Looking for pharma jobs in Hyderabad? Novick Biosciences is hiring experienced professionals for an Executive – Analytical Quality Assurance (AQA) role.
This opportunity is ideal for candidates seeking QA jobs, pharmaceutical careers in India, and growth-oriented positions in a regulated pharmaceutical environment.
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About the Company
Novick Biosciences is a growing pharmaceutical organization committed to delivering high-quality healthcare solutions through innovation, scientific excellence, and regulatory compliance.
The company follows stringent GMP, GLP, and data integrity standards to ensure product quality and patient safety.
With a strong focus on research, development, and quality systems, Novick Biosciences provides professionals with opportunities to work in a compliance-driven environment that supports continuous learning and career advancement.
The organization emphasizes operational excellence, regulatory readiness, and global quality standards.
Job Details
- Company Name: Novick Biosciences
- Position: Executive – Analytical Quality Assurance (AQA)
- Experience: 3–4 Years
- Qualification: M. Pharmacy
- Location: Balanagar, Hyderabad
- Work Type: On-site
- Application Period: 04 June 2026 to 13 June 2026
- Preferred Candidates: Male candidates and immediate joiners
Job Description
Novick Biosciences is seeking a qualified Analytical Quality Assurance Executive to support quality and compliance activities within its analytical research environment.
The selected candidate will play a critical role in ensuring regulatory compliance, reviewing analytical documentation, and maintaining data integrity standards.
Executive – Analytical Quality Assurance (AQA)
- Department: Analytical Quality Assurance (AQA)
- Role: Executive
- Experience: 3–4 Years
- Education/Qualification: M. Pharmacy
- Location: Balanagar, Hyderabad
- Industry: Pharmaceutical Manufacturing & Research
Skills/Qualifications
- M. Pharmacy qualification from a recognized institution
- Experience in pharmaceutical formulation environments
- Knowledge of GMP and GLP requirements
- Understanding of data integrity principles
- Expertise in analytical method validation
- Knowledge of assay, dissolution, and related substance testing
- Familiarity with change control systems
- Experience handling OOS, OOT, deviations, and CAPA
- Strong documentation and record management skills
- Ability to support regulatory inspections and audits
- Effective communication and cross-functional coordination
- Good analytical and problem-solving abilities
Key Responsibilities
- Review analytical method development data.
- Verify stability study analytical results.
- Approve analytical reports and documentation.
- Review specifications and standard testing procedures.
- Maintain GMP and GLP compliance.
- Ensure analytical data integrity practices.
- Manage change controls effectively.
- Handle OOS, OOT, deviations, and CAPA.
- Monitor instrument calibration status.
- Ensure qualification of analytical equipment.
- Maintain laboratory records and logbooks.
- Support internal and external audits.
- Coordinate quality compliance activities.
- Ensure proper GDP documentation practices.
- Manage HPLC data backup activities.
Benefits/Perks
- Competitive pharmaceutical industry compensation
- Career growth opportunities
- Exposure to quality assurance systems
- Learning and development opportunities
- Experience with regulatory inspections
- Collaborative work environment
- Opportunity to work with cross-functional teams
- Long-term career advancement potential
- Exposure to global quality standards
How to Apply
Interested candidates can send their updated resumes directly to the official recruitment team at:
Email: recruitment@novickbio.com
Candidates with relevant formulation experience and immediate availability are encouraged to apply as early as possible before the application deadline.
For additional pharmaceutical job opportunities, career resources, and industry updates, visit Pharma Recruiter: https://pharmarecruiter.in
Apply today and take the next step in your pharmaceutical quality assurance career with Novick Biosciences.
Why You Should Join Novick Biosciences
Novick Biosciences offers professionals the opportunity to work in a quality-focused and compliance-driven pharmaceutical environment. Employees gain valuable exposure to analytical quality systems, regulatory requirements, and cross-functional collaboration.
The organization promotes continuous improvement, professional development, and adherence to international quality standards. This makes it an excellent workplace for professionals seeking long-term career growth in pharmaceutical quality assurance.
FAQs
Who is eligible to apply for this position?
Candidates with an M. Pharmacy qualification and 3–4 years of formulation industry experience are eligible to apply.
How can I apply for the AQA Executive role?
You can submit your updated resume via email to recruitment@novickbio.com before the application deadline.
Is this a walk-in interview opportunity?
No walk-in interview details have been announced. Applications are being accepted through email submissions.
What career growth opportunities are available?
The role offers exposure to quality systems, regulatory audits, analytical compliance, and professional development within the pharmaceutical industry.
