Stanford Laboratories hiring QC and QA Executives in Himachal Pradesh and Rajasthan for pharma candidates with 1 to 5 years experience
Introduction
Stanford Laboratories has opened new career opportunities for professionals in Quality Control (QC) and Quality Assurance (QA). This hiring drive is aimed at candidates with experience in pharmaceutical manufacturing, especially in Oral Solid Dosage (OSD) segments. Individuals looking to strengthen their careers in quality operations and regulatory compliance can benefit from this role.
This opportunity provides hands-on exposure to validation, documentation, and analytical processes within a well-established pharmaceutical environment.
Company Overview
Stanford Laboratories is a recognized pharmaceutical company known for its manufacturing excellence and adherence to regulatory standards. The company operates advanced facilities focused on producing high-quality formulations, particularly in the OSD segment. With a strong emphasis on compliance, innovation, and process efficiency, Stanford Laboratories offers professionals a structured environment to develop expertise in quality systems and pharmaceutical operations.
Job Overview
| Job Title | Executive – Quality Control / Quality Assurance |
|---|---|
| Company Name | Stanford Laboratories |
| Location | Himachal Pradesh & Rajasthan |
| Employment Type | Full-Time |
| Qualification | B.Sc, B.Pharm, M.Sc, M.Pharm |
| Experience | 1–5 Years |
| Salary | ₹2.5 LPA – ₹6 LPA (Approx.) |
| Application Mode | Email & Contact |
Job Location & Employment Type
The selected candidates will be placed at the following manufacturing locations:
- Mehatpur, Himachal Pradesh
- Ghiloth, Rajasthan
This is a full-time, on-site role within the company’s production and quality departments. Candidates must be willing to work at either of the above locations based on organizational requirements.
Open Positions / Department Details
Stanford Laboratories is hiring for the following departments:
- Quality Assurance (QA)
- Quality Control (QC)
Candidates will be assigned responsibilities depending on their prior experience and skill set in either QA or QC functions.
Key Roles & Responsibilities
Quality Assurance (QA) Responsibilities
- Prepare, review, and maintain documentation in accordance with Good Manufacturing Practices (GMP).
- Assist in validation activities including process validation and cleaning validation protocols.
- Perform In-Process Quality Assurance (IPQA) activities during manufacturing.
- Ensure all processes comply with regulatory guidelines and internal quality standards.
- Monitor documentation accuracy and maintain audit readiness.
Quality Control (QC) Responsibilities
- Conduct analytical testing of raw materials, intermediates, and finished products.
- Operate and maintain laboratory instruments used in chemical analysis.
- Follow Good Laboratory Practices (GLP) while performing testing procedures.
- Carry out sampling and stability studies as per defined protocols.
- Maintain proper records of test results and laboratory activities.
Eligibility Criteria
Education:
- B.Sc, B.Pharm, M.Sc, or M.Pharm in relevant disciplines.
Experience:
- 1 to 5 years of experience in pharmaceutical industry
- Experience in OSD (Oral Solid Dosage) manufacturing will be preferred
Skills Required:
Technical Skills:
- Knowledge of GMP and GLP guidelines
- Familiarity with QA documentation and validation processes
- Experience in analytical testing and laboratory instruments
- Understanding of regulatory compliance requirements
Soft Skills:
- Strong attention to detail
- Effective communication skills
- Ability to work in a team environment
- Good documentation and reporting abilities
Salary & Benefits
- Salary: ₹2.5 LPA to ₹6 LPA (depending on experience and skills)
- Work in a regulated pharmaceutical manufacturing setup
- Gain exposure to quality systems and regulatory frameworks
- Opportunity to build expertise in QA/QC domains
- Career growth in pharmaceutical quality operations
Selection Process
The recruitment process may involve the following stages:
- Resume screening
- Technical interview focusing on QA/QC knowledge
- Practical or role-based discussion (if required)
- HR round for final selection
Candidates with a clear understanding of pharmaceutical quality practices and compliance standards will have an advantage during the selection process.
How to Apply
Eligible candidates can apply through the following method:
- Send your updated resume via email
- Ensure your CV highlights your QA/QC experience, analytical skills, and regulatory knowledge
Email: anu.singh@stanlabs.com
Contact Number: +91 7428098777
Why Apply for This Pharma Job?
This job opening at Stanford Laboratories is a valuable opportunity for professionals aiming to establish or advance their careers in Quality Assurance and Quality Control. The role provides practical exposure to GMP-compliant processes, analytical testing, and validation activities within a production environment. Candidates will gain industry-relevant experience, improve their technical capabilities, and develop a strong foundation in regulatory compliance.
Working with an established pharmaceutical company also enhances long-term career prospects and opens doors to higher roles in quality management and regulatory affairs.
Important Note / Disclaimer
PharmaJobHub.in is an independent job information platform. We do not provide any recruitment guarantee and are not affiliated with any company. Candidates are advised to verify details from official sources before applying.
Final Call-to-Action
Interested candidates who meet the eligibility criteria should apply as soon as possible. Early applications can improve your chances of selection for this opportunity in the pharmaceutical quality domain.
