Exciting pharma jobs opportunity! USV Pvt Ltd is hiring a Sterile IPQA Executive for its USFDA-approved injectable site. Ideal for experienced QA professionals seeking growth in sterile formulation. Apply now for pharmaceutical careers in India.
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About the Company
USV Pvt Ltd is a leading Indian multinational pharmaceutical company founded in 1961. Headquartered in Mumbai, it specializes in diabetes, cardiology, and a wide range of healthcare solutions including injectables, biosimilars, peptides, and solid orals.
With a strong focus on innovation, regulatory compliance, and quality, USV serves patients across India and over 60 countries globally. The company maintains USFDA-approved manufacturing facilities and is recognized for its commitment to affordable, high-quality healthcare.
USV ranks among the top players in India’s pharma market, particularly in oral anti-diabetic and cardiac segments. Its emphasis on R&D, cGMP standards, and patient-centric values makes it a preferred employer for professionals in pharmaceutical careers.
Job Details
- Company Name: USV Pvt Ltd
- Experience: 6-8 Years
- Location: USFDA-approved Sterile Formulation Site (Injectable / Sterile)
- Work Type: On-site
Job Description
USV Pvt Ltd is actively hiring experienced professionals for its Quality Assurance department at the sterile injectable manufacturing facility. This role in Sterile IPQA offers a chance to contribute to high-standard aseptic processing in a regulated environment.
Sterile IPQA Executive
- Department: Quality Assurance (IPQA – In-Process Quality Assurance)
- Market: Pharmaceutical – Sterile Formulation / Injectables
- Role: Sterile IPQA Executive
- Experience: 6-8 Years
Skills/Qualifications
- Hands-on experience in aseptic processing and sterile injectable formulation
- Strong knowledge of cGMP and EU Annex 1 guidelines
- Proven expertise in clean room operations, particularly Grade A/B areas
- Experience with USFDA-approved manufacturing sites
- Ability to review Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR)
- Proficiency in handling deviations, investigations, and CAPA management
- Excellent attention to detail and documentation skills
- Strong communication and teamwork abilities for cross-functional coordination
Key Responsibilities
- Oversee Aseptic Processing & Media Fills
- Ensure cGMP & EU Annex 1 Compliance
- Review BMR/BPR documentation
- Conduct IPQA Rounds & Line Clearance
- Manage Deviations & CAPA effectively
Benefits/Perks
- Career growth in a leading pharma company with global presence
- Opportunities for continuous learning and skill development in sterile technology
- Competitive salary and performance-based incentives
- Collaborative work culture focused on quality and innovation
- Exposure to international regulatory standards and best practices
How to Apply
Interested candidates with relevant experience in sterile QA should send their updated CV to sanafatma.khan@usv.in with the subject line: STERILE IPQA.
For more pharma jobs and similar opportunities in the industry, explore listings on Pharma Recruiter.
Apply today and take the next step in your pharmaceutical career with a reputed USFDA-approved organization!
Why You Should Join
Joining USV Pvt Ltd means becoming part of a company with over six decades of excellence in healthcare. The organization fosters a culture of integrity, innovation, and collaboration while maintaining the highest standards of regulatory compliance.
Employees benefit from long-term career stability, exposure to advanced sterile manufacturing technologies, and opportunities to contribute to life-saving injectable products. With a focus on professional growth and a supportive environment, USV empowers talent to build rewarding pharmaceutical careers in India and beyond.
FAQs
Q1: What is the required experience for the Sterile IPQA Executive role at USV?
A: Candidates should have 6-8 years of relevant experience in sterile injectable formulation and IPQA activities.
Q2: Is prior experience in a USFDA-approved site mandatory?
A: Yes, hands-on experience in USFDA-approved sterile manufacturing facilities is highly preferred for ensuring compliance with international standards.
Q3: How can I apply for this pharma job?
A: Email your CV to sanafatma.khan@usv.in with the subject line “STERILE IPQA”. Ensure your profile highlights relevant sterile QA experience.
Q4: What growth opportunities does this QA job offer?
A: The role provides excellent scope for advancement in Quality Assurance, exposure to EU Annex 1 and cGMP practices, and potential for leadership positions in a growing organization.
