Covalent Laboratories Hiring QC Method Validation

• Company Overview
• Job Role & Responsibilities
• Quality Control – Method Validations
• Eligibility / Qualifications
• Location & Salary
• Application Process
• FAQs
• Summary Table

Covalent Laboratories QC Method Validation Vacancy | Sangareddy

Covalent Laboratories, Sangareddy hiring Quality Control professionals for Method Validations. Apply now with experience in pharmaceutical QA/QC.

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Covalent Laboratories Private Limited, a prominent player in the pharmaceutical industry, is seeking experienced and dedicated professionals to join its Quality Control (QC) team focused on Method Validations. This role offers an excellent opportunity to advance your career while contributing to high standards of pharmaceutical quality and compliance.

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Company Overview

Covalent Laboratories Private Limited is a well-established pharmaceutical company dedicated to manufacturing and developing high-quality pharmaceutical products. The organization prides itself on maintaining stringent quality control practices, adhering to regulatory standards, and fostering a culture of scientific excellence. With state-of-the-art facilities in Sangareddy, Telangana, Covalent Laboratories has positioned itself as a trusted name in the pharmaceutical and life sciences sectors.

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Job Role & Responsibilities

Quality Control – Method Validations

• Conduct analytical method development and validation for pharmaceutical products.
• Perform routine testing of raw materials, in-process samples, and finished products.
• Maintain and ensure compliance with cGMP, SOPs, and regulatory guidelines.
• Document all analytical data and generate comprehensive validation reports.
• Troubleshoot and resolve analytical discrepancies to ensure accuracy and reliability.
• Collaborate with production and QA teams to uphold quality standards.

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Eligibility / Qualifications

• Education: B.Pharm, M.Sc (Chemistry/Pharmaceutical Chemistry/Analytical Chemistry)
• Experience: Relevant experience in Quality Control and Method Validation in a pharmaceutical setting.
• Skills Required:
  • Strong analytical and problem-solving capabilities.
  • Hands-on experience with HPLC, UV-Vis, FTIR, and other analytical instruments.
  • Knowledge of cGMP, GLP, and regulatory compliance.
  • Excellent documentation and communication skills.

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Location & Salary

• Job Location: Gundla Machanoor Village, Hathnoor, Sangareddy District, Telangana.
• Salary: Competitive and commensurate with experience.
• Work Mode: Full-time, Onsite.

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Application Process

Interested candidates are requested to share their updated CVs via email to:
hr@covalentlab.com

Contact Numbers: 9100167917 / 9100132004

Apply promptly to join Covalent Laboratories’ dynamic QC team and contribute to pharmaceutical excellence!

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FAQs

1. Who can apply for this QC Method Validation role?
Candidates with a B.Pharm or M.Sc in Chemistry and relevant experience in QC and Method Validation.

2. Are freshers eligible?
No, prior hands-on experience in pharmaceutical QC and method validation is required.

3. What will the candidate be responsible for?
Developing and validating analytical methods, performing routine testing, documenting results, and ensuring compliance with regulatory standards.

4. Where is this position located?
Gundla Machanoor Village, Hathnoor, Sangareddy District, Telangana.

5. How can I apply?
Send your CV to hr@covalentlab.com or contact via 9100167917 / 9100132004.

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Summary Table

Category	Details
Company	Covalent Laboratories Private Limited
Vacancies	Quality Control – Method Validation
Required Education	B.Pharm, M.Sc (Chemistry/Pharmaceutical Chemistry/Analytical Chemistry)
Experience	Relevant experience in QC and Method Validation (Pharmaceutical Industry)