Job Title: Technical Writer II

Job Description

We are seeking a dedicated Technical Writer II with a wealth of experience in technical/scientific writing. This role involves crafting and updating cGMP documentation essential for the production of life-saving clinical and commercial drug products. The successful candidate will collaborate with subject matter experts to ensure the delivery of high-quality documents that support Right-First-Time manufacturing.

Responsibilities

• Craft and update cGMP documentation to support drug product manufacturing.
• Utilize standard batch record templates and collaborate with subject matter experts.
• Identify and correct gaps or misalignments between batch records and SOPs.
• Analyze manufacturing deviations to enhance reference documentation.
• Optimize the layout, organization, and content of technical documents.

Essential Skills

• Proven experience in technical writing within a pharmaceutical environment.
• Bachelor's Degree in a STEM field.
• Minimum of 2 years of experience in a GMP-regulated Biologics or Pharma Industry.
• Experience writing SOPs and pharmaceutical batch record or validation documents.
• Knowledge of Good Manufacturing Practices and US/EU regulations.

Additional Skills & Qualifications

• Success in working with cross-functional teams and providing proactive communication.
• Organizational skills and the ability to work efficiently under pressure.
• Expertise in oral and written communication in English.
• Proficiency in Microsoft Office applications.
• Experience in pharmaceutical operations is advantageous.

Work Environment

The position is within a fast-paced contract manufacturing environment where the ability to manage multiple tasks simultaneously is essential. The role does not involve research and development activities.

Pay and Benefits

The pay range for this position is $34.00 - $43.00/hr.

Eligibility requirements apply to some benefits and may depend on your job

classification and length of employment. Benefits are subject to change and may be

subject to specific elections, plan, or program terms. If eligible, the benefits

available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Saint Louis,MO.

Application Deadline

This position is anticipated to close on Jul 7, 2025.

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.

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 due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.