Specialist QC
West Greenwich, RI · On-site
Specialist QC What you will do Let's do this. Let's change the world. In this vital role you will ... Ensure investigations are completed accurately, on time, and in compliance with GMP requirements ...
Specialist QC
West Greenwich, RI · On-site
Specialist QC What you will do Let's do this. Let's change the world. In this vital role you will ... Ensure investigations are completed accurately, on time, and in compliance with GMP requirements ...
Specialist QC
West Greenwich, RI · On-site
Specialist QC What you will do Let's do this. Let's change the world. In this vital role you will ... Ensure investigations are completed accurately, on time, and in compliance with GMP requirements ...
Specialist QC
West Greenwich, RI · On-site
Specialist QC What you will do Let's do this. Let's change the world. In this vital role you will ... Ensure investigations are completed accurately, on time, and in compliance with GMP requirements ...
Specialist QC
West Greenwich, RI · On-site
$95 - $125/hr
Specialist QC What you will do Let's do this. Let's change the world. In this vital role you will ... Ensure investigations are completed accurately, on time, and in compliance with GMP requirements ...
Specialist QC
West Greenwich, RI · On-site
$95 - $125/hr
Specialist QC What you will do Let's do this. Let's change the world. In this vital role you will ... Ensure investigations are completed accurately, on time, and in compliance with GMP requirements ...
Specialist QC
West Greenwich, RI · On-site
$95 - $135/hr
Lead Quality Control analytical investigations for Out-of-Specification (OOS), Out-of-Trend (OOT ... Ensure investigations are completed accurately, on time, and in compliance with GMP requirements ...
Specialist QC
West Greenwich, RI · On-site
$95 - $135/hr
Lead Quality Control analytical investigations for Out-of-Specification (OOS), Out-of-Trend (OOT ... Ensure investigations are completed accurately, on time, and in compliance with GMP requirements ...
Associate Quality Control What you will do Let's do this. Let's change the world. In this vital ... Perform sample collection and sample handling to support GMP operations * Perform testing and ...
Associate Quality Control What you will do Let's do this. Let's change the world. In this vital ... Perform sample collection and sample handling to support GMP operations * Perform testing and ...
Associate Quality Control What you will do Let's do this. Let's change the world. In this vital ... Perform sample collection and sample handling to support GMP operations * Perform testing and ...
Associate Quality Control What you will do Let's do this. Let's change the world. In this vital ... Perform sample collection and sample handling to support GMP operations * Perform testing and ...
QC for Manufacturing - Team B Associate Quality Control What you will do Let's do this. Let ... Perform sample collection and sample handling to support GMP operations and Environmental/Water ...
QC for Manufacturing - Team B Associate Quality Control What you will do Let's do this. Let ... Perform sample collection and sample handling to support GMP operations and Environmental/Water ...
QC for Manufacturing - Team B Associate Quality Control What you will do Let's do this. Let ... Perform sample collection and sample handling to support GMP operations and Environmental/Water ...
QC for Manufacturing - Team B Associate Quality Control What you will do Let's do this. Let ... Perform sample collection and sample handling to support GMP operations and Environmental/Water ...
Design, develop and implement quality control training programs. * Work with supervisors to ensure ... Practices (GMP), ISO, and FDA requirements. * Must be able to work in and promote a Team ...
Design, develop and implement quality control training programs. * Work with supervisors to ensure ... Practices (GMP), ISO, and FDA requirements. * Must be able to work in and promote a Team ...
Design, develop and implement quality control training programs. * Work with supervisors to ensure ... Practices (GMP), ISO, and FDA requirements. * Must be able to work in and promote a Team ...
Design, develop and implement quality control training programs. * Work with supervisors to ensure ... Practices (GMP), ISO, and FDA requirements. * Must be able to work in and promote a Team ...
... quality control records) and facility records assuring company standards are maintained and product integrity is preserved. RESPONSIBILITIES 1. Provide support to GMP investigations, validation ...
... quality control records) and facility records assuring company standards are maintained and product integrity is preserved. RESPONSIBILITIES 1. Provide support to GMP investigations, validation ...
... quality control records) and facility records assuring company standards are maintained and product integrity is preserved. RESPONSIBILITIES 1. Provide support to GMP investigations, validation ...
... quality control records) and facility records assuring company standards are maintained and product integrity is preserved. RESPONSIBILITIES 1. Provide support to GMP investigations, validation ...
... quality control records) and facility records assuring company standards are maintained and product integrity is preserved. RESPONSIBILITIES 1. Provide support to GMP investigations, validation ...
