Bal PharmaHiring Formulations – Quality Control (QC)
- Exciting Opportunity for Experienced QC Professionals at Bal Pharma Ltd – Bengaluru
- Why Join Bal Pharma Ltd?
- Key Responsibilities for QC Assistant Manager Role
- Stability and Compliance Management
- Analytical and Instrumentation Expertise
- Documentation and Quality Oversight
- Educational Qualifications & Experience Required
- Minimum Qualifications
- Work Experience
- Desired Candidate Profile
- Technical Skills
- Communication & Team Skills
- Preferences
- Work Location & Reporting Details
- How to Apply
- Career Growth at Bal Pharma
- Final Thoughts
- Job Summary Table
QC Assistant Manager Jobs for B Pharm/M.Pharm/MSc – 10+ Years Experience in Bengaluru
Apply for QC Assistant Manager at Bal Pharma Ltd, Bengaluru. B Pharm/M.Pharm/MSc graduates with 10–15 years of experience. Openings in Formulations division
Exciting Opportunity for Experienced QC Professionals at Bal Pharma Ltd – Bengaluru
Bal Pharma Ltd is hiring for a QC Assistant Manager role in its Formulation division at Bengaluru. This opportunity is ideal for seasoned professionals from pharmaceutical, chemistry, or quality control backgrounds who possess strong regulatory and analytical expertise. With the company’s expansion across regulated markets, Bal Pharma is looking for a dedicated individual to strengthen its quality systems and drive compliance in alignment with global standards.
Why Join Bal Pharma Ltd?
Bal Pharma Ltd is a well-established name in the Indian pharmaceutical landscape with a strong presence in the formulations and active pharmaceutical ingredients (API) segment. With regulatory approvals from global bodies like US FDA, EU GMP, and WHO, the company emphasizes top-tier quality and compliance.
Joining Bal Pharma means working in a professionally stimulating environment with opportunities to lead core QC activities and interface with international regulatory frameworks. The selected candidate will be responsible for driving quality assurance across multiple verticals and ensuring the company’s commitment to global quality standards.
Key Responsibilities for QC Assistant Manager Role
The position of QC Assistant Manager involves the independent handling of various quality control functions and stability studies at the formulation plant. Here are the major responsibilities:
Stability and Compliance Management
- Independently manage stability study protocols for domestic and international submissions.
- Ensure compliance with regulatory requirements of USFDA, EU, and WHO.
- Oversee stability chambers, data trending, and investigation of any anomalies.
Analytical and Instrumentation Expertise
- Proficient in operating and troubleshooting HPLC, GC, UV, IR instruments.
- Validate and transfer analytical methods as per GLP and ICH guidelines.
- Supervise documentation for instrument calibration, SOP updates, and usage logs.
Documentation and Quality Oversight
- Strong command of QMS processes – including OOS, OOT, deviations, CAPAs, and change controls.
- Ensure proper documentation and audit readiness for internal and external regulatory audits.
- Apply ALCOA principles in documentation and data integrity.
Educational Qualifications & Experience Required
Minimum Qualifications
- Bachelor’s or Master’s degree in Pharmacy (B Pharm/M.Pharm)
- Bachelor’s or Master’s in Science (BSc/MSc) – Chemistry/Analytical Chemistry preferred
Work Experience
- 10–15 years of experience in pharmaceutical quality control, preferably in formulation plants
- Candidates must have hands-on regulatory exposure and familiarity with submission protocols
Desired Candidate Profile
Technical Skills
- Strong command over analytical techniques, data analysis, and instrument troubleshooting
- Thorough understanding of GLP, 21 CFR Part 11, USP/EP/JP guidelines
Communication & Team Skills
- Must be fluent in English (spoken and written)
- Ability to lead a QC team and coordinate with QA, RA, and production departments
Preferences
- Male candidates preferred as per operational shift requirements
- Immediate joiners will be given priority
Work Location & Reporting Details
- Location: Bengaluru, Karnataka
- Division: Formulations Plant
- Position Type: Full-Time, On-site
How to Apply
If you are a qualified pharmaceutical or chemistry professional ready to take the next step in your quality control career, email your resume to:
placement@balpharma.com
Subject: “QC – Asst. Manager”
Career Growth at Bal Pharma
Joining Bal Pharma means more than just a job—it’s a career path that offers:
- Exposure to international regulatory environments
- Leadership opportunities in Quality and Compliance
- Long-term career stability in a growth-driven organization
Final Thoughts
If you’re a meticulous, analytical, and experienced QC professional looking to drive change in pharmaceutical compliance and quality, Bal Pharma Ltd is the right place for you. Leverage your stability study expertise and join a company that values science, safety, and scale.
Job Summary Table
| Company Name | Bal Pharma Ltd |
|---|---|
| Departments | Formulations – Quality Control (QC) |
| Education Required | B Pharm, M.Pharm, BSc, MSc (Chemistry) |
| Experience Required | 10–15 Years |
| Location | Bengaluru, Karnataka |
To apply for this job email your details to placement@balpharma.com