Looking for pharma jobs in India? Auxilla Pharmaceuticals & Research LLP is hiring experienced Quality Assurance professionals for Research Associate and Senior Research Associate positions.
Explore exciting pharmaceutical careers with excellent growth opportunities, employee benefits, and a dynamic work environment.
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About the Company
Auxilla Pharmaceuticals & Research LLP is a growing pharmaceutical organization focused on quality, innovation, and research excellence. The company is committed to developing high-quality pharmaceutical products while maintaining strict regulatory compliance and industry standards.
With a strong emphasis on analytical excellence, quality systems, and continuous improvement, Auxilla Pharmaceuticals provides professionals with opportunities to contribute to innovative pharmaceutical development projects.
The organization fosters a culture of collaboration, integrity, and scientific advancement, making it an attractive destination for skilled pharmaceutical professionals seeking long-term career growth.
Job Details
- Company Name: Auxilla Pharmaceuticals & Research LLP
- Position: Research Associate / Senior Research Associate
- Department: Quality Assurance (QA)
- Experience: 3–5 Years
- Qualification: M.Sc. / M.Pharm
- Work Type: On-site
Job Description
Auxilla Pharmaceuticals & Research LLP is seeking qualified and experienced professionals to join its Quality Assurance team.
The selected candidates will play a critical role in reviewing analytical documentation, validation reports, and development records to ensure compliance with regulatory and quality standards.
Research Associate / Senior Research Associate
- Department: Quality Assurance (QA)
- Role: Review and compliance of analytical and development documentation
- Experience: 3–5 Years
- Education/Qualification: M.Sc. / M.Pharm
Skills/Qualifications
- M.Sc. or M.Pharm qualification
- Experience in ADL (Analytical Development Laboratory)
- Experience in Analytical Quality Assurance
- Knowledge of pharmaceutical quality systems
- Understanding of analytical validation requirements
- Familiarity with regulatory documentation
- Strong analytical and review skills
- Excellent documentation practices
- Good communication and teamwork abilities
- Attention to detail and compliance mindset
Key Responsibilities
- Review SOPs and quality documents
- Review STPs and analytical procedures
- Verify Certificates of Analysis (COAs)
- Review stability compilation reports
- Evaluate MDR documentation
- Review analytical validation reports
- Assess product development reports
- Ensure regulatory compliance requirements
- Maintain quality documentation standards
Benefits/Perks
- 5-day work week
- Mediclaim facility
- Transportation facility
- Canteen facility
- Professional development opportunities
- Collaborative work environment
- Exposure to pharmaceutical quality systems
- Long-term career growth potential
- Opportunity to work with experienced professionals
- Stable pharmaceutical industry career
How to Apply
Interested candidates who meet the eligibility criteria can apply by sharing their updated CV directly with the company’s HR team.
Email: hr@auxillapharma.com
Applicants should ensure that their resume highlights relevant experience in Analytical Development Laboratory (ADL), Analytical QA, validation activities, and quality documentation review.
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Apply today and take the next step toward building a rewarding career in pharmaceutical quality assurance.
Why You Should Join
Auxilla Pharmaceuticals & Research LLP offers an excellent platform for pharmaceutical professionals looking to advance their careers in Quality Assurance.
Employees benefit from a quality-focused culture, exposure to regulatory-compliant processes, and opportunities to contribute to important pharmaceutical development activities.
FAQs
Who is eligible to apply for this position?
Candidates with M.Sc. or M.Pharm qualifications and 3–5 years of experience in ADL or Analytical QA are eligible to apply.
How can I apply for the job?
Interested candidates can submit their updated CV via email to hr@auxillapharma.com.
Is this a Quality Assurance role?
Yes. The position is within the Quality Assurance (QA) department and focuses on analytical documentation review and compliance activities.
What career growth opportunities are available?
Employees gain valuable exposure to pharmaceutical quality systems, analytical validation, regulatory compliance, and product development processes, supporting long-term career advancement.
