Senior/Quality Assurance Auditor (GLP)
Company: Amplify Bio
Location: West Jefferson
Posted on: November 7, 2024
Job Description:
Are you passionate about significantly improving the future of
medicine? Do you believe that people are the most important asset
of any company? If so, join AmplifyBio!AmplifyBio is a leading
contract research organization with a comprehensive range of
services that span from being an outsourcing partner for discovery
stage R&D work, a preclinical CRO performing safety efficacy
and toxicology studies for small molecules and advanced therapies
alike, and, most recently, an expansion into manufacturing services
for cell, gene, and mRNA-based therapeutics.The AmplifyBio
ecosystem is comprised of three distinct business units: ADOC
(South San Francisco, CA) Amplify's Discovery, Optimization, and
Characterization laboratories: ASET (West Jefferson, OH) Amplify's
Safety, Efficacy, and Toxicology Site; and the most recently opened
AMEC (New Albany, OH) Amplify's Manufacturing Enablement
Center.About ASET West Jefferson, OH: AmplifyBios safety, efficacy,
and toxicology unit (ASET) was launched as a preclinical CRO that
spun out of Battelle in 2021 to address the changing needs of
commercial organizations developing modern therapeutics. AmplifyBio
brings decades of experience to accommodate a wide variety of GLP
and non-GLP studies in all in vivo models and dose routes. Among
the investments that AmplifyBio has made to empower preclinical
assessments of advanced therapies is building a new
state-of-the-art analytical laboratory to include molecular and
immunological assays that assess critical safety and efficacy
indicators for cell and gene therapies during preclinical
studiesAmplifyBiois seeking to hire aSr./Quality Assurance
Auditor(GLP) to join our growing team!!!The Sr./QA Auditor (GLP)
Conducts audits and performs inspections to assure compliance to
federal regulations, AmplifyBio standards, client specifications,
internal policies, and any other applicable guidelines.What Youll
Do Here:
- Audits protocols, raw data, documents, records, reports, and
inspects work being performed to assure compliance to regulatory
requirements, standards, specifications, internal policies, and any
other applicable guidelines.
- Performs inspections of AmplifyBio facilities and corresponding
documentation to assure compliance to requirements. Issues
recommended actions and assesses corrective actions based on
observation(s).
- Reports audit findings to project leadership and
management.
- Advises operations regarding issues observed during inspections
to mitigate risk.
- May review project planning documents (technical protocols,
project plans, test plans, etc.) for compliance with stated
requirements.
- Utilizes knowledge of specific instrumentation and equipment,
laboratory techniques, and current FDA industry guidance to advise
on compliant operations.
- Interprets and applies existing and new regulatory requirements
and industry standards to operations methods and practices.
- Develops and executes Quality Assurance Audit Plans per
project.
- Demonstrates initiative and accountability, with ownership of
complex projects.
- Demonstrates ownership of assignments with accountability and
instills trust in project team.
- Act as regulatory subject matter expert and amongst peers as a
leader in the organization.
- Identifies compliance gaps and actively drives
process/continuous improvement efforts to minimize risk to the
organization.
- Drives change management through use of effective strategies
and own skills in order to facilitate organizational change
initiatives.We Would Love to Hear from You If:
- Bachelors Degree in a related field; 2-10 years of experience
in a quality assurance program and proven communication skills; or
an equivalent combination of education and/or experience in a
related field.
- Experience in a GLP environment or other regulated QA
Operations.Desired But Not Required:
- Experience with System Validation and Method Qualification
- Experience with electronic Quality Management Systems,
Laboratory Information Management Systems and 21 CFR Part 11
compliance.
- Experience interacting with external audits and regulatory
agencies.
- Proven leadership with mentoring responsibilities.
- Proven risk management skills including mitigation
strategies.At AmplifyBio, we're committed to growing and empowering
an inclusive community within our company and industry. This is why
we hire and cultivate diverse teams of the best and brightest from
all backgrounds, experiences, and perspectives across our
organization.AmplifyBio is an equal opportunity employer, and we
value diversity at our company. We don't discriminate based on
race, color, citizenship status, national origin, ancestry, gender
(including gender expression and gender identity), sexual
orientation, age, weight, religion, creed, physical or mental
disability, marital status, veteran status, political affiliation,
or any other factor protected by federal, state, or local law. Why
You Will Love Working Here:
We take the health and happiness of our employees seriously and
consistently evaluate new ways to Amp up our benefits to provide an
amazing place to work. From a wellness program (did we mention we
have an onsite gym with state-of-the-art equipment and ping pong
table?), to financial planning and legal assistance, we make sure
to take care of our own.
- Health, Dental, and Vision insurance that starts on your first
day at AmplifyBio!
- Competitive Compensation Package
- We take work-life balance seriously and we back it up with a
FLEXIBLE PTO policy!
- Generous paid parental leave
- Wellness and Self-Care Programs
- 401(k) match
- Tuition Reimbursement
- EAP/work-life support system
- A fun work environment where everyones voice matters!
- An Opportunity to Change the World!!!When you join our team,
you will be a part of groundbreaking work while collaborating with
our clients, research scientists, study directors, lab technicians,
and specialists across a variety of disciplines. The future for
AmplifyBio is as great as the combination of our imaginations and
actions, and we hold ourselves accountable for our choices and
results. We have a bias for action, excellence, and, especially,
the health and safety of our employees.
PIfe576ece175f-37248-35750412
Keywords: Amplify Bio, Kettering , Senior/Quality Assurance Auditor (GLP), Accounting, Auditing , West Jefferson, Ohio
Didn't find what you're looking for? Search again!
Loading more jobs...