USV Hiring Officer – Analytical Quality Assurance

BPharm MSc Biotech QA Officer Vacancy | USV Navi Mumbai

BPharm, MSc Biotechnology QA Officer vacancy at USV Pharma biologics plant Navi Mumbai. 2–5 yrs experience required.

USV Private Limited is hiring an Officer – Analytical Quality Assurance (QA) for its Drug Substance Biologics Manufacturing facility located in Nerul, Navi Mumbai. This opportunity is open to experienced pharmaceutical and biotechnology professionals who possess strong expertise in analytical quality systems, laboratory data review, and regulatory compliance within biologics manufacturing environments.

Quality Assurance professionals working in biologics and drug substance manufacturing facilities play a critical role in ensuring that pharmaceutical products meet strict regulatory standards before they reach patients. The role involves reviewing analytical testing results, maintaining data integrity, ensuring compliance with Good Manufacturing Practices (GMP), and supporting quality management systems within regulated pharmaceutical environments.

Candidates with experience in analytical review, HPLC analysis, bioassay data evaluation, and microbiology data review will find this role particularly valuable for building a long-term career in pharmaceutical quality systems and biologics manufacturing.

Company Overview

USV Private Limited is one of India’s leading pharmaceutical companies with a strong presence in the development and manufacturing of high‑quality pharmaceutical formulations and active pharmaceutical ingredients. The company has established a reputation for delivering innovative healthcare solutions across multiple therapeutic segments including diabetes care, cardiovascular therapy, and biotechnology-based medicines.

With decades of pharmaceutical expertise, USV operates advanced manufacturing facilities that comply with international regulatory standards including Good Manufacturing Practices (GMP). The company invests heavily in research, biotechnology innovation, and high‑quality pharmaceutical production systems to support global healthcare needs.

The biologics manufacturing plant located in Nerul, Navi Mumbai focuses on the production of complex drug substances used in biotechnology-driven therapies. These facilities require highly specialized professionals who understand analytical quality assurance, laboratory data review, and pharmaceutical regulatory compliance.

Working with USV provides professionals with exposure to advanced biologics manufacturing systems, strict regulatory compliance environments, and modern pharmaceutical quality management frameworks.

Job Role & Responsibilities

The Officer – Analytical QA role focuses on maintaining compliance and reviewing analytical data generated from quality control laboratories within biologics manufacturing operations.

Analytical Data Review

Quality assurance professionals ensure that analytical results generated by QC laboratories meet regulatory and internal quality standards.

Key responsibilities include:

• Reviewing analytical data generated from quality control laboratories
• Evaluating chromatographic results obtained from HPLC analysis
• Reviewing bioassay test results and microbiology testing data
• Verifying analytical documentation accuracy
• Ensuring compliance with regulatory testing protocols

Quality Assurance Compliance

QA professionals ensure that analytical testing activities comply with pharmaceutical regulatory requirements and data integrity standards.

Key responsibilities include:

• Ensuring compliance with Good Manufacturing Practices (GMP)
• Supporting quality management system (QMS) documentation
• Reviewing analytical records for regulatory compliance
• Maintaining laboratory documentation according to SOP guidelines
• Supporting internal audits and quality investigations

Laboratory Data Integrity

Maintaining accurate laboratory data and documentation integrity is critical within regulated pharmaceutical manufacturing environments.

Responsibilities include:

• Verifying laboratory documentation accuracy
• Reviewing analytical reports generated by QC laboratories
• Ensuring traceability of analytical data
• Maintaining compliance with pharmaceutical data integrity guidelines

Collaboration with QC and Manufacturing Teams

Analytical QA professionals work closely with quality control laboratories and manufacturing teams.

Responsibilities include:

• Coordinating with QC teams for analytical data verification
• Supporting microbiology and bioassay data evaluation
• Assisting with regulatory documentation and batch release processes

These activities ensure that biologic drug substances are manufactured according to strict regulatory standards and quality expectations.

