Ontop Pharmaceuticals hiring QC Analyst HPLC
- Ontop Pharmaceuticals hiring QC Analyst HPLC in Bommasandra, Bengaluru. BPharm, MPharm, MSc Chemistry with 1–3 years experience eligible.
- Company Overview
- Job Role & Responsibilities
- Key Responsibilities
- Eligibility / Qualifications
- Required Education
- Experience Requirement
- Required Skills
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- Is hands-on HPLC experience mandatory for this role?
- What dosage forms will I work on?
- Is this role suitable for freshers?
- Will this role involve regulatory audits?
- What software knowledge is preferred?
- Job Summary Table
Ontop Pharmaceuticals hiring QC Analyst HPLC in Bommasandra, Bengaluru. BPharm, MPharm, MSc Chemistry with 1–3 years experience eligible.
Ontop Pharmaceuticals Pvt. Ltd. is hiring a QC Analyst – HPLC for its manufacturing facility located at Bommasandra Industrial Area, Bengaluru. This opportunity is suited for pharmacy and chemistry professionals with hands-on HPLC experience who want to strengthen their careers in pharmaceutical quality control, regulatory compliance, and data integrity–driven laboratory environments. The role offers exposure to oral solid dosage (OSD) and topical formulations within a GMP-regulated setup, making it a strong career move for professionals targeting long-term growth in pharma quality operations.
Company Overview
Ontop Pharmaceuticals Pvt. Ltd. is an Indian pharmaceutical manufacturing organization engaged in the development and production of quality formulations for domestic and regulated markets. The company operates with a strong focus on Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and robust quality systems to ensure product safety, consistency, and regulatory compliance.
With a commitment to analytical excellence and data integrity, Ontop Pharmaceuticals provides a professional environment where quality control professionals can build deep expertise in chromatographic analysis, stability studies, and audit readiness. The organization values accuracy, compliance, and continuous improvement across its quality operations.
Job Role & Responsibilities
As a QC Analyst – HPLC, you will be responsible for executing routine and advanced analytical testing activities in the quality control laboratory. The role demands strong technical knowledge of chromatographic systems, pharmaceutical testing protocols, and regulatory documentation standards.
Key Responsibilities
- Perform analysis of raw materials, intermediates, in-process samples, semi-finished, and finished products as per approved STPs
- Conduct routine QC testing including assay, dissolution, related substances, and stability studies using HPLC
- Execute analytical testing for OSD and topical dosage forms in compliance with GMP and GLP requirements
- Operate and troubleshoot HPLC systems using Empower, LabSolutions, or equivalent software
- Ensure accurate documentation and data integrity compliance as per ALCOA+ principles
- Maintain laboratory instruments, calibration records, logbooks, and analytical documentation
- Support investigations related to OOS, OOT, deviations, and change controls
- Assist during internal, regulatory, and customer audits by providing analytical data and documentation
- Follow internal SOPs, safety guidelines, and quality policies at all times
This role is critical in maintaining product quality, regulatory compliance, and audit readiness across the manufacturing lifecycle.
Eligibility / Qualifications
Required Education
Candidates must possess one of the following qualifications:
B Pharm, M Pharm, MSc Chemistry
Experience Requirement
- 1 to 3 years of relevant experience in pharmaceutical quality control
- Mandatory hands-on experience with HPLC systems
Required Skills
- Strong operational knowledge of HPLC systems (Empower, LabSolutions, or equivalent)
- Experience in testing raw materials, intermediates, semi-finished, and finished goods
- Hands-on exposure to OSD and topical formulation analysis
- Knowledge of stability testing, dissolution, and related substances analysis
- Sound understanding of GDP, GMP, and GLP requirements
- Basic knowledge of OOS, OOT, deviations, and change control processes
- Ability to support regulatory inspections and customer audits
Location & Salary
- Job Location: Bommasandra Industrial Area, Bengaluru, Karnataka
- Department: Quality Control
- Employment Type: Full-time
Application Process
Interested and eligible candidates can apply by sharing their updated CV through the contact details below:
Email ID: amar.hr@ontoppharma.com
Candidates are advised to mention “QC Analyst – HPLC” in the email subject line for faster shortlisting.
Frequently Asked Questions (FAQs)
Is hands-on HPLC experience mandatory for this role?
Yes. Practical experience operating HPLC systems is mandatory.
What dosage forms will I work on?
You will primarily work on oral solid dosage (OSD) and topical formulations.
Is this role suitable for freshers?
No. This role requires 1–3 years of prior QC experience in a pharmaceutical environment.
Will this role involve regulatory audits?
Yes. You will support regulatory and customer audits by providing analytical data and documentation.
What software knowledge is preferred?
Experience with Empower, LabSolutions, or equivalent chromatography data systems is preferred.
Job Summary Table
| Company | Ontop Pharmaceuticals Pvt. Ltd. |
|---|---|
| Vacancies | QC Analyst – HPLC |
| Required Education | B Pharm, M Pharm, MSc Chemistry |
| Experience | 1–3 Years |
To apply for this job email your details to amar.hr@ontoppharma.com
