Covalent Laboratories Private Limited, an ISO 9001:2008 & ISO 14001(2004) accredited pharmaceutical company and WHO GMP certified for all its products, is specialized in the manufacturing of Cephalosporins.

It has a wide range of products and is fast expanding to meet the present and future market demands for the high value, low volume drugs. Covalent Laboratories manufactures the Active Pharmaceutical Ingredient (API) in bulk quantities for both domestic and international markets. All the drugs manufactured me -ets USP / BP / JP standards.

Covalent Laboratories, which is professionally managed and has well equipped Quality Assurance and Quality Control Lab, focuses on higher production standards for superior quality products that surpass the international standards.

Covalent Laboratories aims at reducing the production cost to give the best price to its customers through its aggre- ssive process development lab.

DATE AND TIME:

Dates: 02nd March 2026 – 04th March 2026

Location: Gundla Machnoor, Sangareddy

HR Contact

• Arun HR: 9100 132 004
• Mahesh HR: 7032 131 492
• Email: hr@covalentlab.com
• Website: www.covalentlab.com

Job Details

1.Sterile Production

Experience: Freshers
Qualification: B.Sc

Job Responsibilities:

• Handling sterile injectable manufacturing process
• Maintaining aseptic conditions in cleanroom
• Equipment cleaning and sterilization
• Documentation as per GMP guidelines
• Following SOPs and safety procedures

2.WTP (Water Treatment Plant)

Experience: 3–5 Years
Qualification: B.Tech

Responsibilities:

• Operating and maintaining RO, DM, and purification systems
• Monitoring water quality parameters
• Maintaining logbooks and calibration records
• Troubleshooting plant issues
• Ensuring compliance with GMP standards

3. Solvent Recovery

Experience: 0–3 Years
Qualification: B.Sc / B.Pharm / Diploma / B.Tech (Chemical)

Responsibilities:

• Operating solvent recovery systems
• Monitoring distillation process
• Ensuring safe chemical handling
• Maintaining recovery efficiency
• Documentation and reporting

4. Production

Experience: 2–6 Years
Qualification: B.Sc / B.Pharm / Diploma (Chemical)

Responsibilities:

• Handling API/intermediate manufacturing
• Operating reactors and process equipment
• Batch charging and monitoring
• Maintaining BMR/BPR documentation
• Following safety and GMP norms

 Benefits:

• Subsidized Canteen
• Attendance Bonus
• Free Transportation
• Attractive Salary
• Career Growth Opportunities

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