GLP Compliance (Quality Control) Jobs in Baddi, Himachal Pradesh

Location: Baddi Plant, Himachal Pradesh
Experience: 4–5 Years
Industry: Pharmaceutical – Injectable
Employment Type: Full-Time
Department: Quality Control / Quality Assurance
Qualification: Bachelor’s or Master’s Degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biochemistry, Biotechnology, Life Sciences, or related discipline.

GLP Compliance Jobs in Baddi – Job Details

GLP Compliance Jobs in Baddi are available for experienced pharmaceutical professionals with 4–5 years of relevant experience. ACME HR Consultancy is hiring a GLP Compliance (Quality Control) professional for a pharmaceutical injectable facility at Baddi Plant, Himachal Pradesh. The role involves ensuring compliance with Good Laboratory Practice (GLP) requirements, regulatory guidelines, company SOPs, approved protocols, documentation standards, and quality systems.

GLP Compliance Jobs in Baddi – Key Responsibilities

GLP Compliance

• Ensure laboratory activities comply with applicable GLP guidelines, SOPs, protocols, and regulatory requirements.
• Monitor compliance with approved study protocols and specifications.
• Identify GLP compliance gaps and support appropriate corrective and preventive actions.
• Support the implementation and maintenance of the GLP quality management system.

Quality Assurance & Inspections

• Conduct routine, study-based, facility, and process inspections.
• Review study protocols, amendments, raw data, reports, and supporting documentation.
• Verify that deviations, incidents, and non-conformances are properly documented and investigated.
• Track CAPA implementation and effectiveness.
• Support internal, client, and regulatory audits and inspections.

Documentation & Data Integrity

• Review laboratory records for completeness, accuracy, traceability, and compliance.
• Ensure adherence to ALCOA+ data integrity principles.
• Review SOPs, forms, logbooks, controlled documents, and laboratory records.
• Support appropriate handling, retention, and archiving of GLP records.
• Review electronic data, audit trails, and computerized systems where applicable.

Study & Project Support

• Support Study Directors and laboratory personnel in GLP-compliant study execution.
• Verify availability of qualified personnel, equipment, facilities, and procedures.
• Review study-related documentation and identify discrepancies.
• Ensure proper documentation of protocol deviations and unexpected events.

Training, Audit & Reporting

• Conduct or support GLP awareness and compliance training.
• Maintain training records and identify training gaps.
• Prepare documentation for audits and regulatory inspections.
• Support audit responses and remediation plans.
• Prepare GLP compliance and inspection reports.
• Maintain trackers for deviations, CAPA, audits, inspections, and training.
• Escalate significant quality or compliance issues to management.

GLP Compliance and Quality Control Responsibilities

Candidates should have:

• Bachelor’s or Master’s degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biochemistry, Biotechnology, Life Sciences, or a related field.
• 4–5 years of relevant experience in GLP, Quality Assurance, Quality Control, laboratory operations, analytical testing, or regulatory compliance.
• Experience in the pharmaceutical industry, particularly injectable manufacturing, will be relevant to the role.

Required Skills for GLP Compliance Jobs

• Good understanding of OECD GLP principles.
• Knowledge of laboratory quality systems.
• Understanding of SOPs, protocols, deviations, CAPA, change control, and investigations.
• Knowledge of ALCOA+ data integrity principles.
• Strong documentation and report-writing skills.
• Good analytical and problem-solving abilities.
• Strong attention to detail.
• Good communication and interpersonal skills.
• Ability to work independently and coordinate with cross-functional teams.

Key Performance Indicators

Performance will be evaluated based on:

• GLP compliance status.
• Timely completion of QA inspections.
• Timely closure and effectiveness of CAPAs.
• Audit and inspection readiness.
• Reduction in recurring deviations and compliance gaps.
• Training compliance.
• Timely review and closure of documentation.

Preferred Competencies

• Regulatory and compliance mindset.
• Strong documentation practices.
• Risk-based thinking.
• Investigation and root-cause analysis skills.
• Ability to identify and communicate compliance risks.
• Commitment to data integrity and quality culture.

How to Apply

Interested and eligible candidates can send their updated CV to:

📧 acmetalenthunt@gmail.com

Acme HR consulting website. here

Linkedin