. To prepare Master documents of Analytical Method Development / Analytical reports for submission & validation batches. . Material Master creation of Material code/ Vendor code in ERP of MIC creati
All Jobs : (1-14 out of 14)
Experience: 4 8 Years4 8 years of experience in qualification and validation in OSD pharma Good documentation and communication skills
Proficient in data analysis,interpretation,and documentation3 8 years of relevant experience in a pharmaceutical R&D or CRO environment
and prepare reports. . Support regulatory department for product documentation,filing,etc. . Should have knowledge about SAPExperience: 10- 14 years (Apart from the QA functions,working on new proje
Walter Bushnell Pharmaceuticals is hiring a Senior Research Associate Analytical R&D for its OSD formulation facility in Roorkee.The ideal candidate should have hands-on experience in Analytical Metho
Qualifications & Skills: . Education: M Pharm / B Pharm in Pharmaceutics or related fieldWalter Bushnell is seeking a Research Scientist - Formulations with experience in Solid Oral Products to join
Position DGM/GM Projects | Delhi NCR ExecutionJob Location: Delhi NCR (Base: Delhi)Job Type: Full-Time | PermanentReporting to: Head Projects / COO / CEO – Real Estate / Promoters / DirectorsExperi
To prepare Master documents of MFC / MFR / BMR / BPR /PVP / Development reports for submission & validation batches. . Material Master creation of Material code/ Vendor code in ERP. . MIC creation o
We are hiring a Research Scientist Formulation R&D for its Roorkee facility.The candidate must have strong experience in formulation development,technology transfer,and scale-up activities for regulat
Knowledge of scale-up processes,and familiarity with Good Manufacturing Practices (GMP) and ICH-guideline. . Hands-on experience with bench-scale and pilot-scale synthesis is essential. Preferred ca
Ideal Candidate Profile: . 6-10 years of relevant experience in pharma project managementExperience in tech transfer will be an added advantage
Qualification:- B Pharma Proficient in MS Office and quality management software. Minimum of 3-5 years of experience in IPQA within the pharmaceutical industry,preferably in API manufacturing. Experie
. API Production: Execute and oversee the manufacturing processes of active pharmaceutical ingredients,following approved batch records and standard operating procedures (SOPs)Technology Transfer and
Preferred candidate profile : . Should have good technical skill and knowledge. . Strong organization,prioritization and planning skills. . Good communication skill and interpersonal relationship.
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