What are the responsibilities and job description for the Quality Assurance Specialist position at Net2Source Inc.?
Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth of 300% in the last 3 years with over 5500 employees globally, with over 30 locations in the US and global operations in 32 countries. We believe in providing staffing solutions to address the current talent gap – Right Talent – Right Time – Right Place – Right Price and acting as a Career Coach to our consultants.
Company: One of Our Clients
Job Description:
Job Title: Quality Technical writer
Location: Seattle, WA* 50% Onsite
Duration: 12 Months (Extendable)
Pay Rate: $54.00/hr on W2
Top Skills:
- Bachelor’s degree required - Life Sciences degree preferred
- Minimum of 1-3 years’ experience in a GMP environment.
- 1-3 years’ experience with GMP labelling is preferred.
- Experience with Oracle and/or SAP preferred.
POSITION SUMMARY
The Technical Writer will manage and oversee data input and documentation management and functions as detailed below to ensure delivery of Cell Therapy labelling projects.
Key Responsibilities and Major Duties
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.
Requirements
Minimum of 1-3 years’ experience in a GMP environment.
1-3 years’ experience with GMP labelling is a plus.
Experience with Oracle and/or SAP a plus.
Demonstrated ability to successfully manage competing deadlines and balance priorities.
Ability to track and follow up on multiple workstreams and escalate when appropriate.
Expertise in Microsoft Word.
Proficient in Microsoft outlook, MS team 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
Awards and Accolades:
- America's Most Honored Businesses (Top 10%)
- Awarded by USPAAC for Fastest Growing Business in the US
- 12th Fastest Growing Staffing Company in USA by Staffing industry Analysts in the US (2020, 2019, 2020)
- Fastest 50 by NJ Biz (2020, 2019, 2020)
- INC 5000 Fastest growing for 8 consecutive years in a row (only 1.26% companies make it to this list)
- Top 100 by Dallas Business Journal (2020 and 2019)
- Proven Supplier of the Year by Workforce Logiq (2020 and 2019)
- 2019 Spirit of Alliance Award by Agile1
- 2018 Best of the Best Platinum Award by Agile1
- 2018 TechServe Alliance Excellence Awards Winner
- 2017 Best of the Best Gold Award by Agile1(Act1 Group)
Regards,
Kajal Singh
Senior IT Recruiter (Pharma and Life Sciences)
Net2Source Inc.
Global HQ Address –270 Davidson Ave, Suite 704, Somerset, NJ 08873, USA
Office: (201) 340-8700 x 980 | Cell: (201) 777-4217 | Fax: (201) 221-8131| Email: singh.kajal@net2source.com
Salary : $50 - $54
