Symbiotec Pharmalab Limited, a leading pharmaceutical and API manufacturing company based in Pithampur, Madhya Pradesh, has announced a hiring opportunity for Executive / Senior Executive – Quality Control (QC) professionals. This is an excellent opportunity for experienced candidates looking to build a long-term career in the pharmaceutical and API industry.

The company is seeking talented professionals with hands-on experience in analytical instruments, quality control activities, and laboratory documentation.

Job Details

Company Name: Symbiotec Pharmalab Limited
Location: Pithampur, Madhya Pradesh
Department: Quality Control (QC)
Position: Executive / Sr. Executive
Industry: API / Pharmaceutical Manufacturing

Eligibility Criteria

Candidates should meet the following requirements:

• Experience: 2 to 6 years in API or Pharmaceutical QC
• Educational Qualification:
  • B.Sc. (Chemistry)
  • M.Sc. (Chemistry)
  • M.Pharm (Preferred)
• Good knowledge of LCMS (Liquid Chromatography Mass Spectrometry) and GC (Gas Chromatography)
• Ability to handle analytical instruments independently
• Experience in sample analysis and report preparation
• Strong understanding of GMP and laboratory practices

Key Responsibilities

• Perform routine and stability sample analysis
• Operate and maintain LCMS and GC instruments
• Prepare analytical reports and documentation
• Ensure compliance with GMP, GLP, and SOP requirements
• Investigate laboratory deviations and OOS results
• Support method validation and analytical troubleshooting
• Maintain data integrity and laboratory records

Why Join Symbiotec Pharmalab?

• Supportive and collaborative work culture
• Continuous learning and career growth opportunities
• Competitive salary package
• Safe and healthy work environment
• Long-term career development prospects

Salary

Salary: Depends on interview performance and experience level.

Application Process

Interested candidates can share their updated CV to:

📧 riya.singh@symbiotec.com

Technical FAQs

1. What is LCMS and why is it important in pharmaceutical QC?

LCMS (Liquid Chromatography-Mass Spectrometry) is an advanced analytical technique used for identifying, quantifying, and characterizing pharmaceutical compounds and impurities with high sensitivity and accuracy.

2. What is the role of Gas Chromatography (GC) in API analysis?

GC is used to analyze volatile compounds and residual solvents in APIs. It helps ensure products comply with ICH and regulatory specifications.

3. What is an OOS (Out of Specification) result?

An OOS result occurs when a test result falls outside predefined acceptance criteria. QC professionals must investigate the root cause and document corrective actions according to GMP requirements.

4. What laboratory documentation is required in pharmaceutical QC?

QC laboratories maintain analytical worksheets, instrument logbooks, calibration records, raw data, certificates of analysis (COA), and investigation reports to ensure regulatory compliance and data integrity.

5. What GMP practices should a QC analyst follow?

A QC analyst should follow SOPs, maintain proper documentation, ensure instrument calibration, follow data integrity principles (ALCOA+), and comply with Good Manufacturing Practices (GMP) at all times.

Conclusion

Symbiotec Pharmalab Limited’s recruitment drive for Executive / Sr. Executive (QC) offers a promising opportunity for professionals with experience in API and pharmaceutical quality control. Candidates with expertise in LCMS, GC, analytical testing, and documentation can apply and become part of a growing organization committed to quality and innovation in healthcare.