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Are you ready to elevate your career in the pharmaceutical industry? SYMED Labs Limited, a leading bulk drug manufacturer and a subsidiary of Viyash Life Sciences, is hosting a walk-in interview drive in Choutuppal, Hyderabad. Recognized by USFDA, WHO, EU GMP, and ISO 9001:2015, SYMED Labs offers a dynamic platform for professionals passionate about quality and innovation in Active Pharmaceutical Ingredients (API) manufacturing. Join us and contribute to cutting-edge healthcare solutions!
About SYMED Labs Limited
SYMED Labs Limited, established in 1997 and headquartered in Hyderabad, India, is a prominent manufacturer of Active Pharmaceutical Ingredients (APIs). As a subsidiary of Viyash Life Sciences, we operate state-of-the-art manufacturing facilities in Choutuppal, Bonthapally, Bolarum, Jeedimetla (Hyderabad), Vizag, and Mumbai.
With over 25 years of expertise, SYMED Labs serves more than 600 customers across 30 countries, delivering high-quality APIs across various therapeutic categories. Our commitment to Good Manufacturing Practices (GMP) and innovation makes us a trusted name in the global pharmaceutical industry.
We are seeking dynamic and experienced professionals for our Quality Assurance, Effluent Treatment Plant (ETP), and Environment, Health, and Safety (EHS) departments at our Choutuppal facility. Join us for our walk-in interview from May 26 to May 30, 2025, and take the next step in your pharmaceutical career!
Walk-In Interview Details
- Dates: May 26th to May 30th, 2025 (Monday to Saturday)
- Time: 10:00 AM to 4:00 PM
- Venue: SYMED Labs Ltd Unit-IV (A Subsidiary of Viyash Life Sciences), Sy. No. 163, 163/A & 164/A, Pittampally (V), Chityal (M), Nalgonda (Dist), Telangana-508114
- Contact: Mahesh Reddy
- Phone: +91-9966586837
- Email: maheshwar.s@viyash.com
What to Bring:
- Updated resume
- Current company appointment letter
- Last 3 months’ pay slips
- Last 3 months’ bank statements
- Copies of educational certificates
- Previous company experience letters
- Note: Male candidates are preferred. If unable to attend, email your resume to maheshwar.s@viyash.com.
Available Positions
Explore our open roles in Quality Assurance, ETP, and EHS at our Choutuppal facility. Below is a user-friendly breakdown of the positions, qualifications, experience, and responsibilities. All roles require relevant experience in pharmaceutical API manufacturing.
1. Quality Assurance – Supervisor/Senior Supervisor
- Number of Positions: 1
- Experience: 1-3 years
- Qualification: B.Sc., M.Sc.
- Location: Choutuppal, Hyderabad
- Key Skills:
- Strong experience in documentation for quality assurance processes
- Knowledge of QMS activities, including Change Control, Deviations, and CAPA
- Familiarity with GMP and regulatory compliance
- What You’ll Do:
- Prepare and review QA documentation, including SOPs, BMRs, and BPRs
- Support regulatory inspections and audits
- Ensure compliance with quality standards and procedures
2. Effluent Treatment Plant (ETP) – Trainee Supervisor
- Number of Positions: 4
- Experience: 2-5 years
- Qualification: B.Sc., M.Sc., B.Tech (Chemical)
- Location: Choutuppal, Hyderabad
- Key Skills:
- Expertise in ETP operations and Reverse Osmosis (RO) plant management
- Knowledge of wastewater treatment processes in pharmaceutical manufacturing
- Familiarity with safety and environmental regulations
- What You’ll Do:
- Operate and maintain ETP and RO plant systems
- Monitor and document effluent treatment processes
- Ensure compliance with environmental standards and regulations
3. Environment, Health, and Safety (EHS) – Supervisor/Senior Supervisor
- Number of Positions: 2
- Experience: 2-5 years
- Qualification: B.Sc., M.Sc., B.Tech (Chemical)
- Location: Choutuppal, Hyderabad
- Key Skills:
- Strong experience in process safety and EHS documentation
- Knowledge of risk assessments and safety protocols in API manufacturing
- Familiarity with EHS regulations and GMP
- What You’ll Do:
- Implement and monitor EHS policies and procedures
- Conduct process safety assessments and documentation
- Ensure compliance with environmental, health, and safety standards
Why Join SYMED Labs Limited?
- Global Recognition:
- Work with a USFDA, WHO, EU GMP, and ISO 9001:2015-certified company
- Contribute to high-quality APIs for global markets
- Career Growth:
- Innovation-Driven:
- Be part of a company that serves over 600 customers in 30 countries
- Support cutting-edge API development and production
- Supportive Culture:
How to Apply
Alternative Application:
- Email your CV to maheshwar.s@viyash.com
- Include details of your API manufacturing experience, current salary, and notice period
Contact for Queries:
- Mahesh Reddy: +91-9966586837 or maheshwar.s@viyash.com
- Note: Male candidates are preferred. Ensure your CV highlights relevant API experience.
For more information about SYMED Labs Limited, visit our website.
Frequently Asked Questions (FAQs)
Is API manufacturing experience mandatory?
Yes, candidates must have relevant experience in pharmaceutical API manufacturing to be considered.
What is the work culture like at SYMED Labs?
SYMED Labs is rated 3.9/5 for overall employee satisfaction, with a 3.6/5 work-life balance and 3.4/5 for work culture. Employees appreciate the collaborative environment but note limited skill development opportunities (rated 3.2/5).
Can I apply if I can’t attend the walk-in?
Yes, email your CV to maheshwar.s@viyash.com with details of your experience and qualifications.
Join SYMED Labs Limited in Choutuppal, Hyderabad, and become part of a globally recognized leader in API manufacturing. Attend our walk-in interview from May 26 to May 30, 2025, or apply online to take the next step in your pharmaceutical career