Technical Writer

Technical Writer – Marietta, GA – Pharmaceutical Manufacturing – M-F, 8am-5pm – Direct hire – Competitive compensation package (up to 10% performance company bonus, 401k, health, dental, vision).

We are partnering with a fully integrated US based biopharmaceutical organization focused on advancing specialty treatments. With a growing and diverse product pipeline, including complex generics and specialty formulations, this is an opportunity to step into a leadership role where your work directly supports life‑changing therapies. If you're a hands‑on leader with strong pharmaceutical manufacturing experience, this role offers the chance to drive production excellence, mentor teams, and grow your leadership career in a highly regulated, high‑impact environment.

Create, manage, and oversee the generation of technical documents for the Manufacturing Operations department.

• Interact with technical associates, leads and subject matter experts (SMEs) from other departments and divisions to create and revise GMP Manufacturing Batch Records, investigations, change controls, with a strong emphasis on pharmaceutical processes such as fluid bed granulation, blending, milling, bi‑layer compression, encapsulation, coating & packaging.
• Prepare, write, update, and maintain manufacturing SOPs and FORMs where applicable, including the preparation of any forms or attachments that may accompany the SOP.
• Other duties as assigned.

• Ability to work independently, with effective communication, collaboration, and decision‑making skills.
• Great attention to detail and ability to work on multiple projects.
• Ability to organize and adapt to organizational priority changes and work effectively with minimal supervision / independently with a sense of urgency.
• Computer experience required – proficiency in Microsoft Office (Word, Excel, Outlook).

• Degree (BA/BS) in a technology‑related field (Biology, Chemistry, Pharmacy, Engineering, etc.) and at least 2‑7 years of development or manufacturing experience in a cGMP solid dosage manufacturing environment.
• Understanding of the fundamental processing stages required to create initial batch records and other supporting documentation (protocols, change controls, investigations, deviations, final reports).
• Pharmaceutical experience; oral solid dosage is highly preferred, other dosage forms may be considered.
• Two‑five years of technical writing experience.
• In‑depth background in Bi‑layer Tableting Technology preferred.
• Strong command of the English language and ability to articulate clearly and concisely through written words.
• Strong computer skills, with accurate conveyance of information in spoken and written form.
• Must meet deadlines, be detail oriented, with solid organizational skills and ability to track multiple projects simultaneously.
• Ability to follow‑up with multiple departments is required.

ADA/EOE IND
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