Scientist – Cell & Gene Therapy

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Role Summary:

The Scientist – Cell & Gene Therapy will play a key role in conducting laboratory experiments and ensuring compliance with cGMP standards. The individual will perform routine and non-routine analyses, compile and interpret test data, maintain laboratory equipment, and support quality control and regulatory submissions.

Key Responsibilities:

• Perform experiments and laboratory activities necessary for process development.
• Conduct routine and non-routine analyses of in-process materials, raw materials,      environmental samples, finished goods, and stability samples.
• Interpret test results, compare them to established specifications, and make      recommendations on data release.
• Compile laboratory test data and perform appropriate statistical and technical  analyses.
• Complete documentation to support testing procedures, ensuring accuracy and compliance.
• Calibrate, validate, and maintain laboratory equipment to ensure reliable operations.
• Supply quality control data necessary for regulatory submissions.
• Receive and inspect raw materials, ensuring compliance with specifications.
• Maintain lab cleanliness and safety standards at all times.
• Support cGMP stability and in-process quality control (IPQC) testing activities      for cell and gene therapy products.

Qualifications and Educational Requirements:

• Master’s degree or PhD in Genetics, Biotechnology, or a related field.
• 1 to 2 years of experience working in a cGMP environment.
• Familiarity with cGMP practices and regulatory guidelines.
• Proven ability to write technical reports, protocols, and standard operating      procedures (SOPs) with regulatory understanding.

Desired Qualities:

• Eagerness to learn and adopt new practices.
• Strong organizational skills with attention to detail.
• Problem-solving mindset to address challenges effectively.
• Multitasking capabilities in a fast-paced environment.
• Excellent reporting and documentation skills.
• Exceptional coordination and communication skills.
• Flexibility and adaptability to changing project needs.
• A team player with a collaborative mindset.

Why Join Helix Cell Therapeutics Ltd.?

• Work in a cutting-edge GMP facility contributing to transformative therapies.
• Collaborate with a passionate and innovative team in the biotechnology industry.
• Opportunities for professional growth and development.
• Be part of a mission-driven organization striving to make therapies accessible and affordable to all.

How to Apply:

Interested candidates are encouraged to submit their resume and cover letter to office.helixcell@gmail.com. Please include “Scientist – Cell & Gene Therapy” in the subject line of your email..

Helix Cell Therapeutics Ltd.
Location: Genome Valley, Shameerpet, Hyderabad
Industry: Biotechnology/Pharmaceuticals

Join Us in Transforming Healthcare

Helix Cell Therapeutics Ltd., a leading biotechnology company at the forefront of cell and gene therapy innovation, is seeking an exceptional leader to serve as Chief Scientific Officer (CSO). This is a rare opportunity to shape the scientific vision and strategy of a dynamic organization dedicated to making advanced therapies accessible and affordable for patients worldwide.

About Helix Cell Therapeutics Ltd.:

Our state-of-the-art GMP facility in Genome Valley is designed to develop and manufacture breakthrough cell and gene therapies. With a vision to advance precision medicine for cancer and currently incurable diseases, we are committed to driving innovation and delivering life-changing solutions.

Position Overview:

The CSO will play a pivotal role in defining and driving the scientific and research strategy of Helix Cell Therapeutics. This leadership position requires a visionary scientist with a proven track record in biotechnology, particularly in cell and gene therapy, to guide our research and development programs.

Key Responsibilities:

• Strategic Leadership:
  • Develop and implement the company's scientific and research strategies aligned       with its vision and mission.
  • Oversee all R&D activities to advance the development of cell and gene       therapy products.
  • Identify and evaluate emerging trends and technologies in the biotechnology space       to maintain a competitive edge.
• Innovation and Research Management:
  • Lead cutting-edge research projects in cell therapy, gene therapy, and       precision medicine.
  • Collaborate with cross-functional teams to transition research from concept to       clinical development.
  • Foster innovation by identifying and securing strategic partnerships with       academic, clinical, and industry collaborators.
• Team Leadership:
  • Build, mentor, and inspire a world-class scientific team.
  • Create a culture of scientific excellence and collaboration within the       organization.
• Regulatory and Compliance Oversight:
  • Ensure all scientific programs comply with regulatory requirements and ethical guidelines.
  • Provide scientific leadership in interactions with regulatory agencies and       industry stakeholders.
• Communication and Representation:
  • Represent the company at scientific conferences, industry events, and regulatory meetings.
  • Communicate the company's scientific vision to internal and external stakeholders,       including the board of directors, investors, and collaborators.

