Umedica Laboratories Walk In Interview 2022 M. Pharm/M.sc/B.pharma/B.sc/Diploma for Tablet Packing/Quality Control/Formulation & Development/Analytical Development At Vadodara & Ahmedabad . Umedica Laboratories Notification full details below..Interested and eligible candidates can attend interview on scheduled time and venue.
- Vacancy details:
- Post Name: Tablet Packing/Quality Control/Formulation & Development/Analytical Development
- Qualification: M. Pharm/M.sc/B.pharma/B.sc/Diploma
- Experienced:01 to 10 years
Job Description: Umedica Laboratories Hiring For Tablet Packing/Quality Control/Formulation & Development/Analytical Development !
- Important Details :
- Location: Vadodara & Ahmedabad
- Post of date:25/04/2022
- 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 email@example.comfirstname.lastname@example.org
- Selection Process: The selection will be on the basis of Interview.
- Walk In Date:30th April 2022 (Saturday) & 1st May
- Time:9:00 a.m to 3:00 p.m
Venue:BARODA PRODUCTIVITY COUNCIL 2nd Floor, Productivity House, Baroda Productivity Road, Alkapuri, Vadodara – 390007.
- HOTEL INDER RESIDENCY Opp. Gujarat College, Nr. BVR, Ellisbridge, Ahmedabad, Gujarat 380006.
We are recruiting for our regulatory approved facility
LABORATORIES” at VAPI, GUJARAT for following requirement:
OPENING FOR PLANT LOCATION VAPI:
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 Hanna Software.
Quality Control (Analyst Officer to Sr. Officer Level) Experience – 1 to 4 Years
Qualification – 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:
Formulation & Development (Jr. Research Associate to Sr. Research Associate / Research
Scientist/ Sr. Research Scientist/ Manager (TL/GL))
Experience – 1 to 10 Yrs
Education – 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 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 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 delivery in efficient manner.
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
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 analysis of finished product / Overall Responsible for all Products Stability samples analysis/ 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 data’s, log books, procurements and all other important activities for smooth functioning of AR&D.
UMEDICA LABORATORIES invites dedicated, passionate & competent young professionals to be part of our USFDA, EU GMP and TGA Australia approved formulations manufacturing plant “UMEDICA