AbbVie
Associate Scientist, Quality Control (Wednesday-Saturday 4pm-2:30am)
AbbVie, Worcester, Massachusetts, us, 01609
Associate Scientist, Quality Control (Wednesday‑Saturday 4pm‑2:30am)
Base pay range: $58,656.00/yr – $107,500.00/yr
Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com.
Purpose The Associate QC Scientist performs laboratory testing within a fast‑paced GMP environment in support of one or more of the following areas: raw materials, in‑process product, final bulk product, stability, and/or validation. The role involves analyzing test data, evaluating results, writing procedures, managing time efficiently under the guidance of a supervisor, trending data to support assay performance, and writing laboratory investigation reports.
Responsibilities
Performs test methods as written to support product/material release.
Maintains a safe work environment for self and others in accordance with procedural requirements.
Implements and maintains GMP with respect to laboratory records, procedures, and systems.
Performs a variety of laboratory techniques as trained.
Accepts responsibility for completing assigned tasks as committed and works with others to maintain a positive atmosphere.
Revises procedures as necessary and provides support for the department.
Maintains trend reports that support departmental performance.
Supports investigations.
Executes laboratory techniques with minimal error.
Qualifications
BA/BS in Chemistry, Biochemistry, Medical Technology, Biology, or equivalent science degree.
2+ years of related work experience.
Maintains certifications as needed for assigned job tasks.
Additional Information
The compensation range described above is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting. Individual compensation paid within this range will depend on many factors, including geographic location.
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance, and a 401(k) to eligible employees.
This job is eligible to participate in our short‑term and long‑term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or other form of compensation remain in the Company’s sole discretion.
Senior Level Entry level
Employment Type Full‑time
Job Function Research, Analyst, and Information Technology
Industries Pharmaceutical Manufacturing and Biotechnology Research
Referrals increase your chances of interviewing at AbbVie by 2x.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only – to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html
#J-18808-Ljbffr
Company Description AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com.
Purpose The Associate QC Scientist performs laboratory testing within a fast‑paced GMP environment in support of one or more of the following areas: raw materials, in‑process product, final bulk product, stability, and/or validation. The role involves analyzing test data, evaluating results, writing procedures, managing time efficiently under the guidance of a supervisor, trending data to support assay performance, and writing laboratory investigation reports.
Responsibilities
Performs test methods as written to support product/material release.
Maintains a safe work environment for self and others in accordance with procedural requirements.
Implements and maintains GMP with respect to laboratory records, procedures, and systems.
Performs a variety of laboratory techniques as trained.
Accepts responsibility for completing assigned tasks as committed and works with others to maintain a positive atmosphere.
Revises procedures as necessary and provides support for the department.
Maintains trend reports that support departmental performance.
Supports investigations.
Executes laboratory techniques with minimal error.
Qualifications
BA/BS in Chemistry, Biochemistry, Medical Technology, Biology, or equivalent science degree.
2+ years of related work experience.
Maintains certifications as needed for assigned job tasks.
Additional Information
The compensation range described above is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting. Individual compensation paid within this range will depend on many factors, including geographic location.
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance, and a 401(k) to eligible employees.
This job is eligible to participate in our short‑term and long‑term incentive programs.
Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or other form of compensation remain in the Company’s sole discretion.
Senior Level Entry level
Employment Type Full‑time
Job Function Research, Analyst, and Information Technology
Industries Pharmaceutical Manufacturing and Biotechnology Research
Referrals increase your chances of interviewing at AbbVie by 2x.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only – to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html
#J-18808-Ljbffr