Quality Control Technician I (Manufacturing/Quality) 1st Shift

Immediate need for a talented Quality Control Technician I (Manufacturing/Quality) 1st Shift . This is a 12 Months Contract opportunity with long-term potential and is located in Swiftwater, PA (Onsite) . Please review the job description below and contact me ASAP if you are interested.

Job ID:26-29279

Pay Range: $20 - $26/hour. Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).

Key Responsibilities:

• Knowledge of general Microbiological techniques including aseptic processing and culturing of both bacterial and viral isolates.
• Activities include assisting with maintaining safety and compliance of the laboratory work area; Performing cleaning of laboratories, equipment, and ancillary areas as required;
• Attending/Contributing to scheduled team meetings, department, and safety meetings.
• This position requires proficiency and understanding of the theory related to processes, assays, and equipment as well as the ability to identify issues/trends.
• Develop a working knowledge of appropriate compendia and/or regulatory guidance.
• Participation in various and assigned phases of Quality Control testing.
• Duties may include (but are not limited to): Visual Evaluation of vials, syringes, plates, bottles, and canisters.
• Setup and breakdown of equipment.
• Documentation, waste disposal, cleaning of laboratories, and all other activities as assigned.
• The candidate must pass an eye exam and receive vaccinations to be eligible for this position.

Key Requirements and Technology Experience:

• Must have skills: Knowledge of microbiological techniques
• Experience with tissue culture, sterility, or bioburden
• Familiar with cGMP guidelines
• Bachelor's Degree in Microbiology or Biological Sciences with 1-2 years of experience.
• Prior Quality Control experience is desirable.
• Knowledge of microbiological techniques and experience with tissue culture, sterility, or bioburden is preferred.
• Exceptional attention to detail and strong writing skills are crucial.
• The individual must be familiar with cGMP guidelines.
• The candidate must be able to work in a team environment.

Our client is a leading Pharmaceutical Industry, and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.

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