Get in touch with us
For Sales
Sales & Business
Mo: +91 90814 27292 (India)
Mo:+65 8574 9712 (singapore)
Our Email
inquiry@vitasvpharma.com
Office Time:
Office Time : 10.00 AM to 7.00 PM (MON - SAT)
Locations:
Head Office: 404, sunrise building, Lajamni Chowk, Shanti Niketan Society, Mota Varachha, Surat, Gujarat 394101
Corporate office: 01, Al Musalla Commercial Building, Gold Souk, Meena Bazaar, Bur Dubai- Dubai, UAE
Manufacturing sites:
Manufacturing Unit-1: Plot No. C-345/2, GIDC Saykha, Nr. Argama Village, Tal. Vagra, District Bharuch, Gujarat 392140
Email: smit@vitasvpharma.com
Contact +91 90670 67834
Manufacturing Unit-2: Plot No. CH 18 &CH 19P, Dahej Industrial Estate, Dahej, Gujarat-392130
Email: dr.daniel@vitasvpharma.com
Contact +91 90814 27292
Team
Our Team is your Team
At Vitasv, there are no half measures – we are always on target. When your mission is to be faster and stronger than your competitors, you need a winning team driving your vision forward. You need people that has the industry know how and internal capabilities that align with your business goals. You need a team that has a passion for relentless commitment to you.
Dr. Daniel Tigerstorm (Dhaval Vaghani)
Responsible for Entire Facility VitasV Pharma And Chemical Pvt Ltd. Head, Production Management, Audit Management, Quality Management, Co-ordination with all Department , Safety management, Liaising, Man management, MIS management.
1. Production planning, Production target, Day to Day Review production report, other production related Tasks, c GMP Implementation.
2. Heading the team & successfully facing audit, Implementation of the corrective measures.
3. Recruitment, Motivation, Problem solving, proper utilization of available attrition level, Team
management, Maintain Harmonious relation among all the Employee level.
4. Co-ordination with all dept. Like PPIC, Store, Account, HR, Maintenance, QC, QA.
5. Liaising with different Govt. Agencies like FDA, GPCB, GIDC, GEB, Factory Inspector, Excise.
6. Over all responsibility of running the plant efficiently & with minimum cost/ maximum output.
7. Audit schedule, maintaining premises in clean status round the year to face audit with short notice,
review of audit documents, SOPS day by day working as per cGMP.
8. MIS management all the desired MIS by HO, Reduction of break down, PMS.
9. Process scale up from R&D level to plant level & up to DMF filing of infringing& non infringing route of the product such as cefotaxime acid, ceftriaxone sodium, cefuroxime Axetil etc.
10. Responsible for regular management activities such as manpower allocation to process area as well clean room activities.
11. By process change improves the colors & quality of ceftriaxone sodium & Cefotoxime acid. Also improved the yield resulted the capacity enhancement of the plant
12. I have faced five times US FDA & onetime EDQM & MHRA Audit.
13. Implemented TQM and Employee Suggestion Scheme to make the utility cost- competitive as well as to create cost awareness amongst employees by an effective participation in cost reduction programs
& working environment.
14. Made an effective effort in Manufacturing Cost Reduction Program with joint efforts of Production
function, towards continuous improvements in the yield / batch cycle time & optimization of batch sizes, which almost doubled the production capacity with same infrastructure & reduce the utility cost of product.
15. By process modifications reduced the spray draying time & increase the capacity of production.
16. Achieving budgeted production target with anticipated RMC.
17. Responsible for all operations such as manpower handling, safety, Production and its quality and cost.
18. Responsible for production planning, input and output of material such as issue of raw materials.
AFFAIRS Martina Feitzinger
Martina is leading the Scientific Affairs teams for Vitasv. She brings more than 20 years of experience within the pharmaceutical industry. She has been working across global regulatory setup for over 15 years. Leading teams in all continents, Martina successfully spearheaded several thousands of MA strategies including a number of proprietary, 505b2/hybrid and complex products.
Arni Baldursson
Vyara is leading the Finance & IT teams for Vitasv. She has more than 10 years’ experience in Finance. She started her career in Financial Advisory with Deloitte and has led a number of high profile transactions in various industries, building strong business acumen. During the past 5 years she has been heading Finance and FP&A functions in global pharmaceutical companies. Vyara is highly focused on digital transformation and automation in organisations.
Arni Baldursson
Vyara is leading the Finance & IT teams for Vitasv. She has more than 10 years’ experience in Finance. She started her career in Financial Advisory with Deloitte and has led a number of high profile transactions in various industries, building strong business acumen. During the past 5 years she has been heading Finance and FP&A functions in global pharmaceutical companies. Vyara is highly focused on digital transformation and automation in organisations.
Arni Baldursson
Vyara is leading the Finance & IT teams for Vitasv. She has more than 10 years’ experience in Finance. She started her career in Financial Advisory with Deloitte and has led a number of high profile transactions in various industries, building strong business acumen. During the past 5 years she has been heading Finance and FP&A functions in global pharmaceutical companies. Vyara is highly focused on digital transformation and automation in organisations.
AFFAIRS Martina Feitzinger
Martina is leading the Scientific Affairs teams for Vitasv. She brings more than 20 years of experience within the pharmaceutical industry. She has been working across global regulatory setup for over 15 years. Leading teams in all continents, Martina successfully spearheaded several thousands of MA strategies including a number of proprietary, 505b2/hybrid and complex products.
AFFAIRS Martina Feitzinger
Martina is leading the Scientific Affairs teams for Vitasv. She brings more than 20 years of experience within the pharmaceutical industry. She has been working across global regulatory setup for over 15 years. Leading teams in all continents, Martina successfully spearheaded several thousands of MA strategies including a number of proprietary, 505b2/hybrid and complex products.