biopharm manufacturing associate - level 3 us- second shift.

　　cambridge , massachusetts

　　posted 10 days ago

　　job details

　　summary

　　$48 - $50.04 per hour

　　contract

　　associate degree

　　category life, physical, and social science occupations

　　reference47264

　　job details

　　job summary:

　　We're seeking a motivated individual capable of performing manufacturing processes following current Good Manufacturing Practices (cGMP) and Good Documentation Practices (GDP) within a cleanroom environment. Reporting to the department manager and working on a shift of 12+ individuals, the individual will be expected to demonstrate expertise and breadth of knowledge in operating automated systems, setting up and using single use pharmaceutical systems (mixing, filtration, homogenization), following written procedures (SOPs), performing in process testing (pH, conductivity testing, weighing), and conducting routine sanitization tasks to maintain facility and equipment in a clean controlled state.

　　location: Cambridge, Massachusetts

　　job type: Contract

　　salary: $48.00 - 50.04 per hour

　　work hours: 3 to 11

　　education: Associate

　　responsibilities:

　　Performs hand-on operations (i.e. set-up, cleaning, solution preparation) per approved procedures and under cGMP guidelines

　　With guidance from senior staff, may perform and monitor critical processes

　　May assist in execution of routine validation and engineering protocols

　　May draft and revise routine documents

　　May identify opportunities for improvement and will be able to perform basic troubleshooting activities

　　Elevates issues to senior technicians and/or supervisor for incident reporting

　　May act as a safety representative

　　qualifications:

　　Associate degree in an area of life sciences with a minimum of 1 year of experience in manufacturing production or Bachelors' degree in an area of life sciences with 1 year of experience in manufacturing production preferred.

　　Effective oral and written communication skills required.

　　Experience or understanding of pharmaceutical development preferred.

　　Knowledge of cGMP, GDP, USP, and FDA quality guidelines and regulations preferred.

　　Process organizational skills to ensure production batch completeness preferred.

　　skills: SOP, MS-WORD, MS-EXCEL, MS-Powerpoint, 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 [email protected].

　　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).

　　Applications accepted on ongoing basis until filled.