Annora Pharma Private Limited has announced an excellent career opportunity for experienced pharmaceutical professionals. The company is hiring a General Manager – Quality Assurance (QA Lead) to lead its Quality Assurance function and ensure compliance with global regulatory standards. This senior leadership role is ideal for professionals with extensive experience in Quality Assurance, cGMP compliance, regulatory audits, and pharmaceutical manufacturing.

If you have over 20 years of experience in the pharmaceutical industry, especially in OSD (Oral Solid Dosage) manufacturing, this is a great opportunity to advance your career with one of India’s growing pharmaceutical organizations.

Job Overview

Particular Details

Company Name

Annora Pharma Private Limited

Job Position

General Manager – Quality Assurance (QA Lead)

Department

Quality Assurance (QA)

Reports To

Quality Head

Qualification

B.Pharm / M.Pharm (Preferred)

Experience

20+ Years

Industry

Pharmaceutical

Preferred Background

OSD (Oral Solid Dosage) Manufacturing

About Annora Pharma

Annora Pharma Private Limited is committed to delivering high-quality healthcare solutions by maintaining world-class manufacturing standards and robust quality systems. The organization focuses on innovation, regulatory compliance, and continuous improvement while ensuring patient safety and product quality.

Educational Qualification

Candidates should possess:

B.Pharm or M.Pharm (Preferred)

Strong knowledge of pharmaceutical quality systems

Excellent leadership and communication skills

Experience Required

Applicants should have:

Minimum 20+ years of experience in the pharmaceutical industry.

Experience in OSD (Oral Solid Dosage) manufacturing is highly preferred.

Proven leadership in Quality Assurance operations.

Experience handling global regulatory inspections and audits.

Key Role Overview

The selected candidate will lead the entire Quality Assurance department and ensure:

Compliance with international quality standards.

Development of effective Quality Management Systems.

Continuous improvement initiatives.

Regulatory readiness for domestic and international inspections.

Cross-functional collaboration to achieve operational excellence.

Key Responsibilities

Lead the complete Quality Assurance function.

Ensure compliance with cGMP, GLP, and regulatory requirements.

Manage regulatory inspections and customer audits.

Develop and strengthen Quality Management Systems (QMS).

Review SOPs, validation protocols, and quality documentation.

Drive quality culture throughout the organization.

Coordinate with Manufacturing, QC, Regulatory Affairs, and Engineering teams.

Ensure product quality, compliance, and patient safety.

Preferred Skills

Leadership and team management

cGMP & GLP expertise

Regulatory compliance

Audit management

Risk assessment

Quality documentation

Investigation & CAPA management

Change Control

Validation

Continuous Improvement

Why Join Annora Pharma?

Leadership opportunity in Quality Assurance.

Exposure to global pharmaceutical regulatory standards.

Work in a modern pharmaceutical manufacturing environment.

Career growth with a reputed pharmaceutical organization.

Opportunity to lead quality excellence initiatives.

Contact Details

HR Contact: Dara Ramesh

Designation: DGM – HR

Mobile: 7331150240

Email: ramesh.d@annorapharma.com

Website: www.annorapharma.com

Technical FAQs

1. What is cGMP, and why is it important in pharmaceutical manufacturing?

Current Good Manufacturing Practices (cGMP) are regulatory guidelines that ensure pharmaceutical products are consistently produced and controlled according to quality standards, ensuring safety, efficacy, and compliance.

2. What is the role of Quality Assurance in an OSD manufacturing facility?

Quality Assurance ensures that manufacturing processes, documentation, validation, investigations, and product release comply with regulatory requirements while maintaining product quality and patient safety.

3. What is CAPA in pharmaceutical Quality Assurance?

CAPA (Corrective and Preventive Action) is a quality management process used to identify root causes of deviations, implement corrective actions, and prevent recurrence to improve overall product quality.

4. What documents are commonly reviewed by a QA Lead?

A QA Lead reviews SOPs, Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), validation protocols, change controls, deviations, investigations, audit reports, and CAPA documentation.

5. Which regulatory agencies should a QA Lead be familiar with?

A senior QA professional should have knowledge of regulatory guidelines from agencies such as USFDA, MHRA, EMA, WHO-GMP, PIC/S, and CDSCO, along with ICH quality guidelines.