22 Mass Spectrometry Jobs

Immunology innate immune mechanisms in disease pathogenesis Metabolomics, particularly in the context of aging and metabolic disorders Organoid-Based Cell and Developmental Biology Genomics Informatics Lipid Trafficking Department hosts state-of-the-art research facilities in genomics, mass spectrometry, drug screening, flow cytometry, Drosophila biology, protein expression and characterization, in vivo & in vitro biosafety laboratories and an advanced imaging facility. Additionally, they are home to two major research centers: the Center for Integrative and Translational Research, which support preclinical models of health and disease and the Center of Excellence in Epigenetics. These are further strengthened by university-wide initiatives such as the SNU-Dassault Systems Center that facilitates computational biology studies. Selected candidates will be expected to establish and maintain an independent, externally funded research program, actively engage in undergraduate and graduate teaching, and contribute to the development of interdisciplinary courses and initiatives in collaboration with other departments across the university. Qualification Faculty appointments are open at all levels from Assistant to Full Professor based on the candidate s qualifications, experience, and alignment with the department s strategic vision. Applicants must hold a Ph.D. in the Sciences and have completed a productive postdoctoral tenure that clearly demonstrates strong potential for an internationally recognized and impactful research career.

Walk In Drive For Quality Control Department In Formulation Division @ Bollaram Department:- Quality Control Qualification :-BSC | B Pharmacy | MSC | M Pharmacy Experience :- 2 To 8 Years Division :- Formulation Interview Date:- 08-06-2025 Interview Time :- 9.00AM TO 2.00PM Work Location:- MSNF-II , Kothur | MSNF-V, Rk Puram Venue Location:- Plot No- 42, Anrich Industrial Estate, Bollaram Village, Hyderabad, Telangana 502325 Note:- Candidate should bring Update Resume , Increment Letter, Pay slips, Bank Statement, Certificates, Aadhar Card & Pan Card We are looking for candidate those who have experience in Quality Control Formulation ( HPLC,GC,UV,Dissalution, LCMS, GCMS). About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

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 "

Role & responsibilities 1. generate sample run list from the laboratory's information management system (LIMS). 2. Set up the LCMS system for sample analysis and run samples according to defined methods. Documents activity according to company sops. 3. Process and review instrument data and document all observations according to company sops. 4. Update data into Laboratory's LIMS. 5. Prepare reagents required for routine analysis. 6. Write or contribute to the review of written SOPs in the laboratory. 7. Understand and comply with all safety procedures applicable to the type of work performed. 8. Work with all laboratory personnel to maintain a safe and clean working environment. 9. Work with the QAU and Safety Officer to address and correct issues arising from quality assurance or safety audits. Preferred candidate profile M.SC/M PHARMA ANY GRADUATE/POST GRADUATE

Walk In Drive For Quality Control Department In Formulation Division @ Vizag Department:- Quality Control Qualification :-BSC | B Pharmacy | MSC | M Pharmacy Experience :- 2 To 8 Years Division :- Formulation Interview Date:- 08-06-2025 Interview Time :- 9.00AM TO 2.00PM Venue Location:- Hotel Cygnett Inn Ramachandra , 31-2-4/5, NH16, opp. All India Radio Station, Kurmannapalem, Visakhapatnam, Andhra Pradesh 530046 Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Pay slips, Bank Statement, Certificates, Aadhar Card & Pan Card We are looking for candidate those who have experience in Quality Control Formulation ( HPLC,GC,UV,Dissalution, LCMS, GCMS). About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

Walk In Drive For Quality Control Department In Formulation Division @ Jadcherla Department:- Quality Control Qualification :-BSC | B Pharmacy | MSC | M Pharmacy Experience :- 2 To 8 Years Division :- Formulation Interview Date:- 01-06-2025 Interview Time :- 9.00AM TO 2.00PM Venue Location:- ELITE HOTELS & RESORTSNH44,Bangalore Hyderabad Hwy Jadcherla, Telangana 509301 Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Pay slips, Bank Statement, Certificates, Aadhar Card & Pan Card We are looking for candidate those who have experience in Quality Control Formulation ( HPLC,GC,UV,Dissalution, LCMS, GCMS). About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

Roles and Responsibilities Conduct bioanalytical research activities such as method development, validation, and sample analysis using techniques like HPLC, GC, mass spectrometry, chromatography, spectrophotometry, and polarimeter. Develop and validate methods for bioanalysis of biologics and biosimilars according to regulatory requirements (e.g., USFDA). Collaborate with cross-functional teams to ensure timely delivery of high-quality results. Perform stability testing of biological products under various conditions. Troubleshoot issues related to instrument calibration, maintenance, and operation. Desired Candidate Profile Bachelor's degree in Pharmacy (B.Pharma) or Master's degree in Pharmacy (M.Pharma) from an accredited institution or M.Sc. Strong understanding of analytical instruments such as HPLC/UPLC/GC/MS/ICP-MS/Wet Analysis etc.

