Join Rusan Pharma Ltd., a global leader in addiction and pain management treatments, at our walk-in interview on June 6-7, 2025, for roles in ADL, Quality Control, Engineering, Production, and Quality Assurance at our USFDA-approved API facility in Ankleshwar, Gujarat.
Event Details
- Date: June 6-7, 2025 (Friday-Saturday)
- Time: 9:30 AM to 4:30 PM
- Venue: Rusan Pharma Ltd., Plot No. 6406, Near Hoechst Chowkdi, GIDC, Ankleshwar, Gujarat 393002
- Note: Bring updated resume, educational certificates, last 3 months’ payslips, and Aadhaar/PAN ID proof. Candidates interviewed in the last 3 months need not attend.
Job Opportunities
| Department | Position | Qualification | Experience | Key Responsibilities |
|---|---|---|---|---|
| Analytical Development Lab (ADL) | Jr. Officer / Officer | B.Sc / M.Sc | 2-4 Yrs | Perform analytical testing using HPLC, GC; support R&D for product quality enhancement |
| Quality Control | Jr. Officer / Officer | B.Sc / M.Sc | 1-5 Yrs | Conduct wet lab analysis, HPLC, GC testing; ensure compliance with cGMP standards |
| Engineering | GMP Coordinator | B.Sc / M.Sc | 5-7 Yrs | Manage GMP compliance, maintain API plant equipment, support process optimization |
| Production | GMP Coordinator | B.Sc / M.Sc | 5-7 Yrs | Oversee API production, ensure GMP compliance, manage process safety and documentation |
| Production | Jr. Officer / Officer | B.Sc / M.Sc | 1-3 Yrs | Support API production, operate equipment, maintain cGMP standards |
| Quality Assurance | Sr. Officer / Executive | B.Sc / M.Sc | 3-7 Yrs | Handle IPQA, QMS, change control, deviations, and audit compliance for API manufacturing |
| Analytical Quality Assurance | Executive / Assistant Manager | B.Sc / M.Sc | 5-10 Yrs | Review analytical data, manage method validation, ensure compliance with pharmacopeial standards |
Key Responsibilities
- ADL (Jr. Officer / Officer):
- Perform HPLC and GC testing for R&D batches
- Support analytical method development and validation
- Ensure compliance with GLP and cGMP
- Quality Control (Jr. Officer / Officer):
- Conduct wet lab, HPLC, and GC analysis for raw materials and finished products
- Maintain accurate documentation and regulatory compliance
- Perform stability and in-process testing
- Engineering (GMP Coordinator):
- Oversee maintenance of API manufacturing equipment
- Ensure GMP compliance and process safety
- Coordinate calibration and preventive maintenance
- Production (GMP Coordinator):
- Manage API production processes and documentation
- Ensure GMP compliance and safety protocols
- Supervise production operations and troubleshoot issues
- Production (Jr. Officer / Officer):
- Support API production and equipment operation
- Maintain cGMP standards and documentation
- Assist in process optimization and batch execution
- Quality Assurance (Sr. Officer / Executive):
- Perform IPQA, manage QMS, and handle deviations
- Ensure compliance with USFDA and API standards
- Support audits and market complaint resolution
- Analytical Quality Assurance (Executive / Assistant Manager):
- Review analytical data for compliance with pharmacopeial standards
- Oversee method validation and verification
- Manage CAPA, change control, and analytical QMS
Why Join Rusan Pharma?
Rusan Pharma, established in 1994, is a technology-driven pharmaceutical company specializing in addiction and pain management, with innovative drug delivery systems like transdermal patches. Our Ankleshwar facility is USFDA-approved, offering a dynamic environment for career growth. Learn more at Rusan Pharma.
How to Apply
- Walk-In: Attend with required documents during the specified time.
- Email: Send CV to mitesh.maharaj@rusanpharma.com or monika.prajapati@rusanpharma.com.
- Note: USFDA API manufacturing experience required for non-ADL roles. Freshers not eligible.
Additional Information
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Disclaimer: Rusan Pharma does not charge fees for recruitment. Verify offers through official channels.
Note: Shortlisting based on qualifications, experience, and USFDA API exposure.Show in sidebar
