QA Manager — GLP

Vimta Labs Ltd; Hyderabad; On-site; INR 1,500,000 - 2,100,000; Full time

Job summary

Vimta Labs Ltd in Hyderabad is seeking a QA Manager — GLP to partner with cross-functional teams and deliver measurable impact within the Vimta scientific ecosystem. This role blends hands‑on execution with stakeholder collaboration, contributing to programs that advance pharmaceutical research, clinical insight, and quality assurance for clients across India and global markets.

Reviewed by HR · 365-day retention for unsuccessful applications

Qualifications

• Educational qualification appropriate to the role.
• Hands-on familiarity with industry-standard tools, instruments, or platforms.
• Strong written and verbal communication.
• Ownership mindset, structured problem-solving, and clear documentation.
• Purposeful work contributing to pharma, food, and environment.
• Career growth with cross-domain exposure across Bioanalytical, Clinical, Pharma, F&B, and Environmental services.

Responsibilities

• Own day-to-day delivery of the function, ensuring quality, turnaround, and compliance to internal and regulatory standards.
• Partner closely with adjacent teams (operations, QA, scientific leadership) to plan workloads, elevate blockers, and close out projects on schedule.
• Translate evolving project requirements into clear execution plans, technical documentation, and reporting that stakeholders can act on.
• Mentor and review the work of junior team members, building team capability and continuity over time.

Skills

Strong written and verbal沟通

Education

M.Sc / M.Pharm + QMS certification preferred

Tools

Industry tools familiarity

Job description

• Education M.Sc / M.Pharm + QMS certification preferred

As a QA Manager — GLP, you will partner with cross-functional teams to deliver measurable impact within the Vimta scientific ecosystem. This role blends hands‑on execution with stakeholder collaboration, contributing to programs that advance pharmaceutical research, clinical insight, and quality assurance for clients across India and global markets.

What you’ll own

• Own day-to-day delivery of the function, ensuring quality, turnaround, and compliance to internal and regulatory standards.


• Partner closely with adjacent teams (operations, QA, scientific leadership) to plan workloads, elevate blockers, and close out projects on schedule.


• Translate evolving project requirements into clear execution plans, technical documentation, and reporting that stakeholders can act on.


• Mentor and review the work of junior team members, building team capability and continuity over time.

What we’re looking for

• Educational qualification appropriate to the role (see the Education line in the role-details panel).


• Demonstrated experience in the relevant domain, including hands‑on familiarity with industry‑standard tools, instruments, or platforms.


• Strong written and verbal communication; comfortable engaging with scientific peers, regulators, and clients alike.


• A bias for ownership, structured problem‑solving, and clear documentation — with a quality‑first mindset.


• Purposeful work. Contribute to programs that touch real patient and consumer outcomes across pharma, food, and environment.


• Strong learning curve. Work alongside experienced scientific leaders in one of India's most accredited testing environments.


• Modern infrastructure. Access to NABL / GLP / CAP‑accredited labs and instrumentation that span chromatography, MS, immunoassay, and more.


• Career mobility. Defined growth tracks with cross‑domain exposure across Bioanalytical, Clinical, Pharma, F&B, and Environmental services.

Reviewed by HR · 365-day retention for unsuccessful applications