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QC Microbiology Technician

Dormont Manufacturing Company

Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients. We are PCI. Summary Conducts sampling and testing of production environments, and/or facility clean utilities, as per approved procedures. Performs Lab work and other tasks as assigned by management. Essential Duties and Responsibilities Maintains and adheres to safe work habits and all applicable PCI safety procedures and guidelines. Is proactive in identifying safety risks and alerts management to take corrective action. Completes routine environmental monitoring of clean rooms, as per approved procedures over multiple local production sites. Completes environmental monitoring of clean rooms during manufacturing, as per approved procedures over multiple local production sites. Utility sampling, as per approved procedures over multiple local production sites. Completed daily and weekly assigned tasks in the Microbiology Laboratory Adheres to verbal instructions and written procedures in operating production equipment and performing processing steps; accurately completes appropriate production documentation Complete data verifications checks and/or inputs Other duties as assigned Special Demands This position requires frequent movement between different buildings for various tasks and responsibilities. A key aspect of this role is the need for aseptic gowning and meticulous compliance with gowning procedures during clean room operations PHYSICAL REQUIREMENTS Ability to wear personal protective equipment such as safety glasses/goggles, gloves and safety shoes. Ability to gown and gain entry to controlled manufacturing areas Ability to lift, pull or push equipment requiring up to 15-20 lbs of force Ability to stand for 6 hours in a production suite Ability to work any shift (up to 10 hours) as required dependent on business needs Work Environment Ability to work in a face paced environment Must be able to travel between multiple local production Resilient through operational change Able to work in a highly complex environment with competing demands and priorities Ability to work varied hours as required by the production schedule Qualifications High school Diploma, GED, or equivalent credential required; AS degree or BS degree in Microbiology or related scientific field preferred. 0-2 years’ experience in a cGMP environment; equivalent combination of education and experience will be considered. Exceptional organizational skills Following written instructions Detail oriented Ability to multi-task Word Processing, XL spreadsheets Competent in MS Office Professional verbal and written communication skills required High school diploma or its equivalent Equal Employment Opportunity (EEO) Statement PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status. At PCI, Equity and Inclusion are at the core of our company’s purpose: Together, delivering life-changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity – at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture. #J-18808-Ljbffr

Vacancy posted 2 days ago
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