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Civil Projects Engineer

Posted on 25 Oct

OMGI Consultants

Diploma / BE / BTech Civil for -

1. Building Maint / Project works.
2. GMP & Civil related site documentation works.
3. Safety Awareness for site Job.

Should have worked in manufacturing industry (experience in pharma preferred)

Process Development

Posted on 25 Oct

OMGI Consultants

Technology transfer / Process Engineering, Designing of process equipments, Cost estimation, technical services dept etc in any Fine Chemical / Pharmaceutical / Agro Chemical Mfg Unit.

Mechanical Maintenance Engineer

Posted on 25 Oct

OMGI Consultants

Maintenance of API Plant equipments - SS/GL reactors & Utilities-pumps,centrifuges ,dryers,HVAC,Boilers,Compressors ,Chilling plant etc.

Quality Assurance Formulations

Posted on 25 Oct

OMGI Consultants

M.Sc / B.Pharm with experience in independently handling overall QA function of any reputed Pharamceutical Formulations unit having Tablets & Capsules.
Exposure of handling audits of US FDA,UK MHRA compulsory.

Mechanical Maintenance Executive/am

Posted on 25 Oct

OMGI Consultants

Diploma / BE Electrical/ Mechanical Engineer with experience in Pharma Industry ( Oral solid dosage )

Solvent Recovery

Posted on 25 Oct

OMGI Consultants

experience in API Pharmaceutical industries/Bulk Drugs familiar with solvent recovery/distillation plant.
Optimisation of distillation columns operated thru PLC/DCS.

Quality Control Microbiology

Posted on 25 Oct

OMGI Consultants

Microbial Limit test , Bacterial Endotoxin testing, Water sampling and testing, Sterility testing in any reputed pharmaceutical API co..

Finance & Accounts

Posted on 25 Oct

OMGI Consultants

CA with experience in any reputed manufacturing industry.
Must have handled -Finance & Accounts, Audits , Taxation ,Statutory Compliance - Excise - Central & State, VAT, SEEPZ, Indirect / Direct / Over Head Costingv, MIS & Budget etc.

Validation Manager

Posted on 25 Oct

OMGI Consultants

B.Pharm / M.Pharm with experience in Validation in a reputed Pharmaceutical Sterile Formulations - Injectables unit.
Core expertise - Validations of equipment / instruments / machine.
Exposure of US FDA,UK MHRA compulsory.

Production Formulations

Posted on 25 Oct

OMGI Consultants

Experience of manufacturing of SVP-liquid injectables - vials/ampoules .
Exposure of US FDA,UK MHRA compulsory.
Good team leader with technical knowledge on validation & qualification studies of equipments & processes

Technical Operations Gm/avp

Posted on 25 Oct

OMGI Consultants

Handle 6 formulation sites in India for all operational and technical areas like -
trouble shooting, Tech transfer, Audit, PPIC etc. - having Tablets,Capsules, Ophthalmics,Oral Powders etc.

Analytical Method Development API

Posted on 25 Oct

OMGI Consultants

good exposure in handling and calibration of UV spectro photometer, HPLC(with various detectors) ,GC ,Dissolution apparatus etc. Analytical Method Development of API.

Regulatory Affairs API

Posted on 25 Oct

OMGI Consultants

Preparation of DMFs for APIs.
Exposure to USFDA & UKMHRA markets.

Production API AGM

Posted on 25 Oct

OMGI Consultants

responsible and accountable for all activities related to plant including Safety, productivity, Availability, continuous improvement, environment. Shall have ability to work in Cross Functional teams (CFT) like QA, QC, RA.

Quality Control Formulations Corporate

Posted on 25 Oct

OMGI Consultants

M.Sc. / B.Pharm /' M.Pharm for Corporate QC role handling multiple plant locations.

Project Management Executive Injectables

Posted on 25 Oct

OMGI Consultants

Co-ordinate Project Activities with all stake-holder in R&D, Plant Production and Marketing etc for Injectable ANDA Project.

Sr.manager / AGM - Engineering & Projects (For Biologics / Biopharma)

Posted on 25 Oct

KEMWELL BIOPHARMA PVT. LTD.

Dear Candidates,

We are looking for a candidate having relevant experience in Pharma & Biopharma (Atleast 3-4 yrs) in Engineering & Projects.

