The Advanced Centre for Treatment, Research and Education in Cancer (ACTREC) is a premier cancer research institute under the Tata Memorial Centre (TMC), an autonomous grant-in-aid institution of the Department of Atomic Energy (DAE), Government of India. Established initially as the Indian Cancer Research Centre (ICRC) in 1952, it was later renamed the Cancer Research Institute (CRI) and merged with Tata Memorial Hospital (TMH) to form India’s first comprehensive cancer center.
ACTREC is dedicated to cutting-edge research, education, and advanced treatment in oncology, making it a sought-after institution for professionals in life sciences, pharmaceuticals, and cancer research.
Job Openings at ACTREC – Scientific Assistant (On Project)
ACTREC is hiring Scientific Assistants for two key roles in Cell Therapy Project Management and Regulatory Affairs. These positions offer an excellent opportunity for life sciences postgraduates to work in a high-impact research environment.
1. Scientific Assistant – Project Coordinator (GMP Facility Operations – Cell Therapy)
Post: 02 Vacancies
Job Description:
- Monitor budgets, resource allocation, and procurement for GMP equipment and consumables.
- Lead project meetings, track action items, and report progress.
- Liaise with external stakeholders (vendors, regulatory bodies) and track grant utilization.
- Draft and review MoUs, grant documents, and agreements.
- Coordinate with GMP manufacturing teams for production planning and batch scheduling.
- Manage QC testing, product release, and regulatory documentation timelines.
- Maintain a centralized documentation repository.
- Prepare monthly/quarterly grant progress reports and review dossiers.
Eligibility Criteria:
- Post-graduation (preferably in Life Sciences).
- Minimum 2 years of experience in project management, regulatory compliance, or GMP operations.
- Strong computer and documentation skills.
Salary: ₹27,000 – ₹40,000 per month (consolidated)
Duration: 6 months (extendable)
2. Scientific Assistant – Project Coordinator (Regulatory Affairs – Cell Therapy Product Development)
Post: 01 Vacancy
Job Description:
- Prepare, review, and submit CMC sections of regulatory filings (IND, CTA, BLA).
- Ensure compliance with national and international regulatory guidelines.
- Collaborate with process development, QA, and manufacturing teams for documentation.
- Manage regulatory submissions and lifecycle updates.
- Respond to regulatory queries and deficiencies during review cycles.
- Support facility compliance audits and inspections.
Eligibility Criteria:
- Post-graduation (preferably in Life Sciences).
- Minimum 2 years of experience in regulatory affairs, CMC documentation, or compliance.
- Strong technical writing and communication skills.
Salary: ₹27,000 – ₹40,000 per month (consolidated)
Duration: 6 months (extendable)
How to Apply?
- Walk-in Interview Date: 19th June 2025
- Reporting Time: As per official notification
- Venue: PS-306, Meeting Room, 3rd Floor, Paymaster Shodhika, ACTREC, Kharghar, Navi Mumbai – 410210
Documents Required:
- Updated CV with a passport-size photograph.
- Original and Xerox copies of:
- Educational certificates
- Work experience documents
- Aadhaar Card (as ID proof)
Note: Result-awaited candidates are not eligible. Selected candidates must join immediately.