Supervisor, Manufacturing I

Abbvie Careers
Branchburg, NJ Full Time
POSTED ON 1/14/2022 CLOSED ON 4/15/2022

What are the responsibilities and job description for the Supervisor, Manufacturing I position at Abbvie Careers?

About AbbVie
AbbVie’s 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 people’s lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women’s 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.

Job SUMMARY:

With minimum guidance, provides line supervision, scheduling and hands-on assistance in processing tissue. Prepares and compiles documentation for tissue processing and reviews for completeness and accuracy. Implements new procedures as directed. Assists in developing and revising Standard Operating Procedures. Helps in training of all employees. Responsible for managing inventory of Production supplies by interacting with the Materials Department and ordering supplies as necessary. Responsible for overseeing proper housekeeping of Production areas. Interacts with QA and QC departments to assure safety in the work place and adherence to Quality System.

 Second Shift (4:15pm – 4:30am)

 

 

 

KEY DUTIES AND RESPONSIBILITIES: Describe scope:

% of Time or

Importance

  1. Supervision of Production staff.
  2. Production scheduling and staffing.

25%

  1. Assist in production as necessary.
  2. Develop and review SOPs.
  3. Review of production data.
  4. Inventory control.
  5. Maintain clean facilities.
  6. Maintain safe work place

25%

  1. Helps in maintenance and enforcement of the quality system.
  2. Participates in continued improvement activities.
  3. Collaborate in a team based environment in resolving equipment and process related issues.
  4. Comply with cGMP’s and ISO requirements where applicable in the facility.

25%

  1. Ability to communicate and document technical matters with Maintenance Engineering, Quality, Senior Management Team and Auditors.
  2. Demonstrate a clear understanding of ISO, regulatory requirements and of GMP standards through compliance of the LifeCell Quality Policy

25%

 

 


Qualifications

 

 

• Requires a Bachelor’s degree or equivalent; 3-5 plus years’ experience in all aspects of manufacturing/ production processes
• Computer proficiency and scheduling experience required; good writing skills.
• Working knowledge of safety, quality systems, and cGMPs is required
• Familiarity with industrial automation (e.g., distributed control and PLC-based systems
• Familiarity with equipment and facilities validation
.

 

 


Significant Work Activities
Continuous standing 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.

Salary : $0

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