Valence Labs Pvt. Ltd., a rapidly growing pharmaceutical API manufacturing company, has announced a Walk-In Drive at Derabassi, Punjab for experienced professionals in the Production and Quality Control (QC) departments. Candidates with Chemistry backgrounds and relevant API industry experience are invited to attend the interview.

This recruitment drive offers an excellent opportunity for professionals looking to advance their careers in a quality-driven and innovation-focused pharmaceutical organization.

About Valence Labs Pvt. Ltd.

Valence Labs Pvt. Ltd. is engaged in the manufacturing of high-quality Active Pharmaceutical Ingredients (APIs). The company is known for its commitment to quality, regulatory compliance, innovation, customer satisfaction, and employee development.

The organization provides a professional work environment with opportunities for learning, career growth, and performance-based advancement.

Job Details

Department

Position

Qualification

Experience

Production

Chemist / Sr. Chemist

B.Sc / M.Sc (Chemistry)

2 to 5 Years

Quality Control

Chemist / Sr. Chemist

M.Sc (Chemistry)

2 to 5 Years

Industry

API Manufacturing

Experience Required

2 to 5 Years in API Industry

Walk-In Interview Details

Interview Date: 24 June 2026 (Wednesday)

Interview Time: 10:00 AM to 04:00 PM

Venue: Evergreen Hotel, Ambala–Chandigarh Expressway, Near Bus Stand, Bhagat Singh Nagar, Dera Bassi, Sheikhpur Khurd, Punjab – 140507

Documents Required

Candidates should carry the following documents:

Updated Resume/CV

Latest Salary Slip

Educational Certificates

Government ID Proof

Experience Certificates (if applicable)

Passport-size Photographs

Why Join Valence Labs?

Valence Labs offers several advantages for pharmaceutical professionals:

Opportunity to work in a growing API manufacturing company

Learning and career development opportunities

Professional and collaborative work culture

Performance-based growth opportunities

Employee welfare and engagement initiatives

Exposure to regulatory-compliant manufacturing practices

Key Responsibilities

Production Chemist

Execute API manufacturing operations as per SOPs

Monitor batch processes and maintain production records

Ensure compliance with cGMP guidelines

Handle process equipment safely and efficiently

Support process optimization and troubleshooting

Quality Control Chemist

Perform analysis of raw materials, intermediates, and finished products

Operate analytical instruments such as HPLC, GC, UV, and IR

Maintain laboratory documentation and data integrity

Conduct stability and validation studies

Ensure compliance with regulatory and quality standards

Selection Process

Walk-In Interview

Technical Discussion

HR Discussion

Document Verification

Final Selection and Offer Release

Contact Information

Phone: 96718-91500, 98784-79959

Email: hr@valencelabs.co

Website: www.valencelabs.co

Technical FAQs

1. What analytical instruments should a Quality Control Chemist be familiar with?

A QC Chemist should have hands-on knowledge of HPLC, GC, UV-Visible Spectrophotometer, FTIR, Dissolution Apparatus, and other analytical instruments used in API quality testing.

2. What is cGMP and why is it important in API manufacturing?

Current Good Manufacturing Practices (cGMP) are regulatory guidelines that ensure pharmaceutical products are consistently produced and controlled according to quality standards, ensuring patient safety and product efficacy.

3. What is the role of an HPLC system in Quality Control?

High-Performance Liquid Chromatography (HPLC) is used for identification, purity testing, assay determination, impurity profiling, and stability analysis of pharmaceutical products.

4. What are SOPs in pharmaceutical production?

Standard Operating Procedures (SOPs) are documented instructions that describe how specific operations should be performed to maintain consistency, quality, and regulatory compliance.

5. What is data integrity in pharmaceutical laboratories?

Data integrity refers to maintaining complete, accurate, consistent, and reliable records throughout the data lifecycle. It follows ALCOA+ principles (Attributable, Legible, Contemporaneous, Original, Accurate, Complete, Consistent, Enduring, and Available).

Conclusion

The Valence Labs Walk-In Drive 2026 is an excellent opportunity for experienced Production and Quality Control Chemists seeking growth in the API pharmaceutical sector. Candidates with B.Sc/M.Sc Chemistry qualifications and 2–5 years of API experience are encouraged to attend the walk-in interview on 24 June 2026 at Derabassi, Punjab with all required documents. This recruitment drive offers a chance to join a fast-growing organization focused on quality, innovation, and professional development.