Role & responsibilities Preferred candidate profile

Analytical Support & Method Development Plan and conduct GC-MS, LC-MS, and other analytical techniques for flavors, perfumes, aroma chemicals, and natural products, while contributing to method development and technical growth of the team. Instrument & Lab Management Manage and maintain analytical instruments and lab operations, ensuring SOP compliance, accurate documentation, and inventory control. Cross-Functional Collaboration Work closely with Creation, Application, QA, and global/regional teams to ensure alignment and effective analytical support across functions. Volatile Compound Analysis Apply isolation and analytical techniques particularly GC with various detectors and GC-MS for in-depth volatile analysis. Reporting & Documentation Prepare, review, and manage analytical reports using in-house tools, and clearly communicate findings and recommendations to stakeholders. Scientific Expertise & External Coordination Serve as a subject matter expert in analytical/flavor chemistry, supporting global collaborations, literature research, and coordination with external resources. We bring: A team of diverse employees who aren t afraid to think outside of the box. A truly global and collaborative team that cares about the experience of our employees. The encouragement you need to develop and achieve personal growth. A role that is crucial on projects and allows you to build your brand. A caring and supportive environment where you re empowered to grow and share your ideas. You bring: MSc. (with 5+ years experience) or Ph.D. (with 2+ years experience) in analytical chemistry or a related field. Proven expertise in gas chromatography and method development in commercial or research lab settings. Extensive hands-on experience with mass spectrometry for complex analytical applications. Knowledge of ISO 17025:2017 standards is a strong advantage. A curious, problem-solving mindset with a drive to explore new approaches and deliver innovative solutions. A strong sense of ownership and accountability , with the ability to deliver meaningful results and work collaboratively within diverse teams.

Your key responsibilities: Analytical Support & Method Development Plan and conduct GC-MS, LC-MS, and other analytical techniques for flavors, perfumes, aroma chemicals, and natural products, while contributing to method development and technical growth of the team. Instrument & Lab Management Manage and maintain analytical instruments and lab operations, ensuring SOP compliance, accurate documentation, and inventory control. Cross-Functional Collaboration Work closely with Creation, Application, QA, and global/regional teams to ensure alignment and effective analytical support across functions. Volatile Compound Analysis Apply isolation and analytical techniques particularly GC with various detectors and GC-MS for in-depth volatile analysis. Reporting & Documentation Prepare, review, and manage analytical reports using in-house tools, and clearly communicate findings and recommendations to stakeholders. Scientific Expertise & External Coordination Serve as a subject matter expert in analytical/flavor chemistry, supporting global collaborations, literature research, and coordination with external resources. We bring: A team of diverse employees who aren t afraid to think outside of the box. A truly global and collaborative team that cares about the experience of our employees. The encouragement you need to develop and achieve personal growth. A role that is crucial on projects and allows you to build your brand. A caring and supportive environment where you re empowered to grow and share your ideas. You bring: MSc. (with 5+ years experience) or Ph.D. (with 2+ years experience) in analytical chemistry or a related field. Proven expertise in gas chromatography and method development in commercial or research lab settings. Extensive hands-on experience with mass spectrometry for complex analytical applications. Knowledge of ISO 17025:2017 standards is a strong advantage. A curious, problem-solving mindset with a drive to explore new approaches and deliver innovative solutions. A strong sense of ownership and accountability , with the ability to deliver meaningful results and work collaboratively within diverse teams.

Ensure that the manufactured products consistently meet established standards, customer specifications, and industry regulations Optimize processes and drive continuous improvement initiatives Product Modification/ Development as per customer need Required Candidate profile B. Sc Chemistry with M. Sc Polymer Science mandatory 12+ years' experience in Quality Assurance & Control in a chemical/ polymer manufacturing company (preferably in polystyrene manufacturing)

Walk In Drive For Quality Control In Formulation Division @ Kothur Department :- Quality Control Qualification :- BSc | B Pharmacy | MSc | M Pharmacy Experience:- 2 to 8 Years Division :- Formulation Interview Date:- 05-04-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur Venue Location :- Msn Laboratories Pvt Ltd Formulation Unit -2 Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Payslips, Bank Statement, Certificates, Aadhar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

