Ontop Hiring QC Analyst, Quality Control Executive
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities:
- Eligibility / Qualifications
- Required Education:
- Relevant Courses:
- Experience Required:
- Skills Required:
- Location & Salary
- Application Process
- Application Instructions:
- Why Join Ontop Pharmaceuticals?
- FAQs
- What is the required experience for this role?
- Is HPLC experience mandatory?
- What type of formulations experience is required?
- What regulatory knowledge is expected?
- How can I apply?
- Final Thoughts
QC HPLC Jobs BPharm MSc 5 Vacancies Bangalore
B.Pharm, M.Pharm, MSc candidates apply for QC HPLC roles in Bangalore. Multiple vacancies with 3–5 yrs experience. Apply now.
Ontop Pharmaceuticals Pvt. Ltd. is hiring experienced professionals for Quality Control (QC) Analyst roles with strong expertise in HPLC analysis. This opportunity is ideal for candidates with hands-on experience in pharmaceutical quality control, especially in OSD (Oral Solid Dosage) and topical formulations.
If you are looking to advance your career in analytical testing, GMP compliance, and regulatory-driven pharmaceutical environments, this role offers direct exposure to high-value QC operations.
Company Overview
Ontop Pharmaceuticals Pvt. Ltd. is a growing pharmaceutical company focused on delivering high-quality formulations across regulated and semi-regulated markets. The company emphasizes strong quality systems, data integrity, and compliance with global pharmaceutical standards.
With a focus on analytical excellence and formulation quality, Ontop Pharmaceuticals provides professionals with hands-on exposure to advanced QC techniques, regulatory audits, and real-time pharmaceutical production environments.
Job Role & Responsibilities
The QC Analyst (HPLC) role is critical in ensuring product quality, regulatory compliance, and analytical accuracy in pharmaceutical manufacturing.
Key Responsibilities:
- Perform routine, in-process, and finished product analysis using HPLC
- Conduct stability studies, dissolution testing, and related substances analysis
- Handle raw material (RM) testing and batch release support
- Ensure compliance with GMP, GLP, and data integrity (ALCOA+) principles
- Support investigations related to OOS (Out of Specification) and OOT (Out of Trend)
- Maintain documentation, logbooks, and analytical records
- Assist in regulatory and customer audits
- Perform basic instrument calibration and maintenance
This role directly supports pharmaceutical quality assurance systems and ensures safe, effective medicines reach the market.
Eligibility / Qualifications
Required Education:
- B.Pharm
- M.Pharm
- M.Sc (Chemistry)
Relevant Courses:
Pharmaceutical Analysis, Analytical Chemistry, Quality Control, HPLC Techniques, GMP Compliance, GLP Documentation, Stability Studies, Dissolution Testing, Data Integrity ALCOA+
Experience Required:
- 3 to 5 years in pharmaceutical Quality Control
Skills Required:
- Hands-on experience with HPLC (Empower / LabSolutions)
- Strong knowledge of OSD and topical formulations
- Understanding of regulatory guidelines and audit processes
- Experience in OOS/OOT investigation and deviation handling
- Strong documentation and analytical skills
Location & Salary
- Job Location: Bommasandra Industrial Area, Bengaluru
- Salary: Competitive salary package (based on experience and performance)
- Additional Benefits: Exposure to regulatory audits, analytical systems, and career growth opportunities
Application Process
Interested candidates can apply directly via email.
Email: career@ontoppharma.com
Application Instructions:
- Mention “QC Analyst – HPLC” in the subject line
- Attach updated resume with experience details
- Apply early due to limited openings
Why Join Ontop Pharmaceuticals?
- Strong exposure to pharmaceutical quality control and analytical testing
- Work in GMP-compliant, audit-ready environments
- Hands-on experience with HPLC, stability testing, and regulatory compliance
- Career growth in QC, QA, and regulatory affairs domains
This role plays a key part in maintaining pharmaceutical product quality, ensuring compliance with global regulatory standards, and supporting healthcare delivery.
FAQs
What is the required experience for this role?
Candidates must have 3–5 years of QC experience with HPLC exposure.
Is HPLC experience mandatory?
Yes, hands-on HPLC experience is essential for this position.
What type of formulations experience is required?
Candidates should have experience in OSD or topical formulations.
What regulatory knowledge is expected?
Knowledge of GMP, GLP, ALCOA+, and audit compliance is required.
How can I apply?
Send your updated resume to the provided email with the correct subject line.
Final Thoughts
This Ontop Pharmaceuticals hiring drive is a strong opportunity for experienced QC professionals to advance in pharmaceutical analytical roles. With exposure to HPLC systems, regulatory audits, and GMP environments, candidates can significantly strengthen their technical and compliance expertise.
Apply early to avoid missing out on this opportunity.
| Company | Ontop Pharmaceuticals Pvt. Ltd. |
|---|---|
| Vacancies | QC Analyst, Quality Control Executive (HPLC) |
| Required Education | B.Pharm, M.Pharm, M.Sc Chemistry |
| Experience | 3 to 5 Years |
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