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
All Jobs : (1-16 out of 16)
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
Candidate should address scientific queries received from sales / marketing/doctors with sound scientific back-up Candidate should be from well recognized Reputed Govt InstituteShould be proficient in
Job Description Training the sales team /Medical Representatives of the company on the topics allocated. Literature search in companies brands/products and therapeutic areas of operation.Providing in
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
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
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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