New Jersey and San Francisco Areas

The candidate will be a part of the ICQ Consultants team and will be responsible for the project management activities for small to large projects.

• 2 to 6 years of Project Management (PM) with experience in a regulated, manufacturing environment within the biotechnology, pharmaceutical or medical device industry.
• Experience in scheduling, budgeting, planning, resource loading and overall oversight for the execution of CQV projects for lab processes, equipment and utilities process used in the Biotech or Pharmaceutical Industry.
• Direct experience within the following areas: Project management (PM), P6, Installation and Operational Qualification (IQ, OQ) protocols, Validation, Standard Operating Procedure (SOP), Change Control, Data Analysis, single use technologies.

• Successfully working within a multi-disciplinary team coordinating and delivering project activities meeting schedule, budgetary and quality expectations of the client.
• Customarily and regularly exercises discretionary and independent judgment in performing the job.
• Participate in training to ensure continued accreditation.
• Maintain a safe working environment for self, team members and client staff.
• Other tasks in alignment with your skills and competencies as required by the project, client and/or management.

• Excellent organizational, verbal, and written communication skills; with demonstrated ability to efficiently and effectively, communicate with cross-functional teams and management on recommended course of action, with minimal assistance.
• Proficient computer skills and be experienced using MS Office software (Word, Excel, and PowerPoint) and MS Project (as needed).
• A self-starter, detail oriented and able to work independently with minimal supervision.
• Excellent troubleshooting skills: ability to react quickly to understand and solve problems.

B.S. degree in Biology, Biochemistry, Chemistry, Engineering, or equivalent years’ experience working in FDA-regulated industries.