Bioprocess Technician / Cell Culture
: Job Details :

Position Details:Our client, a world-leading Pharmaceutical Company in Andover, MA is currently looking for a Bioprocess Technician to join their expanding team.Job Title: Bioprocess Technician / Cell CultureDuration: 18 months contract, extendable up to 36 monthsLocation: Andover, MANote:The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.You may participate in the company group medical insurance planJob Description:Cell Bank TechnicianSummary:This role is part of Clients Bioprocess Research & Development Cell Banking team responsible for the manufacturing and testing of GMP cell banks used to produce clinical and commercial biopharmaceutical product.Responsibilities:Conduct cell bank manufacturing operations as required. Follow and adhere to cGMP documentation practices, operational procedures, and compliance proceduresPerform cell bank distribution and shipping activities, as requiredAdhere to safety procedures and guidelines by practicing and promoting safe work habitsReview and Archive GMP documents [SOPs, master batch records and campaign summary reports]Maintain cell banking facility and equipment in a constant state of operational and audit readinessCollaborate with partners from diverse cross-functional lines to effectively resolve events and issuesUnderstand scientific principles in order to identify and solve moderately complex problemsMake sound and compliant decisions with minimal input that may require choosing from limited optionsThink critically and facilitate the drive towards continuous improvementEffectively manage own time and balance workload prioritiesMinimum Qualifications:High School Diploma or GED with a minimum of 1-3+ years of experience in a biotechnology manufacturing or laboratory environmentBachelor's degree in biology or related scientific discipline with 1-3 years of relevant experience preferredKnowledge of mammalian cell culture and/or microbial fermentation processesOperational knowledge of computerized systemsAbility to follow Standard Operating Procedures and work under minimal supervisionUnderstanding of scientific principles, ability to think critically and demonstrate troubleshooting and problem-solving skillsStrong interpersonal, teamwork, and collaboration skills with the ability to work in a complex, multi-discipline organization under minimal supervisionExcellent oral and written communication skillsStrong computer skills in Microsoft Office required, especially MS Word, MS Excel.Preferred Qualifications:Prior experience in a Biological Pilot Plant, cGMP Clinical or Commercial Manufacturing settingFamiliarity with business systems (e.g. Document Management Systems, LIMS, SAP, electronic Notebook, etc.)Experience in mammalian and microbial cell culture in a GMP setting with strong aseptic techniqueExperience in cGMP compliance and regulatory compliance requirements as related to manufacture of biologicsWorkplace Requirements:Must be able to gown into cleanroom environment and be standing for ~1-2 hours at a timeMust be able to manipulate screw-cap vials inside a BSC and aseptically fill at least 200 vials in a single settingMust have practical knowledge of the use of Personal Protective Equipment (PPE) to handle hazardous materials throughout siteMust be able to gracefully manage non-ideal situations under stressMust have a change-agile growth mindset for navigating changing needs and priorities.Location/Schedule:This is a fully onsite role in Andover, MAMonday - Friday; first shit (possibility for off shift hours)