Covalent walk-in Production, QC & Documentation

BPharm MSc Jobs Covalent 3 Roles Hyderabad

B.Pharm/M.Sc candidates apply for Production, QC & Documentation roles in Hyderabad. Multiple vacancies, 1–4 yrs experience required.

Covalent Laboratories is conducting a walk-in interview drive for multiple pharma roles in Production, Quality Control (QC), and Production Documentation at its Sangareddy facility. This is a strong opportunity for candidates with API pharmaceutical experience who want to build a stable and growth-oriented career in manufacturing and quality operations.

If you are targeting high-demand pharma careers such as QC analyst jobs, API production roles, or GMP documentation positions, this opening offers practical exposure in a regulated pharmaceutical environment.

Company Overview

Covalent Laboratories is a well-established pharmaceutical company focused on Active Pharmaceutical Ingredients (API) manufacturing. Known for its quality-driven processes and innovation-led approach, the company contributes to the global healthcare ecosystem by delivering high-quality pharmaceutical products.

With a strong emphasis on GMP compliance, process optimization, and regulatory standards, Covalent Laboratories offers professionals the opportunity to work in a technically advanced and compliance-focused environment.

Job Role & Responsibilities

Production Department

• Execute API manufacturing processes as per standard operating procedures
• Monitor batch operations and ensure process consistency
• Maintain production records and batch documentation
• Follow GMP guidelines and safety protocols during manufacturing
• Coordinate with QA/QC teams for smooth production flow

Quality Control (QC)

• Perform analytical testing using HPLC, GC, and other laboratory instruments
• Conduct raw material, in-process, and finished product analysis
• Ensure compliance with GLP, GMP, and regulatory standards
• Maintain analytical documentation and data integrity (ALCOA+)
• Support stability studies and quality investigations

Production Documentation

• Prepare and review batch manufacturing records (BMR/BPR)
• Maintain documentation as per GMP guidelines
• Ensure accuracy and completeness of production data
• Support audit readiness and regulatory compliance documentation

These roles are critical for ensuring product quality, regulatory compliance, and efficient pharmaceutical manufacturing operations.

Eligibility / Qualifications

Required Education:

• Any Degree (Production)
• B.Sc (Production Documentation)
• B.Pharm, M.Pharm, M.Sc (Quality Control)

Relevant Courses:

Pharmaceutical Analysis, Organic Chemistry, Analytical Chemistry, Pharmaceutics, Quality Assurance, GMP, GLP, Industrial Pharmacy, API Manufacturing, Regulatory Affairs

Experience Required:

• 1 to 4 years
• Mandatory: API Pharma Experience

Skills Required:

• Knowledge of GMP and GLP guidelines
• Experience in API manufacturing or QC analysis
• Strong documentation and compliance understanding
• Analytical skills for QC roles
• Attention to detail and process discipline

Location & Salary

• Location: Sangareddy, Hyderabad (Telangana)
• Salary: Best in industry (based on experience)

Employee Benefits:

• Attendance bonus
• Free transportation
• Subsidized canteen
• Overtime allowances
• Festival bonus

Application Process

Candidates can attend the walk-in interview directly.

Walk-In Details:

• Date: 27 April 2026
• Time: 10:00 AM to 03:00 PM
• Venue: Gundla Machnoor Village, Sangareddy District, Telangana

Contact Details:

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

Candidates should carry updated resume and relevant documents while attending the interview.

Why Join Covalent Laboratories?

• Work in a reputed API pharmaceutical manufacturing company
• Gain exposure to GMP-compliant production and QC processes
• Opportunity to build a long-term career in pharma manufacturing and quality control
• Competitive benefits and employee-friendly work environment

This role directly contributes to ensuring the production of safe, effective, and high-quality pharmaceutical products that support global healthcare systems.

FAQs

What positions are available?

Production, Quality Control (QC), and Production Documentation roles.

What experience is required?

Candidates with 1–4 years of relevant pharma experience.

Is API experience mandatory?

Yes, API pharma experience is required.

What qualifications are eligible?

B.Pharm, M.Pharm, M.Sc, B.Sc, or any degree (depending on role).

How can I apply?

Attend the walk-in interview or email your CV to hr@covalentlab.com.

Final Thoughts

This Covalent Laboratories walk-in drive is a strong opportunity for candidates aiming to grow in API manufacturing, quality control analysis, and GMP documentation. With increasing demand for skilled professionals in pharmaceutical production and compliance, these roles offer solid career stability and growth potential.

If you are looking to advance in pharma manufacturing jobs, QC analyst roles, or regulatory-compliant documentation careers, this opportunity is worth considering.

Company	Covalent Laboratories
Vacancies	Production Executive, QC Analyst, Documentation Executive
Required Education	Any Degree, B.Sc, B.Pharm, M.Pharm, M.Sc
Experience	1–4 Years