Levim Lifetech hiring QA associate in Chennai. Check eligibility, experience, salary, and apply for biopharma quality assurance role now today.
If you are aiming to build a strong career in biopharmaceutical quality systems, the Quality Assurance Associate – Levim Lifetech Jobs 2026 offers a promising opportunity. This role is ideal for candidates with at least one year of QA experience who want to gain hands-on exposure to GMP compliance, audits, and regulatory processes.
Levim Lifetech is inviting applications from qualified candidates who are passionate about quality assurance and compliance in the pharma and biotech sector.
Job Overview
| Field | Details |
|---|---|
| Job Title | Quality Assurance Associate |
| Company Name | Levim Lifetech |
| Location | Chennai, Tamil Nadu |
| Employment Type | Full-Time |
| Department | Quality Assurance |
| Experience Required | Minimum 1 Year |
| Education | Bachelor’s / Master’s in Biotechnology, Microbiology, Biochemistry or related field |
| Salary | As per company norms |
Company Overview
Levim Lifetech is an emerging organization in the biopharmaceutical sector, focused on delivering high-quality and compliant healthcare solutions. The company emphasizes regulatory excellence, innovation, and strong quality systems to meet global standards.
Working at Levim Lifetech provides professionals with exposure to modern QA practices, documentation systems, and regulatory frameworks.
Job Location & Employment Type
This role is based in Chennai, Tamil Nadu, and is a full-time position within the Quality Assurance department.
Open Positions / Department Details
The opening is for the Quality Assurance (QA) Associate role, where candidates will work closely with cross-functional teams to maintain compliance and quality standards across operations.
Key Roles & Responsibilities
As a Quality Assurance Associate, your responsibilities will include:
- Supporting Quality Management System (QMS) activities such as deviation, CAPA, OOS, OOT, and incident handling
- Managing documentation control including SOPs, logs, and master records
- Ensuring proper issuance, tracking, and archival of documents
- Assisting in internal and external audits and ensuring CAPA closure
- Supporting validation, calibration, and qualification documentation
- Preparing QA reports, trend analysis, and management review presentations
- Coordinating with different departments for compliance and documentation updates
- Assisting in vendor qualification and maintaining related records
- Supporting GMP training programs and QA induction activities
- Providing assistance in regulatory submissions and complaint investigations
- Tracking and ensuring timely closure of QA and QMS activities
Eligibility Criteria
Education
- Bachelor’s or Master’s degree in:
- Biotechnology
- Microbiology
- Biochemistry
- Or related life sciences field
Experience
- Minimum 1 year of experience in Quality Assurance within pharma or biopharma industry
Skills Required
- Strong understanding of GMP and GLP guidelines
- Knowledge of QMS systems, CAPA, deviations, audits
- Good documentation and record-keeping skills
- Analytical thinking and problem-solving abilities
- Effective communication and teamwork skills
Salary & Benefits
- Salary: As per company norms
- Opportunity to work in a growing biopharmaceutical company
- Hands-on experience in QMS, audits, and regulatory compliance
- Exposure to documentation systems (DMS) and validation processes
- Career growth in QA and regulatory fields
- Supportive and compliance-driven work culture
Selection Process
The hiring process generally includes:
- Resume screening
- Technical interview (QA and compliance knowledge)
- HR discussion
- Final selection
How to Apply
Interested candidates can apply through email application by sending their updated resume to:
Email: hr@tevim.in
Important Dates
- Applications are currently open
- Apply as soon as possible to increase selection chances
Why Apply for This Job?
This role is a great opportunity for early-career professionals to strengthen their expertise in Quality Assurance. Here’s why you should consider applying:
- Gain practical experience in QMS, audits, and compliance systems
- Work in a fast-growing biopharmaceutical company
- Enhance your knowledge of regulatory requirements and documentation systems
- Build a strong foundation for long-term careers in QA and regulatory affairs
- Collaborate with experienced professionals in the industry
FAQs
1. What experience is required for this job?
Candidates must have at least 1 year of QA experience in pharma or biopharma.
2. What qualifications are needed?
A degree in Biotechnology, Microbiology, Biochemistry, or related fields is required.
3. What skills are important for this role?
Knowledge of GMP, GLP, QMS, CAPA, and audits is essential.
4. Is this a fresher job?
No, this role requires minimum 1 year of experience.
5. How can I apply?
You can apply by sending your resume via email to hr@tevim.in.
Conclusion
The Quality Assurance Associate – Levim Lifetech Jobs 2026 is an excellent opportunity for candidates looking to grow in the biopharma quality domain. With exposure to QMS, audits, and regulatory compliance, this role offers strong learning and career advancement prospects. Apply now and take the next step in your QA career.
Disclaimer
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