Bal PharmaHiring Formulations – Quality Control (QC)

Bal Pharma Limited

Bengaluru

On-site

INR 2,400,000 - 4,000,000

Full time

14 days+

Get more replies from employers

Send a job-specific resume in minutes.

Job summary

Bal Pharma Ltd in Bengaluru is hiring for a QC Assistant Manager in the Formulations Plant. The ideal candidate holds B Pharm/M.Pharm or BSc/MSc with 10–15 years of experience in pharmaceutical quality control, and has hands-on regulatory exposure to US FDA, EU GMP, or WHO guidelines.

The role focuses on stability studies, GLP/ICH compliance, QMS processes, and leading a QC team to ensure data integrity and audit readiness across global standards.

Qualifications

Bachelors or Masters in Pharmacy (B.Pharm/M.Pharm) or BSc/MSc in Chemistry/Analytical Chemistry.
Experience: 10–15 years in pharmaceutical quality control, preferably in Formulations.
Hands-on regulatory exposure and familiarity with submission protocols (USFDA, EU GMP, WHO).

Responsibilities

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 anomalies.
Proficient in operating and troubleshooting HPLC, GC, UV, IR instruments.
Validate and transfer analytical methods per GLP and ICH guidelines.
Supervise documentation for instrument calibration, SOP updates, and usage logs.
Strong command of QMS processes including OOS, OOT, deviations, CAPAs, and change controls.
Ensure audit readiness for internal and external regulatory audits.

Skills

Analytical techniques

Data analysis

Instrument troubleshooting

English fluency

Education

B.Pharm / M.Pharm

BSc / MSc (Chemistry)

Tools

HPLC

Job description

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

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