Urgently Hiring - GMP Technical Writer
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Technical Writer Needed- Urgently Hiring
Actalent is currently hiring a technical writer in the Columbus area. This is a contract position for 6 months, this role requires a relevant four-year Science degree either a bachelors of Science or Masters degree of Science. The ideal candidate would have 1+yrs of Technical Writing experience from a GMP setting preferably from a Life Science/Pharma Company, experience in Biologics, Gene Therapy, or Pharmaceutics and knowledge of GMP, regulatory (FDA) requirements, and understanding of aseptic processes.
Job Description
We are seeking a meticulous Technical Writer to join our team. In this role, you will write deviations when SOPs are not followed, ensuring the product remains compliant with standards. You will also write batch records, update and create SOPs, and create one-point lessons. You will partner with a Senior Documentation Specialist to prioritize workloads and interact with technical staff to gather necessary information. You will exercise discretion, judgment, and personal responsibility while maintaining a positive attitude and high integrity. Compliance with regulatory requirements for cellular and gene therapy products and attention to detail are crucial. You will solve, correct, and prevent problems, perform tasks as assigned by leadership, and assign tasks to junior staff. You will work towards specific measurable objectives with minimal supervision, lead a diverse and collaborative team, and document all activities according to SOPs.
Hard Skills
This is a contract position with a duration of 6 Month(s).
Work Site
This is a fully on-site position in Columbus, Ohio.
Work Environment
This is an office-based environment with a business casual dress code. The position operates on a 1st shift schedule, Monday to Friday, 8:00 AM to 4:30 PM, with some flexibility and occasional overtime.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] for other accommodation options.
Actalent is currently hiring a technical writer in the Columbus area. This is a contract position for 6 months, this role requires a relevant four-year Science degree either a bachelors of Science or Masters degree of Science. The ideal candidate would have 1+yrs of Technical Writing experience from a GMP setting preferably from a Life Science/Pharma Company, experience in Biologics, Gene Therapy, or Pharmaceutics and knowledge of GMP, regulatory (FDA) requirements, and understanding of aseptic processes.
Job Description
We are seeking a meticulous Technical Writer to join our team. In this role, you will write deviations when SOPs are not followed, ensuring the product remains compliant with standards. You will also write batch records, update and create SOPs, and create one-point lessons. You will partner with a Senior Documentation Specialist to prioritize workloads and interact with technical staff to gather necessary information. You will exercise discretion, judgment, and personal responsibility while maintaining a positive attitude and high integrity. Compliance with regulatory requirements for cellular and gene therapy products and attention to detail are crucial. You will solve, correct, and prevent problems, perform tasks as assigned by leadership, and assign tasks to junior staff. You will work towards specific measurable objectives with minimal supervision, lead a diverse and collaborative team, and document all activities according to SOPs.
Hard Skills
- Quality Assurance
- Biology
- Deviations
- GMP
- Technical Writing
- Discretion
- Judgment
- Personal Responsibility
- Integrity
- Positive Attitude
- Attention to Detail
- Operational Planning
- Collaboration
- Clear Communication
This is a contract position with a duration of 6 Month(s).
Work Site
This is a fully on-site position in Columbus, Ohio.
Work Environment
This is an office-based environment with a business casual dress code. The position operates on a 1st shift schedule, Monday to Friday, 8:00 AM to 4:30 PM, with some flexibility and occasional overtime.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
- Hiring diverse talent
- Maintaining an inclusive environment through persistent self-reflection
- Building a culture of care, engagement, and recognition with clear outcomes
- Ensuring growth opportunities for our people
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [email protected] for other accommodation options.
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