, pub-2091334367487754, DIRECT, f08c47fec0942fa0 Quality Control Analyst ( Raw Material) At Viatris

Quality Control Analyst ( Raw Material) At Viatris

 Quality Control Analyst ( Raw Material) At Viatris

Quality Control Analyst ( Raw Material) At Viatris

Every day, we rise to the challenge to make a difference and here’s how the (Quality Control Analyst (Raw Material)) role will make an impact:

Key responsibilities for this role include:

Sampling and performing all physical and chemical tests of raw materials in a timely manner.

Performing the raw material section related documentation.

Preparing and executing the raw material section SOPs and reporting all deviations.

Participate in Method validation for new or old products to be submitted to regulatory.

Keeping the inventories related to the sampling room tools and raw section chemicals.

Review of Production orders.

Performing all required training for different activities.

Stick to CGMP and safety procedures in all activities.

Working on improving process by implementing lean and 6σ projects

Deal with different instruments (HPLC, NIR, UV, etc.)

Participate in out-of-specification and failure investigations.

Supply quality control data necessary for regulatory submissions.

Calibration of raw section laboratory equipment and completion of periodic reviews according to required frequency.

Responsible for ensuring that all results generated follow data integrity requirements.

Participate in out-of-specification and failure investigations through LIRs / QARs.

Routine checking of laboratory documentation and calculations to ensure completeness and accuracy of data.

Update of controlled documents as required.

Responsible Maintain high standards of cleanliness, tidiness and organization of work areas at all times.

Responsibility for implementation of Data integrity program in the relevant work area and ensure following up ALCOA principles all over operations.

The minimum qualifications for this role:

Bachelor’s degree in pharmacy or science.

One to two years Industry/GMP experience is preferred in a related area.

Good command of English language.

Ability to use MS Office applications of MS Word, MS Excel, MS PowerPoint.

Excellent interpersonal, communication and presentation skills.

Demonstrated ability to work independently.

Excellent documentation and technical writing skills.

Ability to work in a team and interact with various priorities.

Active, organized and planner with high attention for details.

Ability to work under stress and meet deadlines.

High observation skills.

Hard worker & self-motivated.

Highly motivated towards achievement and task oriented.

Ability to effectively organize and manage personal work schedule semi-independently.

Hard worker & self-motivated.

Time management skills.

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