R&D Technical Project Manager

This listing was posted on ApplicantPro.

R&D Technical Project Manager

Location:

Cranbury Township

Description:

Experic is an industry-leading contract development and manufacturing organization (CDMO) and clinical trial supply services company. Our vision is to deliver innovative and scalable solutions for every phase of a product's life cycle from clinical to commercial. We offer advanced pharmaceutical manufacturing, packaging, and labeling technologies that can accommodate a variety of dosing and packaging formats. We take pride in our precision capabilities, state-of-the-art filling equipment, advanced technologies, and Class A regulatory compliant cGMP facilities. Our main goal is to provide our clients personalized attention and ensure the smooth and successful completion of their pharmaceutical development programs. We aspire to develop a team culture based on trust, integrity, ethical behavior, and compliance, with a relentless focus on delivering high quality results. If you value a collaborative work environment and are energized by the opportunity to truly make a difference, come and Experience the Experic difference . We believe in fostering a fair and respectful work environment that encourages open communication and continuous improvement. At Experic, you can experience a fulfilling career, do meaningful work, and grow professionally and personally. A successful candidate will bring their unique thinking, expertise, and approach while sharing our core values. The successful candidate will: Under minimal supervision, the incumbent is responsible for the project management of assigned client projects including but not limited to the planning of project resources, assembling or leading the project team, time management, budget, scope, quality and satisfaction, risk management, monitoring progress, documentation and reporting. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Management of project related activities from project inception to completion to ensure that they are delivered on-time, within approved budget and achieve project objectives. Organize and lead project core team meetings. Maintains effective communication and working relationships among project core team. Work with cross-functional team members to assess feasibility of project scope and objectives and develop detailed project timeline to ensure that there is enough flexibility and contingency in the plan to respond to unanticipated difficulties. Define and assign schedules and track cross-functional tasks/activities to ensure that projects progress within expected timings. Lead risk analysis & mitigation planning for projects. Identify, monitor, communicate and resolve issues, scope changes, budget variances or other project objective hurdles that may arise during the project execution. Interface with all functional areas of the business to ensure timely, effective, and efficient execution of project tasks. Prepare and present project progress reports and presentations as required. Prepare and track invoicing and payments in collaboration with accounts payable. ADDITIONAL POSITION REQUIREMENTS Ability to work with customers and internal stakeholders to translate manufacturing needs into an efficient and cost-effective plan including, but not limited to material management. Work with technical leads on the drafting of research and development protocols, material specifications and batch records. Facilitate internal and external team meetings. Understanding of GMP considerations for manufacturing projects including pharmaceutical development, manufacturing operations, validation, analytical development and testing. Carries out duties in compliance with all federal and state regulations and guidelines. Complies with all company and site policies and procedures including but not limited to safety, standard operating procedures, and work instructions. Remains current in profession and industry trends. Makes a positive contribution as demonstrated by: making suggestions for improvement learning new skills, procedures, and processes. Is available for other duties as required. Is available for overtime as needed. QUALIFICATIONS: EDUCATION and/or EXPERIENCE Bachelor's Degree required and five (5) years of project management experience in cGMP Pharmaceutical Manufacturing Project Manager or Project Coordinator; or ten (10) years of project management experience in cGMP pharmaceutical setting as a Project Manager or Project Coordinator. LANGUAGE SKILLS Read and interpret documents such as standard operating procedures, manuals, batch records, work instructions and specifications. Legible Handwriting Communicate clearly in writing and orally. OTHER SKILLS, ABILITIES OR QUALIFICATIONS Demonstrate practical knowledge of 21 CFR 210, 21 CFR 211, 21 CFR Part 11, Eudralex Volume 4 and Annex 13. Demonstrate effective collaboration and teamwork. Demonstrate experience managing contract pharmaceutical projects on time and on budget. Demonstrate experience working in a cGxP environment. Familiar with project management tools and technologies such as Microsoft Project. Knowledge of various project management methodologies. Successfully completes regulatory and job training requirements. Proficient in MS Office Ability to perform repetitive tasks while maintaining speed of work and attention to detail without loss to production. Ability to work with others in a team environment.

Company:

Experic

Posted:

December 26 2023 on ApplicantPro

Visit Our Partner Website

This listing was posted on another website. Click here to open: Go to ApplicantPro

Important Safety Tips

Always meet the employer in person.
Avoid sharing sensitive personal and financial information.
Avoid employment offers that require a deposit or investment.

To learn more, visit the Safety Center or click here to report this listing.

R&D Technical Project Manager | Technical Project Manager in Executive Job at Experic | 7116511

R&D Technical Project Manager

Visit Our Partner Website