Umedica Laboratories Released Job Openings On 13/09/2022.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.Pharma,M.Pharma,M.Sc Candidates with 10-20+ Years of Experience for Mgr/ Sr.Mgr/ AGM – Production ( Injection Dept ).
Important Details :
- Location: Vapi
- No of Vacancies:02
- Details of Salary:NA
- Opening date for online Application: 13/09/2022
- Mode of application :Online
- How To Apply: Only keen interested and dynamic Candidates, seeking opportunity to build career with rapidly growing and stable company, meeting the above-mentioned criteria may share their resume on email-id sunil.parekh@umedicalabs.com Website: http://www.umedicalabs.com.
Job Description/Skills Required
- Accountable for manufacturing of Injectables at Site & contract manufacturing of Site as per Marketing projection ( Sterile manufacturing of Vial, Ampoule & dry powder injectables).
- Check on Material availability in store & follow-up with Purchase Department.
- Timely receive & give instructions to arrange for non availability of Material in advance.
- Development & implementation of system and GMPs Standard.
- Control on optimum resource utilization.
- Planning of capacity upgradation & improvements.
- Control on entire GMP related activities to affect zero product defects and no internal failure.
- Ensure monitoring and controlling of Manufacturing activities.
- To ensure appropriate process validations and calibration of equipment’s.
- Review and approve validation, qualification protocols.
- Provide training to subordinates.
- Periodic department meetings and assessment of the subordinate with superiors.
- Review BMR,BPR, MFR protocols under ETC.
- Conduct Self inspection / Audit of inter departments.
- To participate in meetings/telecommunication.
- Responsible to review and authorize documents related to TT Department.
- To provide internal technical inputs/suggestions towards new product development/improvement.
- Face Regulatory Audits ( FDA/WHO/MOA Audits ).
Click here for notification and Apply
