Executive / Senior Executive – Quality Assurance

Cohance Lifesciences Recruitment: Executive / Senior Executive – Quality Assurance | Visakhapatnam

Company:
Cohance Lifesciences

Role:
Executive / Senior Executive – Quality Assurance (IPQA / Analytical QA)

Job ID:
a6a900ae5bb6dc

Job Type:
Full-Time / Regular

Work Mode:
On-site

Location:
Visakhapatnam (Parwada / JN Pharma City), Andhra Pradesh, India

Salary / CTC:
Best in Industry (Commensurate with experience)

Experience Level:
2 to 6 Years

Qualification:
B.Pharmacy / M.Pharmacy / M.Sc (Chemistry)

Selection Process:
Resume Shortlisting, Technical Interview, and HR Discussion

About the Role
Cohance Lifesciences is seeking dedicated Quality Assurance professionals to join their manufacturing operations in Visakhapatnam.
In this role, you will be responsible for line clearance, in-process quality checks, batch manufacturing record reviews, and ensuring strict adherence to cGMP guidelines across active pharmaceutical ingredient (API) and formulation facilities.

Key Responsibilities
Line Clearance & Monitoring: Conduct thorough line clearance and routine surveillance in manufacturing and packaging blocks.
BMR / BPR Review: Review and verify Batch Manufacturing Records and Batch Packaging Records during daily processing.
Deviation & Change Control: Report, investigate, and document site deviations, incidents, out-of-specification (OOS) results, and change control actions.
Sampling & Inspections: Supervise sampling activities, in-process checks, and ensure continuous compliance with standard operating procedures (SOPs).
Audit Preparedness: Support regulatory inspection readiness and internal quality audits according to national and global regulatory frameworks.

Eligibility & Skills Required
Education: B.Sc, M.Sc (Organic / Analytical Chemistry), B.Pharmacy, or M.Pharmacy from an accredited institution.
Experience: 2 to 6 years of core experience in IPQA, Analytical QA, or Quality Compliance within an API or finished dosage pharmaceutical manufacturing plant.
Regulatory Standards: Solid practical knowledge of cGMP, USFDA guidelines, ICH guidelines, and data integrity principles.
Documentation Skills: Excellent attention to detail in technical documentation, SOP writing, and compliance reporting.
Communication: Good verbal and written communication skills with strong team-coordination abilities.

Perks & Benefits
Competitive industry compensation and performance incentives
Comprehensive health insurance and employee mediclaim policies
Subsidized transportation and on-site cafeteria facilities
Continuous learning programs in global pharmaceutical quality standards
Supportive, safety-oriented, and compliant working culture

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