Masters degree in any branch of Life Sciences from a recognised university with a first class. The candidate must have qualified for at least one national-level examination after the Masters degree.
MSc. Biochemistry with two years of research experience in the reputed research organizations. Skills of drafting editing of scientific documents and publication in peer reviewed journals.
Responsible for developing, executing, and documenting qualification and validation protocols for equipment, utilities, and facilities in a regulated pharma setup.
Manage granulation, compression, coating, palletization and capsule filling area. Ensure compliance with SOPs, cGMP and regulatory standards. Maintain accurate documentation and support continuous improvement initiatives.
Responsible for ensuring that the study is conducted in accordance with AZ Procedures / Applicable SOPs and Guidelines, such as ICH and GCP as well as relevant local regulations.
Aspiro Pharma Specialities Pvt Ltd located at the worlds largest integrated pharma cluster hub of Hyderabad, requires the following personnel for our Injectable facility, located at Karkapatla
Experience in pharmaceutical regulatory affairs, including leadership roles and expertise in global regulatory requirements and guidelines including FDA, EMA, and ICH regulations.
Lead strategic planning and execution of CMO operations aligned with business goals. Oversee end- to-end supply chain coordination, including demand and material planning, ensuring timely production and delivery.