Table of Contents
QA Jobs for Biochem & Microbiology at Arene Life Science Limited
Looking to build a strong career in Quality Assurance within the biosciences sector? Here’s an opportunity you shouldn’t miss. QA Jobs for Biochem & Microbiology at Arene Life Science Limited are now open, offering a promising pathway for candidates skilled in laboratory practices, documentation, and QA compliance standards. This role is ideal for those aiming to grow in pharmaceutical quality systems, regulatory workflows, and product compliance—making it a great fit for biochemistry and microbiology graduates seeking industry exposure and growth.
Company: Arene Life Science Limited
Position: Quality Assurance
Department: Quality Assurance / Corporate QA
Location: Patancheru, Hyderabad
Industry: API/ Bulk Drug Manufacturing
Experience: 1-10 Years
Salary: Open / Based on current CTC & skillset
Interview Mode: Face to Face
Note:
ONLY CANDIDATES FROM IN AND AROUND HYDERABAD SHOULD APPLY
ONLY MALE CANDIDATES ARE ELIGIBLE
Job Description (Roles & Responsibilities):
·Manage and execute QMS activities including:
· Change Control
· Deviations
· CAPA
· OOS / OOT investigations
·Oversee documentation systems ensuring accuracy, traceability, and compliance.
·Review and approve SOPs, STPs, protocols, batch manufacturing records (BMR/BPR).
·Support and coordinate internal, external, client, and regulatory audits.
·Ensure adherence to GMP, GDP, and regulatory compliance guidelines.
·Perform IPQA activities such as line clearance, in-process verifications, and batch documentation review.
·Assist production, QC, Microbiology, and R&D in quality-related queries and compliance activities.
·Participate in training programs, risk assessments, and continuous improvement initiatives.
·Maintain excellent documentation practices ensuring data integrity (ALCOA+).
Requirements:
- Strong experience in Quality Management Systems in an API/Bulk Drug company.
- Good knowledge of GMP, GDP, ICH guidelines, FDA/WHO regulatory expectations.
- Ability to manage audits, face auditors confidently, and close audit observations.
- Proficiency in reviewing technical documents like BMRs, COAs, protocols, and reports.
- Working knowledge of process compliance, change control, risk assessment, and CAPA.
- Excellent documentation, communication, and coordination skills.
- Should be detail-oriented and able to work independently with cross-functional teams.
- Ability to handle pressure, meet timelines, and maintain quality standards.
Qualification:
B.Sc/M.Sc in Chemistry, Microbiology, Biochemistry or Related fields.