... quality control records) and facility records assuring company standards are maintained and product integrity is preserved. RESPONSIBILITIES 1. Provide support to GMP investigations, validation ...
Quality Engineer
West Warwick, RI · On-site
$69K - $90K/yr
Support risk assessments, control plans, and quality metrics reporting. Root Cause Analysis ... Working knowledge of GMP and quality management systems. * Strong analytical, organizational, and ...
Quality Engineer
West Warwick, RI · On-site
$69K - $90K/yr
Support risk assessments, control plans, and quality metrics reporting. Root Cause Analysis ... Working knowledge of GMP and quality management systems. * Strong analytical, organizational, and ...
Quality Engineer
West Warwick, RI · On-site
$69K - $90K/yr
Support risk assessments, control plans, and quality metrics reporting. Root Cause Analysis ... Working knowledge of GMP and quality management systems. * Strong analytical, organizational, and ...
Quality Engineer
West Warwick, RI · On-site
$69K - $90K/yr
Support risk assessments, control plans, and quality metrics reporting. Root Cause Analysis ... Working knowledge of GMP and quality management systems. * Strong analytical, organizational, and ...
... GMP), ISO, and FDA requirements Participate in Risk Management activities Monitor production ... Understands and has applied in practice the concepts of process capability, process control, and ...
... GMP), ISO, and FDA requirements Participate in Risk Management activities Monitor production ... Understands and has applied in practice the concepts of process capability, process control, and ...
... GMP), ISO, and FDA requirements Participate in Risk Management activities Monitor production ... Understands and has applied in practice the concepts of process capability, process control, and ...
... GMP), ISO, and FDA requirements Participate in Risk Management activities Monitor production ... Understands and has applied in practice the concepts of process capability, process control, and ...
Senior Scientist, Analytical Chemistry
$90K - $130K/yr
The Senior Scientist will contribute technical expertise to complex analytical challenges while ensuring QC laboratory activities support GMP manufacturing operations. Key Responsibilities * Support ...
Senior Scientist, Analytical Chemistry
$90K - $130K/yr
The Senior Scientist will contribute technical expertise to complex analytical challenges while ensuring QC laboratory activities support GMP manufacturing operations. Key Responsibilities * Support ...
Senior Scientist, Analytical Chemistry
Coventry, RI · On-site
$90K - $130K/yr
The Senior Scientist will contribute technical expertise to complex analytical challenges while ensuring QC laboratory activities support GMP manufacturing operations. Key Responsibilities * Support ...
Senior Scientist, Analytical Chemistry
Coventry, RI · On-site
$90K - $130K/yr
The Senior Scientist will contribute technical expertise to complex analytical challenges while ensuring QC laboratory activities support GMP manufacturing operations. Key Responsibilities * Support ...
... Control, and Facilities/Engineering staff regarding compliance and quality systems ... Experience working with batch records and other GMP documentation * Knowledge of data integrity ...
... Control, and Facilities/Engineering staff regarding compliance and quality systems ... Experience working with batch records and other GMP documentation * Knowledge of data integrity ...
Gmp Quality Control information
What is the difference between Gmp Quality Control vs Gmp Quality Assurance?
| Aspect | Gmp Quality Control | Gmp Quality Assurance |
|---|---|---|
| Primary Focus | Testing and inspecting products to ensure compliance with standards | Developing and maintaining quality systems and processes |
| Responsibilities | Sampling, testing, and documenting product quality | Auditing, process validation, and quality system oversight |
| Certifications | GMP training, laboratory skills | GMP knowledge, quality management system training |
| Work Environment | Laboratories, manufacturing sites | Quality departments, compliance offices |
Gmp Quality Control focuses on testing products to verify they meet quality standards, while Gmp Quality Assurance involves establishing and maintaining systems to prevent defects. Both roles are essential in ensuring product safety and compliance in the pharmaceutical and biotech industries.
Is GMP Quality Control a good career path?
GMP Quality Control involves testing and inspecting pharmaceutical products to ensure they meet regulatory standards, making it a stable career with demand in the healthcare and biotech industries. It often requires attention to detail, knowledge of Good Manufacturing Practices, and certifications such as GMP training or laboratory skills. The role offers opportunities for advancement into quality assurance, compliance, or management positions.
Is GMP Quality Control a good career?
GMP Quality Control is a stable career in the pharmaceutical and biotech industries, focusing on ensuring products meet regulatory standards. It involves tasks such as testing, documentation, and compliance, often requiring knowledge of laboratory techniques and certifications like GMP training. The role offers opportunities for advancement and consistent employment due to industry regulation requirements.
