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Executive – Logistics

Qualification:       Any graduate

Experience:          3 to 5 Years

Job description

Role & responsibilities

  • Would have knowledge of Preparing / Checking all export related documents such as Invoice, Packing list, Bill of lading.
  • Would have Logistics coordination with Custom broker / Transporter / Inter department.
  • Arrange transportation for goods, including negotiating contracts with carriers, scheduling shipments, and tracking deliveries. Optimize routes to minimize costs and ensure timely delivery.
  • Would have Execute entire consignment on orders basis.
  • Would have experience of export documentation as Pre & Post shipment process.
  • Negotiate the freight, booking of containers, Movement of containers etc.MS office.
  • Good follow-up regarding shipments.
  • Good knowledge of DGFT related work.
  • Excellent Communication Skill to proactively deal with clients on phone call, email and WhatsApp.
Production Chemist ( Urgent )

Qualification:       B. Pharma/ M. Pharm / M. Sc – Chemistry

Experience:          4 to 5 Years

Salary:                  No Bar for Right candidate

Requirement:      (Must have APPROVAL CERTIFICATE in TABLET Section)

Job Description:

  • Responsible for planning day to day activities in Production Department.
  • Responsible for monitoring output of Production.
  • Preparation of Daily Production Report.
  • To take charge of operations from previous shift’s Chemist/Officer and give charge of operations to next shift’s Chemist/Officer.
  • Allocating & managing the men power in Tablet Production Department as & when required.
  • Performing I.P.Q.C. (In Process Quality Control) during the manufacturing of Tablets.
  • Compliance of the requirement of cGMP.
  • Co-ordination with Q.A., Q.C., Maintenance Department.
  • To maintain safety, efficacy, quality and enhance quality during all Pharmaceutical operations.
  • To manufacture all products with the compliance of respective Master Formulae Record.
  • To ensure final completion of BMRs, Log Books & all other records on line and transfer to Q.A.
  • To train the Workers & Operators regarding the SOPs on job training & evaluation of the same.
  • Review of Standard Operation Procedures (SOPs) for the activities of Production Department.
Executive – Accounts ( Urgent )

Qualification:       B. Com / M. Com / Inter -AC/ MBA – Finance

Experience:          3 to 5 Years

Salary:                  No Bar for right candidate

Job Description: 

  • Preparation of Books of Accounts I.e. Cash Book, Bank Book, Sales Register, Purchase, Register, General Ledger etc.,
  • Preparation of Bank Reconciliation Statement.
  • Reconciliation of Debtors and Creditors accounts
  • Finalization of Books of Accounts.
  • Giving parties outstanding ledger, ledgers of parties, stock statement.
  • Vendor ledger Reconciliation, Vendor settlement.
  • Data Preparation & Filing of TDS, GST (GSTR3B-GSTR1-GSTR-2)
  • Act as a liaison for vendors to reconcile any billing discrepancies
  • Prepare MIS reports for Monthly and Quarterly.
  • Prepare export invoice, Shipping bill and other documents related to Logistics.
  • To check order, shipping instruction, coordinating with marketing team for any discrepancy
  • To prepare pre-shipment docs and coordinating with CHA for custom clearance & Other relevant matter
  • To maintain records shipment wise
  • To prepare commercial documents as per buyer’s requirements
  • To maintain records of the export transaction
  • To maintain records of the local sales transaction
  • Any other task as assigned by the Management.
Regulatory Affairs Executive (01 Person)

Qualification: B. Pharm / M. Pharm-RA

Experience: 2 to 3 Years


  •  Preparation and review the dossier of as per current prescribed guidelines of the respective regulatory authority.
  •  Well versed with the guidelines of ICH and other regulatory.
  •  Preparation of documents for license application.
  •  Preparation of documents for COPP, FSC, and other legal documents including product permission
  •  Preparation of registration documents as per ACTD , CTD , country format / Review / Preparation & Compilation
  •  Preparation of text matter and checking of artworks.
  •  Should coordinate with the factory for samples, working standards, document data, license related documents.
  •  Should have knowledge with regard to checking samples.
  •  Courier of documents and samples to the respective customer.
  •  Maintaining status and record of dossiers, and samples legal documents.

Qualification : B. Pharm / MBA – Marketing

Experience: 2 to 3 Years


  • • Working in Stability, WRS and Calibration Department.
    • Day to day calibration of PH meter, Weighing balance.
    • Analysis of Injection, Liquid, Dry syrup and Ointment.
    • Analysis of Tablets and Capsules.
    • Preparation and Entries for protocols.
    • Maintenance of Stability samples.
    • Day to day work on stability chamber data.
    • Good documentation practices and good laboratory practices.
    • Day to day documents management and filing and storage of Documents.
    • Follow GMP, cGMP and GDP.  Raw Material analysis.
    • Water Sampling & testing.
    • Bulk & finish product analysis.
    • Doing analysis on Analytical instrument (UV, Karl Fischer, PH Meter, Polarimeter,
    • Potentiometer, Refractometer, Bulk & Tapped density, Melting Point, fluorometer,
    • Flame photometer.
    • Basic knowledge and Handling of HPLC.
    • To maintain instrument logbook & discipline in laboratory.
  • Preparation and Reviewing and tracking of O.P.
  • Handling of Change control & Deviation
  • Preparation of APQR
  • Preparation, review and tracking of Stability Protocol and Stability Testing Plan
  • Destruction of Raw
  • Conduction of Internal audit
  • Maintaining Training Record
  • Preparation and Review of
  • Issuing & Review of BMR and
  • Receiving, Storage and Destruction of
  • SMF
  • Preparation and review of raw and packing material Specification as per
  • Preparation and review of Process Validation and AMV
  • Preparation and Review of Analytical
  • Tracking of Calibration
  • Review and approval of Art

Shop floor Activity

  • IPQA Activity
  • Handling of control sample (Receiving and Destruction)
  • Line Clearance Activity
  • Final Inspection and Release of The Finished Product
  • Dispensing Of Raw Material

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