Covalent Laboratories Private Limited is a WHO-GMP and USFDA-approved pharmaceutical manufacturing company engaged in the development and production of high-quality Active Pharmaceutical Ingredients (APIs) and pharmaceutical products. The company is committed to maintaining global quality standards, regulatory compliance, and operational excellence while fostering innovation and continuous growth. Covalent Laboratories offers excellent career opportunities for professionals seeking to build a successful career in pharmaceutical quality control and manufacturing.
Job Overview
| Particulars | Details |
|---|---|
| Company Name | Covalent Laboratories Private Limited |
| Job Role | QC Chemist / Senior QC Chemist |
| Department | Quality Control |
| Employment Type | Full-Time |
| Industry | Pharmaceutical Manufacturing |
| Experience Required | 0–5 Years |
Educational Qualification
| Qualification | Eligibility |
| Undergraduate / Postgraduate | B.Sc (Chemistry), M.Sc (Chemistry), B.Pharmacy, M.Pharmacy |
Preferred Experience
- Experience in API, pharmaceutical, chemical, or related manufacturing industries is preferred.
- Freshers and experienced professionals with 0–5 years of relevant experience are encouraged to apply.
Key Responsibilities
- Perform quality control testing and laboratory analysis.
- Ensure compliance with GMP and quality standards.
- Support routine analytical activities in the QC laboratory.
- Maintain laboratory documentation and records accurately.
- Follow safety procedures and regulatory guidelines.
- Contribute to continuous quality improvement initiatives.
- Work effectively with cross-functional manufacturing and quality teams.
Required Skills
- Strong analytical and problem-solving abilities.
- Commitment to quality, safety, and regulatory compliance.
- Good understanding of pharmaceutical quality control practices.
- Ability to work in a dynamic manufacturing environment.
- Teamwork and effective communication skills.
- Attention to detail and accuracy.
Eligibility Criteria
| Criteria | Requirement |
| Qualification | B.Sc / M.Sc (Chemistry), B.Pharm, M.Pharm |
| Experience | 0–5 Years |
| Preferred Industry | API, Pharmaceutical, Chemical Manufacturing |
How to Apply
Interested candidates can send their updated resume to:
| Email ID |
| ta@covalentlab.com |
Why Join Covalent Laboratories?
- Opportunity to work with a WHO-GMP & USFDA-approved pharmaceutical company.
- Gain valuable experience in Quality Control within a regulated manufacturing environment.
- Exposure to global pharmaceutical quality and compliance standards.
- Collaborative workplace with opportunities for professional learning and career advancement.
- Be part of a growth-oriented organization committed to quality, innovation, and operational excellence.
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