    

Qualifications and Experience:

• Education:
  • PhD in Biotechnology, Molecular Biology, Cell Biology, or a related field.       Postdoctoral experience preferred.
• Experience:
  • Minimum 15 years of experience in biotechnology, with a significant focus on cell       and gene therapy.
  • Demonstrated success in leading R&D teams and driving innovative products from       concept to clinical development.
  • Strong understanding of cGMP processes, regulatory requirements, and clinical trials.
• Skills and Attributes:
  • Visionary thinker with exceptional strategic planning abilities.
  • Proven leadership and team-building skills.
  • Outstanding communication and presentation skills.
  • Strong network within the biotechnology and scientific community.
  • Passion for advancing healthcare and making a meaningful impact.

    

Why Join Helix Cell Therapeutics?

• Lead a cutting-edge biotechnology company at the forefront of innovation.
• Collaborate with a team of passionate and talented professionals.
• Work in a state-of-the-art GMP facility designed for groundbreaking research.
• Competitive compensation and benefits package.
• Opportunity to make a transformative impact in healthcare.

How to Apply:

Interested candidates are encouraged to submit their resume, cover letter, and a brief summary of their scientific vision to office.helixcell@gmail.com. Please include “Chief Scientific Officer – [Your Name]” in the subject line.

Helix Cell Therapeutics Ltd.
Location: Genome Valley, Shameerpet, Hyderabad
Industry: Biotechnology/Pharmaceuticals

Drive Operational Excellence in Transformative Biotechnology

Helix Cell Therapeutics Ltd., a leading innovator in cell and gene therapy, is seeking an experienced and visionary Chief Operating Officer (COO) to join our executive leadership team. This role offers the opportunity to shape the operational landscape of a company dedicated to revolutionizing healthcare through cutting-edge therapies.

About Helix Cell Therapeutics Ltd.:

Helix Cell Therapeutics operates a state-of-the-art GMP facility designed to develop and manufacture advanced cell and gene therapies. With a mission to make precision medicine accessible and affordable, we are committed to driving innovation and improving lives.

Position Overview:

As COO, you will oversee and optimize the organization’s operational and business activities, ensuring alignment with the company’s strategic goals. This critical role requires a dynamic leader with exceptional operational, managerial, and strategic planning skills to drive growth and efficiency in a fast-paced biotechnology environment.

Key Responsibilities:

• Operational Leadership:
  • Oversee daily operations across all departments, ensuring efficiency and effectiveness.
  • Develop and implement scalable systems, processes, and best practices to enhance       operational performance.
  • Ensure operational readiness for GMP manufacturing, clinical trials, and       regulatory compliance.
• Strategic Planning and Execution:
  • Collaborate with the CEO and leadership team to develop and execute short- and       long-term strategies.
  • Identify opportunities for business expansion and process optimization.
  • Lead key initiatives to achieve the company’s growth objectives.
• Team Leadership and Development:
  • Build and mentor high-performing teams across functions.
  • Foster a culture of accountability, collaboration, and continuous improvement.
  • Drive organizational change management efforts to support innovation and growth.
• Financial and Resource Management:
  • Work with the finance team to manage budgets, optimize resource allocation, and control operational costs.
  • Oversee vendor relationships and negotiations to maximize value.
• Compliance and Risk Management:
  • Ensure compliance with GMP, regulatory, and safety standards.
  • Develop and maintain risk management protocols to safeguard company assets and  operations.
• Stakeholder Engagement:
  • Collaborate with internal and external stakeholders, including regulators, investors,       and partners.
  • Represent the company at industry events and strategic meetings.

    

Qualifications and Experience:

• Education:
  • Master’s degree in Business Administration, Biotechnology, or related field.       Advanced degrees preferred.
• Experience:
  • Minimum 12–15 years of experience in operations, with at least 5 years in a senior leadership role in the biotechnology or pharmaceutical industry.
  • Proven track record of scaling operations in a high-growth environment.
• Skills and Attributes:
  • Strategic thinker with strong analytical and problem-solving skills.
  • Exceptional leadership and team-building capabilities.
  • Excellent organizational and multitasking abilities.
  • Deep understanding of GMP processes, regulatory compliance, and clinical development.
  • Effective communication and negotiation skills.

    

Why Join Helix Cell Therapeutics?

• Lead operational excellence in a transformative industry.
• Work with a passionate team in a cutting-edge GMP facility.
• Competitive compensation, benefits, and growth opportunities.
• Be part of a mission-driven organization making a global impact.

How to Apply:

Interested candidates are encouraged to submit their resume and cover letter to office.helixcell@gmail.com. Please include “Chief Operating Officer – [Your Name]” in the subject line.