What are the responsibilities and job description for the Project Coordinator position at Profit by RPO?
Client: Abbott
Status: Open
Location: Alameda, CA 94502
Position Title: 33714 Project Coordinator
Duration: 6 months
Position Summary
Provides organizational support to the Artwork and Labeling Development department by working directly with a cross functional team,
external translation suppliers as well as internal Design Production Artist team to coordinate and execute activities related to the
development of packaging and labeling items for the launch and maintenance of Abbott Diabetes Care products.
Main Responsibilities
- Responsible for coordinating with an internal cross functional team to develop packaging and labeling items for new products or revisions
to existing products.
- Responsible for coordinating the efficient use of Department resources to meet deadlines for new product releases and revisions.
- Responsible for coordinating the translation of packaging and labeling items with language translation agencies.
- Responsible for interpreting project schedules and escalating project timeline risks and issues to management.
- Performs labeling coordination tasks using electronic workflow system and product lifecycle management system.
- Support assessment for projects to identify scope and impact to labeling.
Issues Engineering Changes and modifies Bill of Materials in Agile for packaging and labeling components.
Knowledge and Skills
Required Education and Experience
- Bachelors Degree in a related field or an equivalent combination of education and work experience.
Minimum 2 years of work experience including coordinating, organizing and executing project activities.
- Computer literacy with PC platform. Proficient in Microsoft Office applications and Adobe Acrobat.
- Familiarity with product lifecycle management system preferred.
- Accuracy, attention to detail, and strong proofreading skills required.
- Ability to read and interpret project schedules.
- Must demonstrate strong problem solving techniques.
- Exhibits excellent verbal and written communication.
- Strong interpersonal skills, must be service oriented.
- Displays solid organizational skills, with the flexibility to quickly realign priorities to meet changing business needs.
- Ability to work on premises for core working hours of department.
- Excels in a fast paced, deadline-driven environment and is able to focus and follow guidelines with minimal supervision; ability to multi-task and
anticipate resources necessary to complete the work.
- Experience with medical device labeling or labeling for highly regulated industry preferred.
- Experience in print production preferred.
Knowledge and Skills
Required Education and Experiences
- Bachelors Degree, preferably in Communications, Marketing, Business Administration, Academic or minimum of five years of relevant
work experience in lieu of degree.
- 2-4 years of work experience including coordinating, organizing and executing project activities.
- Understanding of AGILE (or similar) documentation approval system.
- Familiar with Engineering Change Orders (ECs) and Bill of Materials (BOM).
- Computer literacy with PC. Proficient in Microsoft Office applications and Adobe Acrobat
- Ability to read and interpret project schedules.
- Demonstrates accountability, strong attention to detail and a commitment to accuracy-Strong proofreading ability and attention to detail is required.
- Must demonstrate strong problem solving techniques.
- Exhibits excellent verbal, written, and interpersonal communication skills when interacting with both internal and external customers
- Strong interpersonal skills, must be service oriented.
- Displays solid organizational skills, with the flexibility to quickly realign priorities to meet changing business needs.
- Highly organized
- Ability to work on premises for core working hours of department.
- Knowledge in legal aspects of packaging, trademarks, and promotions is helpful but not a required.
- Background in print production is preferred but not required.
- Excels in a fast paced, deadline-driven environment and is able to focus and follow guidelines with minimal supervision; ability to multi-task and meet
timeliness and accuracy standards by anticipating resources necessary to complete the work
- Prior experience in the pharmaceutical, healthcare, or medical device industry.
- Experience in a GMP environment, as well as familiarity with FDA and regulatory guidance documents related to Medical device labeling is preferred
Job Type: Contract
Pay: $27.00 - $30.00 per hour
Schedule:
- Monday to Friday
Experience:
- Project management: 1 year (Preferred)
Ability to Commute:
- Alameda, CA 94502 (Required)
Ability to Relocate:
- Alameda, CA 94502: Relocate before starting work (Required)
Work Location: In person
Salary : $27 - $30