Quality Control Laboratory Manager

Company Description

Badrivas Biotech Private Limited is dedicated to delivering high-quality healthcare solutions that positively impact lives. We specialize in manufacturing and distributing trusted pharmaceutical products with a strong emphasis on safety, efficacy, and excellence. Our teams in Production, Quality Assurance, and Quality Control uphold the highest standards at every step of the process. At Badrivas Biotech, we aim to empower health, improve lives, and create a lasting impact within communities through our reliable and innovative offerings.

Role Description

This is a full-time on-site role for a Quality Control Laboratory Manager based in Roorkee, Uttarakhand. The Quality Control Laboratory Manager will oversee the day-to-day operations of the laboratory, implement and monitor quality control processes, ensure compliance with regulatory standards, conduct analytical testing, and provide leadership to laboratory staff. Additional responsibilities include maintaining the functionality of laboratory equipment and collaborating with Quality Assurance teams to maintain high operational standards.

Experience : 10–15 years

Location : Roorkee, Uttarakhand

Key Roles & Responsibilities :

Supervise and manage

all QC laboratory activities

— including testing of raw materials, in-process samples, and finished formulations.

Strong expertise in HPLC

operation, troubleshooting, and method validation; experience with systems like

Agilent and Water.

Review and approve analytical data, chromatograms, and test reports ensuring

data integrity

and regulatory compliance.

Manage analytical techniques such as

GC, UV, IR, Dissolution, and Karl Fischer titration .

Ensure compliance with

GMP, GLP, ICH, WHO, and other regulatory requirements .

Lead

OOS / OOT investigations , implement

CAPA , and conduct root cause analyses.

Prepare and maintain

SOPs, STPs, validation protocols, and stability data .

Coordinate with

QA, Production, R&D, and Regulatory Affairs

for timely product release and process improvements.

Handle and face

regulatory and customer audits , ensuring continual audit readiness.

Train, mentor, and evaluate QC staff to maintain technical excellence and productivity.

Oversee calibration, qualification, and preventive maintenance of analytical instruments.

Drive

continuous improvement initiatives

to enhance testing efficiency, accuracy, and compliance.

Required Skills & Competencies :

Hands-on expertise in

HPLC

and analytical method validation.

Sound understanding of

pharma regulatory guidelines (GMP / GLP / ICH) .

Experience in

stability studies, impurity profiling, and release testing .

Proficiency in

analytical documentation and LIMS / CDS software .

Excellent team management, communication, and leadership skills.

Detail-oriented with strong problem-solving and audit-handling capabilities.