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EUPLOID Pharmaceuticals Private Limited is hiring experienced pharmaceutical professionals for senior-level positions at its manufacturing facility in Mysuru, Karnataka. The company’s Mysuru facility focuses on tablets and capsules/oral solid dosage manufacturing.
1. Production Head
Company: EUPLOID Pharmaceuticals Private Limited
Location: Mysuru, Karnataka
Position: Production Head
Department: Production
Dosage Form: Oral Solid Dosage (OSD)
Experience: 18–22 years
Salary: Best in Industry
Eligibility
- 18–22 years of relevant pharmaceutical manufacturing experience.
- Strong experience in Oral Solid Dosage (OSD) manufacturing.
- Candidates with senior-level production leadership experience are preferred.
- Experience in managing production operations in a pharmaceutical manufacturing environment.
Key Responsibilities
- Lead and manage overall production operations for OSD manufacturing.
- Ensure production activities are carried out as per approved procedures and GMP requirements.
- Drive production planning, productivity, capacity utilization and timely batch completion.
- Manage production teams and coordinate with QA, QC, Engineering and other departments.
- Ensure compliance with safety, quality and manufacturing standards.
- Support continuous improvement and operational efficiency initiatives.
2. Quality Assurance Manager / Sr. Manager
Company: EUPLOID Pharmaceuticals Private Limited
Location: Mysuru, Karnataka
Position: Quality Assurance Manager / Sr. Manager
Department: Quality Assurance
Dosage Form: Oral Solid Dosage (OSD)
Experience: 15–20 years
Market Experience: Regulated markets – USFDA / EU
Salary: Best in Industry
Eligibility
- 15–20 years of relevant pharmaceutical QA experience.
- Strong experience in Oral Solid Dosage (OSD) manufacturing.
- Experience with regulated markets such as USFDA and EU is required.
- Candidates with strong experience in Quality Assurance leadership and GMP compliance are preferred.
Key Responsibilities
- Lead Quality Assurance activities for OSD manufacturing operations.
- Ensure compliance with GMP and applicable regulatory requirements.
- Support regulatory inspections and audit readiness for regulated markets.
- Review and oversee quality systems, deviations, CAPA, change controls and related documentation.
- Coordinate with Production, QC, Engineering and other cross-functional teams.
- Drive a strong quality culture and continuous improvement across manufacturing operations.
How to Apply
Interested and eligible candidates can share their updated CV with EUPLOID Pharmaceuticals.
Email: admin@euploidpharmaceuticals.com
Contact: +91 6366 746254
Note: Candidates should apply only if they meet the specified experience and OSD/regulatory-market requirements.
