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.

Pyramid Consulting, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

By applying to our jobs you agree to receive calls, AI-generated calls, text messages, or emails from Pyramid Consulting, Inc. and its affiliates, and contracted partners. Frequency varies for text messages. Message and data rates may apply. Carriers are not liable for delayed or undelivered messages. You can reply STOP to cancel and HELP for help. You can access our privacy policy here.