Covalent Laboratories is conducting walk-in interviews on 13th and 14th April 2026 for Regulatory Affairs, Quality Control, Production, and Production Documentation roles. Explore these pharma jobs and pharmaceutical careers in India at a USFDA, EU-GMP, and WHO-GMP approved API manufacturing company.
Contents
About the Company
Covalent Laboratories Private Limited is a leading manufacturer of Active Pharmaceutical Ingredients (APIs), specializing in Cephalosporins and their intermediates. Established in 2002, the company supplies high-quality bulk APIs to both domestic and international regulated and semi-regulated markets.
With certifications including ISO 14001:2004, WHO-GMP, USFDA, and EU-GMP, Covalent Laboratories maintains stringent quality and environmental standards. The state-of-the-art facility in Gundla Machnoor, Sangareddy, Telangana, supports innovation, regulatory compliance, and sustainable growth in the pharmaceutical sector.
As part of the respected Virchow group, the company focuses on expanding its portfolio to meet global demands for high-value drugs while delivering superior quality products that meet USP, BP, and other international standards.
Job Details
- Company Name: Covalent Laboratories Private Limited
- Experience: 0–5 Years (varies by role)
- Qualification: B.Sc / B.Pharmacy / M.Pharmacy / M.Sc (Organic Chemistry / Analytical Chemistry)
- Location: Gundla Machnoor, Sangareddy, Telangana
- Work Type: On-site
Job Description
Covalent Laboratories Private Limited is hiring talented professionals across multiple departments for its API manufacturing facility. These walk-in interview opportunities suit freshers and experienced candidates seeking stable pharma jobs in a regulated environment. The company offers roles in quality, production, and regulatory functions to support its growing operations in cephalosporin APIs.
Regulatory Affairs
Department: Regulatory Affairs Experience: 0–4 Years Education/Qualification: M.Sc Organic Chemistry / Analytical Chemistry
Quality Control
Department: Quality Control Experience: 0–5 Years Education/Qualification: B.Sc / B.Pharmacy / M.Pharmacy / M.Sc
Production
Department: Production Experience: 1–5 Years Education/Qualification: B.Sc / B.Pharmacy
Production Documentation
Department: Production Documentation Experience: 0–4 Years Education/Qualification: B.Sc / B.Pharmacy
Skills/Qualifications
- Strong knowledge of GMP, SOPs, and regulatory guidelines
- Experience in analytical techniques (for QC and Regulatory roles)
- Ability to handle production processes and documentation
- Good communication and teamwork skills
- Attention to detail and problem-solving abilities
- Preference for male candidates in certain production-related roles
Key Responsibilities
- Execute and monitor daily production activities as per batch records
- Perform quality control testing and analysis of raw materials and finished products
- Prepare and maintain regulatory dossiers and documentation
- Ensure compliance with cGMP and safety standards
- Handle production documentation and record-keeping accurately
- Support team in achieving departmental targets efficiently
Benefits/Perks
- Subsidized Canteen
- Attendance Bonus
- Free Transportation
- Opportunities for career growth in a certified API manufacturing company
- Exposure to international regulatory standards and global markets
- Positive work culture focused on quality and innovation
How to Apply
Interested candidates can attend the walk-in interviews or send their resumes to hr@covalentlab.com. Please mention the position applied for in the subject line. Bring updated resume, educational certificates, experience letters, and ID proof.
For more pharma jobs and walk-in updates across India, visit Pharma Recruiter.
Apply now and take the next step in your pharmaceutical career!
Walk-in Interview Details
- Date: 13-04-2026 & 14-04-2026
- Venue: Covalent Laboratories, Gundla Machnoor, Sangareddy, Telangana
- Contact: 9100132004 / 9100167917
- Email: hr@covalentlab.com
Why You Should Join
Joining Covalent Laboratories means becoming part of a credible, innovation-driven organization with strong regulatory compliance and global presence. The company offers long-term career stability, continuous learning opportunities, and a supportive work environment.
Employees benefit from exposure to advanced manufacturing practices, international quality standards, and a culture that values quality, safety, and professional growth in the competitive pharma industry.
FAQs
Q1: What is the eligibility for these pharma jobs at Covalent Laboratories?
A: Candidates with B.Sc, B.Pharmacy, M.Pharmacy, or M.Sc (Organic/Analytical Chemistry) and relevant experience (0–5 years) can apply. Male candidates are preferable for some roles.
Q2: How can I apply for the walk-in interview?
A: Attend directly at the venue on 13th & 14th April 2026 or email your resume to hr@covalentlab.com.
Q3: Is prior experience mandatory?
A: No. Freshers (0 years) are eligible for several positions, while experienced candidates (up to 5 years) are preferred for others.
Q4: What are the growth opportunities?
A: The company provides excellent scope for career advancement in a USFDA and EU-GMP approved facility with focus on skill development and global exposure.
