23 days old

Senior Associate- Quality Assurance 2nd shift

Amgen
West Greenwich, RI 02817
  • Job Code
    115671500
Amgen

Job ID: R-88350
Location: Rhode Island, RI, US

The Quality Assurance Sr Associate will be responsible for Plant Quality Assurance (PQA) On the Floor in support of Manufacturing activities. This position provides the opportunity to work directly with Manufacturing staff during bulk drug substance operations to facilitate real-time decision-making regarding quality requirements and deviations. This is a unique opportunity to foster a strong partnership and learning environment between Manufacturing and Quality staff. Amgen's Quality Assurance On-the-Floor position Shift 2 (4 days a week; Tuesday through Friday, 10 hours per day 1pm - 11pm) provides coaching, guidance and direction to Manufacturing, Quality Control and Facilities & Engineering staff in regard to compliance and quality systems.

Responsibilities :
Provide Quality oversight to ensure that operations products are manufactured, tested, stored, and distributed according to current Good Manufacturing Practices (cGMP), Good Distribution Practices (GDP) and other applicable regulations.

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

Performs review of cGMP processes, procedures, documents and records, including but not limited to Standard Operating Procedures (SOP), Batch Records, Nonconformance, Corrective Action/Preventative Actions (CAPA).

Author/review quality documents, such as: SOPs, user requirements, risk assessments, training materials, engineering documents, automation documents, environmental qualification protocols/reports, validation protocols/reports.

Adhere to and enable LEAN practices.

Provide guidance during on-the-floor analytical testing.

Ensure that changes that could potentially impact product quality are assessed according to procedures.

Ensure that deviations from established procedures are investigated and documented per procedures.

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

Alert senior management of quality, compliance, supply and safety risks.

Complete required assigned training to permit execution of required tasks.

Support operational improvement initiatives, programs and projects.

Basic Qualifications

Master's degree

OR
Bachelor's degree and 2 years of Quality, Manufacturing, Validation, Process Development or Process Engineering experience
OR
Associate's degree and 6 years of Quality, Manufacturing, Validation, Process Development or Process Engineering experience
OR
High school diploma / GED and 8 years of Quality, Manufacturing, Validation, Process Development or Process Engineering experience

Preferred Qualifications

Scientific degree in Life Sciences or Physical Sciences or Applied Engineering or Manufacturing Technologies

Previous QA oversight of manufacturing, analytical and engineering activities

Experience in investigations, change controls, and CAPAs processes system knowledge

Direct Validation experience with pharmaceutical or biopharmaceutical processes

Ability to evaluate compliance issues and interact with regulatory inspectors

Experience and training in EDMQ, Trackwise, Maximo, LIMS

Experience in managing multiple, competing priorities in a fast-paced environment

Experience leading and/or managing teams

Direct bulk drug substance and drug product experience

Ability to solve complex problems and make scientific risk-based decisions

Experience representing Amgen while interacting with representatives of regulatory agencies

Experience of trending analysis

Demonstrated proficiency using Excel, Word and PowerPoint

Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology.

Amgen focuses on areas of high unmet medical need and leverages 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.

PI115671500

<strong>Amgen</strong><br /><br /><strong>Job ID: </strong>R-88350<br /><strong>Location: </strong>Rhode Island, RI, US<br /><br />The Quality Assurance Sr Associate will be responsible for Plant Quality Assurance (PQA) On the Floor in support of Manufacturing activities. This position provides the opportunity to work directly with Manufacturing staff during bulk drug substance operations to facilitate real-time decision-making regarding quality requirements and deviations. This is a unique opportunity to foster a strong partnership and learning environment between Manufacturing and Quality staff. Amgen's Quality Assurance On-the-Floor position Shift 2 (4 days a week; Tuesday through Friday, 10 hours per day 1pm - 11pm) provides coaching, guidance and direction to Manufacturing, Quality Control and Facilities & Engineering staff in regard to compliance and quality systems. <br /><br />Responsibilities :<br />Provide Quality oversight to ensure that operations products are manufactured, tested, stored, and distributed according to current Good Manufacturing Practices (cGMP), Good Distribution Practices (GDP) and other applicable regulations. <br /><br />Ensure that facilities, equipment, materials, organization, processes, procedures and products comply with cGMP practices and other applicable regulations. <br /><br />Performs review of cGMP processes, procedures, documents and records, including but not limited to Standard Operating Procedures (SOP), Batch Records, Nonconformance, Corrective Action/Preventative Actions (CAPA). <br /><br />Author/review quality documents, such as: SOPs, user requirements, risk assessments, training materials, engineering documents, automation documents, environmental qualification protocols/reports, validation protocols/reports. <br /><br />Adhere to and enable LEAN practices. <br /><br />Provide guidance during on-the-floor analytical testing. <br /><br />Ensure that changes that could potentially impact product quality are assessed according to procedures. <br /><br />Ensure that deviations from established procedures are investigated and documented per procedures. <br /><br />Ensure that production records and testing results are complete, accurate, and documented according to written procedures and cGMP requirements. <br /><br />Alert senior management of quality, compliance, supply and safety risks. <br /><br />Complete required assigned training to permit execution of required tasks. <br /><br />Support operational improvement initiatives, programs and projects. <br /><br /><strong>Basic Qualifications </strong><br /><br /> Master's degree <br /><br /> OR <br /> Bachelor's degree and 2 years of Quality, Manufacturing, Validation, Process Development or Process Engineering experience <br /> OR <br /> Associate's degree and 6 years of Quality, Manufacturing, Validation, Process Development or Process Engineering experience <br /> OR <br /> High school diploma / GED and 8 years of Quality, Manufacturing, Validation, Process Development or Process Engineering experience <br /><br /><strong>Preferred Qualifications </strong><br /><br /> Scientific degree in Life Sciences or Physical Sciences or Applied Engineering or Manufacturing Technologies <br /><br />Previous QA oversight of manufacturing, analytical and engineering activities <br /><br />Experience in investigations, change controls, and CAPAs processes system knowledge <br /><br />Direct Validation experience with pharmaceutical or biopharmaceutical processes <br /><br />Ability to evaluate compliance issues and interact with regulatory inspectors <br /><br />Experience and training in EDMQ, Trackwise, Maximo, LIMS <br /><br />Experience in managing multiple, competing priorities in a fast-paced environment <br /><br />Experience leading and/or managing teams <br /><br />Direct bulk drug substance and drug product experience <br /><br />Ability to solve complex problems and make scientific risk-based decisions <br /><br />Experience representing Amgen while interacting with representatives of regulatory agencies <br /><br />Experience of trending analysis <br /><br />Demonstrated proficiency using Excel, Word and PowerPoint <br /><br />Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology.<br /><br />Amgen focuses on areas of high unmet medical need and leverages 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.<br /><br />Join Us <br /> <br /> 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. <br /> <br /> 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. <br /> <br /> 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. <br /> <br /> 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.<br /><br /> <img src="https://analytics.click2apply.net/v/z14ApdSXlyKJt7oqibe5x"> <p>PI115671500</p>

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Posted: 2019-11-21 Expires: 2019-12-22

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Senior Associate- Quality Assurance 2nd shift

Amgen
West Greenwich, RI 02817

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