Puerto Hiring QC & Micro Officer

BPharm MSc QC Officer Vacancies Rajasthan

BPharm/MSc QC & Micro Officer vacancies at Puerto Lifesciences, Neemrana Rajasthan. Apply with CTC & notice period.

Puerto Lifesciences is hiring Quality Control Officers and Executives, including QC Microbiology professionals, for its sterile injectable manufacturing facility in Neemrana, Rajasthan. If you have hands-on experience in analytical testing, microbiological evaluation, or cGMP-compliant pharmaceutical quality control, this is a strong opportunity within a globally aligned sterile pharma plant.

Sterile injectable manufacturing demands the highest level of regulatory compliance, data integrity, and quality oversight. Professionals with expertise in HPLC analysis, microbiological testing, environmental monitoring, and deviation investigations are in high demand across regulated pharmaceutical markets.

Company Overview

Puerto Lifesciences operates a sterile pharmaceutical manufacturing facility specializing in SVP (Small Volume Parenterals) and LVP (Large Volume Parenterals) injectables. The plant functions in accordance with global cGMP standards, ensuring compliance with stringent regulatory requirements applicable to injectable drug products.

Sterile manufacturing is one of the most regulated segments of the pharmaceutical industry. Companies operating in this domain must maintain strict aseptic controls, validated cleanroom environments, microbiological monitoring systems, and comprehensive quality management systems (QMS).

Working at a sterile injectable facility provides exposure to:

• Aseptic manufacturing practices
• Regulatory audit readiness
• Data integrity standards (ALCOA principles)
• Sterility assurance and contamination control
• Injectable product quality systems

Puerto Lifesciences offers professionals the opportunity to build expertise in sterile pharma quality control, one of the highest-value technical domains in pharmaceutical manufacturing.

Job Role & Responsibilities

Puerto is hiring for two key Quality Control functions:

Quality Control – Officer / Executive (Analytical QC)

Key Responsibilities:

• Operation and calibration of analytical instruments such as HPLC, UV-Visible Spectrophotometer, and pH meter
• Preparation and standardization of reagents and volumetric solutions
• Documentation in accordance with cGMP guidelines
• Ensuring compliance with data integrity principles (ALCOA)
• Supporting OOS (Out of Specification), OOT (Out of Trend), and deviation investigations
• Maintaining laboratory records and analytical reports

Candidates must demonstrate strong understanding of pharmaceutical analytical chemistry and regulatory documentation practices. Experience in injectable product testing will be preferred.

Analytical QC roles are critical in ensuring batch release compliance and regulatory acceptance in export markets.

Quality Control Microbiology – Officer / Executive

Key Responsibilities:

• Performing microbiological testing for sterile injectable products
• Conducting environmental monitoring in classified cleanroom areas
• Performing Bacterial Endotoxin Test (BET)
• Executing Microbial Limit Testing (MLT)
• Conducting sterility testing
• Managing media preparation and Growth Promotion Test (GPT) activities
• Maintaining microbiology records, trend analysis, and data integrity (ALCOA compliance)

Microbiology professionals in sterile plants play a direct role in contamination control and sterility assurance. Experience in aseptic area monitoring and regulatory audit documentation is highly valuable.

Eligibility / Qualifications

Educational Qualifications (comma-separated):

B.Pharm, M.Pharm, B.Sc Microbiology, M.Sc Microbiology, B.Sc Chemistry, M.Sc Analytical Chemistry, Pharmaceutical Analysis

Experience:

• Experience in pharmaceutical Quality Control (Analytical or Microbiology)
• Prior exposure to sterile injectable manufacturing preferred
• Knowledge of cGMP, ALCOA data integrity, and regulatory documentation standards

Required Competencies:

• Hands-on instrument handling (HPLC, UV, pH meter)
• Understanding of deviation management and OOS/OOT investigations
• Knowledge of environmental monitoring and sterility testing
• Strong documentation and compliance discipline

Candidates without relevant pharmaceutical QC experience may not meet the eligibility criteria.

Location & Salary Insights

Location: Ghiloth, Neemrana, Rajasthan

Neemrana is emerging as an industrial and pharmaceutical manufacturing hub, offering strong infrastructure and growing regulatory-compliant facilities.

Salary will depend on:

• Technical expertise in analytical or microbiology QC
• Experience in sterile manufacturing
• Regulatory compliance exposure
• Current CTC and notice period

Sterile injectable Quality Control roles typically command competitive compensation due to the complexity of aseptic compliance and global regulatory expectations.

Application Process

Interested candidates should share the following details:

• Updated CV
• Current CTC
• Notice Period

Apply via:

Website: https://www.puertolifesciences.com
Email: hr@puerto.in

Ensure your resume clearly highlights experience in sterile manufacturing, HPLC analysis, microbiological testing, environmental monitoring, and deviation handling.

Why Sterile Injectable QC Is a High-Value Career

Sterile injectable manufacturing requires zero-contamination tolerance. Regulatory agencies impose strict oversight on SVP and LVP facilities. As a result, experienced QC and Microbiology professionals in this sector remain in high demand.

Working in sterile QC provides expertise in:

• Aseptic process monitoring
• Sterility assurance systems
• Regulatory audit readiness
• Pharmaceutical data integrity standards
• High-risk product quality validation

These competencies significantly enhance long-term career growth in pharmaceutical quality assurance, regulatory affairs, and compliance leadership roles.

Career Growth Opportunities

Professionals joining Puerto Lifesciences may progress toward:

• Senior QC Officer
• QC Manager – Injectable Plant
• Microbiology Lead
• QA Compliance Officer
• Sterility Assurance Specialist
• Regulatory Compliance Manager

Experience in sterile injectable plants strengthens eligibility for roles in USFDA, EU-GMP, and other regulated market facilities.

Frequently Asked Questions (FAQs)

1. Is experience in sterile manufacturing mandatory?

It is strongly preferred, especially for microbiology roles.

2. What instruments should analytical QC candidates know?

HPLC, UV spectrophotometer, and pH meter handling is expected.

3. What microbiology tests are required?

BET, MLT, sterility testing, environmental monitoring, and GPT.

4. How do I apply?

Send your CV, current CTC, and notice period to hr@puerto.in.

5. Is this opportunity suitable for regulatory market exposure?

Yes. Sterile injectable plants operate under stringent global cGMP standards.

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Job Summary

Company	Puerto Lifesciences
Vacancies	Quality Control Officer / Executive; QC Microbiology Officer / Executive
Required Education	B.Pharm, M.Pharm, B.Sc/M.Sc Microbiology, B.Sc/M.Sc Chemistry
Experience	Relevant QC Experience in Pharmaceutical Manufacturing