AbbVie

Supv, Manufacturing

Employer
AbbVie
Location
Branchburg, NJ, United States
Posted
Nov 18, 2020
Ref
204071
Required Education
Bachelors Degree
Position Type
Full time
Position Overview
The Supervisor, Manufacturing, is responsible for overseeing colleagues in a manufacturing environment. The Supervisor plans and assigns work, implements policies and procedures and recommends improvements in production methods, equipment, operating procedures and working conditions. This individual supports the manager in developing an enthusiastic, motivated and flexible team by building working relationships ensuring that Environmental, Health & Safety requirements are adhered to. The Supervisor manages the team on best practices and SOPs while ensuring all Quality requirements are met.

Main Areas of Responsibilities
    Ability to communicate and document technical matters with Maintenance Engineering, Quality, Senior Management Team and Auditors. Demonstrate a clear understanding of ISO, regulatory requirements and of GMP standards through compliance of the LifeCell Quality Policy Helps in maintenance and enforcement of the quality system. Participates in continued improvement activities. Collaborate in a team based environment in resolving equipment and process related issues. Comply with cGMP's and ISO requirements where applicable in the facility. Assist in production as necessary. Develop and review SOPs. Review of production data. Inventory control. Maintain clean facilities. Maintain safe work place Supervision of Production staff. Production scheduling and staffing.


Qualifications
The following listed requirements need to be met at a minimum level to be considered for the job:
Education and Experience
    Required:
      Bachelor's degree in business, scientific discipline or related field with 2 - 4 years of experience in a manufacturing management High school diploma (or equivalent) with 8+ years' related experience
    Preferred :
      Experience managing teams in a manufacturing environment Experience working within the Pharmaceutical, Biotech, Medical Device field Experience working within a regulated environment Experience with FDA, GMP, GTTP, GDP, and/or ISO

Essential Skills, Experience, and Competencies (includes Licenses, Credentials)
    Experience managing medical device in manufacturing Demonstrated experience managing others and being responsible for coaching, mentoring, developing and performance evaluation Experience managing complex production processes Experience interpreting managing the development of SOP's Demonstrated experience with conflict management Demonstrated communication and presentation skills


Job Type
Standard

Schedule
Full-time

Equal Employment Opportunity
At Allergan, 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.