What is the role of quality control in GMP?
In GMP, quality control (QC) is responsible for testing and inspecting raw materials, in-process samples, and finished products to ensure they meet specified quality standards. QC helps prevent defective or unsafe products from reaching consumers by verifying compliance with regulatory requirements and maintaining proper documentation. QC professionals often use analytical tools and follow strict protocols to support product safety and efficacy.
What are popular job titles related to Gmp Quality Control jobs in Rhode Island?
For Gmp Quality Control jobs in Rhode Island, the most frequently searched job titles are:
What job categories do people searching Gmp Quality Control jobs in Rhode Island look for?
The top searched job categories for Gmp Quality Control jobs in Rhode Island are:
What cities in Rhode Island are hiring for Gmp Quality Control jobs?
Cities in Rhode Island with the most Gmp Quality Control job openings:
Specialist QC
West Greenwich, RI • On-site
Amgen, Inc.
Full-time
Medical, Dental, Vision, Life, Retirement
Posted 15 days ago
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.
Specialist QC
What you will do
Let's do this. Let's change the world. In this vital role you will support analytical investigations ownership within the QC Technical Services team at Amgen.
Responsibilities:
Analytical Investigation Ownership
Quality Systems & Risk Assessment
Cross-Functional Collaboration
Inspection Readiness
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 collaborative teammate with these qualifications.
Basic Qualifications
Preferred Qualifications
What you can expect from 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:
Apply now and make a lasting impact with the Amgen team.
careers.amgen.com
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.
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. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
Salary Range
100,450.45USD -135,903.55 USD
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.
Specialist QC
What you will do
Let's do this. Let's change the world. In this vital role you will support analytical investigations ownership within the QC Technical Services team at Amgen.
Responsibilities:
Analytical Investigation Ownership
- Lead Quality Control analytical investigations for Out-of-Specification (OOS), Out-of-Trend (OOT), atypical, and unexpected analytical results.
- Perform scientifically sound root cause analysis and develop effective corrective and preventive actions (CAPAs).
- Ensure investigations are completed accurately, on time, and in compliance with GMP requirements and internal quality standards.
Quality Systems & Risk Assessment
- Own and support deviations, CAPAs, and effectiveness verifications as assigned.
- Review and approve equipment-related change controls, as applicable.
- Partner with Quality Assurance to ensure investigation outcomes are risk-based and inspection-ready.
- May support additional project-based assignments as required.
Cross-Functional Collaboration
- Collaborate with Quality Control laboratories, Manufacturing, Process Development, Quality Assurance, Supply Chain, and other functional groups to resolve complex quality events.
- Facilitate effective communication among stakeholders to ensure timely investigation progression and issue resolution.
- Engage subject matter experts as needed to support technically complex investigations.
Inspection Readiness
- Support internal and external audits by clearly communicating investigation findings, root cause, and CAPA effectiveness.
- Maintain complete, accurate, and inspection-ready documentation.
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 collaborative teammate with these qualifications.
Basic Qualifications
- High school diploma/GED and 10 years of directly related experience OR
- Associate's degree and 8 years of directly related experience OR
- Bachelor's degree and 4 years of directly related experience OR
- Master's degree and 2 years of directly related experience OR
- Doctorate degree
Preferred Qualifications
- Bachelor's degree in Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, or another Life Science discipline.
- 5-8+ years of Quality Control or Quality Assurance experience within the biotechnology or pharmaceutical industry.
- Demonstrated experience leading complex laboratory investigations, including OOS, OOT, atypical results, and laboratory deviations.
- Strong knowledge of GMP regulations, laboratory quality systems, and deviation management processes.
- Experience performing root cause analysis using structured problem-solving methodologies.
- Strong understanding of analytical laboratory techniques, instrumentation, and data integrity principles.
- Experience authoring and managing deviations, CAPAs, change controls, and effectiveness verifications.
- Ability to evaluate technical data, assess risk, and make sound, science-based decisions.
- Strong written and verbal communication skills with the ability to influence cross-functional teams.
- Experience supporting regulatory inspections and responding to auditor inquiries.
- Experience utilizing digital tools, data analytics, or AI-enabled technologies to improve laboratory processes is preferred.
What you can expect from 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.
Apply now and make a lasting impact with the Amgen team.
careers.amgen.com
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.
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. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status.
Salary Range
100,450.45USD -135,903.55 USD