Meril

Senior Manager / Manager – Development Quality Assurance

Meril

Gujarat, India · Full Time

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Experience
10–15 yrs
Salary
Openings
1
Posted
58 minutes ago
Work mode
In office
Education
Master's Degree in Life Sciences or related discipline
Resume
Required to apply

Where you'll work

Job description

About the Role

We are looking for a Senior Manager or Manager in Development Quality Assurance (DQA) to join our team in Vapi, Gujarat. The position requires a professional with 10 to 15 years of experience who will lead the establishment, maintenance, and enhancement of the Quality Assurance system tailored for Research & Development activities. The ideal candidate should possess deep expertise in Biologics or Cell & Gene Therapy (CGT), with a strong background in quality systems, regulatory adherence, data integrity, and comprehensive quality oversight throughout the product development stages.

Key Responsibilities

  • Create, revise, and periodically update SOPs, templates, and other quality-controlled documents that support R&D functions.
  • Design, apply, and improve Development Quality Assurance systems continuously.
  • Implement quality procedures for process, analytical, and formulation development, along with technology transfer, process characterization, and stability study support.
  • Evaluate various R&D documentation such as SOPs, Work Instructions, Equipment Operating Procedures, specifications, protocols, reports, technical docs, and records related to method qualification, transfer, and technology transfer.
  • Provide independent quality reviews ensuring adherence to approved procedures, Good Documentation Practices (GDP), ALCOA+ data integrity principles, internal standards, and relevant regulations.
  • Oversee quality compliance across product development activities including validation, scale-up, engineering batches, and stability programs.
  • Examine laboratory notebooks, electronic lab records, raw data, chromatograms, calculations, and related documentation to verify accuracy, completeness, traceability, and regulatory compliance.
  • Manage Quality Management System (QMS) functions such as change controls, deviations, investigations, CAPAs, risk analyses, document updates, and validate their effectiveness.
  • Lead investigations involving deviations, Out-of-Specification (OOS), Out-of-Trend (OOT) results, documentation errors, and process-related challenges and ensure appropriate corrective and preventive measures are implemented.
  • Evaluate the quality and regulatory impact of proposed changes using established change management procedures.
  • Organize and conduct internal audits of R&D laboratories and development operations to ensure compliance.
  • Compile audit reports, communicate findings, monitor corrective actions, and ensure timely closure of audit points.
  • Work collaboratively with cross-functional R&D teams to support quality system deployment during product development.
  • Support technology transfer processes by reviewing relevant documentation, risk assessments, and transfer packages.
  • Foster a quality-driven culture by guiding proper documentation practices, enhancing data integrity, managing quality risks, and complying with regulatory standards.

Required Qualifications

  • Master's Degree in Life Sciences or a related field.
  • Minimum of 10 to 15 years’ experience in Development Quality Assurance within pharmaceutical or biotechnology sectors.
  • Essential experience in Biologics or Cell & Gene Therapy (CGT).
  • Comprehensive knowledge of Quality Management Systems (QMS), Good Documentation Practices (GDP), ALCOA+ data integrity principles, and global regulatory standards.
  • Demonstrated expertise in quality oversight of product/process development, analytical methods, technology transfers, and stability assessments.
  • Proven experience handling investigations, CAPA processes, change control, internal audits, and risk evaluations.
  • Strong communication abilities, skilled in documentation, problem resolution, and stakeholder engagement.

Preferred Skills

  • In-depth insight into regulatory expectations for biologics and Cell & Gene Therapy development.
  • Experience collaborating within cross-disciplinary R&D teams.
  • Excellent leadership qualities, with strong teamwork and decision-making skills.
  • Dedication to continuous quality improvement and excellence.

Work styles they’re looking for

Leadership Problem Solving Collaboration Attention to Detail Continuous Improvement ALCOA+ data integrity principles

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