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Meril

Senior Manager / Manager – Development Quality Assurance

Meril

Gujarat, India · Tempo pieno

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Esperienza
10–15 anni
Stipendio
Aperture
1
Pubblicato
16 ore fa
Modalità di lavoro
In ufficio
Istruzione
Master's Degree in Life Sciences or related discipline
Riprendere
È necessario candidarsi

Dove lavorerai

Descrizione del lavoro

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 Risoluzione dei problemi Collaborazione Attenzione ai dettagli Miglioramento continuo ALCOA+ data integrity principles

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