QC Lead Analyst, Environmental Monitoring (EM)

The Role Perform routine Environmental Monitoring of Grade A-D Cleanroom environment, including sampling of viable surfaces, viable air and non-viable particulates in a GMP Manufacturing facilityPerform and assist with Environmental Monitoring Performance Qualifications (EMPQ) of cleanroomsAbility to isolate and sub-culture microorganisms for identificationProvides input on SOP revisions and assist in the creation and editing of protocols, risk assessment etc. Job Summary Cellipont Bioservices is growing, and we are looking for a QC Lead Analyst, Environmental Monitoring who believes in the potential of bridging client's discoveries to patient cures and who wants to challenge the status quo and take Cellipont and its clients to the next level.

Job Summary Cellipont Bioservices is growing, and we are looking for a QC Lead Analyst, Environmental Monitoring who believes in the potential of bridging client's discoveries to patient cures and who wants to challenge the status quo and take Cellipont and its clients to the next level. The QC Lead Analyst, Environmental Monitoring is responsible for Environmental Monitoring sampling, analyzing, and reporting results, and microbiological testing to support manufacturing. Works in a fast-paced environmental supporting the quality control department of a CMO for manufacturing of biologic bulk drug substance, sterile finished drug product, and fill/finish.The QC Lead Analyst, Environmental Monitoring is also responsible for ensuring all personnel activities are executed timely and cost effectively to insure customer and stakeholder satisfaction. This role will also require the individual to demonstrate a strong ability to work cross-functionally and possess strong leadership skills.The Role Perform routine Environmental Monitoring of Grade A-D Cleanroom environment, including sampling of viable surfaces, viable air and non-viable particulates in a GMP Manufacturing facilityPerform and assist with Environmental Monitoring Performance Qualifications (EMPQ) of cleanroomsAbility to isolate and sub-culture microorganisms for identificationProvides input on SOP revisions and assist in the creation and editing of protocols, risk assessment etc.Builds credibility within the lab group by performing high quality workWorks closely with manufacturing and QA to coordinate routine EM, changeover EM, and monitoring to support client campaignsPerforms Aseptic Process Simulations (media fills) and fill/finish monitoring which includes continuous monitoring of air quality, personnel aseptic technique, and environment integrityAbility to perform Gown Qualifications and BSC QualificationsLead the compilation and trending of Environmental Monitoring data for reporting purposesReport and investigate environmental monitoring excursions and OOS resultsEffectively communicates results of own work through discussions and documentation with some input from supervisorFlexibility in following unique campaign requirements that may include off-hour and weekend workAbility to train fellow analysts on Environmental MonitoringLead and own various Environmental Monitoring and other QC projects on an as needed basis in collaboration with other departmentsPoint of Contact for on-the-floor activitiesAssist in inventory management and cost effectiveness for the departmentOther duties as assignedThe Candidate Associates Degree in a Life Sciences discipline or Bachelors Degree preferred and 4-5 years minimum of relevant experience working in cGMP cleanroomsSelf-starter with the ability to produce results in a fast-paced environment to meet client deadlines under minimal supervisionExperience with viable and non-viable Environment Monitoring collection instruments.Creative individual with outstanding trouble shooting skillsConcentration of aseptic technique and contamination controlStreak plating and microbial identificationDocument writing, data interpretation, presentation, statistical analysis and trending a plusMinimum supervision required on day-to-day activities and accomplished tasksEscalates problems and factors impacting work performance or completion of assigned tasks to the area supervisorExperience working in cGMP Quality ControlExperience with Microsoft OfficeStrong attention to detailFamiliarity with Good Manufacturing Practices (cGMP's)Have the knowledge and ability to apply basic scientific and regulatory principles utilized to solve operational, as well as routine quality tasksAbility to work flex schedules (occasional weekend, overtime hours, 2nd shift or holidays as needed)Position BenefitsOpportunities for career growth within an expanding teamDefined career path and annual performance review & feedback processCross-functional exposure to other areas of within the organization Robust benefit package designed for unique Health & Wellness needs, including coverage for your furry family members401K strong employer match Tuition ReimbursementEmployee Referral BonusesFlexible work schedules and PTO based on role/level, increasing 1 PTO day each year and paid holidaysGain experience in the cutting-edge cell therapy space "At Cellipont Bioservices, we look for candidates with an innate desire to serve. Our "family" approach ensures you will get the mentorship you need to develop a satisfying career here!" Notice to Agency and Search Firm RepresentativesCellipont Bioservices is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Cellipont Bioservices employee by a third-party agency and/or search firm without a valid written & signed search agreement will become the sole property of Cellipont Bioservices. No fee will be paid if a candidate is hired for this position because of an unsolicited agency or search firm referral. Thank you.