Analytical Method Development Officer - Roha Tulip Consulting Services

5.0 - 6.0 years

4 - 5 Lacs

Roha

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Knowledge of Method Validation & verification as per Pharmacopiea requirement. To perform Method Validation & verification of Chromatographic GC / HPLC methods. Preparation of specification in DMS & SAP system. SOP preparation related to AMD work. Required Candidate profile Candidate Must be MSc Regular. AMD protocols & report preparation, non-chromatographic methods. Maintain require stds & Impurities stock, list etc. Operation of instruments like HPLC,GC,UV,IR etc.

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AMD Officer (Pharma) - Roha Tulip Consulting Services

5.0 - 6.0 years

4 - 5 Lacs

Roha

Work from Office

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Chemist Quality control Dalas Biotech

2.0 - 7.0 years

1 - 4 Lacs

Dharuhera, Neemrana, Bhiwadi

Work from Office

Urgent Opening for QC Chemist Knowledge of HPLC, GC, Stability , KF, UV, validation, Documentation etc

Posted 3 weeks ago

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Senior Research Associate Syngene

1.0 - 3.0 years

3 - 5 Lacs

Bengaluru

Work from Office

Key Responsibilities: The successful candidate will become a member of a team with overall responsibility for purification and analysis of small compound libraries to support lead optimization in medicinal chemistry programs. Individual responsibilities will include analysis and purification of small molecule library compounds (primarily by analytical and preparative LCMS), HPLC and mass spectrometer instrument maintenance, training, and analytical data management. Optimization and/or troubleshooting of analysis conditions will be required to ensure on time delivery of high purity products. Educational Qualification: M.Sc. in Chemistry/Analytical chemistry with 1-3 years of experience in practical analytical chemistry, including both analysis and purification. Experience: 1-3 Years Required Skills: Knowledge and expertise in preparative HPLC, LCMS, and other chromatographic techniques is desirable. Strong computer skills and good communication skills, are preferable. Demonstrated ability to work in a highly team oriented, multitasking environment with experience in technology enabled analysis and purification will be highly appreciated. Behavioral Skills: Good communication skills, good presentation skills, hardworking, sincere and a team player. Must demonstrate integrity and take accountability of their work

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Assistant Manager - Production/Manufacturing Premas Biotech

7.0 - 9.0 years

7 - 9 Lacs

Manesar

Work from Office

Role & responsibilities : Knowledge in handling and troubleshooting purification chromatography systems & columns at small scale and large scale Various Chromatography techniques like Ion exchange, Affinity, HIC etc. TFF systems , Hollow Fiber/cassette Should be well versed with FPLC, AKTA- Process, AKTA- Pilot. Capabilities for linear scalability of R&D process to Mfg. scale. Batch planning, Resource management, Team Training. Shift Schedule Preparation, Audit readiness Handling QMS, Project management, Deviation, Change control, CAPA, OOS, GDP Plan daily downstream execution activities Drive the qualification activities for all downstream equipment. Execute, troubleshoot, and scale up of purification processes, aseptic Operation. Compliance to cGMP in all the manufacturing activity, and timely closure of executed documents and batch records. Active trouble shooting to minimize the various risks prior to execution and during execution. Preferred candidate profile: Should have good communication and presentation skills (verbal & written) Person with high self-motivation, go-getter, enthusiastic. Leadership skills, with steadfast resolve and personal integrity Should have minimum 7 + years of Experience.

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