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Are you ready to launch or advance your career in the pharmaceutical industry with a globally recognized leader? Covalent Laboratories Private Limited, an ISO 14001:2004, WHO-GMP, USFDA, and EU-GMP certified company specializing in Cephalosporin APIs, is hosting walk-in interviews on 6th August 2025 for Production, Quality Control (QC), and Research & Development (R&D) roles at our facility in Gundlamachnoor, Sangareddy, Telangana.
With 120 openings for freshers and experienced candidates, this is your opportunity to join a dynamic team driving innovation in pharmaceuticals.
Why Covalent Laboratories?
Established in 2002, Covalent Laboratories is a Hyderabad-based leader in manufacturing high-quality Active Pharmaceutical Ingredients (APIs), particularly Cephalosporins, for domestic and international markets.
With certifications from USFDA, EU-GMP, and WHO-GMP, our state-of-the-art facility in Gundlamachnoor is equipped with advanced Quality Assurance and Quality Control labs.
Despite mixed employee reviews on work-life balance (rated 2.9/5 on AmbitionBox), Covalent is known for job security (3.3/5) and offers a platform for skill development in a globally compliant environment.
Walk-In Interview Details
Join us for our walk-in drive to explore exciting opportunities! Here are the details:
| Details | Information |
|---|---|
| Date | 6th August 2025 (Wednesday) |
| Time | 9:00 AM to 4:00 PM |
| Interview Venue | Pharma Jobs Talent Acquisition Center, Bhagyalatha Degree College, 1st Floor, Near IDPL X Roads, Hyderabad, Telangana |
| Work Location | Covalent Laboratories Pvt. Ltd., Gundlamachnoor Village, Hathnoor Mandal, Sangareddy Dist., Telangana – 502296 |
| Contact Number | 9010127054 |
| Contact Email | hr@covalentlab.com |
Note: Bring your updated resume, last 3 months’ payslips, increment letter, educational certificates, Aadhar card, and PAN card. Immediate joiners are preferred.
Open Roles and Responsibilities
We are hiring for the following departments with a total of 120 positions:
Production (80 Positions)
- Experience: 0–8 years (freshers and experienced candidates welcome).
- Qualification: B.Sc./M.Sc. (Chemistry, Biochemistry, or related fields).
- Salary: Up to ₹6 Lakhs per annum, based on experience and skills.
Responsibilities:
- Operate and monitor production equipment for Cephalosporin API manufacturing.
- Ensure compliance with cGMP and safety protocols.
- Troubleshoot real-time production issues and support process optimization.
- Maintain batch production records and cleanroom standards.
- Contribute to innovations for productivity and cost reduction.
Quality Control (QC) (20 Positions)
- Experience: 0–6 years.
- Qualification: M.Sc. (Analytical Chemistry, Organic Chemistry, or related fields).
- Salary: Up to ₹6 Lakhs per annum.
Responsibilities:
- Perform analytical testing using HPLC, GC, UPLC, or LCMS.
- Validate analytical methods and prepare Certificates of Analysis.
- Ensure compliance with USP/BP/JP standards and cGLP practices.
- Maintain QC documentation and support regulatory audits (USFDA, EU-GMP).
- Utilize Laboratory Information Management Systems (LIMS) for data management.
Research & Development (R&D) (20 Positions)
- Experience: 0–6 years.
- Qualification: M.Sc. (Organic Chemistry, Analytical Chemistry, or related fields).
- Salary: Up to ₹6 Lakhs per annum.
Responsibilities:
- Conduct research on Cephalosporin intermediates and APIs.
- Develop and optimize processes to reduce production costs.
- Handle analytical instruments (HPLC, GC, LCMS) for method development.
- Document experimental data and support scale-up activities.
- Collaborate with cross-functional teams for process innovation.
Qualifications and Eligibility
To be eligible for these roles, candidates must meet the following criteria:
Education:
- Production: B.Sc./M.Sc. in Chemistry, Biochemistry, or related fields.
- QC & R&D: M.Sc. in Analytical Chemistry, Organic Chemistry, or related fields.
Experience:
- Production: 0–8 years (freshers welcome for entry-level roles).
- QC & R&D: 0–6 years (prior experience in HPLC, GC, or LCMS preferred).
Skills:
- Knowledge of cGMP, cGLP, and regulatory standards (USFDA, EU-GMP).
- Proficiency in analytical instruments (HPLC, GC, UPLC, LCMS) for QC and R&D roles.
- Strong documentation, problem-solving, and teamwork skills.
- Preferred: Experience in Cephalosporin API manufacturing or regulatory audits.
- Note: Freshers must be from recognized institutions; prior internships in pharma are a plus.
Salary and Benefits
- Salary Range: Up to ₹6 Lakhs per annum, based on qualification, experience, and performance.
- Caution: Employee reviews highlight challenges like a 3-year bond for freshers, limited leaves, and average work-life balance (2.9/5). Candidates should consider these factors.
Benefits:
- Exposure to USFDA, EU-GMP, and WHO-GMP certified operations.
- Opportunities for skill development in Cephalosporin API production.
- Job security, rated 3.3/5 by employees, despite a 3-year bond for freshers.
- Work in a globally compliant facility with potential for international exposure.
Why Gundlamachnoor, Hyderabad?
Covalent’s Gundlamachnoor facility, located in Sangareddy district, is part of Hyderabad’s thriving pharmaceutical hub. Equipped with advanced QA/QC labs, it offers a dynamic environment for professionals to grow. Hyderabad’s excellent connectivity and vibrant industry ecosystem make it an ideal location for career development.
How to Apply
Attend our walk-in interviews on 6th August 2025 from 9:00 AM to 4:00 PM at Pharma Jobs Talent Acquisition Center, Bhagyalatha Degree College, 1st Floor, Near IDPL X Roads, Hyderabad. Bring all required documents listed above.
Unable to attend? Email your resume to hr@covalentlab.com or contact 9010127054 for queries. With 120 openings, act quickly to secure your spot!
Why a Career in Pharmaceuticals?
The global API market is projected to reach $272 billion by 2027, driven by demand for high-quality Cephalosporins. Roles at Covalent offer hands-on experience in production, QC, and R&D, contributing to life-saving medicines while building a stable career.
Despite mixed reviews on work culture, Covalent’s focus on job security and global compliance makes it a viable choice for freshers and experienced professionals.
About Covalent Laboratories
Founded in 2002 by M. Narayana Reddy, Covalent Laboratories is an ISO 9001:2008, ISO 14001:2004, USFDA, EU-GMP, and WHO-GMP certified pharmaceutical company specializing in Cephalosporin APIs.
With a workforce of over 60 employees and a presence in regulated markets, we focus on quality, cost efficiency, and innovation through our aggressive process development lab. Learn more at covalentlab.com.
Final Call to Action
Ready to make an impact in pharmaceutical API manufacturing? Attend Covalent Laboratories’ walk-in interviews on 6th August 2025 in Hyderabad or apply via email. With 120 openings in Production, QC, and R&D, don’t miss this chance to join a USFDA-certified leader! Contact 9010127054 or visit covalentlab.com for more details.