What are the responsibilities and job description for the Technical Writer– Pharma (Hybrid, Seattle, WA) position at Stage 4 Solutions?
We are seeking a Technical Writer - Pharma for a global pharmaceutical company. You will manage and oversee data input and documentation management, and functions as detailed to ensure delivery of Cell Therapy labelling projects.
This is a 40-hour per-week, 12-month contract (extensions possible), 50% onsite role in Seattle, WA.
This is a W2 role as a Stage 4 Solutions employee. Health benefits and 401K are offered.
Responsibilities
Please feel free to forward this project opening to others who may be interested.
Stage 4 Solutions is an equal-opportunity employer. We celebrate diversity and are committed to providing employees with an inclusive environment that is free of discrimination and harassment. All employment decisions are based on the job requirements and candidates’ qualifications, without regard to race, color, religion/belief, national origin, gender identity, age, disability, marital status, genetic information, or other applicable legally protected characteristics.
Compensation: $50/hr - $54.16/hr
This is a 40-hour per-week, 12-month contract (extensions possible), 50% onsite role in Seattle, WA.
This is a W2 role as a Stage 4 Solutions employee. Health benefits and 401K are offered.
Responsibilities
- Write and revise standard operating procedures (SOPs) and specifications for GMP Labelling operations
- Complete intake forms and follow up on item creation process with cross functional stakeholders. Ability to interview cross functional subject matter experts and translate their description into actionable instructions- Work Instructions, Job Aids using the templates prescribed by corporate policy.
- Schedule cross functional team meetings, collect feedback, create draft documents, schedule reviews, collect and resolve feedback.
- Knowledge of electronic document management systems (EDMS) to complete workflow of document to final approval by uploading the word document into EDMS.
- Prepare document periodic review timetable and ensure the review/approval or retirement are completed in support of the procedure lifecycle in timely manner.
- Maintain a good understanding of regulations and other guidelines applicable to GMPs.
- 1 years’ experience in a GMP environment.
- 1 years’ experience with GMP labelling is a plus.
- Experience with Oracle and/or SAP a plus.
- Expertise in Microsoft Word. Proficient in Microsoft Outlook, MS Teams meetings, Share point, EDMS. Able to conduct video conference calls via MS Teams 4-6 hours a day.
- Bachelor’s degree required - Life Sciences degree preferred
Please feel free to forward this project opening to others who may be interested.
Stage 4 Solutions is an equal-opportunity employer. We celebrate diversity and are committed to providing employees with an inclusive environment that is free of discrimination and harassment. All employment decisions are based on the job requirements and candidates’ qualifications, without regard to race, color, religion/belief, national origin, gender identity, age, disability, marital status, genetic information, or other applicable legally protected characteristics.
Compensation: $50/hr - $54.16/hr
Salary : $50 - $54
