Preference: Candidate must be from Pharma Industry Must be proactive,self-driven and energetic Must be a quick thinker,Extrovert,team player,enthusiastic,active listener,learning attitude Qualificatio
All Jobs : (1-16 out of 16)
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
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
Competencies Excellent communication skills in English and Hindi Strong organizational and project management skills with the ability to multi task,prioritize,and manage operations. Education Qualific
Knowledge of regulatory expectations for APIs and CMC documentation preferredExperience: . 1 to 3 years (Research Associate Entry level) . Strong hands-on experience in peptide API process developme
Greenfield project experience preferred (lab setup,equipment qualification,method validation / transfer) Experience: 4 6 Years4 6 years of QC experience in a pharma OSD facility
Ideal Candidate Profile: . 6-10 years of relevant experience in pharma project managementExperience in tech transfer will be an added advantage
. 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
The ideal candidate should have experience in equipment / utility qualification documentation and QMS activities in a pharmaceutical setup. . Key Responsibilities: . 5 8 years of experience in QA Ph
Experience Required: 3 to 6 years of hands-on experience in formulation IPR. . Qualification: M Pharm (Pharmaceutics / Pharmaceutical Chemistry or equivalent). Company name: Walter Bushnell. Work Loc
6 10 years of experience in QC Pharma (OSD preferred) Experience: 610 Years
Preparation and approval of URS (User Requirement Specifications) for production equipment and systems. Experience: 3 10 Years (depending on level)
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
Qualifications: . BE / B Tech or ME / M Tech in Chemical Engineering Professional certification in process engineering or related areasProficiency in process analysis,process modelling and simulation
. API Production: Execute and oversee the manufacturing processes of active pharmaceutical ingredients,following approved batch records and standard operating procedures (SOPs)Technology Transfer and
Proficient in data analysis,interpretation,and documentation3 8 years of relevant experience in a pharmaceutical R&D or CRO environment
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