Chemist, Senior Chemist & Shift In-Charge Jobs at Suraj Laboratories

🏢 About the Company

Established in 2021, Suraj Laboratories Pvt. Ltd. is a cutting-edge manufacturer and service provider in the pharmaceutical sector, specializing in Active Pharmaceutical Ingredients (API) and API intermediates. We excel in the development and production of generic APIs, advanced intermediates, and providing end-to-end solutions for chemistry-related services.

Our state-of-the-art API manufacturing plant, located in Kadechur Industrial Area, Yadgir District, Karnataka, is designed to handle complex and hazardous chemical reactions. The facility complies with current Good Manufacturing Practices (cGMP) and meets all regulatory guidelines, ensuring the highest quality standards. Suraj Laboratories has earned the trust of global regulatory customers, with successful audits showcasing our commitment to compliance and excellence.

As a rapidly growing organization, Suraj Laboratories offers a collaborative and innovation-driven work culture, making it an ideal place for professionals to grow and excel in their careers.

🎯 Role Overview

Position: Chemist/Sr. Chemist, Shift In-Charge
Department: Production
Location: Kadechur Industrial Area, Yadgir District, Karnataka

We are hiring for the Production Department to fill key positions such as Chemist, Senior Chemist, and Shift In-Charge roles. This opportunity is open to skilled professionals with 3 to 10 years of experience in pharmaceutical production or API manufacturing. The selected candidates will play a critical role in driving production efficiency while maintaining strict adherence to safety and quality standards.

Mode of Interview: Telephonic round.
No. of Positions: Multiple openings available.

💼 Key Responsibilities

• Manage and oversee production activities to ensure smooth workflow and timely completion of tasks.
• Conduct and monitor chemical reactions, ensuring compliance with cGMP standards and regulatory guidelines.
• Operate and maintain production equipment and tools, ensuring optimal performance.
• Document production data accurately and update logs for audits and reviews.
• Implement standard operating procedures (SOPs) and ensure compliance with quality control measures.
• Address and troubleshoot production issues, minimizing downtime and delays.
• Coordinate with cross-functional teams, including quality assurance and maintenance, to optimize production efficiency.
• Promote and enforce safety protocols during the handling of hazardous materials and chemicals.

📋 Requirements

Qualification:

• B.Sc. or M.Sc. in Chemistry or related fields.

Experience:

• 3 to 10 years of experience in API manufacturing or pharmaceutical production environments.

Gender:

• Open to Male candidates only.

Key Skills:

• Proficiency in handling complex chemical reactions and manufacturing processes.
• Knowledge of cGMP standards, regulatory compliance, and quality assurance.
• Strong analytical, problem-solving, and organizational skills.
• Effective communication and teamwork abilities.
• Capacity to work under pressure in a fast-paced manufacturing environment.

💰 Compensation & Benefits

• Salary: Competitive package based on experience and qualifications.
• Facilities: Access to world-class production facilities and modern equipment.
• Training: Continuous skill development and professional growth opportunities.
• Regulatory Exposure: Work in a compliant environment, handling audits by regulatory agencies.
• Career Progression: Opportunities for promotion based on performance.

🌟 Work Culture

• Compliance-Oriented: A strong focus on maintaining quality and regulatory standards.
• Innovative Environment: Encourage creative thinking to improve processes.
• Team Collaboration: Foster a supportive and collaborative work culture.
• Safety First: Ensure employee safety at every stage of production.
• Equal Opportunities: Recognize and reward individual contributions.

🎓 Growth Opportunities

• Exposure to advanced API manufacturing technologies and complex chemical processes.
• Professional development through training programs and mentoring by industry experts.
• Opportunities to handle global regulatory audits and interact with international clients.
• Career advancement to senior roles within the organization based on performance.
• Continuous learning through involvement in challenging and innovative projects.

📝 Application Process

1. Telephonic Interview: The initial round of interviews will be conducted over the phone.
2. Resume Submission: Interested candidates can share their updated resumes through the following methods:
   • WhatsApp: 8151830770
   • Email: mahadevappa@surajlabs.com
3. Shortlisting: Qualified candidates will be contacted for further rounds of discussion.

📱 Stay Connected

• WhatsApp: 8151830770
• Email: mahadevappa@surajlabs.com

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