UMEDICA Laboratories Pvt Ltd. was founded in 1982 by late Mr. Umed Doshi, a dynamic entrepreneur whose vision is being spurred further by the able leadership of his son, Mr. Manish Doshi – a true technocrat and an aggressive marketeer. UMEDICA is a manufacturer and exporter of pharmaceutical formulations. Since its inception, UMEDICA has established itself as a company delivering products meeting international quality standards. UMEDICA is a Government recognized Export House, with global business in over 71 countries, covering US, Central & South American countries, Africa, Asian & CIS countries. We are now expanding in Europe, Middle East, Canada & Australia. Recently we have received multiple approvals and marketing authorizations (MA) in US & Europe.
We are recruiting for our regulatory approved facility.
UMEDICA LABORATORIES invites dedicated, passionate & competent young professionals to be part of our USFDA, EU GMP and TGA Australia approved formulations manufacturing plant UMEDICA LABORATORIES at VAPI, GUJARAT for following requirement;
1st Walk In Interviews @ Baroda Location:-
Date: – 30th April 2022 (Saturday)
Time : 9 AM to 3 PM.
Venue: – Baroda Productivity Council
2nd Floor, Productivity House, Baroda Productivity Road, Alkapuri, Vadodara – 390007
2nd Walk In Interviews @ Ahmedabad Location:-
Date: – 1st May 2022 (Sunday)
Time : 9 AM to 3 PM.
Venue: – Hotel Inder Residency Opp. Gujarat College,Nr. BVR, Ellisbridge, Ahmedabad, Gujarat 380006
Opening for Plat Location Vapi : –
Department – Tablet Packing (Technical Associate to Sr. Officer Level)
Experience – 1 to 4 Years
Qualification – ITI / D.Pharm / Diploma Engineering / B.Sc / M.Sc / B.Pharm
Skill Set – Should have sound knowledge require in following machine – Strip Pack / Auto Cartonator WKH 100 / IC 150 C / Blister Pack – Elmach FB 3000 / 3015 PDA / CVC Primary Bulk Packing Line. / Should have sound knowledge require in primary & secondary packing activity for bulk, blister & strip packing and QMS Document + Handling SAP S4 Hana Software.
Department: Quality Control (Analyst Officer to Sr. Officer Level)
- Experience – 1 to 4 Yrs
- Education – B.Sc / M.Sc / B.Pharm / M.Pharm
Skill Set – Should have sound experience of handling troubleshooting during HPLC analysis, To have experience of working on HPLC software like LC Solution, Lab Solution ,Effective utilization of HPLC system, Individual handling of FP / RM / Section / Malvrn / AMV / Stability.
Opening for R&D Lab Location at Mumbai : –
Department Formulation & Development (Research Associate / Sr. Research Associate / Research Scientist Officer to Sr. Research Scientist / Asst. Manager Level)
- Experience – 1 to 12 Years
- Qualification M.Pharma (Pharmaceuticals)
Skill Set Literature search (Intellectual search for technical information through a variety of resources including internet) / To perform RLD characterization / Planning and execution of Lab trials (Design and development of pharmaceutical dosage forms) / Documentation of test results, Data compilation / Perform reformulation and Stability study as per current guidance and Regulatory expectations / Execution and monitoring of Scale up and Exhibit batches / Supervise, Guide the team members / scientists for development trials / Utilization of resources (manpower, raw materials) in efficient manner / Data compilation and interpretation to decide the way forward / Strategy finalization (IP, Lit search, Experimental trial data) / Co-ordination with CFT’s (SCM/AD/BE/IP/QA/QC/TT/Production) for product delivery in efficient manner / Team management / Ensure delivery of product as per stipulated timelines
Department: Analytical Development (Jr. Research Associate to Sr. Research Associate / Research Scientist/ Sr. Research Scientist/ Manager (TL)
- Experience – 1 to 10 Years
- Qualification M.Sc (Organic Chemistry)
Skill Set To support for Dissolution / To perform routine and stability support for development batches. / To maintain online documentation. / To perform CDP analysis / To monitor cGLP in the lab / To develop the Assay, Dissolution and Related substance method. / Multimedia method developments. / Execution of Routine analysis of finished product / Overall Responsible for all Products Stability samples analysis / Validation of Analytical methods / To develop the Assay, Dissolution and Related substance method including Multimedia developments / Monitoring and prioritizing the day to day Planning and regular routine analytical work / Reviewing and approving all projects Analytical method validations protocols, reports and respective specifications with MOA’s / Imparting necessary guidance to Analytical method development and AMV team for all new products / Literature search, DMF Review and Coordination with vendors and different stake holders / Review and Approval of all AR&D documents like protocols, reports, stability datas, log books, procurements and all other important activities for smooth functioning of AR&D.
Note: – Pharma formulation experience must. Candidate should be well versed in English language.
Those who are not able to attend walk-in, may forward their resume on below given mail id –/
(Candidates not permitted in Walk In Interview Without Facemask)
More Job Updates Join What’s App Group –
Join Telegram Group –