Cipla Hiring QA Validation (DPI) – Hauppauge, New York | Pharma Quality Jobs
Cipla Hiring QA Validation (DPI) – Hauppauge, New York
Company Overview
Cipla is a globally respected pharmaceutical company with a strong legacy of delivering high-quality, affordable medicines across regulated markets. In the United States, Cipla operates through its subsidiary InvaGen Pharmaceuticals, Inc., supporting the development and manufacturing of generic prescription medicines under strict regulatory standards.
InvaGen’s Hauppauge, New York facility plays a critical role in pharmaceutical manufacturing, validation, and quality assurance—supporting products that directly impact patient health and regulatory compliance.
Job Summary
Cipla is seeking a QA Validation professional (DPI) to support equipment, facility, and utility validation activities at its Hauppauge, NY manufacturing site. This role focuses on ensuring compliance with cGMP regulations through structured validation programs, documentation control, and audit readiness.
The position is ideal for professionals early in their pharma quality careers who want hands-on exposure to regulated manufacturing environments, FDA interactions, and validation lifecycle management.
💼 Why Cipla Is Hiring for This Role
As Cipla continues to expand its regulated manufacturing footprint in the United States, the company is strengthening its quality and validation teams to support new product introductions, regulatory readiness, and continuous compliance with FDA expectations. This role supports long-term manufacturing stability and inspection preparedness.
💭 Jobs for All Note: QA Validation roles are foundational in pharmaceutical manufacturing. This position offers strong long-term career value by building expertise in cGMP compliance, audits, and validation systems—skills that are always in demand across the global pharma industry.
Eligibility & Qualifications
- Bachelor’s degree in a scientific discipline (Biology, Chemistry, Pharmacy or related field).
- 1–2 years of experience in pharmaceutical manufacturing or validation environments.
- Exposure to DPI, MDI, oral solids, or injectable manufacturing preferred.
- Strong documentation, analytical, and communication skills.
- Comfort working in regulated, fast-paced manufacturing settings.
👥 Who Should Apply / Who Should Avoid
- Best suited for: QA or validation professionals seeking hands-on experience in cGMP environments, FDA audits, and pharmaceutical manufacturing compliance.
- Not ideal for: Candidates seeking remote roles, non-regulated industry work, or non-quality positions.
Job Details
| Job Title | QA Validation (DPI) |
|---|---|
| Company | Cipla – InvaGen Pharmaceuticals, Inc. |
| Location | Hauppauge, New York, USA |
| Employment Type | Full-Time (Professional, Exempt) |
| Work Schedule | General shift (8:30 AM – 5:00 PM; may vary) |
| Salary Range | $68,000 – $74,600 (as per employer disclosure) |
| Req ID | 96138 |
Key Responsibilities
- Support and maintain cGMP-compliant validation programs for equipment, facilities, and utilities.
- Coordinate commissioning, qualification, and validation activities across manufacturing systems.
- Prepare and review validation documents such as protocols, reports, SOPs, URS, FAT/SAT records.
- Oversee calibration and preventive maintenance documentation from external vendors.
- Participate in validation lifecycle activities including process validation and requalification.
- Support internal, customer, and FDA audits by providing validation documentation and responses.
- Assist with deviation investigations, change control processes, and remediation efforts.
📈 Career Growth & Advancement at Cipla
Professionals starting in QA Validation roles at Cipla can grow into advanced quality and leadership positions based on performance and experience. Typical career paths include:
- Senior QA Validation Specialist
- Quality Systems or Compliance Lead
- Validation Manager
- Quality Assurance Management Roles
Work Environment & Compliance
- On-site role only (no remote or hybrid option).
- Work performed in cGMP laboratory or manufacturing environments.
- Use of PPE such as lab coats, safety glasses, and protective equipment is mandatory.
- Weekend or holiday work may be required based on business needs.
How to Apply
Application Safety Notice: This is a local U.S. hiring role. Applications must be submitted only through Cipla’s official careers website. Cipla does not charge any fees at any stage of recruitment.
Apply on Cipla CareersFAQs
Is this role open for global transfers?
No. This position is strictly for local U.S. applicants and not for global assignments.
Is remote work available?
No. This is a fully on-site role at the Hauppauge, NY facility.
Does Cipla charge any recruitment fee?
No. Cipla never charges candidates for job applications or offers.
Resources & References
✍️ About the Author
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Company Disclaimer: Cipla is an Equal Opportunity Employer and conducts recruitment only through official channels. All qualified applicants will receive consideration without discrimination.
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