Technical Writer

SEEKING A STRONG TECHNICAL WRITER FOR A CONTRACT ROLE

We are seeking a detail-oriented and skilled Technical Writer to join our team for a key project involving the implementation of two new isolation lines equipped with high-speed fillers. This role is integral to the successful transfer and customization of existing procedures and standard operating procedures (SOPs) from an external facility to our Shirley site. The project is expected to last approximately six months, with a possibility of extension based on operational needs.

Key Responsibilities:

• Review, adapt, and customize 17 existing procedures/SOPs for implementation at the site
• Collaborate closely with the project management team and subject matter experts (SMEs) to ensure accurate information is captured and conveyed.
• Utilize Veeva electronic documentation systems for writing, editing, and managing documentation.
• Ensure that all documentation adheres to industry standards and regulatory requirements, including FDA guidelines as applicable.
• Coordinate with cross-functional teams to gather information, clarify technical content, and validate procedural accuracy.
• Maintain comprehensive records of revisions and ensure all documents are up to date and accessible.
• Provide training and support to end-users on new procedures, as needed.
• Participate in project meetings to provide documentation updates and address any writing-related concerns.

Qualifications:

• Bachelor’s degree in English, Technical Communication, Life Sciences, or a related field.
• Previous experience in technical writing, preferably within the pharmaceutical or biotechnology industries.
• Familiarity with Veeva or similar electronic documentation systems.
• Strong understanding of Good Manufacturing Practice (GMP) and regulatory requirements in pharmaceutical manufacturing.
• Excellent written and verbal communication skills with a strong attention to detail.
• Ability to work independently and collaboratively in a fast-paced environment.
• Strong organizational skills and the ability to manage multiple tasks and deadlines.

What We Offer:

• Competitive salary and benefits package.
• Opportunities for professional development and growth within the company.
• A supportive and collaborative work environment.
• The chance to contribute to the development of innovative pharmaceutical solutions.

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.

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

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

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 actalentaccommodation@actalentservices.com for other accommodation options.