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Work Schedule
12 hr shift/days
Environmental Conditions
Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
Job Description
Position Title: QA Technician II, Day shift
Schedule: 12-hour Days, 6AM – 6PM on 2-2-3 schedule
Location/Division Specific Information: Greenville, NC
Pharmaceutical Services Group - Quality on the Floor, Sterile Facility
Location: Greenville, NC
How will you make an impact?
You will ensure quality execution of sterile operations with respect to quality inspections for production packaging and inspection for both commercial and product development. Additionally, this position will participate in quality implementation of practical process improvements and continuous improvement initiatives. Primary responsibilities require oversight inspections for acceptable quality limits (AQL) in production packaging and inspection areas. The role necessitates physical fitness for prolonged standing, walking, and repetitive bending, proficiency in non-aseptic gowning, and related knowledge of current good manufacturing processes (cGMP).
What will you do?
Follow all job-related safety and other training requirements. It is the responsibility of each employee to work in a safe and responsible manner in order to build an injury-free and incident-free workplace.
Perform daily AQL inspections in steriles processes, complete and complete supporting documentation. Provide quality mentorship to uncover any errors or deficiencies to assure quality and compliance as required by site procedures and cGMPs.
Take appropriate actions during quality assurance activities (e.g. AQL results) to ensure adequate controls in relation to the level of product quality, safety and business risks.
Communicate and coordinate with production and other quality assurance as required to resolve issues and compliance concerns per procedural requirements.
Participate in troubleshooting quality issues through data review and analysis to resolve next actions or critical issues
Ensures concern of quality issues / events to the appropriate production area and quality management
Participates in practical process improvement initiatives
How will you get here?
Education: High School diploma / equivalent minimally required.
Equivalent combinations of education, training, and meaningful work experience may be considered.
Experience:
Knowledge, Skills, Abilities
Hard-working, confirmed ownership & responsibility; Ability to self-motivate, provide QA mentorship to production colleagues and communicate daily with team members on the quality AQL inspection team
Position requires day shift schedule and some overtime as business requires
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $25 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving analytical challenges, improving patient diagnostics and therapies or growing efficiency in their laboratories, we are here to support them. Our distributed team consists of more than 75,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services and Patheon. For more information, please visit www.thermofisher.com.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.