50 Openings : Umedica Laboratories Walk In 30 April – 1st May 2022 For B.Sc,M.Sc,B.Pharma,M.Pharma,Diploma

Umedica Laboratories Released Job Openings On 20/04/2022.UMEDICA is a part of the Amoli Group of Companies, manufacturing and exporting a wide range of formulations viz; Injectables, Tablets, Capsules, Suspensions, Dry Syrups, etc. UMEDICA offers a diverse product portfolio comprising of antibiotics, non-steroidal anti-inflammatory (NSAIDs), analgesics, antifungal, antiviral, anti-malarials, antituberculosis agents, antihistaminics, psychotropic, antihypertensives, lipid-lowering agents, drugs for sexual dysfunction, multivitamins etc.

Vacancy Details:

Umedica Laboratories Recruiting B.Sc,M.Sc,B.Pharma,M.Pharma,Diploma Candidates with 01-06+ Years of Experience for Tablet Packing/Quality Control / R&D/Analytical Development Departments.

Important Details :

• Location:Vapi, Mumbai
• No of Vacancies:50
• Details of Salary:NA
• Opening date for online Application:20/04/2022
• Mode of application :Walk In
• Time and Venue:  30 April – 1st May , 9.00 AM – 3.00 PM
  1st one in Baroda – BPC Hall and 2nd one in Ahmedabad Hotel Inder Residency Opp. Gujarat College,Nr. BVR, Ellisbridge, Ahmedabad, Gujarat 380006
  Contact – MR. PARIMAL BRAHMBHATT ( 02262811800 )

Related Job : Latest BPharm,MPharm,B.Sc,M.Sc,Diploma,ITI,Any Graduate Fresher And Exp Jobs In Hydaerbad,Ahmedabad,Mumbai,Delhi,Bangalore,Visakapatnam,Noida,Chennai,Pune,Goa,Vadodara,Vapi,Indor Etc 

Job Description/Skills Required

• Opening for Plat Location Vapi : –
• Department – Tablet Packing (Technical Associate to Sr. Officer Level)
• Experience – 1 to 4 Years
• Qualification – ITI / D.Pharma / Diploma Engineering / B.Sc / M.Sc / B.Pharma
• 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.Pharma / M.Pharma
• 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 YearsQualification 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 – parimal.hr@umedicalabs.com / hrd@umedicalabs.com(Candidates not permitted in Walk In Interview Without Facemask)

Click here for Official notification and Apply