We began our journey 17 years ago in 2007 with the vision to make a meaningful impact in the management of chronic lifestyle related diseases. Today Chronic and Sub-chronic therapies account for ~ 86% of our revenue, and our product range spans ~ 90% of India’s Rs. 55,000+ crore chronic care market.
Apply:
- Apply Now: recruitment@eristotherapeutics.com
- WhatsApp: 9558001555 / 9414100208
Positions:
Quality Control
- Designation: Officer / Sr. Officer (Ointment / RM / Intermediate / FP / FG / SFG / RM)
- Qualification: M.Sc. (Chemistry) / B.Pharm
- – Experience: 2–5 Years
- – Requirements: Strong analytical skills, experience in HPLC/GC/Dissolution/DT/FRI & other QC instruments, handling tablets, capsules, oral suspensions, injectables & external preparations.
Injectable Department
- Assistant Manager – Manufacturing
- – Qualification: M.Sc. (Chemistry) / B.Pharm
- – Experience: 5–7 Years
- – Requirements: Exposure to injectable manufacturing, in-process checks, manpower handling, GMP documentation, machine breakdown & troubleshooting, audit compliance.
Ampoule Operator – Filling Machine
- – Qualification: ITI / B.Pharm
- – Experience: 2–5 Years
- – Requirements: Operation of ampoule filling & sealing machines, real-time BMR/BPR documentation, basic machine knowledge.
Oral Solid Dosage (OSD)
• Dy. Manager / Asst. Manager – Liquid
- – Qualification: B.Pharm / M.Pharm / B.Sc. / M.Sc.
- – Experience: 8–10 Years
- – Requirements: Syrup preparation, filtration systems, suspension stabilization, BMR/BPR review, GDP, SOP compliance, production planning & batch execution.
• Capsule Operator (Corrected — now under OSD)
- – Qualification: ITI / B.Pharm
- – Experience: 1–2 Years
- – Requirements: Knowledge of capsule filling machines, operation, and breakdown management.
External Preparation
• Sr. Officer – QMS
- – Qualification: B.Pharm / M.Pharm / B.Sc. / M.Sc.
- – Experience: 2–4 Years
- – Requirements: Experience in external preparation manufacturing, documentation practices, machine operation knowledge & troubleshooting.
Quality Assurance (QA)
• Officer – IPQA Parenteral
- Qualification: B.Pharm / M.Pharm
- Experience: 1–2 Years
- Requirements: In-process checks, sampling, inspections, review of BMR/BPR, compliance with SOPs, validation protocol review, monitoring critical parameters, approval of batch records.
Positions:
Quality Control
- Designation: Officer / Sr. Officer (Ointment / RM / Intermediate / FP / FG / SFG / RM)
- Qualification: M.Sc. (Chemistry) / B.Pharm
- – Experience: 2–5 Years
- – Requirements: Strong analytical skills, experience in HPLC/GC/Dissolution/DT/FRI & other QC instruments, handling tablets, capsules, oral suspensions, injectables & external preparations.
Injectable Department
- Assistant Manager – Manufacturing
- – Qualification: M.Sc. (Chemistry) / B.Pharm
- – Experience: 5–7 Years
- – Requirements: Exposure to injectable manufacturing, in-process checks, manpower handling, GMP documentation, machine breakdown & troubleshooting, audit compliance.
Ampoule Operator – Filling Machine
- – Qualification: ITI / B.Pharm
- – Experience: 2–5 Years
- – Requirements: Operation of ampoule filling & sealing machines, real-time BMR/BPR documentation, basic machine knowledge.
Oral Solid Dosage (OSD)
• Dy. Manager / Asst. Manager – Liquid
- – Qualification: B.Pharm / M.Pharm / B.Sc. / M.Sc.
- – Experience: 8–10 Years
- – Requirements: Syrup preparation, filtration systems, suspension stabilization, BMR/BPR review, GDP, SOP compliance, production planning & batch execution.
• Capsule Operator (Corrected — now under OSD)
- – Qualification: ITI / B.Pharm
- – Experience: 1–2 Years
- – Requirements: Knowledge of capsule filling machines, operation, and breakdown management.
External Preparation
• Sr. Officer – QMS
- – Qualification: B.Pharm / M.Pharm / B.Sc. / M.Sc.
- – Experience: 2–4 Years
- – Requirements: Experience in external preparation manufacturing, documentation practices, machine operation knowledge & troubleshooting.
Quality Assurance (QA)
• Officer – IPQA Parenteral
- Qualification: B.Pharm / M.Pharm
- Experience: 1–2 Years
- Requirements: In-process checks, sampling, inspections, review of BMR/BPR, compliance with SOPs, validation protocol review, monitoring critical parameters, approval of batch records.
For More JOB Updates Join Our Whatsapp Group Click Here
