Capital Project Planner/Scheduler - Los Angeles Metro Area
Compli

Los Angeles, California

This job has expired.


Capital Project Planner/Scheduler - Los Angeles Metro Area

(Pharmaceutical/Biotech)-Competitive Salary, Work/Life Balance!

On-Site

Previous Pharmaceutical/Biotech/Medical Device experience is mandatory for these roles.

Are you looking to be a part of a close-knit work community? Do you have experience in the Life Science industry? Will you represent Compli, LLC. as an experienced Capital Project Planner / Scheduler for our pharmaceutical manufacturing, biotech, and medical device client projects? Do you enjoy traveling the country and making a difference? If so, this could be the right opportunity for you!

The Capital Project Planner / Scheduler position is responsible for our clients growing company. Please review the list of responsibilities and qualifications below and apply.

Important: Our Client has mandated COVID-19 vaccination for their workforce, effective October 1st, 2021. All external personnel providing services to Compli' s client are required to comply with this requirement.

Responsibilities:

  • Create, monitor, and analyze project schedules in accordance with standard of best project practice
  • Track, analyze, and report information appropriately to allow the project teams to manage their projects and evaluate weekly reports
  • Ensure accuracy of project schedules and performed version control
  • Co-ordinate project schedules, tasks, meeting updates, and efficient distribution of reports
  • Prepare, implement, and monitor scopes of work using Work Breakdown Structure (WBS) for control and integrity
  • Monitor projects' progress, including identifying critical activities and reviewing forecasts and progress achieved to date
  • Maintain project risk register to ensure that risks are effectively managed to minimize their impact on schedule, scope, and budget of projects
  • Track baselines, perform what-if analysis, and develop contingency plans
  • Developing conceptual models for Business Capability traceability matrix to explain processes to all levels of users
  • Perform coordination of cross-functional departments to identify project issues, monitor action items, and work with the project manager to ensure resolution.


Requirements:
  • Minimum of five years related-work experience in the construction industry, or as a project scheduler
  • Minimum of two years of Pharmaceutical or Bio-Tech Industry experience
  • Strong communication skills - written and verbal
  • Good analytical and planning skills.
  • Ability to learn quickly and work under pressure in a fast-paced environment
  • Proficiency in word processing and spreadsheet applications
  • Proficiency in the use of project scheduling software such as Primavera P6 or Microsoft project
  • Must have good attention to details
  • Excellent organizational and time management skills
  • Good working ethics and ability to treat documents with confidentiality
  • Ability to work effectively within a team setting and also to provide leadership when required to do so.
  • All candidates must be legally eligible to work in the United States
  • Must be willing to travel up to 100% of their work time; regionally and/or nationally throughout the U.S.


Education:

B.S./B.A degree and three years experience or Masters degree plus one year experience or an equivalent combination of education and experience. Degrees are preferably in relevant scientific discipline and experience is in pharmaceutical or biopharmaceutical industry.

Compli, LLC was founded in 2001 to provide commissioning, validation, and regulatory support services, CQV, asset management, reliability engineering, and staff augmentation services to the life sciences industry. We serve pharmaceutical companies across the U.S. Regarding regulations and compliance, it has never been more important to understand the documentation and quality assurance activities as they relate to vendors, engineering, construction, and contractors, which is why clients trust the Compli team.

Perks of the Job:
  • Competitive Pay commensurate with experience
  • Work / Life Balance
  • Working with a small, close-knit team where you are valued as an individual
  • A learning environment and continuous advancement opportunities


Feel overqualified? Feel underqualified? Apply anyway if this sounds like the fit you are looking for! We have flexibility in how we hire the role.

To learn more and APPLY NOW: http://www.ucompli.com/careers

Agencies, Compli welcomes your qualified candidates. Please email compli-opportunities@ucompli.com to establish a relationship with our firm.

We are an equal opportunity employer M/F/D/V

Job Keywords: United States, Laverne, CA, Los Angeles, CA, Los Angeles County and Surrounding Area, California, Validation Engineer, Technical Writing, CQV, qualification, vial packing, C&Q, packaging equipment, serialization and aggregation processes, vial packing line


This job has expired.

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