- This role is part of the Bioprocess Research & Development Cell Banking team responsible for the manufacturing and testing of GMP cell banks used to produce clinical and commercial biopharmaceutical product
location: Chesterfield, Missouri
job type: Contract
salary: $23.26 - 27.00 per hour
work hours: 9 to 5
education: High School
responsibilities:
- Conduct cell bank manufacturing operations as required. Follow and adhere to cGMP documentation practices, operational procedures, and compliance procedures.
- Perform cell bank distribution and shipping activities, as required.
- Adhere to safety procedures and guidelines by practicing and promoting safe work habits.
- Review 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 readiness.
- Collaborate with partners from diverse cross-functional lines to effectively resolve events and issues.
- Understand scientific principles in order to identify and solve moderately complex problems.
- Make sound and compliant decisions with minimal input that may require choosing from limited options.
- Think critically and facilitate the drive towards continuous improvement.
- Effectively manage own time and balance workload priorities.
- Cell Bank testing team
- QA
- PharmSci Cell Bank team
- Shipping and logistics teams
- Calibration and validation colleagues
qualifications:
Education
Required:
- High School Diploma or GED with 1-3 years of experience in a biotechnology manufacturing or laboratory environment.
- Bachelor's degree in biology or related scientific discipline with 1-3 years of relevant experience
Required:
- Knowledge of mammalian cell culture and/or microbial fermentation processes.
- Operational knowledge of computerized systems.
- Ability to follow Standard Operating Procedures and work under minimal supervision.
- Understanding of scientific principles, ability to think critically and demonstrate troubleshooting and problem-solving skills.
- Strong interpersonal, teamwork, and collaboration skills with the ability to work in a complex, multi-discipline organization under minimal supervision.
- Excellent oral and written communication skills.
- Strong computer skills in Microsoft Office required, especially MS Word, MS Excel.
- Prior experience in a Biological Pilot Plant, cGMP Clinical or Commercial Manufacturing setting.
- Familiarity 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 technique.
- Experience in cGMP compliance and regulatory compliance requirements as related to manufacture of biologics
skills: Biology, Laboratory Information Management Systems (LIMS), Cell Cultures, GMP (Good Manufacturing Practice)
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).
This posting is open for thirty (30) days.