Veeda Lifesciences is inviting applications from experienced professionals for the position of Auditor – Analytical Quality Assurance (QA) at its Peenya, Bangalore, Karnataka location. Candidates with 5 to 8 years of relevant experience in analytical quality assurance, analytical characterization, and biosimilar development can apply for this opportunity.

This position is suitable for professionals with expertise in analytical data review, regulatory compliance, quality audits, and analytical comparability assessments in the pharmaceutical and biotechnology sectors.

Job Details

• Company Name: Veeda Lifesciences
• Job Title: Auditor – Analytical QA
• Department: Analytical Quality Assurance (QA)
• Job Location: Peenya, Bangalore, Karnataka
• Required Experience: 5–8 Years
• Qualification: Not specified in the recruitment notice. Candidates should confirm the required educational qualifications with the employer.
• Job Type: Experienced Professional
• Salary: Not mentioned
• Application Mode: Email
• Official Contact Email: Mahendra.t3705@veedalifesciences.com

Job Responsibilities

Selected candidates will be responsible for the following activities:

1. Perform quality assurance reviews and audits of analytical characterization studies supporting biosimilar development.
2. Review study protocols, analytical reports, raw data, and supporting documentation to ensure compliance with Good Laboratory Practice (GLP), where applicable, ALCOA+ principles, internal procedures, and data integrity requirements.
3. Ensure compliance with applicable regulatory requirements, including FDA, EMA, and relevant ICH guidelines such as Q5E, Q6B, Q2(R2), Q9, and Q14.
4. Review analytical characterization data involving HOS, SPR, NMR, FTIR, CD, DSC, DLS, peptide mapping, glycan profiling, and analytical comparability assessments.
5. Conduct internal audits of CMC R&D functions and participate in sponsor audits, regulatory inspections, and due diligence audits.
6. Evaluate analytical comparability assessments and associated statistical analyses to ensure scientific validity and support appropriate biosimilarity conclusions.
7. Provide QA guidance and support during biosimilar development activities and regulatory filing programmes.
8. Review and approve analytical study protocols, validation protocols and reports, characterization reports, technical reports, change controls, deviations, OOS/OOT investigations, CAPAs, and risk assessments.

Required Technical Knowledge

Candidates applying for this role should have relevant experience in analytical quality assurance, laboratory documentation, regulatory compliance, and quality system management.

Knowledge of the following analytical techniques and concepts will be relevant:

• Higher-order structure (HOS) characterization
• Surface Plasmon Resonance (SPR)
• Nuclear Magnetic Resonance (NMR)
• Fourier Transform Infrared Spectroscopy (FTIR)
• Circular Dichroism (CD)
• Differential Scanning Calorimetry (DSC)
• Dynamic Light Scattering (DLS)
• Peptide mapping and glycan profiling
• Analytical method validation and comparability assessments
• ALCOA+ data integrity principles
• Deviation management, CAPA, and risk assessment
• ICH guidelines and pharmaceutical regulatory requirements

How to Apply for Veeda Lifesciences Recruitment 2026

Interested and eligible candidates can apply by sending their updated CV to the email address provided in the recruitment advertisement.

Email your CV to: Mahendra.t3705@veedalifesciences.com

Applicants should mention “Application for Auditor – Analytical QA” in the email subject line and highlight their relevant experience in analytical QA, biosimilar characterization, regulatory compliance, and quality audits.

Candidates are advised to verify the job details and any additional eligibility requirements with the employer before applying.

Frequently Asked Questions (FAQs)

1. What is the job role offered by Veeda Lifesciences?

Veeda Lifesciences is hiring for the position of Auditor – Analytical QA. The role involves auditing analytical characterization studies, reviewing laboratory documentation, ensuring data integrity, and supporting biosimilar development and regulatory compliance.

2. How much experience is required for the Auditor – Analytical QA position?

Candidates should have 5 to 8 years of experience in a relevant field. Experience in analytical quality assurance, analytical characterization, pharmaceutical quality systems, or biosimilar development would be relevant to the advertised responsibilities.

3. Which analytical techniques are relevant to this position?

The advertised role includes reviewing analytical data from HOS characterization, SPR, NMR, FTIR, CD, DSC, DLS, peptide mapping, and glycan profiling. Candidates should be familiar with interpreting analytical study documentation and assessing the reliability and scientific validity of results.

4. Which regulatory guidelines are mentioned in the recruitment notice?

The advertisement refers to FDA and EMA requirements and relevant ICH guidelines, including Q5E, Q6B, Q2(R2), Q9, and Q14. Knowledge of GLP, where applicable, ALCOA+ data integrity principles, and quality risk management is also relevant to the position.

5. How can candidates apply, and what is the salary for this job?

Candidates can send their updated CV to Mahendra.t3705@veedalifesciences.com. The recruitment notice does not specify the salary or educational qualification requirements, so applicants should confirm these details directly with the employer.