ScieGen Pharmaceuticals India Recruitment 2026: Analytical Quality Assurance Career Opportunity in Jadcherla
The pharmaceutical industry continues to be one of the fastest-growing sectors in India, creating excellent opportunities for professionals specializing in quality assurance, regulatory compliance, and analytical sciences. Companies are increasingly investing in robust quality systems to meet global regulatory standards, resulting in a growing demand for skilled Analytical Quality Assurance professionals.
If you have experience in pharmaceutical quality systems and are looking for an opportunity to advance your career, ScieGen Pharmaceuticals India Pvt. Ltd. has announced a recruitment opportunity for the position of Executive/Senior Executive – Analytical Quality Assurance at its Jadcherla facility in Telangana.
This opening is ideal for candidates who possess strong knowledge of laboratory quality systems, GMP compliance, pharmaceutical documentation, and regulatory requirements.
About ScieGen Pharmaceuticals India
ScieGen Pharmaceuticals India is recognized for its commitment to quality, innovation, and regulatory compliance in pharmaceutical manufacturing. The company focuses on maintaining high-quality standards while ensuring that products meet domestic and international regulatory expectations.
Working with an organization that emphasizes quality and continuous improvement provides professionals with valuable exposure to modern pharmaceutical operations, advanced quality systems, and global compliance practices.
For experienced quality professionals, this opportunity offers a platform to enhance technical expertise while contributing to the delivery of safe and effective pharmaceutical products.
Job Details
Position
Executive / Senior Executive – Analytical Quality Assurance
Company
ScieGen Pharmaceuticals India Pvt. Ltd.
Location
Jadcherla, Telangana, India
Experience Required
3 to 5 Years
Educational Qualifications
Candidates possessing any of the following qualifications may apply:
- B.Pharm
- M.Pharm
- B.Sc.
- M.Sc. (Chemistry)
- M.Sc. (Analytical Chemistry)
Applicants with relevant pharmaceutical industry experience and exposure to quality assurance functions will be preferred.
Role Overview
Analytical Quality Assurance professionals are responsible for ensuring that laboratory operations comply with internal quality systems and regulatory requirements. They help maintain the integrity of analytical data, review quality documentation, and support investigations related to laboratory events.
The role serves as an important link between Quality Control, Quality Assurance, Manufacturing, and Regulatory Affairs departments. Professionals in this field play a vital role in ensuring product quality and maintaining compliance with current Good Manufacturing Practices (cGMP).
Key Responsibilities
Documentation Review and Verification
One of the primary responsibilities of the role involves reviewing laboratory documents and analytical records to ensure accuracy, completeness, and compliance.
Activities may include:
- Reviewing analytical reports
- Verifying laboratory notebooks
- Checking test records
- Reviewing chromatographic data
- Ensuring documentation follows GMP requirements
Accurate documentation is critical for maintaining product quality and regulatory compliance.
Quality Compliance Monitoring
Candidates may be involved in monitoring compliance activities across analytical laboratories.
Responsibilities may include:
- Reviewing GMP compliance practices
- Ensuring adherence to approved procedures
- Monitoring quality systems implementation
- Supporting laboratory quality initiatives
- Ensuring compliance with regulatory expectations
Maintaining a strong quality culture is a key aspect of pharmaceutical manufacturing operations.
Investigation Management
Analytical Quality Assurance teams frequently handle investigations related to laboratory events and deviations.
These may include:
- Out of Specification (OOS) investigations
- Out of Trend (OOT) investigations
- Laboratory deviations
- Incident management
- Root cause analysis
Candidates should possess strong analytical and problem-solving skills to effectively support investigation activities.
CAPA Review and Monitoring
Corrective and Preventive Actions (CAPA) are essential components of pharmaceutical quality systems.
Responsibilities may include:
- Reviewing CAPA records
- Monitoring CAPA implementation
- Tracking effectiveness checks
- Supporting continuous improvement initiatives
Effective CAPA management helps prevent recurring quality issues.
