Senior Executive - QC
Senior Executive - QC
Posted on :
20-01-2025
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1 Vacancy
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Job Description
Job Title: Senior Executive QC (Analytical LCMS)
Job Location: Hyderabad Telangana India
Job Location Type: Onsite
Job Contract Type: Fulltime
Job Seniority Level: MidSenior level
PopVax is an Indian fullstack biotechnology company developing novel mRNA vaccines and therapeutics using computational protein design. Our first vaccine is a nextgeneration COVID19 booster which will enter a firstinhuman Phase I clinical trial in the U.S. early this year. This vaccine is intended to broaden protection against both current and predicted future SARSCoV2 variants reducing the possibility of a new mutation in the virus suddenly causing another massive wave of infection. We have a preclinical pipeline of 6 additional novel vaccine candidates built on our mRNALNP platform that we will be taking into clinical trials over the next few years. Our work to date has been funded primarily via project agreements totalling 10 million USD with the Bill & Melinda Gates Foundation and Vitalik Buterin's public health & biosecurity organisation Balvi.
We have seen up close that there are incredible capabilities in vaccine design testing and optimization just waiting to be unlocked that will enable us to pursue and perhaps even succeed at realizing wildly ambitious agendas such as ending TB preventing future pandemics via broadlyprotective vaccines tackling the deadly scourge of antimicrobial resistance eliminating debilitating degenerative diseases like multiple sclerosis and curing fiendishly tricky chronic conditions such as ME/CFS and Long COVID. We are initiating multiple new vaccine programs this year to go after a number of these opportunities.
We are seeking an Senior Executive QC (Analytical LCMS) to join our team in Hyderabad (note: inperson only; we do not offer remote work) to play a key role in helping develop optimize and document analytical protocols and assays for our mRNALNP vaccines and therapeutics.
Candidates Must Have
We have seen up close that there are incredible capabilities in vaccine design testing and optimization just waiting to be unlocked that will enable us to pursue and perhaps even succeed at realizing wildly ambitious agendas such as ending TB preventing future pandemics via broadlyprotective vaccines tackling the deadly scourge of antimicrobial resistance eliminating debilitating degenerative diseases like multiple sclerosis and curing fiendishly tricky chronic conditions such as ME/CFS and Long COVID. We are initiating multiple new vaccine programs this year to go after a number of these opportunities.
We are seeking an Senior Executive QC (Analytical LCMS) to join our team in Hyderabad (note: inperson only; we do not offer remote work) to play a key role in helping develop optimize and document analytical protocols and assays for our mRNALNP vaccines and therapeutics.
Candidates Must Have
- MS in Analytical Chemistry Biochemistry or a related field with a minimum of 3 years of experience in analytical method development preferably related to biologics.
- Handson experience of chromatography instrument HPLC/UHPLC with PDA/UV or CAD detector.
- Handson experience of data analysis and reporting on Empower Lab Solutions and Chromeleon software.
- Experience in handling and data analysis on LCMS/MS and/or HRMS platforms for quantitative analysis of large biomolecules (biologics/biosimilars/peptides).
- Proven track record of QC analytical work planning and execution on daily basis
- Understanding of cGMP requirements and its compliance
- Working understanding of global guidelines on analytical method validation 21 CFR Part 11 compliance quality control checks to ensure data quality.
- Working knowledge of MS office tools for data compilation and preparation of report
- Experience in writing clear and precise analytical protocols for newly developed methods and keeping said protocols updated as methods are further developed.
- Excellent problemsolving organizational and communication skills.
- A demonstrated ability to collaborate effectively across departments and with external partners.
- A deep commitment to ethical principles particularly in data collection and analysis.
- Experience in execution of analytical methods for nucleic acids—in particular mRNA & pDNA—or related cell & gene therapy (CGT) materials using techniques including but not limited to HPLC capillary electrophoresis and gel electrophoresis.
- Experience in the use of LCMS for the characterization of chemicals and biomolecules preferably including some experience in the use of LCMS/MS.
- Knowledge of GDP GLP and GMP practices.
- The ability to perform and document instrument validation.
- Experience in the use of compendial methods for biopharmaceutical product testing in a cGMP environment.
- Experience in performing and documenting stability studies for biopharmaceutical products.
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Employment Type
Full Time
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