Qc Analyst Ii - Lexington, United States - ARIAD

ARIAD

Verified Company

Lexington, United States

2 weeks ago

Posted by:

Mark Lane

beBee recruiter

Description

At Takeda, Quality has always been a priority for us, throughout our long history. Today, what we do in Global Quality touches every part of our diverse organization.

It's reflected in our end-to-end Quality Management System that encompasses R&D, Manufacturing & Distribution, Commercial, Vaccines and our BioLife Plasma collection network.

When you're a part of our team, you'll do meaningful work that makes an impact on the lives of patients.

Learn more about us and explore the opportunities to build a remarkable career.

Job ID R0122905
Date posted 05/13/2024
Location Lexington, Massachusetts
Job Title: QC Analyst II

Location:
Lexington, MA

About the role:

As a QC Analyst II, you will focus on the daily lab operations and execution of testing to support manufacturing operations /validation/or development studies.

You will also test samples from drug substance and drug product manufacturing, stability and multiple protocol studies using approved test methods or test methods derived from QC technical protocols.

You will also help with sampling activities. You will report to the Quality Control Supervisor.

How you will contribute:

Maintain operational and GMP readiness of the QC areas and maintain important reagent inventory such as antibodies and cell banks at business appropriate quantities.
Participate in more complex projects, and multiple quality systems with general guidance.
Support commercial and clinical testing for defined sitebased and external programs, and method transfer and validation. Introduce new equipment and technology to improve sustainability and compliance is expected.
Establish and recommend changes to policies which effect subordinate organizations.
Test execution, participate in training analysts, trouble shooting of methods.
QC operations support which requires data review, data trending, OE/5S/LEAN programs, maintenance of equipment and reagents, lab house keeping, support for other QC groups. Compliance and quality systems (SOP revisions, input to quality systems records).
Involvement in multiple departmental and teams and programs; inspection and regulatory support.
Product Testing: Area focuses on techniques such as SDS-PAGE Silver, QPCR, Potency, Kinetics assay, Enzyme Activity, pH, Osmo, A280 etc., to support inprocess, release and stability testing.
May refer to established precedents and policies.

What you bring to Takeda:

Typically requires a bachelor's degree and a minimum of 5+ years of related experience. (science related degree would be ideal).
Previous experience in a GMP QC role would be ideal.
Main Skills: Microsoft Office, Laboratory Information Management System, SAP, Trackwise, compliance and science understanding.

Important Considerations:

At Takeda, our patients rely on us to deliver quality products.

As a result, we must follow strict rules in our manufacturing facilities to ensure we are not endangering the quality of the product.

In this role, you may:

May be required to wear personal protective equipment (PPE) and other clean room garments daily. This may include safety shoes, safety glasses, aprons, face shields, lab coats, full body gowns, hair nets and gloves and hearing protection.
Repetitive bending and reaching to setup and breakdown equipment (if required by specific activity).
Ability to work around chemicals (if working around the laboratories).
Ability to wear personal protective equipment such as gloves, gowning, and respiratory protection in some cases.
Ability to walk and stand for periods of time.
Individual may be required to participate in environmental chamber monitoring program which would include the use of an oncall mobile phone as well as onsite support during nonbusiness hours.
Need to remove all makeup, jewelry, contact lenses, nail polish and/or artificial fingernails while in the manufacturing environment.
Work in a cold, wet environment.
Work multiple shifts, including weekends, or be asked to work supplemental hours, as necessary.
Work around chemicals such as alcohol, acids, buffers and Celite that may require respiratory protection.

More about us:

At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs.

Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work.

Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do.

We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world.

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Takeda Compensation and Benefits Summary
We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all em