Puerto Hiring QC GLP Executive

Puerto Lifesciences QC GLP Executive Hiring

Puerto Lifesciences hiring QC GLP Executive for sterile injectable operations. B.Pharm, M.Pharm, BSc, MSc candidates can apply.

Puerto Lifesciences has announced a new pharmaceutical hiring opportunity for experienced Quality Control professionals in its sterile injectable manufacturing division. The company is recruiting for the position of Quality Control (GLP) Executive for candidates with strong exposure to sterile pharmaceutical quality systems, laboratory compliance, analytical documentation, and GMP-regulated manufacturing operations.

This latest pharma QC recruitment is ideal for professionals looking to grow their career in sterile injectable manufacturing, pharmaceutical quality assurance systems, regulatory compliance, analytical laboratory operations, and data integrity management.

Candidates searching for:

• Pharma quality control jobs
• GLP executive jobs in pharma
• Sterile injectable QC jobs
• WHO GMP pharmaceutical jobs
• Quality assurance and QC careers
• Analytical laboratory pharma jobs
• OOS investigation jobs
• Data integrity pharma jobs
• cGMP pharmaceutical manufacturing careers
• Regulatory compliance jobs in pharma

can explore this latest Puerto Lifesciences opportunity.

The company is specifically looking for dynamic and motivated professionals who can support laboratory compliance systems, analytical operations, documentation practices, and regulatory audit readiness in a sterile pharmaceutical environment.

Company Overview

Puerto Lifesciences is a sterile pharmaceutical manufacturing company specializing in SVP (Small Volume Parenteral) and LVP (Large Volume Parenteral) injectable products.

The organization operates according to global cGMP standards and focuses on maintaining strong pharmaceutical quality systems aligned with international regulatory requirements.

The company’s manufacturing and laboratory operations emphasize:

• Sterile injectable manufacturing
• WHO-GMP compliance
• Global cGMP standards
• Quality control systems
• Regulatory audit readiness
• Pharmaceutical laboratory excellence
• Data integrity practices
• Analytical testing compliance

Puerto Lifesciences continues expanding its pharmaceutical operations and is actively hiring experienced professionals capable of supporting regulated manufacturing and laboratory environments.

The company provides opportunities for pharmaceutical professionals to work in:

• Sterile manufacturing facilities
• Quality control laboratories
• Regulatory compliance operations
• Pharmaceutical analytical testing
• Laboratory documentation systems
• Quality assurance coordination

Job Role & Responsibilities

Position: Quality Control (GLP) – Executive

Experience Required

• 3 to 7 Years

The selected candidate will be responsible for supporting pharmaceutical laboratory operations, ensuring GLP and GMP compliance, managing analytical documentation, and participating in regulatory quality systems.

Laboratory Compliance & Regulatory Support

Candidates will be responsible for:

• Ensuring laboratory compliance with GLP, GMP, WHO-GMP, and safety guidelines
• Supporting sterile pharmaceutical quality systems
• Maintaining compliance with regulatory standards
• Ensuring laboratory operations follow global cGMP requirements

Analytical Data Review

Key responsibilities include:

• Reviewing analytical raw data
• Reviewing audit trails and laboratory records
• Monitoring documentation as per data integrity requirements
• Verifying analytical documentation accuracy

Laboratory Inventory & Reagent Control

The candidate will manage:

• Volumetric solutions
• Laboratory reagents
• Standards and cultures
• Laboratory consumables
• Proper labeling and validity tracking

Investigation Handling

The role involves handling:

• OOS (Out of Specification) investigations
• OOT (Out of Trend) investigations
• Laboratory deviations
• Incident investigations
• Root Cause Analysis (RCA)
• CAPA implementation

Documentation & SOP Management

Candidates should be capable of:

• Preparing and reviewing SOPs
• Reviewing STPs and specifications
• Managing protocols and analytical documents
• Maintaining pharmaceutical laboratory records
• Supporting regulatory documentation systems

Instrument Calibration & Qualification

The selected professional will support:

• Instrument calibration
• Qualification activities
• Verification processes
• Preventive maintenance coordination
• Analytical equipment monitoring

Cross-Functional Coordination

The role requires collaboration with:

• Quality Assurance teams
• Production department
• Microbiology department
• Regulatory teams
• Audit support functions

Audit & Inspection Readiness

Responsibilities include:

• Supporting internal audits
• Participating in customer audits
• Preparing for regulatory inspections
• Maintaining inspection readiness

Laboratory Safety & Housekeeping

Candidates will ensure:

• Laboratory housekeeping compliance
• Safety standard implementation
• Quality laboratory discipline
• Compliance within QC and Microbiology labs

Technical Knowledge Requirements

Candidates should possess knowledge of:

• ICH Guidelines
• IP/USP/EP/BP pharmacopeia
• GLP practices
• Sterile pharmaceutical operations
• Data integrity systems
• Audit trail review
• Laboratory compliance procedures

Software & Documentation Skills

Applicants should have proficiency in:

• MS Word
• MS Excel
• Laboratory documentation
• Audit trail review systems
• Pharmaceutical reporting systems

Why This Pharma QC Job is Valuable

Quality Control and GLP roles in sterile pharmaceutical manufacturing are among the most in-demand positions in India’s regulated pharmaceutical industry.

