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. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Parenteral and Eyecare Operations S&T organization is responsible for the technical transfer and support of marketed and pipeline injectable products. This person will support the AbbVie Technical Operation functions and the AbbVie Technical Centers worldwide. Identify and resolve manufacturing issues for commercial and Research and Development products. Provides technical support to cross-functional teams during development, commercial launch or problem solving for a given drug product through investigational experimental approach, and optimization. The work would include support of both drug product process, analytical testing, and test method development activities. This person will also support process development lab management in partial capacity. The person is expected to demonstrate experimental precision and should possess general understanding of core disciplines supporting parenteral processes. Responsibilities: + Highly autonomous and productive in performing laboratory research and/or method development. + Liaison between functional groups as well as sister divisions (ie Operations, Quality, Regulatory, Validation, Materials Management, R&D, Analytical Test Labs, Stability and API) + Capable of working totally independently and providing technical support to a project team. + Provide individual technical support of all scale-up activities and maintain timelines for on-going projects. + Write/co-author process memos and scientific reports in support of Regulatory Submissions, Regulatory Field Alerts and supportive quality control and manufacturing documents. + Responsibility of writing and/or reviewing deviations, NCMRs and investigations in terms of the technical content. + Anticipate, recognize and resolve problems. + Provides guidance/mentoring for summer interns in the department. + Provides technical support for introduction of new products and for process improvements to existing products. + Understand and adhere to corporate standards regarding code of conduct, safety, appropriate handling of materials, controlled drug and radioactive compounds, GxP compliance, and animal care where applicable. Qualifications + Bachelors, Masters, or PhD in chemical engineering, pharmaceutical sciences, chemistry, pharmaceutics, or related disciplines with 10+ (Bachelors), 8+ (Masters), or 0-3+ (PhD) years of relevant industry experience. + Strong technical background in pharmaceutical dosage forms. Developed problem solving abilities. Scientific report writing skills. Knowledge and experience in working in a cGMP environment. Knowledge of regulatory issues involved with CMC. Good organizational skills. Excellent communication (oral and written) and interpersonal skills. 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. 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 Salary: $91,500 - $173,500