What are the responsibilities and job description for the Associate Manufacturing Days - West Greenwich, RI position at VetJobs?
Job Description
ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post.
Salary Range
70,985.20USD -96,038.80 USD
Associate Manufacturing - Days
What you will do
Let’s do this. Let’s change the world. In this vital role you will perform operations within the Manufacturing area, specifically purification, at Amgen's 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.
This role is expected to work a 12-hour shift on a rotating schedule. The shift pattern will be 7AM-7PM (A shift), with a two-week rotation covering 7 days per rotation (A Shift). The rotating shift offers several benefits, with an average of 14 days on shift per month with every other weekend off.
Responsibilities
Efficiently perform and monitor critical GMP manufacturing operations in accordance with Standard Operating Procedures (SOPs).
Effectively use and perform basic troubleshooting within the site’s electronic systems (e.g., and Manufacturing Execution System (MES), Delta V, and Enterprise Resource Planning (ERP) system).
Execute routine validation protocols, and regularly draft and revise documents such as Manufacturing Procedures, SOPs, and technical reports.
Contribute to the culture of safety and quality by participating in and leading team safety and quality initiatives.
Understand and contribute to the team’s Lean Manufacturing goals and objectives by identifying improvement opportunities and implementing solutions.
Work with diverse teams.
Escalate issues appropriately.
Ownership of corrective and preventative action and non-conformance records.
Auto req ID
482003BR
Minimum Education Required
High School/GED
Additional Qualifications/Responsibilities
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The dedicated professional we seek is a great teammate with these qualifications.
Basic Qualifications
High school/GED 2 years of manufacturing or operations work experience OR
Associate’s 6 months of manufacturing or operations work experience OR
Bachelor’s Degree in a related field
Preferred Qualifications
Knowledge of large-scale Purification operations, chromatography, TFF, aseptic processing, etc.
Knowledge of large-scale cell culture operations.
CFR and Regulatory knowledge.
Mechanical ability/expertise on fed-batch manufacturing equipment.
Knowledge of WIP lab equipment and computers, with LIMS access.
Demonstrated strong work ethic and positive attitude.
Basic statistical mathematical skills.
Ability to interpret and apply GMP knowledge.
Understanding of analytical methods for manufacturing area.
Ability to demonstrate technical writing capability with Trackwise access.
Able to demonstrate project management skills and presentation skills.
Independently collaborate with outside resources.
Ability to understand, apply and evaluate basic chemistry, biology and physical principles.
Experience with Delta V, RD’s.
Experience with lab equipment/testing.
What you can expect of us
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.
In Addition To The Base Salary, Amgen Offers a Total Rewards Plan, Based On Eligibility, Comprising Of Health And Welfare Plans For Staff And Eligible Dependents, Financial Plans With Opportunities To Save Towards Retirement Or Other Goals, Work/life Balance, And Career Development Opportunities That May Include
A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.
City*
West Greenwich
State*
Rhode Island
Job_Category
Management
Job Code
Pharmaceutical Pharmaceutical
Affiliate Sponsor
Amgen
Salary Range
>$100,000
ATTENTION MILITARY AFFILIATED JOB SEEKERS - Our organization works with partner companies to source qualified talent for their open roles. The following position is available to Veterans, Transitioning Military, National Guard and Reserve Members, Military Spouses, Wounded Warriors, and their Caregivers. If you have the required skill set, education requirements, and experience, please click the submit button and follow the next steps. Unless specifically stated otherwise, this role is "On-Site" at the location detailed in the job post.
Salary Range
70,985.20USD -96,038.80 USD
Associate Manufacturing - Days
What you will do
Let’s do this. Let’s change the world. In this vital role you will perform operations within the Manufacturing area, specifically purification, at Amgen's 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.
This role is expected to work a 12-hour shift on a rotating schedule. The shift pattern will be 7AM-7PM (A shift), with a two-week rotation covering 7 days per rotation (A Shift). The rotating shift offers several benefits, with an average of 14 days on shift per month with every other weekend off.
Responsibilities
Efficiently perform and monitor critical GMP manufacturing operations in accordance with Standard Operating Procedures (SOPs).
Effectively use and perform basic troubleshooting within the site’s electronic systems (e.g., and Manufacturing Execution System (MES), Delta V, and Enterprise Resource Planning (ERP) system).
Execute routine validation protocols, and regularly draft and revise documents such as Manufacturing Procedures, SOPs, and technical reports.
Contribute to the culture of safety and quality by participating in and leading team safety and quality initiatives.
Understand and contribute to the team’s Lean Manufacturing goals and objectives by identifying improvement opportunities and implementing solutions.
Work with diverse teams.
Escalate issues appropriately.
Ownership of corrective and preventative action and non-conformance records.
Auto req ID
482003BR
Minimum Education Required
High School/GED
Additional Qualifications/Responsibilities
What we expect of you
We are all different, yet we all use our unique contributions to serve patients. The dedicated professional we seek is a great teammate with these qualifications.
Basic Qualifications
High school/GED 2 years of manufacturing or operations work experience OR
Associate’s 6 months of manufacturing or operations work experience OR
Bachelor’s Degree in a related field
Preferred Qualifications
Knowledge of large-scale Purification operations, chromatography, TFF, aseptic processing, etc.
Knowledge of large-scale cell culture operations.
CFR and Regulatory knowledge.
Mechanical ability/expertise on fed-batch manufacturing equipment.
Knowledge of WIP lab equipment and computers, with LIMS access.
Demonstrated strong work ethic and positive attitude.
Basic statistical mathematical skills.
Ability to interpret and apply GMP knowledge.
Understanding of analytical methods for manufacturing area.
Ability to demonstrate technical writing capability with Trackwise access.
Able to demonstrate project management skills and presentation skills.
Independently collaborate with outside resources.
Ability to understand, apply and evaluate basic chemistry, biology and physical principles.
Experience with Delta V, RD’s.
Experience with lab equipment/testing.
What you can expect of us
As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.
The expected annual salary range for this role in the U.S. (excluding Puerto Rico) is posted. Actual salary will vary based on several factors including but not limited to, relevant skills, experience, and qualifications.
In Addition To The Base Salary, Amgen Offers a Total Rewards Plan, Based On Eligibility, Comprising Of Health And Welfare Plans For Staff And Eligible Dependents, Financial Plans With Opportunities To Save Towards Retirement Or Other Goals, Work/life Balance, And Career Development Opportunities That May Include
A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.
City*
West Greenwich
State*
Rhode Island
Job_Category
Management
Job Code
Pharmaceutical Pharmaceutical
Affiliate Sponsor
Amgen
Salary Range
>$100,000
Salary : $100,000