AbbVie

Sr Mgr, Quality Laboratories

Posted on: 15 Jan 2021

Branchburg, NJ

Job Description

About AbbVie
AbbVies mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on peoples lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, womens health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn.

Envision working with energetic colleagues and inspirational leaders. Now, place yourself in that mix; leading discussions, asking the right questions and driving results.

Mgr, Quality Laboratories

What Your New Manager Wants You To Know

I am looking for an experienced Sr. Manager, QC Labs will act as subject matter expert (SME) on microbiology, sterilization, and production clean room controls including aseptic processing and environmental monitoring.

Sincerely,

Sr. Mgr, Quality Laboratories

YOU ARE more than just a title, YOU ARE

A strategic thinker: Align and excite internal stakeholders to facilitate success through strong leadership, strategic thinking and personal drive.

First class team player: Collaborate across multiple disciplines to ensure compliance and ability to influence cross-functional teams and senior leadership.

You Will

* Management of Quality Control Laboratory personnel and activities, including QC Testing, Finished Product Testing, Microbiology Testing and the LIR/NCR/CAPA/Change Control processes as they relate to the laboratory.
* Responsible for bringing innovative solutions to complex problems, especially in the areas of improved efficiencies and automation.
* Ensure there is adequate, trained staff to accomplish Quality objectives, and ensure the collection, organization, analysing and reporting on data regarding non conformances (OOS), and other quality issues, as determined by the Sr. Mgr. Quality Control.
* Establish in-house capability of microbiological testing and microbial identification. Provide hands on guidance and training to junior level associates on laboratory testing and assure overall compliance to cGMPs and GDP.
* Design and lead sterilization and microbiological needs of project teams based on regulation and guidelines, which includes autoclave loading pattern, terminal (ebeam) sterilization of product, in-process bioburden reduction and testing.
* Assist with the development and implementation of policies and procedures as they pertain to all QC and Microbiology laboratories supporting the overall Quality program.

Qualifications

You Bring

* 5-10 yrs. with Ph.D.
* >10 yrs. with a Bachelor or Masters Degree
* Daily management of 4 direct and approximately 36 indirect laboratory staff
* Extensive knowledge/experience of sterilization process, aseptic processing and clean room regulations, industry practices, quarterly dose audit and related ISO standards.
* Experience with Microsoft Office Applications including Word, Excel, PowerPoint, and Outlook. Experience and knowledge in Data Integrity and governing regulations.
* Ability to serve as a senior technical advisor. Ability to communicate at all levels and deliver highly technical information in clear and easy-to-understand terms.
* Demonstrated organizational development skills. Able to identify, challenge and mentor department associates providing feedback, guidance and direction supporting individual development.
* Organize and prioritize tasks and effectively communicate priorities to direct reports, peers and management.
* In-depth knowledge in FDA, ISO, AATB, and USP regulations/guidelines.
* Demonstrated experience working with internal and external customers. i.e. vendors, collaborating investigators, contract test labs. Comprehensive understanding of microbiology, aseptic processing and sterilization.
* Willingness to work with potentially bio-hazardous materials including human and animal tissues and a variety of media.
* Reviews sterilization microbiological practices against current industry regulations.
* Experience developing sterilization methods; steam sterilization, radiation, aseptic processing.
* Experience with regulatory guidelines for sterilization, microbiological, analytical and histological practices relating to clean room manufacturing, aseptic processing, and sterilization of human tissue, medical devices or pharmaceuticals.
* Demonstrated mathematical, statistical, communication, technical writing, presentation, critical thinking and problem-solving skills.

Significant Work Activities
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)
Travel
No
Job Type
Experienced
Schedule
Full-time
Job Level Code
IC
Equal Employment Opportunity
At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis 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, protected veteran status, or any other legally protected characteristic.

AbbVie

Chicago, IL

AbbVie Inc. discovers, develops, manufactures, and sells pharmaceutical products in the United States, Japan, Germany, Canada, Italy, Spain, the Netherlands, the United Kingdom, Brazil, and internationally. The company offers HUMIRA, a therapy administered as an injection for autoimmune and intestinal Behçet's diseases; IMBRUVICA to treat adult patients with chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), mantle cell lymphoma, waldenström’s macroglobulinemia, marginal zone lymphoma, and chronic graft versus host disease; VENCLEXTA, a BCL-2 inhibitor used to treat adults with CLL or SLL; VIEKIRA PAK, an interferon-free therapy to treat adults with genotype 1 chronic hepatitis C virus (HCV); TECHNIVIE to treat adults with genotype 4 HCV infection; and MAVYRET to treat patients with chronic HCV genotype 1-6 infection.

It also provides KALETRA, an anti-human immunodeficiency virus (HIV)-1 medicine used with other anti-HIV-1 medications to maintain viral suppression in HIV-1 patients; NORVIR, a protease inhibitor indicated in combination with other antiretroviral agents to treat HIV-1; and SYNAGIS to prevent respiratory syncytial virus infection at-risk infants. In addition, the company offers AndroGel, a testosterone replacement therapy for males; CREON, a pancreatic enzyme therapy for exocrine pancreatic insufficiency; Synthroid to treat hypothyroidism; and Lupron to treat prostate cancer, endometriosis, and central precocious puberty, as well as anemia.

Further, it provides Duopa and Duodopa, a levodopa-carbidopa intestinal gel to treat Parkinson’s disease; Sevoflurane, an anesthesia product; and ORILISSA, a non-peptide small molecule gonadotropin-releasing hormone antagonist for women with moderate to severe endometriosis pain. It has collaborations with Alector, Inc.; Janssen Biotech, Inc.; Galapagos; Bristol-Myers Squibb Company; and Calico Life Sciences LLC. The company was incorporated in 2012 and is headquartered in North Chicago, Illinois.

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