This job has expired

You will need to login before you can apply for a job.

Front Line Manager - Night Shift

Juncos, PR
Start date
Nov 21, 2022
You need to sign in or create an account to save a job.

Job Details


Youve earned your degree. How will you use that achievement to reach your goals? Do more with the knowledge youve worked hard to acquire and the passion you already have. At Amgen, our shared missionto serve patientsdrives all that we do. It is key to our becoming one of the worlds leading biotechnology companies, reaching over 10 million patients worldwide. Become the professional you are meant to be in this meaningful role.

Front-Line Manufacturing Manager (Non-Standard Shift - Night Shift)


What you will do

Lets do this. Lets change the world! In this vital role, the Front-Line Manufacturing Manager is responsible for leading and supervising either small manufacturing or a section of a larger production area in an Inspection and Packaging facility. You will lead and empower employees to perform a production process to fulfill business goals.

As the leader of the manufacturing floor, you will also provide mentorship, instruction, motivation, and feedback to the employees on a day-to-day basis within a non-standard shift structure. Your scheduled workweek may include extended shifts, Saturday and/or Sunday and/or 12hrs, second or third shift on a regular basis, based on business need. **Several positions available**.

Specific responsibilities include but are not limited to:

  • Evaluate and approve reports and protocols
  • Evaluate current operating procedures and recommend changes to management to optimize production.
  • Assure achievement schedule adherence with Supply Chain requirements
  • Creates and enforces quality integrity checks and ensures regulatory compliance of operating areas
  • Ensure that all non-conformances are triaged within the established goal, in addition, to act as a lead for Human Performances Deviations
  • Assure corporate change control procedures are followed, and that the Regulatory and Quality Assurance partners are advised prior to the changes
  • Interact with regulatory agencies for internal and external audits
  • Ensure maintenance and re-validation of systems
  • Collaborate with cross-functional teams (i.e. Quality Assurance/Quality Control, Production Planning & Inventory Control (PPIC), Clinical Manufacturing, Process Development, Regulatory, etc.) in completing production activities
  • Applies analytical skills to identify and solve business and technical problems
  • Responsible for selection, training, performance evaluations, staff relations, and development of staff as the best talent, to assure personnel consistently follows HR policies, SOPs, business practices, business conduct expectations, and Amgen Values.
  • Lead CI Activities of his/her functional group to improve productivity; be a Role Model regarding the Continuous Improvement Culture by means of daily use of his/her Standard work (Purpose Presence On the Floor); Foster / develop multi-year real/effective initiatives that significantly impact the changeover time (CHO) and Overall Equipment Effectiveness (OEE) of the area.
  • Lead Functional Area metric; Report and provide action plans to improve performance in Uptime Meetings and during Work Center Team Meetings. Aligned with plant goals.
  • Active & effective presence on the floor during his/her scheduled shift to ensure an active role in the day-to-day activities.
  • Decision maker and possess good sound judgment and inform resolution to Senior Manager
  • Control and supervise budget area expenses, including meal penalty and overtime
  • Ensure plant safety through auditing and evaluations
  • Lead the process to maintain the focus of the group on continuous improvement and the use of ideas initiative or/and kaizen process in the inspection/packaging areas


What we expect of you

We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a strong leader with these qualifications.

Doctorate degree


Masters degree and 3 years of regulated industry experience


Bachelors degree and 5 years of regulated industry experience


Associates degree and 10 years of regulated industry experience


High school diploma / GED and 12 years of regulated industry experience


Previous managerial experience directly managing people and/or experience leading teams, projects, programs or directing the allocation of resources.

Beyond that, additional Preferred Qualifications are:
  • Experience in the pharmaceutical, medical device, biotechnology or other regulated industries with proficiency in biopharmaceutical compliance knowledge
  • Strong Managerial skills and ability to successfully prioritize a diverse workload to meet targets
  • Experience Managing Deviations and CAPA
  • Verbal and written communication skills in Spanish and English that will include technical terminology
  • Analytical problem-solving, project management, and presentation skills
  • Experience with regulated systems to perform job duties (SAP/MES, QMTS, LMS, Maximo, Trackwise, etc.)
  • Be a Subject Matter Expert of the processes, systems, and equipment from his/her areas.


Some of the vast rewards of working here

As we work to develop treatments that take care of others, so we work to care for our teammates professional and personal growth and well-being.

  • Full support and career-development resources to expand your skills, enhance your expertise, and maximize your potential along your career journey
  • A diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
  • Generous Total Rewards Plancomprising health, finance and wealth, work/life balance, and career benefitswith compensation and benefits rated above 4 stars (out of 5) on Glassdoor

Apply now for a career that defies imagination

Objects in your future are closer than they appear. Join us.

Join Us

If you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen.

Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses.

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 but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients.

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, or disability status.

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.

Amgen requires all staff in the United States, Puerto Rico and Canada to be vaccinated from COVID 19 as a condition of employment. In accordance with applicable law, Amgen will provide reasonable accommodations to staff members who qualify on the basis of a medical reason or a sincerely held religious belief, practice, or observance. Such accommodation may not pose an undue hardship to Amgen, its operations, or its staff.


We are all different, yet we have this in common: our mission to serve patients. This sense of shared purpose is key to our becoming one of the world’s leading biotechnology companies. It guides us as we continue to launch new medicines and reach millions of patients worldwide.

We live the mission.

We win together.

We thrive on continual challenge.

Our team of 22,000+ scientists and professionals worldwide bring distinct perspectives and experiences to all we do. We leverage our global talent to achieve together—to research, manufacture and deliver ever-better products and greater depth to our mission.

At Amgen, there is a strong correlation between our high level of diversity and performance. Because addressing issues with a wider range of perspectives and approaches leads to more creative problem-solving. Together, we’re transforming the promise of science and biotechnology into therapies that have the power to restore health.

Connect with us to explore how you can Win, Live, and Thrive at Amgen.


Find Us
Corporate Headquarters
One Amgen Center Drive
Thousand Oaks
You need to sign in or create an account to save a job.

Get job alerts

Create a job alert and receive personalized job recommendations straight to your inbox.

Create alert