. 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 : (1-16 out of 16)
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
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
Experience: 4- 10 years of experience in a manufacturing plant setup,preferably in the pharmaceutical or chemical industry. Education: Graduate / Post-Graduate in HR / Labour Welfare / Industrial Rela
Job Description Position: HR Recruiter(Executive) (Talent Acquisition) Location: Delhi Summary of Job : As a recruiter, your analytical skills, enthusiastic attitude and process oriented exec
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
Masters degree in Human Resources Oversee the filing of contracts and identify and implement actions required to Must be aware of full transition from manual to automation Education Qualification : E
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