Key Responsibilities: Lead the design, development and validation of new analytical methods for evaluating the quality, safety, nutritional content of Food & Nutra products. Manage & oversee the analytical laboratory operations, including equipment, personnel workflows to ensure accurate and reliable results. Collaborate closely with R&D Quality Assurance, Regulatory teams to ensure analytical method align with product development goals and regulatory requirements. Drive continuous improvement of analytical methodologies to enhance efficiency, accuracy and precision in food & nutra-analysis. Ensure compliance with local and international food safety and quality standards such as FSSAI, FDA or ISO. P Provide technical expertise including chromatography, spectroscopy, mass spectrometry and microbiological testing. Conduct troubleshooting and root cause analysis to resolve analytical issues in food & nutra product analysis. Maintain accurate documentation of analytical procedures, method validation reports and other relevant records. Stay updated with the latest advances in food & nutra-analysis technologies and incorporate cutting edge methods into the labs practices.

Walk In Drive For Quality Control In Formulation Division @ Kothur Department :- Quality Control Qualification :- BSc | B Pharmacy | MSc | M Pharma Experience:- 2 to 8 Years Division :- Formulation Interview Date:-29-03-2025 Interview Time:- 9AM TO 2.00PM Work Location :- MSNF-II, Kothur Venue Location :- Msn Laboratories Pvt Ltd Formulation Unit -2 Survey Nos.1277 & 1319 to 1324, Nandigama (Village), Kothur (Mandal, Mahbubnagar, Telangana 509001) Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Payslips, Bank Statement, Certificates, Aadhar Card & Pan Card About Company:- MSN Group is the fastest growing research-based pharmaceutical company based out of India. Founded in 2003 with a mission to make health care affordable, this Hyderabad-based venture has Fifteen API and Six finished dosage facilities established across India & USA. The group has an integrated R&D center for both API and formulation under one roof, dedicated to research and development of pharmaceuticals to make them more accessible. With core focus on speed and consistency in delivery, MSN has achieved the following: More than 900+ national and international patents Product portfolio featuring over 450 + APIs 300+ Formulations, covering over 35 major therapies Won the trust of more than 40 Million patients across 80+ countries globally Innovation and speed form the crux of our business strategy. Backed by a dedicated and experienced team of over 14,000 the organizational environment at MSN integrates multiple disciplines and functions by effective implementation of goals and objectives through technology, coupled with Integrity, Imagination and Innovation.

Greetings from Atria Power!! (www.atriapower.com). We are hiring for B.Tech Mechanical or Chemical Engineering Graduate with 5 + years of Experience in Bio Mass Power Plant for Atria Power. About Atria Group. Atria Group was established in 1950. We are one of the most eminent business groups in South India. Atria Group is with business verticals which includes Power(Atria Power), Internet Technology(ACT Broadband), Media Services(ACT cable TV), Hospitality (Atria Hotels), Education (Atria Institute of Technology & Xceler) and Real Estate. Should be capable of first principles design of Biomass based power plants including fuel handling system and boilers. Should generate Specification and RFQ for procurement of Biomass system. Proficient in Testing and Acceptance of Biomass systems. Requirements. Tech Graduate Mechanical or Chemical Engineering. 5+ years of Relevant Experience. Hands on Experience in AutoCAD. Proficient in MS project. Proficient in MS Office. Fluent communication skills both verbal and written. Sujitha Balan. 073386 99681 (ref:mfg.careers). Show more Show less

The responsibility of the Applications Specialist / Scientist, India MS Applications is to provide full portfolio application support for mass spectrometry based solutions and instrumentation offered by Bruker and its associated applications in the region , whilst maintaining and developing existing and new relationships with clients and ensuring Bruker s high quality standards are maintained. One should have a hands-on experience using Mass Spec for Proteomics, metabolomics, lipidomics applications from sample preparation to data interpretation. The individual should have a pleasing manner, excellent communication skills, computer literacy, especially with regard to modern scientific user interfaces, document and presentation preparation and report writing. The person should have the tenacity and self-motivation inspired by success, enthusiasm, drive and initiative with a high degree of personal integrity. The personality of a natural team player, willing and able to build confidence and to establish cooperative relationships with personnel throughout the Company. He/ she should have the ability to operate independently and as part of the greater business group with self-discipline and to decide priorities in a rapidly changing commercial environment. Providing telephone, remote and on-site support to users of Bruker MS products specifically in "OMICS" applications. Provide specialized technical sales support to sales organization approaching new and existing clients for product and solution. Conduct training and follow-up visits to Bruker clients presenting to key specialist and technical staff. Draw upon your mass spectrometry application experience to assist users to implement and maximize Bruker instrumentation usage in their environment Maintain existing and develop new relationships through maximising assigned application expertise with clients Maintain relationships with key Bruker collaborators, partners and colleagues. Maintain a high level of product knowledge. Maintain CRM database. Present scientific presentations on Bruker MS solution at conferences or seminars. Prepare all reports required by management including monthly reports and expenses in time. Work closely with other application colleagues in the region and willingness to support the team extensively online or at site as required. Qualifications Masters (minimum) degree in science subject (Chemistry / Biochemistry / Microbiology / Biotechnology). Laboratory working experience in either Research Life Science or industrial laboratory. Experience in full understanding of various MS platforms like QQQ, Ion Trap, MALDI TOF, MALDI TOF-TOF and any other advanced MS techniques. Expert knowledge of analytical Mass spectrometry, complete OMICS workflow and routine applications. Clear understanding of the India research, pharma, life science and clinical markets together with a proven track record of working with technology-based products in those markets. Understanding of the SouthEast Asia region would be advantageous. Good market intelligence with respect to competitive products and vendors. Presentation, data interpretation and sample preparation skills and willingness to travel extensively are essential.

