12 days old

Supervisor of Manufacturing

Salt Lake City, UT
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Company Info

Teva is a global pharmaceutical leader and the worlds largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide.  Our employees are at the core of our success, with colleagues in over 80 countries delivering the worlds largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and weve built a promising pipeline centered around our core therapeutic areas.  We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation.  This is how we improve health and enable people to live better, healthier lives.  Join us on our journey of growth!

Job Description

SummaryUnder general supervision, directs and oversees the manufacturing process operations.  Ensures that all phases of manufacturing activity are performed in a safe manner and in compliance with cGMP and Standard Operating Procedures (SOP's).  Ensures that Company and government compliance are adhered to.

 

Essential Job Functions: This is not intended as a comprehensive list; it is intended to provide a representative summary of the major duties and responsibilities. Incumbent(s) may not be required to perform all duties listed, and may be required to perform additional, position-specific tasks.

  • Carries out supervisory responsibilities in accordance with the organizations policies, procedures, and state, federal and local laws.
  • Supervises and coordinates the manufacturing work schedule to meet production requirements.
  • Assigns and delegates work assignment responsibilities to subordinate hourly personnel.
  • Performs on-going cGMP and safety training to department process operators.
  • Assures that manufacturing operations are performed in compliance with batch records, SOP's, and cGMP's.
  • Revises batch records and SOP's as required.
  • Coordinates with Quality Control Department for timely release of intermediate sample results and packaging final product release.
  • Reviews and approves time sheets for hourly subordinate personnel.
  • Performs responsibilities associated with department hiring, training, problem resolution, work assignment delegation and attendance tracking; applies effective implementation of employee disciplinary corrective action programs; conducts performance evaluations.
  • Ensures compliance with Company equipment and safety rules and regulations.
  • Ensures compliance with all Company policies and procedures.
  • Maintains management presence in the manufacturing area through the monitoring and control of manufacturing process.
  • Apprises Manufacturing Manager of all current manufacturing process issues.
  • Improves the efficiency of the operation by analyzing and correcting production equipment and processing problems; troubleshoots equipment by making minor adjustments to compensate for product processing problems.
  • Coordinates with materials management scheduling and quality assurance documentation to ensure scheduling efficiency and batch record audit completion.
  • Interfaces with external contacts/vendors to facilitate the introduction of new equipment.
  • Performs related duties as assigned

Qualifications

Knowledge of

  • Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirement.
  • Effective oral and written communication skills.
  • Proper English, grammar and punctuation.
  • Principles of supervision and training.
  • Manufacturing processes, equipment procedures and systems.
  • Principles of safety, workers' compensation, OSHA and related principles and practices.
  • Current Company policies and procedures, including safety rules and regulations.
  • Pharmaceutical principles, practices, and their application.
  • FDA, SOP, cGMP and other standards, guidelines, and pertinent regulatory compliance requirements.
  • Principles of mathematics and statistical computations.

 

Minimum Qualifications:  Bachelors Degree in chemical engineering, pharmacy, chemistry or related field from an accredited college or university, and three (3) five (5) years of responsible supervisory experience, preferably in pharmaceutical, food, or cosmetic manufacturing environment; or an equivalent combination of education and experience.

Function

Manufacturing

Sub Function

Manufacturing/Operations

Reports To

In process of validation

Tevas Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.

Posted: 2019-02-05 Expires: 2019-03-08

Join us at the forefront of pharmaceutical research and production. With state-of-the-art facilities, highly skilled colleagues, and a high-powered organizational culture, Teva offers you countless possibilities to make a real difference in people's lives and add value to your career.

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Supervisor of Manufacturing

Teva Pharmaceuticals
Salt Lake City, UT

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