Mon. Jun 10th, 2024

About Us

Founded in 1986 by Mr. P. V. Ramprasad Reddy, Mr. K. Nityananda Reddy and a small group of highly committed professionals, Aurobindo Pharma was born of a vision. The company commenced operations in 1988-89 with a single unit manufacturing Semi-Synthetic Penicillin (SSP) at Pondicherry.

Aurobindo Pharma became a public company in 1992 and listed its shares on the Indian stock exchanges in 1995. In addition to being the market leader in Semi-Synthetic Penicillins, it has a presence in key therapeutic segments such as neurosciences, cardiovascular, anti-retrovirals, anti-diabetics, gastroenterology and anti-biotics, among others.

Vacancy Details

  2. Education: B.Pharma / M.Pharma in Any Specialization
  3. Experience: 20 to 25 year(s) of experience
  4. salary:  ₹ 25,00,000 – 35,00,000 P.A.
  5. Location: Jadcherla

Roles and Responsibilities

Responsible for overall manufacturing activities.

  • To ensure that products are produced and stored according to the appropriate documentation.
  • To approve the instructions relating to production operations (SOPs, Batch processing and packaging records) and ensure their strict implementation.
  • To ensure that production records are evaluated and signed by authorized person before they are sent to Quality Assurance department.
  • To evaluate proposed changes in product, process or equipment and ensure that appropriate validations are done.
  • Assist in the investigation of Batch failures, Market complaints and Product recalls.
  • To ensure that the production operations are carried out as per cGMP regulations.
  • To ensure that required initial and continuing training of the department personnel are carried out.
  • To ensure that requisite documentation like monthly stock statements, production reports are made.
  • To coordinate with Engineering Department.
  • To ensure that calibrations and preventive maintenance are done at regular intervals.
  • To coordinate with PPIC regarding production schedule.
  • To coordinate with QA, QC and stores for implementation of planned production schedule.
    overview activities related to raw material, Packaging material and finished goods stores.
  • To Monitor the activities related to Raw material, Packing material and finished goods stores.
  • To participate in vendor qualification process and also in vendor audits, wherever necessary.
  • To ensure that plant hygiene including cleaning and sanitation are performed and maintained.
  • To ensure the implementation of Safety, Health and Environment policy requirements in the plant

Desired Candidate Profile

  • Candidates from pharmaceutical manufacturing ( preferably Oral Solid Dosage(OSD) Tablets, Capsules ) is mandatory
  • Deep knowledge of production management
  • Understanding of quality standards and health & safety regulations
  • Knowledge of performance evaluation and budgeting concepts
  • Experience in reporting on key production metrics
  • Proficient in MS Office and ERP software
  • Outstanding communication ability
  • Excellent organizational and leaderships skills
  • Attention to detail

By Sivamin

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