Company
pharmaceutical
ExpertScience&Technology
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Expert Science &Technology. Skills: analytical development, oligonucleotide/peptide analytics, chromatography techniques, mass spectrometry, GMP. performing method feasibilities. validate robust analytical methodologies applied to innovative Oligonucleotides/peptide therapeutics”
Industry & Context.
investigations on SST failures, OOX/Deviations/Change controls as needed.
based in the Genome Valley, Hyderabad
What They're Looking For.
Must Have
Ph.D. in Analytical Chemistry or an equivalent qualification with a minimum of 1–3 years of experience, or M. pharm/M. Sc. with at least 8 years of experience within the pharmaceutical industry, specifically in analytical development., expertise in oligonucleotide/peptide analytics, Understanding of general regulatory and quality expectations., GMP experience is a must, Good scientific background, Good knowledge of software and computer tools such as Office package, LIMS, chromatography data-evaluation software (e.g. Chromeleon) etc., Profound expertise in liquid chromatography separation techniques such as (RP, IEX and HILIC) is a must.
Nice to Have
Experience in mass spectrometry applied to biological molecules would be an asset, Experience in Mass Spectrometry (ranging from mass confirmation to actual quantitative analysis of impurities and sequencing) is an asset
What You'll Do.
performing method feasibilities
validate robust analytical methodologies applied to innovative Oligonucleotides/peptide therapeutics
and document scientific experiments
documentation and submission of raw data in an appropriate data system
execution of laboratory activities
Support in evaluation and interpretation of results
Responsible for assigned laboratory related area/activities
implementation and maintenance of lean/efficient/environmentally sustainable practices in the laboratory
Proactively communicate key issues and any other critical topics
meet KQI (Key quality indicators) and KPI (Key performance indicators) for all assigned activities
Support internal and external audits
How You'll Work.
Team & Collaboration
Proactively communicate key issues and any other critical topics in a timely manner to the manager and/or to any other relevant project team member(s).
Communication Scope
communication skills including presentation and scientific/technical writing.
Process & Methodology
Plan, organize, execute, and document scientific experiments (e. g. , analytical method developments/ validations/ transfers/ stability/ release testing, formulation development analytics etc. ) according to the agreed timelines and appropriate quality standards.
Full Job Description
**Job Description Summary** As part of this group, you design, plan and/or perform scientific/technical studies. By bridging analytical science to the clinical performance, you will drive the transformation of our molecules into medicines that improve and extend patient’s lives. The position is based in the Genome Valley, Hyderabad, within the Technical Research and Development Organization (TRD) of Development **Job Description** **Key Responsibilities** * Responsible for performing method feasibilities and validate robust analytical methodologies applied to innovative Oligonucleotides/peptide therapeutics. Strong experience in various chromatography techniques is a pre-requisite. Experience in mass spectrometry applied to biological molecules would be an asset. * Plan, organize, execute, and document scientific experiments (e.g., analytical method developments/ validations/ transfers/ stability/ release testing, formulation development analytics etc.) according to the agreed timelines and appropriate quality standards. * Accountable for documentation and submission of raw data in an appropriate data system (for e.g., LIMS test activation and results entry). * Responsible for good documentation practices (GDP) and good laboratory practices (GLP) during execution of laboratory activities. * Support in evaluation and interpretation of results including investigations on SST failures, OOX/Deviations/Change controls as needed. * Responsible for assigned laboratory related area/activities (e.g., chemical/reagents/consumables/samples/column/ glassware management etc.). Responsible for implementation and maintenance of lean/efficient/environmentally sustainable practices in the laboratory. * Proactively communicate key issues and any other critical topics in a timely manner to the manager and/or to any other relevant project team member(s). * Responsible to meet KQI (Key quality indicators) and KPI (Key performance indicators) for all assigned activities. Support internal
Applying for this Expert Science &Technology role?
Most applicants get filtered before a human reads their resume. See if yours makes the cut.
How to Apply on Workday
- Workday has a multi-step form — save your progress after every section.
- "Apply With LinkedIn" can fail or lose data; manual entry is more reliable.
- Watch for the "Submit for Review" final step — hitting "Save" alone does not submit.
- Job requisition numbers are useful when following up with HR by email.
ANONYMOUS · UNFILTERED
What do employees actually say about this company?
Real rants from real employees. Read before you apply.