The Opportunity : Avantor
, a Global Fortune 500 company is looking for a
dedicated Quality Assurance Senior Technician for our
biopharmaceutical’s organization.
This Aurora, OH role is
full-time on-site, Monday through Friday 3 – 11 : 30 PM
with potential overtime.
Minimum Education :
bachelor’s degree preferred.
Required Experience (1+ yrs) :
Collaboration skills (IE :
Microsoft Office)
Quality software (IE : ETQ,
SAP, LIMS).
Record keeping skills.
Ability to adhere to manufacturing
procedures.
Ability to follow standard
operating procedures (SOPs) and accurately complete paperwork.
Analytical / problem-solving skills.
Understanding of root cause analysis.
Understanding of statistical sampling plans,
and analysis of quality assurance data .
Preferred Experience :
Business level interpersonal, oral and written communication skills
Detail oriented
Working effectively in a team
environment
How you
will thrive and create an impact :
Avantor® is a leading life sciences company and global provider of
mission-critical products and services to the life sciences and
advanced technology industries. A GMP manufacturing facility, the
Aurora, OH location specializes in manufacturing of biochemicals.
With the ability to adapt readily to change and
manage multiple priorities the Quality Assurance Sr. Technician
will :
Provide support to our
customers, quality management system programs (including cGMP and
ISO), and the entire manufacturing operation.
Play a vital role in helping Avantor achieve success through
quality monitoring, modification, and continuous improvement.
Inspect shipments, reconciles labels, review
and release finished product and other paperwork.
Reviews QC testing documentation and results
for conformance.
Confirm expiration dating
and issue certificates of analysis for each lot.
Review and approve / reject quality-related
documents.
Assist in planning, developing,
and implementing quality assurance programs.
Respond to customer requests, including but not limited to
investigating complaints and completing required paperwork for
corrective and preventive actions and associated follow-up.
Assist in changing and maintaining ISO and
cGMP paperwork
Implement and oversee
training.
Ensure the quality requirements of
all departments are being followed and are accurately documented.
Complete preventative maintenance (P)
calibration documentation files
Manage out of
service equipment
Oversee / assure validations
are performed according to approved protocols and samples provided
as requested.
Interpret, understand and
manage a variety of technical information.
Prepare routine, technical, and special presentations / reports to
staff and management.
Oversee the writing and
maintenance of owner process manuals.
Coordinate and perform quality assurance system internal audits
Investigate non-conformances and determine
root cause analyses.
determining and documenting any areas that may need quality
improvements.
Perform other duties as
assigned.
Disclaimer :
The above statements are intended
to describe the general nature and level of work being performed by
employees assigned to this classification. They are not intended to
be construed as an exhaustive list of all responsibilities, duties
and skills required of employees assigned to this position. Avantor
is proud to be an equal opportunity employer.
Why
Avantor?
Dare to go further
in your career. Join our global team of 14,000+
associates whose passion for discovery and determination to
overcome challenges relentlessly advances life-changing science.
The work we do changes
people's lives for the better. It brings new
patient treatments and therapies to market, giving a cancer
survivor the chance to walk his daughter down the aisle. It enables
medical devices that help a little boy hear his mom's voice
for the first time. Outcomes such as these create unlimited
opportunities for you to contribute your talents, learn new skills
and grow your career at Avantor.
We are
committed to helping you on this journey through our diverse,
equitable and inclusive culture which includes learning experiences
to support your career growth and success. At Avantor, dare to go
further and see how the impact of your contributions set science in
motion to create a better world. Apply
today!
EEO
Statement : We are an Equal
Employment / Affirmative Action employer and VEVRAA Federal
Contractor. We do not discriminate in hiring on the basis of sex,
gender identity, sexual orientation, race, color, religious creed,
national origin, physical or mental disability, protected Veteran
status, or any other characteristic protected by federal,
state / province, or local law.
If you need a reasonable
accommodation for any part of the employment process, please
contact us by email at recruiting@avantorsciences.com and let us
know the nature of your request and your contact information.
Requests for accommodation will be considered on a case-by-case
basis. Please note that only inquiries concerning a request for
reasonable accommodation will be responded to from this email
address.
For more
information about equal employment opportunity protections, please
view the Know Your Rights poster .
3rd
Party Non-Solicitation Policy :
By
submitting candidates without having been formally assigned on and
contracted for a specific job requisition by Avantor, or by failing
to comply with the Avantor recruitment process, you forfeit any fee
on the submitted candidates, regardless of your usual terms and
conditions. Avantor works with a preferred supplier list and will
take the initiative to engage with recruitment agencies based on
its needs and will not be accepting any form of solicitation.
Qa Technician • Aurora, OH, Portage County, OH; Ohio, United States