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 : (1-17 out of 17)
6-11 Yrs
₹ Not disclosed
Roorkee
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
6-10 Yrs
₹ Not disclosed
Gurugram
Ideal Candidate Profile: . 6-10 years of relevant experience in pharma project managementExperience in tech transfer will be an added advantage
7-11 Yrs
₹ Not disclosed
Gurugram
. 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
6-10 Yrs
₹ Not disclosed
Gurugram
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
5-10 Yrs
₹ Not disclosed
Gurgaon/ Gurugram
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
5-10 Yrs
₹ 3-4 Lacs PA
Charkhi Dadri
Maintaining Schools bank accounts,monitoring the transactions,and processing public and non-public fund purchases and payments at the Institute Ensure that all administrative duties,checks,documentati
3-8 Yrs
₹ Not disclosed
Roorkee
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
3-6 Yrs
₹ Not disclosed
Gurugram
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
6-11 Yrs
₹ 5-7 Lacs PA
Greater Noida
Problem solving,Eye for details,should be flexible to work in pressure . Ensure that all administrative duties,checks,documentation,reports and returns (internal and external) are completed accurately
6-11 Yrs
₹ Not disclosed
Roorkee
6 10 years of experience in QC Pharma (OSD preferred) Experience: 610 Years
5-10 Yrs
₹ Not disclosed
Roorkee
Preparation and approval of URS (User Requirement Specifications) for production equipment and systems. Experience: 3 10 Years (depending on level)
8-12 Yrs
₹ Not disclosed
Roorkee
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
1-5 Yrs
₹ Not disclosed
Gurugram
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
1-3 Yrs
₹ 1-3.5 Lacs PA
Ganganagar
. API Production: Execute and oversee the manufacturing processes of active pharmaceutical ingredients,following approved batch records and standard operating procedures (SOPs)Technology Transfer and
3-8 Yrs
₹ Not disclosed
Kolkata(Ganganagar)
Proficient in data analysis,interpretation,and documentation3 8 years of relevant experience in a pharmaceutical R&D or CRO environment
6-8 Yrs
₹ Not disclosed
New Delhi, Gurugram
Key ResponsibilitiesAudit Planning and ExecutionDevelop and implement a risk-based annual audit plan in collaboration with the Head of Internal Audit.Lead and manage internal audit projects, ensuring
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