Company Jobs

Preparation and review of test procedure, development reports, method validation protocol and LNBs. Perform calibration of the analytical instruments as per calibration schedule. Analytical method development, validation, and sample analysis for Extractables and Leachables using HPLC, LCMS, GCMS and ICPMS. Identification and characterization of unknown impurities by LCMS.

Capture critical unit operation parameters and ensure accurate representation in business process flow mappings. Facilitate workshops and discussions to align stakeholders on current workflows and identify gaps or improvement areas. Data Analysis and Technical Insights.

B.Sc. / B.Pharm/ M.Sc.; Hands-on experience in Analytical Method Validation, Method Transfer, Protocol Review, Analysis of CU, BU, Assay on HPLC & UV Spectrophotometer, BD, TD, PSD & Water Content, Tests are performed daily to daily on job.

B.Sc./ B.pharmacy graduate with MBA or equivalent qualification. Proven track record of leading a large, geographically diverse sales team, including at least 2 years of experience overseeing half of India with consistent performance, growth and positive P&L outcome.

Must know process validation cleaning validation verification and hold time studies. Candidate should also have exposure to EU, MHRA, and USFDA regulatory audits.

Plan and coordinate with various departments like QA, QC and Production, to project the document requirements for appropriate submissions. Co-ordination with clients for the tracking and status update of project plans.

Candidates having hands-on experience in Analysis of Raw Material, Packaging Material, Finished Goods, Stability, Method Transfer and Laboratory Investigations. Should have sound knowledge of QMS like Deviations, Change Control, Vendor Management etc.

Achieve sales targets and execute growth plans for East Africa. Develop and implement strategies to expand market share in the region. Identify and negotiate business partnerships in untapped territories.

To author and gain approval of scientific and regulatory submission documents that comply with global regulatory standards. To maintain key business relationships with appropriate cross-functional product team members.