What are the responsibilities and job description for the Manufacturing Contractor I position at BioPharma Consulting JAD Group?
Under direct supervision, the Manufacturing Contractor I will perform routine clinical manufacturing operations at the manufacturing facility, ensuring all activities are executed safely, efficiently, and in compliance with current Good Manufacturing Practices (cGMP). This role supports the production of clinical products through hands-on operation of manufacturing equipment and close collaboration with cross-functional support teams.
Key Responsibilities
- Perform routine clinical manufacturing operations in a cGMP-regulated environment
- Operate production equipment according to approved SOPs for clinical product manufacturing
- Execute activities in areas including:
- Weighing and dispensing
- Solution preparation
- Equipment CIP/COP
- Small parts cleaning
- Materials stocking within manufacturing suites
- Accurately document all manufacturing activities using existing forms and records
- Maintain a safe, clean, and compliant manufacturing environment at all times
- Interact with cross-functional support groups such as Facilities, Quality Control (QC), Quality Assurance (QA), Materials Management, and EHS to ensure timely and accurate completion of activities
- Follow manufacturing schedules and shift requirements as assigned
Physical & Work Environment Requirements
- Ability to perform strenuous and sometimes repetitive physical work in a classified cleanroom environment
- Ability to lift up to 50 lbs and push/pull bulk materials up to 250 lbs with assistance
- Ability to wear half-face respirators, full-face respirators, and/or PAPR as required for chemical processing
- Willingness to work assigned manufacturing shift schedules
Education
- Biotech Certificate or Associate’s degree preferred
- 1 year of industry experience preferred
Required Skills & Qualifications
- 0–3 years of manufacturing or related industry experience
- Mechanical and scientific aptitude with the ability to follow detailed procedures
- Strong attention to detail in both operations and documentation
- Commitment to safety and maintaining a compliant manufacturing environment
- Ability to clearly and thoroughly document work activities
- Strong time management skills and ability to work effectively in a team environment
- Excellent verbal and written communication skills
- Shift: 4x10 Weds-Sat 6am-4pm
- 1 year contract