Intas Careers: Gene Therapy Assistant Manager | Apply now
Are you looking for exciting Chemistry Jobs in the pharmaceutical industry? Intas Pharmaceuticals is hiring an Assistant Manager / Manager in Gene Therapy (QA) at their Daskroi, Gujarat facility. Join Intas careers and contribute to innovative cell and gene therapy developments while ensuring the highest standards of quality and compliance. This is a unique opportunity for professionals seeking a rewarding career in pharmaceutical quality assurance, process development, and GMP-compliant operations, all within a global leader committed to excellence and innovation in healthcare.
About Intas
Intas Pharmaceuticals is a global leader in the development, manufacturing, and marketing of high-quality pharmaceutical formulations. With operations in over 85 countries under the brand Accord Healthcare, Intas focuses on addressing unmet medical and societal needs through innovation in areas like Biosimilars, Cell & Gene Therapy, and New Chemical Entities. Committed to the highest quality standards, its products are approved by major regulatory authorities, including the USFDA, MHRA, and EMA. Through Intas careers, the company attracts and nurtures top talent, fostering an empowering environment where employees drive excellence, innovation, and growth in global healthcare.
Details
- Job Title: Assistant Manager / Manager- Gene Therapy (QA)
- Requisitions No.: 15966
- Location: Daskroi, Gujarat
- Qualification Required: MSc, MPharm, MTech
Job Description
This role is ideal for professionals seeking Chemistry Jobs in the pharmaceutical sector. The Assistant Manager supports the implementation and maintenance of GMP-compliant systems in R&D and manufacturing facilities for Cell and Gene Therapy. The position ensures compliance during product development, operational readiness, and regulatory documentation.
Skill Required
- Good understanding of GMP regulations and quality systems.
- Strong documentation and compliance skills.
- Ability to work collaboratively with cross-functional teams.
- Familiarity with aseptic techniques and cleanroom operations.
Roles and Responsibilities
- Providing QA oversight for development and manufacturing activities.
- Provide QA input during equipment qualification, commissioning, and validation.
- Review qualification and validation documentation for compliance.
- Review and support method and process development, technology transfer, and process validation activities.
- Review batch records and ensure adherence to GMP requirements.
- Assist in documentation for process development and comparability studies.
- Assist in deviation management, CAPA tracking, and change control processes.
- Maintain training records and ensure timely completion of GMP training.
- Promote adherence to quality standards across teams.
- Promote Good documentation practices and data integrity principles.
Relevant Skills
- Equipment qualification, Facility commissioning, and validation.
- Process development and comparability studies.
- Deviation management, CAPA tracking, and change control processes.
- Good documentation practices and data integrity principles.
- Awareness of GT and CGT
