Manager Manufacturing (12hr PM)

BioSpace; New Albany (OH); On-site; USD 110,000 - 150,000; Full time

Benefits offered by this job

Retirement plan

Medical coverage

Life insurance

Bonus program

Stock incentives

Time off

Flexible work

Job summary

Amgen in Columbus-area Ohio is seeking a Manager of Manufacturing to lead a 12-hour PM production shift in an Inspection and Packaging facility. You will supervise staff, ensure cGMP compliance, and drive production schedules in a fast-paced biotech environment.

Key qualifications include a doctorate or equivalent leadership experience in pharma/biotech, strong project management and regulatory skills, and the ability to partner with QA, Regulatory, and FDA as needed.

Qualifications

• Doctorate degree with leadership experience in pharma/biotech.
• Experience managing people and leading teams or projects in pharma/biotech.
• Knowledge of cGMP/Regulatory requirements in manufacturing.

Responsibilities

• Manage and lead all aspects of a manufacturing area in an Inspection and Packaging facility with cGMP compliance.
• Hire, train, evaluate staff and ensure production schedules are completed.
• Coordinate development and revision of SOPs and change controls; interact with FDA as needed.
• Oversee safety, budgeting, and cross-functional collaboration with QA/QC, PPIC, Reg, Regulatory.

Skills

Leadership

Project Management

Analytical Problem Solving

Verbal Communication

Written Communication

Conflict Resolution

Coaching Mentoring

Scheduling

Regulatory requirements

Education

Doctorate degree

Masters degree

Bachelors degree

Associates degree

High School Diploma

Job description

Join Amgens Mission of Serving Patients

At Amgen, if you feel like youre part of something bigger, its because you are. Our shared missionto serve patients living with serious illnessesdrives all that we do.

Since 1980, weve helped pioneer the world of biotech in our fight against the worlds 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, youll 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, youll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

Manager, Manufacturing- 12 Hour PM (6:00pm - 6:30am)

What you will do

Lets do this. Lets change the world. In this role you will be managing and leading all aspects of either a small manufacturing production area, or a section of a larger production area in an Inspection and Packaging facility. Responsibility includes maintaining production in full cGMP compliance. Supervises, hires, and develops staff and ensures production schedules are completed.

Compliance

• Evaluate and approve reports and protocols.
• Ensure cGMP and CFR compliance of manufacturing areas.
• Revise, update, and review procedures
• Coordinate the development and revision of SOPs.
• Evaluate current manufacturing procedures and recommend changes to management to optimize production.
• Assure all corporate change control procedures are followed, and Regulatory and QA are made aware prior to the changes.
• Interact with the FDA.
• Ensure Amgen policies are followed

Process/Equipment/Facilities

• Ensure maintenance and re validation of systems.
• Collaborate with cross-functional teams (i.e. QA/QC, PPIC, Clinical Mfg, PD, Regulatory, etc.) in completing production activities.
• Develop, implement and assess solutions for problems.
• Responsible for resolving problems during operation.
• Coordinates set up of critical new manufacturing processes.

Staff Supervision

• Responsible for selection, training, evaluation, staff relations and development of staff.
• Ensure training programs are maintained
• Ensure scheduling of production and maintenance activities.
• Interacts with management in optimizing organizational structure and responsibilities
• Ensure plant safety through auditing and evaluations.

Administrative

• Interacts with management in planning, developing and maintaining budget.
• Assist in developing and maintaining department goals

Shift

This position will be supporting a rotating 12hr schedule which cycles every two weeks; 3 days one week and 4 days the next.

What we expect of you

We are all different, yet we all use our outstanding contributions to serve patients. The professional we seek will possess these qualifications.

Basic Qualifications

• Doctorate degree
• Masters degree and 3 years of experience in the pharmaceutical, medical device or biotechnology industry
• Bachelors degree and 5 years of experience in the pharmaceutical, medical device or biotechnology industry.
• Associates degree and 10 years of experience in the pharmaceutical, medical device or biotechnology industry.
• High School Diploma/GED and 12 years of experience in the pharmaceutical, medical device or biotechnology industry.

In addition to meeting at least one of the above requirements, you must have experience directly managing people and/or leadership experience leading teams, projects, programs, or directing the allocation or resources. Your managerial experience may run concurrently with the required technical experience referenced above

Preferred Qualifications

• Educational background in Science, Engineering or Business Administration
• Availability to work on an overnight shift
• Strong Managerial skills
• Non-Conformance and CAPA
• Ensure that all Non-conformance are triage within the established goal.
• Leadership and team building
• Verbal communication
• Written Communication including technical writing skills
• Conflict Resolution
• Analytical Problem Solving
• Project Management
• Coaching, Mentoring and Counseling
• Ability to be flexible and manage change
• Regulatory requirements
• Scheduling
• Presentation Skills

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, well 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

Benefits

• 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, including remote and hybrid work arrangements, where possible

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.

In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.