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Randstad US biopharm manufacturing associate - level 2 us- first shift in cambridge, Massachusetts

biopharm manufacturing associate - level 2 us- first shift.

  • cambridge , massachusetts

  • posted 2 days ago

job details

summary

  • $46 - $48.33 per hour

  • contract

  • bachelor degree

  • category life, physical, and social science occupations

  • reference48389

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: $46.00 - 48.33 per hour

work hours: 7 to 3

education: Bachelors

responsibilities:

  • Assist with set-up and operates new complex processing equipment

  • Identify and propose solutions to complex problems

  • Act in a leading and/or SME capacity for equipment / process operations and may perform supervisory role in the absence of immediate supervisor

  • May assist with recruiting activities

  • May interact with outside agency inspectors

  • Demonstrates independent project management

  • Drafts, revises, reviews and may own complex documents (i.e. Batch Records, Form Preps)

qualifications:

Basic Qualifications:

  • Bachelor's degree with 2+ years' experience in GMP manufacturing production

  • OR, HS Diploma or GED with 3+ years' experience in GMP manufacturing production

Preferred Qualifications:

  • Facilitation and demonstration skills

  • Basic knowledge of CFRs and regulatory trends

  • Independent collaboration with outside resources

  • More advanced knowledge / proficiency with business software (i.e. Excel, Visio) and industry systems (LIMS, ERP)

Must Have:

  • 2-3 Years' Experience in GMP manufacturing product

  • TFF Experience

skills: SOP, CRF, MS-EXCEL, GMP (Good Manufacturing Practice), LIMS (Laboratory Information Management System

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).

Applications accepted on ongoing basis until filled.

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