biopharm manufacturing associate - level 2 us- first shift.
cambridge , massachusetts
posted today
job detailssummary
$46 - $48.33 per hour
contract
bachelor degree
category life, physical, and social science occupations
reference48389
job detailsjob 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, Massachusettsjob type: Contractsalary: $46.00 - 48.33 per hourwork hours: 7 to 3education: Bachelorsresponsibilities:
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 SystemEqual 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] 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.