The key responsibilities would be: Responsible for an Analytical team involved in Method development, Method Transfer, and Validation for various stages of drug development. Method Validation of analytical methods per internal and country-specific regulatory guidelines and execution through proper protocols. Responsible for reviewing and approving analytical data in the CMC section of regulatory files. Effective method development ensures that laboratory resources are optimized while methods meet the objectives required at each stage of drug development. Responsible for ensuring delivery timelines and adherence to customer quality and standards and customer Relationship management. Facilitating scientific and technical discussions with team members and external collaborators to resolve issues. Participating with group members to explore innovative and improved ways for meeting the group's deliverables while contributing to the scientific depth of the group Demonstrated experience in designing and writing stability protocols, investigational or registration studies, and analyzing and trending large sets of data. Desired Candidate Profile Build a highly talented team to drive the successful integration of objectives. Coach and develop staff; engage in the recruitment, training, and retaining talented scientific pool and provide cross-training wherever required. Mentor and coach the existing team and develop a pipeline of high-caliber and talented professionals with the right skill sets. Drive career advancement plans, objective/goal setting, deciding on the Goals & Objectives for direct reports, and ensuring a similar approach for down-the-line reporting in the organization. Structure /improve processes and systems to ensure operational excellence in the organization. Direct and guide the team to engage in proposal writing, contract negotiation, sales presentations, and support of client relations As a part of the senior leadership team, participate in formulating and reshaping strategies that affect Sipra's Lab's growth, operations, and future plans. Influence the external environment through thought leadership; build visible and active engagement with key opinion leaders, professional societies, academic institutions, and, most importantly, current and future clients to align research to areas of mutual interest. Develop productivity metrics and initiatives to improve productivity year on year through a combination of talent, processes, and technology. Note: This is a senior Leadership role Interested candidates can also send their resumes to hr@sipralabs.com.

Role & responsibilities :- 1) Knowing HPLC/ GC, Dissolution, UV, FT-IR, Potentiometer Troubleshooting, Calibration, Method Validation and Method Development. 2) Perform the analysis individually for In process and stability samples as per plan. 3) Follow Good manufacturing practices, Good laboratory practices and Good documentation practices in ADL. 4) Method Development of new products for test like Cleaning, Assay, Residual solvent, Dissolution & organic impurities. 5) Preparation, storage and usage of Volumetric / Reagent / Standard / Indicator solution. 6) Perform the calibration and verification of all instrument / equipment as per calibration scheduled. Preferred candidate profile :- Post Graduation in M.Sc. Analytical Chemistry ./M. Pharma From Pharma Background Industry. Knowing GCMS, LCMS is added advantage Perks and benefits :- As per company

Key Responsibilities Need to have strong theoretical knowledge (HPLC/LCMS/Prep.HPLC/SFC) Plan and conduct the analysis with required skills. Record the observations meticulously and update to the TL/SME. Share and discuss the observations with supervisor. Independent in maintaining the instrument and setting up the instrument for analysis. Expected to be aware of basics in analytical chemistry (basic analytical techniques Theory and application) as well as handling of laboratory equipment / instruments with basic understanding. Expected to be aware and working in a safety compliant manner

