- Location
- Durham, NC
- Type
- Full-time
- Department
- IT
- Education
- Associate
- Closing date
- Today
- Source
- ApplyToJob
Description
Position Summary
The Manufacturing Operator is responsible for executing a wide range of operations in a cGMP-compliant biopharmaceutical manufacturing environment. This role involves operating, maintaining, and troubleshooting production equipment, performing and documenting complex and critical processes, and supporting equipment validation activities. The operator ensures compliance with standard operating procedures, safety regulations, and documentation standards while contributing to continuous improvement initiatives. Ideal candidates will have an A.A.S. in a scientific discipline or equivalent experience, along with 3–6 years of hands-on manufacturing experience. The role also requires strong communication skills, proficiency with MS Office and electronic systems, and the ability to adapt in a dynamic team environment while meeting strict quality and safety standards.
Essential Functions
Supervisory responsibilities
Key Relationships (examples: Depts or Individual positions that this position will be working closely with):
Knowledge, Skills, and Abilities
Physical Demands and Work Environment
While performing the duties of this job, there may be certain physical demands required for the position.
Other Duties
You may be asked to take on any other responsibilities or tasks that are within your skills and abilities whenever reasonably asked.
Limitations and Disclaimer
The above job description is meant to describe the general nature and level of work being performed; it is not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required for the position. The Company is committed to making reasonable adjustments to the workplace to ensure the role is accessible to all candidates, including those with disabilities. To perform the job successfully, the employee must possess the abilities or aptitudes to perform each duty proficiently.
The Manufacturing Operator is responsible for executing a wide range of operations in a cGMP-compliant biopharmaceutical manufacturing environment. This role involves operating, maintaining, and troubleshooting production equipment, performing and documenting complex and critical processes, and supporting equipment validation activities. The operator ensures compliance with standard operating procedures, safety regulations, and documentation standards while contributing to continuous improvement initiatives. Ideal candidates will have an A.A.S. in a scientific discipline or equivalent experience, along with 3–6 years of hands-on manufacturing experience. The role also requires strong communication skills, proficiency with MS Office and electronic systems, and the ability to adapt in a dynamic team environment while meeting strict quality and safety standards.
Essential Functions
- Operate manufacturing equipment and instruments.
- Complete assigned tasks in a timely manner.
- Conduct daily activities in an organized, efficient manner.
- Perform simple, routine, complex, and critical operations.
- Troubleshoot equipment issues, when necessary.
- Ensure process equipment is appropriately maintained for operation.
- Perform and document operations in accordance with cGMP’s.
- Execute equipment qualification protocols and validation protocols.
- Routinely draft and revise standard operating procedures and master batch records.
- Provide management with performance operation updates and shift reports
- Recognize and initiate process deviations.
- Support continuous improvement initiatives by identifying areas needing improvement, recommending strategies for improvement, and implementing those strategies once approved.
- Communicate effectively, both in written and verbal formats.
- Maintain training compliance.
- Ensure a safe working environment for all staff.
Supervisory responsibilities
- Direct Reports: No
- Indirect Reports: No
Key Relationships (examples: Depts or Individual positions that this position will be working closely with):
- Quality Control
- Quality Assurance
- Process Development/ Formulation R&D
- Facilities
- No
- A.A.S. in a scientific discipline, or equivalent experience preferred
- 3-6 years’ experience in a cGMP biopharmaceutical manufacturing environment required
- Previous experience as subject matter expert and training others
- Existing knowledge of equipment in a manufacturing/production environment
Knowledge, Skills, and Abilities
- Must be able to work within and adapt to electronic systems
- Able to function, with guidance, in a rapidly changing environment while balancing multiple priorities simultaneously
- Must be able to be PAPR and Respirator qualified
- Able to work independently and as part of a team
- Must be able to read, write and converse in English
- Must have a good working knowledge of MS Office (Outlook, Word and Excel)
Physical Demands and Work Environment
While performing the duties of this job, there may be certain physical demands required for the position.
- Requires constant standing, walking, seeing, & hearing
- Requires occasional sitting
- Requires constant carrying & lifting; frequently under 20 LBS, 20-60 LBS, & occasionally over 60 LBS
- Requires frequent bending, twisting, gripping, & reaching
- Requires frequent pushing & pulling under 20 LBS, 20-60 LBS, & occasionally over 60 LBS
Other Duties
You may be asked to take on any other responsibilities or tasks that are within your skills and abilities whenever reasonably asked.
Limitations and Disclaimer
The above job description is meant to describe the general nature and level of work being performed; it is not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required for the position. The Company is committed to making reasonable adjustments to the workplace to ensure the role is accessible to all candidates, including those with disabilities. To perform the job successfully, the employee must possess the abilities or aptitudes to perform each duty proficiently.
Skills
ExcelCompliance