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Executive Quality Control

Acme Generics

Baddi, Himachal Pradesh

Department: Quality Control

Experience: 2-6 Years

Industry: Pharmaceutical

Education: MSc/B Pharma

Job Description

Job Description

Executive Quality Control – Quality Control | Acme Generics | Baddi, Himachal Pradesh, India

Acme Generics is seeking qualified professionals for the role of Executive Quality Control at its pharmaceutical manufacturing facility located in Baddi, Himachal Pradesh, India. This full-time opportunity is ideal for candidates with 2 to 6 years of experience in pharmaceutical analytical testing, laboratory operations, quality control systems, documentation management, and regulatory compliance within GMP manufacturing environments. The selected candidate will conduct analytical testing activities, maintain laboratory records, support quality assurance coordination, ensure compliance with pharmaceutical standards, and participate in quality investigations and operational reviews. Candidates with expertise in analytical instruments, laboratory procedures, pharmaceutical quality systems, and compliance documentation will be preferred. This role offers valuable exposure to pharmaceutical analytical laboratories, quality-driven manufacturing operations, compliance systems, and regulated healthcare production environments focused on testing accuracy, product quality, operational reliability, and continuous quality improvement.

Location
Baddi, Himachal Pradesh, India

Employment Type
Full-time

Experience Required
2 to 6

Compensation & Benefits
Competitive salary package with analytical laboratory exposure, pharmaceutical quality experience, and long-term technical growth opportunities.

About Acme Generics
Acme Generics operates in the pharmaceutical industry specializing in healthcare manufacturing, quality systems, analytical operations, and regulated production environments.

Position Overview
The Executive Quality Control will manage laboratory testing operations, analytical documentation systems, and pharmaceutical compliance activities.

Key Responsibilities

Perform analytical testing of pharmaceutical samples.
Maintain laboratory records and quality documentation.
Support quality control and compliance operations.
Ensure compliance with GMP and laboratory standards.
Coordinate with production and quality assurance teams.
Monitor analytical equipment and laboratory systems.
Participate in investigations and deviation handling activities.
Support audit preparation and regulatory inspections.
Maintain sample management and reporting procedures.
Assist in continuous quality improvement initiatives.


Required Skills & Competencies

Strong understanding of pharmaceutical analytical systems.
Knowledge of laboratory operations and testing procedures.
Documentation and reporting management expertise.
Communication and technical coordination abilities.
Problem-solving and analytical thinking skills.
Awareness of GMP and pharmaceutical compliance standards.
Ability to manage laboratory workflows efficiently.
Attention to analytical accuracy and quality standards.
Operational planning and testing coordination capabilities.
Adaptability to regulated pharmaceutical environments.


Educational Qualification
MSc/B Pharma

About the Project & Industry
The pharmaceutical quality control industry relies on advanced analytical testing systems and laboratory operations to maintain healthcare product quality, compliance, and manufacturing reliability.

Why Join Acme Generics?
Acme Generics offers opportunities to work in modern pharmaceutical analytical environments with exposure to quality systems and regulated manufacturing operations.

How to Apply
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