Technical Writer

Aptask Global Workforce (AGW) is seeking a Technical Writer for an Onsite position with a Global Biotechnology Company located in New Albany, OH. This is a 24+ month contract opportunity.

In this role, you will support the manufacturing team and provide technical expertise to draft and revise documents such as Standard Operating Procedures (SOPs), protocols, technical reports, and training materials in a GMP regulated environment. You will liaise with cross-functional departments regarding documentation changes and support continuous process improvement projects. Shift hours: 8 AM - 5 PM

Responsibilities:

Develop, review, and update technical content including standard operating procedures, work instructions, risk assessments, protocols, and reports

Provide technical and clerical support to the manufacturing team in the preparation of documentation and collation of data

Liaise with the manufacturing team and other cross-functional departments regarding documentation changes

Collaborate with multiple departments to support new/revised training documentation

Support process owners and participate in continuous process improvement and troubleshooting projects

Generate, own, and provide subject matter expertise to Quality System records such as minor deviations, CAPA, and change control records

Develop protocols for Manufacturing to support change controls, deviations, and troubleshooting investigations

Liaise with Quality Assurance to ensure that GMP standards are maintained

Requirements:

Master's Degree in Science and/or Engineering

OR Bachelor's Degree in Science and/or Engineering and 2 years in Manufacturing, Packaging, or Quality experience in pharmaceutical, medical device, or biotechnology companies

OR Associate's Degree in Science and/or Engineering and 5 years in Manufacturing, Packaging, or Quality experience in pharmaceutical, medical device, or biotechnology companies

OR High School Diploma / GED and 8 years in Manufacturing, Packaging, or Quality experience in pharmaceutical, medical device, or biotechnology companies

Desired skills:

Previous Veeva experience

Prior deviation and CAPA experience

Experience working in a Good Manufacturing Practices (GMP) environment and a background in technical writing

Experience with device assembly and packaging of final product

Ability to translate highly technical information into easily understandable information for manufacturing operators

A fact-based problem solver with strong troubleshooting and problem-solving skills

Excellent written and oral communication skills

Pay range: up to $38.21 per hour

Only candidates available and ready to work directly as Aptask Global Workforce (AGW) employees will be considered for this position.

If you have the described qualifications and are interested in this exciting opportunity, apply today!

Aptask Global Workforce (AGW)

ApTask Global Workforce (AGW) is a certified Minority and Veteran workforce solutions company. AGW delivers operational, clinical, lab and professional talent with a strong focus on healthcare and life sciences. The company supports clients with reliable staffing, program expertise and a commitment to quality, speed and consistent delivery.

Benefits of working with ApTask Global Workforce include:

Medical

Dental

Vision

Sick Pay (for applicable states/municipalities)

Our team stays close to the process and is here to guide you every step of the way. To learn more, please visit our website

ApTask Global Workforce is an Equal Opportunity Employer. Candidates will receive consideration without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability or status as a protected veteran.