Associate Scientist, Quality Control (2nd shift, Wed-Sat, 4pm-2:30am)

Initial Therapeutics, Inc.; Worcester (MA); On-site; USD 50,000 - 80,000; Full time

Job summary

An established industry player is seeking an Associate QC Scientist to join their dynamic team in a fast-paced GMP environment. In this role, you will perform critical laboratory testing, analyze data, and ensure compliance with industry standards. You will have the opportunity to work with a variety of laboratory techniques while contributing to the success of innovative health solutions. If you are passionate about science and eager to make a significant impact in the field of healthcare, this position offers a rewarding career path with comprehensive benefits and a supportive work culture.

Benefits

Paid Time Off

Medical Insurance

Dental Insurance

Vision Insurance

401(k)

Short-term Incentive Programs

Qualifications

• 2+ years of related work experience required.
• Ability to perform various laboratory techniques with minimal error.

Responsibilities

• Perform test methods to support product/material release.
• Maintain a safe work environment and comply with GMP regulations.
• Assist in writing lab investigation reports and maintaining trend reports.

Skills

Laboratory Testing

Data Analysis

GMP Compliance

Problem Solving

Education

BA/BS in Chemistry

BA/BS in Biochemistry

BA/BS in Medical Technology

BA/BS in Biology

Job description

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 atwww.abbvie.com. Follow @abbvie onX,Facebook,Instagram,YouTube,LinkedInandTik Tok.

Job Description

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. Analyzes test data and evaluates results. Writes procedures with guidance. Works under the guidance of a supervisor but can manage time efficiently in achieving timely completion of assigned duties. Assists in trending data to support assay performance. Assists in writing lab investigation reports.

The work schedule and hours for this position are Wednesday through Saturday, 4:00pm to 2:30am.

Responsibilities:

• Performs test methods as written to support product/material release.
• Understands and maintains a safe work environment for themselves and others in accordance with procedural requirements.
• Understands, implements and maintains GMP with respect to laboratory records, procedures and systems in accordance with procedural requirements.
• Will perform a multitude of laboratory techniques for which they are trained.
• Accepts responsibility to complete assigned tasks as committed and works with others to maintain a positive atmosphere to accomplish business objectives.
• Revises procedures as necessary and provides support for the department.
• Helps maintain trend reports, which support departmental performance.
• Support investigations.
• Will effectively perform a multitude of laboratory techniques for which they are trained on with minimal error.

Qualifications

• BA/BS in Chemistry, Biochemistry, Medical Technology, Biology or equivalent science degree.
• 2+ years of related work experience.
• Maintains their certifications as needed for assigned job tasks.

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

• The compensation range described below 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 based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.

• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.

• This job is eligible to participate in our short-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 any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie's policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.

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