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Job Title: Pharmaceutical Technical Writer

Duration: 08+ Months Contract

Notes from HM:

• Role will be Onsite
• Bachelor's Degree required
• Should have GMP facility/environment experience and knowledge
• Resolving non-conformances (nice to have)
• Project experience is ideal
• Experience in validations
• Experience with writing protocols
• Working knowledge of Change Controls (Comet, Salesforce, Truevault)
• Must be able to communicate clearly
• Must have at least 4 years of experience
• Technical Writing experience a must
• Should be proficient in MS Office
• Should be comfortable with working with Stakeholders to get work done and to get communications out

General Summary:

Produces complex technical written communications used for projects assigned to department. Projects may include marketing tools, technical manuals, and presentations. May participate in special projects.

Duties & Responsibilities:

1. Prepares work to be accomplished by reviewing delivery schedules and prioritizing work, gathering, organizing, and analyzing technical information from various relevant sources.
2. Verifies facts and clarifies information as needed.
3. Develops, writes, edits, and proofs complex assignments for various internal customers.
4. Ensures Company publications meet established standards of style and format.
5. Reviews photographs, drawings, sketches, diagrams, and charts selected for specific publications to ensure relevance to content.
6. Generates and reviews text for nontechnical documents upon request.
7. Serves as editing consultant to other staff.
8. Suggests format, layout, and graphics for materials reviewed.
9. Reviews published materials and recommends revisions or changes in scope, format, and content.
10. Produces rough draft of revised versions.
11. Mentors less experienced employees by providing guidance and input on work assignments.
12. Reviews drafts for adherence to business standards.
13. Investigates and resolves customer complaints and concerns.
14. Responds to complicated inquiries.
15. Participates in or leads projects as assigned.
16. Provides input into project parameters and timelines.
17. Makes recommendations on method and materials for optimum results.

Work Experience:

Generally requires 4-6 Years

Seniority level

Associate

Employment type

Contract

Job function

Writing/Editing and Quality Assurance

Industries

Pharmaceutical Manufacturing and Hospitals and Health Care