Bachelors degree or Masters degree in chemistry or Pharmacy with 1-5 years of relevant experience in Quality control department.

Knowledge of the establishment and operation of data monitoring committees, dose review teams, and independent response adjudication committees

Support initiatives to maintain or improve quality performance and compliance of Novartis PV activities including case processing, medical safety, risk management, Health Authority reporting, PV IT systems and device vigilance. Champion the quality mindset.

M. Sc/ Integrated M. Sc in Microbiology/ Biotechnology/ Life Science (specialization in Microbiology)/ Biochemistry/ Food Science and Technology/ Molecular Biology

Macleods is one of the fastest growing pharmaceutical company, having strong presence in various therapeutics segments. Ranked amongst the top 10 companies.

Having Injectable Experience of Shop floor supervising activities like Filtration, Filling, Sealing, Stoppering, Garment Washing, Vial Washing, Autoclave, Ophthalmic, Suspensions, Lyophilizes. Operations and Training and QMS.

Handling & maintaining of fully auto mated Glatt integrated line (Horizontal)/Octagonal Blender/Bin Blender/Sifter/Mill Fette Compression machine/Capsule filling machine with line equipment/Automated Tablet and Capsule visual inspection machine/Auto coater machine Countec Bottle filling line.

Diploma in Pharmacy or its equivalent. Registration with the State Pharmacy Council. Age Not more than 36 years as on 01.01.2025.

L.N. College of Pharmacy, established in 2023 under Saraswathi Educational Trust, Dharmapuri, Tamil Nadu, is dedicated to shaping future pharmaceutical professionals.

Degree with life Science background, trained in Clinical Research e.g. Diploma in Clinical Research ,or MSC Clinical Research and PharmD.

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.

Openings in Analytical Research Laboratories, Formulation & Development

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.

Candidate should have thorough knowledge on regulatory guidance, literature search applicable for sterile formulation development.

Openings in Production / Packing / Warehouse / Engineering / Quality Assurance / Quality Control & QC Micro / EHS