Sr Mgr QA _ AML 1 Inspection And Packaging

Amgen Inc. Juncos , PR 00777

Posted 2 months ago

Are you looking for a meaningful new opportunity to test and growth your QUALITY skills? We have an immediate need for a SR MANAGER QUALITY ASSURANCE to join AML's Inspection & Packaging a Non Standard Shift Organization. This is an outstanding opportunity to seek a variety of challenges and responsibilities in support to our manufacturing facility at Amgen Manufacturing Limited in Juncos, Puerto Rico.

THE ROLE

The Sr Mgr QA role will lead the Quality Operations for AML1 Packaging Lines and will support the Inspection Lines. Sr Mgr QA will provide oversight to the Quality Operations, ensuring staff is well trained and execution is in compliance with procedures and regulations. Actively engaged with projects and deviations impacting Packaging to ensure requirements are complete and Plant QA staff is knowledgeable and trained to timely execute. Accountable for the Quality and Compliance state of the Packaging Processes in a NON STANDARD SHIFT Operations

AML1 Inspection and Packaging Operations consist of 16 lines working 7 days a week. Area is very dynamic, with a high number of production lots, investigations and projects, required in an expedited timeline.

SPECIFIC RESPONSIBILITIES INCLUDE BUT ARE NOT LIMITED TO:

  • Responsible for leading and directing the Quality Assurance functions for assigned plant(s) or functional area(s)

  • Responsible for providing Quality oversight to ensure that operations for clinical and licensed pharmaceutical products are manufactured, tested, stored, and distributed according to current Good Manufacturing Practices (cGMP) and other applicable regulations

  • Ensures that facilities, equipment, materials, organization, processes, procedures and products comply with cGMP practices and other applicable regulations

  • Responsible for Quality disposition (approval or rejection) of raw materials and components, bulk drug substances, bulk drug products, and finished product for assigned areas

  • Ensures the Quality unit provides review, approval and tracking of cGMP processes, procedures, assays, documents and records, including Non conformance, CAPAs, and validations

  • Supports Continual Improvement initiatives, programs and projects

  • Ensures that changes that could potentially impact product quality are assessed according to procedures

  • Ensures that deviations from established procedures are investigated and detailed per procedures

  • Ensures that production records and testing results are complete, accurate, and documented according to written procedures and cGMP requirements

  • Ensures that GMP functions are periodically audited to assess compliance to cGMP regulations and to identify potential risks

  • Ensures that Quality Assurance personnel are qualified and trained to perform assigned functions in accordance with cGMP with requirements

  • Ensures the Quality Management System is implemented, maintained and reviewed in accordance with cGMP regulations

  • Alerts senior management of significant quality, compliance, supply and safety risks

  • Develops area budget and handles expenditures

BASIC QUALIFICATIONS

Doctor degree and 2 years of Quality or Manufacturing experience in pharmaceutical, medical device or biotechnology industry

Or

Master's degree and 6 years of Quality or Manufacturing experience in pharmaceutical, medical device or biotechnology industry

Or

Bachelor's degree and 8 years of Quality or Manufacturing experience in pharmaceutical, medical device or biotechnology industry

AND 2 years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources.

PREFERRED QUALIFICATIONS

  • Educational background in Life Sciences or Engineering

  • Demonstrated ability to manage supervisors.

  • Experience working with Quality Systems

  • Ability to delegate wisely and effectively.

  • Works effectively with diverse departmental groups.

  • Excellent team development and leadership skills.

  • Skill and knowledge of and experience with processes involved in manufacturing and distribution, QA, Quality Control, validation, and process development.

  • Commands respect from team, peers, and management.

  • Detailed knowledge of CFRs, GMPs and pharmaceutical processing and demonstrated ability to apply.

  • Able to make sound, quality decisions independently.

  • Excellent communication (both written and verbal), facilitation, and presentation skills in English and Spanish

  • Skilled in risk management

  • Demonstrate the Amgen Values/Leadership Practices

  • Work under pressure, adapt to changes in priorities

  • Negotiations skills to influence staff and peers to ensure deliverables and results are timely met.

The benefits

Our broad approach is one of the reasons why we are regularly recognized as a 'Best Place To Work'. We offer an outstanding benefits package that includes an award-winning retirement and stock plan. And between the paid time off, and wellness program - and on-site child care and fitness facilities - you will find us

Our culture is what makes Amgen a special place to work. We have a powerful shared purpose around our mission - to serve patients. We respect one another, recognize contributions, and have embedded collaboration, trust, empowerment and inclusion in all that we do.

We equip all our staff members to live well-rounded, healthy lives. Most recently, Amgen added benefits for transgender employees and continues to pride itself on industry-leading, family-friendly offerings for families of all compositions.

Amgen focuses on areas of high unmet medical need and uses its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.

Our culture is what makes Amgen a special place to work. We have a powerful shared purpose around our mission - to serve patients. We respect one another, recognize contributions, and have embedded collaboration, trust, empowerment and inclusion in all that we do.

We equip all our staff members to live well-rounded, healthy lives. Most recently, Amgen added benefits for transgender employees and continues to pride itself on industry-leading, family-friendly offerings for families of all compositions.

Amgen focuses on areas of high unmet medical need and uses its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential.

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.

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Sr Mgr QA _ AML 1 Inspection And Packaging

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