POSITION SUMMARY :
The purpose of the EM Technician I is to perform routine environmental monitoring to assess the viable and nonviable particulate levels within classified manufacturing rooms and support rooms.
ESSENTIAL FUNCTIONS :
The responsibilities of this role include, but are not limited to, the following :
- Conduct viable and nonviable environmental monitoring throughout facility, including aseptic processing areas and classified manufacturing areas (Compounding, Component Preparation, Vial Wash, and Dispensary)
- Collect facility waters and submit for testing and accurately record results of above testing and promptly report any discrepancies or out of limit conditions to supervisor
- Perform Aseptic Gowning Training and certification sampling
- Requisition of materials, maintaining inventory and receive and store prepared media
- Prepare environmental monitoring plates and EM test reports for aseptic processing area
- Perform disinfection of incubator rooms weekly
- Follow safety requirements and maintains good housekeeping of laboratory area
- Incubate and inspect media fill units and incubate and examine samples for microbial growth
- Enumerate bacteria and report excursions
- Temperature charts for incubators and refrigerators in the Microbiology Laboratory
- Ensure processes and products are in compliance with all local, state, and federal rules and regulations. Oversee that processes are in cGMP compliance and establish systems that identifies opportunities for improvement and makes constructive suggestions for change to improve process effectiveness to heighten quality. Develop knowledge of and understand regulatory requirements such as 21CFR Parts 210 and 211, cGMP’s, FDA, OSHA and other regulatory agencies.
- Assume additional duties and responsibilities as assigned
MINIMUM QUALIFICATIONS :
Bachelor’s degree in Chemistry, Microbiology, Biology or other related Science from an accredited universityMay consider an Associate’s degree from an accredited university with minimum 3 (three) years of experience in the pharmaceutical industry (cGMP environment) and aseptic techniqueMay consider a High School Diploma with minimum 5 (five) years of experience in the pharmaceutical industry (cGMP environment) and aseptic techniqueMinimum 1 (one) year’s experience in the pharmaceutical industry (cGMP environment) and aseptic techniqueAbility to get gowning certified within 30 daysPhysical Requirements include - standing and walking up to 8 hours (4 hours at a time for aseptic processing area), lifting or moving up to 35 pounds and reaching with hands and arms up to 6 hours. Must be able to climb or balance, stoop, kneel, crouch, or crawl up to 1 hour.Must be flexible for working across shifts (nights and / or weekends) as neededCOMPETENCIES / CONDUCT :
In addition to the minimum qualifications, the employee will demonstrate :
A ‘See it, Own it, Make it Happen’ attitude.Excellent problem solving and critical thinking skills.Strong attention to detail and ability to follow standard procedures.Team collaboration and professional behaviors to align with Indivior guiding principles and core values.Good interpersonal and communication skillsBENEFITS :
Indivior is committed to providing a culture driven by guiding principles and top-tier benefits that match the importance of the work we do. The Indivior experience includes :
3 weeks’ vacation plus floating holidays and sick leave
401(k) and Profit Sharing Plan- Company match of 75% on your first 6% of contributions and profit sharing contribution equal to 4% of your eligible pay
U.S. Employee Stock Purchase Plan- 15% Discount
Comprehensive Medical, Dental, Vision, Life and Disability coverage
Health, Dependent Care and Limited Purpose Flex Spending and HSA options
Adoption assistance
Tuition reimbursement
Concierge / personal assistance services
Voluntary benefits including Legal, Pet Insurance and Critical Illness coverage
Gym, fitness facility and cell phone discounts