Covalent Laboratories walk ins for Freshers & Experienced in Production, Quality Control Department from 20th – 22nd July’ 2026

Covalent Laboratories Private Limited is conducting a Walk-in Interview for Quality Control and Production positions at its manufacturing facility in Gundla Machnoor, Sangareddy, Telangana. This hiring drive is open to professionals with 0–5 years of experience who are looking to build their careers in the pharmaceutical manufacturing industry. The interviews will be held from 20th July to 22nd July 2026.

About Covalent Laboratories

Covalent Laboratories Private Limited is a leading pharmaceutical manufacturing company with WHO-GMP, USFDA, EU-GMP, and ISO 14001:2004 certifications. The company specializes in the development and manufacturing of high-quality pharmaceutical products while maintaining global quality and regulatory standards. Covalent Laboratories provides employees with a professional work environment, continuous learning opportunities, and strong career growth prospects.

Job Overview

Open Positions

Eligibility Criteria

Quality Control

• 2–5 years of experience in pharmaceutical quality control.
• Qualification: B.Pharmacy, M.Pharmacy, or M.Sc.

Production

• 0–5 years of experience.
• Qualification: Any Graduate.

Key Responsibilities

Quality Control

• Perform analytical testing of raw materials, in-process samples, and finished products.
• Ensure compliance with GMP and laboratory quality standards.
• Maintain laboratory documentation and analytical records.
• Follow standard operating procedures (SOPs) and quality guidelines.
• Support investigations related to laboratory deviations and out-of-specification (OOS) results.

Production

• Operate and monitor pharmaceutical manufacturing processes.
• Ensure adherence to production schedules and GMP requirements.
• Maintain production records and documentation.
• Follow safety procedures and standard operating practices.
• Support continuous improvement initiatives within manufacturing operations.

Required Skills

• Pharmaceutical Manufacturing
• Quality Control
• GMP Compliance
• SOP Documentation
• Production Operations
• Analytical Skills
• Documentation
• Attention to Detail
• Teamwork
• Communication Skills

Walk-in Interview Details

Employee Benefits

• Subsidized Canteen
• Attendance Bonus
• Company-Provided Bus Transport

Note: Male candidates are preferred for these positions, as mentioned in the recruitment advertisement.

Documents to Carry

Candidates should bring:

• Updated Resume/CV
• Passport-size Photographs
• Educational Certificates and Marksheets
• Experience Certificates (if applicable)
• Government-issued Photo ID Proof

Contact Details

Why Join Covalent Laboratories?

• Work with a pharmaceutical company approved by WHO-GMP, USFDA, and EU-GMP.
• Opportunity to build a career in quality control or pharmaceutical production.
• Employee-friendly benefits, including transportation and attendance incentives.
• Exposure to global manufacturing standards and regulatory compliance.
• Continuous learning and career advancement opportunities in a growing pharmaceutical organization.