 
Key skills : Experience in handling Biopharma equipments like Bioreactors, Autoclaves, Chromatography techniques, Lypholizhers,Fill Finish etc.,

Job descriptions as follows,

Ensures utility services on time for production
Ensures machine up - time by providing men and material
Optimises the consumption of utilities (power, steam, air and water)
Ensures energy savings
Ensures compliance w.r.t. CGMP, regulatory and statutory requirements
Manages and develops Team Members
Coordinates with all functions
Ensures skill up gradation for team and self
Monitors daily/ frequent breakdown and resolves them.
Analyses the root cause of frequent failures
Monitors (on an on-going basis), the utility operation and consumption vis-a-vis budget
Suggests improvements to production to increase volume/ efficiency
Ensures capacity enhancement/ up-gradation to meet new challenges in production
Serves as a CFT (Cross functional team) member for New Product Development
Provides appropriate training for CGMP and EHS and ensures compliance
Supports SCM team on technical parameters whenever required and certifying the suitability
Monitors and provides the budget Vs. actual and other MIS related information to management on
pre-determined time frames.
Utilizes SAP and IT tools by updating 100% accurate Master data and performs the transactions
without errors
Allocates functionally experienced team members for implementation & validation of SAP and IT
tools
Ensures that the team members are attending the training and obtaining full knowledge of SAP and
IT tools as per the business requirement
Maintains Data Security and Integrity

Dy.manager / Manager - DQA

Posted on 25 Oct

KEMWELL BIOPHARMA PVT. LTD.

 1. Compliance to QA and cGMP systems at Pharmaceutical Development Unit

2. To define Systems, Standards and Procedures to be followed.

3. To verify implementation of systems / procedure.

4. To ensure release of batches based on the review of batch documents and quality control reports.

5. To comply with company policies, procedures, quality standards to achieve quality goals.

6. To monitor compliance with the requirements of current Good Manufacturing Practice and also to conduct

management review meeting.

7. To ensure that required initial and continuing training of personnel is carried out and adopted according to the

need.

8. To have co-ordination with FD, AD, Production, Quality Control, Engineering and Stores department for

improving various quality concerned aspects.

9. To co-ordinate in completion of validation and qualification activities for all equipments, instruments, facility

and SAP.

10. To identify, audit, approve and monitor material suppliers.

11. To identify, audit, approve and monitor service providers and contract analysts.

12. To plan and conduct Internal audits, initiate and approve the corrective action plans.

13. To handle out of specification results and complaints.

14. To approve change control, deviations, CAPAs, Batch documents. To review implementation of proposed

changes and deviations and also closure of the same.

15. To approve process and cleaning validation / qualification documents, BMR, MFR, written procedures,

specifications, test procedures and other documents including amendments.

16. To approve or reject intermediate, bulk and finished products.

17. To take decisions for rejecting starting and packing materials in case of failure in test results.

18. To approve and release the artwork.

19. To ensure satisfactory arrangements exist to ensure as far as possible that the medicinal products are stored

and distributed so that quality is maintained throughout its storage period in the manufactured premises.

20. To check and approve SOPs of all departments.

21. To review the master batch documents and BOM.

22. To approve the analytical related activities such as Test request, analytical method development and validation

protocol and report.

23. To provide Certificate of Conformance for each batch produced.

24. To review and update Master documents like VMP, VMP for Computerized system, organogram and

drawings.

25. To perform SAP related activities related to QM Module.

26. To coordinate with quality council meeting.

27. To assist SAP activities like, IQ, OQ, PQ of SAP system.

28. To coordinate for various audits, Regulatory and customer.

Regional Manager/ Area Manager-ortho at Hyderabad/ Bangalore

Posted on 25 Oct

CVZ MANAGEMENT CONSULTANT Pvt. LTD.

Responsibilities:

The (RSM) /ASM) is responsible for the overall performance of their assigned region providing leadership to their sales team that creates a motivational environment and sets the expectation of success.

The RSM/ASM will review, modify if necessary, and approve strategically targeted, account-specific business plans developed by each sales representative in their region, that reflect an in-depth understanding of local, regional and national market forces impacting product sales.


The RSM/ASM schedules ride-a-longs and works one-on-one with sales representatives on product knowledge, call planning, territory management, relationship building and selling skills including opening, probing, supporting, overcoming objections and closing.

In addition, the RSM/ASM will work closely with sales head to assist in the development of marketing plans, targeting strategies, incentive plans etc.

  1. No. of Reportees:6-10 TBM, Task Force
  2. Therapy Area: Super Specialty Ortho
  3. Brands- Are leading ranks in ORG with very exclusive portfolio
  4. Coverage: Andhra Pradesh, Karnataka, Telengana
  5. Reporting to National Sales manager



Facilities Engineer - (A Pharma Company @ Formulation) in Chennai

Posted on 25 Oct

BVR People Consulting

Position: Sr.Executive to Manager
Qualification: BE / B.Tech(Mech)
Experience: 3 to 8 Years
Location: Chennai
Note: Candidate must have experience in Process Industry for Maintenance works of Mechanical, Electrical & Civil also. Mainting all office.

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