PharmEng Technology

Equipment Project Manager

PharmEng Technology  •  Bloomington, IN (Onsite)  •  7 days ago
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Job Description


The Equipment Project Manager is responsible for overseeing and managing all aspects of equipment projects related to packaging and inspection. This includes ensuring that equipment meets user requirements, process parameters, and global regulatory guidelines. The role provides Operations, Quality Assurance, and regulatory bodies with scientifically sound, documented evidence that systems and processes will perform as required, ensuring a quality, compliant manufacturing environment.

Key Responsibilities:

  • Manage and oversee equipment projects related to packaging and inspection from initiation to completion.
  • Ensure equipment validation and maintenance in compliance with user requirements, process parameters, and regulatory guidelines.
  • Develop and execute project plans, timelines, and budgets.
  • Collaborate with cross-functional teams, including Operations, Quality Assurance, and Engineering, to ensure project objectives are met.
  • Conduct risk assessments and identify potential project issues and mitigation strategies.
  • Provide scientifically sound, documented evidence to support equipment validation and project activities.
  • Maintain accurate and comprehensive documentation of project activities and deliverables.
  • Ensure effective communication and coordination between project stakeholders.
  • Provide training and support to team members and other departments as needed.

Qualifications:

  • Bachelor's degree in Engineering, Packaging Technology, or a related field.
  • Minimum of 7 years of experience in equipment project management, with a focus on packaging and inspection.
  • Strong understanding of GMP regulations and validation principles.
  • Excellent project management and organizational skills.
  • Strong analytical and problem-solving abilities.
  • Effective communication and interpersonal skills.
  • Ability to work independently and as part of a team.

Preferred Qualifications:

  • Master's degree in Engineering, Packaging Technology, or a related field.
  • Experience with packaging and inspection equipment in a regulated manufacturing environment.
  • Knowledge of current Good Manufacturing Practices (cGMP) and Good Laboratory Practices (GLP).
PharmEng Technology

About PharmEng Technology

PharmEng Technology, now part of Efor Group, leader in Compliance Engineering, is a leading provider of technical services and solutions to the pharmaceutical, biotechnology, and healthcare industries. With over 25 years of experience, we specialize in Commissioning, Qualification, and Validation (CQV) services for facilities, utilities, equipment, and processes.

As part of Efor’s global network of 3,000 experts across 12 countries, we are better equipped than ever to deliver innovative and comprehensive solutions tailored to the unique needs of clients worldwide. This integration strengthens our ability to combine global expertise with local proximity, positioning PharmEng as a strategic partner for the industry’s most prominent players.

Our team of highly skilled professionals brings a wealth of industry expertise and knowledge to every project, ensuring that our clients receive the highest quality services and solutions. We pride ourselves on our ability to provide flexible, innovative, and cost-effective solutions that meet our clients' unique challenges.

At PharmEng Technology by Efor, we are committed to delivering excellence in everything we do. We work closely with our clients to understand their goals and objectives, developing customized solutions that deliver measurable results. Our focus on quality, safety, and compliance ensures that our clients can trust us to meet their most critical needs.

Specialties: PharmEng Technology specializes in the planning, design, construction, and validation of Health Care, Laboratory, API Pharmaceutical, and Biotechnology facilities and equipment, including computer systems. We provide professional services that meet both regulatory and business demands, following current Good Manufacturing Practices (cGMP), Good Engineering Practices (GEP), and Good Laboratory Practices (GLP).

Industry
Chemicals & Materials
Company Size
201-500 employees
Headquarters
Toronto, CA
Year Founded
Unknown
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