Hiring for Technical officer - Mass spectrometry facility Applications are invited for technically qualified candidates for Technical Officer position at Amity Lipidomics Research Facility (ALRF). Period of Engagement: Initially for a period of one year which can be extended as per performance of the candidate. Essential qualification: Candidate must have postgraduate degree of M.Tech/M.Sc. in Chemical Sciences/Pharmacy/Life Sciences/Instrumentation with demonstrable research experience. Desirable qualification: Candidate should have handled LCMS and GCMS, preferably handling triple stage quadrupole/linear ion trap mass spectrometer, Q-Trap 4500 (SCIEX). How to apply: Interested candidates may submit their resumes at sgoel@ggn.amity.edu latest by 24th March, 2025 with the following details - Details of Academic & Professional/Technical Qualifications Details of past experience & present employment Present Pay/emoluments Names and complete addresses along with E-mail and Phone No. of three independent responsible persons as referees who can comment on the candidates suitability and temperament. https://www.amity.edu/gurugram/lipidomics-research-facility.aspx Amity Institute of Biotechnology, Amity University Haryana, Gurgaon (Manesar) - 122413

Mass Spectrometry specialist Location: Pune Date posted: 06 Aug 2024 Apply until: 31 Dec 2025 Position: Regular Experience: 2-7 years Job function: Analytical Services Role: Full time Job Description Responsible for method development, sample preparation, chromatography, data acquisition, data analysis and data interpretation using a variety of mass spectrometry and software platforms Writing standard operating procedures, scheduling sample analysis, analyzing data, maintaining accurate records, and preparing reports Design and execute protocols and experiments, modify protocols as needed. Responsible for overall laboratory organization management. Planning for equipment maintenance and replacement. Assist in procurement of equipment and related consumables. Following Good Laboratory Practices EHS policies in the operations of the lab. Interacting with the clients and understanding their testing requirements Conceptualize and plan Technical Workshops especially those with hands-on sessions Requirements and preferences Qualification: Ph.D (Analytical Chemistry) Experience with proteins; especially, intact mass analysis, peptide mapping, sequencing, qualitative and quantitative proteomics, synthetic peptides 5+ years of hands-on experience with mass spectrometry techniques and related computational tools Orientation and interest in setting up and operating service facilities of use to industry and startups. Strong people management skills Solid interest and skills in hands-on work in lab management, equipment handling and maintenance of the same. Strong written and oral communication skills, attention to detail, persistence, and resilience. About the Team Center for BioPharma Analysis (CBA) is an initiative of Venture Center supported by the National BioPharma Mission , BIRAC (Government of India). CBA supports with complete characterization of Biopharmaceutical Product/Biosimilar as per the ICH Q6B guidelines with GLP Compliant workflows and our state-of-the-art techniques like Surface Plasmon Resonance, SEC-MALS and more. For more information: https://bioanalysis.in/ General requirements and expectations from Venture Center employees: Venture Center is a non profit organization with aim to benefit society by promoting entrepreneurs and start ups. Thus, Venture Center seeks employees and consultants with a strong interest and passion in seeing technology innovators, entrepreneurs, and start ups succeed, and a strong "service" ethos. A strong feature of Venture Center jobs is the rich learning environment and opportunity provided to employees to experiment, take initiative and be creative. The work of most employees has visible impact which can be satisfying. All employees benefit from access to high quality facilities and work environments. Compensation packages can be flexible but are often conservative due to Venture Center s non profit status. General requirements include: a) strong ethical standards and work ethics, b) comfort with computers, computer applications and internet, c) strong communication skills spoken and written. Venture Center s working hours are 9 AM 6.00 PM (Monday to Saturday) and are designed to keep operations of Venture Center convenient for the start ups, entrepreneurs, inventors and others that the organization serves. Managers in certain functions are provided the opportunity to avail of flexible hours. All jobs are located in Pune, Maharashtra, India. Venture Center is an equal-opportunity employer and does not discriminate against any employee or applicant based on age, color, disability, gender, national origin, race, religion, sexual orientation or parental status.

Roles and Responsibilities Develop analytical methods for biochemistry samples using GC-MS, LCMS, and other relevant techniques. Conduct method validation, optimization, and transfer to ensure accuracy and reliability of results. Collaborate with cross-functional teams to resolve method-related issues and improve overall efficiency. Maintain accurate records of experiments, data analysis, and reporting in accordance with regulatory requirements. Stay up-to-date with industry developments in mass spectrometry technologies and apply this knowledge to improve laboratory operations. Desired Candidate Profile 2-7 years of experience in Analytical Method Development & Validation (GC-MS & LCMS). MS/M.Sc(Science) degree in Bio-Chemistry or Chemistry from a recognized university. Strong understanding of chromatography principles, including HPLC/UPLC systems. Proficiency in developing analytical methods for biochemistry samples using various instruments such as GC-MS/MS.