1+ months

Manufacturing Engineer II

SAIC
Sunrise, FL
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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

Essential Duties:

  • Trouble shoots equipment and processes in the Packaging areas.
  • Interfaces with Quality Assurance and Research and Development on Process requirements for new and current products.
  • Identify recurrent problems and to recommend and implement the upgrades of current equipment and the purchase of new equipment and regulatory requirements.
  • Assist manager with on-site transfer projects and product scale-up activities.
  • Researches and recommends improvements in Packaging and control systems.
  • Complies with all Company policies and procedures, including safety rules and regulations and all department Standard Operating Procedures (SOPs).
  • Prepares capital expenditure requests.
  • Performs related duties as assigned.

 

Responsibilities:

 

  • In depth knowledge of Programmable Logic Controllers (PLC) technology. Preferably Allen Bradley and Siemens.
  • Superior Mechanical and Electrical Troubleshooting skills- Preferably packaging equipment. Identifying root causes and correcting and preventing recurrence, implementing TPM techniques.
  • Experience in identification, recommendation, procurement, qualification and validation of Packaging equipment and new components.
  • Identify and implement plant improvements through equipment reliability, equipment. changes- Demonstrated success improving Safety, Quality, OEE of operations.
  • Experience managing engineering change processes Workflows, Controls and Documentation.
  • Demonstrated success in knowledge transfer to team.

 

Qualifications

Knowledge of:

  • Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements.
  • Pharmaceutical packaging validation/qualification of unit dose packaging equipment practices and procedures.
  • Installation, operation, performance and maintenance of packaging equipment.
  • Advanced electronic/optical verification systems installation and maintenance.
  • Advanced research, analysis, and interpretation of technical scientific packaging engineering information and design practices and methods.
  • Project team leadership, supervision and training methods and techniques.
  • Business, scientific and personal computer hardware and software applications.
  • Business English usage, spelling, grammar and punctuation.
  • Current Company policies, practices and procedures, including safety rules and regulations.

Skill in:

  • Analyzing problems, identifying solutions, recommending and implementing methods, procedures and/or techniques for resolution.
  • Designing packaging engineering processes for pharmaceutical products.
  • Communicating clearly and concisely, both orally and in writing.
  • Managing multiple projects, duties and assignments.
  • Leading, coordinating and reviewing the work of multiple project team activities, delegating assignments, and providing training to less experienced staff.
  • Operating scientific and personal computers.
  • Interpreting and applying Federal, state and local policies, procedures and regulations.
  • Establishing and maintaining cooperative working relationships with others.

Physical Requirements and Working Conditions: Incumbents in this class are subject to extended periods of sitting, standing, walking, vision to monitor, lifting materials weighing up to 25 pounds and moderate to loud noise levels. Incumbents may be exposed to toxic materials, toxic gases, electrical hazards, dangerous tools and equipment and the antibiotics penicillin and cephalosporin. Work is performed in a pharmaceutical manufacturing environment.

Minimum Qualifications: Bachelors Degree in Packaging Engineering or related engineering field from an accredited college or university, and seven  (7)  ten (10) years related engineering experience, or at least three (3) years satisfactory performance as a Packaging Engineer, Senior; or an equivalent combination of education and experience may be substituted. Open to industries including consumer goods, automotive,etc.

Function

Manufacturing

Sub Function

Packaging Engineering

Reports To

Associate Director Site Engineering

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: 2018-12-17 Expires: 2019-02-16

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Manufacturing Engineer II

SAIC
Sunrise, FL

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