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位置: Olde West Chester, 俄亥俄州, 美国
职位 ID R-054171
发布日期: Jun. 25, 2019

AtAstraZeneca we work together across global boundaries to make an impact and find answers to challenges. We do this with the upmost integrity even in the most difficult situations because we are committed to doing the right thing. We continuously forge partnerships that help pursue world-class medicines in new ways, combining our people’s exceptional skills with those of people from all over the globe.

Position Summary:

As the PET Process Facilitator, you will be a leader for the Process Operation (ie. Manufacturing/Packaging). In this capacity, the Process Facilitator manages the Process / Package Operation to produce high quality product in accordance with the PET operating strategy. As a responsible leader for the operation (potentially with other Process Facilitators), this must be done while maintaining effective employee relations and compliance to cGMP, other regulatory, and SOX requirements, as well as SHE obligations and AstraZeneca standards.

Main Responsibilities:

  • Provides direction to PET personnel in the efficient use of equipment and
  • materials to produce quality products in accordance with the PET Plan or Rhythm Wheel
  • Responsible for all PET activity to include coordination of support staff,
  • scheduling and improvement.
  • Promotes the use of safe work practices during all aspects of production and
  • ensures all external and AstraZeneca SHE standards are met on a daily basis.
  • Accountable for training of PET personnel on equipment, processes and
  • Standard Operating Procedures. Partners with PET Coach to develop training
  • plans and assist in providing resources for training.
  • Ensures that cGMP’s are used and followed during production of products so
  • that all FDA and international regulations are met. Responds to monthly internal audit observations.
  • Promotes a positive work environment by effectively administering AstraZeneca Human Resources policies and procedures including Performance Management and by communicating information to employees and responding to their concerns.
  • Ensures proper documentation practices are maintained consistently to company standards in manufacturing documents, training documentation, production logs, etc.
  • Generates reports for deviations, assists in the investigations, and
  • recommends/implements solutions to resolve deviations. Approves deviation investigations as appropriate. Responds to product defect notifications.
  • Authors, reviews, and approves Standard Operating Procedures and other documents to ensure integration of cGMPs and improve process efficiencies.
  • Promotes and encourages continuous improvement in efficiency, quality,
  • production, and safety through the use of team driven processes and key
  • performance indicators and recognition and rewarding high performance.
  • Collaborates with OE Engineers & PET Engineers to optimize process
  • performance.
  • Participates in the design, selection, installation and qualification of new
  • equipment, facilities, and processes.
  • Reviews, approves, and implements change control.
  • Provides career development and performance management for direct reports.
  • Co-owns life cycle management of PET/facility assets
  • Works collaboratively within and across PETs to ensure flow of product, sharing of best practices, and lean behaviors.
  • Maintains presence across multiple operating shifts.
  • Occasionally performs rolls for PET Lead when designated.

Minimum Requirements:

  • Bachelor of Science in Engineering, Pharmacy, related Science or business.
  • Minimum 5 years’ experience in GMP or regulated production environment
  • Minimum of 1-3 years previous supervisory experience.
  • Knowledge of FDA cGMP’s.
  • Strong communication and leadership skills.
  • Problem solving skills.


Preferred Background:

  • Experience working in a LEAN manufacturing environment
  • Working knowledge of LDMS or AZDocs, Microsoft applications, SAP, Trackwise
  • Training or experience in formulation, filling, packaging, validation, technology

transfer, change control.

  • Knowledge or previous experience in managing technical programs/projects
  • Strong mechanical, electrical, troubleshooting and problem solving abilities.
  • Ability to direct and participate in cross-functional teams.
  • Project management skills.

To be considered for this exciting opportunity, please complete the full application on our website at your earliest convenience – it is the only way that our Recruiter and Hiring Manager can know that you feel well qualified for this opportunity.  If you know someone who would be a great fit, please share this posting with them.

AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law

Senior Process Facilitator
制造

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