Review of Technical Documents
The selected candidates may also review various quality and technical documents, including:
- Standard Operating Procedures (SOPs)
- Analytical Specifications
- Stability Protocols
- Stability Reports
- Method Validation Reports
- Method Transfer Documents
- Quality Risk Assessments
These activities ensure consistency and compliance throughout analytical operations.
Audit and Inspection Support
Analytical QA professionals often participate in audits and inspections.
Potential involvement may include:
- Internal quality audits
- Customer audits
- Supplier audits
- Regulatory inspections
Exposure to audit processes can significantly strengthen professional expertise and career growth.
Essential Skills for Success
Employers typically seek candidates who combine technical knowledge with strong professional skills.
Technical Skills
Preferred knowledge areas include:
- Current Good Manufacturing Practices (cGMP)
- Data Integrity principles
- FDA regulations
- ICH guidelines
- USP standards
- Pharmaceutical quality systems
- Laboratory compliance practices
- Analytical documentation review
Candidates with hands-on experience in these areas often stand out during the selection process.
Professional Skills
Important soft skills include:
- Attention to detail
- Analytical thinking
- Problem-solving abilities
- Communication skills
- Teamwork and collaboration
- Time management
- Documentation accuracy
Strong professional skills help ensure smooth coordination with multiple departments.
Why Choose a Career in Analytical Quality Assurance?
Analytical Quality Assurance remains one of the most stable and rewarding career paths within the pharmaceutical industry.
Some benefits include:
Exposure to Global Standards
Professionals gain experience working with internationally recognized regulatory guidelines and compliance requirements.
Strong Career Stability
Quality-related roles remain essential regardless of market conditions because pharmaceutical companies must maintain compliance at all times.
Continuous Learning Opportunities
The field offers ongoing learning through audits, investigations, regulatory updates, and quality improvement initiatives.
Cross-Functional Experience
Professionals interact with multiple departments, enhancing overall pharmaceutical industry knowledge.
Future Career Growth
Analytical QA experience can open doors to advanced leadership and compliance-focused roles.
Career Progression Opportunities
Professionals working in Analytical Quality Assurance can progress into various senior-level positions.
Potential career paths include:
- Senior Executive – Quality Assurance
- Assistant Manager – Quality Assurance
- Deputy Manager – Quality Assurance
- Quality Compliance Specialist
- Regulatory Compliance Manager
- Analytical Quality Assurance Manager
- Global Quality Operations Lead
Candidates who continue upgrading their knowledge through certifications and training programs often experience faster career advancement.
How to Apply
Interested candidates should prepare an updated resume highlighting:
- Relevant pharmaceutical industry experience
- Analytical Quality Assurance exposure
- GMP and regulatory knowledge
- Investigation handling experience
- CAPA management experience
- Documentation review expertise
Apply Now
Email Your Resume To:
Before applying, ensure that your resume clearly demonstrates your quality assurance experience, technical competencies, and achievements in pharmaceutical compliance activities.
Frequently Asked Questions (FAQs)
What qualification is required for this role?
Candidates with B.Pharm, M.Pharm, B.Sc., or M.Sc. (Chemistry/Analytical Chemistry) qualifications may apply.
How much experience is needed?
The company is seeking professionals with approximately 3–5 years of relevant pharmaceutical industry experience.
Where is the job located?
The position is based in Jadcherla, Telangana.
What quality systems knowledge is preferred?
Knowledge of GMP, Data Integrity, OOS, OOT, CAPA, FDA regulations, and ICH guidelines is highly desirable.
Is this position suitable for freshers?
No. The opportunity is intended primarily for candidates with relevant pharmaceutical quality assurance experience.
Final Thoughts
Analytical Quality Assurance professionals play a crucial role in ensuring that pharmaceutical products consistently meet quality and regulatory standards. As pharmaceutical companies continue expanding their operations and regulatory expectations become increasingly stringent, demand for skilled QA professionals remains strong.
The Executive/Senior Executive – Analytical Quality Assurance opportunity at ScieGen Pharmaceuticals India offers experienced professionals a chance to work in a compliance-driven environment while advancing their careers in pharmaceutical quality management.
If you possess the required qualifications and experience, this could be an excellent opportunity to take the next step in your pharmaceutical career journey.
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