Covalent Laboratories Walk-In Production, QC, API Industry | Fresher Eligible
- Covalent Laboratories Walk-In Drive 2026 | Freshers & Experienced Pharma Jobs in Production, QC, API Industry
- Company Overview
- Job Role & Responsibilities
- Production Documentation
- Quality Control (QC)
- Solvent Recovery
- Production
- Eligibility / Qualifications
- Educational Qualification:
- Relevant Courses:
- Experience Required:
- Skills Required:
- Location & Salary
- Benefits:
- Application Process
- Walk-In Details:
- Contact Details:
- Email:
- Frequently Asked Questions (FAQs)
- 1. Can freshers apply?
- 2. What qualifications are accepted?
- 3. Is this a direct walk-in?
- 4. What benefits are offered?
- Summary
Covalent Laboratories Walk-In Drive 2026 | Freshers & Experienced Pharma Jobs in Production, QC, API Industry
Covalent Laboratories is conducting a walk-in interview drive for multiple roles in Production, Quality Control, Solvent Recovery, and Production Documentation departments. This is a strong opportunity for freshers and experienced candidates to enter or grow in the API pharmaceutical manufacturing sector.
The company is hiring across multiple departments with experience ranging from 0 to 5 years, making it suitable for both fresh graduates and early-career professionals. The walk-in drive will be conducted on 23rd and 24th March 2026 at Sangareddy.
Company Overview
Covalent Laboratories is a well-established name in the API pharmaceutical manufacturing industry, known for its focus on innovation, quality compliance, and regulatory standards. The company operates with modern manufacturing facilities and follows global quality systems aligned with GMP guidelines.
With a strong presence in active pharmaceutical ingredients (API) production, Covalent Laboratories contributes to the global healthcare ecosystem by ensuring consistent quality, process efficiency, and regulatory compliance.
Working here gives candidates exposure to industrial-scale pharmaceutical manufacturing, quality systems, and real-time production environments.
Job Role & Responsibilities
The responsibilities vary based on the department, but all roles are aligned with pharmaceutical manufacturing, quality assurance, and compliance-driven operations.
Production Documentation
- Maintain batch manufacturing records and documentation
- Ensure compliance with GMP and SOP guidelines
- Support audit documentation and regulatory inspections
Quality Control (QC)
- Perform testing of raw materials, intermediates, and finished products
- Handle analytical instruments like HPLC, UV, and other QC equipment
- Ensure data integrity and laboratory compliance
Solvent Recovery
- Monitor solvent recovery processes and equipment
- Ensure safety and process optimization in chemical operations
- Maintain documentation for process validation and compliance
Production
- Execute API manufacturing processes as per SOPs
- Monitor production parameters and ensure batch consistency
- Maintain safety, quality, and compliance standards
Eligibility / Qualifications
Educational Qualification:
B.Sc, B.Pharmacy, M.Pharmacy, M.Sc, Diploma (Chemical), B.Tech (Chemical)
Relevant Courses:
Pharmaceutical Chemistry, Industrial Pharmacy, Organic Chemistry, Analytical Chemistry, Chemical Engineering, Process Engineering
Experience Required:
- Production Documentation: 0–2 Years
- Quality Control: 1–4 Years
- Solvent Recovery: 0–4 Years
- Production: 0–5 Years
Skills Required:
- Knowledge of GMP, GLP, and pharmaceutical manufacturing processes
- Familiarity with API production and quality systems
- Strong documentation and compliance skills
- Ability to work in a regulated environment
- Good teamwork and communication skills
Location & Salary
- Location: Gundla Machnoor, Sangareddy, Telangana
- Job Type: Full-time (On-site)
- Salary: As per industry standards
Benefits:
- Subsidized canteen facility
- Attendance bonus
- Free transportation
Application Process
Candidates can directly attend the walk-in interview on the given dates.
Walk-In Details:
- Date: 23rd & 24th March 2026
- Time: As per interview schedule (recommended morning attendance)
- Venue: Covalent Laboratories, Gundla Machnoor, Sangareddy
Contact Details:
- Arun HR: 9100132004
- Mahesh HR: 7032131492
Email:
Candidates are advised to carry updated resumes, educational documents, and ID proof for the interview.
Frequently Asked Questions (FAQs)
1. Can freshers apply?
Yes, freshers are eligible for multiple roles including Production and Documentation.
2. What qualifications are accepted?
B.Sc, B.Pharm, M.Pharm, M.Sc, Diploma Chemical, and B.Tech Chemical candidates can apply.
3. Is this a direct walk-in?
Yes, candidates can directly attend the interview without prior application.
4. What benefits are offered?
Subsidized canteen, attendance bonus, and free transportation are provided.
Summary
| Category | Details |
|---|---|
| Company | Covalent Laboratories |
| Vacancies | Production, Quality Control, Solvent Recovery, Production Documentation |
| Required Education | B.Sc, B.Pharm, M.Pharm, M.Sc, Diploma, B.Tech Chemical |
| Experience | 0–5 Years |
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