Rusan Walk-In Production, QA, QC & AQA
- Company Overview
- Job Role & Responsibilities
- Production – GMP Coordinator (Officer / Junior Officer)
- Production – Shift Incharge (Executive)
- Quality Control (Junior Officer / Officer)
- Analytical Quality Assurance (Executive / Senior Officer)
- Quality Assurance – API (Junior Officer to Senior Officer)
- Quality Assurance – API (Assistant Manager)
- Eligibility / Qualifications
- Required Education
- Experience Requirements
- Location & Salary
- Walk-In Interview Details
- Application Process
- Why Build Your Career at Rusan Pharma
- Frequently Asked Questions (FAQs)
- Who can attend this walk-in interview?
- Is this walk-in suitable for freshers?
- What departments are hiring?
- Can I apply if I cannot attend in person?
- Summary Table
Rusan Walk-In – BSc/MSc API Roles – Ankleshwar
Rusan Pharma hiring Production, QA, QC & AQA professionals in Ankleshwar. 1–9 years experience. Walk-in 28 Dec 2025.
Rusan Pharma Ltd has announced a walk-in interview for experienced professionals across Production, Quality Assurance, Quality Control, and Analytical Quality Assurance at its API manufacturing facility in Ankleshwar, Gujarat. This hiring drive targets candidates with hands-on exposure to regulated API environments who want to advance their careers in GMP-driven pharmaceutical operations.
The walk-in covers multiple designations from Junior Officer to Assistant Manager, offering opportunities for professionals at different career stages. Candidates with strong documentation skills, QMS exposure, and practical API manufacturing or analytical experience will find this opportunity aligned with long-term growth in the pharmaceutical industry.
Company Overview
Rusan Pharma Ltd is a reputed pharmaceutical company with a focused presence in active pharmaceutical ingredient (API) manufacturing and regulated market supply. The company is known for its compliance-oriented operations, quality-first culture, and commitment to delivering safe and effective pharmaceutical products.
Rusan operates GMP-compliant manufacturing facilities and emphasizes strong quality systems, analytical robustness, and continuous improvement. Working at Rusan provides professionals with exposure to regulatory expectations, disciplined manufacturing practices, and stable career progression in the API sector.
Job Role & Responsibilities
Multiple roles are open across core API manufacturing and quality functions. Selected candidates will contribute directly to compliant production, quality oversight, and analytical assurance activities.
Production – GMP Coordinator (Officer / Junior Officer)
- Coordinate GMP activities on the shop floor in API manufacturing units
- Ensure adherence to SOPs, batch manufacturing records, and cGMP guidelines
- Support documentation control, deviations, and corrective actions
- Coordinate with QA and QC teams for smooth production execution
Production – Shift Incharge (Executive)
- Lead shift-wise API manufacturing operations
- Monitor critical process parameters and manpower allocation
- Ensure timely batch execution and compliance with safety and quality standards
- Handle shift documentation, handovers, and production reporting
Quality Control (Junior Officer / Officer)
- Handle QC documentation and QMS-related activities
- Support routine testing, data review, and laboratory compliance
- Coordinate with QA for investigations and corrective actions
- Maintain accurate laboratory records as per GMP and GDP requirements
Analytical Quality Assurance (Executive / Senior Officer)
- Review analytical data for compliance and accuracy
- Support analytical investigations, method-related issues, and documentation
- Ensure adherence to data integrity principles and QMS requirements
- Coordinate with QC and QA teams for analytical compliance
Quality Assurance – API (Junior Officer to Senior Officer)
- Support IPQA and batch review activities in API manufacturing
- Handle deviations, CAPA, change control, and QMS documentation
- Perform on-floor QA monitoring and compliance checks
- Support internal audits and regulatory inspection readiness
Quality Assurance – API (Assistant Manager)
- Lead QA operations and ensure end-to-end GMP compliance
- Review batch release documentation and quality decisions
- Oversee QMS systems, audits, and continuous improvement initiatives
- Mentor junior QA team members and coordinate cross-functional quality activities
Eligibility / Qualifications
Required Education
B.Sc, M.Sc (Chemistry or relevant life sciences disciplines)
Experience Requirements
- Production (GMP Coordinator / Shift Incharge): 5–7 years in API manufacturing
- Quality Control: 1–3 years with QMS and QC exposure
- Analytical Quality Assurance: 3–5 years with analytical experience
- Quality Assurance (Officer to Senior Officer): 1–4 years in Pharma API QA
- Quality Assurance (Assistant Manager): 7–9 years in Pharma API QA
Location & Salary
- Job Location: Rusan Pharma Ltd, GIDC, Ankleshwar, Gujarat
- Employment Type: Full-time
- Salary: Competitive and aligned with industry standards, based on experience and role level
Walk-In Interview Details
- Date: 28th December 2025 (Sunday)
- Time: 09:30 AM to 04:30 PM
- Venue:
Rusan Pharma Ltd
Plot No. 6406, Near Hoechst Chowkdi
GIDC, Ankleshwar, Gujarat – 393002
Application Process
Interested and eligible candidates may directly attend the walk-in interview with updated resumes and relevant documents.
Candidates unable to attend can share their profiles via email:
Why Build Your Career at Rusan Pharma
Rusan Pharma offers a structured environment for professionals to strengthen their expertise in API manufacturing, quality systems, and analytical compliance. Exposure to GMP-driven operations and regulated market expectations makes Rusan a strong platform for long-term career development in pharmaceutical production and quality leadership.
Frequently Asked Questions (FAQs)
Who can attend this walk-in interview?
Candidates with B.Sc or M.Sc qualifications and relevant API manufacturing or quality experience can attend.
Is this walk-in suitable for freshers?
No. All roles require prior pharmaceutical industry experience.
What departments are hiring?
Production, Quality Control, Analytical Quality Assurance, and Quality Assurance.
Can I apply if I cannot attend in person?
Yes. You may email your resume to the HR contacts provided.
Summary Table
| Company | Rusan Pharma Ltd |
|---|---|
| Vacancies | Multiple |
| Required Education | B.Sc, M.Sc |
| Experience | 1–9 years (Role-dependent) |
To apply for this job email your details to monika.prajapati@rusanpharma.com
