Technical Project Manager

Prinova US LLC

$75K — $95K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • High School Diploma or equivalent with 4+ years experience, or 2-year degree with 2+ years experience in a business-related field.
  • Proficient in MS Office, especially Excel, Word, and Outlook.
  • Strong computer skills with MRP systems, internet, and email.
  • Familiarity with cGMP regulations.
  • Ability to work effectively in a team environment.

Responsibilities

  • Own and manage Data Control processes for compliance with cGMP and internal SOPs.
  • Serve as the primary liaison between R&D, Quality, Sales, and Operations for new business opportunities.
  • Lead cross-functional product development projects, managing timelines and coordinating tasks.
  • Oversee accuracy and updates of Item Master and BOM data in the MRP system.
  • Facilitate the compilation and maintenance of formula and packaging specifications in collaboration with R&D.
  • Coordinate the flow of critical information across departments for smooth project development.
  • Manage change control processes and document any client-initiated changes.

Benefits

  • Medical, Dental, and Vision insurance.
  • Employer-paid Short-term and Long-term Disability.
  • Health Savings Account (HSA) and Flexible Spending Account (FSA) options.
  • Paid Maternity and Paternity Leave.
  • Paid Time Off (PTO).
  • Employer-paid Basic Life Insurance.
  • 401(k) & Roth with employer match.
  • Eight Paid Holidays plus 3 Floating Holidays.
  • Voluntary options for Critical Illness, Hospital Indemnity, and Accident insurance.
  • Training and development opportunities for personal growth.
Full Job Description
Technical Project Manager Department: Research & Development Location: Spring Hill, TN The Technical Project Manager serves as the primary point of contact for all aspects of new and changing products within assigned accounts. Working closely with the Product Development, Sales, R&D, and cross-functional teams, they are responsible for the coordination, compilation, and documentation of all relevant product development details throughout the project lifecycle. Main Duties & Responsibilities • Own and manage Data Control processes, ensuring compliance with cGMP and internal SOPs. • Serve as a primary liaison between R&D, Quality, Sales, and Operations to support the development and commercialization of new business opportunities with new or existing customers. • Lead cross-functional product development projects, including creating and managing timelines, coordinating tasks, and ensuring timely execution across the product lifecycle. • Oversee the compilation, entry, and maintenance of Item Master and BOM data in the MRP system for assigned accounts, ensuring accuracy and timely updates. • Lead the compilation and maintenance of formula and packaging component specifications in collaboration with R&D. • Facilitate the flow of critical information across departments, ensuring seamless communication and documentation throughout project development. • Manage change control processes, including the investigation and documentation of deviations and client-initiated changes (e.g., CCFs). • Compile, track, and coordinate approval of Finished Product Specifications (FPS) and other project documentation for future reference. • Coordinate formulation development or redevelopment efforts with R&D as needed. • Attend and facilitate cross-functional meetings and participate in relevant internal and external training programs to enhance knowledge and skills. • Perform other duties as assigned to support departmental and organizational goals. • Support training of new employees Requirements and Skills • High School Diploma or equivalent with 4+ year experience in a related field, or 2-year degree with 2+ year experience in a business related field; • Proficient in use of MS Office, particularly Excel, Word, Outlook; • Strong computer skills in MRP system, internet and email required; • Must be familiar with cGMP's; • Must possess the ability to function professionally and effectively in a teamwork environment; • Ability to read and comprehend simple instructions, short correspondence, and memos; • Ability to write professional correspondence; • Ability to add, subtract, multiply and divide all units of measure, using whole numbers, fractions and decimals; • Ability to write and prepare professional business letters, memorandums, documents, and reports. • Ability to wear any required PPE such Ability to sit for extended hours; • Ability to view a computer screen and type for extended hours; • Work environment is normally in an office setting. Must be able to make frequent rounds in a warehouse environment; • Ability to work around a variation of different smells and aromas; • Other physical requirements include occasional squatting, bending, twisting, and bi-lateral hand and wrist movement; • This position may require infrequent travel; • Ability to adjust to work schedule as business needs require. Benefits: • Medical, Dental, Vision • Employer paid STD and LTD • HSA and FSA • Paid Maternity and Paternity Leave • PTO • Employer paid Basic Life Insurance • 401(k) & Roth with employer match • Eight Paid Holidays + 3 Floating Holidays • Voluntary - Critical Illness, Hospital Indemnity, Accident • Personal growth including training and development opportunities

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