Executive Quality Control

Executive Quality Control Jobs at Jubilant Generics | Roorkee

BSc/MSc Chemistry QC Executive vacancy at Jubilant Generics, Roorkee. Apply for Quality Control pharma jobs at USFDA-approved facility.

Jubilant Generics Limited is hiring Executive – Quality Control professionals for its advanced pharmaceutical manufacturing facility. This opportunity is ideal for candidates looking to build a long-term career in quality control within a globally regulated pharma environment. The role offers hands-on exposure to regulatory documentation, analytical validation, and compliance activities aligned with USFDA, MHRA, WHO, and other international standards. Candidates with a strong foundation in analytical chemistry, pharmaceutical quality systems, and regulatory documentation will find this position both challenging and rewarding.

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Company Overview

Jubilant Pharma Limited is a globally integrated pharmaceutical company with a strong presence across specialty pharmaceuticals, generics, and active pharmaceutical ingredients. The organization operates through two major business segments: Specialty Pharmaceuticals and Generics & APIs. Its operations span radiopharmaceuticals, contract manufacturing of sterile injectables, non-sterile formulations, allergy therapy products, solid dosage forms, and complex APIs.

Jubilant Generics Limited (JGL), a wholly owned subsidiary of Jubilant Pharma, plays a critical role in the company’s generics and API manufacturing operations. In India, JGL operates advanced R&D centers in Noida and Mysore, supported by two world-class manufacturing facilities located in Mysore, Karnataka and Roorkee, Uttarakhand. These facilities cater to regulated markets including the US, Europe, Japan, Canada, and emerging global markets.

The Roorkee manufacturing facility is a state-of-the-art, fully backward-integrated plant approved by major global regulatory authorities such as USFDA, Japan PMDA, UK MHRA, TGA, WHO, and Brazil ANVISA. The site follows strict GMP, GLP, and data integrity standards, making it an excellent environment for quality professionals seeking exposure to international regulatory compliance.

Jubilant’s API and dosage portfolio focuses on lifestyle-driven therapeutic areas such as cardiovascular and central nervous system disorders. The company holds leadership positions in multiple APIs, supported by strong intellectual property, regulatory filings, and in-house bioequivalence and clinical research capabilities. With consistent revenue growth and a strong R&D backbone, Jubilant Generics continues to strengthen its position as a trusted global pharma partner.

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Job Role & Responsibilities

The Executive – Quality Control role at Jubilant Generics Limited is a documentation-intensive and compliance-focused position supporting regulatory submissions and manufacturing quality systems. The selected candidate will be responsible for reviewing, validating, and ensuring accuracy of analytical, manufacturing, and validation documents as per global regulatory expectations.

Key Responsibilities

Document Validation

• Review analytical and quality documents intended for regulatory submissions
• Ensure compliance with applicable pharmacopoeial and regulatory guidelines
• Verify data integrity, accuracy, and completeness of QC documentation

Raw Material and Packaging Material Review

• Review raw material specifications and standard test procedures in line with pharmacopoeial requirements
• Review packaging material specifications and test procedures
• Ensure alignment with approved quality standards and regulatory filings

Manufacturing Documentation Review

• Review batch manufacturing records and batch packaging records
• Verify documentation intended for regulatory submissions and audits
• Identify discrepancies and ensure corrective actions are implemented

Analytical Method Validation

• Review analytical method validation protocols and reports
• Ensure methods comply with ICH, USFDA, and global regulatory expectations
• Support quality assurance for validated analytical procedures

Analytical Method Transfer

• Review analytical method transfer documentation
• Ensure successful transfer of methods between laboratories or sites
• Verify compliance with internal SOPs and regulatory standards

Process, Cleaning, and Equipment Validation

• Review process validation, cleaning validation, and equipment qualification documents
• Ensure validation activities meet regulatory and internal quality requirements
• Support inspection readiness and audit responses

This role directly contributes to regulatory compliance, product quality, and patient safety, making it a critical function within the quality organization.

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Eligibility / Qualifications

Candidates applying for this Quality Control Executive position should meet the following eligibility criteria:

Educational Qualification

• BSc in Chemistry
• MSc in Chemistry
• BPharmacy
• MPharmacy (Pharmaceutical Analysis, Quality Assurance)

Relevant Courses: BSc Chemistry, MSc Chemistry, BPharmacy, MPharmacy, Pharmaceutical Analysis, Quality Assurance, Analytical Chemistry, Industrial Chemistry

Experience

• Experience in pharmaceutical quality control, analytical validation, or regulatory documentation is preferred
• Exposure to USFDA, MHRA, WHO, or other regulated market audits is an added advantage
• Freshers with strong academic knowledge and internship exposure may also be considered, depending on internal requirements

Key Skills

• Strong understanding of GMP, GLP, and data integrity principles
• Knowledge of pharmacopoeias such as IP, USP, BP, and EP
• Familiarity with analytical techniques and validation protocols
• Excellent documentation review and compliance skills
• Attention to detail and regulatory mindset

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Location & Salary

Job Location: Roorkee, Uttarakhand

The Roorkee facility offers a professionally managed work environment with exposure to global regulatory standards. The location is well connected and known as a growing pharmaceutical manufacturing hub.

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Application Process

Interested and eligible candidates can apply online through the official Jubilant career portal using the link below:

👉 Apply Online: https://jubilantcareer.jubl.com/jobprofile/39655/linkedin

Candidates are advised to apply early, as shortlisting may begin immediately based on profile suitability.

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Frequently Asked Questions (FAQs)

Q1: Who can apply for the Executive – Quality Control role at Jubilant Generics?
Candidates with BSc/MSc Chemistry or Pharmacy qualifications and relevant QC or documentation experience can apply.

Q2: Is this role suitable for freshers?
Freshers with strong academic backgrounds and exposure to pharmaceutical quality systems may be considered.

Q3: What type of regulatory exposure does this role offer?
The role involves documentation and validation aligned with USFDA, MHRA, WHO, PMDA, and other global regulators.

Q4: What is the work location for this job?
The position is based at Jubilant Generics’ Roorkee manufacturing facility in Uttarakhand.

Q5: How do I apply for this pharma quality control job?
Applications must be submitted online through the official Jubilant career link provided above.

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Job Summary Table

Category	Details
Company	Jubilant Generics Limited
Vacancies	Executive – Quality Control
Required Education	BSc Chemistry, MSc Chemistry, BPharmacy, MPharmacy
Experience	Pharma Quality Control / Documentation (Freshers may apply)