Ready to make an impact with a leader in sterile products? Puerto Life Sciences Pvt. Ltd., committed to delivering world-class sterile solutions, is hiring Manager / Assistant Manager roles for our Quality Assurance and Quality Control teams at our Neemrana, Rajasthan facility. With a focus on aseptic manufacturing and strict adherence to global GMP standards, we’re looking for experienced professionals to join our mission of ensuring quality in healthcare.
Job Details
| Field | Details |
|---|---|
| Job Title | Manager / Assistant Manager – Quality Assurance, Quality Control |
| Company | Puerto Life Sciences Pvt. Ltd. |
| Job Type | Full-Time |
| Location | Neemrana, Rajasthan |
| Department | Quality Assurance, Quality Control |
| Experience | 5–8 Years |
Job Description
Manager / Assistant Manager – Quality Assurance
- Qualifications: B.Pharm / M.Pharm / M.Sc.
- Experience: 5–8 years in pharmaceutical QA, preferably in sterile facilities
- Vacancies: Multiple
- Location: Puerto Life Sciences Pvt. Ltd., Plot No. F-41, RIICO Industrial Area, Neemrana, Alwar, Rajasthan – 301705
Responsibilities
- Oversee QA operations and ensure compliance with global GMP standards
- Lead CAPA and deviation management processes
- Support regulatory audits and ensure readiness
- Strategize and implement QA processes
- Manage team performance and foster a culture of quality
Required Skills
- Expertise in QA operations for sterile manufacturing
- Strong knowledge of cGMP, GLP, and regulatory guidelines (USFDA, MHRA)
- Experience with CAPA, deviations, and audit support
- Leadership and team management skills
Manager / Assistant Manager – Quality Control
- Qualifications: B.Pharm / M.Pharm / M.Sc.
- Experience: 5–8 years in pharmaceutical QC, preferably in sterile facilities
- Vacancies: Multiple
- Location: Puerto Life Sciences Pvt. Ltd., Plot No. F-41, RIICO Industrial Area, Neemrana, Alwar, Rajasthan – 301705
Responsibilities
- Lead the QC team and ensure lab operations meet regulatory compliance
- Manage internal and external audits
- Strategize and implement QC processes
- Oversee lab supplies and ensure accurate documentation per standards
- Maintain peak lab performance and quality metrics
Required Skills
- Expertise in QC operations for sterile products
- Knowledge of cGMP, GLP, and regulatory standards (USFDA, MHRA)
- Experience with audits, lab management, and documentation
- Strong leadership and analytical skills
Application Details
- Date: Apply by April 30, 2025
- Time: Contact for interview scheduling
- Contact: Email your details to hr@puerto.in
Documents Required
- Updated Resume
- Current CTC
- Notice Period
- Photocopy of Educational Certificates
- Experience Certificates
Important Notes
- Eligibility: Candidates must have 5–8 years of experience in pharmaceutical QA/QC
- Preference: Experience in sterile facilities is preferred
- Pre-Apply: Submit your details via email
How to Apply
- Email Application: Send your resume, current CTC, and notice period to hr@puerto.in with the subject “Application for Manager/Assistant Manager – [Department] – Neemrana – April 2025”.
- Pro Tip: Highlight your experience with sterile manufacturing, audits, or CAPA in your resume!
- Application Deadline: Apply by April 30, 2025.
Don’t wait! Join Puerto Life Sciences Pvt. Ltd. in Neemrana and contribute to world-class sterile products today! 🚀🌍
Eligibility Reminder: Candidates must have 5–8 years of relevant experience, preferably in sterile facilities. Ensure your application includes all required details.