In 1978, Centaur Pharmaceuticals, commenced pharmaceutical manufacturing operations in Mumbai and has now evolved into a vertically integrated pharmaceutical company. Centaur House, our corporate headquarters, is located in Mumbai, the commercial capital of India. Centaur has a strong matrix of capabilities across the pharmaceutical value chain including API, formulations, Contract Research and Manufacturing Services, Clinical Research, R&D, regulatory and marketing.
Centaur's USFDA & MHRA approved plant is seeking deserving candidates, having experience in Formulation / Oral solid dosage and regulated markets.
For Pune Plant (Formulation)
Quality Control - Officer / Executive
Core Area : Raw Material / In Process / Finished Product / Packing Material / Stability /AMT/AMV/QMS
Qualification : M.Sc (Chemistry)
Experience : 04 to 08 Years
Job Profile : 1. Experience must include analysis of Raw Material, In Process. Finished goods, Packing Material; Stability Testing & Stability sample handling (Tablets / Capsules).
2. Hanging of HPLC. dissolution & other sophisticated instruments.
3. The person applied for AMT1AMV should have exposure to AMT/AMV testing.
4. Handling of Laboratories Error. Deviation, OOS and OOT
Quality Control - Sr. Executive / Asst. Manager
Core Area : 1. AMV/AMT, Validation.
2. RM/PM/ Stability
Qualification : M.Sc. (Chemistry)
Experience : 08 to 14 years
Job Profile : 1. Knowledge of QC Instruments.
2. Handling of Investigate (OOS, OOT Deviation and CAPA)
3. Team player with leadership skills
4. Planning and execution of work related to QC.
5. Maintenance of QC records. Specification and all QMS documents
6. Need expertise on Section handing.
7. USP Tech transfer projects including AMV. AMT and ANDAquery handling
8. Have exposure of Commercial Validation
Quality Assurance - Sr. Officer/ Executive
Core Area : QMS/IPQA/validation
Qualification : B.Pharm. / M.Pharm
Experience : 04 to 08 years.
Job Profile : 1. Carry out In process Quality Assurance activity m Production and warehouse area. Candidate must have exposure of Validation activities of QA department.
2. Execution and reporting. Process validation, BMR BPR - Preparation and review. Cleaning Validation, Review of Batch manufacturing record and maintaining data.
3. Ensures quality assurance and regulatory compliance throughout the investigation, deviation, complain], CAPA, and planned deviation management process while adhenng to applicable regulatory statute and standards
4. Preparation of Investigation Report for Lab QMS. Handling of Method Development and Method Verification activities
5. Review of Audit trial electronic data of QC instrument.
Quality Assurance - Asst. Manager
Core Area : QMS. IPQA, Validation, Audit Compliance
Qualification : B.Pharm / M.Pharm
Experience : 10 to 14 years.
Job Profile : 1. Person Must be well versed with current quality, regulatory trends and industry practices such as QbD, Quality Risk Management an their implementation, CAPA management, complaint handling, failure investigation. OOS Investigation, Deviation Management. Ability to handle Team of 15 employees
2. Expertise of handling USFDA, MHRA. EUGMP, Customer audits and other regulated markets audit is essential
3. Ability to handle entire gamut of QA Dept in regulatory market
For Goa Plant (Formulation)
Quality Control - Officer / Executive
Core Area : Raw Material / Lab support/AMT / AMV
Qualification : M.Sc. (Chemistry)
Experience : 04 to 09 Years
Job Profile : 1. Experience in FP / IP Handling of instruments like HPLC, GC.
2. Knowledge of Lab support activities like Calibration of instruments. Qualification and maintenance of standards.
3. Knowledge of LIMS software.
4. Method validation / transfer activity
Production / Packing-Officer/ Sr. Officer
Core Area : Granulation/ Compression / Packing
Qualification : B.Pharm / M.Pharm
Experience : 03 to 05 years
Job Profile : 1. Ensure proper planning and execution the batches In accordance with the plan.
2 Handling of all activities related to manufacturing of OSD formulations
3.Tram operators and workers on cGMP, Data Integrity and Personal Hygiene along with Good Documentation Practices.
4. Handling of Qualification and Validation activities m manufacturing.
Mumbai Location (Head Office)
CQA-Vendor Management
Core Area : Vendor Audit
Qualification : B.Pharm / M.Pharm / MSc
Experience : 10-15 Years
Job Profile : Supplier Audit. Audit, CQA, SAP, Vendor Management. KSM, RM, Packing material, components
CQA- Oversite Sight
Core Area : CQA, QMS, Audits
Qualification : B.Pharm / M.Pharm / M.Sc
Experience : 12-17 Years
Job Profile : Audit and Compliance, GMP, Change Control (CC), OOS, Deviation, CAPA, Site Support, Risk Management, Gap Assessments. SOPs. Corporate policy.
CQA-Audit & Compliance
Core Area : CQA, QMS
Qualification : B.Pharm / M.Pharm / M.Sc.
Experience : 12-17 Years
Job Profile : Audits, Regulatory Compliance, GMP, Change Control (CC), OOS, Deviation, CAPA, Risk Management. SOPs. ICH Guideline, USFDA, MHRA, WHO, Corporate policy.
CQA-Culture Transformation
Core Area : Survey Quality Circle Awareness.
Qualification : BPharm / MPharm / MSc
Experience : 10-15 Years
Job Profile : Quality Mindset, Transformation, Quality culture, Quality Circle, daily hurdles, Interaction, awareness session, Campaign
COA-QCSME
Core Area : CQA,CQC,QC
Qualification : B.Pharm/ MPharm/MSc
Experience : 10-15 Years
Job Profile : 21CFR Part 11, Audit Trial, CAPA, Global CAPA, Regulatory Compliances, troubleshooting
Only experienced candidates can attend the interview.
Walk in Interview
Saturday 07th October & Sunday 08th October 2023 between 09:30 am to 05:00 pm
At : Kesarval Garden Retreat, Main Highway, Opp. Toyota showroom, Vema-Plateau, Cortalim-Goa.
Interested candidate for Head office can only send their resume on E-mail ID - nrane@centaurlab.com
Important Note :
1 .Candidates should have experience in Formulations regulated manufacturing company such as USFDA & MHRA.
2. Exposure to regulatory audits like USFDA. MHRA is mandatory Interested candidates can walk in along with their detailed resume and recent passport size photograph.
Candidates who are not being able to attend the interview can send their resume on
For Pune Plant (Formulation) : Email: hrpune@centaur.co.in.
For Goa Plant (Formulation): Email: akshay.pednekar@centaurgoa.com
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