Analytical Development Supervisor
Adcock Ingram
Midrand, ZA
7d ago

Required Learning :

Minimum 2 years’ experience in sampling in a pharmaceutical / FMCG environment

Experience of pharmaceutical analysis (NIR) in a highly regulated environment is preferred

Basic cGMP / cGLP

Must possess good knowledge of analysis methods and tools

Ability to work with a high degree of autonomy with strong attention to detail.

Ability to produce accurate work of a superior standard.

Ability to work successfully under time constraints / meeting project deadlines.

Excellent verbal and written communication skills

Strong ability to analyse data

Computer literacy / MS Office

Ability to work overtime when required

Key Outputs :

Sampling incoming raw materials

Evaluates incoming raw materials

Undertake the point of receipt inspection / sampling of incoming raw materials.

Cleaning / housekeeping of the Sampling Areas

Work independently with minimal supervision and complete assigned task in a timely manner and on schedule

Meet production needs by timely and effectively inform the status of the sampling activities to the Supervisor / Manager

Review data for GMP compliance

Identify correct stock for sampling

Verify supplier info against approved vendor and manufacturer lists

Daily decisions of prioritizing of workload with Supervisor

Follow all SOP’s and taking necessary decisions at all times

Be alert at all times and notice deviations immediately.

Ensuring all cGMP, cGLP and SOP’s are followed at all times

Ensuring correct amounts of consumables are used

Taking care not to break or loose sampling tools and / or samples or cause any accidents or incidents or breakdowns

Core Competencies :

Strategic thinking ability

Problem Solving

Thorough understanding and working knowledge of Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP)

Uncompromising on integrity and ethical responsibility

Committed to quality

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