Salary: NegotiableAge: 25 – 35yrsReporting relationship: Lead ScientistITC is firmly committed to utilizing Research and Development as a key driver of business growth and competitive success and towards this allocates resources to create and sustain a highly innovative and rewarding work environment. It also employs a large number of reputed scientists and researchers at its facilities in Bangalore, where scientists are engaged in multiple state of the art research wings like Genomics, Cell Biology, Proteomics, Chemicaland Material Science, Measurement and Delivery Science, Consumer and Sensorial Science, Ingredient Science, to name a few. One of the focus areas of ITC is using the genome information for improving industrially important traits in crop plants. In the view of the above, ITC is seeking a highly capable Junior Research Associate specialized in Genetics & Plant Breeding, who can develop/utilize contemporary techniques for attaining the desired traits in Tobacco. The role holder will work with the team of Agrisciences and will be working on Wheat improvement through Plant Breeding.
M.Sc. in Genetics / Plant Breeding
Desirable that the candidate has exposure/training from an Institute of repute.
Plant breeding &Coordinating field experiments.
Development of RIL’S or mapping population & Molecular markers for specific traits of interest in Wheat.
Development of variety or hybrid for specific traits of interest in Wheat.
Marker assisted selection and pyramiding of multiple traits.
Specific expertise in the area of development of RIL’s / mapping populations.
Development of plant variety or hybrid preferably using MAS.
Should have recently published in peer reviewed journals.
Should be able to create a hypothesis, design and execute experiments, maintaining the highest standards.
Good Team Player .
High energy level \ Enthusiasm.
Curiosity to Experiment and Learn.
Job location: Life Sciences & Technology Centre, Bangalore – Corporate R&D Agri-SciencesApply for this job
Min 2+ yr Exp.
Salary: Upto 5Lac PATo generate sales by contacting potential customers, identifying their needs, persuading them that your products or services (rather than those of competitors) can best satisfy those needs; closing the sale by agreeing the terms and conditions; and providing an after-sales services.
Implement strategy prescribed by product management team and provide them inputs for new products after gathering feedback from customers.
Meet key opinion leaders for own region and maintain cordial relationships with them.
Collect competitor information and doctor's prescription trends through pharmacy managers.
Conduct and manage CME and other such initiatives to maintain company's brand image.
Plan weekly targets at doctor, product and total volume level.
Collect queries from doctors and get response for them within timelines.
Current Openings are with one of the Flagship division of Emcure.
B Pharma and BSc Freshers are eligble to Apply.
Graduates with previous experience as a Medical Representative can also apply.
Deputy Manager/Sr.Executive Manufacturing (Biosimilar Fill Finish)
Min 3+ yr Exp.
Salary: NegotiableObjective: To ensure,facilitate to biosimilars drug product manufacturing and timely completion of drug product manufacturing process.
To facilitate Operation & changeover of process systems, debottlenecking of process hurdles.
Regular interaction with Operation team, QAD and supporting functions to achieve the desired manufacturing activities.
Focus on plant goals in order to attain expected products over all batch yield.
Coordinate and monitor the manufacturing schedule to ensure proper utilisation of process units, utilitiesetc.
Hands on experience with vial filling line ,Pre filled syringe line and lyophilser process.
High preference will be given to person has experience with Grohninger vial and pre filled syringes line and EDWRDS Lyophilisers.
Any international filling line systems experience also preferable (Ex: Baush & strobble, Seidenadar Germany, Optima, steriline,Spami Italy filling lines).
To ensure the preparation of the cleaning / disinfectant solution and cleaning/fumigation of area/equipment as per the schedule and respective SOPs.
To ensure entire manufacturing activities to be performed as per respective SOP's /guidelines.
To ensure that on- line entries in GMP documents like BMRs, BPRs, log-books etc. are performed as per Good Documentation Practice.
To ensure that all documents are updated/revised periodically to meet cGMP standards and as per QAD requirement.
Ability to mainly evaluate schedule in accordance to manufacturing processes, and determine the most efficient method of accomplishing goals in order to meet the targets.
Supervise, coach and train new and current employees (i.e. job, safety, etc.) to meet performance expectations by providing strong leadership skill set.
To co-ordinate and support for timely completion of calibration, preventive maintenance, qualification/ validation revalidation of process units as per schedule.
Ensure that safety, Good Manufacturing Practices (GMPs) and sanitation policies and procedures are met.
Processsystems and manufacturing area readiness for GMP.FDA,WHO and international audits.
Preparation of BMR’s and BPR’s.
Validation protocols preparation and its execution.
Having USFDA ,ENVISA,ENVIMA audits experience would be added advantage.
Injectable manufacturing FDA approval would be highly preferable ( specifically Maharashtra state any zonal region FDA approved candidate in injectable manufacturing domain).
Post graduate in microbiology/ biotechnology or B Pharm having minimum 5 to 8 years’ experience in biotech injectable manufacturing domain or any OLD ( oral liquid dosage) and LVP
( low volume parenteral) manufacturing domain.
Demonstrated ability to effectively supervise, lead and build relationships at all levels within the company.
Self-motivated; has accurate self-insight; builds team spirit by teaching and, maintains a positive disposition and persuasive.
Salary: 5 Lac (PA)EDUCATION: Master of Pharmacy (Pharmaceutics)
Candidate should have relevant experience in Formulation development for Solid oral projects for regulated and semi-regulated markets. Candidate should have sound knowledge of regulatory guidelines / directives, GMP practices and relevant system SOPs. Should be able to properly plan and execute daily activities including pre formulation trials and laboratory batches
Candidate must have a profound understanding of complete product development cycle, must have been actively involved in the technology transfer and execution of exhibit batches. Previous experience in oncology molecules will be preferred and thorough understanding of formulation and analytical instruments is expected. Proficient in computer skills including internet search, MS office required for day to day activity is required.
Will be reporting to the Team Leader for his day to day activities.
Complete literature search to be performed on the projects allotted.
Planning & execution of lab scale batches and stability loading.
Planning & execution of Pre-formulation studies.
Complete product development of the product as per QbD approach.
Documentation including Research Lab notebook writing, calibration of instruments.
Daily interactions with the analytical department for results and interpretation of the results.
Execution of scale up and machine suitability trial batches at plant.
Execution of Exhibit and pre-exhibit batches at plant.
Preparation of Technology transfer document product development report.
Responding to Regulatory queries post filling.
Problem solving of the production batches.
Procurement of the R&D machines and equipments required and preparation of their URS.
IQ/OQ/PQ of the R&D instruments and Preparation of relent system and equipment SOPs.