About the Job

We are seeking a pharma QC, QA, R&D, AR&D Fresher to join our team on a Full-time basis with OnSite work arrangements. In this role, you will support quality and research activities that help ensure products meet required standards and regulatory expectations. You’ll work closely with experienced professionals across QC/QA and R&D functions, gaining hands-on exposure to documentation, laboratory workflows, sample handling, and basic analytical support. This position is designed for freshers who are eager to learn, follow SOPs meticulously, and contribute to a culture of quality and continuous improvement.

Roles & Responsibilities

• Support Quality Control (QC) activities by assisting with sample receipt, labeling, and preparation.
• Contribute to Quality Assurance (QA) tasks such as compiling and maintaining departmental documentation and batch-related records.
• Assist with routine R&D / AR&D activities under supervision, including preparing materials, monitoring trial progress, and recording observations.
• Follow SOPs, safety procedures, and lab compliance requirements during all activities.
• Perform basic checks for data integrity and assist in reviewing entries for completeness and accuracy.
• Coordinate with internal teams to ensure timely completion of assigned lab and documentation tasks.
• Participate in training sessions and shift handovers to stay aligned with quality and operational standards.

Required Skills & Qualifications

• Strong foundation in pharmaceutical quality concepts and willingness to learn QC/QA/R&D processes.
• Core practical knowledge/interest aligned with Digital Subscriber Line (e.g., basic familiarity with connectivity concepts used for training systems and data access, if applicable).
• Good attention to detail and ability to follow instructions precisely.
• Basic understanding of laboratory documentation practices (good record-keeping mindset).
• Clear communication skills and comfort working on-site in a structured environment.
• Relevant academic background in Pharma, Biotech, Chemistry, or a related field.
• Eagerness to learn compliance, GMP-oriented thinking, and quality-driven workflows.