Stallion Laboratories Pvt. Ltd. is inviting applications for multiple positions in its Quality Control (QC) department within pharmaceutical formulations.
The available roles include Officer, Senior Officer, Executive, Assistant Manager, and Deputy Manager across different QC functions.
Candidates with 2–14 years of relevant experience can apply for positions involving analytical method validation, QC documentation, HPLC analysis, GC operations, GLP documentation, and raw material and finished product planning.
Interested candidates can submit their updated resumes to the recruitment email addresses provided below.
Company Overview
Stallion Laboratories Pvt. Ltd. operates in the pharmaceutical formulations sector and is seeking experienced professionals to strengthen its Quality Control team. The openings cover analytical testing, laboratory documentation, LIMS management, and QC planning activities.
Stallion Laboratories QC Department Vacancies
1. Officer / Senior Officer – AMV/AMT / QC Documentation
- Department: Quality Control (QC)
- Experience: 2–4 years
- Job Function: Analytical Method Validation (AMV), Analytical Method Transfer (AMT), and QC documentation.
2. Executive – GLP Documentation & LIMS Master
- Department: Quality Control (QC)
- Experience: 5–8 years
- Required Knowledge: Specifications (SPECs), Standard Testing Procedures (STPs), and Test Data Procedures (TDPs).
- Job Function: GLP documentation and LIMS master management.
3. Officer / Senior Officer – HPLC Analysis / GC Operations
- Department: Quality Control (QC)
- Experience: 2–4 years
- Job Function: HPLC analysis and gas chromatography (GC) operations.
4. Assistant Manager / Deputy Manager – RM/PM Section & FG/FP Planning
- Department: Quality Control (QC)
- Experience: 10–14 years
- Job Function: Raw Material (RM), Packaging Material (PM), and Finished Goods/Finished Product (FG/FP) planning activities.
Eligibility & Qualifications
Educational Qualifications
Candidates with relevant educational qualifications for pharmaceutical Quality Control roles may apply. The recruitment announcement does not specify particular degrees or academic streams.
Experience Requirements
- Officer / Senior Officer – AMV/AMT / QC Documentation: 2–4 years.
- Executive – GLP Documentation & LIMS Master: 5–8 years.
- Officer / Senior Officer – HPLC Analysis / GC Operations: 2–4 years.
- Assistant Manager / Deputy Manager – RM/PM Section & FG/FP Planning: 10–14 years.
Required Skills
- Knowledge of pharmaceutical Quality Control processes.
- Understanding of analytical method validation and method transfer.
- Familiarity with GLP documentation and LIMS master management.
- Knowledge of specifications, STPs, and TDPs.
- Experience in HPLC analysis and GC operations for relevant positions.
- Understanding of raw material, packaging material, and finished product planning for relevant managerial roles.
- Commitment to pharmaceutical quality standards and regulatory compliance.
Location & Salary
Job Location
The recruitment announcement does not specify the job location.
Salary Details
The salary package has not been disclosed. Compensation may vary depending on the position, relevant experience, and company policies.
How to Apply
Interested candidates can send their updated resumes to either of the following email addresses:
- Email: aarti.oberoi@stallionlabs.com
- Email: paresh.patel@stallionlabs.com
Application Instructions
- Prepare an updated resume highlighting relevant pharmaceutical QC experience.
- Mention the exact position applied for in the email subject line.
- Send the application to one of the email addresses listed above.
- Ensure your experience and technical skills match the requirements of the selected position.
Frequently Asked Questions
1. Which company is hiring for Quality Control jobs?
Stallion Laboratories Pvt. Ltd. is recruiting professionals for multiple Quality Control positions.
2. What positions are available?
The openings include Officer / Senior Officer – AMV/AMT / QC Documentation, Executive – GLP Documentation & LIMS Master, Officer / Senior Officer – HPLC Analysis / GC Operations, and Assistant Manager / Deputy Manager – RM/PM Section & FG/FP Planning.
3. Can freshers apply for these vacancies?
The advertised positions require 2–14 years of experience. Freshers are not eligible based on the stated experience requirements.
4. What qualifications are required?
Specific educational qualifications have not been mentioned in the recruitment announcement. Candidates should have relevant qualifications and experience for their chosen QC role.
5. How can candidates apply?
Candidates can email their updated resumes to aarti.oberoi@stallionlabs.com or paresh.patel@stallionlabs.com. The position applied for should be mentioned in the email subject line.
6. What is the salary offered?
The salary details have not been disclosed in the recruitment announcement.
Job Summary
| Category | Details |
|---|---|
| Company | Stallion Laboratories Pvt. Ltd. |
| Vacancies | Officer / Senior Officer – AMV/AMT / QC Documentation; Executive – GLP Documentation & LIMS Master; Officer / Senior Officer – HPLC Analysis / GC Operations; Assistant Manager / Deputy Manager – RM/PM Section & FG/FP Planning |
| Required Education | Relevant qualifications for pharmaceutical Quality Control roles; specific degrees not stated |
| Experience | 2–4 years, 5–8 years, 2–4 years, and 10–14 years, respectively |