Novick Biosciences in Hyderabad urgently hiring experienced professionals for Formulation Analytical Development (FAD) and Development Quality Assurance (DQA) roles. Apply now for high-paying pharma jobs in India 2025.
Novick Biosciences Urgent Hiring | High-Paying FAD & DQA Pharma Jobs in Hyderabad 2025
Novick Biosciences Pvt. Ltd., a rapidly growing Contract Research Organization (CRO) located in Hyderabad, India, is urgently recruiting experienced pharmaceutical professionals for its Formulation Analytical Development (FAD) and Development Quality Assurance (DQA) departments. These are high-paying pharma R&D positions offering excellent career growth for skilled professionals in India’s booming pharmaceutical industry.
About Novick Biosciences
Founded with a vision to provide cutting-edge research services to global pharmaceutical companies, Novick Biosciences has established itself as a trusted CRO partner for drug discovery, formulation development, analytical research, and quality assurance. Novick supports both domestic and multinational pharma clients with advanced GMP-compliant contract manufacturing and analytical services.
Located in Balnagar, Hyderabad, Novick’s facility is equipped with modern laboratories, analytical instrumentation, and regulatory-compliant infrastructure aligned with US FDA, EMA, MHRA, and WHO standards. Novick Biosciences specializes in oral solid dosage (OSD) forms, liquid orals, and complex formulations.
👉 Learn more at: Novick Biosciences Careers
Current Openings – Apply Before 30th June 2025
Position 1: Formulation Analytical Development (FAD) Scientist
Location: Balnagar, Hyderabad
Experience: 7–8 years (Formulation Experience – OSD & Liquid Orals)
Eligibility Criteria
Qualifications:
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M. Pharmacy (Analytical Chemistry) / M.Sc. (Analytical Chemistry)
Key Skills Required:
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Hands-on experience in Analytical Method Development for CRO/in-house formulation projects.
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Expertise in Assay, Uniformity of Dosage Units (UOD), Related Substances, Dissolution Testing, Cleaning Validation, Water Content Analysis, etc.
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Preparation of Analytical Test Methods, Specifications, Method Development Reports.
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Conduct Method Validations, Protocol Preparations, and Report Documentation.
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Strong compliance with Good Documentation Practices (GDP) and Good Laboratory Practices (GLP).
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Familiarity with GMP compliant oral liquid and solid dosage manufacturing processes.
Position 2: Development Quality Assurance (DQA) – Sr. Executive
Location: Balnagar, Hyderabad
Experience: 7–8 years (Formulation Experience)
Eligibility Criteria
Qualifications:
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M. Pharmacy (Pharmaceutics)
Key Responsibilities:
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Preparation of Product Development Reports (PDR).
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Responsible for SOP Preparation, Review, and Approval across Development QA and other departments.
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Management of Change Controls, Deviations, Incidents.
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Review and approval of Master Formula Cards, Drug-Excipient Compatibility Studies, Method Development Reports, Validation Reports, and Method Transfer Documents.
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Actively participate in regulatory inspections (US FDA, WHO, EMA, MHRA) and client audits.
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Approval of specifications, test procedures, stability protocols, development protocols, and scale-up batch protocols.
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Responsible for obtaining Test Licenses and Narcotic-related Licenses for regulated products.
Why Choose Novick Biosciences?
✅ US FDA, WHO & EMA-Compliant CRO:
Work in globally recognized, regulatory-compliant laboratories.
✅ Top Salaries for Experienced Pharma Professionals:
Competitive salary packages aligned with industry benchmarks. Senior-level FAD and DQA professionals in Hyderabad typically earn between ₹9–15 LPA, with growth prospects based on performance.
✅ Exposure to Global Clients & Projects:
Collaborate on formulation development projects for both domestic and international pharmaceutical companies.
✅ Advanced Analytical Techniques:
Work with modern equipment: HPLC, UPLC, GC, FTIR, UV-Vis Spectroscopy, Dissolution Testers, Water Content Analysis (KF), Stability Chambers.
✅ Strong Compliance Culture:
Experience Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), ICH guidelines, and global regulatory standards.
✅ Job Security & Growth:
Novick Biosciences offers long-term career opportunities in one of India’s fastest growing CRO environments.
Why These FAD & DQA Roles Matter
These high-paying formulation analytical development and quality assurance roles are critical to ensuring:
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Safe, stable, and effective formulations.
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Regulatory compliance for global filings.
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Accurate method validation for batch release.
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Successful regulatory audits from US FDA, WHO, MHRA, EMA and client inspections.
With India’s CRO/CDMO sector growing rapidly, skilled scientists with analytical method development and QA experience are in high demand, particularly in Hyderabad, India’s pharma capital.
Growth Opportunities at Novick Biosciences
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Hands-on training in advanced analytical instrumentation.
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Involvement in complex global formulation projects (NDAs, ANDAs, EU filings).
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Cross-functional exposure to R&D, Regulatory Affairs, and Manufacturing teams.
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Leadership grooming for Manager and Sr. Manager roles in CRO/CDMO sector.
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Opportunities to work on high-value, IP-protected formulation projects.
With the global CRO industry projected to reach $90 billion by 2027, CRO professionals in Hyderabad can expect strong salary hikes and global career exposure.
Work Environment at Novick Biosciences
Novick Biosciences provides:
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Modern analytical laboratories.
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Fully air-conditioned, GMP-compliant research environment.
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Collaborative culture emphasizing scientific excellence and compliance.
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Continuous upskilling programs in advanced formulation and regulatory standards.
Employees rate Novick highly for stability, global exposure, learning opportunities, and salary transparency.
How to Apply
📅 Application Period:
19th June 2025 – 30th June 2025
📩 Send Your Resume To: recruitment@novickbio.com
📍 Location:
Novick Biosciences Pvt. Ltd., Balnagar, Hyderabad
🔔 Note: Male candidates are preferred for these specific positions.
📝 Application Checklist:
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Updated Resume
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Educational Certificates
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Experience Letters
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Previous Salary Slips
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Government-issued ID Proof
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Passport-size Photos
Preparation Tips for Walk-In Interviews
✔ Highlight your analytical method development and method validation experience.
✔ Mention previous exposure to regulatory inspections (US FDA, WHO, EMA).
✔ Showcase expertise in GMP-compliant documentation, deviation handling, change control management.
✔ Prepare to discuss recent formulation projects or analytical challenges you handled successfully.
✔ Bring complete documentation for faster evaluation.
Why Hyderabad’s Balnagar is a Pharma Hotspot
Hyderabad’s Balnagar Industrial Zone has emerged as a key hub for:
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Contract Research Organizations (CROs)
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API Manufacturing Units
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Formulation Development Facilities
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GMP-Compliant Pharma Clusters
With excellent connectivity to Genome Valley, Gachibowli, and International Pharma clients, Hyderabad remains the top destination for high-paying pharma careers in India.
Important Disclaimer
Novick Biosciences maintains a transparent, ethical recruitment process. The company:
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Does not charge any recruitment fees.
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Does not use personal email accounts (like Gmail/Yahoo) for recruitment communications.
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Communicates job offers exclusively via recruitment@novickbio.com
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Encourages applicants to report any suspicious recruitment activity directly to HR.
Take the Next Step – Apply Today!
If you’re a highly experienced formulation or analytical scientist looking for stable, well-paying, growth-oriented pharma jobs in Hyderabad, Novick Biosciences offers the perfect platform to elevate your career.
👉 Apply before 30th June 2025 and secure your place in India’s thriving pharma research sector.
