Associate Manufacturing Nights (D shift) - West Greenwich, RI
Associate Manufacturing Nights (D shift) - West Greenwich, RI
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Not Disclosed
Salary Not Disclosed
1 Vacancy
Job Description
What you will do
Lets do this. Lets change the world. In this vital role you will perform operations within the Manufacturing area specifically solutions at Amgens innovative Rhode Island facility. You will be required to know comprehend and apply Good Manufacturing Practices (GMP) as well as understand follow and document in batch records.
Responsibilities Include:
Perform batching and transfer of Buffers and Media in appropriate areas according to Standard Operating Procedures (SOPs).
Follow and monitor critical processes complete routine validation protocols and regularly draft and revise documents such as Manufacturing Procedures SOPs and technical reports.
Conduct basic troubleshooting and assist in the review of documentation for assigned functions.
May also have the responsibility of initiating and owning area Deviations revising SOPs and performing LEAN functions.
Identify recommend and implement improvements related to routine functions.
In this role you will be expected to work a 12-hour shift (7PM-7AM) on a rotating schedule (D- Shift). This includes extra benefits such as receiving an added 15% shift differential and also getting premium pay for any Sundays worked. The schedule during the initial on-boarding/training phase (2-6 weeks) will be administrative (Monday through Friday approximately 8am to 5pm).
What we expect of you
We are all different yet we all use our unique contributions to serve patients. The driven professional we seek is a self-starter with these qualifications.
Additional Qualifications/Responsibilities
What we expect of you
We are all different yet we all use our unique contributions to serve patients. The driven professional we seek is a self-starter with these qualifications.
Basic Qualifications:
High school/GED 2 years of manufacturing or operations work experience OR
Associates 6 months of manufacturing or operations work experience OR
Bachelors Degree in a related field
Preferred Qualifications:
Bachelors degree in Science or Engineering
Knowledge of large-scale biotechnology operations such as purification cell culture aseptic processing etc.
Knowledge of Single-use-Systems
CFR and Regulatory knowledge
Mechanical ability/expertise
Basic statistical mathematical skills
Ability to interpret and apply GMP knowledge
Understanding of analytical methods for manufacturing area
Demonstrated technical writing capability
Able to demonstrate project management skills and presentation skills
Ability to understand apply and evaluate basic chemistry biology and physical principles
Basic troubleshooting skills on production equipment
Experience with Delta V
Experience with lab equipment/testing
Required Experience:
IC
Employment Type
Part-Time
