshooting, and performance verification. Your responsibilities will also include preparing and reviewing SOPs, STPs, protocols, reports, and analytical records to comply with regulatory requirements. You will need to maintain accurate documentation in laboratory notebooks and electronic systems. Furthermore, you will participate in internal and external audits and provide analytical data to support regulatory submissions. Collaboration with cross-functional teams including R&D, Quality Control, and Regulatory Affairs will be essential in supporting product development and lifecycle management. You will offer technical support during investigations, deviations, and CAPAs, as well as train junior analysts and new team members on analytical techniques and laboratory practices. To excel in this role, you should hold an M.Sc. / M.Tech / M.Pharm in Biotechnology, Biochemistry, or a related life sciences discipline, along with 4-8 years of relevant experience in analytical development or QC of biopharmaceuticals. Hands-on experience with HPLC method development and ELISA-based techniques is required, as well as familiarity with regulatory guidelines such as ICH, FDA, and EMA, and quality systems. Key skills for this position include strong analytical and problem-solving abilities, attention to detail and data integrity, excellent documentation and communication skills, proficiency in software tools like Empower, Chromeleon, SoftMax Pro, and the capability to manage multiple projects and meet deadlines.,

By joining Bio-Techne, you will become part of a company with a strong and positive mission to support cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, along with all its brands, offers tools to researchers worldwide to further the treatment and prevention of diseases. This is an exciting opportunity for a motivated and dynamic individual to join the fast-paced global Life Sciences organization of Bio-Techne, with the position based in India. As an Application Manager/Specialist, your responsibilities will include providing scientific expertise, application support, and training to customers and channel partners. You will collaborate with the commercial team in pre-sales and post-sales customer support activities, effectively resolving customer escalations. Acting as a trusted expert, you will enhance customer satisfaction and loyalty, contributing to the success of the Bio-Techne Protein Simple business in the Indian sub-continent region. In the role of Application Manager/Specialist, some of your key responsibilities will include: - Performing product demonstrations and Proof of Concepts (POC) experiments - Conducting seminars, conferences, and workshops for various audiences - Supporting technical training for Sales Representatives and channel partners - Developing technical selling strategies in collaboration with Sales Representatives - Monitoring market dynamics and implementing strategies for market proficiency - Participating in marketing activities such as roadshows, tradeshows, and workshops to promote Bio-Techne products - Providing post-sales support including customer training and troubleshooting assistance - Coordinating cross-functional engagements for urgent responses - Assisting customers with experimental design and setup guidance Education and Experience requirements: - PhD/MSc./M. Tech in Biotechnology or Biochemistry - Minimum 5-10 years of laboratory or related technical experience - Experience in Analytical method development, Proteins, Monoclonal Antibody analysis - Previous experience in support or training-related roles preferred - Knowledge of Cell culture, Immunoassays, Proteins, Antibodies - Hands-on experience with Flow cytometry, PCR, and Bioassays preferred Key Skills and Abilities: - Strong communication and presentation skills - Effective teamwork abilities - Problem-solving aptitude - Self-motivated and proactive approach - Ability to manage multiple priorities - Fluent in English, additional language skills are a plus - Willingness to travel locally up to 50% of the time - Proficient in computer and internet usage Bio-Techne offers competitive wages, extensive benefits, retirement programs, and opportunities for career development and advancement. The company fosters an empowering and innovative culture where employees are valued and encouraged to contribute new ideas. To protect the interests of all, Bio-Techne does not accept unsolicited resumes from any source other than candidate applications. Unsolicited resumes will be considered Bio-Techne property.,