Aspiro Pharma Hiring Assistant Manager / Manager – Production-QMS

Assistant/Manager Production-QMS Vacancies – Aspiro Pharma Hyderabad

Apply for Production-QMS vacancies at Aspiro Pharma, Hyderabad. Openings for B.Pharm/M.Pharm/M.Sc with 10–15 years’ experience.

Aspiro Pharma Ltd., a leading injectable manufacturing company, is hiring experienced professionals for its Production-QMS department at the Karakapatla, Hyderabad facility. This is an excellent opportunity for B.Pharm, M.Pharm, or M.Sc graduates with strong backgrounds in QMS and injectable manufacturing compliance to join a globally recognized pharmaceutical company.

Company Overview

Aspiro Pharma Ltd. is part of the esteemed Hetero Group, known for its extensive presence in formulations, APIs, and injectables across global markets. With its USFDA, EU, MHRA, and WHO-approved facilities, Aspiro Pharma has earned a reputation for excellence in regulatory compliance, quality manufacturing, and pharmaceutical innovation. Working here ensures exposure to global regulatory frameworks and large-scale injectable operations.

Job Role & Responsibilities

As an Assistant Manager/Manager – Production-QMS, you will be responsible for:

• Ensuring compliance with cGMP, regulatory, and company quality standards across injectable operations.
• Reviewing and approving QMS documents: SOPs, change controls, deviations, CAPAs, risk assessments, and batch manufacturing records.
• Leading investigations into deviations and market complaints while implementing CAPA measures.
• Driving shop floor compliance, conducting internal audits, and supporting regulatory inspections (USFDA, EU, MHRA, WHO).
• Coordinating with cross-functional teams for QMS implementation and continual improvement.
• Monitoring production processes to identify compliance gaps.
• Training and mentoring team members on QMS procedures, cGMP practices, and data integrity principles.
• Supporting technology transfer, process validation, and regulatory submissions from a QMS perspective.

Eligibility / Qualifications

• Education: B.Pharm, M.Pharm, or M.Sc. Related courses include Pharmaceutical Technology, Industrial Pharmacy, Pharmaceutical Chemistry, Quality Assurance, Regulatory Affairs.
• Experience: 10–15 years of experience in injectable manufacturing with strong exposure to QMS functions.
• Strong knowledge of cGMP, regulatory standards, data integrity, and QMS documentation.
• Proven leadership skills with the ability to guide teams through audits and compliance improvements.

Location & Salary

• Location: Injectable Manufacturing Facility, Karakapatla, Hyderabad.
• Salary: Competitive package as per industry standards with benefits and career growth opportunities.

Application Process

Interested candidates can apply by sending their updated resumes to:

Hemasundar.i@hetero.com
Subject Line: Production-QMS

Apply before 23rd August 2025 to secure your opportunity. Early applications will be given preference.

Why Join Aspiro Pharma?

• Work with a USFDA and EU-approved injectable facility.
• Exposure to global regulatory frameworks and QMS best practices.
• Be part of a dynamic team contributing to world-class injectable manufacturing.
• Competitive salary, professional development, and long-term career opportunities.

FAQs – Aspiro Pharma Production-QMS Vacancies

Q1: What positions are open?
Assistant Manager and Manager roles in Production-QMS.

Q2: Who can apply?
B.Pharm/M.Pharm/M.Sc graduates with 10–15 years of injectable QMS experience.

Q3: What is the job location?
Karakapatla, Hyderabad.

Q4: What regulatory exposure is required?
Candidates must have worked with facilities inspected by USFDA, EU, MHRA, or WHO.

Q5: How do I apply?
Send your updated CV to Hemasundar.i@hetero.com with the subject line “Production-QMS”.

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