Laboratory Technician VI

AbbVie Inc.; Waco (TX); On-site; USD 65,000 - 95,000; Full time

Benefits offered by this job

Paid time off

Medical/dental/vision insurance

401(k)

Short-term incentive programs

Job summary

AbbVie Inc. in Waco is seeking a Specialist in Chemistry to support the manufacturing process of Rx and OTC pharmaceutical products. Knowledge of GMPs and technical writing skills is required. The role involves stability testing, materials handling, and collaboration with QA and production teams to ensure product quality.

The position emphasizes working in a GMP-regulated environment with aseptic requirements and requires strong analytical abilities and precise documentation skills.

Qualifications

• Bachelor's Degree with an emphasis in Chemical or related science.
• 5 years of experience in pharmaceutical manufacturing chemistry lab or similar laboratory experience.
• Intermediate knowledge of Microsoft Office. Experience with LIMS and Trackwise preferred.
• Experience working in a GMP regulated environment preferred.
• Experience working in an aseptic environment preferred.
• Excellent analytical skills and problem-solving skills.
• Strong math skills, including the comprehension of metric weights and measures, performing complex calculations, and spreadsheet management.
• Ability to read, comprehend, write, and communicate effectively in English.
• Ability to work with minimal supervision.
• Ability to provide direction for functional area.

Responsibilities

• Provides technical support to Chemistry Laboratory staff in executing stability protocols and conducting testing. Supports laboratory operations and manufacturing activities related to raw materials, in-process materials, and finished products.
• Conducts investigations on out of specification test results.
• Organizes and may perform testing of raw materials (including USP water), bulk samples, and finished product to assure the chemical quality of the product.
• Evaluates stability of raw materials, bulk samples, and finished product per established protocols.
• Interfaces with QA counterparts to optimize laboratory support of QA and production activities.
• Works effectively with chemists to complete special sample analyses as required.
• Preforms other duties as assigned and assists on special projects as required.
• Ensures compliance with governmental and regulatory requirements including FDA, ISO 13485, MDD, OSHA, and EPA.
• Works to ensure environmental, health and safety compliance.

Skills

Analytical skills

Problem solving

Math skills

English communication

Education

Bachelor's Degree in Chemical or related science

Tools

SAP

Microsoft Office

LIMS

Trackwise

Job description

About AbbVie

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 including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube.

Job Summary

The Specialist in Chemistry is responsible for supporting the manufacturing process of Rx and OTC pharmaceutical products in Waco. Knowledge of GMPs and technical writing skills.

Responsibilities

This position is responsible for the following:

• Provides technical support to Chemistry Laboratory staff in executing stability protocols and conducting testing. Supports laboratory operations and manufacturing activities related to raw materials, in-process materials, and finished products.


• Conducts investigations on out of specification test results.


• Organizes and may perform testing of raw materials (including USP water), bulk samples, and finished product to assure the chemical quality of the product.


• Evaluates stability of raw materials, bulk samples, and finished product per established protocols.


• Interfaces with QA counterparts to optimize laboratory support of QA and production activities.


• Works effectively with chemists to complete special sample analyses as required.


• Preforms other duties as assigned and assists on special projects as required.

Regulated Responsibilities (including cGMP and EHS)

Incumbent is expected to be fully compliant with all criteria established by governmental agencies, Ministry of Health, and legislative requirements including, but not limited to: the FDA, European Community (EC), ISO 13485 - Medical Devices, European Economic Community Medical Device Directive (MDD), Canadian Medical Device Regulations (CMDR), OSHA, Sarbanes-Oxley, EPA, DOT, EEOC, and ADA.

Incumbent will work to ensure that the company is in compliance with all environmental, health and safety requirements and assure our business practices enhance the welfare of our customers, employees and the community in which we operate.

Qualifications

• Bachelor's Degree with an emphasis in Chemical or related science.


• 5 years of experience in pharmaceutical manufacturing chemistry lab or similar laboratory experience.


• Intermediate user knowledge of Microsoft Office. Experience with LIMS and Trackwise preferred.


• Experience working in a GMP regulated environment preferred.


• Experience working in an aseptic environment preferred.


• Excellent analytical skills and problem-solving skills.


• Strong math skills, including the comprehension of metric weights and measures, performing complex calculations, and spreadsheet management.


• Ability to perform detailed tasks and document activities accurately.


• Able to work in an aseptic controlled environment which includes wearing PPE, aseptic gowning qualifications, and subsequent gowning requalification's.


• Specific vision requirements include 20/20 near vision (can be corrected with eyeglasses or contacts).


• Ability to work and communicate with others in a professional and effective manner, within a team-oriented environment.


• Ability to read, comprehend, write, and communicate effectively in English.


• Intermediate user knowledge and understanding of Windows based computer systems such as Microsoft Office, with an ability to learn other computer-based systems. Experience with SAP preferred.


• Strong written and verbal communication skills.


• Ability to work with minimal supervision.


• Ability to provide direction for functional area.

Compensation

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.

Benefits

• 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.

Equal Opportunity

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