QC Associate I

Duration: 12 Months+

100% onsite RTP Pharma

The QC Associate I is responsible for supporting key functional, tactical, and operational aspects of the QC Microbiology. Responsibilities include, but are not limited to, training, water and environmental sampling, support for testing. A fundamental understanding of the Client Quality Systems and able to apply it in their daily support functions. Adherence to all GMP requirements, effective interactions/ communication with Quality Control management and support of investigations. The Associate I should possess skills to work effectively, attention to detail, work with oversight from team/manager, within a team framework, across all business areas and levels of the organization. This position requires good written and verbal communication skills.

Principal accountabilities:

• Performs sampling & testing support
• Provides timely review/ corrections for data and documentation generated by QC Microbiology. Initiates exceptions/ deviations as required.
• Supports maintenance of effective laboratory systems to ensure integrity of all laboratory results.
• Participates in basic technical problem solving and seeks guidance on resolution.
• And other job duties that may be assigned from time to time.

Minimum Education Requirements:

• AS degree, BS degree, or technical degree (1–2-year college)

Minimum Experience Requirements:

• 0-2 years in comparable/ related role with scientific laboratory experience and some cGMP experience

Scope Accountability: Within Team Area; Routinely works within own work group and responsible for managing self/ activities as assigned under less frequent to intermittent supervision/ guidance. Responsible for managing assignments through to completion by agreed upon timelines. Prioritizing workload according to direction given with understanding of business needs.

Shift: Day