Eligibility / Qualifications

USV is seeking candidates with relevant pharmaceutical or biotechnology qualifications along with experience in analytical laboratory data review.

Required Educational Background

B.Pharm, M.Sc Biotechnology, M.Sc Microbiology, M.Sc Biochemistry, M.Sc Life Sciences, M.Pharm Pharmaceutical Analysis, M.Pharm Quality Assurance

Candidates with strong knowledge of analytical laboratory practices and pharmaceutical regulatory documentation will be preferred.

Experience Requirement

2 to 5 years of experience in pharmaceutical or biotechnology quality assurance or quality control environments.

Relevant experience may include:

• Analytical QA data review
• HPLC chromatographic analysis
• Bioassay and microbiology data review
• Pharmaceutical laboratory documentation systems

Preferred Candidate Skills

Ideal candidates should demonstrate:

• Strong understanding of pharmaceutical analytical testing
• Hands‑on exposure to HPLC analysis
• Experience reviewing analytical laboratory data
• Knowledge of GMP and pharmaceutical regulatory guidelines
• Attention to detail and documentation accuracy

Candidates with experience in biologics manufacturing environments may have an additional advantage.

Location & Salary

Job Location

USV Private Limited
Drug Substance Biologics Manufacturing Plant

Nerul
Navi Mumbai
Maharashtra, India

Navi Mumbai is one of India’s major pharmaceutical and biotechnology manufacturing hubs with several global pharmaceutical companies operating research and production facilities.

Salary

Salary packages depend on candidate experience, technical expertise, and previous exposure to pharmaceutical quality systems. Professionals working in biologics manufacturing facilities typically receive competitive compensation due to the specialized nature of biotechnology manufacturing operations.

Application Process

Interested candidates can apply by sharing their updated resume with the recruitment team.

Send your CV to:

ankit02.kumar@usv.in

Candidates should mention the following details while applying:

• Current CTC
• Expected CTC
• Notice period

Applicants are encouraged to highlight their analytical QA experience, HPLC exposure, and laboratory data review expertise in their resume.

Why Build a Career in Biologics Quality Assurance

Biologics manufacturing represents one of the fastest growing segments in the pharmaceutical industry. Biologic drugs are used in advanced therapies such as oncology treatments, immunology drugs, and complex biologically derived medicines.

Quality assurance professionals working in biologics manufacturing gain valuable expertise in analytical quality systems, regulatory compliance, and advanced biotechnology manufacturing processes. These skills are highly valuable within the global pharmaceutical and biotechnology industries.

Career progression opportunities may include:

• Analytical Quality Assurance Specialist
• Quality Compliance Manager
• Biologics Manufacturing QA Lead
• Pharmaceutical Regulatory Affairs Specialist
• Quality Systems Manager

Because biologic drugs require extremely strict regulatory oversight, professionals trained in biologics QA and analytical compliance are in strong demand worldwide.

Frequently Asked Questions (FAQs)

Who can apply for the USV Analytical QA Officer role?

Candidates with BPharm or MSc Biotechnology qualifications and 2–5 years of pharmaceutical QA or QC experience can apply.

What analytical techniques should candidates know?

Candidates should have hands‑on experience with HPLC analysis and analytical data review within pharmaceutical laboratories.

What type of facility is hiring for this role?

The position is based at USV’s biologics drug substance manufacturing facility located in Navi Mumbai.

Is biologics experience mandatory?

Biologics experience is preferred but candidates with pharmaceutical analytical QA experience may also apply.

How can candidates apply for the job?

Applicants can send their updated resume to the official recruitment email mentioned in the job announcement.

Job Summary

Company	USV Private Limited
Vacancies	Officer – Analytical Quality Assurance
Required Education	BPharm, MSc Biotechnology, MSc Microbiology, MSc Biochemistry, MPharm Pharmaceutical Analysis
Experience	2–5 Years