Puerto Life Sciences Hiring QA, QC & Microbiology

Puerto Life Sciences QA, QC, Micro Jobs – Neemrana, Rajasthan

Puerto Life Sciences hiring QA, QC & Microbiology professionals in Neemrana. M.Pharm, B.Pharm, MSc candidates with sterile experience apply now.

Puerto Life Sciences Pvt. Ltd. is expanding its sterile manufacturing operations at its Neemrana facility and is inviting experienced pharmaceutical professionals to join its Quality Assurance, Quality Control, and Microbiology teams. These roles are designed for candidates who want to work in a regulated, compliance-driven environment where product quality, patient safety, and regulatory excellence are non-negotiable. If you are seeking long-term pharma careers in Rajasthan with exposure to GMP, QMS, and global quality standards, this opportunity offers both stability and growth.

Company Overview

Puerto Life Sciences Pvt. Ltd. is a pharmaceutical organization focused on delivering high-quality sterile products that meet stringent domestic and international regulatory requirements. With a strong emphasis on GMP compliance, data integrity, and continuous improvement, the company has built a reputation for operational excellence and ethical manufacturing practices. Its Neemrana facility supports sterile production and quality operations, offering professionals hands-on exposure to audits, validations, and regulated market expectations.

Job Roles & Responsibilities

Quality Assurance Department

Senior Executive – Quality Assurance (5+ Years)

• Review and approve Batch Manufacturing Records (BMR) and Batch Packing Records (BPR).
• Ensure line clearance, IPQA oversight, and compliance during sterile manufacturing operations.
• Handle deviations, change control, and CAPA activities within the QMS framework.
• Coordinate internal, external, and regulatory audits.
• Support validation activities, training programs, and cross-functional quality initiatives.

Officer – Quality Assurance (Up to 4 Years)

• Support routine QA activities including documentation review and shop-floor compliance.
• Assist in deviation investigations, SOP management, and GMP audits.
• Ensure adherence to data integrity and quality systems.

Regulatory Affairs Department

Executive – Regulatory Affairs (4+ Years)

• Compile, review, and submit CTD/eCTD dossiers for domestic and international markets.
• Manage regulatory submissions, license renewals, and post-approval changes.
• Coordinate with QA, QC, and manufacturing teams for timely regulatory compliance.
• Liaise with regulatory authorities to address queries and approvals.

Quality Control Department

Senior Executive – QC Reviewer (5+ Years)

• Perform chemical analysis of raw materials, finished products, and stability samples.
• Operate and review data from analytical instruments such as HPLC, UV, FTIR, and KF.
• Ensure compliance with pharmacopeial standards and regulatory guidelines.
• Handle method validation, instrument calibration, and audit readiness.

Executive / Officer – Quality Control (Up to 4 Years)

• Conduct routine QC testing and documentation as per SOPs.
• Maintain data integrity and support investigations related to OOS and OOT.

Quality Control – Microbiology

Senior Executive – Microbiology (5+ Years)

• Perform microbiological testing of water, environment, raw materials, and finished products.
• Conduct sterility testing, BET, MLT, and environmental monitoring.
• Ensure aseptic practices, media preparation, and EM compliance.
• Support validation activities and GMP audit readiness.

Executive / Officer – Microbiology (Up to 4 Years)

• Assist in routine microbiological analysis and documentation.
• Support aseptic monitoring and laboratory compliance activities.

Eligibility & Qualifications

• Education: B.Pharm, M.Pharm, B.Sc, M.Sc (Chemistry / Microbiology / Life Sciences).
• Experience: Relevant experience as mentioned for each role.
• Mandatory: Sterile pharmaceutical manufacturing experience.
• Strong knowledge of GMP, QMS, data integrity, and regulatory compliance.

Location & Salary

• Job Location: Ghiloth, Neemrana, Rajasthan.
• Salary: Competitive compensation with performance-based bonuses.
• Benefits include career growth opportunities and a collaborative work environment.

Application Process

Interested candidates should send their updated CV along with current CTC and notice period details to:

Email: hr@puerto.in

Only candidates with prior sterile industry experience will be considered.

FAQs

Who can apply for these roles?
Candidates with relevant QA, QC, Microbiology, or Regulatory Affairs experience in sterile pharmaceutical manufacturing.

Is sterile experience mandatory?
Yes. Only candidates with sterile industry exposure are eligible.

What qualifications are accepted?
B.Pharm, M.Pharm, B.Sc, and M.Sc in relevant disciplines.

Where is the job location?
Ghiloth, Neemrana, Rajasthan.

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Company                              Puerto Life Sciences Pvt. Ltd.
Vacancies                              Multiple openings across QA, QC, Micro & RA
Required Education              B.Pharm, M.Pharm, B.Sc, M.Sc
Experience                            Up to 4 Years / 5+ Years depending on role