Process Engineer in Wilson

Energy Jobline ZR; Wilson (NC); On-site; USD 75,000 - 120,000; Full time

Job summary

Pharma-Bio Serv is seeking a Process Engineer in Wilson, North Carolina for work in a regulated pharmaceutical/biologic manufacturing environment.

The role requires a engineering degree and 4+ years in industry with experience in tech transfer, process validation, and downstream operations.

Fluency in English and Spanish is required; visa sponsorship is not offered; strong data analysis and communication skills are essential.

Qualifications

• Bachelor’s degree in Engineering or related field is required.
• At least 4 years in pharma/biologic manufacturing or regulated industry with 2 years in Tech Transfer.
• Knowledge of quality systems and regulatory requirements (FDA/EMEA).
• Data collection/analysis to inform decisions for studies.
• Support New Product Introduction/process validation in downstream manufacturing.
• Strong communication skills in English and Spanish.

Skills

Data analysis

Independent worker

Communication skills

Education

Bachelor’s degree in Engineering or related field

Job description

Job DescriptionJob Description

Pharma-Bio Serv, a global consulting firm headquartered in Puerto Rico, has been dedicated exclusively to providing services to the largest biotechnology & bio-engineering companies within the regulated industry for over 30 years. Since our inception, our services have resulted in project experience level and personnel resource base ranking among the highest worldwide.

We are looking candidates with experience within regulated environment for aProcess EngineerinWilson, North Carolina.

Requirement:

• Bachelor’s degree in Engineering in Engineering, Science or related scientific field, required.
• At least 4 years of experience in the pharmaceutical/Biologic manufacturing industry or regulated industry experience and a minimum 2 years of experience in Technical Transfer process.
• Proven knowledge quality systems and continuous improvement practicesand application of industry regulations including those of FDA, EMEA, and other authorities.
• Ability to collect, process, and analyze data to draw meaningful conclusions and make informed decisions for studies
• Supporting New Product Introduction/ process validation in Downstream manufacturing facility.
• Ability to work independently with minimum supervision, having a good sense of prioritization of goals and good time management.
• Excellent verbal and written communication skills, including ability to effectively communicate with internal and external customers.

Please note: This position does not offer visa sponsorship. Applicants must be fluent in both Spanish and English. Kindly refrain from applying if you do not meet these requirements.We do not provide H1B Visa support / No C2C available.

Company Description

Pharma-Bio Serv, a global consulting firm headquartered in Puerto Rico, has been dedicated exclusively to providing services to the largest biotechnology & bio-engineering companies within the regulated industry for more than 30 years. Since our inception, our services have resulted in a project experience level and personnel resource base ranking among the highest worldwide.

Company Description

Pharma-Bio Serv, a global consulting firm headquartered in Puerto Rico, has been dedicated exclusively to providing services to the largest biotechnology & bio-engineering companies within the regulated industry for more than 30 years. Since our inception, our services have resulted in a project experience level and personnel resource base ranking among the highest worldwide.