Rusan Pharma Ltd., a globally recognized pharmaceutical company specializing in addiction treatment and pain management, is excited to announce multiple job openings at our US FDA-approved Active Pharmaceutical Ingredient (API) manufacturing facility in Ankleshwar, Gujarat.
With a commitment to innovation and quality, we are seeking talented professionals to join our Research & Development (R&D), Quality Assurance (QA), Quality Control (QC), Analytical Development Laboratory (ADL), and Production departments. If you have expertise in API manufacturing, HPLC/GC analysis, or GMP compliance, this is your chance to advance your career with a leader in the pharmaceutical industry.
Event Details
- Venue: Rusan Pharma Ltd., Plot No. 6406, Nr. Hoechst Chowkdi, GIDC, Ankleshwar, Gujarat – 393002
- Application Process: Send your updated CV to mitesh.maharaj@rusanpharma.com or monika.prajapati@rusanpharma.com
- Website: www.rusanpharma.com
- Note: Mention the position title in the email subject line for faster processing.
Open Positions
We are hiring for the following roles at our Ankleshwar API manufacturing facility:
1. Executive – Research & Development (R&D)
- Department: Research & Development
- Experience: 5+ years in API R&D
- Qualification: B.Sc. / M.Sc. (Chemistry or related field)
- No. of Positions: 1
- Responsibilities:
- Lead API development projects, focusing on innovative formulations like transdermal patches and injectables.
- Conduct process optimization and scale-up trials.
- Collaborate with cross-functional teams for regulatory compliance.
2. Executive / Assistant Manager – Quality Assurance
- Department: Quality Assurance
- Experience: 8–10 years in API production and analytical background
- Qualification: B.Sc. / M.Sc. (Chemistry or related field)
- No. of Positions: 1
- Responsibilities:
- Oversee QA processes to ensure compliance with US FDA and cGMP standards.
- Review analytical data and manage quality audits.
- Handle deviations, change controls, and CAPAs.
3. Officer – Quality Control
- Department: Quality Control
- Experience: 3–5 years in API Quality Control with expertise in HPLC or GC
- Qualification: B.Sc. / M.Sc. (Chemistry or related field)
- No. of Positions: 1
- Responsibilities:
- Perform HPLC and GC analysis of in-process, intermediate, and finished API samples.
- Conduct stability testing to ensure product shelf-life integrity.
- Ensure adherence to QC protocols and regulatory standards.
4. Jr. Officer / Officer – Analytical Development Laboratory (ADL)
- Department: Analytical Development Laboratory
- Experience: 2–4 years in API ADL
- Qualification: M.Sc. (Chemistry or related field)
- No. of Positions: 1
- Responsibilities:
- Develop and validate analytical methods for APIs.
- Perform pharmacopoeial testing (USP, EP) using HPLC, GC, and volumetric analysis.
- Prepare specifications, STPs, and documentation for regulatory submissions.
5. Executive (GMP Coordinator) – Production
- Department: Production
- Experience: 5–8 years in API production
- Qualification: B.Sc. / M.Sc. (Chemistry or related field)
- No. of Positions: 1
- Responsibilities:
- Coordinate GMP-compliant production activities for API manufacturing.
- Monitor batch manufacturing processes and ensure adherence to SOPs.
- Support scale-up and validation activities in the production unit.
Why Join Rusan Pharma?
- Global Leader: Work with a company supplying APIs to US-based firms for orphan drugs, addiction treatment, and obesity medications, with approvals from US FDA, Health Canada, EU, and ANVISA.
- Innovation-Driven: Contribute to niche API development, including controlled substances like Buprenorphine, Methadone, and Fentanyl, at a facility with 21-CFR-compliant systems like SAP and LIMS.
- Career Growth: Benefit from a culture that nurtures talent, with opportunities for skill development and professional advancement.
- Work Environment: Join a team of 500+ employees in a collaborative, technology-driven setting with a 3.7/5 rating for skill development on AmbitionBox.
How to Apply
Interested candidates should send their updated CV to:
- Email: mitesh.maharaj@rusanpharma.com or monika.prajapati@rusanpharma.com
- Subject Line: Specify the position (e.g., “Executive – R&D” or “Officer – Quality Control”).
- Documents: Include your CV, relevant certifications, and experience details.
Note: Only candidates meeting the specified qualifications and experience will be contacted. Shortlisted candidates may be invited for interviews at the Ankleshwar facility.
About Rusan Pharma
Founded in 1994, Rusan Pharma Ltd. is a fully integrated global pharmaceutical company headquartered in Mumbai, India. Specializing in addiction treatment and pain management, we operate advanced manufacturing units in Ankleshwar, Dehradun, and Kandla, with approvals from MHRA (UK), MCC (SA), and US FDA.
Our Ankleshwar facility, recently GMP-approved by the US FDA in May 2024, is a cornerstone of our global API supply chain, supporting markets in Europe, South Africa, Russia, and the US.
Rusan Pharma is an equal opportunity employer committed to diversity, equity, and inclusion. We encourage applications from all eligible candidates to join our mission of improving global healthcare.