Sr Associate Mfg - Nights

Amgen; West Greenwich (RI); On-site; USD 86,000 - 116,000; Full time

Benefits offered by this job

Stock-based long-term incentives

Award-winning time-off plans

Retirement and Savings Plan

Total rewards program

Job summary

Amgen is seeking a Senior Associate Manufacturing - Nights to lead on the production floor in the Inoc/Seeds area. The role requires following SOPs, performing critical processes, and drafting technical documents.

You may own NC/CAPA and drive improvements across quality, equipment, and process functions. The position features a 12-hour rotating night shift (7PM–7AM) with a 15% shift differential and premium pay for Sundays, plus an onboarding period of Monday–Friday hours.

Qualifications

• High school diploma / GED and 4 years of Manufacturing or Operations experience OR
• Associate’s degree and 2 years of Manufacturing or Operations experience OR
• Bachelor’s degree and 6 months of Manufacturing or Operations experience OR
• Master’s degree

Responsibilities

• Lead manufacturing operations on the production floor.
• Ensure all safety and compliance procedures are followed at all times.
• Participate in the development, implementation, and issue resolution associated with process equipment Commissioning, Qualification, and Validation.
• Provide troubleshooting, technical support, and resolution of equipment, automation, and process issues on the manufacturing floor.
• Write, revise, and own controlled documentation (SOPs, Manufacturing Procedures (MPs), Forms, Technical Reports, etc.)
• Serve as SME for functional area operations.
• Provide training to manufacturing staff on process and equipment.
• Own deviations and Corrective and Preventive Actions (CAPA)
• Champion Lean Transformation and OE initiatives; facilitate the drive towards continuous improvement in all Manufacturing areas.
• Collaborate with Quality, Engineering, Process Development, Validation, and Operations to resolve manufacturing events in a timely manner.
• Assure appropriate escalation to different levels of management when personnel and environmental safety, equipment functionality, product supply, or quality are at risk.
• Collaborate with Quality, Manufacturing Managers, Plant Engineering, Process Development, and Regulatory Compliance staff in multi-functional teams.
• Participate in the design, development, and implementation of processes in support of the manufacturing floor.

Skills

Troubleshooting

Technical writing

Project management

Collaboration

GMP knowledge

Education

High school diploma / GED with 4 years experience

Associate’s degree with 2 years experience

Bachelor’s degree with 6 months experience

Master’s degree

Tools

LIMS access

DeltaV

Job description

Career Category

Operations

Job Description

Join Amgen’s Mission of Serving Patients

At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.

Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

Senior Associate Manufacturing - Nights

What you will do

Let’s do this. Let’s change the world. In this vital role you will perform operations in the Manufacturing area, specifically Inoc/Seeds. Operations will be performed according to Standard Operating Procedures (SOPs). Senior Associate will perform and monitor critical processes, execute routine validation protocols, and regularly draft and revise documents such as Manufacturing Procedures, SOPs, and technical reports. Senior Associate will also perform basic troubleshooting and assist in the review of documentation for assigned functions. May participate on cross-functional teams and represent the Inoc/Seeds group. Senior Associate may also have the responsibility of owning NC/CAPA’s and Change Control records. In addition, Senior Associate may identify, recommend, and implement improvements related to routine function.

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 phase for this role (2-6 weeks) will be administrative (Monday through Friday, approximately 8am to 5pm).

Job Responsibilities:

• Lead manufacturing operations on the production floor.
• Ensure all safety and compliance procedures are followed at all times.
• Participate in the development, implementation, and issue resolution associated with process equipment Commissioning, Qualification, and Validation.
• Provide troubleshooting, technical support, and resolution of equipment, automation, and process issues on the manufacturing floor.
• Write, revise, and own controlled documentation (SOPs, Manufacturing Procedures (MPs), Forms, Technical Reports, etc.)
• Serve as SME for functional area operations.
• Provide training to manufacturing staff on process and equipment.
• Own deviations and Corrective and Preventive Actions (CAPA)
• Champion Lean Transformation and OE initiatives; facilitate the drive towards continuous improvement in all Manufacturing areas.
• Collaborate with Quality, Engineering, Process Development, Validation, and Operations to resolve manufacturing events in a timely manner.
• Assure appropriate escalation to different levels of management when personnel and environmental safety, equipment functionality, product supply, or quality are at risk.
• Collaborate with Quality, Manufacturing Managers, Plant Engineering, Process Development, and Regulatory Compliance staff in multi-functional teams.
• Participate in the design, development, and implementation of processes in support of the manufacturing floor.

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 self-starter with these qualifications.

Basic Qualifications :

• High school diploma / GED and 4 years of Manufacturing or Operations experience OR
• Associate’s degree and 2 years of Manufacturing or Operations experience OR
• Bachelor’s degree and 6 months of Manufacturing or Operations experience OR
• Master’s degree

Preferred Qualifications :

• Knowledge of small-scale bioreactors, wave bioreactors, and aseptic processing.
• CFR and Regulatory knowledge
• Mechanical ability/expertise
• Knowledge of WIP lab equipment and computers, with LIMS access
• Basic statistical mathematical skills
• Ability to interpret and apply GMP knowledge
• Understanding of analytical methods for the 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
• Basic troubleshooting skills on bioreactors
• 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.

Application deadline

Amgen does not have an application deadline for this position; we will continue accepting applications until we receive a sufficient number or select a candidate for the position.

Sponsorship

Sponsorship for this role is not guaranteed.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Salary Range

86,048.05USD -116,417.95USD