Troikaa Group Jobs in India

Candidate Having Minimum 5 to 10 Years of Experience in API Pharma/Chemical Industries. · Having knowledge of projects and plant maintenance. · Having knowledge of DG sets, HT/LT panels, breakers, transformers, VFD, and UPS systems. · Having exposure to electrical breakdown and p ...

Candidate having a minimum of 10 to 20 years of experience in pharmaceutical industries. · Having good Knowledge of plant maintenance, utility systems, water systems, Equipment qualification, etc. · Having knowledge of engineering liaisoning-related work. · Having good exposure t ...

Sr. No. · Responsibilities · 1 · To involve in production planning and to monitor inventory. · 2 · To manage the day-to-day manufacturing operation activities of the plant. · 3 · To coordinate with functional departments such as warehouse/Quality control/Quality Assurance/Enginee ...

Male candidate is required for operation of vial or ampoule washing and tunnel, autoclave, disinfectant preparation, filtration and filter integrity related activity. Should have knowledge of documentation and should be able to work in shift. · ...

Manufacturing · Documentation · Operation of API Equipment  · GMP and GDP Knowledge  · Safety Awareness  · Handling of Material · Operation of Powder Processing Area. · ...

Perform routine and non-routine analysis of finished products using various analytical techniques · (e.g., HPLC, UV-VIS, Dissolution). · ➢ Design, execute, and interpret stability studies to assess the shelf life of products, including degradation · pathways and product performan ...

Male candidate is required for autoclave operation, disinfectant preparation related activities. The candidate should have English knowledge and having injectable document related experience. Should be able to work in shifts. · ...

Method developments and validation of analytical method on said sophisticated instruments like HPLC , Gas chromatograph UV Spectrophotometry , autititratour , dissolution etc. as per ICH / Pharmacopeia guideline. · Preparation of protocol and report there off. · Very well versed ...

I.T Turnkey Projects. · Active Directory, Domain controller, GPO, DNS, DHCP. · Managed Hyper-V technology. · Knowledge about hyper converged and tradition architecture. · Veeam Backup & Replication · Administration of Office 365. · Manage IT infrastructure like, high performance, ...

Technical Supervisor  - Autoclave and GMP washer operator requirement for parenteral production department  (ITI persons available) · ...

Training Co-ordination – Manage stakeholders of Corporate Training responsibilities at head office and plant locations for smooth conduct of the planned Corporate Training team activities without affecting the important events and activities of the scheduled location. · Training ...

Manufacturing · API Production · Bulk drugs & Reactor handling · BMR & BPC Filing · Production & Manufacturing · ...

Candidate should haveing min. 5 to 15 years of pharma/chemicla industries experienec. He should have GMP and good documnetation knoladge. · ...

Candidate must be able to read & type on portal in English. If he can speak in English can be an additional skill but not compulsory. Data entry speed in English is essential. · ...

Filling & MDLI · Meter Dose & Liquid Inhilation · Filling & Washing · Machine Handling · BMR BPR Filling · Documentation Process · ...

Packing department, · Labeling machine setting, · Leaflet unit setting,  · cartoon magazine setting & HMI setting. · Tack & Trace System · ...

Sr. No. · Responsibilities · 1.0 · Analytical method Validation/Verification and method transfer · 1.1 · To review, method transfer documents received from ADL prior to execution of method validation at site. · 1.2 · Execution of Method validation/Verification and Method transfer ...

HPLC analysis and documentation, · Assay and RS analysis, · FP / Stability analysis. · LIMS · Documentation. · Viscosity and chemical analysis,  · Particle size distribution. · ...

Product Development of Oral Solid Dosage Forms. · Basic knowledge about different pharmaceutical dosage forms. · Writing/reviewing Standard Operating Procedures (SOPs) ,  · Observing and complying with Good Manufacturing Practice (GMP) and Good Distribution Practice (GDP). · ...

Preparation of the Dossiers for New/RenewalVariations/Query response/Tender for Europe, UK,  US, Canada and Australia Market · ...