Sr Officer Quality Control – Quality Control | Oxalis Labs | Baddi, Himachal Pradesh, India
Oxalis Labs is inviting applications for the position of Sr Officer Quality Control at its pharmaceutical manufacturing facility in Baddi, Himachal Pradesh, India. This full-time opportunity is ideal for candidates with 1 to 7 years of experience in pharmaceutical quality control, analytical testing, laboratory operations, GMP compliance, documentation management, and regulated pharmaceutical manufacturing environments. The selected candidate will perform analytical testing activities, maintain laboratory records, coordinate with quality assurance and production teams, support compliance operations, and ensure adherence to pharmaceutical quality standards and regulatory guidelines. Candidates having exposure to analytical instruments, laboratory procedures, sample testing, pharmaceutical documentation systems, and quality-focused manufacturing operations will be preferred. This role provides excellent exposure to pharmaceutical analytical laboratories, compliance-driven quality systems, testing technologies, and regulated manufacturing environments focused on operational reliability, product quality, analytical accuracy, and continuous quality improvement.
Location
Baddi, Himachal Pradesh, IndiaEmployment Type
Full-timeExperience Required
1 to 7Compensation & Benefits
Competitive salary package with analytical laboratory exposure, pharmaceutical quality learning opportunities, and long-term career growth.About Oxalis Labs
Oxalis Labs operates in the pharmaceutical industry specializing in healthcare manufacturing, analytical testing, quality systems, and regulated pharmaceutical production operations.Position Overview
The Sr Officer Quality Control will support analytical testing activities, maintain quality documentation systems, and ensure laboratory compliance operations.Key Responsibilities
- Perform pharmaceutical analytical testing and laboratory activities.
- Maintain laboratory records and quality documentation systems.
- Support quality control and compliance operations.
- Ensure compliance with GMP and pharmaceutical standards.
- Coordinate with production and quality assurance teams.
- Monitor analytical instruments and laboratory equipment.
- Participate in investigations and deviation handling processes.
- Maintain sample management and reporting systems.
- Support audits and regulatory inspections.
- Assist in continuous quality improvement initiatives.
Required Skills & Competencies
- Strong understanding of pharmaceutical quality control systems.
- Knowledge of analytical testing and laboratory operations.
- Documentation and reporting management expertise.
- Communication and 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.