Thursday 25 June 2020
Lee Pharma Limited-Walk-In Interviews for Multiple Positions (45 Openings) On 28th June 2020
Job Description
•Qualification : B.Sc / M.Sc/ B.Pharm / M.Pharm/ ITI Operators/ Technicians
•Experience :01-06 years
•Department: QC, AR&D,R&D And Production (API)
•Openings : 45
•Experience :01-06 years
•Department: QC, AR&D,R&D And Production (API)
•Openings : 45
Time And Venue Details: Walk-In On 28th June 2020 From 9:30 AM to 5:30 PM
Venue:Unit I, Lee Pharma Ltd,Survey No 10/G-1, Gaddapotharam Village, Jinnaram Mandal
Sangareddy District, Pincode : 502319, Telangana, India, Contact – (9154030588).
Venue:Unit I, Lee Pharma Ltd,Survey No 10/G-1, Gaddapotharam Village, Jinnaram Mandal
Sangareddy District, Pincode : 502319, Telangana, India, Contact – (9154030588).
Tuesday 23 June 2020
Glenmark Pharmaceuticals Ltd - Hiring Principal Scientist / Senior Principal Scientist - Apply Now
Principal Scientist / Senior Principal Scientist @ Glenmark Pharmaceuticals Ltd
Job description
Planning and management of the assigned in-vitro projects specifically handling Molecular Biology and Protein Sciences function.
· Overall supervision of existing projects-training and guiding.
· Setting up and standardization of new experiments in cloning, sequence verification, RT-PCR analysis, protein expression optimization, purification and scale up for assigned projects
· Evaluation of new potential targets for drug discovery through literature Review. To track Competitive intelligence for the target of interest/project
· Taking stock of inventory and accordingly placing order for new reagents and consumables. Maintenance and procurement of various machines and equipment in the lab.
· Budget projection and optimum utilization of both manpower and material requirements annually for the project.
· Communication of final results for the project to other departments - Making presentations and representing in cross functional Project/drug discovery meetings.
· Interaction with the scientific advisor for scientific queries related to the project.
Required Candidate profile
Require 10+ years of experience in molecular biology, providing molecular and cell biology support, biomarker evaluation, generation of bioactive proteins and stable cell lines, gene expression analysis, assay development, target conceptualization, project design and operational management.
Knowledge and Skills (Functional/Technical)
· Sound technical knowledge of Standard Molecular Biology Techniques & Tissue culture and cell based assay
Leadership/Managerial Attributes
· Should have managed projects in molecular and cell biology from both execution as well as people and project management perspective.
· High on Team working and ability to motivate the team.
If the above job description matches with your profile then please email your CV at varun.jain@glenmarkpharma.com
Sun Pharmaceuticals-Walk-In Interviews for Production On 27th June - 2020 @ Vapi
Job Description
Vacancy for Production Department
•Production: Officer / Sr. Officer
Candidate having educational qualification of B. Pharm / M. Pharm with 2 to 5 years of experience in manufacturing section Granulation / Compression / Coating & Packing.
Candidate having educational qualification of B. Pharm / M. Pharm with 2 to 5 years of experience in manufacturing section Granulation / Compression / Coating & Packing.
•Production Technician: Candidates having educational qualification of ITI (Any Trade) / D.Pharm , DME , Diploma in I & C ,Diploma in E & C etc with 2 to 5 years of experience in Compression, Coating, Granulation, Packing.
Post Name: Production Manager
Experience: 2-5 years
Location : Dadra and Nagar Haveli
Time And Venue Details : Walk-In On 27th June 2020 (Saturday) From 10 :00 AM to 09. 00 PM, Venue :- Plot No.C/1-2710, 3rd Phase, GIDC, Vapi, Gujarat – 396195
Vacancies: 20
Urgent Openings for Officer / Executive / Sr. Executive - Quality Assurance @ Hemmo Pharmaceuticals Pvt. Ltd
Officer / Executive Quality Assurance
Job description:
· Preparing and reviewing Site Master File, Validation master plan, Master Batch Records.
· Preparing and reviewing cleaning validation, process validation and Hold time study protocols and reports.
· Reviewing of Batch Manufacturing Records, Batch Packing Records and Bill of material
· Ensuring adherence to quality standards & maintaining all the related documents; conducting inspections at various stages to ensure safety & quality specifications are met without any slippages.
· Steering the implementation of cGMP for all operational activities.
· Conducting audits and ensuring compliance and audit readiness; reviewing production documents.
· Participating in Internal Audits to ensure quality in other departments like Production, Stores, Engineering etc.
· Addressing market complaints, deviation, CAPA, and change management systems.
· Preparing and reviewing of Annual product Quality Review.
· Imparting training, conducting online on job as well as classroom trainings for cGMP, cGDP to support subordinates
· Preparing and reviewing SOPs related to Quality Assurance, Production, Stores and Engineering
Required Candidate profile:
Minimum 4 to 6 years of hands on experience in Quality Assurance and handling QMS system and Risk analysis
Executive QA / Sr. Executive QA
Job description:
1. Establishing and ensuring the compliance of all systems as per GMP.
2. Handling of Customer complaints.
3. Conducting self-inspection and internal audit.
4. Facing Customer and Regulatory agencies audits
5. Ensuring proper responses to the customer or regulatory agencies including making report for audit compliance.
6. Taking plant rounds daily to ensure the compliance as per GMP.
7. Sound knowledge of evaluation of Risk analysis as per ICH Q 9 and implementation of CAPA.
8. Sound knowledge of elemental impurities analysis as per ICH Q 3D and USP
9. Performing risk analysis as part of Corrective and Preventive action for OOS / Change control and Deviations
10.Sound knowledge of Implementation Change control Deviation, OOS and generating risk analysis wherever required and closure of the same.
Required Candidate profile:
Minimum 7 to 9 years of hands on experience in Quality Assurance and handling QMS system and Risk analysis, Audit and Compliance.
Experience having worked in API plant with regulatory approval from USFDA, MHRA, EDQM.
Shall have good knowledge and requirement QMS, and ICH Q 9.
Skills / Knowledge/Abilities:
· Strong technical background and knowledge of Quality management Systems.
· Good oral and written communication skills.
· Good knowledge of Microsoft office programs.
· Ability to adapt and learn to ensure good decision making in fast pace environment.
Location: Navi Mumbai
Resume shall include following details:
· Current CTC
· Expected CTC
· Notice Period.
Interested Candidates can send CV to hr@hemmopharma.com
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