ROLE RESPONSIBILITIES

• Perform all physical and chemical tests for in-process, finished product and related tasks in a timely manner.
• Perform all physical and chemical tests for stability studies of finished products and related tasks in a timely manner.
• Participate in testing of method validation for new or old products to be submitted to regulatory authorities.
• Analysis stability testing samples as per effective stability plan with COA documentation.
• Trained on  Standard Operating Procedures (SOPs) related to department.
• Implementing the PQS requirements regarding the chemical laboratory
• Perform and execute analytical method validation protocols.
• Back-up for Incoming Materials (PM/RM) activities (Sampling and testing of PM only).

Qualifications

BASIC QUALIFICATIONS

• Basic scientific degree.
• 1-2 years’ experience in similar position.
• Ability to read English and interpret documents such as cGMP/ FDA regulations, standard operating procedures, and Pfizer corporate policy manuals.
• Ability to report results clearly and concisely.  Sound reasoning and ability to quickly analyze and solve complex problems.
• Excellent attention to detail and time management skills.
•  Ability to work independently and with other teams.
• PC literate with the following applications:  MS Excel, Word, PowerPoint.

PREFERRED QUALIFICATIONS

• Basic scientific degree.

• 2 years’ experience in similar position

PHYSICAL/MENTAL REQUIREMENTS

• Good command of English both written and spoken.
• Knowledgeable with interpersonal learning.
• Communication and team work.
• Logic way of thinking.
• Management and decision-making skills.
• High analytical skills.
• Professional in reports writing.

PC literate with the following applications:  MS Excel, Word, PowerPoint.

Work Location Assignment: On Premise

Tagged as: Pharmaceuticals