This opportunity provides exposure to:

• Sterile injectable manufacturing
• Regulatory audit systems
• Global pharmaceutical compliance
• Data integrity practices
• WHO-GMP operations
• Pharmaceutical laboratory investigations
• Analytical quality systems
• cGMP documentation practices

Professionals with experience in sterile pharmaceutical quality systems are highly valued across:

• Injectable manufacturing companies
• Global pharma plants
• USFDA-regulated facilities
• EU-GMP pharmaceutical organizations
• Clinical manufacturing units
• Contract manufacturing companies

Eligibility / Qualifications

Educational Qualification

The company has not specified exact qualification criteria in the notification, but relevant candidates from pharmaceutical and life sciences backgrounds are generally preferred.

Suitable educational backgrounds may include:

• B.Pharm
• M.Pharm
• B.Sc Chemistry
• M.Sc Chemistry
• Pharmaceutical Analysis
• Microbiology
• Life Sciences

Experience Required

• 3 to 7 years

Preferred Candidate Profile

Candidates with the following profile may receive preference:

• Experience in sterile pharmaceutical operations
• Strong analytical documentation skills
• Exposure to GLP and GMP systems
• Knowledge of data integrity requirements
• Experience in OOS/OOT investigations
• Regulatory audit exposure
• Pharmaceutical QC laboratory experience

Relevant Courses

Pharmacy, Pharmaceutical Analysis, Pharmaceutical Chemistry, Analytical Chemistry, Industrial Pharmacy, Quality Assurance, Microbiology, Biotechnology, Regulatory Affairs, Pharmaceutical Quality Systems, Drug Regulatory Compliance

Career Growth Opportunities

Professionals joining Puerto Lifesciences may later advance into roles such as:

• Senior QC Executive
• Quality Assurance Executive
• Data Integrity Specialist
• Validation Officer
• Regulatory Compliance Executive
• Laboratory Compliance Lead
• Audit Coordinator
• QC Manager
• Quality Systems Specialist
• Pharmaceutical Regulatory Affairs Professional

The sterile injectable manufacturing segment offers strong long-term career growth due to increasing global demand for high-quality pharmaceutical products.

Location & Salary

Job Location

India

Approximate Salary

Based on current pharmaceutical industry standards for Quality Control GLP Executive roles in sterile pharmaceutical companies, the expected salary range may be:

• ₹5.5 LPA to ₹10 LPA

Salary may vary depending on:

• Experience level
• Sterile injectable exposure
• Audit handling experience
• Regulatory knowledge
• Technical expertise in QC systems

Application Process

Interested candidates should share the following details:

• Updated CV
• Current CTC
• Notice Period information

Email Application

Email ID: hr@puerto.in

Candidates are advised to mention relevant sterile manufacturing and QC experience clearly in the resume.

Important Skills That Can Improve Selection Chances

Candidates with practical experience in the following areas may have an advantage:

• Sterile pharmaceutical operations
• Analytical laboratory compliance
• Audit trail review
• CAPA implementation
• Deviation investigations
• cGMP documentation
• Regulatory inspection handling
• Pharmaceutical SOP systems
• Instrument qualification
• Data integrity compliance

Why Sterile Pharma Jobs Are Growing Rapidly

India’s sterile pharmaceutical manufacturing sector is witnessing rapid growth due to increasing demand for:

• Injectable products
• Hospital formulations
• Export-oriented pharmaceuticals
• Regulatory-compliant manufacturing
• Global pharmaceutical outsourcing
• Contract manufacturing services

This growth is creating strong demand for experienced Quality Control and Quality Assurance professionals.

Sterile pharmaceutical QC professionals with expertise in GLP, data integrity, audit systems, and regulatory compliance are among the highest-demand profiles in the healthcare and pharmaceutical industry.

FAQs

1. Which company is hiring for this role?

Puerto Lifesciences is hiring for the Quality Control (GLP) Executive role.

2. What experience is required?

Candidates with 3 to 7 years of experience can apply.

3. What type of pharmaceutical company is Puerto Lifesciences?

Puerto Lifesciences is a sterile pharmaceutical manufacturing company specializing in SVP and LVP injectables.

4. Which skills are required for this role?

Candidates should have knowledge of GLP, GMP, OOS investigations, CAPA, audit trails, data integrity, and laboratory documentation.

5. Is regulatory audit exposure important?

Yes. Experience with internal audits, customer audits, and regulatory inspections is valuable.

6. How can candidates apply?

Interested candidates can send their updated CV to hr@puerto.in.

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