To Perform and review Method Transfer/verification/validation of Assay, Dissolution, Related compound and Residual solvents etc. for new projects using instruments like HPLC,UV, IC ,GC, Autotitrator and AAS etc. Preparation of Method Transfer/Verification/Validation protocol (API, Excipients and Finish product) like HPLC,
Extractables & Leachables (E&L) Execute extractables and leachables studies for pharmaceutical packaging materials, process contact materials, and device components. Perform sample preparation, extraction studies, and analytical testing as per study protocols. Support identification and characterization of unknown
Description: Prepare and review qualification protocols and reports for equipment, utilities, and systems (DQ, IQ, OQ, PQ, as applicable). Coordinate and monitor qualification activities with Engineering, Production, and Validation teams. Ensure qualification documentation complies with GMP and
Description: Analytical Development - Injectable & Complex Injectable This role supports the development of drug substances and drug products by contributing to the design and execution of analytical methods used to evaluate quality attributes across various Injectable dosage forms.
Description: Analytical Development - Injectable / Complex Injectable The position supports peptide and oligonucleotide drug substance (DS) and drug product (DP) development through the development, optimization, validation, transfer, and application of advanced analytical methods to evaluate critical quality attributes (CQAs).
Description: To plan and perform method development, analysis and validation activity by using Particle size analyser. To plan and perform method development, analysis and validation activity by Titration,TLC,UV,XRPD,ICP-MS, Potentiometric. Responsible for Handling and analysis for Qualification of PRS, WS and
Description: The position is responsible for in-process and final product quality analyses and inspection in compliance with approved standards and regulatory requirements. The role involves interpreting and evaluating analytical results for accuracy and precision against established specifications.
Be the First to Apply DivisionPiramal Pharma Solutions Piramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a
Review analytical data for Raw Materials (RM), Packaging Materials (PM), in-process samples, Finished Products (FP), stability samples, working standards, reference standards, and other test samples. Review and approve Certificates of Analysis (COAs) for RM, PM, in-process samples,
Description: This role supports the development of drug substances and drug products by contributing to the design and execution of analytical methods used to evaluate quality attributes across various dosage forms, with a specific focus on inhalation chemistry,
This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in
Job TitleProject Engineer Job Description Summary Job Description Requisition Field Description Example Job Posting Title Market appropriate job title Mechanical Billing Engineer Job Description Summary Purpose of the role in 1-2 sentences This Role is part
Job TitleProject Engineer Job Description SummarySupport the PMC team in mechanical quantity verification, contractor billing validation, progress monitoring, and coordination of mechanical works for an industrial project. Ensure accurate measurement certification, compliance with project specifications, and timely
This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in
This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in
JOB TITLE Assistant Manager- Quality Control, Chemistry REQUIREMENTS Education / Experience Post Graduate in Science (Organic or Analytical Chemistry ) 8 to 10 years in chemical & instrumental testing laboratory with exposure to GMP, GLP. Technical skills
Lead and maintain the Pharmaceutical Quality System (PQS) by establishing, implementing, monitoring, and continuously improving quality systems in compliance with ICH Q7, ICH Q9(R1), ICH Q10, applicable cGMP regulations, and company quality policies to ensure a
About the Company Ajanta Pharma is a specialty pharmaceutical company committed to developing, manufacturing, and marketing high-quality, affordable medicines. Headquartered in Mumbai, India, the company has a strong presence across India and international markets, with operations
JOB TITLE Sales & Operations Planning (S&OP) JOB ROLE Responsible for executing End-to-End S&OP Cycle FUNCTION / DEPARTMENT Procurement SUB-FUNCTION Supply Chain Management REPORTING TO DGM – Sales and Operations Planning JOB LOCATION Sanand, Ahmedabad, Gujrat
Job Description Manager / Senior Manager – Quality Assurance (Vendor Qualification & Supplier Quality Management) Department- Quality Assurance (Corporate QA) Location - Vapi, Gujarat Qualification M.Pharm / M.Tech / M.Sc. (Pharmaceutical Sciences or Life Sciences) Candidates