Indoco Remedies Ltd., is a fully integrated, research-oriented pharma company engaged in the manufacturing and marketing of Formulations (Finished Dosage Forms) and Active Pharmaceutical Ingredients (APIs). We have seven decades of presence in the Indian Pharma market and a strong foothold in the international market across 55 countries. Indoco has carved a place for itself in the international arena and is exporting a number of generic products in the Regulated and Emerging Markets.
Indoco Remedies Ltd., is a leading pharma Company with global presence in 55 countries and international regulatory approvals including USFDA and UKMHRA. WALK-IN-INTERVIEWS For our tablet manufacturing facility in Goa.
Below positions are for candidates to work in all shifts:
- OFFICER / SR. OFFICER / EXECUTIVE – PRODUCTION
- SR OFFICER / JR EXECUTIVE – (LIQUID MFG/PKG)
- OFFICER PACKING
- QC-ANALYST,
- QA – QMS,
- QA – INVESTIGATOR,
- QA – IPQA
For job description please click on the below link: https://www.indoco.com/job-description/Goa-Walk-in-drive-Aug2023.pdf
Job Description:
OFFICER / SR. OFFICER/EXECUTIVE – PRODUCTION:
- Qualification : B. Pharm / M. Pharm
- Job Profile : 1 to 9 years’ experience in granulation, compression & coating areas for regulated market. FDA approval in tablet manufacturing would be preferred. Having machine exposure of FETTE, Sejong for compression and FBD, FBE, RMG for Granulation.
SR. OFFICER / Jr. EXECUTIVE – (Liquid MFG/PKG):
- Qualification : B. Pharm / M. Pharm
- Job Profile : 2 to 5 years’ experience in Liquid Manufacturing and Liquid Packing departments to manage routine manufacturing and packing activities. Experience in handling of Track and Trace system, coordination of shifts and batch reconciliation.
OFFICER – PACKING :
- Qualification : B. Pharm / M. Pharm
- Job Profile : 2 to 4 years’ of experience in tablet packing department to manage routine packing activities on high speed blister packaging lines equipped with cartonators and bottle packing line. Experience in handling Track and Trace system, coordination of shifts and batch reconciliation.
QC – ANALYST :
- Qualification : BSC / MSC in (Chemistry/ Analytical)
- Job Profile : 3 to 7 years’ experience in stability, validation, finished product, in process, raw material and GLP. Software knowledge of Empower, Lab Solution & Tiamo Caliber LIMS. Experience in handling instruments like HPLC, UV, IR, KF GC, Malvern. Exposure of regulatory audits like USFDA, MHRA, EU, WHO.
QA-QMS :
- Qualification : B. Pharm / M. Pharm
- Job Profile : 4 to 5 years’ experience in handling change controls, deviations, market complaints, CAPA. Review of quality risk management. Preparation/review of SOPs. To carry out activities related to training. Candidate must have experience in regulatory plants.
QA-INVESTIGATOR:
- Qualification : B. Pharm / M. Pharm
- Job Profile : 7 to 8 years’ experience in handling market complaints, investigation related to deviations and CAPA. Preparation/Review of APQR. Quality alert notification, field alert and handling product recall related activities. To carry out activities related to training. Candidate must have experience in regulatory plants.
QA-IPQA:
- Qualification : B. Pharm / M. Pharm
- Job Profile : 2 to 3 years’ experience in handling of IPQA related activities like Line clearance, sampling, in process checks, batch record review, QA rounds, batch release (Semi Finished), material verification, swab sampling, IPQC instrument handling, etc. Candidate must have experience in regulatory plants..
Above positions are for candidates to work in all shifts
