Fresher Walk-In for R&D, QC, Production & Regulatory Jobs | Covalent Laboratories
- Covalent Laboratories Walk-In Drive 2026 | R&D, QC, Production & Regulatory Jobs Apply Now
- Company Overview
- Job Role & Responsibilities
- Research & Development (R&D)
- Regulatory Affairs
- Quality Control (QC)
- Production
- Production Documentation
- Eligibility / Qualifications
- Educational Qualification:
- Experience:
- Skills Required:
- Location & Salary
- Benefits:
- Walk-In Interview Details
- Application Process
- Frequently Asked Questions (FAQs)
- Who can apply for this walk-in drive?
- Are freshers eligible?
- What departments are hiring?
- Is prior experience mandatory?
- What documents should I carry?
Covalent Laboratories Walk-In Drive 2026 | R&D, QC, Production & Regulatory Jobs Apply Now
Covalent Laboratories is conducting a walk-in interview drive for multiple pharmaceutical roles across Research & Development (R&D), Regulatory Affairs, Quality Control, Production, and Production Documentation departments. This hiring drive is open for candidates with 0 to 5 years of experience, making it a strong opportunity for freshers and early-career professionals looking to enter or grow in the pharma industry.
The company is offering multiple vacancies across departments at its Sangareddy facility, providing candidates with exposure to pharmaceutical manufacturing, analytical testing, regulatory compliance, and drug development processes.
Company Overview
Covalent Laboratories is a well-established pharmaceutical company known for its commitment to quality, innovation, and regulatory compliance. The organization focuses on developing and manufacturing high-quality pharmaceutical products while maintaining strict adherence to global standards such as GMP and regulatory guidelines.
With a strong infrastructure and a focus on continuous improvement, Covalent Laboratories provides professionals an opportunity to build a long-term career in pharmaceutical research, quality assurance, and production operations.
Job Role & Responsibilities
Research & Development (R&D)
- Assist in formulation development and analytical method development
- Support research activities aligned with product development
- Maintain accurate laboratory documentation and reports
Regulatory Affairs
- Prepare and review regulatory documents and dossiers
- Ensure compliance with domestic and international regulatory guidelines
- Coordinate with cross-functional teams for submission activities
Quality Control (QC)
- Perform analytical testing using instruments such as HPLC, GC, and UV
- Ensure compliance with GLP and GMP standards
- Maintain documentation and laboratory records
Production
- Handle pharmaceutical manufacturing processes
- Ensure adherence to batch manufacturing records and SOPs
- Maintain production efficiency and quality standards
Production Documentation
- Prepare and maintain batch records and documentation
- Ensure compliance with regulatory and GMP documentation practices
- Support audit and inspection readiness
Eligibility / Qualifications
Educational Qualification:
M.Sc (Organic Chemistry, Analytical Chemistry), B.Sc, B.Pharmacy, M.Pharmacy
Relevant Courses: B.Sc Chemistry, M.Sc Organic Chemistry, M.Sc Analytical Chemistry, B.Pharm, M.Pharm, Pharmaceutical Sciences, Industrial Pharmacy
Experience:
- R&D: 0–2 Years
- Regulatory Affairs: 0–4 Years
- Quality Control: 2–5 Years
- Production: 1–5 Years
- Production Documentation: 0–4 Years
Skills Required:
- Knowledge of GMP, GLP, and regulatory compliance
- Analytical and problem-solving skills
- Good documentation and communication skills
- Understanding of pharmaceutical manufacturing and quality systems
Location & Salary
- Job Location: Gundla Machnoor, Sangareddy
- Interview Location: Covalent Laboratories, Sangareddy
- Salary: Not disclosed (as per industry standards)
Walk-In for R&D, QC, Production & Regulatory Jobs
B.Sc, M.Sc (Organic/Analytical Chemistry), B.Pharm, M.Pharm
0–5 Years (Role Dependent)
Benefits:
- Subsidized canteen
- Attendance bonus
- Free transportation
Walk-In Interview Details
- Dates: 21st & 22nd April 2026
- Venue: Covalent Laboratories, Gundla Machnoor, Sangareddy
Application Process
Candidates can directly attend the walk-in interview with updated resume and required documents.
For queries or prior application:
Phone: 9100132004 / 9100167917
Email: hr@covalentlab.com
Frequently Asked Questions (FAQs)
Who can apply for this walk-in drive?
Candidates with B.Sc, M.Sc, B.Pharm, or M.Pharm qualifications with relevant experience can apply.
Are freshers eligible?
Yes, freshers can apply for R&D and Production Documentation roles.
What departments are hiring?
R&D, Regulatory Affairs, Quality Control, Production, and Production Documentation.
Is prior experience mandatory?
Some roles require experience, but entry-level roles are also available.
What documents should I carry?
Updated resume, educational certificates, ID proof, and passport-size photographs.
| Category | Details |
|---|---|
| Company | Covalent Laboratories |
| Vacancies | R&D Executive, Regulatory Affairs Executive, Quality Control Analyst, Production Executive, Documentation Executive |
| Required Education | B.Sc, M.Sc (Organic/Analytical Chemistry), B.Pharm, M.Pharm |
| Experience | 0–5 Years (Role Dependent) |
