Job Description
QC Lead – Quality Control | Maya Biotech | Baddi, Himachal Pradesh, India
Maya Biotech is hiring experienced professionals for the role of QC Lead for its pharmaceutical quality control operations in Baddi, Himachal Pradesh, India. This full-time opportunity is suitable for candidates with 9 to 15 years of experience in pharmaceutical quality control, laboratory management, analytical testing, GMP compliance, quality systems management, laboratory coordination, documentation management, quality audits, analytical workflow supervision, and pharmaceutical compliance operations.
The selected candidate will support quality control and laboratory management activities related to pharmaceutical manufacturing operations. Responsibilities include supervising laboratory testing and analytical quality workflows, monitoring compliance with GMP and pharmaceutical quality standards, maintaining laboratory documentation and operational records, coordinating with production and quality assurance departments, supporting quality audits and compliance verification activities, monitoring analytical instruments and laboratory process systems, participating in operational review meetings and laboratory coordination discussions, assisting in troubleshooting and corrective action implementation, supporting workflow management and quality reporting activities, and contributing to continuous improvement initiatives related to pharmaceutical quality control systems. Candidates should possess strong understanding of pharmaceutical laboratory systems and analytical quality workflows.
This opportunity provides valuable exposure to pharmaceutical laboratory systems, analytical quality operations, GMP workflows, compliance management systems, laboratory supervision activities, and large-scale pharmaceutical manufacturing environments within a reputed pharmaceutical organization. Professionals interested in pharmaceutical quality control and laboratory management can strengthen their technical and operational expertise through this opportunity.
Location
Baddi, Himachal Pradesh, India
Employment Type
Full-time
Experience Required
9 to 15
About Maya Biotech
Maya Biotech operates in the pharmaceutical industry specializing in pharmaceutical manufacturing systems, healthcare product development, laboratory quality operations, and compliance management activities.
Key Responsibilities
Supervise laboratory testing and analytical workflows.
Monitor compliance with GMP and quality standards.
Maintain laboratory documentation and operational records.
Coordinate with production and quality assurance teams.
Support quality audits and compliance verification.
Monitor analytical instruments and process systems.
Participate in quality review and coordination meetings.
Assist in troubleshooting and corrective actions.
Support workflow management and quality reporting.
Contribute to continuous improvement in QC systems.
Required Skills
Strong understanding of pharmaceutical QC systems.
Knowledge of analytical testing and GMP workflows.
Awareness of laboratory compliance and documentation.
Communication and coordination management expertise.
Problem-solving and analytical thinking abilities.
Documentation and laboratory reporting skills.
Time management and workflow planning capabilities.
Attention to operational accuracy and compliance.
Team coordination and multitasking expertise.
Adaptability to pharmaceutical manufacturing environments.
Educational Qualification
M.Sc / B.Pharm
Industry
Pharmaceutical
Why Join Maya Biotech?
Maya Biotech offers professionals opportunities to work in advanced pharmaceutical manufacturing environments with exposure to modern laboratory systems and quality management practices.
How to Apply
Candidates need to register on our portal to apply for this opportunity. Already registered candidates can directly login and apply.
Check our website — www.ackjobs.com — regularly for the latest updates in the job market. Join our WhatsApp and social media groups from the website.
Maya Biotech is hiring experienced professionals for the role of QC Lead for its pharmaceutical quality control operations in Baddi, Himachal Pradesh, India. This full-time opportunity is suitable for candidates with 9 to 15 years of experience in pharmaceutical quality control, laboratory management, analytical testing, GMP compliance, quality systems management, laboratory coordination, documentation management, quality audits, analytical workflow supervision, and pharmaceutical compliance operations.
The selected candidate will support quality control and laboratory management activities related to pharmaceutical manufacturing operations. Responsibilities include supervising laboratory testing and analytical quality workflows, monitoring compliance with GMP and pharmaceutical quality standards, maintaining laboratory documentation and operational records, coordinating with production and quality assurance departments, supporting quality audits and compliance verification activities, monitoring analytical instruments and laboratory process systems, participating in operational review meetings and laboratory coordination discussions, assisting in troubleshooting and corrective action implementation, supporting workflow management and quality reporting activities, and contributing to continuous improvement initiatives related to pharmaceutical quality control systems. Candidates should possess strong understanding of pharmaceutical laboratory systems and analytical quality workflows.
This opportunity provides valuable exposure to pharmaceutical laboratory systems, analytical quality operations, GMP workflows, compliance management systems, laboratory supervision activities, and large-scale pharmaceutical manufacturing environments within a reputed pharmaceutical organization. Professionals interested in pharmaceutical quality control and laboratory management can strengthen their technical and operational expertise through this opportunity.
Location
Baddi, Himachal Pradesh, India
Employment Type
Full-time
Experience Required
9 to 15
About Maya Biotech
Maya Biotech operates in the pharmaceutical industry specializing in pharmaceutical manufacturing systems, healthcare product development, laboratory quality operations, and compliance management activities.
Key Responsibilities
Supervise laboratory testing and analytical workflows.
Monitor compliance with GMP and quality standards.
Maintain laboratory documentation and operational records.
Coordinate with production and quality assurance teams.
Support quality audits and compliance verification.
Monitor analytical instruments and process systems.
Participate in quality review and coordination meetings.
Assist in troubleshooting and corrective actions.
Support workflow management and quality reporting.
Contribute to continuous improvement in QC systems.
Required Skills
Strong understanding of pharmaceutical QC systems.
Knowledge of analytical testing and GMP workflows.
Awareness of laboratory compliance and documentation.
Communication and coordination management expertise.
Problem-solving and analytical thinking abilities.
Documentation and laboratory reporting skills.
Time management and workflow planning capabilities.
Attention to operational accuracy and compliance.
Team coordination and multitasking expertise.
Adaptability to pharmaceutical manufacturing environments.
Educational Qualification
M.Sc / B.Pharm
Industry
Pharmaceutical
Why Join Maya Biotech?
Maya Biotech offers professionals opportunities to work in advanced pharmaceutical manufacturing environments with exposure to modern laboratory systems and quality management practices.
How to Apply
Candidates need to register on our portal to apply for this opportunity. Already registered candidates can directly login and apply.
Check our website — www.ackjobs.com — regularly for the latest updates in the job market. Join our WhatsApp and social media groups from the website.