Covalent Walk-in Production, QC & ETP

B.Sc, B.Pharm QC & Production Walk-in – Sangareddy

Covalent Laboratories hiring for Production, QC & ETP roles. B.Sc, B.Pharm, M.Sc eligible. Walk-in interviews at Sangareddy.

Covalent Laboratories has announced a multi-day walk-in interview drive for its manufacturing and quality operations at Sangareddy, Telangana. This hiring initiative is aimed at both freshers and experienced professionals seeking stable, long-term careers in pharmaceutical manufacturing, quality control, and environmental operations. The openings are ideal for candidates actively searching for pharma jobs in Sangareddy, QC analyst roles, production documentation jobs, and API manufacturing careers in regulated facilities.

With a strong presence in the Indian pharmaceutical industry, Covalent Laboratories continues to invest in talent across production, quality, and utilities to support its growing operations. This walk-in drive offers direct interview opportunities, fast-track selection, and immediate exposure to regulated pharma manufacturing environments.

Company Overview

Covalent Laboratories is a well-established pharmaceutical company known for its expertise in API manufacturing and strong compliance with global regulatory standards. The organization operates advanced manufacturing facilities and follows strict quality systems aligned with GMP, GLP, and environmental compliance norms.

The Sangareddy facility plays a critical role in Covalent’s production and quality operations, supporting domestic and international supply chains. Employees benefit from structured processes, a safety-focused culture, and consistent opportunities for technical and career growth within the pharmaceutical industry.

Job Role & Responsibilities

Production – Documentation

Candidates joining production documentation will support batch manufacturing and compliance activities. Key responsibilities include:

• Preparation, review, and maintenance of batch manufacturing records (BMR)
• Documentation control in line with GMP requirements
• Coordination with production and quality teams for record reconciliation
• Supporting audits and inspections through accurate documentation

Production – Manufacturing

Production roles focus on day-to-day manufacturing operations within API or formulation units. Responsibilities include:

• Executing manufacturing activities as per approved SOPs
• Handling equipment and production processes safely and efficiently
• Maintaining process documentation and logbooks
• Supporting shift operations and meeting production targets

ETP / ZLD Operations

ETP-ZLD professionals ensure environmental compliance and sustainable operations. Responsibilities include:

• Operation and monitoring of Effluent Treatment Plant and Zero Liquid Discharge systems
• Maintaining compliance with pollution control norms
• Recording operational data and coordinating with utility teams
• Supporting audits related to environmental and safety standards

Quality Control – Instrumentation

QC Instrumentation roles focus on analytical testing and equipment handling. Responsibilities include:

• Operation and calibration of analytical instruments
• Performing routine and stability testing as per specifications
• Maintaining data integrity and analytical documentation
• Supporting method validation and audit activities

Quality Control – Validation

QC Validation professionals support method and process validation activities. Responsibilities include:

• Execution of analytical method validation protocols
• Documentation and reporting of validation studies
• Ensuring compliance with regulatory guidelines
• Supporting internal and external audits

Eligibility / Qualifications

Candidates must meet the following educational and experience criteria based on the department:

• Production – Documentation: B.Sc, 0–1 year experience
• Production – Manufacturing: B.Sc, B.Pharmacy, Diploma (Chemical), 0–6 years experience
• ETP / ZLD: B.Sc, M.Sc, Diploma, 2–8 years experience
• QC – Instrumentation: M.Sc, M.Pharmacy, B.Pharmacy, 2–6 years experience
• QC – Validation: M.Sc, M.Pharmacy, B.Pharmacy, 2–6 years experience

Relevant courses include B.Sc Chemistry, B.Sc Life Sciences, B.Pharmacy, M.Pharmacy, M.Sc Chemistry, Diploma in Chemical Engineering.

Location & Salary

• Interview Venue & Job Location: Covalent Laboratories, Gundla Machnoor, Sangareddy, Telangana
• Salary: Competitive and commensurate with experience and role

Benefits & Work Culture

Covalent Laboratories offers a supportive and employee-focused work environment with benefits including:

• Subsidized canteen facility
• Attendance-based incentives
• Free transportation facilities
• Stable employment in a regulated pharma setup

Walk-in Interview Details

• Dates: 30 December 2025 to 03 January 2026
• Location: Covalent Laboratories, Gundla Machnoor, Sangareddy

Candidates are advised to carry updated resumes and relevant documents during the interview.

Application Process

Interested candidates who are unable to attend the walk-in may share their resumes in advance:

• Email: hr@covalentlab.com
• Contact: 9100132004

Shortlisted candidates will be contacted for further steps.

FAQs

Who can apply for this walk-in interview?
Candidates with B.Sc, B.Pharmacy, M.Sc, M.Pharmacy, or relevant diplomas meeting the experience criteria can apply.

Are freshers eligible?
Yes. Freshers are eligible for Production Documentation roles.

Is prior pharma experience mandatory for all roles?
Experience requirements vary by department. Some roles accept freshers, while others require up to 8 years of experience.

What type of company is Covalent Laboratories?
Covalent Laboratories is a reputed pharmaceutical manufacturer with strong regulatory compliance and global exposure.

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Company                       Covalent Laboratories
Vacancies                       Multiple
Required Education       B.Sc, B.Pharm, M.Sc, M.Pharm, Diploma
Experience                     0–8 Years