Production Supervisor for Manufacturing (Temporary 6 months)

Heredia - Costa Rica

Monthly Salary: Not Disclosed

Posted on: Yesterday

Vacancies: 1 Vacancy

Job Summary

POSITION OBJECTIVE: Efficiently manage resources product control and implementation of improvements adding value to all production processes according to the companys defined quality and safety standards and regulations to achieve the goals and objectives established for the manufacturing area.

SUPERVISORY RESPONSIBILITIES: This position may have supervisory responsibility over Manufacturing personnel.

KEY RESPONSIBILITIES:

Collaborate in in-process product control on all production lines under your charge to ensure priority compliance and identify possible restrictions.
Ensure production line results to monitor compliance with the Production Plan.
Evaluate and implement changes in procedures catalogs First Article First Shipment First Article and other process improvement opportunities to ensure they are carried out efficiently and adequately aiming for operational cost reduction.
Act as Subject Matter Expert (SME) for the production lines under your charge clarifying procedures techniques and processes to ensure the correct execution of tasks within the production line as well as supporting projects.
Provide support in production capacity management to agree on production commitments with the logistics department.
Support during internal or external audit processes required by the regulatory entity acting as SME for the areas under your charge.
Lead departmental improvement initiatives such as SWAT Operating Supplies and any others responding to objectives set by the company leading improvement teams and meeting departmental targets.
In case of deviations from procedures in your area investigate the event and identify preventive and corrective actions to eliminate the root cause of these.
Ensure timely disposition of retained material according to the companys quality system always ensuring product quality and prudent resource management.
Provide support to Human Resources to contribute to induction processes position changes and other cases in your area.
Ensure the motivation of employees under your charge by timely reinforcing and recognizing formally and informally behaviors that promote AbbVies culture.
Guarantee compliance with corporate and legal EHS requirements by adhering to policy and internal procedures and ensure compliance through strategies internal controls communication and necessary trainings.
Perform all other functions inherent to the position and those assigned by the immediate supervisor to make the best use of the areas resources.

Qualifications :

Bachelors Degree in Industrial Engineering Industrial Production Engineering Chemical Engineering or Industrial Chemistry.
Advanced English.
At least 2 years of knowledge and experience in the medical industry.
At least 2 years of experience managing personnel in a manufacturing environment.
At least 1 year of experience in the quality area (desirable).
Ongoing Masters studies in fields related to Manufacturing (desirable).
Available to work full on site in Heredia shift A1 (monday to friday from 6:00 am to 3:30 pm)

Additional Information :

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 & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

Employment Type :

Full-time

POSITION OBJECTIVE: Efficiently manage resources product control and implementation of improvements adding value to all production processes according to the companys defined quality and safety standards and regulations to achieve the goals and objectives established for the manufacturing area.SUPER...

SUPERVISORY RESPONSIBILITIES: This position may have supervisory responsibility over Manufacturing personnel.

KEY RESPONSIBILITIES:

Collaborate in in-process product control on all production lines under your charge to ensure priority compliance and identify possible restrictions.
Ensure production line results to monitor compliance with the Production Plan.
Evaluate and implement changes in procedures catalogs First Article First Shipment First Article and other process improvement opportunities to ensure they are carried out efficiently and adequately aiming for operational cost reduction.
Act as Subject Matter Expert (SME) for the production lines under your charge clarifying procedures techniques and processes to ensure the correct execution of tasks within the production line as well as supporting projects.
Provide support in production capacity management to agree on production commitments with the logistics department.
Support during internal or external audit processes required by the regulatory entity acting as SME for the areas under your charge.
Lead departmental improvement initiatives such as SWAT Operating Supplies and any others responding to objectives set by the company leading improvement teams and meeting departmental targets.
In case of deviations from procedures in your area investigate the event and identify preventive and corrective actions to eliminate the root cause of these.
Ensure timely disposition of retained material according to the companys quality system always ensuring product quality and prudent resource management.
Provide support to Human Resources to contribute to induction processes position changes and other cases in your area.
Ensure the motivation of employees under your charge by timely reinforcing and recognizing formally and informally behaviors that promote AbbVies culture.
Guarantee compliance with corporate and legal EHS requirements by adhering to policy and internal procedures and ensure compliance through strategies internal controls communication and necessary trainings.
Perform all other functions inherent to the position and those assigned by the immediate supervisor to make the best use of the areas resources.

Qualifications :

Bachelors Degree in Industrial Engineering Industrial Production Engineering Chemical Engineering or Industrial Chemistry.
Advanced English.
At least 2 years of knowledge and experience in the medical industry.
At least 2 years of experience managing personnel in a manufacturing environment.
At least 1 year of experience in the quality area (desirable).
Ongoing Masters studies in fields related to Manufacturing (desirable).
Available to work full on site in Heredia shift A1 (monday to friday from 6:00 am to 3:30 pm)

Additional Information :

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 & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

Work :

Employment Type :

Full-time

Key Skills

Lean Manufacturing
Six Sigma
Continuous Improvement
FDA Regulations
Lean
Packaging
Production Planning
cGMP
Cell Culture
Leadership Experience
Supervising Experience
Manufacturing

Apply Now

About Company

AbbVie

AbbVie is a global biopharmaceutical company focused on creating medicines and solutions that put impact first for patients, communities, and our world. We aim to address complex health issues and enhance people's lives through our core therapeutic areas: immunology, oncology, neuro ... View more

View Profile View Profile

AI AutoApply

Apply to 100+ jobs with one click