Trainee

0 years

0 Lacs

Posted:13 hours ago| Platform: GlassDoor logo

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Work Mode

On-site

Job Type

Part Time

Job Description

Major accountabilities:

  • Maintains applicable Standard Operating Procedures (SOPs), GxP compliant documentation and records within the Sandoz Quality Management System.
  • Ensures the integrity of all Quality Systems records and data, as applicable and collaboration of own team with other functions and departments.
  • Ensures an adequate level of education, GxP knowledge.
  • Updates and maintains relevant information in electronic systems (e.g. Change Control, Documentation, Training).
  • Follow up and monitoring of e.g. CAPAs, actions, metrics, Quality plan).
  • Supports Quality Audits and Health Authority inspection.
  • Reporting of technical complaints / adverse events / special case scenarios related to Sandoz products within 24 hours of receipt -Distribution of marketing samples (where applicable)

Key performance indicators:

  • Customer satisfaction -Punctuality rate -Jobs done on time, following the specified cycle time -Consistent compliance with GMP and Health, Safety and Environment guidelines and Standard Operating Procedures -No complaints with regulatory inspections

Minimum Requirements:
Work Experience:

  • Functional Breadth.
  • QC/ QA in pharmaceutical ind./ biotech with environmental monitoring &.
  • Collaborating across boundaries.
  • cleanliness zones.

Skills:

  • Continuous Learning.
  • Dealing With Ambiguity.
  • Gmp Procedures.
  • QA (Quality Assurance).
  • Quality Control (Qc) Testing.
  • Quality Standards.
  • Self-Awareness.
  • Technological Expertise.
  • Technological Intelligence.

Languages:

  • English.

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Sandoz

Pharmaceuticals

Basel

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