Covalent walk-in QC, AR&D, Production & Documentation

Covalent Labs Hiring QC & Production | Sangareddy

Covalent Laboratories hiring for QC, AR&D, Production & Documentation roles in Sangareddy. B.Pharm, M.Pharm, B.Sc, M.Sc eligible.

Covalent Laboratories has announced a major walk-in hiring drive for experienced pharmaceutical professionals at its Sangareddy manufacturing facility. The company is recruiting candidates for Quality Control, Analytical Research & Development (AR&D), Production, Production Documentation, and CWTP departments.

The walk-in interviews will be conducted from 25th May 2026 to 30th May 2026 at the company’s facility in Gundla Machnoor, Sangareddy. Candidates with pharmaceutical manufacturing experience, analytical laboratory exposure, production operations knowledge, and formulation industry backgrounds are encouraged to attend.

This recruitment drive is suitable for professionals looking for pharma manufacturing jobs, QC analyst jobs, AR&D openings, production executive careers, pharmaceutical documentation roles, and regulated pharma industry opportunities in Telangana.

Covalent Laboratories is also offering employee benefits including subsidized canteen facilities, attendance bonuses, and free transportation support for selected candidates.

Company Overview

Covalent Laboratories is a pharmaceutical manufacturing company involved in formulation development, analytical operations, production management, and quality systems. The organization focuses on maintaining pharmaceutical manufacturing standards aligned with GMP compliance and regulated industry requirements.

The company recruits professionals for pharmaceutical production, analytical research, quality control testing, engineering support, and documentation management to support ongoing manufacturing and development activities.

Candidates working at pharmaceutical manufacturing facilities gain practical exposure to quality systems, analytical instruments, formulation manufacturing operations, validation systems, and pharmaceutical compliance processes.

Job Role & Responsibilities

Quality Control Department

Candidates selected for Quality Control roles will support analytical testing and quality verification activities within pharmaceutical manufacturing operations.

Key responsibilities include:

• Performing raw material and finished product analysis
• Operating analytical instruments such as HPLC and laboratory systems
• Supporting GMP and GLP laboratory practices
• Handling pharmaceutical analytical documentation
• Conducting stability and quality testing activities
• Preparing analytical reports and quality records
• Supporting regulatory compliance requirements
• Maintaining laboratory data integrity systems

AR&D (Analytical Research & Development)

The AR&D department is hiring professionals with analytical development experience in pharmaceutical research environments.

Responsibilities include:

• Analytical method development and validation
• Supporting formulation development activities
• Conducting laboratory investigations and analytical studies
• Preparing analytical documentation and reports
• Performing method transfer activities
• Supporting pharmaceutical research operations
• Ensuring compliance with quality and regulatory standards

Candidates with analytical laboratory exposure and pharmaceutical development experience will be preferred.

Production Department

Production professionals will be responsible for pharmaceutical manufacturing operations and batch execution activities.

Key responsibilities include:

• Handling pharmaceutical manufacturing operations
• Monitoring production activities and process parameters
• Maintaining batch manufacturing records
• Supporting GMP-compliant production systems
• Coordinating with quality assurance and engineering teams
• Monitoring equipment cleaning and production processes
• Ensuring production targets are achieved safely and efficiently

Production Documentation

Candidates selected for production documentation roles will manage pharmaceutical documentation and production records.

Responsibilities include:

• Preparation and review of production documents
• Maintaining batch manufacturing records
• Supporting documentation compliance activities
• Handling SOP-related documentation
• Maintaining production logbooks and records
• Supporting audit and inspection readiness
• Coordinating with QA and production departments

CWTP (Water Treatment Plant)

The company is also hiring professionals for water treatment plant operations.

Key responsibilities include:

• Monitoring water treatment systems and utilities
• Maintaining plant operations and documentation
• Supporting pharmaceutical utility management
• Handling preventive maintenance coordination
• Ensuring compliance with pharmaceutical utility standards
• Monitoring system performance and quality parameters

Eligibility / Qualifications

Covalent Laboratories is hiring candidates from pharmaceutical, analytical, and engineering backgrounds.

Educational Qualification

Eligible qualifications include:

• B.Pharmacy
• M.Pharmacy
• M.Sc
• B.Sc
• B.Tech

Experience Required

• Quality Control: 2 to 5 Years
• CWTP: 4 to 6 Years
• AR&D: 1 to 4 Years
• Production: 1 to 5 Years
• Production Documentation: 2 to 5 Years

Required Skills

Candidates with the following skills may receive preference:

• Pharmaceutical manufacturing experience
• GMP and GLP knowledge
• Analytical laboratory operations
• Documentation and compliance handling
• Production process knowledge
• Pharmaceutical quality systems
• Analytical method validation
• Regulatory compliance awareness
• Strong communication and coordination skills

The company has mentioned preference for male candidates for these openings.

Location & Salary

Job Location: Sangareddy, Telangana

Interview Venue: Covalent Laboratories, Gundla Machnoor, Sangareddy

Salary: Approx. ₹2.8 LPA to ₹8 LPA depending on role and experience

Interview Dates: 25th May 2026 to 30th May 2026

Application Process

Interested candidates can directly attend the walk-in interview at the company venue.

Candidates may also share their updated resumes through the official company email.

Email ID: ta@covalentlab.com

Contact Numbers: 9100132004, 9100167917

Candidates attending the interview should carry:

• Updated Resume
• Educational certificates
• Experience documents
• Government ID proof
• Passport-size photographs

Employee Benefits

Covalent Laboratories has mentioned several employee benefits for selected candidates.

Benefits include:

• Subsidized canteen facility
• Attendance bonus
• Free transportation
• Exposure to pharmaceutical manufacturing systems
• Career growth opportunities in pharma operations

FAQs

What qualifications are required for Covalent Laboratories hiring?

Candidates with B.Pharmacy, M.Pharmacy, M.Sc, B.Sc, and B.Tech qualifications can apply.

What departments are hiring at Covalent Laboratories?

The company is hiring for Quality Control, AR&D, Production, Production Documentation, and CWTP departments.

Is pharmaceutical experience mandatory?

Yes. Relevant pharmaceutical industry experience is preferred for all positions.

What is the interview location?

The walk-in interview will be conducted at Covalent Laboratories, Gundla Machnoor, Sangareddy.

What employee benefits are offered?

Selected candidates may receive subsidized canteen access, attendance bonuses, and free transportation facilities.

How can candidates apply for these openings?

Candidates can directly attend the walk-in interview or share their resumes at ta@covalentlab.com.

Summary Table

Company	Covalent Laboratories
Department Vacancies	Quality Control, CWTP, AR&D, Production, Production Documentation
Qualification	B.Pharmacy, M.Pharmacy, M.Sc, B.Sc, B.Tech
Experience	1 to 6 Years
Location	Sangareddy, Telangana